New pyridyl-functionalized organoiron alkynyl complexes. Easy access to polymetallic architectures featuring an electroactive site by simple co-ordination reactions

被引：37

作者：

Le Stang, S ^{[1
]}

Lenz, D ^{[1
]}

Paul, F ^{[1
]}

Lapinte, C ^{[1
]}

机构：

[1] Univ Rennes 1, Dept Chem, UMR CNRS 6509, F-35042 Rennes, France

来源：

JOURNAL OF ORGANOMETALLIC CHEMISTRY | 1999年 / 572卷 / 02期

关键词：

organoiron(II); organoiron(III); iron acetylide; Sonogashira-coupling; substituted pyridine; pyridinium salt; dinuclear complex;

D O I：

10.1016/S0022-328X(98)00961-9

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

The functionalized complexes 3a-d [(dppe)Cp*Fe(C=C-L)] (L = 4-Py, 3-Py, 2-Py) were isolated with good yields from the alkynyl complex 1 [(dppe)Cp*Fe(C=CH)1 (dppe = 1,2-bis(diphenylphosphino)ethane) from the corresponding bromopyridines using a Sonogashira-coupling reaction. These redox active compounds are stable under two redox states and react as usual pyridyl ligands towards methyl iodide or (THF)W(CO)(5). They allow easy access to the corresponding pyridinium salt 4a or to the dimetallic iron-tungsten complex 5a. (C) 1999 Elsevier Science S.A. All rights reserved.

引用

页码：189 / 192

页数：4

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