Photochemical studies of binuclear phenoxysubstituted phthalocyanines containing catecholate bridges

被引:13
作者
Seotsanyana-Mokhosi, I [1 ]
Maree, S [1 ]
Maree, MD [1 ]
Nyokong, T [1 ]
机构
[1] Rhodes Univ, Dept Chem, ZA-6140 Grahamstown, South Africa
关键词
binuclear phthalocyanines; phenoxyphthalocyanine; singlet oxygen quantum yield; photobleaching; fluorescence; zinc phthalocyanine;
D O I
10.1142/S1088424603000239
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Binuclear ZnPc complexes covalently bridged by catechol units have been synthesized and their absorption and photochemical properties examined. The complexes studied are 1,2-bis-2',9',16',23'-triphenoxyphthalocyaninatozinc benzene (6a), 1,2-bis-2'-9',16',23'-tri-4-carboxyphenoxyphthalocyaninatozinc benzene (6b), 1,2-bis-2',9',16',23'-tri-4-nitrophenoxyphthalocyaninatozinc benzene (6c) and 1,2-bis-2'-9',16',23'-tri-4-tert-butylphenoxyphthalocyaninatozinc benzene (6d). Larger intramolecular coupling was observed for 6b and 6c, containing the carboxyphenoxy and nitrophenoxy substituents, respectively, than for 6a and 6d. A single Q band peak was observed for the fluorescence spectra of 6b and 6c, whereas, 6a and 6d showed a split Q band. The absence of the high energy fluorescence peaks corresponding to absorbance peaks in the 640 nm region, suggests that the intramolecular coupling is broken by excitation for complexes 6b and 6c. Copyright (C) 2003 Society of Porphyrins & Phthalocyanines.
引用
收藏
页码:167 / 175
页数:9
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