Reductive elimination of halogens assisted by phosphine ligands in Fe(CO)4X2 (X = I, Br) complexes

被引：24

作者：

Bellachioma, Gianfranco ^{[1
]}

Cardaci, Giuseppe ^{[1
]}

Macchioni, Alceo ^{[1
]}

Venturi, Chiara ^{[1
]}

Zuccaccia, Cristiano ^{[1
]}

机构：

[1] Univ Perugia, Dipartimento Chim, I-06123 Perugia, Italy

来源：

JOURNAL OF ORGANOMETALLIC CHEMISTRY | 2006年 / 691卷 / 18期

关键词：

reductive elimination; carbonyl halide iron complexes; phosphonium salts; radical mechanism;

D O I：

10.1016/j.jorganchem.2006.05.041

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

Fe(CO)(4)X-2 complexes [X = I (1), Br(1')] react with phosphine ligands L (L = PMe3, PEt3, PMe2Ph, PMePh2, PPh3) via a two-step mechanism: in the first step fac-Fe(CO)(3)LX2 Complexes are formed; in the second step two parallel pathways, a and b, are observed; in pathway a, reductive elimination with formation of equimolar amounts of Fe(CO)(3)L-2 (5) and phosphonium salts [LX]X-+(-) is observed; in pathway b, disubstituted dihalide complexes cis,trans,cis-Fe(CO)(2)L2X2 are formed. The relative weights of pathways a and b depend on the basicity, steric hindrance and concentration of ligand L, on the nature of the halogen and on temperature. A radical mechanism which accounts for most of the experimental results is proposed. (c) 2006 Elsevier B.V. All rights reserved.

引用

页码：3881 / 3888

页数：8

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