Phosphine substituted Ru3(μ-dppm)(CO)10:: structural trends within [Ru3( μ-dppm)(PR3)(CO)9] (R=Et, Ph, Cy and Pri)

被引：21

作者：

Torabi, AA ^{[1
]}

Humphreys, AS ^{[1
]}

Koutsantonis, GA ^{[1
]}

Skelton, BW ^{[1
]}

White, AH ^{[1
]}

机构：

[1] Univ Western Australia, Dept Chem, Nedlands, WA 6009, Australia

来源：

JOURNAL OF ORGANOMETALLIC CHEMISTRY | 2002年 / 655卷 / 1-2期

关键词：

ruthenium; carbonyl substitution; cluster; phosphine;

D O I：

10.1016/S0022-328X(02)01567-X

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

The complexes [Ru-3(mu-dppm)(PR3)(CO)(9)] (R=Et, Ph, Cy, Pr'} were prepared from [Ru-3(mu-dppm)(CO)(10)] by simple phosphine substitution reactions at room temperature and their structures determined by single crystal X-ray studies. Variations in the Ru-Ru bond adjacent to the phosphine ligand suggest the enhanced reactivity of [Ru-3(mu-dppm)(CO)(10)] over the parent carbonyl [Ru-3(CO)(12)] to be consequent on the inability of [Ru-3(mu-dppm)(CO)(10)] to effectively relieve steric congestion imposed by the presence of the bulky, bidentate dppm ligand. (C) 2002 Elsevier Science B.V. All rights reserved.

引用

页码：227 / 232

页数：6

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