Transition-metal hydrides as hydrogen atom donors: Stronger metal-hydrogen bonds can be advantageous

被引：15

作者：

O'Connor, Joseph M. ^{[1
]}

Friese, Seth J. ^{[1
]}

机构：

[1] Univ Calif San Diego, Dept Chem & Biochem 0358, La Jolla, CA 92093 USA

来源：

ORGANOMETALLICS | 2008年 / 27卷 / 17期

基金：

美国国家科学基金会;

关键词：

D O I：

10.1021/om800551d

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

The tungsten hydride complex (eta(5)-C5H5)W(CO)(3)H (1-W) functions as a hydrogen atom donor in the [(eta(5)- C5Me5)Ru(NCMe)(3)]PF6-mediated Bergman cycloaromatization reaction of (Z)-dodeca-4,8-diyn-6-ene. The strong M-H bond in 1-W does not react with the enediyne substrate but does react with the diradical arising from cyclization, thereby demonstrating the advantages of strong metal-hydrogen bonds in the hydrogen atom transfer reactions of metal hydrides with substrates involving alkenes and alkynes.

引用

页码：4280 / 4281

页数：2

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