PRIMARY PHOTOCHEMICAL PROCESSES IN FAC-CLRE(CO)3L2 (L=4-PHENYLPYRIDINE AND 4-CYANOPYRIDINE) - A STEADY-STATE AND FLASH PHOTOCHEMICAL STUDY OF REACTION-PRODUCTS AND INTERMEDIATES

被引：35

作者：

FELIZ, M ^{[1
]}

FERRAUDI, G ^{[1
]}

ALTMILLER, H ^{[1
]}

机构：

[1] UNIV NOTRE DAME,RADIAT LAB,NOTRE DAME,IN 46556

来源：

JOURNAL OF PHYSICAL CHEMISTRY | 1992年 / 96卷 / 01期

关键词：

D O I：

10.1021/j100180a050

中图分类号：

O64 [物理化学（理论化学）、化学物理学];

学科分类号：

070304 ; 081704 ;

摘要：

The photochemistry of fac-ClRe(CO)3L2, L = 4-phenylpyridine and 4-cyanopyridine, has been investigated by monochromatic steady-state and flash photolyses between 400 and 229 nm. Two parallel photoprocesses, the photogeneration of the emissive MLCT state and the photoredox dissociation in {ClRe(CO)3L+, L .-} products, have been observed with both compounds. A third photoprocess, namely, the photogeneration of a Re(I)-ligand biradical, has been observed only in photolyses of the 4-phenylpyridine complex. While this Re(I)-ligand biradical reduces Cu(II)(TIM)2+ to the corresponding Cu(I) species, no such reaction is undergone by the MLCT state. Differences between the electronic structures of these complexes, shown by extended Huckel MO calculations, were related to their intrinsic photochemical behavior.

引用

页码：257 / 264

页数：8

共 44 条

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