SYNTHESIS AND RING-OPENING REACTIONS OF CATIONIC RUTHENIUM BIARYL THIONOLACTONE COMPLEXES

被引：18

作者：

BRINGMANN, G

SCHONER, B

SCHUPP, O

SCHENK, WA

REUTHER, I

PETERS, K

PETERS, EM

VONSCHNERING, HG

机构：

[1] UNIV WURZUBRG,INST ANORGAN,HUBLAND,D-97074 WURZBURG,GERMANY

[2] UNIV WURZBURG,INST ORGAN CHEM,D-97074 WURZURG,GERMANY

[3] MAX PLANCK INST FESTKORPERFORSCH,D-70506 STUTTGART,GERMANY

来源：

JOURNAL OF ORGANOMETALLIC CHEMISTRY | 1994年 / 472卷 / 1-2期

关键词：

RUTHENIUM; CRYSTAL STRUCTURE; THIONOLACTONE; RING OPENING; FLUXIONALITY;

D O I：

10.1016/0022-328X(94)80213-0

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

The preparations of novel thionolactone-bridged configuratively labile biaryls and their [Cp(R3P)2Ru]+-complexes are described. The dynamics of helimerization of these complexes and their reactivity towards nucleophiles have been investigated. Hydride transfer reagents lead to a cleavage of the thionolactone bridge to give the corresponding thiolate complexes, apparently via intermediate exothiolactolate ruthenium complexes. A similar lactolate analog is formed upon addition of a mild S-nucleophile.

引用

页码：275 / 284

页数：10

共 26 条

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