Synthetic, structural, electrochemical and electronic characterisation of heterobimetallic bis(acetylide) ferrocene complexes

被引:127
作者
Colbert, MCB
Lewis, J
Long, NJ
Raithby, PR
White, AJP
Williams, DJ
机构
[1] UNIV LONDON IMPERIAL COLL SCI TECHNOL & MED,DEPT CHEM,LONDON SW7 2AY,ENGLAND
[2] UNIV CAMBRIDGE,DEPT CHEM,CAMBRIDGE CB2 1EW,ENGLAND
来源
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS | 1997年 / 01期
关键词
D O I
10.1039/a605177d
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A series of novel heterobimetallic bis(acetylide) ferrocene complexes featuring a bis[1,2-bis(diphenylphosphino)-methane]ruthenium centre and seven variously substituted aromatic acetylene ligands have been synthesised and characterised. The crystal structure of trans-[Ru(dppm)(2){C=C(C5H4)Fe(C5H5)}(2)] shows the ruthenium centre in a distorted-octahedral environment bound to two ferrocene units in a linear fashion by 'rigid-rod'-like acetylene linkages. The conformation is stabilised by strong intramolecular CH ...pi(C=C) interactions Electrochemical studies showed that incorporation of donor-substituted aromatic acetylide ligands causes a cathodic shift in the Ru-II/III redox potential. Conversely, an anodic shift is observed when electron-withdrawing substituents are present in the acetylide systems. Electronic spectral measurements indicated that the systems belong to the Robin and Day 'Class II' mixed-valence species and suggest that greater electronic interaction occurs in the bis(acetylide) complexes than in the corresponding monoacetylide chloro-complex.
引用
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页码:99 / 104
页数:6
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