THE PHOTOCHEMICAL FORMATION OF ORGANOMETALLIC RADICALS FROM ALPHA-DIIMINE COMPLEXES HAVING A METAL-METAL, METAL-ALKYL OR METAL-HALIDE BOND

被引：14

作者：

STUFKENS, DJ

VANOUTERSTERP, JWM

OSKAM, A

ROSSENAAR, BD

STOR, GJ

机构：

[1] Anorganisch Chemisch Laboratorium, Universiteit van Amsterdam, J.H. van 't Hoff Instituut, 1018 WV Amsterdam

来源：

COORDINATION CHEMISTRY REVIEWS | 1994年 / 132卷

关键词：

D O I：

10.1016/0010-8545(94)80034-0

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

This article describes the homolytic splitting of metal-metal, metal-alkyl and metal-halide bonds by visible excitation of alpha-diimine complexes into their MLCT transitions. It is shown that mechanistic information about these reactions can best be obtained from the alkyl complexes which show a strong dependence of their quantum yield on the alkyl group. A detailed mechanism is presented for the photochemistry of fac-XMn(CO)3 (alpha-diimine)(X = halide) which complexes, quite unexpectedly, photodecompose into radicals Mn+(CO)3(alpha-diimine.-) via their mer-isomers.

引用

页码：147 / 154

页数：8

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