Affiliation:
1. Anorganisch-Chemisches Institut der Technischen Universität München
Abstract
Reduction of paramagnetic L4Co (L = (CH3)3P) (d9) by alkali metals affords salts of L4Co- (d10). These are strong reducing agents, powerful bases and very able nucleophiles. They rapidly exchange three of their phosphine ligands for CO. Their reactions with a variety of inorganic and organic halides are shown to be effectively oxidative additions. From the distinct thermochromic behaviour of these salts both in the solid state and in solution a reversible formation involving different states of solvation is deduced.
Cited by
46 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献