Professional Documents
Culture Documents
Kenzo Hirayama
Fuji Photo Film Research Laboratories
Odawara, Japan
Introduction ......................................................................................................................... 1
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viii Contents
(VI) 4-methyl-6-(2,6,6-trimethyl-2-
(V) cholesta-7,14-dien-3-one cyclohexenyl)-3,5-hexadien-2-one
X
maxH 242ra
^ (loB£4'°) xJaJH 285my (loge 4.2)
Studies of ultraviolet and visible absorption spectra started long before the study
of infrared absorption spectra, and a far larger number of spectral measurements is
available. Still, they have not been fully utilized for the identification of organic
compounds and the most important reason for this state of affairs is that these data have
not been organized from the point of view of the absorbing system, as outlined above.
Having realized the need for such a collection of data, the writer collected,
classified, and published such data as a part of "Yuki Kagaku Teisu Binran," a volume in
"Dai Yuki Kagaku" (Series of Comprehensive Organic Chemistry, 25 vols. with an index
volume, Asakura Shoten, Tokyo, 1960-1963).
In that publication, rules were proposed for notation and for the order of the ab-
sorbing systems. The collection of data was certainly useful in utilizing ultraviolet and
visible absorption spectra, but it included only a table for identifying absorption maxima
from absorbing systems and no table in which the absorbing systems could be found from
the absorption maxima, which would be the most convenient method for structural identifi-
cation.
This shortcoming has now been corrected, and the revised and enlarged version that has
been compiled for the present edition does contain a tabulation according to absorption
maxima.
Table I is a list from which absorption maxima can be found from the absorbing systems,
i.e., from the chemical structure. In general, the absorption of strongest intensity in a
range of about 50my in wavelength was taken as the absorption maximum. Consequently, the
distance between two absorption maxima is usually more than 50my.
This table is used in the following manner. To look for the absorption maximum of
O' C~C' C~-C' C-C
cholesta-4,6-dien-3-one (I), we look under the absorbing system 'i *±
The order of the arrangement of absorbing systems is explained in detail under "Explanation
of Notation and Arrangement." The desired absorbing system can be found directly from
Table I by following this order of arrangement, or the chromophore group in this absorb-
ing system (O!C-C'.C—C'.C in the above example) can be found from the "List of Chromophores"
from which the compound number of (0:C)(C:C)2 is found as 772-831.
Table II is a reverse index of Table I. It is a list of absorbing systems to be
found from the wavelengths of absorption maxima.
Ultraviolet and visible absorptions of organic compounds can be determined approxi-
mately from the absorbing system, but the solvent used and measurement error must also be
taken into account. Consequently, it is better to examine the wavelength regions around
the desired wavelength.
For example, if an unsaturated ketone having no substituent other than one keto
group has an absorption maximum at 285my (loge 4.42) in ethanol, the following absorption
maxima in a range of 285±5my can be found from Table II.
807, 808, 812, 813, and 815, i.e., a dienone of °:9"°:C~~°:C type, with two or three
alkyl auxochromes, or a trienone of type (VII) with a steric hindrance like compound 850.
These conclusions are based on the chemical observation that there is no hetero-atom
in the molecule other than the oxygen atom in the keto group and on spectral observations
of the absorption maximum and intensity, but the possible absorbing systems can be further
narrowed by comparing ultraviolet absorption curves.
Kenzo Hirayama
EXPLANATION ON NOTATION AND ARRANGEMENT
ABSORBING SYSTEM
An absorbing system consists of a chromophore or conjugated chromophores, printed in
bold face type in Table I, and an atom or atoms, if any, joined to the chromophore or con-
jugated chromophores, and sometimes, consists merely of auxochromic atoms.
Rules determine the notation and sequence of absorbing systems, as mentioned below.
When there is a choice, the direction is so chosen as to make the symbol of the most
predominant auxochromic atom, and if there is a choice, that of the subsequent predomi-
nant auxochromic atom(s), come as early as possible.
e.g. C-CiC-CiC (not CiC-CiC-C)5 CiC-CiC (not CiC-CiC)
Cl Cl
CiC-CiC-C (not C-CiC-CiC), C-CiC-CiC (not CiC-CiC-C)
ii ii ii 61 ci ci
NOTATION OF LONG CONJUGATED ABSORBING SYSTEMS
In addition to the above measures, sometimes, long conjugated absorbing systems may
be denoted in an abbreviated manner.
e.g. (CiC)5~C4 instead of C-CiC-CiC-CiC-CiC-CiC-C
£ i
&-[CiC]5-6 instead of 6-CiC-CiC-CiC-CiC-CiC-S
Criteria (c) to (f) determine the predominancy of absorbing systems by the nature
of auxochromic atoms joined to the chromophores. When applying these criteria, the pre-
dominancy of C atoms of carboaromatic and heteroaromatic unit chromophores is -regarded
as same as that of C atoms of CiC, and the predominancy of hetero-atoms of heteroaromatic
unit chromophores is regarded as higher than that of C atoms of CiC and lower than that
of C atoms of CiCiC, in order to make the determination by these criteria accord with the
optical properties of absorbing systems.
e.g. C-S-CiC-CiCiC < S-CiC-CiCiC-C, Br-S-CiN-N < Cl-fr-CiN-0
A alcohol
AA acetic acid
Ac acetone
B benzene
C chloroform
cH cyclohexane
CD carbon dioxide
D dioxan
E ether
EA ethyl acetate
H hexane
Hp heptane
iO isooctane or trimethylpentane
iP isopropanol
L liquid
M methanol
PB petroleum benzine
PE petroleum ether
Py pyridine
THF tetrahydrofuran
V vapor
W water
T
Numbers in the column solv.T indicate pH-value.
(N45)(N:N) 7031-7035 Part 44. (05)- & (X:05:X)- (05) (6)4 7530-7542
(N45)(6) 7036-7045 Chromophores (05) (6) (NrC) (CrC)
(N45)(6)(OrN) 7046-7047 (05) 7400-7410 7543-7544
O (05)(C:C) 7411-7413 (05)(6)3(OrC) 7545-7546
(N4SrN) 7048-7053 (05) (NrC) 7414-7423 (05)(6)4(OrC)2 7547
(N465) 7054-7170 (05)2(N:C)2 7424-7426 (05) (6) (OrC) (CrC)
(N465)(6) 7171-7177 (05) (N:C) (C:C) 7427-7430 7548-7549
(N465:0) 7178-7247 (05)2(N:C)2(C:C)2 7431 (05)(6)2(OrC) 7550-7551
(N465:0)(6) 7248 (05)2(N:C)2(C:C)4 7432 6
(0:N465:0) 7249-7291 (05)2(N:C)2(C:C)6 7433 (05)(6)3(OrC)(OrC) 7552
(05) (6) (NrC) (CrC) 7434 6
(°;N465rO) 7292-7305
(05)(0:C) 7435-7439 (05) (N26) (NrNrN) 7553
(N466) 7306-7315 (05) (OrC)2 7440 (05)(OrN26rO) 7554
(N466:0) 7316-7320 (05)2(0:C)2 7441 (Or05rC)(6)2 7555-7562
(N466:0)(0:C) 7321-7328 (05)(0:C)(C:C) 7442-7444 (Or05rO)(6)3 7563
6 (05) (OrC)(CrC)2 7445-7446 (Or05rO)(66)(6) 7564
(0:N466:0) 7329-7336 (05) (OrC) (CrC)3 7447-7448
(0:N466:0)(0:C) 7337-7341 (05)(0:C)(C:C)4 7449 Part 45. (06)- and (06:X)-
(05) (OrC) (CrC)5 7450 Chromophores
(0:N466:0)(6) 7342 (05) (OrC) (CrC)6 7451 (06)(6)3 7565-7581
(°;N466rO) 7343-7346 (05)2(OrC) (CrC) 7452 (06)(6)3(CrC) 7582-7585
(OS)2(OrC)(CrC)4 7453 (06) (6)3(CrC)2 7586-7587
(05)2(OrC) (CrC)6 7454 (06)(6)4(CrC) 7588-7590
(°-N466rO)(OrC) 7347
(OS)2(OrC)2(CrC)2 7455 (06rO) 7591-7606
(OS)2(OrC)2(CrC)4 7456 (06rO)(OrC) 7607-7610
(°;N466;°) 7348-7352
(05)2(OrC)2(CrC)6 7457 (06rO)(OrC) 7611-7620
(N4665) 7353-7356 (05) (Or(J:) 7458-7460 6
(0:N463:0) 7357-7360 N (06.-O)(OrC)2 7621-7622
(N4635) 7361-7362 (05) (OrC) 7461-7472 6
(N4635)(6) 7363-7367 6 (06rO)(6)2 7623
(N4635)(6)(0:C) 7368 (05) (OrC)2 7473-7476
O O Part 46. Other aromatic
(N465) 7369-7370 (05) (OrC) (CrC) 7477-7484 Chromophores with
6 O Hetero-atom(s)
Part 42. Other aromatic (05) (OrC) (CrC)2 7485-7487 (065) 7624-7629
Chromophores with 6 (065) (OrC) 7630
N Hetero-atoms (05) (OrC) (CrC)3 7488-7489 A
(N565) 7371-7379 O (065) (6)2 7631-7632
(N565)(6) 7380-7382 (05)(0:C)2(C:C)2 (065) (6)4 7633-7634
(N565)(6)(0r(p 7383 O 7490-7491 (Or065rC)(6) 7635-7641
(05) (OrN) 7492-7495 (066) (6) 7642-7670
(N565:0) 7384-7389 O (066rO) 7671-7679
(N565:0)(6) 7390 (05) (OrN)2 7496 (066rO)(OrC) 7680-7683
(N565:0)(6)(0:C) 7391 O 6
ti (05) (OrN) (CrC) 7497 (066rO)(6) 7684-7745
(N565:0)(6)(0:C) 7392 (066rS)(OrC) 7746
O (05) (OrN) (NrC) 7498-7506 A
(0:N565:0) 7393-7395 (0665) 7747-7759
(N565) 7396-7397 (05) (O rN) (OrC) 7507-7508 (0665)(Or05rC)(6) 7760
O (Or0665rO) 7761-7762
Part 43. Aromatic Chromo- (05) (OrN) (OrC) 7509-7511 (063)(6)(0r9) 7763-7765
phores with P or As O
Hetero-atom(s) (05) (6) 7512 (063rC)(6) 7766-7767
(0:P665:0) 7398 (05)(6)2 7513-7524 (063rO) 7768-7774
(0:As665:0) 7399 (05)(6)3 7525-7529
chromophore no . chromophore no . chromophore no .
C methane V no W30u 1
^
s<
c
O cyclohexyl methyl sulfoxide
methyl sulfone
215
<180
3.S K47c
G12
20
21
L 257.5 2.6 Hl 6 38
i-c<Cl
F
1-chlorohexaf luoro-1-iodopropane L 286 2.5 H16 52
system compound solv. max. loge ref. no.
2,3-dihydrothiophene 1-dioxide no F6 78
1 , 2-dimethylenecyclobutane
H
H
226
237
4.3
4.0
S18
W52
89
90
c2-c: c-c : c-c l-methyl-4- (1 , 5-dimethyl-2 , 4-hexadien- A 235.5 3.7 B93 110
yl)cyclohexene; zingiberene
oc-c : c-c: C-C2 5H-6 ,7,8, 8a-tetrahydro-2 ,5,5, 8a-tetra- A 286 3.9 B151 141
methylchromene
s c-c: CH^: c-c 3- (2-hydroxyethylthio) androsta-3 , 5-dien- A 268 4.4 R33 147
C 17-one
C2-C i c-c ic~9i c-c 4 , 8-dimethyl-10- (2 , 6 , 6-trimethyl-l , 3- PE 284 4.7 111 165
C cyclohexadienyl) -4,6, 8-decatrien-l-yn-
3-ol
C2-C i C-C i9~C. C-C choles ta-3 , 5 , 7-triene iP 315 4.2 S28 166
C
C2-Ci c-ci 9~cic ergocalciferol; calciferol; vitamin D2 A 265 4.3 R4n 167
c-c : c-c : c-c:c-c 2-acetoxy-3 , 7 , 7-trimethyl-l , 3 , 5-cyclo- 207 4.1 C97 174
heptatriene 273 3.5
[enol acetate of eucarvone]
O-Ci C-Ci C-Ci C-C l-ethoxy-2- (2 , 6 , 6-trimethyl-l , 3-cyclo- PE 284 4.5 112 176
hexadienyl) ethylene
iO
226
269
304
4.4
4.2
4.3
R27
N4
181
182
C C'l pentaene; ergosta-5,7,9(ll) ,14,22-
£:£: >cic-cic-c2 pentaene
C-CiC-CiC-CiC-CiC-C - 1
6 , 6-diethoxy-3-methyl-l- (2 , 6 , 6-tr imethy PE 318 112 186
2-cyclohexenylidene) -2 , 4-hexadiene
E
313
355
4.7
4.1
B163
W38
188
189
choles ta-4 ,6,8, ll-tetraen-3 3-ol
(CiC)9-C2 B
2 , 4 , 6 , 8 , 10 , 12 , 14 , 16 , 18-eicosanonaene 412 5.3 B88 211
system compound solv. max. loge ref. no.
C-CiC-CiC-C2 3-methy 1-1- (2,6, 6-trimethy 1-1-cy clo- H 230 4.5 A41 256
hexenyl) -4 , 6-octadien-l-yn-3-ol
Si-Ci C-C: C-C 3-methyl-l- (triethylsilyl) -3-penten- H 234 4.2 B98 257
1-yne
c2-c: c-c; c-c: c-c di-1-cyclohexeny !acetylene A 252 4.8 B86 264
275 4.8
c-ci c-c: c-c: c-c 6-methy 1-3 , 5-octadien-7-yn-2-ol A 260 4.6 C28n 267
c2-c :9~ci c-c: c-c: c-c 6-methyl-8- (2,6, 6-trimethyl-l-cyclo- H 226 4.1 A41 269
C C hexenyl) -3 , 5-octadien-7-yn-2-ol 301 4.3
c-c ; c~9 : c-c : c-c : c-c 9- (l-hydroxy-2 , 2 , 6-trimethylcyclohexyl) -A 302 4.7 A41 271
3 , 7-dimethyl-2 , 4 , 6-nonatrien-8-yn-l-ol
c2-c:c:9— CiCiC-C2 E
2 , 3-dibromo-l , 4-bis (2 , 2 , 6 , 6-tetramethyl- 231 4.7 B92 298
Br Br cyclohexylidene) -1 , 3-butadiene
*1 0.2N NaOH/A+C(9:l)
system compound solv. max. loge ref. no.
C-N: c-c : N-C bis (cyclohexylimino) ethane ; glyoxal M 217 4.3 C12 376
biscyclohexylimide 267 2.4
C-N !9-9: N-C 2,3-bis (butylimino) butane; diacetyl A 209 4.3 B26 377
disbutylimide
N-N: c-c : N-N 2,3-dihydrazonobutane; diacetyl di- A 265 4.2 B27 380
hydrazone; butanedione dihydrazone
N-N: c-c: c-c2 2-f ormyl-1 , 3 , 3-tr imethylcyclohexene 2 , 4-A 225 4.1 B120 421
C dinitrophenylhydrazone ; 3-cyclocitral 255 4.2
2 , 4-dinitrophenylhydrazone 387 4.4
*1 0.2N NaOH/A+C(9:l)
system compound solv. max. loge ref. no.
*1 0.2N NaOH/A+C(9:l)
system compound solv. max. loge ref. no.
s;^«* 33-acetoxy-5a-cholesta-8,14-dien-7-one
2 , 4-dinitrophenylhydrazone
cholesta-l,4-dien-3-one 2 ,4-dinitro-
C
C
393
400
4.4
4.5
D32
D28
475
476
phenylhydrazone
*»^£?
cholesta-1 , 4-dien-3-one semicarbazone C 302 4.3 15 477
: :
»-" <i £> 2 , 6-dimethyl-2 , 5-heptadien-4-one 2 , 4-di-A
nitrophenylhydrazone; phorone 2, 4-di-
nitrophenylhydrazone
226
258
388
4.3
4.2
4.4
B120 478
N-N: c-c !9-0: c-c 24-methylcholesta-4, 6-dien-3-one 2 , 4-di- C 400 4.6 B38 499
C C nitrophenylhydrazone; 4,6-ergostadien-
3-one 2, 4-dinitrophenylhydrazone
N-N : c«c : c-c : C-C2 4- (2 , 6 , 6-trimethyl-l-cyclohexenyl) -3- M 294 4.2 B84 503
C C buten-2-one p-nitrophenylhydrazone ; 408 4.5
3-ionone p-nitrophenylhydrazone
N-N : c~c : C-CiC-C :c-c2 7 , 11-dimethy 1-2 ,4,6, 10-dodecatetraenal A 325.5 4.4 B156 515
semicarbazone; 12-apolycopenal semi-
carbazone
N-N: c-c: c-c: c-c: C-C2 4-methyl-6- (2,6, 6-trimethylcyclo- PE 236 4.3 112 517
C hexylidene) -2 , 4-hexadienal phenylsemi- 340 4.9
carbazone
N-N : c-c . c-c : c-c : C-C2 8-methoxy-2 , 7-dimethyl-2 , 4 , 6-octatrienalC 407 4.6 A12 518
C 2 , 4-dinitrophenylhydrazone
N-N: c-c: c-c: c-c: c-c 2,6-dimethyl-8-(2,6,6-trimethyl-l-cyclo- PE 234 4.2 112 520
C C hexenyl) -2,4, 6-octatrienal phenyl- 332 4.9
semicarbazone
N-N: c-c: c-c: c-c: c-c 2-methyl-4- (2,6, 6-trimethyl-2-cyclo- PE 335.5 4.7 112 521
hexenylidene) crotonaldehyde semi-
carbazone
N-N: c-c: c-c: c-c: c-c 5 , 6-dihydro-6-hydroxy-13-apocarotenone A 235 3.7 A41 523
semicarbazone 325 4.8
*1 tetrachloroethylene
system compound solv. max. loge ref. no.
N-N: c-c:.c-c 2-butynal 2 , 4-dinitr opheny lhydr azone ; C 363 4.4 L32 553
tetrolaldehyde 2 , 4-dinitrophenyl-
hydrazone
N-N .C-Ci C-Ci C-C 6 , 6-dimethyl-2 , 4-hep tadiynal 2 , 4- M 365 4.5 B90 555
dinitr opheny Ihydrazone
S-N. c-c; c-c: c-c 6 ,6-dimethyl-4-hepten-2-ynal semi- M 290 4.5 B90 558
carbazone
N-N: c-c :c-ci c-(p: c-c2 3-methyl-5- (2 , 6 , 6-trimethyl-l-cyclo- M 265 4.2 14 560
C C hexenyl) -2-penten-4-ynal 2 , 4-dinitro- 395 4.5
pheny lhydr azone
(N: c) (c; c) (C !O3-NC5 6-methyl-8- (2,6, 6-tr imethy 1-1-cyclo- A 342 4.6 A41 563
hexenyl) -3 , 5-octadien-7-yn-2-one
semicarbazone
PART 6. (NiC)-, (N:C:N)-, AND (N:N:C)-CHROMOPHORES
Nic-c:c-c:c-c2 3 B-acetoxy-17 3-cyano-5 3-andros ta-14 , 16- A 286 4.3 R48 576
Vj diene
Next Page
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PART 7. (OrC)-CHROMOPHORES
o:c-c:c-c2 3 , 7 -dime thy 1-2 , 6-octadienal ; citral A 238 4.1 B156 637
324 1.8
0 3-one
W 2-methyl-l-penten-3-one
l-cyclopropyl-2-methyl-2-propen-l-one
A 220
319.5
215
3.9
1.4
4.0
E21
H9
662
663
. 305 1.6
E
244
236
4.2
4.2
W26
18
773
774
TT?"
o: :c <:c C2
methyl 3a-hydroxy-12-oxo-5 3-chola-
7,9(ll)-dienoate
A 238
290
3.6
4.1
F32 813
2- (cyclohexylideneethylidene) cyclo- E
307
297
4.2
4.4
P29
F48
814
815
hexanone
4,6-dibromocholesta-3,5-dien-6-one A
C 296
303
4.3
4.0
J2
J2
829
830
; : Brc
° Ht rrc 4,6, 7-tribromocholes ta-4 , 6-dien-3-one C 313 4.2 J2 831
»:%br
? : c
3-acetoxy-4,4~dimethylcholesta-5 ,8,11-
trien-7-one ; 3-acetoxylanosta-5 , 8 , 11-
trien-7-one
A 258
326
3.9
3.9
B39 833
° %b °-
0 0C
Br- '
2 , 4-dibromocholesta-l , 4 , 6-tr ien-3-one
A
326
233
4.1
4.2
13
F29
834
835
o-t%~ trien-11-one; 3-acetoxyergosta-
6,8, 14-tr ien-11-one
326 3.9
237
3.9
4.1
C97
C31
905
906
methano-1 , 4-naphthalenedione 354 1.8
o:
ra£f° 4 , 5-dichloro-4-cyclopentene-l , 3-dione cH 258
327
4.2 Ml
1.7
912
"raw :o
4-bromp-5-chloro-4-cy clopentene-1 , 3--
dione
cH 269 4.1 Ml 914
(o:j)2(c:c)9-c4 6 , 6 , 10 , 14 , 19 , 23 , 27 , 27-octamethyl-8 , 10
C , - 489 KIl 932
12 , 14 , 16 , 18 , 20 , 22 , 24-dotr iacontanona-
ene-2 ,7,26 , 31-tetraone ; 3-carotenone CD 499 KIl 933
o:
s
OiD-C
formamide
N,N-dimethylf ormamide
V
V
<180
<180
H89
H89
974
975
N
acetamide M ^207 S2g 976
*1 O.IN NaOH/W
PART 9. (O :C) -CHROMOPHORES
6
system compound solv. max. loge ref. no.
o:
s formic acid W
V
206.5
205
1.7
1.7
L18
B98
999
1000
ethyl methacrylate
M
A
^227
214 3.8
S2g
U3
1020
1021
system compound solv. max. loge ref. no.
ethyl 3-aminocrotonate
A
A
245
274
3.7
4.3
K32
G16
1040
1041
*1 alkaline solution
system compound solv. max. logs ref. no.
cic
o:c-c:c-c 2-chlorocrotonic acid A 222 4.0 B98 1073
°w6 ci
o:c-c:c-c
6 Br
3 , 4-dichlor o-2 , 5-dihydro-2-oxof uran ;
a , 3-dichlorocrotonolactone
2-bromocrotonic acid
A
A
225
228
4.1
3.8
M59u
B98
1074
1075
*1 O. IN NaOH/W
system compound solv. max. loge ref. no.
*1 Na salt in water
system compound solv. max. logs ref. no.
C no A29 1113
M no S2g 1114
°'iTT
0
methylmalonic acid; mesaconic acid no J30 1115
5.8
294
291
3.6
3.7
V7
V7
1116
1117
*1 Na salt in water
system compound solv. max. loge ref. no.
o: : :o
XT~ n 2 , 5-dimethyl-trans-2 , trans-4-hexadiene- M
dioic acid; 2, 5-dimethyl- trans , trans-
muconic acid
282 4.5 E16 1129
(o:c)2(c:c)4 methyl 2,5, 9- tr imethy 1-2 ,4,6, 8-deca- H 350 4.3 K74 1143
tetraenedioate
(OiC) (c;c) (CiO4-C5 3 , 7-dimethy 1-9- (2,6, 6-trimethy 1-1-cyclo- H 265 4.1 A41 1155
hexenyl) -2,4, 6-nonatrien-8-ynoic acid 351 4.5
n" 2-(2,4-dinitrophenylhydrazono)butanoic
acid
A 243
254
364
4.1
4.1
4.4
B120 1158
6
SiI ^ 2-cyanocrotonic acid
methyl 2-cyanocrotonate
A
A
215
220
4.0 A28
3.9 A28
1174
1175
o:? .
N:C>C. C-C. C-C2
2-cyano-5-methyl-2 , 4-hexadienoic acid A 295 4.3 A28 1184
(o:c)(o:c)(c:c)6-c3 methyl 13-f ormy 1-4 , 8 , 13- tr imethy 1- A 440 KIl 1200
2 , 4 , 6 , 8 , 10 , 12- tr idecahexaenoate ;
apo-3-norbixinal methyl ester CD 455 KIl 1201
(o:c)(o:c)(c:c)7-c3 methyl 15-f ormy 1-4 ,8,13, 13-tetramethyl- CD 483.5 KIl 1203
2 , 4 , 6 , 8 , 10 , 12 , 14-pentadecaheptaenoate ;
apo-2-norbixinal methyl ester PE 450 KIl 1204
(o:c)(o:c)(c:c)8-c4 methyl 17-f ormy 1-4 ,8,13, 17-tetramethy 1- A 458 KIl 1208
2 , 4 , 6 , 8 , 10 , 12 , 14 , 16-heptadecaoctaen-
oate; apo-1-norbixinal methyl ester CD 478 KIl 1209
°i
4-acetoxy-l-butenyl ethanethiolate
o:
r acetyl chloride H
Lq
235
234.5
1.7
1.7
L18
K18
1234
1235
system compound solv. max. loge ref. no.
o:
0
n;° oxalyl chloride no K55 1236
*1 0.014% KOH/W
system compound solv. max. loge ref. no.
*1 O. IN NaOH/W
system compound solv. max. loge ref. no.
*1 O. IN HCl *2 O. IN NaOH/W
system compound solv. max. loge ref. no.
*1 NaCl/W
system compound solv. max. loge ref. no.
*1 O. IN HC1/W *2 IN NaOH/W
system compound solv. \nax. loge ref. no.
*1 bivalent anion
system compound solv. max. loge ref. no.
2- (N-me thy !methane s ulf onamido) f luorene A 269-70 4.4 S13 1892
302 4.0
*1 dihydrochloride in water
system compound solv. max. loge ref. no.
OC2-6-6-OC2 5 , 5T -di- ter t-buty 1-4 , 4 ' -dihydroxy-3 , 3 'H- 263 S2g 1918
dimethylbiphenyl
FN-S-S-FN 4 , 4 ' -diamino-2 , 2 ' -dif luorobiphenyl A 267 4.4 B66 1934
6-[6]3-6 I,!1 :2f ,1'^2",I1" : 2"' ,!""-quinquephenyl C 234 4.7 W48 1972
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*1 0.1% AA/ A
system compound solv. max. logs ref. no.
c>c :e 1,3, 5-tr ichloro-2 , 4 , 6-triviny !benzene 238 4.6 R36 2059
£e*«Ci3
6-c:c-c:c-c:c-c:c-c2 3-methyl-6-phenyl-l-(2,6,6-trimethyl- A 338 S39 2060
t t cyclohexenyl) -1 , 3 , 5-hexatr iene
*1 0.1% AA/A
system compound solv. max. loge ref. no.
(6)3(c:c)4
i~«i
p-bis (4-phenyl-l, 3-butadienyl)benzene A 328 4.7 B74 2125
fr-c^-^a
5/C.C-6
1,2,3, 4-tetraphenyl-l , 3-butadiene D 356 4.6 H67 2127
6-c ; c-ci c-c; c-c ;c-e dipheny loctatetrayne A 285 5.1 S21n 2140
365 4.5
397 4.3
*1 acid A
system compound solv. max. loge ref. no.
*1 H2SO4
system compound solv. max. loge ref. no.
F-&-Ni N-S-N 4! - (dime thy lamino) -2-f luoro-trans- *2 321 4.2 C34 2325
azobenzene 510 4.2
*1 Na salt/W *2 acid A
system compound solv. max. loge ref. no.
Cl3-S-N: N-S-OC2 2,4, 6- trichloro-4 ' -hydroxy-2 ' , 6T - B 334 3.9 B131 2346
dime thy 1-cis-azobenzene 455 3.3
2,4, 6-tr ichloro-4 ' -hydroxy-2f , 6 ' - B 338 4.2 B131 2347
dime thy 1-trans-azobenzene 460 3.0
*1 cone. H2SO^
system compound solv. max. loge ref. no.
Br-S-N ! N-6-N i N-S-Br p-bis (p-bromophenyl-trans-azo) benzene THF 371 4.7 D2 2378
*1 cone. H2SO^
PART 17. (6)(N:C)-SYSTEM
*1 no M18 2413
ci-e-c : N-N :c-e-ci bis (o-chlorobenzylidene) hydrazine A 307 4.6 B26 2539
o-s-c: N-N: c-s-o bis (o-hydroxy-a-methylbenzylidene) - A+W 293 4.2 B75 2548
C b hydrazine 362 4.1
O-S-N: c-c : N-S-O bis (p-hydroxyphenylimino) ethane A 236 4.2 F16 2557
301 2.8
388 4.0
Br- 6-N: C-C !N-S-Br bis (p-bromophenylimino) ethane A 254 4.5 F16 2559
299-302 3.3
Br-S-N: C-C .'N-S-Br 2 , 3~bis (p-bromophenylimino) butane A 236 4.6 F16 2561
c6 336 3.7
*1
360
358
4.7
4.3
B125
B125
2563
2564
422 4.5
*1 hydrochloride (N-phenylauramine)
system compound solv. max. loge ref. no.
N
>C:IY-N:C<|-N bis [p- (dimethylamino) -a-phenylbenzyl-
idene ] hydr az ine
A 260-3
315-7
4.4
4.3
S85 2573
357-8 4.4
N :N N:C
N-> - <|:N
bis [bis (p-dimethylaminophenyl)methylene] - A 241 4.5 S85 2574
hydrazine 265-6 4.5
S
-|>C:N-N:C<|~S bis (a-phenyl-p-phenylthiobenzylidene) -
hydrazine
A 253 4.5 S85 2576
CI
-|>C:I*-N:C<|-CI bis (p-chloro-a-phenylbenzylidene) -
hydrazine
A 280 4.3 S85 2578
N-6-C: CHp !N-C2 3-ethyl-2- [p- (dimethylamino) styryl] -2- 477 B135 2584
S thiazolinium iodide
*?tt**
o3-6-c: c-c : N-N
l-phenyl-2- (phenylacetyl) cyclohexene
2 , 4-dinitrophenylhydrazone
388
4.3
4.5
Pl
L28
2593
2594
trimethoxyphenyl)-2-cyclohexene~l-one
2 , 4-dinitrophenylhydrazone
*1 0.2N NaOH/A+C(9:l)
PART 18. (6)(N:C)-, (6)(N:C:C)-, AND (6)(P:P)-SYSTEM
*1 0.014% KOH/W
system compound solv. max. logs ref. no.
*1 2N HCl
system compound solv. max. loge ref. no.
N2-e--c: o 6- [bis (2-cyanoe thyl) amino ] -1- (2-cyano- A 247 4.4 B123 2719
C ethyl) -1 ,2,3, 4- tetrahydro-4-quinolinone 424-31 3.5
*1 50% A *2 0.1N HCl -1- 50% A (1:1) *3 O. IN NaOH + 50% A (1:1) *4 H2SO4
system compound solv. max. loge ref. no.
°r
09-6
o:c-6-c:o
2-methoxy-4-pyruvoy !phenol
phthalaldehyde
A
*4
H
324
370
255
3.9
4.4
4.0
LlO
LlO
G33
2837
2838
2839
297 3.4
0:9-6—9:0
C No C
4,7-bis(2-cyanoethyl)-l,2,3,4,7,8,9,10-
octahydro-4 , 7-phenanthroline-l , 10-
A 284-51
492-6
4.3
3.7
B123 2846
dione
0:9-6— 9:0 6-anilino-l ,2,3, 4-tetrahydro-5 , 8-di- A 265 4.3 B148 2856
C O2N C hydroxy-l , 4-naphthalenedione 417 4.2
*1 ,H2SO4 + AA (2:8)
system compound solv. max. logs ref. no.
0 10
I* 4-methylbenzophenone M 259 4.2 K3 2860
2 , 2T , 4 , 5f , 6-pentamethylbenzophenone
cH
cH
244
248-53
4.2
4.1
F49
F49
2871
2872
c23>:°
4-(dimethylamino)benzophenone A 247 4.2 S85 2873
">:o 255-7 4.4
*1 A containing O. IN KOH/W
system compound solv. ^max. loge ref. no.
1- (m-methoxyphenyl) -2-phenylethanedione
A
A
257
323
255
4.3
3.6
3.9
L13
L13
2920
2921
319 4.1
365 3.3
: 4 , 4! -dipheny Ibenzophenone
t> ° *1 300
339
4.8
4.8
A22 2935
*1 1,2-dichloroethane
system compound solv. ^max. loge ref. no.
*1 H2SO4
system compound solv. ^max. loge ref. no.
A
2 , 3 , 3a , 4 , 5 , 6-hexahydrobenz [ e ] azulen-2- 224 4.0 K38 2988
one 274 4.1
233
287
4.5
4.2
3.9
L28 3008
B 296 T6 3033
404
M 290 T6 3034
408
*1 259 T6 3035
580
B 425 T6 3037
M 425 T6 3038
*1 630 T6 3039
?
: 2- (N-benzyl-N-methylamino) -1 , 3-diphenyl- Hp 248 4.2 CIlO 3057
" S>c:o 2-propen-l~one 286 4.2
392 3.2
H 3- [p- (dime thylamino) phenyl] -1-pheny 1-2- Hp 254 4.2 CIlO 3064
-«:J>c:o propen~l-one 385 4.5
6-c:c>r>co
.n 1 , 5-dipheny 1-1 , 4-pentadien-3-one iO 228 4.2 A17 3092
e-c:c 328 4.5
C1-6~~C - C^f» ' * 2 , 6-bis (p~chlorobenzylidene) cyclohexan- A 236 4.3 H87 3095
ci-6-c:c~'0 one 332 4.5
M 430 T6 3118
*1 735 T6 3119
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TO
o:c-6— c:o
N-ethyl-4 , 5-methylenedioxyphthalimide
tetrachlorophthalimide
A
A
245
302
234
4.6
3.3
3.9
W4
R32
3147
3148
AtI 4 * 330 3.4
s
~i '
a- (p-chlorophenyl) -cis-cinnamamide A 292 4.4 C71 3158
*1 cH + D (9:1)
system compound solv. max. loge ref* no.
*1
274
281
229
3.0
3.1
4.0
M56
D35
3304
3305
276 3.2
*1 O. IN HC1/W *2 IN NaOH/W
system compound solv.. max. loge ref. no.
£
h° benzene-l,2,4-tricarboxylic acid 1,2-
anhydride
M 289 S2g 3322
:;
°n°
o? 6:0 benzene-l,2,4,5-tetracarboxylic acid W 297 3.4 B62n 3323
n
c-6-e-c:o ethyl f luorene-1-carboxylate A 245
263
4.4
4.3
F49 3324
3-methylcinnamic acid
M
A
265
265
S2g
R19
3336
3337
^:c^:o
e-c:c-c:o 2-phenyl-l-cyclohexene-l-carboxylic acid 245 3.9 Pl 3338
d c6
c2-6-c: c-c : o cH
3- (5 , 6 , 7 , 8-tetrahydro-2-naphthyl) acrylic 228 4.2 F49 3339
O acid 292 4.4
:
~ rr ct-benzamidocinnamic acid
ethyl a-benzamidocinnamate
A
A
222
279
222
4.3
4.2
4.3
B51
B51
3342
3343
282 4.3
*3
227
310
240
4.0
4.2
4.1
C4
C4
3346
3347
325 4.1
(6)(o:c)2(c:c)2-c 4-benzylidene-3-me thy 1-2 -pent enedioic cH 271 4.2 PIl 3370
acid
l*-tt°
: :o
2- (carboxymethyl) -3 , 3-diphenylacrylic
acid
A 264 4.0 F49 3382
°> n
ci-e-c:c-6-c:o
2- (carboxymethyl) -3 , 3-bis (p-methoxy-
phenyl) acrylic acid
methyl p-(p-chloro-cis-styryl)benzoate
A
A
236
278
236
4.2
4.2
4.2
K36
C72
3383
3384
O 296 4.4
*1 Na salt/W *2 anion
system compound solv. ^max. loge ref. no.
(6)2 (0'.C)(NiC) (CiC)-Ci p-chloro-a- (p-ethoxycarbonylphenyl) -cis- A 236 4.3 C72 3404
6 cinnamonitrile 322 4.4
*1 KOH/A *2 anion
system compound solv. max. loge ref. no.
°-n
o-oSrc** acid
*2 275 4.2 L35 3427
c-e-c:c_.
8: 0 methyl 2-oxo-4-(p-tolyl)-3-butenoate M 233.5 3.8 S64 3438
*1 KOH/A *2 anion
system compound solv. ^max. loge ref. no.
*1 10% HC1/W
system compound solv. max. loge ref. no.
*1 Na salt in W *2 alkaline M
system compound solv. max. loge ref. no.
*1 O. IN HC1/M
system compound solv. max. loge ref. no.
^~r B 303
370
3.6
2.2
S31u 3721
: :o
o:K
° rn 2,4, 6-trinitrophenol A
D
355-62
366
4.2
4.2
F49
VlO
3732
3733
SC-G-GH)JiO 2-me thy lsulf onyl-5-nit rof luorene A 258 S15 3751
C O ^33O
*1 pH 10.4 in A
system compound solv. max. loge ref. no.
*1 Na salt in M
system compound solv. max. loge ref. no.
°fe
o: :o
rm 2-acetyl-7-nitrof luorene A 261
400
4.1
4.3
S16 3877
4-hydroxylamino-3-nitrobenzoic acid
410
^56O
2.7
3.8
B99
B99
3890
3891
o: :o
m 5-nitrosalicylic acid
methyl 3-nitrosalicylate
M
M
217.5
305
286
S2g
S2g
3892
3893
E
433.5
573
4.6
2.9
B155
B155
3906
3907
C2-N.'6:C-6-N p-benzoquinone-1- [p- ( dime thy lamino ) - *3 610 5.1 B139 3936
pheny lmethine ] -4-dimethylimmonium
perchlorate
c2-N:e:c<5-N
£. O
p-benzoquinone-1- [ a- (p-dimethylamino-
phenyl) pheny lmethine] -4-dimethyl-
W 320
425
4.2
4.3
S35n 3939
N-fi-r<66_~NNC
PO2-N.6.C< p-benzoquinone-1- [ a- (p-aminophenyl) -a- A 485 5.0 M34 3941
C (4-amino-m-tolyl) ]methine-4-immonium
chloride; Fuchsin W 543 4.9 M34 3942
*1 IN HC1/W
system compound solv. max. loge ref. no.
'3
0:6:0 t rime thy 1-p-benzoquinone C 258.5
338
434
4.3
2.6
1.6
B114 3967
*4
o:e:o tetramethyl-o-benzoquinone
tetramethy 1-p-benzoquinone C
446
264
339
435
4.3
2.4
1.5
S49
B114
3969
3970
*1 0.01N HC1/W
system compound solv. max. loge ref. no.
*1 0.01N HC1/W
system compound solv. max. loge ref. no.
o:e:c-6-N p-benzoquinone~l- [p- (dime thy lamino) - B 470 4.3 H88 4008
phenylmethine]
C 490 4.3 H88 4009
Next Page
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*1 acid A
system compound solv. ^max. loge ref . no.
*1 acid A
system compound solv. max. loge ref. no.
OC2-66 A
6-methoxyestra-l, 3 , 5 (10) , 6 , 8-pentaen-17- 240 4.6 J13 4179
one 303 3.8
*1 acid A
system compound solv. max. loge ref. no.
*1 acid A
system compound solv. max. loge ref. no.
*1 IN HC1/W
system compound solv. ^max. loge ref. no.
00-66-9:0-0 6-methoxyestra-l ,3,5 (10) ,6,8, 14-hexaen- A 259.5 4.7 J13 4239
C 17-one 302 3.9
330 3'. 6
c2-66-9:N-o cH
1 , 2 , 3 , 3a, 4 , 5-hexahydropyren-5-one oxime 240 4.7 F49 4252
C 310 3.9
C-N : c-^6—66-c : N-C 1,1' ,6,6' ,7,7'-hexahydro-5,5'-diiso- C 255 4.9 S43n 4253
C
°3 2 ^3 2 C propyl-3 , 3f -dimethyl-2 , 2 ' -binaphthyl- 385-92 4.4
8,8' -dicarboxaldehyde bis (dodecylimine)
66-c: N-N :c-66 bis [ 1- (1-naphthyl) ethylidene ] hydrazine A 293 4.3 B75 4256
c £
bis[l-(2-naphthyl)ethylidene]hydrazine D 262 4.7 B75 4257
305 4.5
*1 50% A
system compound solv. ^max. loge ref. no.
*1 O. IN NaOH/W
system compound solv. \nax. loge ref . no.
A
methyl 1, 2 , 3 , 3a , 4 , 5-hexahydro-6-methoxy- 221 4.4 T16x 4283
3-methyl-5-oxo-3-acephenanthrylene- 299 3.8
carboxylate 372 3.6
0-66-9^-9:0 gona-1 ,3,5 (10) ,6,8, 14-hexaen-16-one A 218 4.8 W25 4288
C C 276 4.6
306 4.5
6
TSt0 gona-1, 3, 5 (10) ,6,8,13-hexaen-17-one A 219
280
334
4.6
4.7
4.2
W25 4291
system compound solv. ^max. loge ref. no.
*1 O. IN NaOH/50% A
system compound solv. max. loge ref. no.
*1 0.2N NaOH/50% A
system compound solv. ^max. loge ref. no.
*1 0.5N Na2C03/W
system compound solv. max. loge ref. no.
*1 NaOH/A
system compound solv. max. loge ref. no.
*1
334
445
4.7
4.7
B125 4419
B125 4420
*1 Na salt in W
system compound solv. max. loge ref. no.
*1 acid/A
system compound solv. max. loge ref. no.
*1 acid/A *2 O. IN NaOH/W
system compound solv. max. loge ref. no.
*1 acid/A
system compound solv. max. loge ref. no.
*1 Ice O. IN NaOH/24cc A
system compound solv. max. loge ref. no.
*1 50% H2S04/W
system compound solv. max. logs ref. no.
*1 50% H2S04/W
system compound solv. max. loge ref. no.
c4-75-c : o ethyl 4,5:7, 8-bis ( trimethylene) -6- cH 587-94 2.8 TIl 4586
azulenecarboxylate 630 2.8
696 2.4
665:c:c:c:c:665 di- (9-f luorenylidene) butatr iene ; B 500 4.8 K75 4607
l,l,6,6-di(2,2'-biphenylylene)- 543 5.3
hexapentaene
(665! O)(O! Iy)3 2,4, 7-trinitrof luoren-9-one A 280 4.5 F49 4619
O 336-48 3.9
63 phenanthrene A 250
293
4.7
4.1
M23 4621
330 2.5
346 2.5
*1 P with KOH/M
system compound solv. max. loge ref. no.
G
4-63 1,2,7, 8- tetramethy lphenanthrene PE 264 4.8 R43 4660
307 4.2
340 2.7
*1 2N HCl/50% A *2 5% NaOH/W
system compound solv. max. loge ref. no.
63
T 9-isopropylphenanthrene A 252
294
330
4.8
4.1
2.5
F49 4695
348 2.5
63
T 1-acetylanthracene A 241
254
385
4.8
4.8
3.7
J25 4700
63
T methyl 2-phenanthrenecarboxylate 263
344
361
4.9
2.9
2.9
W42n 4704
n° 9-nitroanthracene A 251
348
363
383
5.1
3.6
3.6
3.6
J18 4708
*1
452
415
4.2 B125
4.3 B125
4724
4725
*1 HCl salt
system compound solv. max. logs ref. no.
1-hydroxyanthraquinone
M
M
600-29
252 4.5
P9
P8
4787
4788
327 3.5
402 3.7
413.5 3.7
1,2,3,5,6, 7-hexahydroxyanthraquinone ;
M 552
213 4.2
P9
B67
4816
4817
°6 rufigallic acid 295 4.6
349 3.9
438 3.9
°:KT 2-benzamido-l-nitroanthraquinone Ac
EA
505
470
4.0
3.8
B105
B105
4842
4843
o:e3:c-6-N anthraquinone 9-{ [p- (dime thy lamino)- Ac 450 4.1 H88 4847
phenyl]methide}
B 442 4.1 H88 4848
anthraquinone 9-{ 1- [p- (dime thy lamino) - Ac 420 3.9 H88 4852
o:*c4* phenyl ] -1-phenylme thide }
445
4.1
4.1
H88
H88
4857
4858
*1 HC104/M
PART 30. CHROMOPHORES CONSISTING OF 4 CARBOAROMATIC CONDENSED RINGS
635: c-c :o benzo [a] f luoren-11-ylidenesuccinic acid A 263 4.8 F49 4892
293 4.2
314 4.0
344 3.2
63s : N-N benzo [a] f luoren-11-one 2,4-dinitro- D 256 3.7 F49 4893
phenylhydrazone 415 3.4
*1 2N HCl/50% A
system compound solv. max. loge ref. no.
*1 IN NaOH/50% A
system compound solv. max. loge ref. no.
n-o N- (benz [a] anthracene-5-carbonyl) glycine 8.3 292 4.7 J20 5029
343.5 3.9
350 3.0
:
°f
6
*:>r-n benz[a]anthr~7-ylglyoxalic acid A 296
351
390
4.8
3.8
3.5
B8 5039
6
*r 6-nitrochrysene
505 4.1
6
'I*- 5-phenoxy-6 , 11 , 12-triphenylnaphthacene B 299
460
490
525
5.0
3.8
4.1
4.1
B12 5049
X4 5,6,11, 12-tetraphenylnaphthacene ;
rubrene
B 303
465
495
5.1
3.8
4.1
B12 5050
530 4.1
530 4.1
system compound solv. \nax. loge ref. no.
763 M;
benzo [ a] naphtho [ 1 , 8a , 8-cd] cycloheptene 208 4.6 A8g 5058
pleiadiene 230 4.4
248 4.4
342 3.9
424 2.6
449 2.6
480 2.6
Next Page
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310 4.5
376 2.8
C2-S5 A
6H-naphtho [ 3 , 4 , 4a , 5 , 6~def g ] naphthacene 300.5 4.9 C49 5084
369 3.9
390 3.9
*1 IN NaOH/50% A *2 trichlorobenzene
system compound solv. ^max. loge ref. no.
*1 1-methylnaphthalene
system compound solv. max. logs ref. no.
6
S tribenzo [de ,kl , rst ] pentaphene B 301 4.6 C46z 5162
352 3.9
365 3.9
483 4.6
516 4.7
O2-S8 B , 8-624
4 , 11-diacetoxyphenanthro [ 1 , 1Oa , 10 , 9 , 8a 4.2 B130 5179
fghij ]perylene 678 4.6
6752 diindeno [1,2, 3-cd : 1 , 2 , 3-lm] perylene ; B 297 4.5 C36 5182
periflanthene 498 4.7
537 4.8
69 B 327.5
anthra [ 9 , 9a , 1 , 2-cde ] benzo [ r s t ] pentaphene ; 4.8 C45u 5183
violanthrene 458 4.6
492 4.9
6952 B
dibenzo [ a , j ] diindeno [1,2, 3-cd : 1 , 2 , 3-lm] -294 4.5 C36 5192
perylene 312 4.5
324 4.5
448 4.5
*1 1-methy !naphthalene
PART 32. (NS)-CHROMOPHORES
TO ethyl 4,5-dimethylpyrrole-2,3-
dicarboxylate
A 213
293
3.9
4.0
C89 5212
*1 hydrochloride in A
system compound solv. \nax. loge ref. no.
*1 O. IN HC1/W *2 O. IN NaOH/W
system compound solv. max. loge ref. no.
iron (II) complex of 5, 5 '-dime thy 1-2,2'- 510 3.9 H78u 5390
bipyridyl
copper (I) complex of 6,6 '-dime thy 1-2,2'- 455 3.8 H78u 5391
bipyridyl
NSH:: c-c 3- (2-pyrrolin-2-yl) pyr idine ; myosine A 234 4.1 S83 5399
N 266 3.6
*1 acid A
system compound solv. max. loge ref. no.
2,4, 6-tris [p- (dime thy lamino) phenyl] -1- 436 W44g 5454
methylpyridinium perchlorate
N^6-N
N&-C :c-e 2-styrylpyridine A 275-85 B74 5455
310 4.4
N6-c:c-e-N 2- [p- (dime thy lamino) styryl] pyridine A 460 4.6 C68 5457
N-6-c:c-N6-c:c-e-N 2, 4-bis[p- (dime thylamino) styryl] pyridine A 510 4.8 C68 5465
NSHMlN-S-N 2- [p- (dime thy lamino )phenylazo] pyridine 1.2 457 4.6 K41 5471
525-50 4.0
system compound solv. ^max. loge ref. no.
IU43_JUC
no—wo 3- (2-pyrrolyl)pyridine ; nornicotyrine A 229 3.8 S83 5489
294 4.2
*1 HCl salt in A
system compound solv. max. loge ref. no.
C-N65-|0:6:0|-N65-C 2 , 5-bis (2-me thy 1-3-indo IyI) -p-benzo- Ac 498 3.8 B153 5587
quinone
*1 nitromethane
system compound solv. ^max. loge ref. no.
*1 242 M9 5599
298
416
An 630 S2 5614
C 605 S2 5615
*1 601 S2 5617
*2 591 S2 5618
*3 678 S2 5619
V 546 S2 5620
*1 1,1,2, 2-tetrachloroethane
system compound solv. \nax. loge ref. no.
*1 10% A *2 O. IN HC1/W
system compound solv. ^max. loge ref. no.
*1 O. IN HC1/W
system compound solv. max. loge ref. no.
*1 HCl salt/A
system compound solv. ^max. loge ref. no.
N66-C:C-6-N 2- [ p- (dime thy lamino ) s tyry 1 ] quinoline M 396 4.6 B139 5832
N66-c:c-c:c-6-N 2-{ 4- [p- (dime thy lamino )phenyl] -1 , 3- M 411 4.6 B139 5836
butadienyl}quinoline
c-N66i c-ci c-c :N-6 2- (4-anilino-l , 3-butadienyl) -1-ethyl- M 528.5 5.0 B139 5850
quinolinium iodide
c-N66i C-Ci c-c iN-6 1-e thy 1-2- [ 4- (N-methy lanilino ) -1 , 3- 515 5.0 B139 5851
C butadienyl]quinolinium iodide
c-N66iC-Ci SiN-C2 2- [p- (dimethylamino) styryl] -1-methyl- M 522 4.8 B139 5852
quinolinium iodide
C-N66 : C-C : C-CiSiN-C2 2-{ 4- [p- (dimethylamino)phenyl] -1 , 3- M 558 4.7 B139 5854
butadienyDquinoline methiodide
*1 0.01N HC1/W
system compound solv. \nax. loge ref. no.
*1 IN HC1/A
system compound solv. ^max. loge ref. no.
*1 M with 0.01 M HCl *2 O. IM HC1/W *3 Ac wtih 0.01M HCl *4 C with 0.0001M HCl
*5 dil. HC1/W
system compound solv. *max. loge ref. no.
*1 5N HC1/W
system compound solv. ^max. loge ref. no.
*1 5N HC1/W
system compound solv. ^max. loge ref. no.
C-NS3 i C-C iN-C2 1f , 3-diethyl-5 ' , 6 ' -benzothiazolino-2 ' - 437 B135 6036
S cyanine iodide
C-NS3 i C-NS-C 1 , 1 ? -die thy 1-3 ' , 4 ' -benzo-2-pyrido-2 ' - 475 B137 6037
cyanine iodide
C-NS3 i C-NS3-C 1 , 1 f -die thyl-5 , 6 , 5! , 6 ' -dibenzo-2 , 2 ' - 524 B137 6041
cyanine iodide 554
C-NS3 i C-Ci C-NS3-C 1 , 1 f -diethy 1-5 , 6 , 5 ' , 6 ' -dibenzo-2 , 2 ' - 589 B137 6043
carbocyanine iodide 625
o.:N2^:c-6-o 5-(p-methoxybenzylidene)-l,3-dimethyl-
2 , 4-imidazolidinedione ; 5- (p-methoxy-
C
2 benzylidene) -1 , 3-dime thy lhydantoin
stable isomer A 231 4.0 S37 6119
331 4.2
*1 0.01N NaOC2H5/A
system compound solv. ^max. loge ref. no.
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4- (dime thy lamino) pyr imidine 3.2 262 4.2 B147 6169
system compound solv. max. loge ref. no.
*1 monohydrochloride/W
system compound solv. ^max. loge ref. no.
*1 monohydrochloride
system compound solv. ^max. loge ref. no.
*1 O. IN HC1/A *2 O. IN NaOH/ A
system compound solv. ^max. log e ref. no.
*1 hydrochloride/A
system compound solv. max. loge ref. no.
*1 monohydrochloride *2 5N HC1/W
system compound solv. ^max. loge ref. no.
ClNC2-N2S 4-amino-6-chloro-2-me thy 1-5- (piper idino- 240 3.9 H65 6343
methyl) pyrimidine 277 3.7
*1 acid solution
system compound solv. ^max. loge ref. no.
NC-N2S-CiN 4-amino-5-cyano-2-me thy lpyr imidine 3.0 242 4.0 S74 6367
293 3.7
*1 O. IN HC1/W *2 O. IN NaOH/W
system compound solv. ^max. loge ref. no.
N26-c: c-c:c-s 4- (4-pheny 1-1, 3-butadienyl) pyrimidine C 344 4.6 K49 6386
N2S-[CiC]7-S 4- (14-pheny 1-1 ,3,5,7,9,11, 13- tetradeca- C 447 5.0 K49 6391
heptaenyl) pyrimidine
*1 10% A/W
system compound solv. max. loge ref. no.
*1 O. IN NaOH /W
system compound solv. ^max. loge ref. no.
*1 O. IN NaOH/W
system compound solv. ^max. logs ref. no.
*1 O. IN NaOH/W
system compound solv. ^max. loge ref. no.
*1 O. IN NaOH/W
system compound solv. max. loge ref. no.
*1 O. IN HC1/W
system compound solv. \nax. loge ref. no.
*1 O. IN HC1/W *2 O. IN NaOH/W
system compound solv. max. loge ref. no.
OiN2^iO 5-amino-l ,2,3, 4-tetrahydr o-2 , 4- 3.0 260 4.1 S74 6581
pyrimidinedione; 5-aminouracil
7.0 225 4.0 S74 6582
290 3.8
OiN 2 SiOI-NiO 1,2,3, 4-tetrahydro-5-nitro-2 , 4-- 3.0 235 3.8 S74 6604
pyrimidinedione; 5-nitrouracil 300 4.0
*1 0.05N NaOH/W
system compound solv. \nax. loge ref. no.
*1 NaOCH3 /M
system compound solv. ^max. loge ref. no.
*1 50% AA/W
system compound solv. \nax. loge ref. no.
*1 O. IN HC1/W
system compound solv. ^max. loge ref. no.
*1 O. IN HC1/W
system compound solv. max. loge ref. no.
*1 NaOH/A (1:1)
system compound solv. max. loge ref. no.
C2-N3S-S 1 , 5-dime thy 1-3-pheny 1-1H-1 , 2 , 4-triazole A 245 4.2 A38 6871
*1 cation *2 KOH/A
system compound solv. max. loge ref. no.
*1 KOH/A *2 85 mol. excess of HCl *3 420 mol. excess of HCl *4 12,300 mol. excess of
HCl
system compound solv. max. loge ref. no.
tris (dime thy lamino) -1,3, 5-triazine W 216 4.7 H69 6917
*2 no K39 6933
*1 50% AA/W
system compound solv. max. loge ref. no.
C3-N4SS 2 -e thy 1-5 , 6 -dimethyl- IH-I ,3,4, 7-tetraza- 247 3.2 S21 7068
indene 306 4.2
*1 O. IN HC1/W
system compound solv. ^max. loge ref. no.
N-N4SS ! O 6-amino-l , 2 (or 2,3) -dihydro-2-purinone ; 2.0 284 4.0 M18 7192
6-amino-2-hydroxypur ine ; isoguanine
7.0 240 3.9 M18 7193
286 3.9
*1 sulfate in W *2 O. IN HC1/W
system compound solv. \nax. loge ref. no.
o:N4$5:o 1,2,3, 6-tetrahydro-l, 3-dimethy 1-2 , 6- 6.4 270 4.0 T17n 7268
C2 purinedione; theophylline
1,2,3, 6-tetrahydro-l , 3 , 9-trime thy 1-2 , 6- 5.0 267 4.0 G40 7275
purinedione; isocaffeine
10.0 269 4.0 G40 7276
OiN4^SiO 8-amino-l , 2,3, 6-tetrahydro-2 , 6-purine- 2.3 233 3.9 C20 7282
N dione ; 8-amino-2 , 6-dihydroxypurine 285 4.1
5 0
Z-w -C
4
perhydro-1 , 3,7, 9-tetramethyl-2 ,6,8-
purinetrione
240
293
3.8
4.0
F51 7305
N2-N4ee: o -c:o 2-amino-7 , 8-dihydro-4- (methylamino) - 1.0 263 4.1 Ell 7321
7-oxo-6-pteridinecarboxylic acid 360 4.2
ethyl 2-amino-3 ,4,7, 8- tetrahydro-8- (2- 1.0 270 3.9 Ell 7340
hydroxyethyl) -4 , 7-dioxo-6-pteridine- 292 3.9
carboxylate; ethyl 2-amino-7,8-dihydro- 378 4.4
4-hydroxy-8- (2-hydroxyethyl) -7-oxo-6-
pteridinecarboxylate 11.0 265 4.2 Ell 7341
380 4.3
*1 O. IN NaOH/W
system compound solv. max. loge ref. no.
Cl2-N4S3S-S A
6 , ll-dichloro-2-phenyltetrazolo [ f ] -5 , 6- 505 JlOn 7366
phenanthrolinium nitrate 680
*1 3.2N ECl/ A
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N-N5SS 7-amino-l , 2 , 3-tr iazolo [ d] pyrimidine 2.0 265 3.7 C21 7374
Nc65.0|-6-C:0
5 5-amino-2- (p-carboxypheny 1) -6 , 7-dihydro- *1 225 4.3 B54 7392
A 6 1,2 , 3-triazolo[d]pyrimidin-7-one;
5-amino-2- (p-carboxyphenyl) -1 ,2,3-
triazolo [d]pyrimidin-7-ol
o:N565:o 4,5,6, 7-te trahydro-1 , 2 , 3- 1 riazolo [ d ] - 2.0 265 3.8 C21 7393
pyrimidine-5, 7-dione; 1,2,3-triazolo-
[d]pyrimidine-5,7-diol 6.5 265 3.8 C21 7394
W <220 R2 7402
*1 0.2N NaOH/A+C(9:l)
system compound solv. ^max. loge ref. no.
^ *VC:N-O
0-Ni(K05
2-furil dioxime nickel *2 480 YOn 7424
(OS)2(NiC)2(CiC)6 bis [ 7- (2-f uryl) -2,4, 6-heptatrienyl- D 300 4.2 B76 7433
idene] hydrazine 430 5.0
444 5.0
05-[CiC]5-CiO 11- (2-f uryl) -2,4,6,8, 10-undecapentaenal D 260 3.9 B76 7450
300
412 4.9
•**&•••
05-ClC-CiC-C-O
1- (2-f uroyl) -2- (2-f uryl) ethylene
410
3.6
4.8
4.3
S89
K5
7452
7453
05-CiC-CiC^ one
£!£§*« l,13-di(2-furyl)-l,3,5,8,10,12-trideca-
hexaen-7-one
426 4.4 K5 7454
*£&=• c:c-05
1, 6-di (2-f uryl) -1 , 5-hexadiene-3 , 4-dione 400 4.1 K5 7455
2-furoic acid A
W
244
245
4.0
4.1
H84
M6
7461
7462
o: :o
m 5-(3,4-dicarboxy-2-furyl)pentanoic acid A 263 3.4 H73 7474
:o
°TO ethyl 3,4-dihydroxy-2,5-furandi-
carboxylate
*2
*3
287
317
4.4
4.4
El
El
7475
7476
05-c:c-c:o 2-benzamido-3- (2-f uryl) acrylic acid A 228 4.1 B51 7480
N O 311 4.3
(OS)(OiC)2(CiC)2-C 4-carboxy-5- (2-f uryl) -3-me thyl-2 , 4- iP 300 4.5 PIl 7490
pentadienoic acid
*1 0.5N Na2C03/W
system compound solv. ^max. loge ref. no.
W <200 R2 7511
305 4.0
Co-6
3 2 , 5-dimesityl-3-phenylf uran A 266 4.2 K30 7528
6X)6-6-C3
s~s
ci
tetraphenylfuran B 342
512
3.8
3.1
S40 7530
340
3.9
2.9
3.8
S40
S40
7531
7532
510 3.2
S^'O
(05) (S)4(OiC)2 3 , 4-dibenzoyl-2 , 5-diphenylf uran A 258 4.5 K26 7547
:
H§ ° 3- (a-hydroxybenzyl) -2 , 5-diphenyl-4-
furancarboxylic acid
3- (a-hydroxybenzyl) -2 , 5-diphenyl-4-
A
A
297
345
4.3
4.4
S25
S25
7550
7551
furancarboxylic lactone
(05) (6)3(0:5) (o:c) 4-benzoyl-2 , 5-diphenyl-4-f urancarboxylic A 399 4.4 S25 7552
6 acid
*1 0.1% HC1/M
system compound solv. max. loge ref. no.
*1 NaO Ac /A
system compound solv. ^max. loge ref. no.
*1 O. IN NaOH/W
system compound solv. max. loge ref. no.
*1 H2SO4
system compound solv. ^max. loge ref. no.
06
BV:? 9- (perhydro-2 , 4 , 6-trioxopyrimidin-5-
ylidene)xanthen
*1 560 D3 7783
*1 1% H2S04/dil. AA
system compound solv. \nax. loge ref. no.
o3-6-c:oN5:o -S-N:O 2- (o-nitrophenyl) -4- (3,4 , 5-trimethoxy- AA 400 4.4 B40 7884
benzylidene) -2-oxazolin-5-one ; 2- (o-
nitrophenyl) -4- (3 , 4 , 5-trimethoxy-
benzylidene) -5-oxazolone
*1 IN HC1/W *2 IN NaOH/W
system compound solv. max. loge ref. no.
C 3-ON65 : C-C . C-ONSS-C 3 3 , 3 T -diethy 1-9-methy 1-5 , 5T , 6 , 6 f -tetra- M 501 B28 7934
C me thy loxa car bo cyanine iodide
S-ON^S : c-c : C-ON^S-S 3 , 3 T -diethy l-9-methyl-5 , 5 ' -diphenyl- M 500 B28 7936
C C C oxacarbocyanine iodide
OC3-ON2SS 5-acety 1-2 , 6 , 7-trimethy lpyrido [ 3 , 2-d ] -A 232 4.0 A18 7945
oxazole 279 4.0
Next Page
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ss-c: IY-N: c-ss bis [ 1- (2-thienyl) ethylidene] hydrazine ; A 265 4.1 S88 7991
C ^ 2-acetylthiophene azine 335 4.2
*2
290
330
308
4.2
3.8
4.2
El
El
8010
8011
V375 3.5
AA
266
%354
268
3.9
3.5
4.2
El
El
8013
8014
<350 4.0
SS-N4S-C N, N-dime thy 1-2- [5- (2-thienyl) -2H- *1 271 3.9 E13u 8057
tetrazol-2-yl] ethylamine
*1 HCl salt
system compound solv. ^max. loge ref. no.
*1 AcOH + HClO4
system compound solv. max. loge ref. no.
C2-SS3S 7 , 11-dime thy lphenan thro [2 , 3-b ] thiophene A 279 4.8 J17 8158
345 4.2
*1 1% H2S04/dil. AA
PART 49. AROMATIC CHROMOPHORES WITH S AND N HETERO-ATOMS
*2 280 V3 8173
*1
306
288
4.0
3.6
C77
C77
8191
8192
*3 471 K9 8197
C3-SNS! C-C iNS-6 l-ethyl-2 ' , 5T -dimethy 1-1f -pheny 1-6 , 7- 440 S59 8205
*2 dihydro-4H-pyrano [4 , 3-d] thiazolo-3f -
pyrrolocarbocyanine iodide
SC2-SNSiC-CiNS-S l-ethyl-2f , 5 ' -dime thy 1-1f -phenyl-6 , 7- 450 S59 8206
*2 dihydro-5H-thiopyrano [3 , 2-d] thiazolo-3f
pyrrolocarbocyanine iodide
C3-SNS. C-C .C-ON65-C 3,3' -die thy 1-4 ' , 5 ' , 6 ' , 7 ' -tetrahydro- 514 S59 8211
oxathiacarbocyanine iodide
c-SN65iC-c:N-6 3-ethy 1-2- [2- (phenylimino) ethylidene]- M 394 4.6 B141 8295
benzothiazoline
c-SN65i c-c: C-CiINhS 3-ethy 1-2- [ 4- (phenylimino) -2-buten- M 448 4.8 B141 8298
ylidene]benzothiazoline
c-SN65i c-Ci c-c. N-e 3-ethy 1-2- [ 4- (N-methy lanilino) -1 , 3-buta-M 496.5 5.0 B141 8300
4 dienyl] benzothiazolium iodide; 3-ethyl-
2- [ 4- (N-methylphenylimino) -2-butenyl-
idene]benzothiazoline perchlorate
c-SN65i c- [Ci C]2-CiN-S 3-ethy 1-2- (6- (phenylimino) -2 , 4-hexadien- M 485 4.8 B141 8301
ylidene )benzothiazoline
C-SN65 : C- [C : C]2-C N-S 3-ethyl-2- [ 6- (N-methy lanilino) -1,3,5- M 597.5 5.1 B141 8303
C hexatrienyl]benzothiazolium iodide;
3-ethyl 2- [ 6- (N-methylphenylimino) -
2 , 4-hexadienylidene ] benzothiazoline
hydroiodide
system compound solv. ^max. loge ref. no.
C-SN65 .'C-CiSiN-C2 2- [2- (p-dimethylaminophenyl) vinyl] -3- M 524 4.8 B139 8307
methylthiazolium iodide
*1 528 4.8 B139 8308
C3-SNSS i C-C i C-ON^S-S 3 , 3f -die thy 1-5f , 6-dimethyl-5-phenyl- M 530 B28 8312
C oxathiacarbocyanine perchlorate
*1 nitromethane *2 HO-CH2-CH2-O-C2H5
system compound solv. max. loge ref. no.
C2-SNSS : c-c : C-SNSS-C2 3 , 3f -diethy 1-6 , 6f -dime thy ldithiacarbo- M 562 B28 8324
cyanine iodide
C-SNSS . C- [C i C] 2-SN65 3-ethyl-2-[ 5- (2-thiazolyl) -2, 4-penta- M 490 4.8 B140 8330
dienylidene] thiazoline
C-SNSS : c- [ c : c]3-SNss-c
3 , 3T -diethyldithiatricarbocyanine iodide M 758 5.4 B140 8332
C3-SN665 8-me thy lacenaphtheno [5, 4-d] thiazole 240 4.6 S2n 8349
305 3.9
C-SN665 i C-C ! C-SNSS-C2 3 , 3 f -diethy l-6-methyl-4f , 5 ' -benzothia- M 580 B28 8358
carbocyanine iodide
f
C-SN665 : C-C : C-SNSS-C2 3 , 3 ' -diethyl-6 , 9-dimethyl-4 , 5 ' -benzo- M 551 B28 8359
C thiacarbocyanine iodide
C-SNSSS : c-c : C-SNSSS-C 3 , 3 T -die thy 1-4 , 5 : 4 ' , 5 ' -dibenzothiacarbo- 596 5.1 K28 8361
cyanine iodide
C-SNS3S :C-N66-C 1 ' , 3-diethyl-4 ,5:6, 7-dibenzothia-2f - 510 4.7 K28 8378
cyanine iodide
c-sN635 : c-c : c-SN63s-c 3 , 3 f -diethyl-4 ,5:4',5f:6,7:6',7f -tetra- 614 4.1 K28 8380
benzothiacarbocyanine iodide
*1 l.ON HC1/W
system compound solv. \nax. loge ref. no.
*1 50% H2SO4M
system compound solv. max. logs ref. no.
*1 NaOH/W
system compound solv. \nax. loge ref. no.
*1 NaOH/W
TABLE II
ABSORBING CHROMOPHORE FROM ABSORPTION MAXIMUM
X :
max <199-5my (6) (NrC) 4.6 2626 (6)(0:C) 4.1 3172
(6) (OrC) 4.6 3142 6 4.1 3173
none 3.4 4 N 4.1 3174
3.0 5 (6)(0:C) 3.9 3165 4.4 3202
3.1 8 6 4.2 3178 4.2 3217
(C:C) 4.0 55 4.6 3203 4.3 3279
3.9 56 4.4 3207 4.4 3287
3.9 57 4.2 3211 4.5 3288
4.0 61 4.3 3276 4.2 3296
80 4.6 3280 4.2 3298
(C:C) 3.8 230 4.2 3282 4.5 3301
3.6 231 4.5 3285 (N25) (6) (0:N) 4.1 6090
3.8 232 (6)(0:N) 4.1 3481 6
(C:C:C) 293 O 4.2 3484
4.4 294 4.2 3514 Amax : 206-207. 5my
4.3 295 (N5) 3.8 5197
(N:C) 3.7 373 3.9 5198 (C:C) 3.6 65
(N-C) 564 (N265) 4.4 6632 3.5 66
(OrC) 1.8 1002 (N365) 4.4 6950 4.4 83
O (05) 4.0 7400 (CrC)3 4.1 174
(OrC)2 3.6 1011 (05MOrCp 3.5 7468 4.1 175
O O (C-C)3 5.1 237
(OrC)2(CrC) 3.9 1107 (065)(0:C) 4.3 7630 (0:C) 3.0 617
O O (0:C) 976
(6) 3.9 1323 N
4.4 1355 Amax : 204-205. 5my (O: C) 1.7 999
4.4 1372 6
4.6 1510 none 3 (6) 3.9 1326
5.2 1538 2,3 35 4.4 1394
(6)(0:C) 4.3 2682 (C:C) 3.1 59 4.6 1448
4.2 2692 3.6 67 3.9 1477
4.5 2693 4.2 71 1576
(6)(0:C)2 4.6 3307 (NrC)2 4.1 375 3.9 1578
O 4.6 3312 (OrC) 1.7 1000 4.5 1682
(N66) 4.5 5678 O 1.6 1001 (6)2 4.6 1866
4.3 5679 1.7 1003 (6) (CrC) 4.0 2048
1.6 1004 (6) (OrC) 4.4 3208
1.8 1005 6 4.1 3212
A :
max 200-203. 5my 2.0 1008 4.2 3215
(OrC)(CrC) 4.0 1014 4.4 3216
(CrC) 2.8 58 O 4.1 1015 4.4 3267
3.4 60 (OrC)2(CrC) 4.1 1109 4.4 3297
3.6 63 O 4.6 3302
3.5 64 (6) 4.3 1392 (6) (OrN) (OrC) 4.0 3866
3.7 84 4.1 1412 6
(CrC)2 4.0 94 4.1 1641 (N6) 4.3 5337
(OrC)(CrC) 4.0 1016 1686 (N25) 3.7 6069
O 3.8 1708 (N36) 4.9 6909
(6) 3.9 1399
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
x
max.: 208-209. 5my (6) (OrN) 4.1 3585 (66)(0:C) 4.5 4271
6 4.1 3639 (66) (6) 4.6 4355
(C:C) 3.7 68 (6) (0:N) (0:C) 4.2 3869 4.5 4356
4.0 69 O 4.1 3872 (N66) 4.3 5673
4.1 82 (N5) 4.2 5194 4.1 5679
(N:C)2 4.3 377 (N5)(OrC)2 4.1 5211 (N26) 4.3 6250
(0:C)(C:C) 4.1 634 O (05) (OrN) (0:C) 4.0 7509
(OrC)2(CrC) 4.1 1106 (N65) 5569 6 6
6 4.2 1108 5570
(S:C:0) 1.7 1317 (N66) 4.5 5746 Amax. : 213-213. 5my
(6) 4.5 1684 (N26) 3.6 6278
(6)(0:C) 4.3 2723 3.6 6279 (CrC)(CrC) 4.0 242
4.2 2737 (0:N26:0) 3.8 6588 (OrC)(CrC)2 3.9 809
4.2 2754 (ON5)(6)2 4.4 7794 (OrC) 1.9 1007
4.3 2783 O
(6) (OrC) 4.4 3186 (OrN) 4.0 1284
O 4.4 3189 Xmax : 211-211. 5my i
4.2 3218 ' (6) 1572
(6)(OrC)2 4.6 3309 (OrN) 3.9 306 1637
O O 3.8 1664
(6) (OrN) 4.2 3575 (OrC)(CrC) 1017 4.0 1688
O 4.1 3578 O 1692
4.1 3627 (6) 2.6 1366 1767
4.2 3629 4.0 1389 (6)(CrC) 4.3 2010
(6MOr^)(OrC) 4.0 3867 3.9 1510 (6)2(NrC)2 4.2 2527
O O (6) (CrC) 4.0 2049 (6) (OrC) 3138
(763) 4.6 5058 (6)(N*rC) 4.5 2627 N
(N5)(6) 4.2 5225 (6) (OrC) 4.2 2781 (6) (OrN) 3.8 3571
4.2 5227 (6) (OrN) 4.2 3632 O 4.2 3588
(N6) 4.3 5332 O 4.3 3634
(N6rO) 3.9 5524 (7665) 4.6 5056 (6) (OrN) (OrC) 4.1 3870
(N26) 3.3 6149 (N26) 3.9 6299 6
4.2 6181 3.7 6300 (Or63rO) 4.2 4817
(N26rS) 3.9 6535 4.3 6342 (N5) (OrC)2 3.9 5212
(N35) 3.6 6857 A
(N6) 3.7 5352
A
max.: 212-212. 5my 3.7 5355
Xmax r 210-210. 5my 3.8 5356
(OrC)(CrC) 4.1 1028 (N66) 4.6 5674
none 3.0 9 O 4.0 1031 4.1 5708
(CrC) 2.4 76 (OrC)(CrCrC) 1157 (N26) 4.1 6247
(O:?) 1.7 1006 O 3.7 6263
O (6) 3.9 1358 3.7 6265
(OrC)(CrC) 3.8 1039 4.3 1754 3.8 6281
O (6)(NrC) 4.1 2625 3.8 6282
(OrC)(CiC) 3.8 1151 (6)(OrC) 4.2 2743 3.8 6309
O 4.0 2744 (N26rO) 4.1 6406
(6) 3.9 1357 4.3 2780 (05) (OrN) (OrC) 4.1 7510
4.6 1450 4.2 2784 6 6
3.8 1544 (6) (OrC) 3199 rO
3.9 1718 6 3286 <S:SN5sC) (66) 4.6 8238
3.9 1802 (6) (OrN) 4.0 3625
(6) (OrC) 4.2 2753 O
(66)2 4.7 4222
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
A
max.: 214-214. 5mjj (N5) (OrC)2 3.9 5215 (SN65) 4.8 8249
O
(C:C) 4.0 81 (N65) 4.3 5557
(N:C) 3.7 317 (N26) 3.8 6277 Xmax.r 217-217. 5mu
(0:C)(C:C) 3.9 636 (N26rO) 4.0 6397
(OrC)(CrC) 3.7 947 (N26rS) 4.0 6542 (CrC)2 4.3 86
(OrC)(CrC) 4.0 1019 (05) 7404 (NrC) 3.9 336
O 3.8 1021 (05) (OrC) 4.5 7466 (NrC)2 4.3 376
(OrC)(CrC)2 3.9 1076 O (OrC) 1.7 1010
O O
(6) 4.2 1348 Amax. r 216-216. 5my (OrC)(CrC) 4.1 1023
3.8 1534
(6)(OrC) 4.5 3143 (OrC)(CiC) 4.0 1022 (6) 1574
N O 4.0 1027 3.8 1649
(6)(OrC) 3294 (6) 3.9 1521 4.0 1652
O (6)(N:.C) 4.5 2623 3.9 1656
(6) (OrN)2 4.1 3694 (6) (OrC) 4.4 2710 3.9 1672
O 4.1 2736 1738
(6) (OrN) (OrC) 4.0 3873 4.2 2827 1744
O (6)(OrC)(CrC) 4.1 2985 4.1 1772
(6G)2(NrN) 4.9 4244 (6) (OrC) 4.3 3185 (6) (OrC) 4.3 2822
4.6 4246 O 4.4 3210 (6) (OrC) 3258
(66) (OrC) 4.3 4270 3234 4.2 3270
(66) (6) (NrN) 4.6 4417 (6MOrC)(CrC) 4.2 3335 3.9 3274
O O (6) (OrC) (CrC) 4.0 3358
(63) 4.1 4646 (6) (OrN) 3.7 3573 6
(N6) 3.5 5311 O 3.9 3630 (6) (OrN) 3.8 3486
(N26) 3.4 6276 3.9 3644 O 3.9 3631
(N26rO) 4.1 6484 (6)(OrN)2(CrC) 3804 (6) (OrN) (OrC) 4.2 3875
(N26rS) 3.9 6562 O O
(N35)2 3.8 6860 (6MOrN)3(OrC) 3899 (6) (OrN) (OrC) 3892
(ON65)(6)(OrN) 4.2 7922 O O O O
6 (66)2(NrN) 4.8 4245 (66) (OrC) 4.4 4273
(66)2(OrN) 4.8 4248 (63) (OrC) (CrC) 4.4 4703
\nax.: 215-215. 5my 4.7 4249 (N6) 3.7 5331
(66) (6) (NrN) 4.5 4416 3.7 5366
(NlC)(CrC) 1.7 571 O (N6rO)(6) 4.1 5550
(OrC) 2.6 596 (N5) 3.9 5195 (N65)(Or6rO) 4.4 5584
(OrC)(CrC) 4.0 663 (N6) (OrC)2 5435 4.4 5589
3.1 711 O (N66) 4.6 5672
(OrC)(CrC) 4.0 985 (N65) 4.5 5552 (N26) 3.9 6310
N 4.4 5571 3.8 6311
(OrC)(CrC) 4.0 1033 (N65)(OrC) 4.5 5580 3.9 6347
O (N26) (NrC) 4.4 6366
(OrC)(NrC)(CrC) 4.0 1174 (N66) 4.5 5697 (N26rO) 4.4 6482
6 (N66rO) 4.6 5877 (N26rS) 4.1 6548
(6) 1577 (N25) (6)(OrN) 4.0 6087 (N36) 4.7 6914
1654 O (N45)(6)(OrN) 3.9 7047
4.0 1751 (N26) 4.0 6348 O
3.9 1773 (OrN^rO)(OrC,:) 4.1 6601 (0665) 4.4 7749
(6)(Nr*C) 4.3 2492 O 4.1 6602
(6) (OrC) 4.2 2725 (N35) 3.7 6858
(6) (OrC) 4.2 3273 (N36) 4.7 6917
6 (065) 4.5 7629
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
x
max.: 218-218. 5my (063:0) 4.6 7770 (SN65)(0:N) 4,2 8276
(SN65) 4.3 8250 6
(C:C)(C:C)2 4.0 260 (SN65)(0:N) 4.3 8277
x
(0:C)(C:C) 4.2 1057 max.: 220-220. 5my
O
(0:N) 3.2 1259 *max.: 219-219. 5my (C:C) 85
(6) 1353 (CiC)2 4.4 87
4.5 1542 none 2.9 10 4.0 92
3.8 1620 (C:C)(C:C) 4.0 247 (N:C) 2.8 312
3.9 1665 (N:C) 3.0 319 4.6 324
4.3 1695 (0:C)(C:C) 3.6 658 3.7 328
1794 (0:C)2(C:C) 3.8 913 (N:C)(C:C) 4.4 393
3.9 1811 (0:C) (CiC) 3.9 948 (NiC)2 0.3 570
(6)(C:C) 4.3 2010 (0:C) 3.3 1220 (N-C)2(CrC) 4.1 579
(6)(N:C) 4.4 2455 S (0:C)(C:C) 4.2 635
(6)(0:C) 4.0 2729 (6) 4.0 1546 3.9 662
4.2 2828 1653 3.7 680
(6)(0:C)(C:C) 4.2 2967 3.6 1719 (0:CN2) 998
(6)(0:C) 4.4 3184 1731 (0:C)(C:C) 4.0 1034
O 4.1 3188 1783
4.0 1038
(6)(0:C) 4.1 2669
3.9 3190 4.1 2734 (0.-C)(CiC)3 4.8 1153
3201 4.3 2825 O
4.3 3295 (6)(0:C)(C:C)2 3.5 3014 (0:C) (NiC) (C:C) 3.9 1175
(6)(0:C)(C:C) 4.0 3361 (6)(0:C) 4.0 3192 O
O 6 (0:C)(0:C)(C:C) 4.1 1196
(6)(0:N) 4.4 3568 (6)(0:C)(C:C) 4.3 3341 O
O (6) 3.7 1351
(6)(0:N) 4.2 3652 (6)(0:N) 3.9 3669 3.8 1352
O O 4.9 1538
(6) (OrN)2 4.1 3695 (6) (OrN)2 4.3 3682 3.9 1646
O O 4.0 1659
(66)2 5.1 4228 (66) 5.0 4136 4.5 1707
(66)2(N:N) 4.9 4247 (66)2 4.8 4221 (6)(C:C) 4.4 2028
O (66)(0:C)(C:C) 4.4 4289 (6) (0:C) 4.0 2727
(66)(0:C)(C:C) 4.8 4288 4.6 4291 4.3 2821
(75) 4.1 4559 (66)2(0:C)2 4.8 4315 4.3 2824
(64) 4.7 4903 6 (6)(0:C)(C:C) 4.1 2964
(N6) 3.9 5303 (66)(6)(N:N) 4.6 4376 (6)(0:C) 4.3 3187
3.9 5370 4.5 4378 O 4.4 3221
3.9 5372 (66)(6)(0:C) 4.6 4426 (6)(0:C)(C:C) 4.3 3359
(N6)(C:C) 4.1 5395 4.7 4427 O 4.3 3362
(N65) (0:6:0) 4.4 5585 (75)(0:N) 4.3 4588 (6)2(0:C)(C:C) 4.2 3375
(N26) 4.1 6186 O O
4.0 6353 (N65) 4.4 5563 (6)(0:N) 4.3 3633
3.6 6360 (N6)4 4.7 6059 O 4.3 3641
3.5 6361 (N26) 4.2 6305 4.2 3654
(N26:0) 3.8 6429 4.2 6306 4.2 3655
4.0 6436 3.9 6349 4.2 3657
(N275) 4.3 6762 4.1 6354 4.3 3658
(N4S) 3.5 7018 (N263) 4.5 6794 4.2 3659
(05) 7403 (N465) 3.9 7056 (6)(0:N)(C:C) 3796
4.4 7407 (0635) 4.7 7784 O
(05) (6)2 4.4 7518 (064) 4.2 7785 (7:0) 4.4 4040
(0665) 4.5 7747 (SS)(N4S) 4.2 8058 (66) 5.0 4098
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
A
5.0 4101 max.: 221-221. Smy (CrC)(CrC) 4.0 243
4.9 4127 (NrNrN) 2.2 308
4.9 4130 (N: N) 3.8 305 (NrC) 3.8 334
4.9 4134 O (NrC)(CrC)2 4.2 556
4.6 4143 (N:C) 3.7 327 (OrC)2 2.1 627
(66)(0:C)(C:C) 4.7 4325 (0:C) 2.8 980 (OrC)(CrC)3 4.1 832
O N (OrC)2(CrC) 4.1 904
(66) (6) (NrN) 4.5 4415 (0:C)(N:C) 3.9 991 (OrC)(NrC)(CrC) 3.9 971
O N (0:C) 2.6 979
(63) 4.0 4648 (0:C)(C:C) 4.4 1026 N 4.0 981
(64) 4.6 4902 O 4.3 1072 (0:C)(N:C) 3.1 989
4.7 4905 (6) 4.3 1350 N
4.6 4917 4.3 1532 (OrC)(CrC) 4.2 1025
4.6 4936 (6)(C:C) 4.3 2016 O 4.1 1029
4.6 4950 (6)2(N:C)2 4.1 2542 4.0 1073
4.5 4956 (6)(0:C) 4.1 2662 (0:C)(C:C)3 4.0 1090
4.6 4997 (6)(OrN) 4.0 3609 O
(64)(0:C) 4.5 5031 O (O: N) 3.2 1260
O (6XOrIjO2 4.4 3708 (6) 4.1 1524
(N5)(0:C) 4.2 5219 O 4.3 3712 (6) (OrC) (CrC) 3.9 3010
(6)2(0:N) 4.1 3742 (6)(0:C) 4.5 3144
(N6) 3.6 5333 O N
(N65) 4.4 5561 (0:6:0) 4.4 3975 (6) (OrC) 4.1 3220
(N65)(0:C) 4.3 5577 (66) 5.2 4099 O
4.3 5578 5.0 4102 (6)(0:C)(C:C) 4.3 3342
4.2 5579 4.9 4151 O 4.3 3343
(N66) 4.3 5678 4.9 4152 (S)(OrN) 4.0 3528
(N66)2 4.9 5806 (66)(0:C) 4.4 4283 O 4.3 3661
(N25)(6)(0:N) 4.0 6089 (66)(6)(0:C) 5.0 4431 4.2 3662
O 5.0 4433 (6) (OrN)2 4.2 3696
(N26) 4.1 6155 (64) 4.6 4939 O 4.2 3706
(N26:0) 4.1 6407 4.6 4996 4.3 3715
3.8 6417 (64X0:9) 4.6 5032 (6) (OrIJf)(CrC) 3785
4.5 6483 O O
(N26:S) 4.0 6551 (NS)(OrC) 4.4 5213 (66) 4140
(N266) 4.6 6661 O 4.2 5214 4.7 4168
(N36) 4.2 6902 (N6) 3.7 5312 (66) (OrC) 4.1 4272
(N45) 4.2 7017 (N66) 4.7 5665 (6) (OrC) (CrC) 4.4 4290
(N465) 4.2 7150 (N26:S) 3.9 6541 (66)2(0:C)2 4.9 4314
(0:N465:0) 4.2 7254 4.2 6554
(N466) 4.2 7315 (N263) 4.5 6796 (66) (6) (OrC) 4.9 4432
(0:N463:0) 4.9 7359 (N4S) (6) 4.0 7038 (66) (6) (OrC) 4.4 4438
(063:C)(6) 4.8 7766 (N465) 4.2 7091 O 4.8 4440
4.8 7767 4.3 7110 (75) 4.2 4529
(063:0) 4.6 7774 (N465:0) 4.1 7198 (7S)(OrN) 4.4 4589
(0:ON5:C)(6) 4.0 7796 (0:N463:0) 3.9 7358 O
(0:ON5:C)(6)2 4.3 7828 (S665) 4.5 8138 (0:63:0) 4.6 4819
4.3 7841 (635) 4.6 4888
(ON65)(6) 4.4 7919 (64) 4.5 4913
(0:865:0) 4.0 8115 *max.: 222-222. 5my 4.5 4928
(S665)(0:N) 4.5 8147 4.5 4929
O (CrC)2 139 (64) (CrC) 4.5 5012
(Se665)(0:N) 4.5 8419 (CfC) 3.7 231 (65) 4.8 5071
O 3.7 232 (N6) 3.5 5298
absorbing absorbing absorbing
chromophore logs no. chromophore loge no. chromophore loge no.
(6)2(0:C)(C:C) 4.4 3381 (OrC)(CfC) 3.4 946 (7 :0) (6) (0:N) (C:C) 4.2 4091
6 (OrC)(CfC)(CrC)2 4.1 956 6
(6)(0:N) 4.2 3663 (OrC)(CrC) 4.1 1030 (7 :0) (6) (O: N) (0:C) (C:C)
O 4.2 3666 6 3.9 1035 6 6 4.3 4093
(6) (OrN)2 4.3 3709 4.1 1074 (66) 4.6 4158
6 (0:C) 3.4 1221 4.6 4190
(7:0)(6)(0:C)(C:C) 4.3 4089 S (66)(C:C) 4.7 4236
O (0:N) 3.8 1274 4.5 4237
(66) 4142 O (66) (OrC) 4.6 4278
4.8 4191 (OrN)(CrC) 3.5 1290 (66) (OrC)2 4310
(66) (OrC)(CrC) 4.5 4286 O 3.6 1297 6
(66) (6) 4.8 4366 (6) 1343 (66) (OrC) (CrC) 4.5 4322
(66)2(6) 5.0 4370 3.7 1429 6 4.8 4357
(75) 4.3 4531 4.0 1547 4.7 4365
(Or63rO) 4.4 4826 1558 (75) 4.1 4533
(64) 4.6 4926 4.1 1650 (63) 4.8 4668
4.6 4927 4.2 1706 (Or63rO) 4.6 4799
4.5 4930 4.1 1721 4.6 4818
4.6 4938 3.9 1781 (635) 4.6 4884
4.6 4952 1798 (64) 4.6 4951
4.5 5007 (6)2(CrC)2 4.4 2099 4.6 4975
(65) 4.7 5085 (6)3(NrN)2 4.2 2364 (64)(OrC) 4.6 5025
(N6) (CrC) 4.1 5405 4.3 2377 (65) 4.4 5073
(N6)(OrC) 3.8 5413 ^)5(NrN)4 4.4 2391 (N5) 3.7 5196
O (6)3(NrN) (NrN) 4.2 2405 (N6) 4.0 5284
(N75) 4.2 5920 6 4.5 2406 (N6) 4.0 5284
(N26) 4.1 6268 (6) (NrC) 4.2 2415 (N6) (OrC) (CrC) 3.8 5414
4.1 6269 (6) (NfC) 4.0 2619 (N66) 4.5 5656
4.3 6285 (6) (OrC) 4.3 2724 4.8 5748
(N26rO) 3.8 6427 3.7 2730 4.1 5761
(N266) 4.6 6679 4.4 2764 (N66)(OrN) 4.4 5816
(N3S) (6) 4.0 6864 (6)2(OrC) (CrC) 3.8 3068 6
3.9 6869 4.0 3089 (N665)(OrN) 4.5 5952
(N36) 4.2 6938 (6) (OrC) 4.0 3131 6
(05) (OrC) (CrC) 3.7 7482 N (N64) 4.6 6055
O (6) (OrC) 3286 (N26) 4.0 6154
(OrON5rC)(6)2 4.2 7804 6 4.1 6219
4.4 7840 (6)(OrC)2 4.0 3306 4.4 6287
(ON65)(0:N) 4.4 7903 6 4.3 6288
O (6)2(OrC)2(NrN) 4.1 3397 4.1 6312
(SN65) 4.4 8264 O 4.2 6346
(SN65)(6)(OrN) 4.4 8289 (6) (OrN) 4.2 3518 (N26rO) 4.2 6399
A 6 4.4 3552 (N26rS) 3.9 6550
4.1 3553 (OrN26rO) 4.0 6582
A
max.: 225-225. 5my 3.9 3580 (N266) 4.4 6680
3.8 3581 4.7 6681
(CrC) 4.2 74 4.2 3665 (N266rO) 4.5 6735
(CfC)(CrC) 4.2 253 (6) (OrN)2 4.3 3714 (N263) 4.5 6797
(NrC) 1.4 320 O (N45) 3.5 7019
4.3 337 (6) (OrN)3 4.2 3720 (N45) (6) (OrN) 4.1 7046
4.0 365 O 4.4 3731 6
(NrC)(CrC) 4.1 421 (6)2(OrN)2(NrC)2 4.2 3851 (N465) 3.8 7135
(OrC)(CrC) 4.2 660 O 4.2 3854 3.9 7136
4.3 671 (7:0) 4.5 4048 (N466) 4.3 7311
absorbing absorbing absorbing
chromophore loge no. chromophore logs no. chromophore loge no.
(6) (OrC)2 3.9 3307 (N63) (6) 4.5 6032 (6)2 4.2 1954
(!) 4.2 3308 (N26) 4.2 6153 (6)(C:C) 3.7 1991
(6) (OrC) (CrC) 4.3 3340 3.9 6256 3.7 2015
6 4.0 3346 (N26:0) 4.0 6400 (6)2(C:C) 4.1 2082
(6)(0:C)(0:C)(C:C) 3.8 3437 4.0 6401 (6)2(N:N) 4.2 2156
6 4.0 6496 (6)3(N:N)2 4.4 2365
(6) (OrC) (OrC) 3442 (N26:S) 3.9 6564 4.2 2369
6 N (N36) 4.4 6930 (6)4(NrN)3 4.3 2384
(6) (OrN) 4.3 3553 (N45) 3.5 7026 4.4 2386
O 4.2 3576 (N465rO)(6) 4.3 7248 (6)2(N:N) (N:N) 4.3 2407
(6)(OrN)2 4.4 3717 O: rO_ . . __9 6
O X):N466:0; ^'^ /J" (6)(N:C) 3.9 2412
(6) (OrN)3 4.3 3725 (05)(N:C) 4.2 7414 (6)2(N:C)2 4.4 2560
6 (05)2(0:C)2 4.0 7441 (6) (N-C) 4.0 2618
(6)2(0:N)2 4.2 3757 (05)(6)2 4.3 7521 (6)(0:C) 4.1 2753
6 (066:S)(0:C) 4.3 7746 4.1 2754
(6)(OrN)(CrC) 4.0 3763 O 4.2 2755
O 3777 (0665) 4,. 6 7759 (6) (OrC)2 4.5 2848
3799 (0:ON5:C)(6)2 4.3 7816 4.1 2851
(6) (OrN)2(OrC) 4.4 3898 (S5) (OrC) (CrC) 4.1 8022 4.2 2853
O O (S5)(6) 4.0 8033 (6)2(OrC) (CrC)2 4.2 3092
(6) (OrN) (OrC) (CrC) 3900 (S65) 4.5 8102 (6) (OrC) 4.0 3165
O 6 (SN2S :N) (6) 4.2 8393 6 4.0 3168
(Or6rO) 4.4 3977 3.7 3172
4.4 3978 (6)(0:C)(C:C) 4.2 3339
(7:0) 4.3 4044 Xmax r 228-228. 5my 6
(66) 5.1 4104 * (6)2(OrC)(CrC) 4.1 3374
4.9 4105 (CrC) 4.0 70 6 4.1 3378
5.1 4106 (CfC)(CrC) 4.1 254 (6) (OrC) (OrC) 3406
5.1 4108 (CrC)(CrC)4 4.3 272 6
5.1 4111 (NrC) 3.8 329 (6)(OrN) 3.8 3501
5.0 4113 4.2 340 6 4.2 3549
4.9 4150 4.3 348 3.9 3578
4178 4.1 369 3.9 3585
4189 3.9 370 4.1 3667
5.0 4192 (NrC)(CrC) 4.2 394 (6) (OrN)2 3701
5.0 4193 4.2 446 6 4.0 3702
4.8 4194 (NrC)(CrC)2 4.2 495 (7:0) 4.4 4039
4201 (NrC)(CrC)3 4.3 512 4.3 4043
(66)(OrC) 4.7 4277 (OrC)(CrC) 4.0 641 (66) 5.1 4103
(66) (6) (OrC) 4.6 4430 4.0 659 4.9 4114
(75) 4.3 4535 4.0 763 4.2 4141
4.4 4542 (OrC)(CrC) 3.8 1075 4.8 4146
4.4 4546 O 4159
4.3 4553 (OrN) 3.9 1276 4.9 4160
(63)(66)2 5.1 4729 O 4.3 1285 4.7 4187
(64) 4.5 4924 (6) 3.9 1417 (66)2 4.6 4220
(65) 4.5 5081 1440 5.1 4225
(66) 4.6 5110 4.5 1679 (66) (CrC) 4.7 4233
(N6) 3.9 5310 1741 (66) (OrC) (CrC) 4.4 4292
3.9 5315 3.8 1756 (66) (OrC) (CrC)2 4.7 4294
(N6rO) 4.0 5504 1792 (66) (6) 4.8 4354
(N65) 4.4 5574 4.2 1803 4.7 4362
(N66rO) 4.3 5868 1839
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
(66) (6) (OrC) (CrC) 4.8 4446 (0:C)(C:C) 4.1 643 (N26:0) 4.3 6512
O 4.1 666 (N266)(0:N) 4.7 6697
(75) 4.2 4537 4.0 682 6
4.4 4544 (0:C)(C:C)2 4.1 780 (N45) (6) 4.0 7036
(6552) 4.8 5138 4.1 781 3.8 7042
(N6) 3.8 5373 (OrC)(NrC) 4.1 965 (N465) 3.9 7132
(N6)(OrC) 3.9 5412 (OrN) 3.8 1255 3.9 7132
(N6) (6) (CrC) 4.1 5456 (OrN)(CrC) 4.0 1289 4.3 7147
(N6:0) 3.8 5521 O 4.3 7147
3.8 5526 (6) 3.9 1611 (N466) 4.4 7306
(N65) 3.9 5556 4.1 1827 Or rO
4.5 5573 1840 ^rV6S0) 4 3
' 7349
(N65)(6)(OrC) 4.3 5583 (6)2(CrC)2 4.4 2098 (N65rO) (6) (OrC) 4.3 7391
(N26) 4.2 6164 4.2 2100 N
4.2 6188 (S)2(NrN) 4.0 2159 (063rO) (6) (OrC) 4.7 7778
3.8 6212 (6) (NrC) 4.0 2411 6
(N26:0) 3.9 6410 (S)2(NrC)2 4.2 2533 (0:ON5 rC) (S)2 4.3 7807
3.8 6420 (S)(NrC)(CrC) 4.4 2597 (SSS)(OrC) 4.3 8110
(N266:0) 4.3 6730 (6) (NiC) 4.0 2620 O
(N263) 4.6 6789 4.2 2621 (SN25:N)(6) 4.3 8391
4.6 6793 (S)(OrC) 4.2 2745 (S06) 3.6 8403
(N364) 4.4 7015 (6) (OrC) 3.8 3277
(N4S)(S) 4.1 7033 O
4.0 7039 (S)(OrC)2 4.0 3305 Xmax : 230-230. 5my
4.1 7044 O 4.3 3543
(N465) 4.5 7086 4.0 3577 (CrC)2 3.8 98
4.0 7137 (6) (OrN)2 4.4 3718 3.9 100
4.1 7140 O (CrC)4 3.8 185
4.3 7162 (6)(OrN)2(CrC)2 3808 (CrC)5 3.3 198
(05) 3.3 7405 O (CrC)(CrC) 4.5 256
(05) (OrC) (CrC) 4.1 7480 (6) (OrN) (OrC) 4.0 3868 (CrCrCrC) 4.0 300
O 4.1 7481 O (NrC) 3.4 326
(OS)(OrN)(CrC) 7497 (66) 5.0 4109 4.1 368
O 4.7 4117 (NrC)(CrC) 4.3 471
(OS)(S)2 4.3 7523 4.8 4161 (NrCrN) 2.3 581
(OS)(S)3 4.4 7527 4.8 4206 (OrC)(CrC) 4.0 661
(05) (6) (OrC) (CrC) 2.9 7548 (75) 4.2 4539 4.1 665
(063rO)(6) 4.7 7777 4.0 4551 (OrC)(CrC)3 4.2 849
(OrONSrC) (S)2 4.2 7813 (Or63rO) 4771 (OrC)(CrC) 4.3 1024
(OrON5rC)(6)2(OrN) 4.3 7849 4.3 4797 6 4.0 1037
O 4.3 7851 (N6) 4.0 5269 3.6 1039
4.2 7853 (NS)(NS) 3.8 5489 (OrC)(NiC)(CrC) 4.0 1176
(OrONSrC) (05) (6) 4.1 7896 (N65) 4.3 5575 6
(ONSS)(S) 4.3 7913 (N66) 4.5 5667 (OrN) 3.8 1275
(SNSSrN) 4.2 8334 (N66rO) 4.2 5862 6
4.2 5884 (6) 3.9 1396
(N2S) 3.9 6211 3.9 1398
Amax.r 229-229. 5my 4.3 6232 4.1 1431
4.1 6329 4.0 1449
(NrC) 4.1 313 4.1 6330 4.1 1658
3.8 345 (N26rO) 4.0 6409 (S)2 4.8 1873
4.0 367 3.8 6412 4.1 1932
3.9 371 3.8 6421 (S)(CrC)2 4.5 2056
(NrC)(CrC) 4.2 464 4.4 6471 (S)2(CrC) 4.2 2081
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
(6) (NiC) 3.9 2627 (75) (6) 4.2 4592 (ON65) (6) 3.8 7911
'(G)(OrC) 4.1 2648 (0:63:0) 4.5 4813 3.8 7912
3.8 2664 4.6 4815 (ON2665) 4.2 7950
2668 (635) 4.7 4887 (S6:0) 3.9 8101
3.7 2681 (G4)(NrC) 4.5 5018 (S665)(0:N) 4.4 8143
4.1 2682 (645) 4.8 5060 6
4.0 2701 (N6) 4.0 5271 (SN5) 3.6 8160
4.1 2715 4.2 5278 (SN5:0) 3.8 8220
3.3 2756 4.1 5304 3.7 8222
(6)(0:C)(C:C) 4.0 2943 (N6:0) 3.9 5523 (SN665) 4.6 8349
4.0 2951 (N66) 4.6 5689 (S2N26655) 4.5 8402
3.9 2955 4.0 5701 (0:80655:0) 4.5 8404
4.3 2986 4.3 5705 (Se665)(0:N) 4.4 8416
(6)2(0:C)(C:C) 4.1 3070 4.4 5726 O
(6)2(0:C)(C:C)2 4.4 3097 4.3 5753
(G)2(OrC)(NrC)(CrC) 5755 *max.: 241-241. 5my
4.1 3130 (N66:0) 4.1 5893
(6) (OrC)(CrC) 3.8 3157 (N665) 4.6 5945 none 3.3 30
N (NG4) 4.5 6066 (CrC)2 4.4 120
(6) (OrC) 3.9 3186 (0:N25:C)(6) 4.1 6100 4.3 142
O 3263 4.1 6106 (NrC)(CrC) 4.2 394
3.9 3264 r Or N
c.rWAx / 9 A1 -, o 4.3 411
(
4.1 3298 0: 23-C)(6)
N 4 2 6113
' (OrC)(CsC) 4.2 639
(6) (OrC)
A 2 3321 R:)(6)
(S:N 5. °WM / i 6124
4.1 AIO/ 4
-° 647
2 C 4>2 6?4
(7:0) 4.4 4054 (ON65) (6) (O: N) 4.1 7923 (6)(0:N) 4.0 3479
4.9 4059 6 6 3.8 3643
(66)(0:C) 4.6 4273 (SS)(Or(^)2 4.0 8017 (6) (O: N) (0:C) 4.0 3889
(66)(0:N) 4.9 4327 O 6 6
(63) 4.7 4632 (S5)(6) 4.0 8033 (N:6:N:N) 3.9 3931
4.8 4635 (SN5) 8171 3.7 3932
4.8 4636 3.8 8178 (66)(C:C) 4.7 4239
4.8 4642 (SN5:N) 3.9 8218 (66)(0:C) 4.3 4285
4.8 4657 (SN5:0)(6)(C:C) 4.1 8225 (66)(0:N) 4.3 4333
(63)(0:C) 4.5 4705 (SN65) (6) 3.7 8285 (66)(6)2 4.7 4369
6 (SN665) 4.6 8352 (66) (6) (N:N) 4.2 4417
(0:63:0)(0:N) 4.6 4841 6
6 (75) 4.4 4529
(66) 4.6 5127 Amax :259-259.5my (665:0) (0:C) 4.7 4615
(N6) 3.5 5345 * N
(N6)2 4.0 5387 none 3.2 40 (665:0) (0:C) 4.7 4616
(N6)(0:C) 3.2 5410 (N:C) 4.3 309 6 4.6 4617
(N6:0)(6) 3.6 5550 (N:C)(C:C) 4.3 434 4.8 4618
(N66) 4.3 5688 4.4 450 (63) 4.8 4634
(N63) 5.0 5968 4.2 459 4.8 4650
4.8 5988 (OrC)2 1.3 625 (63)(6)2 5.0 4721
4.8 6011 (0:C)(C:C) 4.0 697 (635) 4.6 4884
(N25)(6)2 4.4 6080 4.1 709 (64) 4.5 4969
(N26) 6184 4. ,4 723 4.5 4970
3.9 6241 4.2 725 (N5)(0:C) 3.7 5205
3.3 6298 3.8 768 6
3.4 6299 (0:C) (CiC)2 4.4 775 (N6) 3.6 5314
3.7 6304 (OrC) 1.8 977 (N6)(6)(N:N) 4.1 5481
3.7 6322 N (N6:0) 3.8 5520
(N26)(6) 4.3 6380 (OrC)(CrC)2 1081 3.8 5529
(N26:0) 3.8 6434 O (N66) 4.0 5691
4.0 6479 (6) 2.7 1342 4.0 5700
(0:N26:0) 3.9 6565 2.3 1349 (N66) (6) (0:C) 5840
3.9 6566 1354 6
4.0 6577 3.0 1393 (N63) 5.3 5978
(N265) 3.6 6634 2.6 1436 4.9 5980
(0:N266:N) 4.2 6761 4.2 1462 4.9 5992
(N2665) 4.6 6776 3.3 1510 (N26) 3.6 6201
(N2635) 4.6 6840 3.8 1642 (N26:0) 3.7 6420
(N3S) (6) 3.9 6877 4.3 1691 3.8 6440
(N36) 3.6 6904 1733 3.6 6547
(N36)(0:C) 4.3 6941 (6)2 4.4 1952 4.3 6472
6 (6)(C:C) 4.2 1992 3.7 6473
(N36)(6) 4.2 6944 3.9 2013 (0:N26:0) 3.8 6576
(N365) 3.8 6957 4.3 2019 (N266)(0:N) 4.3 6703
3.7 6963 4.5 2052 6
(N45:N) 3.1 7050 (6)(N:N) 3.9 2147 (N266) (6) 4.6 6707
(N465:0) 4.1 7183 (6)(0:C) 3.8 2717 (N2635) 4.6 6833
4.2 7208 (6)2(0:C) 4.2 2860 (N3S) (6) 2.5 6875
(0:N466:0) 3.9 7336 (6)2(0:C)2 4.3 2911 (N365) 3.8 6952
(OS)(NiC) 4.3 7415 (6) (0:C) (CrC)5 3035 3.8 6953
(05)(6)3 3.9 7529 (6)2(OrC) (CrC) 3044 (N466) 7309
(OS)(S)4(OrC)2 4.5 7547 (S)4(OrC)4(CrC) 4.6 3126 (0:N466:0) (OrC) 3.9 7337
(S)(OrN) 3.6 3461 O
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
4.4 2899 (N6) (Or^)2 5435 (0:C) (CiC) (CrC)3 4.0 1154
(6)2(0:C)2 4.1 2926 O 6
(6)2(0:C) 4.3 3151 (0:N65:C) (OrC) 4.4 5612 (6) 3.3 1386
N 6 1494
(6)(0:C) 3.8 3296 (N66) 3.6 5661 4.1 1495
6 3.0 3301 3.4 5743 4.2 1499
(6) (OrC) (OrC) (CrC) 4.1 3418 (N66rO)(6) 4.4 5911 2.7 1522
O (N63) 4.8 5996 2.7 1525
4.1 3435 4.8 5998 2.6 1526
(6) (OrN) 3.9 3509 (N64) 4.9 6052 3.2 1532
O 3.7 3634 (N25rC)(6)4(OrC)2 4.7 6093 3.2 1542
(6) (OrN) (OrC) 4.1 3862 (N26) 4.2 6169 2.8 1655
O 4,2 3866 3.2 6318 2.6 1751
(6)2(SrC) 3908 3.8 6325 2.3 1811
(Nr6rC)(6)2 4.3 3938 4.6 6360 (6)2 4.3 1905
(Or6rC)(6)2 4.4 4010 (N26:0) 3.6 6412 1918
(7:0) 4.3 4055 3.7 6423 1949
4.4 4060 3.8 6480 (6)(CrC) 4.2 2032
(66)2(N:N) 4.3 4246 (0:N26:0) 3.6 6583 (6)2(CrC) 4.0 2065
(6G)2(NrN) 4.1 4247 (N265)(0:N) 4.4 6652 (6)2(NrN) 3.8 2250
6 4.3 4248 O 4.3 6654 (G)2(NrC) 4.2 2520
(66)2(N:C)2 4.7 4257 (N3G) 3.3 6938 (G)(OrC) 3.9 2740
(GG)(OrC)(CrC) 4.0 4292 (N365) 3.8 6964 2818
(6G)(OrC)(CrC) 4.6 4326 3.8 6971 4.3 2834
O (N365)(0:N) 4.3 7000 (6) (OrC)2 4.1 2854
(66) (6) (NrN) 4.1 4400 O 4.0 2855
(Nr66rN) 4.3 4450 (N465) 3.8 7065 (6)2(OrC) 4.3 2865
(Or66rO) 4.3 4469 4.1 7072 (6) (OrC) (CrC) 3127
4.5 4493 4.0 7099 (6) (OrC) 4.1 3267
(75) 4.4 4533 4.2 7119 6 3275
4.4 4535 4.2 7120 (6)2(OrC) 4.3 3324
(63) 4.9 4652 4.2 7121 A
(63)(OrC) 5.1 4699 (N465rO) 4.0 7233 (6) (OrC) 3448
(64) (NrC) 4.6 5020 (OrN465rO) 4.0 7253 Cl
(6452) 4.6 5106 (OrN466rO) 3.7 7335 (6) (OrN) 3.7 3535
(N6) 3.5 5245 (OrN466rO) (OrC) 4.1 7339 O 3.8 3550
3.6 5248 6 4.2 3567
3.7 5257 (N565)(6) 3.7 7381 3.8 3570
4.0 5275 (066rO)(6) 4.6 7717 4.0 3635
3.6 5319 4.6 7720 (7rO) 4.5 4058
3.6 5321 (OrONSrC) (6)2 4.2 7806 (7rO) (6) (OrN) (CrC) 4.2 4092
3.5 5348 (S5)(6)2 8043 6
3.8 5349 (SeS) (6)2 8405 (66)2(NrN) 4.4 4249
3.5 5350 (Se5)(6)2(OrC) 8408 6
(N6) (CrC) 3.7 5401 (66) (OrN) 4.4 4330
3.7 5404 4.1 4337
(N6)(OrC) 3.4 5416 Amax. r 263-263. 5my (66) (6) 4.9 4359
N 4.8 4360
(N6)(OrC) 3.6 5425 none 2.5 28 (Or66rO) 4.3 4463
6 3.7 5426 (CrC)2 3.4 104 (63) 4.9 4663
3.5 5427 (NrC)(CrC) 4.3 431 (63)(OrC) 4.9 4704
3.6 5429 (OrC)(CrC) 3.7 758 6
3.5 5432 (OrC)(CrC)2 4.4 792 (635rC)(OrC) 4.8 4892
(OrC)(CrC)5 4.0 860 6
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
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(6)2(0:C)2(N:N) 4.1 3399 (0:N466:0) (0:C) 3.9 7338 (75) 4.3 4542
6 6 6 (63) 4 . 9 4665
(6) (OrC) 3.9 3443 (066:0) (6) 7722 (64) 5.1 4907
S 4.1 7724 5.2 4908
(6)(0:N) 3.8 3584 (0:0665:0) 4.5 7761 5.1 4909
6 4.3 3620 (S5)(0:C) 3.9 8002 5.2 4912
3.7 3653 (S5)(0:C) 4.2 8014 5.0 4937
(66) (OrC)(CrC) 4.5 4316 6 (64)(C:C) 5.1 5012
6 4.4 4320 (S5)(N6)4 4.4 8054 (65) 4.8 5089
(66) (OrN) 4.3 4336 (S5) (N4S) 4.0 8055 (655) 4.6 5107
(66) (6) (NrN) 4.3 4401 (S665)(0:N) 4.2 8151 (N6) 3.9 5262
(66) (6) (NrC)2 4.9 4418 O 3.4 5351
(0:66:0) 4.2 4487 (SN5) 3.9 8167 3.9 5352
(75) 4.3 4546 (N6)2 4.0 5377
(63) (6) 5.0 4709 (N65) 3.8 5569
(635:0) 4.8 4896 Xmax : 269-269. 5my (N66) 3.6 5764
(65) (NrCrO) 4.7 5096 " (N66:0) 3.6 5862
(655) 4.8 5108 (CrC)4 4.2 182 (N665)(0:N) 4.4 5954
(N6) 3.6 5260 (CrC)(CrC)2 4.5 268 6
3.4 3566 (OrC)(CrC) 3.9 752 (N63) 4.5 5982
(N65) 4.1 5557 (OrC)2(CrC) 3.9 910 (N26) 3.7 6225
(N66:0) 3.8 5876 4.1 914 3.9 6327
(N66:0)(6) 4.5 5910 (OrN)(CrC) 3.7 1297 (N26:0) 4.0 6506
(N63) 4.8 5987 O (N26:S) 4.2 6543
4.3 6005 (S-Fe)(OrC) 3.9 1319 4.3 6549
(N635) 4.8 6049 (6) 2.8 1597 4.2 6554
(N26) 3.6 6157 3.2 1643 (N265)(0:N) 4.4 6657
3.7 6159 3.1 1665 6
3.7 6180 4.3 1696 (N266:0) 4.0 6738
3.6 6187 2.5 1719 (N263) 4.4 6789
6192 (6)2 4.4 1892 (N3S) (6) 4.1 6881
3.6 6210 (6) (NrC) 2.9 2631 (N36) 4.2 6923
3.6 6228 (6) (OrC) 4.1 2753 (N465) 4.2 7113
3.6 6267 (6)2(0:C)2(C:C) 4.3 3120 4.2 7114
4.2 6290 (6) (OrC) (CrC) 4.1 3128 4.1 7115
3.5 6305 (6) (OrC) 3134 4.0 7170
(N26:0) 3.5 6408 N (0:N465:0) 4.0 7262
3.6 6427 (6) (OrC) 2.5 3181 4.0 7276
6454 6 4.3 3268 4.0 7278
6455 (6) (OrC) (OrC) 3.9 3407 (05) 7404
3.9 6478 6 (06:0) 3.9 7598
3.9 6481 (6) (OrN) 4.7 3494 (0:065:C)(6) 3.9 7636
3.8 6482 O 3.8 3590 (066:0) (6) 7711
(N26:S) 4.5 6563 (6) (0:N) (CrC) 3.8 3780 7721
(0:N26:0) 4.0 6575 O (0645) 4.6 7786
4.0 6580 (0:6:0) 4.3 3990 (ON65) (6) (OrN) 4.5 7922
(N465) 4.2 7081 (0:6:N:N) 3.5 4038 6
3.9 7129 (66) 3.7 4161 (SN65) 4.2 8260
3.9 7130 (66) (OrC) 3.7 4309 4.2 8272
4.1 7156 6
(0:N465:0) 4.0 7269 (66) (6) (NrN) 4.1 4377
(N466:0)(0:C) 4.0 7327 (66) (6) (IjTrN) 4.1 4415 Amax : 270-270. 5mU
O O
(0:66:0) 4.3 4466 (CrC)3 4.3 157
absorbing absorbing absorbing
chromophore loge no . chromophore loge no. chromophore loge no.
(S5)(0:C) 3.9 8005 3.7 4148 (S5) (0:ON5:C) (6) 4.1 8073
6 3.7 4152 (SN5)(0:£) 4.1 8189
(S5)(0:ON5:C)(6) 4.0 8071 3.7 4192 O
4.0 8072 (66) (6) 3.9 4358 (SN5) (6) 3.8 8386
(SN65) 4.4 8267 (0:63:0) 4.5 4802 (SeN265)(6)2 4.5 8441
(SN63:0) 4.0 8374 4.2 4834
(64) 4.8 4919
4.6 4920 Amax r 275-275. 5my
*max.: 274-274. 5my 4.7 4921
5.1 4935 (C:C) 3.7 75
(CiC)2 3.5 96 5.0 4936 (C:C)2 3.8 111
(C:C)3 4.5 160 5.1 4954 3.7 128
(CrC)3(CiC)3 4.8 289 4.6 4965 (CrC)3 3.7 164
(NrC)(CrC) 4.5 410 (N6) 3.6 5365 (CrC)(CrC)2 4.8 264
(OrC) 2.0 616 (N6)2(OrC)2 3.9 5437 (CiC)4(CrC)2 5.0 290
2.4 617 O (NrC)2(CrC)2 4.6 541
(OrC)(CrC) 4.0 754 (N66) 3.3 5744 4.6 542
(OrC)(CrC)2 4.0 788 3.4 5781 (OrC)(CrC) 3.3 718
4.5 796 (N75rO) (NrC) 4.6 5924 (OrC) (CrC) (CrC) 4.1 950
(OrC)(CrC) 4.3 1041 (N665) 4.6 5943 (OrC)(CrC) 4.3 1046
O (N63) 4.3 5973 6
(6) 3.3 1361 4.6 5979 (OrC)(NiC)(CrC)3 3.9 1189
2.9 1363 (N26) 3.7 6243 6
2.9 1409 3.6 6312 (OrN) 2.2 1273
1613 3.9 6350 6
3.7 1662 3.9 6351 (6) 2.9 1375
1736 (N26rO) 4.0 6431 4.1 1411
(6)2 4.4 1880 3.7 6490 3.4 1550
4.4 1891 3.8 6503 3.4 1561
4.5 1955 (SrN26rO) 4.0 6609 3.3 1567
(6)5 4.6 1973 (N266rO)(OrN) 3.6 6749 3.3 1568
(6) (CrC) 4.3 2036 6 3.0 1570
(6)2(CrC)2 4.4 2104 (N365) 3.8 6954 3.3 1584
(6) (OrC) 3.0 2690 4.0 6955 3.4 1716
4.0 2747 3.9 6959 1741
3.9 2751 4.0 6962 1783
4.1 2824 (N365)(OrN) 4.2 6992 (6)2 4.2 1923
4.1 2825 O 4.1 6996 2.8 1940
(6) (OrC) (CrC) 4.1 2988 (N465) 3.9 7062 (6) (CrC) 4.0 2035
(6) (OrC) 3.0 3166 3.9 7164 (6)2(N:N) 3.8 2204
O 3262 (N465rO) 3.9 7198 3.9 2262
2.7 3287 4.3 7205 (6)2(NrC) 4.2 2499
(6)(OrC)2 3.0 3304 4.3 7206 4.3 2518
6 3.1 3313 (OrN465rO) 4.0 7273 (6)2(NrC)2 4.3 2545
(6)2(OrC)(CrC) 4.2 3375 4.0 7274 (6)(N:C) 3.0 2645
O 3.9 7280 (6)(OrC) 4.0 2672
(6)(0:N) 4.3 3568 4.0 7281 4.2 2729
O 3.5 3666 (N565:0) 3.8 7389 4.0 2771
(6) (OrN)2 3688 (066) (6) 4.3 7649 4.1 2803
O 4.2 3695 (066rO) 4.0 7672 4.1 2822
(6) (OrIjO (O: (JJ) 4.0 3888 (0-.ON5 rC) (6)2 4.1 7839 W2(OrC)2 4.2 2916
O O (ON65) (OrIp) 3.8 7905 (6)3(OrC)2 4.3 2934
(Or6rO) 4.4 3987 O (6)(0:C) 3.4 3171
(66) 3.7 4111 (ON65rO) 3.7 7937 O
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
(N26) (NiC) 3.6 6369 3.2 1602 (N66) (6) (C:C) 4.3 5827
(N26:0) 3.6 6395 3.5 1605 (N75) (NrC) 4.7 5922
6463 3.5 1608 (N665) 4.6 5943
4.1 6464 1725 (N665) (Orljf) 4.4 5953
(N26:0)(6) 3.9 6524 1779 O
(N265) 4.2 6638 3.2 1824 (N26:0) 4.0 6458
3.7 6643 1825 3.9 6459
(N266:0) 4.4 6734 1848 3.7 6460
(N266:0)(0:N) 4.2 6753 (6)2 4.6 1948 (S:N26:0) 4.3 6614
O (6)4(N:C)2 4.3 2579 (N266) 3.8 6677
(N2635) 4.5 6832 (6) (NrC) 3.2 2617 (N2665) 4.5 6771
(N264)(6) 4.6 6850 (6)(0:C) 3.1 2701 (N365) 3.8 6976
(N35:0)(6) 3.9 6899 4.0 2793 3.8 6977
(N365)(0:N) 4.1 6994 (6)2(0:C)2 4.0 2930 4.0 6978
6 (6) (OrC) 3.2 3179 (N365)(0:N) 3.9 6991
(N465:0) 4.0 7184 6 3.9 3288 O
3.8 7202 (6)(0:C)2 3.1 3304 (N465) 4.3 7091
4.3 7207 O 3.1 3306 (N465:0) 3.9 7227
(0:N465:0) 4.1 7291 (6)2(0:C) (0:C) 3.8 3411 3.8 7234
/°:M AA m QQ 7*// ° (066:0) (6) 7695
(0.N466:0) 3.9 7344 (6)(0:N) 3.5 3604 4.0 7723
(05) (OrC)(CrC)6 4.0 7451 6 (0665) 4.3 7748
(066) (6) 4.2 7650 (Or6rO) 2.7 3951 (0:ON5:C) (6)2 4.2 7816
(066rO) 4.0 7675 2.6 3954 (S5) (6) 4.2 8038
(066rO)(6) 7716 4.3 3991 (SN5) 4.3 8176
(0665) 4.2 7747 (Or6:N) 4.5 4037 (SN5:S) (6)2(C:C) 4.1 8230
(S5) (CrC) 4.1 7987 (66) 3.7 4101 (SN665) 4.1 8348
(SN5) 8171 3.8 4129 (Se665) 4.3 8412
8173 4208
(SN65) 8251 (66) (CrC) 3.9 4237
4.1 8264 (66) (Or C)2 3.7 4312 Xmax r 282-282. 5my
4.3 8274 6
(SN25)(6) 3.7 8388 (66) (6) (NrN) 4.2 4398 none 3.0 48
(Or66rNrN) 4.0 4527 (CrC)2 4.1 125
(63)(6) 4.8 4712 (NrC)(CrC) 4.5 419
Amax.r 281-281. 5mu (Or63rO) 4.0 4806 (OrC) 1.1 586
4.2 4813 (OrC)2 1.4 620
(CrC)2 4.4 136 4.3 4814 621
(CrCrC)(CfC)2(CrC)2 4.3 4827 (OrC)(CrC) 4.4 727
4.8 299 (64) 4.9 4903 3.3 757
(NrC)2 386 4.7 4959 (OrC)(CrC)2 4.4 804
(OrC) 1.5 598 4.8 4962 (OrC)(CrC) 4.3 1043
1.4 600 4.9 4991 6
1.4 608 (64)(CrC) 4.8 5014 (OrC)2(CrC)2 4.5 1129
1.3 614 (64)(OrC) 4.4 5026 6
(OrC)(CrC) 4.4 1050 (6452) 4.7 5106 (OrC)(NrC)(CrC)2 4.3 1183
6 (N6) 3.9 5315 6
(OrN) 1270 4.0 5328 (6) 3.2 1593
6 (N6rO) 4.1 5531 1738
(6) 1341 (N65) 3.8 5553 1739
1482 3.7 5555 3.0 1829
1490 3.8 5556 1832
3.3 1583 3.9 5563 3.2 1846
1596 (N65)(Or6rO) 4.0 5585 (6)2 4.4 1893
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
(6)2 4.4 1890 4.0 5281 (6) (0:C) (CrC)2 3.5 3013
(6)2(C:C) 4.5 2066 5291 (6)2(0:C) (C:C) 3082
(6)(N:N) 3.8 2151 4.5 5336 (6)(0:C) 4.3 3190
(6)(N:C)(C:C) 2591 (N6) (N5) 4.0 5492 6 3201
(6) (OrC) 3.1 2709 (N65) (0:6:0) 4.1 5584 4.2 3269
4.0 2779 (N66) (0:1(1) 5813 3286
3.9 2804 O 2.8 3290
(6) (OrC)(CrC) 4.4 3003 (N64) 5.0 6059 (6) (OrC)3 3322
(6)2(OrC)(CrC) 4.2 3051 4.5 6063 O
3078 (N26) 4.0 6246 (6) (OrN) 4.0 3607
3079 (N26:S) 4.0 6545 O 3.8 3658
3083 (N2665) 4.2 6765 (66) 3.8 4114
(6) (Or (JJ)2 3149 4.1 6775 3.7 4117
N (N465) 4.2 7075 4.0 4118
(6)(OrC)(CrC) 4.5 3154 (0:N465:0) 4.2 7283 (66) (6) (OrC) 4.0 4441
A 4.5 3155 (05) (6) 4.1 7512 6
4.5 3156 (0:05:C)(6)2 4.2 7559 (76) 4.6 4555
(6)(0:C)2 3315 (0:05:C)(6)3 3.5 7563 4.5 4567
6 3.3 3318 (06:0) (OrC) 3.8 7609 4.6 4570
(6)(0:C)(C:C) 4.3 3361 (06rO)(Or£) 3.6 7612 (0:63:0) 4.3 4819
6 4.3 3363 O 3.9 4820
(6)2(0:C)(C:C) 4.4 3380 (066:S)(0:C) 4.0 7746 3.8 4821
6 O (635) 4.4 4877
(6) (OrIjI) 3.7 3536 (0:ON5:C) (6)2 4.2 7818 (635)(0:C) 4.4 4890
O 3.8 3555 4.2 7820 N
(0:6:0) 4.1 3976 (ON65) 4.4 7901 (64) 4.9 4924
4.2 3979 (S65) 4.0 8104 4.9 4929
(66) 3.8 4105 (SN5)(0:C)2 3.6 8192 4.9 4930
3.8 4184 O 4.7 4949
<«)2
(66)(0:j)
4.i «» (•=«»;>
3.8 42,9 (SiSB5|0)(s5)
3.' «37
^^
l;l Uf1
4.9 4973
(66) (OrIjO 3.9 4348 (SN65) (6) 4.1 8284 (65) 4.7 5074
O 4.6 5088
(66) (6) 4.0 4353 4.5 5089
4.0 4354 Xmax : 289-289. 5my (66) 4.7 5131
(0:66:0) 4.1 4497 * (N6) 4.1 5311
(75) 4.6 4560 (CrC)4 4.3 187 4.2 5359
(0:63:0) 4.3 4822 (OrC)(CrC)2 4.4 807 (N6)2(CrC) 3.9 5407
(635) 4.3 4879 4.4 808 (N65) 3.6 5575
4.5 4885 (SrC) 4.0 1312 (0:N65:N65:0) 5643
(64) 5.0 4927 (6) 3.5 1448 (N66) (NrN) 4.0 5810
5.0 4931 3.3 1450 (N665) 4.2 5944
5.0 4952 1702 4.1 5949
4.8 4961 3.0 1829 (N64) 4.9 6058
4.7 4982 1832 4.9 6065
4.9 4988 (6)2 4.5 1947 (N25)(6)4 4.6 6082
(64)(N:C) 4.8 5018 (6) (NrN) 4.2 2150 (N26) 3.9 6178
4.9 5019 (6)2(N:C)2 4.6 2555 3.6 6219
(64) (OrIjO 4.7 5041 (6)2(OrC) 4.2 1877 4.1 6352
O 4.4 2883 (N26:0) 3.7 6419
(65) 4.7 5081 4.1 2886 (N265) 4.0 6639
(N6) 3.5 5270 (6) (OrC) (CrC) 3.5 2962 (N266:0) 3.4 6731
absorbing absorbing absorbing
chromophore loge no . chromophore loge no. chromophore loge no.
(65) 4.9 5067 (Se665)(0:N) 4.4 8416 (N5) (OrC)2 4.0 5212
(6452) 5.1 5106 6 O
(66) 4.6 5111 (N6) 3.8 5305
(N5) (OrC)2(OrC) 3.9 5222 Amax. : 293-293. 5my (0:N65:N65:0) 4.6 5642
O (N66)2 4.0 5806
(N6) 3.9 5316 (0:C) 1.3 613 (N665) 4.2 5927
(N6)(C:C) 3.6 5397 1.5 615 4.2 5928
(N6)(6)2 4.7 5446 (0:C)(C:C) 4.3 720 4.2 5941
(0:N65:N65:0) 4.6 5638 4.3 771 (N63) 3.9 5974
(N66) 3.6 5668 (0:C) (CiC)2 3.9 811 (N26) 3.6 6230
3.8 5680 (Or^)(NrC) (CrC)2 4.2 1187 2.5 6298
3.8 5695 O (N26) (NrC) 3.7 6367
3.7 5785 (6) 3.6 1447 3.7 6368
3.7 5788 2.5 1449 (N26:0) 3.9 6484
(N66:0) 4.0 5893 3.1 1469 (N26:0)(6) 6516
4.0 5894 1614 (N26:S) 4.0 6540
(N65) 4.8 6067 3.3 1685 4.3 6552
(0:N25:C) 3.9 6097 (6)2 3.9 1915 (0:N26:0) 4.0 6598
(N26) 3.1 6151 4.0 1916 (N265) 3.8 6637
3.7 6341 3.7 1917 (N266:0) (6) (0:N) 4.0 6756
(N26:0) 3.6 6444 (6)(C:C) 2.9 1987 6
(N26:S) 4.2 6546 (6)2(N:C)2 4.1 2532 (N26/) 4.6 6849
4.1 6556 4.2 2548 (N465) 4.1 7111
4.2 6557(6)3(N:C) 4.4 2565 ,0.- , .
(
(N265) 3.9 6644(6)(0:C) 3.4 2706 0:V5-0) 4
'° 7305
(N265)(0:C) 3.9 6649(6) (0:C) (CrC)2 4.4 3015 (ON65) (6) 4.3 7917
O (6)(OrC)(CrC)5 3032 (S5) (Or(^) (CrC) 4.4 8024
(N266) 3.8 6681 (6) (OrC) 3.4 3216 O
(N2635) 4.7 6830 O (S5)(6)(0:C) 4.1 8048
4.6 6831 (6) (OrN) (CrC) 4.1 3766 (S665)(OrN) 3.6 8149
(N365) 3.8 6963 O O
(N365)(OrN) 3.8 6986 (Nr6rC)(6)3 4.4 3944
6 (66) 3.8 4149 Xmax.: 294-294. 5mp
(OrN465rO) 3.9 7288 (66) (CrC) 4.0 4232
f°:N «• m 4 1 7294
^ (66)2(NrC)2 4.3 4256 (NrC)2 391
H)r 4D3'u; 3.9 7302 (66) (OrC) 3.8 4270 (NrC)(CrC)2 4.2 503
(OrN466rO)(OrC) 3.9 7340 (66)(OrC)2 3.7 4312 (OrC) 1.7 605
O O (OrC)(CrC) 4.2 1044
(06.-O)(OrC) 3.7 7614 (66) (6) (NrN) 4.2 4396 O
O (665rO) 3.5 4610 (OrC)(CrC)o 4.6 1088
(065) (6)4 4.6 7633 (63) 4.1 4621 6
(066rO)(6) 7697 4.2 4622 (OrC)-(CrC) 3.6 1116
(OrON5rC)(6)2 4.3 7807 (6655) (NrC)2 4.6 4871 6 *"
4.4 7842 (635) 4.4 4882 (6) 1513
(ON65)(6) 4.3 7910 (635:C)(0:9) 4.2 4892 3.5 1555
4.3 7918 O 3.6 1609
(S65)(OrON5rC)(6) 4.3 8113 (64) 5.0 4925 1636
(SN5) 4.3 8180 4.0 4951 1726
(SN5)(6)(CrC) 4.3 8198 4.9 4991 3.5 1785
:0 3.8 8240 4.9 4995 3.6 1850
(SrSN5:C)(S5) 3.8 8242 4.9 4998 (6)2 4.0 1907
(SN65)(OrN) 4.1 8277 (6)7 4.7 5141 (6)2(C:C) 4.4 2071
O 5.0 5155 (6) (NrN) 3.8 2151
(SN65rO) 3.6 8339 (6) (NrC) 3.6 2626
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
(N265) (NiC) 4.0 6648 (0:63:0) 3.6 4824 Xmax : 297-297. 5my
(N266)(0:N) 3.9 6700 (635) 4.6 4887
6 (64) 4.9 4947 none 2.4 25
(N365) (0:1)1) 3.8 6987 4.9 4950 (CiC)5(CrC)2 5.2 291
O 4.6 4983 (0:C) 1.5 604
(N465) 4.1 7112 4.9 5000 (0:C)? 1.5 628
4.1 7216 4.9 5008 (OrC)TCrC)2 4.4 805
r°:N A^. m 1 Q 4
'9 501 (6) 4
'3 141?
(0.N465.0) 3.9 79QA
7296 (64)(N.:C) 4.8 °
5017 4.0 1515
(ON65)(6)(0:N) 4.3 7925 (64) (OrC) 4.7 5037 3.4 1684
O 6 3.7 1827
(ON365)(6) 4.5 7951 (64) (OrC) (OrC) 4.8 5039 (6)(C:C) 3.9 2021
(S5)(0:C) 4.1 7999 O 3.4 2028
(SN65) 3.9 8259 (64) (6) 5.1 5045 (6)2(C:*C) 4.3 2137
(SeN65) 3.3 8424 (64) (6)3 5.1 5048 (6)(N:C) 4.4 2435
(65) 5.2 5071 3.9 2461
4.7 5073 (6) (OrC)2 3.4 2839
Amax.r 296-296. 5my 4.9 5085 (6) (OrC) (CrC)2 4.3 3012
(Or65rO) 4.8 5105 (6)(OrC) 3.5 3240
(OrC)(CrC)2 4.5 798 (66) 4.6 5110 O 3.7 3265
4.3 829 (69) 4.6 5188 (6) (OrC)4 3.4 3323
(OrC)(CrC)3 4.2 832 (N6) 3.6 5268 O
(OrC)2(CrC) 1122 (N6)(OrC) 5434 (65rC) (6) (CrC) 4.3 4097
O O (66) 4.0 4125
(OrN) 1242 (N6rO) 3.9 5517 4201
(6) 3.6 1615 (N65) 4.1 5562 (66) (6) (CrCrC) 4.4 4375
3.2 1750 (N66) 3.8 5710 (Or 66rO) (CrC) 4.4 4516
1770 (N66)(OrN) 3.9 5818 (665rO)(OrC) 3.5 4616
1790 O O
(6)2 3.8 1925 (N66) (6) (CrC)2 4.4 5833 (63) 4.0 4627
(6) (OrC) 2660 4.4 5834 4.1 4628
2668 (N665)(OrC) 4.7 5950 4.0 4637
(6) (OrC) (CrC)5 3033 N (64) 4.9 4956
(6)2(OrC)(CrC) 4.2 3054 (N26) 3.6 6329 4.9 4957
(6) (OrC) 3.5 3204 3.6 6330 (6A)(0:C) 4.8 5036
O 3.4 3208 (N26rO) 3.8 6406 O
3293 (N2665) 4.2 6779 (64) (NrCrO) 4.9 5042
(6)2(OrC) (CrC) 4.4 3384 (N365) 6956 (645rO) 5.0 5065
O (N465) 4.2 7083 (65) (NrC) 4.7 5092
(6) (OrC1:) (OrC) (CrC) 3.1 3423 4.3 7094 (66) 4.8 5116
O 4.3 7150 5.0 5133
4
(6) (O: J) 3.9 3552 (0:^65:0) 4. 0 7300 ^2) -5 5182
(Or6rO) 2.6 3950 (05) (6)3(OrC) 4.4 7545 (N6) (6) 4.0 5442
4.0 4003 (065) (6)4 4.6 7634 (N6rO) 3.8 5504
(66) 3.9 4123 (066rO) 3.9 7673 3.6 5536
4.3 4128 (066rO)(6) 4.0 7686 (0:N65:0) 3.5 5598
(66) (CrC) 4.0 4233 (0:ON5:C) (6)2(OrN) 4.1 7882 (0:N65rN65rO) 4.5 5645
4.1 4235 O 4.5 5646
(66) (OrC)2 4310 (ON65) (6) 4.4 7913 (N63) 4.6 5981
O (SN65) 3.0 8261 (N64) 4.3 6052
(66) (6) 4.2 4359 (SN65) (6) 4.2 8281 (N2S) (6) (OrN) 3.7 6091
(66SrO)(OrCp 3.5 4618 0
O (N26) 3.6 6153
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
(6) (OrC) 3.3 3189 (N265)(OrC) 3.9 6650 (6) 3.4 1619
O 3.8 3237 6 (6)2 4.0 1866
3260 (N265)(0r^) 3.8 6655 (6)2(NrN) 3.9 2289
(6) (OrC)2(OrC) 3408 O (6)2(NrC)2 4.6 2527
O (N266) 3.6 6689 2.8 2557
(6) (OrN) 3660 (N266)(OrN) 3.9 6702 (6) (OrC) 1.8 2728
O O (6) (OrC1:) 3.4 3207
(6)2(OrN)2 4.1 3757 (N266rO) 2.8 6715 O 3.4 3256
O 2.9 6716 (6) (OrC) (CrC) 4.1 3344
(6) (OrN) (CrC) 3792 3.9 6717 O
O 3799 3.6 6720 (6)2(OrN) 4.2 3742
(6) (OrI^)2(CrC) 3806 (N2665) 4.1 6767 6
O 4.2 6780 (6) (OrN) (CrC) 3774
(N:6:C)(6)2 4.4 3940 (N264) 4.6 6849 O
(66) 3.5 4141 (N35)(6)2(CrC) 4.7 6894 (6) (OrN)2(CrC)2 3807
3.9 4203 ,Or , . O
(66) (OrC) 2.8 4282 \)r 4 D ' J
'y /JU4 (Or6rO) 4.1 4002
(75) 4.4 4567 (N466rO) (OrC) 3.9 7323 (Or6rN) 4.2 4025
(665rN) 4.0 4609 O 4.0 7325 (66) 2.5 4098
(63) 4.1 4625 (05) (NrC) 3.9 7414 (66) (6) (OrC) 3.9 4439
4.1 4631 4.4 7422 O
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
(665:0) (0:<jO 3.7 4617 (OrC)2(CrC)2 4.4 1133 Amax. : 305-3 05. 5my
(63) 4.1 4632 (6) 3.4 1414 (N:C) (CrC)2 4.7 484
4.2 4636 (6)2 3.9 1891 4.7 488
4.2 4643 4.0 1915 (N:C) (C-C)2 4.5 556
(0:63:0) 4.3 4748 4.2 1928 (NrC) 565
(64)(OrC) 4.7 5023 (6)2(N:N) 3.9 2275 (0:C) 1.2 585
(64) (6)4 5.1 5050 (G)3(NrN)2 4.5 2364 (0:C)(C:C) 4.5 656
(65)(N:C:0) 5.2 5095 (6)2(N:C) (C:C) 4.5 2605 1.6 663
(65:0) 4.3 5100 (6)(0:C) 3.5 2710 2.0 668
4.1 5102 (6)(0:C) 4.2 3266 746
(66) 4.8 5111 6 4.0 3268 (OrC)(CrC)7 3.9 875
(67) 4.8 5160 (6)(0:N) 4.1 3471 (OrC)(CrC)(CrC)2 4.4 955
(N5) (OrC) (OrC) 4.3 5220 (6) (0:N)2(C:C) 4.3 3804 (OrC)2(CrC)2 4.0 1136
o O o
(N6) 3.6 5278 (Or6rN) 3.9 4031 (6) 1635
3.4 5279 (66) 3.5 4205 1769
(N6rO) 4.0 5539 (66) (OrC) 3.8 4279 (6)2 3.9 1871
(N66) 3.5 5772 (75) (OrC) 4.5 4574 (6) (CrC) 4.1 2015
3.4 5774 (63) 4.1 4653 (6)2(CiC)2 4.5 2138
3.5 5784 4.1 4654 (6)2(NrN) 3.9 2287
(N26) 3.7 6189 4.1 4686 4.2 2315
(N26) (6) (OrI^) (NrC) 4.3 6394 (63) (6) 4.6 4710 3.9 2340
O (Or63rO) 4.4 4792 3.9 2344
(N26rO) 3.7 6445 (64) (6)4 5.1 5051 (6) (NrC) 3.6 2483
(OrN26rO) 3.8 6600 (65) 5.1 5072 (6)2(NrC)2 4.3 2545
(N266) 3.9 6676 (65) (OrCrN) 4.8 5096 (6) (OrC) 2808
(N266rO) 3.1 6726 (66) 5.1 5112 (6) (OrC)2 3.4 2848
3.1 6727 (68) 4.8 5165 (6) (OrC)2(CrC) 4.4 3042
3.9 6740 (N6)2 3.7 5392 (6)2(OrC) (CrC) 4.4 3049
(N275) 3.8 6762 (N6rO) 3.9 5518 (6) (OrC) 3.8 3144
(N2665) 4.2 6784 (N65) 3.9 5574 N
(N2665rO) 3.9 6788 (N66) 3.3 5740 (6) (OrC) 3272
(N465) 3.8 7071 3.2 5754 6
(OrN465rO) 4.2 7286 3.4 5782 (6) (OrN) 4.1 3586
(N466) 3.9 7315 Or 6 3.2 3661
(05) (OrC) (CrC) 4.7 7478 V/V'LM°; ^'J 01ZZ (6) (OrN)2 3.0 3670
O (N26) 3.9 6181 O 3.2 3710
(066:0) (6) 7693 3.7 6277 (6)2(OrN)2 4.4 3756
7702 2.7 6302 O
(0665) 4.3 7753 (N266) (6)2(CrC)2 4.6 6712 (6) (OrN) (CrC) 4.1 3765
(S5)(OrC) 4.0 8001 (N266rO) 3.9 6739 O 3775
(SN65) 4.1 8258 (N263) 6805 (6) (OrN) (OrC) 3892
(Se665) 4.3 8412 (N365) 4.0 6979 O O
(N465)(6) 4.4 7171 (Nr6rC)(6)2 3.3 3938
4.4 7173 (Or6rO) 2.5 3962
Xmax r 304-304. 5my (OrN465rO) 4.2 7285 (7:0) (6) 4.1 4070
(N466) 3.9 7311 (7rO) (6) (OrC) (CrC) 4.4 4089
(CrC)4 4.3 182 (066rO)(6) 4.4 7684 O
(NrC)(CrC)2 4.7 486 4.0 7687 (66) 3.7 4133
4.5 502 (063rO) 4.0 7772 3.9 4174
(NrC)2(CrC)6 4.1 548 (S5) (6) 4.2 8039 (66)2 3.3 4222
(OrC)(CrC) 1.7 703 (S665)(OrN) 4.0 8143 (66)2(NrC)2 4.5 4257
(OrC)(NrC)2 4.4 970 O (63) 3.8 4655
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
(N665)(6)(0:C) 4.6 5960 (66) 3.9 4187 (6) (OrN) (CrC) 4.2 3763
N (635:N) 4.1 4894 O
(N26) 3.9 6345 (64) (NrC) 4.9 5020 (66)2(OrC)2 4.1 4315
4.0 6352 (64)(0:C) 4.7 5028 O
(N26:0) 4.0 6428 (645) 4.8 5060 (66) (6) (N:N) 4.4 4385
(0:N26:0) 3.7 6589 3.9 5061 (66)(6)(0:C) 3.8 4432
(N265)(0:(p 3.9 6651 (65) 4.9 5076 (7S)(OrN) 4.3 4588
O 5.0 5085 O
(N263) 6806 (66) 4.8 5110 (65:0) 4.4 5104
(05)(6)3(0:C) 4.4 7546 (N5) 4.3 5201 (66) 5.3 5113
(SS)(CrC)2 4.3 7989 (NS)(OiC)2 4.4 5217 4.7 5130
(S65) 3.5 8107 O (67) 4.9 5147
3.2 8108 (N6) 3.5 5306 (N6:0) 3.9 5515
(N6)2(6)(C:C)2 4.7 5468 4.0 5533
(0:N65:C) 3.9 5611 (0:N65:C) 4.2 5609
x
max.: 308-308. Smy (N66) 3.9 5673 (N64) 4.4 6054
3.5 5746 (N26) 2.5 6316
(CrC)12 4.5 221 3.6 5747 3.1 6350
(NrC)(CrC)2 4.6 485 (OrN2SrC) (6) 4.2 6102 (N26) (6) (NrNrN)2 4.2 6393
4.6 490 (N266) 3.5 6661 (N26rO) 3.8 6396
(OrC)(CrC) 4.1 732 (N263) 4.0 6798 (N26rO)(6) 3.7 6520
(OrC)(CrC)2 4.3 820 (N365) (6) 4.5 7005 (N266) 3.9 6680
4.4 824 4.4 7006 (N2665) 4.4 6776
(OrC)(CiC) 1.3 947 (OS)(OrN) 4.1 7495 (N263) 2.8 6792
(OrC)2(CrC) 4.0 1121 O (N465) 3.7 7097
O (OrONSrC) (6)2 4.3 7813 4.0 7161
(6) 1744 (OrONSrC) (6)2(OrljO 4.1 7874 (06rO)(OrC) 4.0 7618
(6)2 4.4 1930 O O
(6)(CrC)2 4.5 2058 4.1 7877 (066rO)(6) 4.6 7727
(6)2(CrC)4 4.4 2115 (SS)(OrC)2 4.2 8011 (SN65-.N) 3.7 8336
(6)2(NrC)2 4.6 2535 O (SeSN26655) 3.6 8443
(6) (NrC) (CrC) 2585 (SN65) (6) (OrN) 8288
(6) (NrC) 3.4 2623 0
(6) (OrC) 4.1 2674 An^x r 310-310. 5my
3.4 2725 Amax.: 309-309. Smy
(6)2(OrC) (CrC) 3.3 3047 (CrC)7 5.7 241
4.3 3074 (CiC)3(CrC) 4.2 286 (NrC)(CrC) 4.1 500
(6)(0:(p 4.4 3194 (NrC)(CrC)2 4.3 496 (OrC)(CrC) 1.6 659
O 3.6 3226 (NrC)(CrC)3 4.5 510 1.7 672
3.5 3252 (OrC)2(CrC)2 4.4 1130 1.6 682
3263 6 4.2 733
3.6 3264 (OrC)(OrC)(CrC) 4.0 1195 (OrC)(CrC)2 3.8 782
3.5 3302 O 4.5 821
(6)(OrC)(CrC) 4.2 3354 (6) 3.3 1467 (OrC)(CrC)7 4.0 874
O 1830 (6) 1559
(6)(OrN) 4.1 3475 (6)2(NrN) 4.1 2283 (6)2 4.6 1868
(6)(0:N)(C:C) 3795 (6) (OrC) (CrC) 4.2 2995 (6)5 4.8 1975
6 4.1 3004 (6)5(NrN)4 4.2 2391
(6) (OrN) (NrC) (NrN) 4.2 3859 (6) (OrC) 3227 (6) (NrC) 2440
O 6 3.5 3245 (6)2(NrC)2 4.6 2541
(Or6rO) 2.9 3959 (6)(0rl{0 4.3 3529 (6)4(NrC)2 4.1 2570
2.6 3960 O 3.2 3645 (6)2(N:C) (CrC) 2601
4.2 4005 (6)2(0:ljO 4.3 3753 (6) (OrC) 4.0 2672
(Or6rN) 3.9 4034 O 2.7 2687
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
(6) (OrC) 4.5 3195 Amax. : 313-313. 5my Xmax : 314-314. 5my
O 3.8 3196
3.4 3210 (C:C)4 4.7 188 (CiC)3 4.4 179
(6)(0:C)(0:C)(C:C) 4.2 3437 (CrC)2(CrC)4 4.3 284 (N:C)(C:C) 4.6 412
O (N:C)(C:C)2 4.7 492 (N:C)(C:C)2 4.8 491
(6)(0:N) 4.0 3466 (NrC)(CrC)3 4.4 512 (OrC)(CrC)2 3.5 810
(6)(OrN) 4.0 3580 (NrC)(CrC)(CrC)2 4.7 559 (OrC)(CrC)3 4.1 839
O 2.8 3614 (OrC)(CrC) 1.4 641 (OrC)(CrC)(CrC)2 4.2 956
(6) (OrN)2 3.4 3698 1.8 664 (6) 3.6 1699
O 3.4 3707 (OrC)(CrC)2 3.7 826 (6)2 3.8 1911
3.2 3711 4.2 831 3.8 1912
3.2 3714 (OrC)(CrC)3 4.8 843 (6)(CrC) 3.5 2016
(6)2(OrIj02(NrC)2(CrC)2 (OrC)(CrC)(CrC)2 4.4 954 (6)2(NrN) 4.1 2225
O 4.6 3857 (6)2 4.1 1890 4.3 2335
(6)(OrN)(OrC) 3.9 3871 (6)2(CrC)2 4.5 2100 (6)(N:C) 4.3 2439
O (6)2(NrN) 4.3 2160 (6) (OrC) 3.5 2667
(Nr6rN) 4.6 3916 (6)3(NrN) 4.0 2355 (6) (OrN) 4.0 3454
(7rO)(6)(CrC) 4.4 4082 (6)(OrC) 3.9 2758 (6)(OrN) 3.2 3633
(66) 4138 (6)2(OrC) 4.4 2906 O
2.3 4151 (6)(OrC)2(CrC)3 4.5 3372 (Nr6rN) 4.6 3919
(66)(OrC) 3.9 4278 O (Or6rO) 4.3 4004
(66) (6) 4.2 4363 (6) (OrN) 4.2 3528 (66) (OrC) 4298
(63)(6) 4.5 4714 O 3.1 3629 O
(Or63rO) 3.8 4747 3.2 3665 (66) (OrC) (CrC) 4.5 4325
(7665) (OrN) 4.4 5057 (6) (OrIjI) (CrC) 3777 O
O O (66) (6) 2.8 4357
(6952) 4.5 5192 (66) (OrC) (CrC) 4.1 4324 (63) 4.2 4639
(N6) 5290 O (635rC)(OrC) 4.0 4892
(N66) 3.5 5764 (66) (6) 4.2 4361 O
3.7 5769 (Or63rO) 3.7 4789 (65) 5.0 5078
3.7 5775 (65) 5.2 5119 (N6)2(6) (CrC)2 4.7 5467
3.6 5795 (N6) 3.5 5297 (N66) 3.5 5656
(N66)(6) 4.0 5823 (N6) (OrC) (CrC) 4.1 5414 3.3 5665
(N66) (6) (CrC)3 4.4 5837 (N6:0) 4.0 5541 3.4 5668
(N665) 3.8 5942 (N66) 3.0 5682 3.9 5671
(N26rO) 3.6 6512 3.8 5773 3.9 5716
(N26rS) 4.3 6544 3.2 5774 3.1 5741
3.7 6554 Or 4.3 6117 3.3 5768
(S:N26:0) 3.8 6610 C0.N25rC)(6) 4<3 611g 3>5 5?94
(N266rO) 2.8 6715 (N26:0)(6) 3.8 6515 (N66:0) 3.6 5868
(OrN266rO) 4.0 6760 (N265) 3.7 6641 3.8 5881
(N275)(6) 4.0 6764 (N266) 3.8 6672 (N66rO)(6) 4.2 5913
(N465) 4.2 7137 3.7 6679 (N266) 3.9 6677
(N466rO) 3.8 7316 3.5 6687 (N465) 3.6 7069
(05) (OrC) (CrC) 4.4 7443 (N465) 4.4 7140 3.6 7142
(066rO)(6) 4.6 7733 4.4 7145 O: „
(0665) 4.5 7759 4.0 7162 (0rN466:0) 3 7
' 7343
(065) 4.2 7787 (N465rO) 3.7 7180 (05) (OrC) (CrC) 7442
(OrON5rC)(05)(6) 4.3 7896 (05) (OrC) 1.8 7435 (05) (OrN) (OrC) 4.1 7510
(SN65-.S) 4.4 8345 (05) (OrC) (CrC) 4.3 7481 6 O
O (05)(6)2 4.4 7524
(0665) 4.2 7749 (0665) 4.0 7752
(S665)(0rlp 4.0 8151 (S5)(0:C) 4.2 8000
O (S5)(6)4 4.2 8044
absorbing absorbing absorbing
n chromophore loge no.
chromophore loge no. chromophore loge °-
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(N26:0)(6)(0:N) 3.9 6532 (6) (OrC) (CrC)2 4.8 3369 (N26:0) 3.8 6485
6 6 (N26rO)(6)(OrN) 3.8 6531
(N266rO)(OrN) 3.9 6743 (6)2(0:C) (N:N) 3388 6
O A (N265) 3.7 6645
(N266) 4.4 6855 (6) (OrN) 3.1 3481 (N266:0) (O: N) 4.0 6747
CN365) 3.7 6974 6 3.4 3584 6
(N465) 4.2 7135 (6) (OrN) (CrC) 3767 (N2635) 4.2 6840
O: rO O 3785 (N465) 4.3 7136
(
0: 4 :0; ^1 /J^y (6) (O :N) (O :C) 3.8 3870 4.1 7153
(05) (OrC) (CrC) 4.3 7482 6 (N466) 3.9 7310
6 (7:0) 4.0 4046 X):N 66'-0\ 3.8 7350
(05)(6)2 4.5 7514 (7 :0) (6) (0:C) (C:C) 4.4 4088 O: 4 :0 3,8 7351
(05) (6) (OrC)(CrC) 4.0 7548 6 (05) (OrN) (NrC) 4.2 7506
(ON65)(6)(OrN)2 4.3 7928 (7 rO) (6) (OrN) (CrC) 4.2 4092 O
O 6 (05) (6)3 4.4 7526
(SN65rS) 4.4 8346 (7 rO) (6) (O: IjJ) (OrC) (CrC) (05) (6)4 3.7 7537
O 6 4.5 4094 (066rO)(6) 4.4 7691
(66) 3.3 4122 (0:ON5:C) (6)2 4.2 7826
:
Vax 325-325. 5my 4159 (S5) (OrC)2 4.1 8018
(66) (6) (OrC) 3.8 4434 O
none 3.8 18 (0:66:0) 3.1 4476 (0:865:0) 3.4 8115
(CrC)3 163 (63) (6) 4.3 4715 (S665) 3.6 8133
(CrC)5 4.7 202 (0:63:0) 3.8 4732 (SN65:S) 4.4 8340
([Cr]9C) 5.4 302 3.7 4738 4.2 8342
(NrC)(CrC)3 4.3 513 3.8 4744 4.6 8347
4.4 515 3.4 4798 (Se665) 3.3 8415
4.8 523 3.6 4834
(OrC)(CrC)4 4.5 1096 (0:63:0) (N-C) 3.7 4838
6 3.7 4839 Xmax r 326-326. 5my
(OrC)2(CrC)2 4.7 1132 (Or63rO) (OrN) 3.6 4840
O 6 (CrC)5 4.9 199
(OrCrC) 1.2 1239 (64) 4.0 4911 (OrC)(CrC) 1.6 665
(SrC) 4.3 1306 (Or64rO) 4.2 5053 1.4 681
(6)2(N:N) 4.1 2154 (66) 5.4 5126 (OrC)(CrC)3 3.9 833
3.7 2204 (67) 5.2 5154 4.1 834
4.3 2214 (N6) (6) (CrC) 4.4 5459 3.9 835
4.4 2215 (N6rO) 4.2 5537 (6)2(CrC)2 4.5 2138
4.3 2233 (N66) 3.6 5695 (6)2(NrN) 4.0 2170
(6)2(NrC)2 4.4 2530 3.2 5743 (6)(NrC) 3.8 2460
(6)(N:C)(C:C) 4.5 2597 3.5 5779 (6) (OrC) 3.7 2768
(6)2(NrC) (CrC) 4.4 2605 (N66) (OrC) (NrNrN) 3.6 5811 3.9 2769
(6) (OrC) 3.5 2656 (N66rO) 3.4 5864 3.4 2793
4.2 2730 3.4 5890 1.9 2834
(6)2(OrC) 4.1 2888 3.4 5891 (6) (OrC) (CrC) 2972
4.0 2901 (N66rO)(OrC) 3.9 5906 (6)2(OrC) (CrC) 4.6 3385
4.0 2902 6 6
(6)(OrC)(CrC) 4.1 3006 (N66rO)(6) 3.6 5911 (6)2(OrN) 3.4 3750
(6) (OrC) (CrC)2 4.6 3016 (N75) (NiC) 3.9 5921 6
(6)2(OrC)(CrC) 3.8 3091 3.9 5922 (7:0)2 4.2 4062
(6)2(OrC) (NrN) 3162 (N665) 3.6 5948 (7 rO) (6) (CrC) 4.3 4084
N (N665)(OrN) 3.9 5951 (66) 3.2 4119
(6)(OrC)(CrC) 4.1 3347 (OrN25rC) 3.7 6099 (63) 2.6 4637
O (N25) 3.3 6174 (63) (6) 4.5 4714
(N26) 3.6 6333 (64) 4.1 4937
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
(N26:0)(6) 3.7 6521 3.6 5742 (05) (OrC) (CrC)2 4.5 7486
(SrN26rO) 4.0 6618 (N66) (N:N) 3.4 5809 O 7487
(N266) 3.4 6685 (N665) 3.7 5943 (066:0) (6) 7701
(N266)(6) 4.1 6706 (N64) 4.0 6063 7711
(N266:0)(OrN) 4.1 6751 (S:N26:0) 4.2 6613 4.4 7742
6 4.0 6754 (N265)(0:N) 3.5 6653 (0:ON5:C)(6) 4.5 7800
(0:N266:N) 3.6 6761 O (S665) (OrIjI) 3.6 8148
: (N
(
V ° N 66-0) 4 2 7344 2665) 3
- 7 6773 °
0r 4 ' (063:0) 4.0 7768 (SN665) 3.8 8348
(05)2(N:C)2 4.6 7425 (0:ON5:C)(6) 4.5 7802 (SN26655) 4.0 8401
(05)(0:C)(C:C) 4.3 7483 (S5) (6) 3.9 8037
6
(0:ON5:C)(6) 4.4 7798 Xmax> : 338-338. 5my
4.3 7799 Amax : 337-337. 5my
(S5)2(N:C)2 4.2 7991 " (NrC)2(CrC)4 4.9 545
(0:SN5:C)(6) 4.4 8231 (NrC) 4.0 361 (OrC)(CrC) 1.6 647
(OrC)2 1.5 629 4.0 715
(6) 4.0 1485 (OrC)2(CrC) 1.8 903
Amax.: 336-336. 5my (6)2 (NrN) 4.5 2351 (OrC)(CrC)3 4.3 1090
(6) (OrC) 3.5 2681 6
(OrC)(CrC) 1.7 638 4.4 2718 (Or(^)(CrC)(CrC)3 4.2 1154
(6)2(CrC) 4.5 2080 4.4 2770 O
(6)2(N:N) 4.5 2220 (6) (OrC) (CrC) 3.3 2963 (6) (CrC)4 2060
4.2 2336 (6KOrC)(CrC)3 4.4 3023 (6)4(CrC)2 4.6 2130
(6)2(NrC)2 3.7 2561 (6) (OrC) 3.7 3184 (6)2(NrN) 4.4 2171
(6) (OrC) 4.3 2829 6 4.4 2231
(6)2(OrC)(CrC)2 4.5 3097 (6) (OrC)2(CrC)2 4.3 3371 4.2 2347
(6)(OrC)(OrC)(CrC) 4.4 3441 6 (6)2(NrC)2(C rC) 4.7 2608
6 (6) (OrN) 4.1 3618 (6) (NfC) (NrN) 4.3 2642
(6)(OrN)2 4.2 3676 6 3,2 3666 (6)(OrC) 4.4 2785
(!) (6) (OrN)2 3.2 3712 (6)2(OrC) 4.1 2884
(6) (OrN)3 4.2 3727 6 (6)3(OrC)2 4.2 2934
6 (6)2(OrN)2 4.3 3755 (6)2(OrC) (CrC) 4.3 3068
(7rO) 3.8 4057 O (6) (OrC) 3234
(66) 2.9 4190 (6) (OrN) (CrC) 3770 6
(66) (OrC) 3.5 4300 6 (6) (OrN) (OrC) 3.9 3867
6 (Or6rO) 2.4 3999 6
(66) (OrN) 3.9 4335 (7rO) 4.1 4043 (Nr6rN) 4.6 3925
(Or66rO) 3.5 4482 (7rO)(6) 3.9 4079 (Or6rO) 2.6 3967
4512 (66) 4189 3.0 3996
(63) 2.7 4633 (66) (OrC) 3.6 4277 (66) 3.3 4129
2.6 4641 (66) (6) (OrC) 3.4 4426 3.4 4132
2.5 4642 (63) 3.0 4643 3.5 4210
2.7 4651 2.6 4653 (66) (OrC) 3.2 4309
2.5 4654 2.6 4656 6
(635rO) 3.3 4898 3.0 4668 (66) (OrC)2 4.2 4313
(64) 4.7 4920 (Or63rO) 3.7 4758 6
4.6 4921 (64) 4.7 4978 (66) (6) 4.3 4363
3.8 4987 (67) 5.0 5152 (66) (6) (CrC)2 4.7 4372
(65) 4.0 5070 (N6rO)(6) 3.9 5551 (66) (6) (NrN) 3.5 4412
(N66) 3.8 5699 (N66) 3.5 5677 (Or66rO) 3.5 4455
4.2 5712 4.0 5801 3.4 4459
4.2 5720 (N66rO) 4.1 5892 3.5 4468
3.7 5725 (N26) 3.6 6231 3.4 4483
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
3.4 4487 (N26) 2.6 6131 (66) (6) (CrC)2 4.8 4373
(665)(0:C)2 4.2 4599 (N266:0) (0:C) 4.1 6741 (66)(6)(N:N) 4.3 4416
4.1 4600 6 6
(63) 3.7 4623 (N465) 4.7 7369 (0:66:0) 3.5 4453
2.7 4650 (N565)(6) 4.5 7380 3.1 4458
2.5 4652 (N565)(6)(0:C) 4.3 7383 (63) 2.7 4660
2.5 4655 6 (64) 3.9 4905
(64) 4.7 4941 (06:0) (OrCj)) 4.0 7619 3.9 4926
4.5 4966 O 3.8 4931
3.9 4982 (65) 4.2 5086
(645) 4.0 5062 Amax : 340-340. 5my (N5) 2.5 5194
(65) 4.2 5072 " (N6:0)(6) 4.0 5550
(67) 5.2 5153 none 2.4 26 (N66) 3.4 5690
(N66:0) 4.1 5883 (N:C) (CrC)3 4.9 517 4.0 5705
4.2 5886 4.8 522 3.3 5759
(N66:0)(6) 4.2 5912 (OrC)(CrC) 4.4 712 (N66) (OrC) (NrNrN) 3.6 5811
(N26:S) 3.5 6542 (OrC)(CrC)(CrC)3 4.4 957 (N66) (6) (OrN)2 4.1 5844
(0:N26:0)(0:N) 4.0 6605 (6) 1673 6 4.2 5846
6 (G)2(NrN) 4.4 2279 (N66:0) 4.0 5900
(N266) 2.5 6686 4.4 2280 (N64) 3.7 6056
(N266:0) 4.1 6719 4.3 2290 ,0: r-.rWM 4.2 6111
(N365)(0:N) 3.8 7000 (6)2(NrC) 4.3 2514 \)r 2 M ' 2.5 6130
O (G)2(NrC)2 4.3 2532 (N2G) 3.4 6337
(OS)(G)3 4.5 7529 (G)(OrC) 0.5 2685 (S:N26:S) 4.1 6624
(05) (6)4 4.5 7539 3.3 2712 3.9 6627
(066:0) (6) 7721 3.5 2747 (N266:0) (OrN) 4.0 6753
(0645) 4.5 7786 (G)2(OrC) 4.1 2893 6
(SN2665) 3.4 8397 (G)4(OrC)2 2.7 2938 (N2665) 3.8 6766
(G)(OrC)(CrC)2 4.3 3019 3.7 6781
(G)(OrC) 3.4 3295 (N264) 3.7 6845
A
max.: 339-339. 5mu 6 (N465) 3.5 7086
(G)(OrC)(CrC)2 4.3 3368 (N465:0) 4.3 7239
(C:C:C:C:C:C) 4.5 301 6 (N466:0) 3.8 7317
(OrC)(CrC)2 4.4 778 (G)(OrN) 3.4 3524 (0:N466:0) 4.0 7333
(G)4(OrC) 4.8 2935 O 4.1 3615 .0.- ,, _. , n „. .
(
(0:6:0) 2.4 3970 3.2 3647 0:V6:0) 4
'° ?345
(7:0) (6) 3.8 4080 4.1 3649 (05) (OrN) (NrC) 4.1 7504
(0:66:0) 3.2 4477 (G)(OrN)2 4.1 3702
(63) 3.7 4624 O (OS)(G)2 4.4 7519
3.6 4664 (G)2(OrN)(NrN) 4.3 3821 (05) (6)4 3.8 7532
3.4 4667 O 3.9 7538
(635:0) 3.6 4897 (G)(OrIjO(OrC) 3.5 3865 (OGGrO)(G) 4.3 7737
(64) 4.6 4965 O 3.9 3873 (063:0) 4.0 7770
3.9 4992 (G)(OrN)(OrN)(OrC) 3.7 3902 (ONS)(OrC) 4.3 7790
(G4)(OrC) 4.6 5034 6 6 4.3 7791
6 (7:0) 4.0 4060 (SN665) 4.0 8352
(NG)(G)(OrC)(CrC) 4.3 5488 (GSrC)(G) 4.3 4096
(N66) 3.5 5683 (66) 3.5 4165
4.2 5703 4211 Xmax : 341-341. 5my
3.8 5763 (GG)(OrC) 3.2 4267
3.5 5804 (GG)(Or(J) 3.2 4308 (G)2(CrC)8 5.4 2142
(N66:0) 4.0 5882 O (G)2(NrN) 4.4 2229
4.2 5887 (GG)(OrN) 4.8 4345 4.4 2232
4.0 5901 (GG)(G) 3.9 4360 (G)2(NrC)(CrC)2 4.6 2607
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
(6) (NiC)(NrN) 4.5 2644 (6)4(CrC)2 4.5 2128 (OrC)(CrC)4 4.6 855
(6)(0:C) 3.7 3200 (6)2(N:N) 4.2 2345 4.4 858
6 (6)(NrC) 4.3 2426 (OrC)(CrC)5 4.7 1098
(6) (OrN) 4.2 3619 4.6 2443 A
6 2445 (6) 3.9 1495
(6)2(OrN)2(NrN) 4.5 3844 (6)(OrC) 4.5 2654 (6)2(NrC)2 4.6 2538
O 4.4 2792 (6)(OrC) 3.4 2778
(Or6rO) 2.8 3989 (6)2(OrC) 3.2 2876 (6) (OrC) (CrC) 4.4 2950
(66) (OrC) 3.8 4285 3.2 2878 2977
(66) (OrC) (CrC) 4.0 4292 3.2 2891 (6)2(OrC) (CrC)2 4.6 3098
(66)(0:C) 3.3 4305 (6)4(OrC)2 2.5 2941 (6) (OrN)2(CrC)2 3808
O (6)2(OrC)(CrC)2 4.6 3099 O
(75) 3.6 4528 4.6 3100 (Or6rO) 4.6 3972
(63) 3.1 4669 (6) (OrN) (CrC) 3786 (7:0) (6) 4.3 4068
(64) 3.9 4922 6 (66) (OrN) 3.9 4336
3.9 4943 (Or6rNrN) 4.5 4038 (66)(6)(C:C) 4.3 4371
(67) 4.2 5145 (66) 3.6 4185 (Or66rO) 3.4 4452
4.7 5151 3.2 4209 3.4 4460
(N6) 4.1 5340 (66) (OrC) 3.4 4269 (75) 3.6 4536
(N6)(0:C) 3.3 5410 (66) (OrC) 3.6 4299 3.5 4549
(N6) (6) (OrC) (CrC) 4.4 5484 O 3.7 4550
4.4 5486 (66) (OrN) 4.1 4344 (75) (OrC) 3.7 4584
(N66) 4.3 5797 (63) 2.8 4661 6
(N66)(OrN) 3.7 5818 (63) (OrC) 3.7 4701 (63) 3.7 4629
O (635) 3.9 4875 (64) 4.7 4919
(N66)(6) 4.7 5826 (64) 3.9 4923 3.8 4924
(N63) 3.4 6010 3.8 4927 3.8 4930
(N265)(OrN) 3.8 6655 (763) 3.9 5058 4.2 4981
O (65) 4.3 5129 3.9 4993
(N266) 3.5 6673 (N6) (6) (OrC) (CrC) 4.3 5485 4.8 5004
(N266rO)(OrN) 4.0 6745 4.3 5487 (64)(0:C) 4.6 5027
O (N6rC)(6) 4.1 5496 (64)(OrC) 3.9 5029
(N2635) 4.0 6832 4.0 5497 N
(N365)(OrN) 3.8 7001 (N66) 4.2 5723 (65)(6)2 4.7 5097
O 3.2 5743 (N66) 3.5 5686
(OrN466rO) 4.1 7334 (N665) (6) 4.2 5959 (N66)(OrN) 3.6 5817
(05)(6)4 3.9 7536 (N64) 3.8 6054 A
(063:C)(6) 4.1 7766 (N26) 3.7 6216 (N66rN) (N66) (NrC) 5861
4.1 7767 (N266:0) 3.7 6730 (N665) 3.6 5941
(063rO) 3.8 7774 (N2665) 3.8 6770 (N25rO) (6) (OrN) 3.9 6096
(OrN466rO) 4.1 7332 (SrN26rO) 4.0 6619
: (0:N fifi-m L n 7^6 (N266)(OrN) 3.8 6695
Vax 342-342. 5my (^66.0) 4.0 7346 4
(05) (OrN) (CrC) 7497 (N2635) 4.3 6835
(CrC)5 4.6 200 6 (05) (6)4 4.5 7541
(CrC)3(CrC)3 4.6 289 (05) (6)4 3.8 7530 (066:0) (6) 7722
(NrC) 3.9 360 (SN5) (6)2(CrC) 4.2 8201
(NrC)2(CrC)4 4.8 546
(NrC)(CrC)(CrC)3 4.6 563 Amax.r 343-343. 5my
(OrC)(CrC) 4.6 651 Xmax r 344-344. 5my
4.6 652 (CrC)5 4.9 199
(OrC)(CrC)4 5.0 853 (NrC)2(CrC)2 544 (NrN) 1.0 303
(Or(^)2(CrC)2 4.1 1134 (NrC)2(CrC)8 3.6 549 (NrC) 4.1 362
O (OrC)2 1.3 630 (6)2(CrC)2 4.7 2105
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
(6)4(C:C)2 4.6 2129 (6)(0:C) 3.5 2741 (05) (0:N) (N:C) 4.1 7503
(6)(0:C) 3.4 2739 (6) (0:C) (C :C) 4.5 2948 O
3.5 2774 (6)2(0:C)(C:C) 4.4 3069 (05)(6)4 3.9 7534
(6)(0:C)2 4.0 2844 (6)2(OrC) (NrC) (CrC) (05) (6)2(0:C) 4.4 7551
(6)2(0:C)(C:C)2 4.4 3093 6 4.4 3403 A
(6)2(0:C)(N:C) (CrC) (6) (OrIjO 3.2 3531 (066:0) (0:C) 3.4 7682
6 4.5 3402 O 4.1 3591 O
(6)(0:N) 3.9 3589 (6) (OrN)2 4.1 3677 (066:0) (6) 7708
O 6 3.1 3716 4.2 7725
(6)2(S:C) 4.5 3911 (6) 3 (Or IjO (N:N) 4.5 3845 4.3 7741
(7:0) 4.1 4050 O (ON65) (6) 4.7 7915
(7:0) (6) 3.9 4081 (66) 3.0 4135 (S5) (6) (0:C) (C:C) 4.3 8052
(66) (OrC) (CrC) 4.2 4318 3.2 4154 (S635) 4.2 8158
6 4.2 4323 3.4 4176 (Se5) (6)2(0:C) 8408
(0:66:0) 3.5 4502 (66)(0:N) 3.6 4333
(75) 3.7 4538 3.9 4334
3.7 4552 (66) (6) 3.1 4359 Amax : 346-346. 5my
(75) (OrC) 3.6 4577 (66) (6)2(N:C) 4.8 4422
O 4.5 4424 none 2.5 54
(63) (OrC) 2.9 4704 (0:66:0) 3.3 4479 (OrC)(CrC) 4.7 653
6 (75) 3.7 4564 (OrN) 2.0 1251
(63) (6) 3.5 4714 (63) 2.6 4644 (6)3(N:C)2 4.4 2568
(635) 3.7 4889 2.6 4662 (6)2(OrC) (CrC) 4.3 3059
(635:0)(0:C) 3.2 4892 (64) 4.3 4935 (6) (OrN) 3.5 3574
O 3.9 4952 6
(64) 3.9 4925 (64) (CrC) 4.5 5014 (6) (OrN) (CrC) 3768
3.2 4963 (64)(6) 4.0 5044 6
3.8 4968 (65) 4.5 5078 (66)2 3.8 4226
4.5 4979 (67) 4.6 5142 (66)2(N:N) 4.4 4249
3.9 4990 (68) 5.1 5169 6
(6)n 4.8 5193 (69) 4.7 5189 (66) (OrC) (CrC)2 4.0 4294
(N66) 3.3 5732 (610) 5190 (66) (6) (NrN) 3.9 4386
(N66)(6) 4.4 5821 (N6)(6)(0:C) 5483 (0:66:0) 3.5 4488
4.2 5823 (N65)(0:66:0) 3.3 5588 (75) 3.7 4534
(N66:0)(0:C) 4.0 5903 (N66) 4.6 5689 (63) 2.5 4621
(N66:0)(0:C) 4.0 5904 3.7 5726 2.4 4622
O (N66)(6) 4.3 5822 (63) (0:C) (OrC) 3.0 4707
(N63) 3.5 5962 (N66) (6) (OrC) 5841 Cl
(N26) (6) (CrC)2 4.6 6386 6 (0:63:0) 3.2 4809
(N2665) 3.7 6778 (N63) 4.5 5974 (635) 3.9 4877
(05) (6) (OrC) (CrC) 4.4 7549 3.6 5983 3.9 4880
(063:0)(0:C) 3.8 7775 3.6 5987 (64) 3.9 4929
O 3.9 6000 3.9 4932
(0:ON5:C)(6)2(0:N)2 3.9 6021 4.6 4942
O 4.4 7891 (N64) 3.5 6053 4.4 4984
3.8 6058 4.4 4985
Vax.: 345-345. 5my r° : STWM LL AUR (64)(N:CrO) 4.9 5042
(0.N2N5.C)(6) 4.4 6115 (N«.N) 3<5 550Q
(SS)3 4.3 7979 (CrC)(CrC)6 4.7 274 (66) (OrC) 3.7 4278
4.4 7981 (NrC) 4.3 340 (63) 2.8 4661
(SS)(OrC)2 3.7 8015 (OrC)(CrC) 4.8 655 3.1 4669
O 3.7 8019 (OrC)(NrC) 4.2 964 (Or63rO) 3.9 4829
(S5)2(6)2(NrC)2 4.1 8046 (OrC)2(CrC)3 4.4 1139 (635) 3.9 4875
(SS) (05) (OrC) (CrC) 4.7 8062 O (64) 4.0 4945
(S65) 3.9 8106 (G)2(Or(JJ)(NrN) 3164 3.9 4950
N (6fi) 5.2 5134
(OrN) 1.7 1259 (N66) 3.7 5714
X
max.: 356-356. Smy (6) 4.0 1484 (N66) (6) (CrC)2 4.5 5833
3.8 1538 (N63) 3.3 6006
(CrC)4 4.2 192 (6)2(NrN) 2323 4.3 6007
(OrC)(CrC)4 856 (G)4(NrC)2 4.4 2573 3.5 6010
(OrN) 1.9 1260 (6) (OrC) 3.5 2775 (OrN2GrO)(OrN) 4.2 6606
(6)4(CrC)2 4.6 2127 3.7 2800 6
(G)2(NrN) 4.4 2259 (6) (OrN) 4.3 3459 (N266rO) 4.0 6723
(6)3(NrN)2 4.3 2368 (NrGrNrN) 4.5 3929 4.2 6732
(6) (OrC) 3.7 2799 4.7 3930 (N2665) 3.6 6779
(G)2(OrC) 4.4 2873 (66) (G-) (NrN) 3.7 44OV (N465) 4.2 7156
(OrGrO) 2.7 3992 (Nr66rN) 3.9 4451 (N466rO) 3.8 7319
(7rO) 3.7 4040 (63) 3.9 4623 (066rO)(6) 7703
(66)2(CrC)2 4.9 4243 3.8 4664 (OrONSrC) (6)2(OrN)2
(66) (6) (NrN) 4.5 4398 (64) 2.7 4914 6 4.4 7888
(7S)(OrC) 3.6 4576 2.5 4916
O 3.9 4955
(G3) 3.9 4624 (G4) (6)2 4.1 5046 Xmax r 359-359. 5my
(Or63rO) 3.5 4815 (NG3) 3.7 5964
(G4) 2.5 4915 4.3 6025 (NrC) 4.3 357
2.6 4917 (N266) 3.7 6721 (OrC)(CrC)5 4.6 1099
4.0 4946 (N2665) 3.6 6787 6
3.9 5006 (N4S) 4.1 7023 (G)2(NrN) 4.3 2236
(64) (NrC) 3.9 5021 (OrN466rO) 4.0 7336 4.2 2266
(65) 4.5 5078 (OS)(OrC)(CrC)3 7489 4.0 2283
4.2 5086 O (6)3(NrN)2 4.6 2369
(N6rC)(6)2 4.1 5498 (SN63rO) 4.0 8374 (6) (OrC) 3.7 2724
(N63) 4.0 5966 (Or SN2665rC) (6) 4.2 8394 (7rO)(6) 4.1 4065
4.3 5984 (66) (OrN) 3.6 4328
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
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A :
max 366-366. 5my (6,)(0:N) 3.9 5040 7716
O 4.8 7728
(N:C) 4.4 349 (65) 4.0 5077 (0:ON5:C) (6)2(0:N) 4.4 7864
4.4 354 (66) 4.9 5111 O 4.5 7866
(N:C)(C:C) 4.4 394 (N64) 3.7 6056
(N:C) (CrC)4 4.9 525 (N266:0) 4.0 6740
(0:N) 2.0 1252 (0:N466:0) (0:C) 4.2 7339 Xmax : 369-369. 5my
(6)2(N:N) 4.4 2244 6
4.1 2267 (0:ON5:C)(6)2 4.6 7821 (N:C)(C:C)4 5.0 524
4.1 2269 4.6 7822 (0:C)(C:C)5 4.7 866
(6)3(N:N)2 4.2 2367 4.6 7834 (6)2(N:N) 4.4 2258
(6)(0:lp3 4.2 3733 (6)4(N:N)2 4.7 2382
O (0:66:0) 3.8 4506
(6)2(0:N) 4.3 3748 Xmax : 368-368. 5my (75) 3.9 4565
6 * (75)(0:C) 3.9 4581
(66)(0:C) 3.7 4274 (6) 4.1 1503 6
3.8 4276 (6)2(C:C)5 4.4 2141 (63) 3.9 4672
(66X0:9) 3.4 4307 (6)2(N:N) 4.5 2239 (64) 2.9 4958
O 4.4 2247 (645) 3.9 5062
(75) 4.0 4531 4.3 2268 (65) 3.9 5084
(63) 3.9 4630 3.7 2270 (N63) 3.8 5978
3.8 4671 4.3 2271 (N266:0) 4.1 6724
(63) (6) 3.3 4712 4.7 2306 4.1 6739
3.0 4718 (6)3(N:N)2 4.6 2370 (0:SN2655 :C) (6) 4.3 8395
(635) 3.9 4879 4.5 2373
4.0 4882 (6)(N:C) 4.3 2470
(64) 2.8 4910 4.3 2471 Xmax : 370-370. 5my
(64) (NiC) 3.9 5019 (6) (OrN) 3.2 3549
(65) 2.9 5074 6 3.6 3617 (CiC)6 4.9 205
(65)(N:C:0) 4.2 5095 (6)3(0:N)2(N:N)2 4.6 3846 (N:C) 4.4 355
(N645) 4.4 6066 O (0:C)(C:C)5 4.8 863
(N26:S) 3.2 6541 (N:6:N:N) 4.4 3931 (0:C)(N:C) 4.3 959
(N2665) 3.8 6777 (0:6:0) 4.4 3974 (6)4(C:C:C:C:C:C) 4.4 2145
(05) (0:C) (CiC)3 4.4 7448 (7:0) 3.8 4052 (6)2(N:N) 4.4 2176
(0:ON5:C)(6)2 4.5 7812 (66)(0:C) 3.4 4303 (6)(0:C) 4.4 2675
(0:ON5:C)(6)2(0:N) 4.5 7859 6 (6)(0:C)2 4.4 2838
O (0:66:0) 3.6 4505 (6)2(0:C) 4.3 2874
(75) 4.0 4542 4.3 2875
*max.: 367-367. 5my (75) (6) 3.9 4591 (6)2(0:C)2 1.9 2911
(63) 3.8 4647 (6)2(0:C)(C:C) 3075
(N :C) 4.4 352 3.9 4659 (6)2(0:C) (CrC)2 4.2 3101
(NrC)(CrC) 4.4 395 (0:63:0) 3.6 4791 (6)2(OrC) (CrC)3 4.7 3104
4.3 456 (635) 4.0 4881 (6) (OrC) (CrC) 4.3 3352
(6)2(N:C) 3.8 2521 (64) 4.0 4983 6
(6)2(N:C)2 4.6 2536 3.9 4992 (6) (OrN) 4.1 3561
(6) (OrN)3 4.1 3728 (64) (NrC) 3.8 5020 6 3565
6 (64) (OrC) 2.9 5032 3.7 3609
(0:66:0) 2.6 4507 6 (7:0)(6) 4.1 4070
(0:63:0) 3.6 4756 (66) 3.1 5112 (66) (OrC) 3.7 4263
(635) 4.0 4883 4.5 5117 (66) (OrN) 4.0 4339
(64) 2.9 4911 C;:OWAN 4 5 6128
- (66) (6) (NrN) 4.1 4377
2.7 4954 ^.w2D:CMt>; 4<5 6129 (0:66:0) 3.8 4471
3.9 4994 (N2665) 3.7 6772 (75) 4.3 4533
(066:0) (6) 7712 (63) 3.9 4674
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
(OrC)2(NrC)(CrC) 4.2 1173 (66)(0:N) 3.3 4338 A1^x. •' 378-378 .5my
O 5.0 4341
(0:C:C) 1.3 1240 (65) 2.8 5066 (OrC)(CrC)2 4.7 819
(6)2(CrC)4 5.0 2112 3.0 5069 (6)2(N:N) 4.5 2249
5.0 2113 (65) 3.8 5131 4.4 2254
(6)2(N:N) 2208 (N65) 4.0 6067 4.4 2255
(6)2(N:C) 4.5 2526 (N266rO) (OrN) 4.2 6747 (6) (OrC) 3.6 2779
(6)2(0:C) (CrC)4 4.6 3107 6 (6) (OrC) (CrC)4 4.8 3029
(6) (OrN) 3.2 3499 (OrN463rO) 3.2 7358 (6) (OrN) 2.9 3512
O 3.1 3548 (OrON5rC)(6)2 4.6 7843 6 4.1 3546
(6)(OrN)2 4.1 3686 (OrON5rC) (6)2(OrN) 4.6 7854 (6) (OrN)2 4.0 3699
6 6 6
(6J2(OrN)2(NrC)2 3.5 3856 (S5)(OrN)2 4.0 8027 (Or6rO) 2.4 4005
6 6 (7:0) (6) 4.0 4075
(0:6:0) 3.2 3948 (SN5)2(6)4 4.3 8194 (66) (6) (NrN) 4.1 4415
3.2 3949 6
2.8 4003 (665rO) 2.4 4610
(7:0) 3.7 4048 Xmax r 377-377. 5my 2.4 4611
(66) (OrC) 3.7 4281 " (63) 4.0 4648
(66)(6)2(0r£) 3.5 4445 (NrC)(CrC) 4.4 425 3.9 4682
O 4.4 444 (Or63rO) 3.7 4793
(63) 3.9 4623 4.4 446 (64) 3.0 4941
3.8 4665 4.4 448 3.2 4942
(Or63rO) 3.8 4763 (OrC)(CrC)2 4.5 779 3.5 4981
(64) 2.7 4914 (OrC)(CrC)5 4.7 860 (64) (CrC) 3.0 5014
(64) (NiC) 3.9 5016 (OrC)(NrNrC) 1.2 1191 (64) (NrC) 4.0 5017
(65) 2.6 5070 (6)2(N:N) 4.4 2175 (64) (6) 3.9 5045
(66) 4.7 5116 (6) (NrC) 4.5 2430 (66) 4.3 5114
(N66)(6)(CrC) 4.5 5830 4.5 2431 (N65)(Or6rO) 3.7 5584
(N275)(6) 4.4 6763 4.4 2455 (N26rS) 3.2 6535
(N263) 3.9 6814 (6)2(NrC)2(CrC)3 4.9 2611 (N466) 2.1 7314
(N365)(OrN) 3.6 6992 (6) (OrC) 3.6 2717 (OrN466rO) (OrC) 4.4 7340
O (6) (OrN)3 4.2 3729 6
(05) (OrN) (NrC) 4.2 7498 O (OS)2(NrC)2(CrC)2 4.8 7431
A 4.1 7501 (Or6rO) 4.4 3977 (OrON5rC) (6)2(0:N) 4.5 7881
(066rO)(6) 3.3 7736 4.4 3978 6
(065) 4.1 7787 (66) (6) (NrN) 3.4 4385 (OrS65rC) (S65) 4.5 8126
(S5) (OrC)2 3.5 8011 (63) 3.9 4629
6 3.7 4664
(S6)(6)3 8076 4.0 4676 Amax r 379-379. 5my
(63) (CrC) 4.0 4696
(63)4(0:0) 4.6 4697 (CrC)6 204
x
max.: 376-376. 5my (Or63rO) 2.1 4733 (NrC)(CrC) 4.4 435
(64) 2.4 4918 (6) (NrC) 4.3 2469
(NrC)(CrC) 4.5 414 (67) 4.6 5147 (6)2(N:C) 4.4 2510
(6)2(NrN) 4.3 2180 (N66) 3.6 5710 (6) (OrC) 3.7 2658
4.0 2242 3.4 5724 (6) (OrN) 4.2 3533
4.4 2246 (N66) (6) (CrC)3 4.7 5837 6
4.4 2253 (N665) 4.3 5930 (6)2(0:N) 4.2 3741
(6) (NrC) 4.4 2473 (N266) (6) 4.0 6707 6
(6)2(OrC) (CrC)3 4.5 3103 (66) (OrN) 4.0 4330
(6) (OrN) (CrC) 4.2 3779 (66) (6) (NrN) 3.6 4413
O (75) 4.1 4561
(Nr6rNrN) 4.6 3934 (75) (6) 4.0 4594
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
Amax : 385-385. 5my (66) 3.7 4116 (N466:0) (0:£) 4.3 7326
(66)2(N:N) 4.2 4248 O
(NrC)(CrC) 4.4 449 O (0:ON5:C) (6)2(0:N) 4.4 7862
(NrC)(CrC)2 4.4 504 (66) (OrC) 3.2 4280 6
(NrC)2(CrC)6 4.9 547 (63) 3.9 4630 (S5)(OrC)2 4.0 8012
(6)2(NrN) 4.3 2292 3.8 4647 O
4.3 2295 3.7 4671 (S5) (OrON5rC) (6) 4.2 8072
(6)2(NrC)(CrC) 4.0 2606 (64) 3.1 4929
(6)2(NrC)2(CrC)4 4.9 2612 3.1 4932
(6)2 (Or C) (Cr C) 4.5 3064 3.1 4948 Xmax r 388-388. 5my
(6) (OrN) 3.0 3511 3.2 4952
O 4.0 4976 (NrC)(CrC)2 4.4 478
(6)2(OrN) (NrN) 4.5 3822 (64) (OrC) 4.0 5024 4.4 505
O 4.0 5028 (OrC)(CrC)3 4.1 851
(Nr6rN) 4.2 3920 (0:64:0) 3.8 5054 (6) (NrC) 4.4 2463
(0:6:0) 2.8 4002 (66) 3.9 5128 (6)2(NrC)2 4.0 2557
(66)2(NrC)2 4.3 4259 3.2 5130 (6) (NrC) (CrC) 4.5 2594
(66) (OrN) 3.9 4347 (N366rO) 7010 (6) (OrC)2(CrC)3 4.6 3373
O 3.6 4351 (N466rO)(OrC) 4.2 7327 O
(0:66:0) 3.4 4454 A (0:6:0) 3.4 3957
(63) 4.0 4685 (05) (OrC)2(CrC)2 4.8 7491 4.2 3973
(63)(OrC) 3.7 4700 6 (66)2(NrC)2 4.4 4253
(64) 2.7 4924 (OrON5rC)(6)2 4.5 7811 (Or66rNrN) 3.8 4525
3.2 4927 4.6 7821 (64) 3.2 4923
2.5 4930 3.0 4925
2.9 5005 3.1 4926
(64) (OrC) 2.9 5032 Xmax r 387-387. 5my 3.1 4974
6 4.1 5033 ' (66) 3.0 5112
(65) 3.8 5077 (NrC)(CrC) 4.4 421 3.9 5126
(68) 4.8 5166 4.4 447 3.9 5127
(N64) 3.5 6054 4.4 459 (N65)(Or6rO) 3.7 5585
(N266) 3.4 6668 (6)2(NrN) 4.4 2174 (N263) 3.9 6817
(N266) (6) (CrC)2 4.5 6710 4.3 2294 (N466) 3.8 7306
(N266rO) 3.6 6718 (6) (OrC) (CrC)4 4.8 3028 (05) (NrC) 4.4 7415
(N2635) 3.6 6835 (6)2(OrC) (CrC) 4.4 3061 (OrON5rC) (6)2(0:If[) 4.5 7873
(0:N466:0) 3.4 7329 4.4 3086 O 4.5 7880
(05) (OrN) (NrC) 4.2 7500 (66) (6) (OrC) 3.6 4429 (SN65rC) (NrC) 4.7 8291
6 (75) 3.9 4559
(OrON5rC)(6)2 4.4 7831 (Or63rO) 4.0 4808
4.5 7832 (64) 3.2 4922 Xmax r 389-389. 5my
(0:ON5:C)(6)2(0:]{0 4.5 7868 3.2 4931
O 3.1 4943 (NrC)(CrC) 4.4 422
(S5)4 4.5 7984 3.5 4949 4.4 426
(S665)(OrN) 3.8 8144 3.0 4973 4.4 436
6 2.9 4989 (OrC)(CrC)5 4.6 865
(SN63rO) 4.0 8376 (64) (OrC) 3.1 5035 (6)2(NrN) 4,4 2177
A (6) (NrC) 4.3 2457
(64)(OrN) 3.5 5041 (7:0) 3.7 4056
Xmax r 386-386. 5my O (66) (6) (NrN) 4.2 4400
(6452) 4.4 5106 3.8 4408
(6)2(NrN) 4.5 2303 (66) 5.0 5111 (75) (6) 4.2 4592
(6)2(OrC) (CrC) 3082 (N66) 3.0 5691 (63) 4.0 4659
(6) (OrN) 4.3 3505 (N64) 3.6 6056 (6655) 4.0 4870
O 4.3 3514 (N265) 3.2 6854 (64) 3.1 4928
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
(SN65:C)(6)(N:C) 4.6 8295 (0:ON5 :C) (6)2 (0:1(0 4.4 7855 Vax.: 400-404. 5my
O
(SN5)2(6)8 4.3 8196 (CrC)13 4.6 224
*max.: 395-395. 5my (SN65:C) (SN65) 4.8 8318 (NrC)2 4.4 384
(NrC)(CrC) 4.5 398
(NrC)2 4.6 382 4.4 416
(NrC)(CrC)2 4.4 479 Amax. r 397-397 .5my (NrC)(CrC)2 4.5 476
4.5 495 " 4.7 485
(NrC)(CrC)(CrC)2 4.5 560 (NrC)(CrC) 4.3 404 4.6 499
(OrC)(CrC)6 4.8 873 (6)2(CrC)4 4.3 2140 4.5 500
(OrC)(NrC)(CrC)2 4.5 1160 (6)2(CrC)5 4.4 2141 (OrC)(CrC)6 4.7 872
6 (6)2(OrC) (CrC) 3083 (OrC)(OrC)(NrC) 4.1 1216
(6)2(NrC)(CrC) 4.6 2600 (66) 4.9 5116 A
(6)2(OrC) (CrC)4 4.8 3109 (N6:0) 3.8 5513 (6) (CrC) 3.6 2030
(6)(0rl^) 3.4 3560 (Or05rC)(6)2 4.5 7557 (6)2(CrC)5 5.0 2116
O 3.7 3563 4.5 7558 W4(CrC)4 4.9 2131
(7rO)(6) 3.8 4080 4.5 7560 (6) (NrN) 1.9 2147
(66) (OrC) 3.9 4264 (Or065rC)(6) 4.5 7637 (6)2(NrN) 2181
(66) (6) (NrN) 4.2 4394 (0:ON5rC) (6)2(OrN) 4.5 7885 2200
(Or66rO) 3.3 4473 (s-SN5:0) (S5) ° 4 5 8239 22 6
°
3.5 4481 Cb.bN5sC)(S5) 4.5 8239 (6)3(N:N)2 3.1 2367
(0:66:0) (CrC) 3.1 4518 (6)5(NrN)4 4.8 2389
(63) 3.8 4679 4.8 2391
(64) 3.9 4972 Amax.: 398-398. 5my 4.1 2393
3.3 4986 (6) (NrC) 4.5 2429
(64)(OrC) 3.3 5034 (N266rO) 3.6 6736 4.3 2433
6 (05)2(NrC)2(CrC)4 4.9 7432 4.5 2454
(65rO) 4.1 5099 (Or065rC)(6) 4.4 7636 (6)2(NrC)2 4.8 2528
(66) 4.3 5110 (066rO)(6) 7722 (6)2(OrC)2 1.9 2912
(OrN65rC) 3.7 5611 (OrON5rC) (6)2 4.5 7824 2.0 2913
(N64) 3.8 6057 fc.cNS:0)Wqft^
(S SN5
L s «9A* 1 9 2914
^
(N266)(6)2(CrC)2 4.3 6712 ' rC (S65) 4 5 8246
' 1.9 2916
(N266rO) 3.5 6727 (6) (OrC) (CrC)2 4.3 3019
(N2635) 4.2 6842 (6) (OrC) (CrC)5 3033
(0:05:C)(6)2 4.5 7556 Xmax r 399-399. 5my (6)2(OrC) (CrC)4 4.8 3108
(0:ON5:C)(6)2(0:N) 4.5 7883 " 4.8 3110
O (OrC)(CrC)6 4.7 868 (6) (OrN) 3.3 3468
(6)2(NrC)(CrC) 4.6 2601 3.8 3472
*max.: 396-396. 5my (6) (OrC)2 4.0 2854 (6) (OrN) 3.7 3495
(6)(OrN)2 4.1 3691 6 3.7 3496
(6)2(NrC)(CrC) 4.5 2604 A 3.1 3510
(6) (OrN) 4.4 3650 (Or6rN) 4.4 4026 4.6 3519
6 3.8 4029 4.4 3521
(7rO)(6) 4.0 4066 (75) (6) 4.2 4594 3.5 3542
(Or63rO) 3.3 4820 (63) 3.9 4682 3.3 3543
(64) (NiC) 3.8 5016 (64) (CrC) 2.9 5014 4.3 3582
(65) (OrC) 4.4 5094 (64) (6) 4.0 5045 (6) (OrN)2 4.4 3682
(66) 4.1 5120 (65) 3.0 5078 O 3.7 3695
(N66)(6)(C:C) 4.6 5832 (68) 4.1 5163 (6)2(0:N) 4.3 3743
(N63) 3.7 6012 (0:N266:N) 4.1 6761 O
(N65) 4.3 6067 (05) (6)3(0:C) (OrC) 4.4 7552 (6)2(0:N) (NrN) 4.3 3832
(N3635) 3.7 7014 A O 4.3 3833
(Or05rC)(6)2 4.4 7562 (Se665)(OrN) 3.7 8418 (6)2(OrN) (Or£) 4.3 3877
(OrON5rC)(6)2 4.5 7825 O O O
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
(N:6:N) 4.8 3921 (N266)(0:N) 3.9 6693 (N:6:N) (6)2(0:N)2 4.5 3928
(0:6:N) 3.0 4022 O 6
3.8 4032 (N266)(6)(C:C)3 3.5 6711 (7:0)(6) 4.1 4069
3.8 4035 (N266:0) 3.5 6715 4.3 4073
(7.'O)(S)(OrN)(CrC) 3.9 4091 3.5 6725 3.9 4081
O 3.5 6726 (7:0)(6)(0:N)(C:C) 4.1 4092
(66) 2.8 4175 (N2665) 3.2 6770 6
2.8 4176 (05)(N:C)(C:C) 4.6 7427 (66)2(N:C)2 4.5 4258
(66)2(C:C) 4.5 4240 (05)2 (0:C)2(C:C)2 4.1 7455 (66)(0:C) 4.0 4262
(66)2(N:N) 4.2 4244 (05) (6) (N:C) (C:C) 4.6 7543 (66)(6)(N:N) 4.1 4393
(66)(0:C) 3.8 4273 (0:05:C)(6)3 4.5 7563 (0:66:0) 3.7 4485
(0:66:0) 3.3 4452 (0:ON5 :C) (6)2(0:N) 4.5 7876 3.6 4500
3.5 4453 O 4.4 7884 3.6 4501
3.3 4460 (S5)(0:05:C)(6) 4.5 8063 (0:66:0) (CrC) 3.2 4519
:0
3.4 4480 rs-SN5
S UM A s «907 (0:66:0)(66) 3.4 4523
(75)(0:N) 4.0 4588 ( -SN5:C)(6) 4.5 8237 ^ 4>3 ^
:0 4 5
O VCS-SN5 wqs^ ' 8244 3
- 6 4665
(63) 3.9 4680 ' :CM ' 4.6 8246 3.9 4685
3.9 4681 (SN65)(6)(C:C) 4.4 8286 (0:63:0) 2.0 4732
3.7 4683 (SN65:C)(6)(N:C) 5.7 8297 5.0 4735
3.8 4684 3.8 4760
(63) (6) 4.0 4717 3.6 4813
(0:63:0) 3.7 4754 Amax.: 405-409. 5my 3.7 4827
3.7 4788 " (0:63:0)(6) 3.0 4846
3.9 4805 (CrC)15 4.2 228 (64) 3.9 4969
(64) 3.2 4966 (NrC)(CrC) 4.5 413 4.0 4970
3.4 4993 (NrC)(CrC)2 4.5 496 4.3 4977
3.6 4999 4.5 503 3.5 4979
3.8 5018 (NrC)(CrC)3 4.7 512 3.3 4982
(645) 4.2 5060 4.6 513 4.2 5001
(645)(0:C)2 4.1 5064 4.6 518 (65) 4.8 5075
N (NrC)(CrC)7 533 (65)(6)2 4.6 5097
(64) (OrC) 3.9 5023 (S)2(NrN) 4.3 2190 (65rO) 4.2 5098
(65) 3.6 5073 2194 (655) 4.0 5107
3.1 5076 2202 (66) 4.5 5124
(S5)(NrCrO) 4.5 5096 4.5 2305 3.3 5130
(65rO) 4.1 5100 (S)3(NrN) 4.6 2358 (6?) 4.7 5157
4.0 5102 (S)5(NrN)4 4.9 2392 4.7 5160
(S6) 3.3 5113 (S)(NrC)(CrC) 2588 (0:N65:0) 5606
4.1 5121 (S)(OrC) 3.4 2804 5607
4.2 5122 3.7 2807 (N665) 4.1 5936
(S7) 3.3 5142 (S)2(OrC)2 1.7 2915 (N665)(0:N) 3.9 5952
(S8) 4.7 5172 XS)(OrC)(CrC)5 3034 O
(NSrC)(NrC) 5495 (S)(OrN) 4.4 3458 (NS3) 3.7 5986
(N65)(0:66:0) 3.4 5588 4.3 3461 4.0 5998
3.1 5590 4.0 3476 (NS4) 3.9 6060
(0:N65:0) 5604 (S)(OrN) 3.6 3539 , Q W c-'O w _ ,, ^107
(N66:S) 5914 6 3.9 3551 (S:N25.C)(6) 4.4 6127
5916 4.3 3653 (N266) 3.5 6669
(NSSrS)(S) 5918 (S)2(OrN)(NrN) 4.3 3826 (N263) 3.5 6815
(NS3) 3.5 5992 O 4.4 3827 3.6 6816
4.0 5997 (S)(OrI)O(OrC) 4.2 3868 (N264) 3.9 6849
3.5 6010 O (OS)(NrC)(CrC) 4.5 7429
(N63:0) 3.9 6045 (0:05:C)(6)2 4.5 7559
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
(6)2(NrC) 4.4 2507 (SN65:C) (SN65) 4.9 8319 (645) 3.9 5061
(6)3(N:C) 4.5 2564 (65) 4.0 5079
(6) (OrC) (CrC) 2975 (67) 3.3 5142
(6)2(OrC) (CrC) 3077 Amax : 425-429. 5my (N66:C)(N:C) 5847
(6) (OrN) 4.5 3457 * (N75:0)(N:C) 4.3 5924
(6) (OrIjO 4.3 3515 (CrC)7 208 (N75:0)(0:C) 4.2 5926
O 4.3 3516 (NrC)(CrC)3 4.7 511 6
4.0 3518 (Or^)(CrC)7 4.6 1100 (N63) 3.6 5979
4.2 3590 O 3.5 6007
2.9 3605 (OrC)(NrC)(CrC)5 1162 (OS)(OrC)(CrC)6 4.9 7451
(6)2(0:N)(N:N) 4.4 3824 O (OS)2(OrC) (CrC)6 4.4 7454
O * 4.2 3837 (OrC)(NrC)(CrC)6 1164 (066:0) (6) 4.4 7729
(N:6:N)(6)2 4.6 3924 O (0:ON5:C) (6) (OrN) 4.5 7874
(0:6:0) 1.4 3963 (OrC)(OrC)(CrC)6 1202 6
(7:0) 3.9 4061 6 (SS) (0:ON5:C) (6) 4.6 8071
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
:
Vax 465-469. 5my (OrC)(NrC)(CrC)7 1165 (6)2(N:N) 3.3 2163
6 4.5 2320
(CrC)11 5.1 220 (Or(^)(OrC)(CrC)7 1206 (6)(NrC) 4.6 2445
([Cr]9C) 4.2 302 O 4.5 2447
(NrC)(CrC)8 536 (OrN) 1261 (6) (NrC) (CrC) 2584
(OrC)2 1.5 624 (6)2(NrN) 3.1 2288 (6)(OrC)2 3.7 2847
(OrC)(CrC)9 891 3.1 2290 (6)(OrN)3 4.4 3723
(OrC)2(CrC)9 930 3.6 2335 O
934 (6)3(NrN) 3.7 2360 (6)2 (OrN) (NrN) 4.5 3816
(6)2(NrN) 3.3 2289 (6)3(NrN)2 4.8 2376 6
2.4 2309 (6)2(OrC)2 1.7 2918 (Or6rO) 1.1 3954
4.4 2319 (6)(OrC)(CrC) 2978 1.1 3959
(6)2(OrC)2 1.7 2917 (6)2(OrC) (NrN) 3163 (7:0) (0:C) 3.1 4063
(6)(OrC)(CrC)3 4.6 3027 & O
(6)2(OrC) (NrN) 4.4 3391 (0:6:C)(6) 4.3 4008 (66) (6) (NrN) 4.1 4389
O (0:6:C)(6)2 4.5 4012 4.2 4404
(6)2(0:N) (NrN) 3817 (0:6:N) 3.8 4023 4.2 4406
6 (7.-O)(OrC)(CrC) 3.0 4064 (0:63:0) 3.8 4740
(66) (6) (NrN) 4.2 4385 O 2.9 4742
4.2 4388 (66) (OrN) 3.5 4350 3.8 4751
4.2 4408 O (Or63rO)(6)2 4.1 4861
(0:66:0) 4511 (66) (6) (NrN) 4.5 4410 (N63:C)(N6) 6037
(75)(OrC)2 4.4 4587 (Or66rO) 3.2 4479 (0:N365:0) 3.1 7008
O (0:63:0) 3.8 4738 (05) (NrC) 4.4 7416
(Or63rO) 4775 3.8 4750 4.4 7421
3.7 4792 4.1 4753 (06)(6)3 7573
(64) (6)4 3.8 5050 4777 (OrON5rC) (6)2 4.5 7808
(68) 3.4 5169 4779 (SN5)2(6)4 8195
(N6) (6) (NrN) 4.3 5475 3.8 4780
(N66rC)(N6) 5855 4.0 4798
(N63) 4.1 6009 (Or63rO)(Orl^) 3.8 4843 Amax. r 480-484 .5my
4.0 6015 O
(OrN365rO) 3.3 7007 (64) 4.1 4906 (NrC)2(CrC)8 550
(OrS65rC)(S65) 8119 (64)(6)3 3.9 5047 551
(S665)(OrN) 3.5 8146 4.1 5048 (NrC)2(CrC)9 552
O (N6)2(NrN) 2.3 5409 (OrC)2 1.6 625
(SN5rC)(N66) 8208 (N6) (6) (NrN) 4.3 5474 (OrC)(CrC)8 878
(OrON5rC)(6)2 4.7 7809 881
(SN5)2(6)g 8197 (OrC)(CrC)9 887
(SN5rC)(N66) 8209 (OrC)(CrC)n 899
*max.: 470-474. 5my (OrC)2(CrC)8 924
926
(CrC)9 215 Amax.: 475-479. 5my (OrC)2(CrC)9 933
(CrC)10 5.1 217 (OrC)2(CrC)10 938
(CrC)12 5.2 221 (CrC)9 213 (OrC)(NrC)(CrC)7 1168
(NrC)(CrC)7 532 (CrC)10 5.0 217 O
(NrC)(CrC)9 538 (CrC)n 5.0 218 (OrC)(NrC)(CrC)8 1169
(OrC)(CrC)9 884 (OrC)2 1.6 625 O
888 (OrC)(CrC)9 889 (OrC)(OrC)(CrC)7 1203
(OrC)(CrC)10 896 (OrC)(NrC)(CrC)8 1171 O 1207
(OrC)(CrOi2 901 (!) (6) 4.5 1485
(OrC)2(CrC)9 1149 (OrC)(OrC)(CrC)8 1209 (6)2(NrN) 4.5 2321
O 6 1212 4.5 2322
(6) 4.5 1496 4.7 2337
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
(N263) 3.4 6816 Amax : 505-509. 5my (7665) (O: N) 3.4 5057
(066)(6) 4.9 7657 " O
(ON65:C)(ON65)(C:C) 7933 (C:C)10 5.0 217 (66) 4.7 5109
(SN65:C)(6)(N:C)(C:C) (C:C)13 5.2 223 3.9 5135
5.0 8300 (CrC)15 5.1 228 (6Q) 5167
(OrC)(CrC)9 883 (N6)2 3.9 5390
(OrC)(CrC)11 898 (N6) (6)2(CrC)2 4.8 5465
*max.: 500-504. 5my (OrC)2(CrC)11 940 (N263) 4.0 6803
(OrC)(NrC)(CrC)8 1170 (05) (6)4 3.1 7530
(CrC)10 5.0 217 O 3.2 7532
(CrC)13 5.2 223 (6)2(NrN) 4.6 2205 3.1 7534
(OrC)2(CrC)9 929 3.8 2330 3.2 7536
(6) 4.6 1484 (6)2(NrC)(C:C) 4.5 2602 3.1 7538
(6)2(N:N) 4.4 2179 (6)2(0:N)2(N:N) 4.4 3843 (05) (6) (NrC) (C:C) 4.6 7544
4.6 2204 O (066) (6) 4.7 7646
4.1 2331 (Or6rC)(6)2 4.6 4016 4.6 7659
4.6 2333 (0:63:0) 4831 (Or S65rC) (S65) 8123
3.7 2336 (Or63rO)(OrN) 4.0 4842 (SN5 rC) (ON65) (CrC) 8211
(6)3(NrN)2 4.7 2371 O (SN635rC) (N66) 4.7 8378
(6)5(NrN)4 4.9 2394 (64) (6)3 4.1 5047
(6) (OrN) (CrC) 4.4 3780 4.1 5048
6 (68) 4.9 5164 Amax : 515-519. 5my
(6)2(OrN)2(NrN) 3840 5.0 5178
O (N65)(Or66rO) 3.9 5589 (OrC)2(CrC)10 936
(Or6rC)(6)2 4.5 4013 (N66rC)(N6) 5857 (OrC)(CrC)12 1103
(0:66:0) 4511 ,0: . ,rO. 6
(665rCrCrCrCr665) 4.8 4607 X): 6 :0; 4 U bUbb
- (6) 4.5 1504
(Or63rO) 3.9 4747 (N4635) (6) 7366 (6)2(N:N) 4.6 2189
3.7 4749 (06)(6)3(CrC) 7584 4.4 2199
3.8 4767 (066) (6) 4.6 7642 (6)2(0:N) (NrN) 4.6 3831
4.1 4773 (SN5rC)(Nr6rC) 8204
4774 (SN63rO) 3.9 8374 Or . , * , nn
(67) 4.4 5145 <Or 7:N > 4 6
' 4095
4.0 5158 (Or66rO) 3.7 4504
(N665)(OrN) 3.5 5954 Amax r 510-514. 5my (Or63rO) 3.8 4757
O * 3.9 4824
(N63rC)(N66) 6039 (CrC)13 225 (67) 4.2 5154
(N4635)(6) 7363 (NrC)2(CrC)8 551 (68) 4.7 5162
(05) (6)4 3.3 7537 (NrC)2(CrC)9 552 3.3 5168
(066) (6) 4.4 7649 (OrC)2(CrC)12 943 (69) 5185
4.0 7651 (6)2(N:N) 2182 (N65) (Or66rO) 3.5 5588
7652 2201 (N66)(OrC) 2.5 5812
7664 2207 6
(ON65rC)(ON65) (CrC) 7934 4.2 2325 (N66) (6)2(OrC) 2.6 5842
(ON65rC)(ON65)(6)2(CrC) 4.6 2326 6
7936 4.7 2328 (N66 rC) (6) (NrC) (CrC)
(OrS65rC)(S65) 8121 4.4 2332 5.0 5851
(SN65rC)(N66) 4.9 8310 (6)2(NrN)2 4.9 2383 (N66rC)(N6) 5856
(SN665rC)(N66) 4.7 8354 (6) (NrC) (CrC) 2589 (N63rC)(N6) 6038
4.7 8355 (Or66rO) 3.9 4486 (066) (6) 3.2 7644
3.8 4498 7656
(Or66rO)(CrC) 3.2 4516 7662
(0:63:0) 3.8 4804 (063) (6) (OrC) 7763
(7665) 3.6 5056 6
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
(OrC)2(CrC)11 941 (SN5rC) (ON65) (CrC) 8212 (SN65rC) (SN65) (CrC) 8322
(OrC)2(CrC)12 944 (SN65.-C) (ON65) (6) (CrC) (SeN65rC) (ON65) (6) (CrC)
(6) (OrC) (CrC)4 4.7 3031 8312 8426
(6)2(OrN)2(NrN) 3839 (SN63:0) 4.0 8376
O 4.5 3841 (SeN65rC)(ON65)(6)(CrC)
(0:6:0) 2.7 3974 8427 ^max.: 545-549. 5my
(0:6:N) 0.1 4024
(Or66rO)(CrC) 3.4 4513 (CrC)19 4.9 229
(665rO) 3.2 4613 (0:66:0) (6) (C:C) 3.4 4522
2.8 4614 (75) 2.6 4561
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
(N65) (0:6:0) 3.7 5585 (SN665 :C) (SN65) (C :C) 8359 (6) (OrN)3 3724
(N65) (0:66:0) 3.8 5592 (SN63:N) 4.1 8367 A
(0:N65:N65:0) 5620 (SeN65 :C) (SeN65) (C:C) 8429 (6)2(OrN) (N:N) 4.4 3825
(S:N65:N65:S) 5655 8430 O
(S6)(6)4(C:C) 8093 (6)2(S:C) 2.9 3907
(0:S65:S65:0) 8127 2.6 3909
(S:SN5;°)(SN5:C) 8248 W.' 560-569.5my (75) 2.5 4547
(SN65:C)(SN65)(C:C) 8323 (6)4(N:N)3 4.9 2387 (75)(C:C) 4572
8325 (6) (OrN)2 3671 (75) (6) 4592
(SN63:0) 4.3 8377 6 (75) (6) (OrC) 2.7 4596
(6) (OrIjI) (OrC) 3.8 3891 (765) 2.6 4864
O 6 (65) 4.1 5080
x
max.: 550-559. 5my (0:6:0) 1.5 3948 2.6 5083
(0:66:0) 4524 (63) 5170
(6)4([C:]7C) 2146 (75) 2.4 4532 4.2 5173
(0:6:0) (6)2 4.5 4015 2.6 4534 4.2 5174
4.9 4019 2.5 4538 4.3 5178
(0:6:C)(6)2(0:C) 4.4 4021 (75)(0:C) 2.7 4575 (N6) (6) (NrN) 5476
O (7S)(OrC) 2.5 4576 (0:N65:N65:0) 4.0 5628
(75) 2.44548 O 2.6 4578 4.1 5631
(7S)(CrC) 4573 (63) 4678 (0:N65:N65 rO) (6)2(0 rC)2
(7S)(OrC) 2.5 4574 (0:63:0) 4.2 4797 5654
(7S)(OrC) 2.5 4580 4811 (N665) 4.7 5933
O 2.5 4582 (68) 4.2 5164 (N63) 3.0 6011
(0:63:0) 4.2 4769 (N65) (0:66:0) 3.2 5590 (N4635) (6) 7367
4.1 4770 (0:N65:N65:0) 3.9 5632 (06)(6)3 7567
4816 (N66rC)(N66) (CrC) 4.9 5859 (ON63:N) 4.9 7939
3.9 4824 (N665) 4.5 5936 (ON6^:N) 7941
(7665) 3.4 5056 (N63) (NrC) 4.3 6026 (S6)(6)3 8081
(7665) (OrN) 3.2 5057 6027 (O :S65:C) (S65) 8125
O (N263)(0:C) 6826 (SN5:C) (SN5) (C rC) 8213
(66) 4.1 5135 O 8214
(67) 5144 (06) (6)3 7565 (SN65:C) (N66) (CrC) 8311
0: 8314
4.1 5146 7577 /cw«.rw Qwq o*r n^
(N6) (6) (NrN) 4.6 5472 (066) (6) 7665 ^«"-W tc.b*O:b.b:>ro; 8316
4.5 5473 7669 (SN65:C) (SN65) (CrC) 8327
5480 /063: -.0. (SN665 rC) (SN665) (CrC) 8363
V
(N65rC)(6) 4.6 5594 Or 2 rO; 8364
(N66:C)(N:6:C)(C:C) (O: S65 rC) (S65) 8118 8365
4.7 5854 (SN5:C)(SN5)(6)4(C:C) 8216 8366
(N63:C)(N6a) 6041 8217 (SeN5:C) (SN65) (CrC) 8423
(066) (6) 7666 (SN65 rC) (SN65) (CrC) 8324
7668 (SN665:C)(SN65)(C:C) 8360
(063)(6)(OrC) 7763 (SeN5 rC) (SN65) (CrC) 8422 Xmax.: 580-589. 5my
O (SeN65rC)(SeN65) (CrC) 8428
(0:S65:S65:0) 8128 8432 (6)2(NrN) 3.1 2314
8130 (6) (OrC) (CrC)5 3035
(S63:N65) 8153 (6)2(OrC) (C :C)4 4.7 3111
(SN65:C)(SN65)(C:C) Amax : 570-579. 5my (75) 2.5 4528
5.2 8321 " 4562
8326 (6) (OrN)2 3674 4563
8328 O 2.7 4564
8329 2.5 4566
absorbing absorbing absorbing
chromophore loge no. chromophore loge no. chromophore loge no.
1 Abe, Harukawa, Ishikawa, Miki, Sumi, and Toga, J. Am. Chem. Soc., 78, 1416
2 Abe, Harukawa, Ishikawa, Miki, Sumi, and Toga, J. Am. Chem. Soc., 78, 1422
3 Acheson, Hoult, and Barnard, J. Chem. Soc., 1954, 4142
4 Acheson and Robinson, J. Chem. Soc., 1952, 1127
5 Adams, Cain, and Wolff, J. Am. Chem. Soc., 62, 732
6 Adams and Gold, J. Am. Chem. Soc., 62, 2038
7 Adams and Van Duuren, J. Am. Chem. Soc., 75, 4631
8 Adams and Van Duuren, J. Am. Chem. Soc., 75, 4638
8g Adams and Whitaker, J. Am. Chem. Soc., 78, 653
9 Adkins and Coonradt, J. Am. Chem. Soc., 63, 1563
10 Adler and Stenemur, Chem. Ber., 89, 291
11 Agallidis, Fromherz, and Hartmann, Ber., 71, 1391
12 Ahmad and Weedon, J. Chem. Soc., 1953, 2125
12c Ahmad and Weedon, J. Chem. Soc., 1953, 3286
13 Ainlery, Davies, Gudgeon, Harland, and Sexton, J. Chem. Soc., 1944, 147
14 Albert, Brown, and Cheeseman, J. Chem. Soc., 1952, 4219
15 Albert and Short, J. Chem. Soc., 1945, 760
15n Alder, Schafer, Esser, Krieger, and Reubke, Anal. Chem., 593, 23
16 Alford and Schofield, J. CHem. Soc., 1953, 1811
17 Allen and vanAllan, J. Org. Chem., 18, 882
17n Allenby and Collier, Arch. Biochem., 38, 147
18 Ames, Bowman, and Grey, J. Chem. Soc., 1953, 3008
19 Anchel, J. Am. Chem. Soc., 74, 1588
20 Anderson, J. Am. Chem. Soc., 55, 2094
21 Anderson and Geiger, J. Am. Chem. Soc., 54, 3064
22 Anderson and Gooding, J. Am. Chem. Soc., 57, 999
23 Anderson and Roedel, J. Am. Chem. Soc., 67, 955
24 Anderson and Seeger, J. Am. Chem. Soc., 71, 340
25 Anderson and Seeger, J. Am. Chem. Soc., 71, 343
26 Anderson and Steedly, J. Am. Chem. Soc., 76, 5144
27 Anderson, Nelson, and Tazuma, J. Am. Chem. Soc., 75, 4980
28 Andrews, Cristol, Lindenbaum, and Young, J. Am. Chem. Soc., 67, 715
29 Andrews and Keefer, J. Am. Chem. Soc., 75, 3776
30 Andrews and Linden, J. Am. Chem. Soc., 69, 2091
3On Andrisano and Pappalardo, Atti accad. naz. Lincei, [8] 15, 64
31 Arends, Ber., ^4, 1936
32 Armarego and Turner, J. Chem. Soc., 1957, 13
33 Armitage, Cook, Entwistle, Jones, and Whiting, J. Chem. Soc., 1952, 1998
34 Armitage and Whiting, J. Chem. Soc., 1952, 2005
35 Armitage, Cook, Jones, and Whiting, J. Chem. Soc., 1952, 2010
36 Armitage, Jones, and Whiting, J. Chem. Soc., 1952, 2014
37 Aronoff, J. Org. Chem., _5, 561
37n Askew, J. Chem. Soc., 1935, 509
37q Askew, J. Chem. Soc., 1935, 512
38 Atkinson, Parkes, and Polya, J. Chem. Soc., 1954, 4256
39 Atkinson, Komzak, Parkes, and Polya, J. Chem. Soc., 1954, 4508
40 Attenburrow, Elkes, Elliott, Hems, Harris, and Brodrick, J. Chem. Soc., 1954, 571
41 Attenburrow, Cameron, Chapman, Evans, Hems, Jansen, and Walker, J. Chem. Soc., 1952,
1094
42 AuIt, Hirst, and Morton, J. Chem. Soc., 1935, 1653
43 Austin, J. Am. Chem. Soc., 56, 2141
B
1 Cairns, Engelhardt, Jackson, KaIb, and Sauer, J. Am. Chem. Soc., 74, 5636
2 Calderbank and Le Fevre, J. Chem. Soc., 1948, 1949
2n Caldin and Long, Proc. Roy. Soc. (London), 228A, 263
3 Calvin and Wood, J. Am. Chem. Soc., 62, 3152
4 Campaigne and Cline, J. Org. Chem., 21, 32
5 Campaigne and Cline, J. Org. Chem., 21, 39
6 Campaigne, Cline, and Kaslow, J. Org. Chem., 15, 600
7 Campaigne and Diedrich, J. Am. Chem. Soc., 73, 5241
8 Campbell, Ginsig, and Schmid, HeIv. Chim. Acta, 36, 1489
8n Campbell, Linden, Godshalk, and Young, J. Am. Chem. Soc., 69, 880
9 Campbell and McCaIl, J. Chem. Soc., 1951, 2411
9g Camps, Ber., 25, 233
9n Carlin and Forshey, Jr., J. Am. Chem. Soc., 72, 793
9u Carlin and Landerl, J. Am. Chem. Soc., 75, 3969
10 Carmack and Leavitt, J. Am. Chem. Soc., 71, 1221
11 Carroll and Bader, J. Am. Chem. Soc., 75, 5400
12 Carson, J. Am. Chem. Soc., 75, 4337
13 Cason and KaIm, J. Org. Chem., 19, 1947
14 Cason and Phillips, J. Org. Chem., 17, 298
15 Cason and Sumrell, J. Org. Chem., 16, 177
16 Casten and Eisen, J. Am. Chem. Soc., 75, 4451
17 Castill and Ruppol, Bull. soc. chim. biol., IQ5 623
18 Castille and Ruppol, Bull. soc. chim. biol., 44, 351
19 Cava and Napier, J. Am. CHem. Soc., 78, 500
20 Cavalieri and Bendich, J. Am. Chem. Soc., 72, 2587
21 Cavalieri, Bendich, Tinker, and Brown, J. Am. Chem. Soc., 70, 3875
22 Cavallito, Martini, and Nachod, J. Am. Chem. Soc., 73, 2544
22x Celmer and Solomons, J. Am. Chem. Soc., 74, 3838
23 Celmer and Solomons, J. Am. Chem. Soc., 75, 1374
24 Cerniani and Passerini, J. Chem. Soc., 1954, 2261
25 Chaco and Iyer, Chem. & Ind. (London), Mar. 3. 1956. 155
25n Cheng and Riddick, Anal. Chem., 26, 536
26 Chanley and Sobotka, J. Am. Chem. Soc., 71, 4140
27 Charles and Freiser, J. Org. Chem., 18, 422
28 Charlesworth and Robinson, J. Chem. Soc., 1934, 1619
28n Cheeseman, Heilbron, Jones, Sondheimer, and Weedon, J. Chem. Soc., 1949, 2031
28u Cherbuliez and Giddey, HeIv. Chim. Acta, 35, 160
29 Chopard-dit-Jean and Heilbronner, HeIv. Chim. Acta, 35, 2170
30 Chuang and Han, Ber., 68, 876
31 Chuang and Han, Ber., 68, 876
32 Cilento, J. Am. Chem. Soc., 71, 1112
33 Cilento, J. Am. Chem. Soc., 75, 3748
34 Cilento and Miller, J. Am. Chem. Soc., 78, 1718
35 Cilento and Walter, J. Am. Chem. Soc., 76, 4469
36 Clar, "Aromatische Kohlenwasserstoffe, Polycyclische System", Springer-Verlag, 1952
37 Clar, Ber., 65, 848
38 Clar, Ber., 65, 848
39 Clar, Ber., 65>, 1417
40 Clar, Ber., j>9, 608
41 Clar, Ber., 69., 1671
42 Clar, Ber., 72,, 2139
43 Clar, Ber., .73, 596
44 Clar, Ber., 75, 1330
45 Clar, Ber., T^9 149
45g Clar, Ber., 76, 261
45n Clar, Ber., .76, 332
45u Clar, Ber., 76, 462
45x Clar, Ber., 76, 465
46 Clar, Ber., 76, 609
46a Clar, Ber., 76, 611
46b Clar, Ber., 7j>, 614
46z Clar, Chem. Ber., 81, 53
47 Clar, Chem. Ber., 81, 63
48 Clar, Chem. Ber., _8J^, 169
49 Clar, Chem. Ber., _81, 520
50 Clar, Chem. Ber., 82, 46
5Og Clar, Chem. Ber., 82, 495
51 Clar, J. Chem. Soc., 1949, 2013
52 Clar, J. Chem. Soc., 1949, 2168
53 Clar, J. Chem. Soc., 1949, 2442
54 Clar, Spectrochimica Acta, ^4, 116
54n Clar and Furnari, Ber., 65, 1421
55 Clar and Frdmmel, Chem. Ber., 81, 163
56 Clar and Kelly, J. Am. Chem. Soc., 76, 3502
57 Clar and Lombardi, Ber., 65, 1415
58 Clar and Stewart, J. Am. Chem. Soc., 74, 6235
59 Clar and Stewart, J. Am. Chem. Soc., 75, 2667
60 Clar and Stewart, J. Chem. Soc., 1951, 687
61 Clar and Stewart, J. Chem. Soc.. 1951, 3215
62 Clayton, Crawshaw, Henbest, Jones, Lovell, and Wood, J. Chem. Soc., 1953, 2009
63 Clemer and Solomons, J. Am. Chem. Soc., 75, 1372
63u Clemo and Cocker, J. Chem. Soc., 1946, 30
64 Clemo and Felton, J. Chem. Soc., 1951, 671
65 Clemo and Felton, J. Chem. SOc., 1952, 1658
66 Clemo and Legg, J. Chem. Soc., 1947, 545
67 Clemo and Mcllwain, J. Chem. Soc., 1938, 479
68 Clemo and Swan, J. Chem. Soc., 1938, 1454
69 Cocker, O'Meara, Schwarz, and Stuart, J. Chem. Soc., 1950, 2052
70 Codington and Mosettig, J. Org. Chem., 17, 1027
71 Codington and Mosettig, J. Org. Chem., 17, 1027
72 Codington and Mosettig, J. Org. Chem., 17, 1033
73 Cohen, Ostberg, Sparrow, and Blout, J. Polymer Sci., _3, 264
74 Cole and Ronzio, J. Am. Chem. Soc., 66, 1584
75 Colton, Jones, and Audrieth, J. Am. Chem. Soc., 76, 2572
76 Compton and Bergmann, J. Org. Chem., 12, 363
77 Conover and Tarbell, J. Am. Chem. Soc., 72, 5221
78 Conrad-Billroth, Z. physik. Chem., 29, 170
79 Conroy and Denton, J. Org. Chem., 18, 1489
80 Cook, Dansi, Hewett, !ball, and Mayneord, J. Chem. Soc., 1935, 1319
81 Cook, Gibb, Raphael, and Somerville, J. Chem. Soc., 1951, 503
82 Cook, Hewett, Mayneord, and Roe, J. Chem. Soc., 1934, 1727
83 Cook, Jones, and Polya, J. Chem. Soc., 1939, 1315
84 Cook, Jones, and Whiting, J. Chem. Soc., 1952, 2883
85 Cooke and Macbeth, J. Chem. Soc., 1938, 1408
86 Cooke, Macbeth, and Winzor, J. Chem. Soc., 1939, 878
87 Cookson, J. Chem. Soc., 1953, 1328
88 Cookson, J. Chem. Soc., 1953, 2789
89 Cookson, J. Chem. Soc., 1953, 2789
90 Cooper, Partridge, and Short, J. Chem. Soc., 1951, 391
91 Cope and Burg, J. Am. Chem. Soc., 74, 168
92 Cope, Burg, and Fenton, J. Am. Chem. Soc., 74, 173
93 Cope and Campbell, J. Am. Chem. Soc., 74, 179
94 Cope and Estes, Jr., J. Am. Chem. Soc., 72, 1128
95 Cope, Haven, Jr., Ramp, and Crumbull, J. Am. Chem. Soc., 74, 4867
96 Cope and Overberger, J. Am. Chem. Soc., 70, 1433
96n Corbett, Metcalf, and Soper, J. Chem. Soc., 1953, 1927
97 Corey and Burke, J. Am. Chem. Soc., 78, 174
98 Corey, Burke, and Remers, J. Am. Chem. Soc., 78, 180
99 Cornforth and Huang, J. Chem. Soc., 1948, 1988
100 Cosgrove and Waters, J. Chem. Soc., 1951, 388
101 Cosulich, Seeger, Fahrenbach, Collins, Roth, Hultquist, and Smith, J. Am. Chem. Soc.,
JT^, 4675
102 Craig, J. Chem. Soc., 1946, 534
102n Craig, Jacobs, and Lavin, J. Biol. Chem., 139, 277
103 Craig and Short, J. Chem. Soc., 1945, 419
103n Cram, J. Am. Chem. Soc., 71, 3953
104 Cram and Cranz, J. Am. Chem. Soc., 72, 595
105 Cram and Daeniker, J. Am. Chem. Soc., 76, 2743
106 Cram and Hatch, J. Am. Chem. Soc., 75, 33
107 Crawford and Smyth, J. Chem. Soc., 1952, 4133
108 Crombie and Manzoor-i-Khuda, Chem. & Ind. (London), 1956, 409
109 Cromwell, Barker, Wankel, Vanderhorst, Olson, and Anglin, J. Am. Chem. Soc., 73, 1044
109n Cromwell and Graff, J. Org. Chem., 17, 414
109u Cromwell and Hoeksema, J. Am. Chem. Soc., 71, 716
110 Cromwell and Watson, J. Org. Chem., 14, 411
111 Crow, Haworth, and Jefferies, J. Chem. Soc., 1952, 3705
112 Crowe and Nord, J. Org. Chem., 15, 81
113 Crowe and Nord, J. Org. Chem., 15, 1177
113n Cunningham, Newbold, Spring, and Stark, J. Chem. Soc., 1949, 2092
114 Curtin and Crawford, Chem. & Ind. (London), Apr. 28, 1956, 313
115 Cymerman, Heilbron, Jones, and Lacey, J. Chem, Soc., 1946, 500
1 Jackman, Bolen, Nachod, Tullar, and Archer, J. Am. Chem. Soc., 71, 2301
2 Jackson and Jones, J. Chem. Soc., 1940, 659
3 Jacobs and Singer, J. Org. Chem., 17, 477
4 Jaeger and Smith, J. Chem. Soc., 1955, 165
4u Jaffe*, J. Am. CHem. Soc., 77_, 4451
5 Jaffe, J. Chem. Phys. , 2:2, 1431
6 Jaffe and Freedman, J. Am. Chem. Soc., 74, 1069
7 Jander and Haszeldine, J. Chem. Soc., 1954, 912
8 Jander and Haszeldine, J. Chem. Soc., 1954, 919
9 Jarowski and Hess, J. Am. Chem. Soc., 71, 1711
10 Jaunin, Piccoli, and Charalambous, HeIv. Chim. Acta, 37, 216
1On Jerchel and Fischer, Ann., 590, 217
11 Johnson and Buell, J. Am. Chem. Soc., 74, 4517
12 Johnson, Erickson, and Ackerman, J. Am. Chem. Soc., 74, 2251
13 Johnson, Gutsche, Hirschmann, and Stromberg, J. Am. Chem. Soc., 73, 322
13n Johnson, Langemann, and Murray, J. Chem. Soc., 1953, 2136
14 Johnson and Mathews, J. Am. Chem. Soc., 66, 210
15 Johnson, Woroch, and Mathews, J. Am. Chem. Soc., 69, 566
16 Jones, J. Am. Chem. Soc., 67, 2021
17 Jones, Cancer Res., ^, 237
18 Jones, Chem. Revs., 41, 353
19 Jones, J. Am. Chem. Soc., 62, 148
20 Jones, J. Am. Chem. Soc., 63, 151
21 Jones, J. Am. Chem. Soc., 63, 313
21n Jones, J. Am. Chem. Soc., 63, 1658
22 Jones, J. Am. Chem. Soc., 63, 2528
23 Jones, J. Am. Chem. Soc., 65, 1815
24 Jones, J. Am. Chem. Soc., 65, 1818
24u Jones, J. Am. Chem. Soc., 67, 2021
25 Jones, J. Am. Chem. Soc., 67, 2127
26 Jones, Holmes, and Steigman, Anal. Chem., 28, 191
27 Jones and Letham, Analyst, 81, 16
28 Jones and Lindsey, J. Chem. Soc., 1950, 1836
29 Jones and McCombie, J. Chem. Soc., 1943, 262
29n Jones, Jr. and Taylor, Anal. Chem., 27, 228
30 Jones, Whitham, and Whiting, J. Chem. Soc., 1954, 1865
3Oc Jones, Whitham, and Whiting, J. Chem. Soc., 1954, 3201
31 Jones and Whiting, J. Chem. Soc., 1949, 1423
32 Jones, Whiting, Armitage, Cook, and Entwistle, Nature, 168, 900
33 Jones, Wilkinson, and Kerlogue, J. Chem. Soc., 1942, 391
33n Juday, J. Am. Chem. Soc., 75, 4071
34 Julian, Cole, and Schroeder, J. Am. Chem. Soc., 71, 2368
35 Julian and Printy, J. Am. Chem. Soc., 75, 5301
36 Julian, Printy, Ketcham, and Doone, J. Am. Chem. Soc., 75, 5305