REACTIONS OF LEWIS BASES WITH METHYLMANGANESE PENTACARBONYL

被引:63
作者
KRAIHANZEL, CS
MAPLES, PK
机构
[1] Department of Chemistry, Lehigh University, Bethlehem
关键词
D O I
10.1021/ic50067a021
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The reactions of a variety of Lewis bases with CH3Mn(CO)5 were examined as a function of time by H1 nmr and infrared spectral methods. Triphenylphosphine, triphenylarsine, and trimethyl phosphite react with CH3Mn(CO)5 to yield a mixture of cis- and trans-CH3COMn(CO)4L complexes. Other phosphorus donor ligands, triphenylstibine, and various amines yield exclusively cis-CH3COMn (CO)4L derivatives. All acetylmanganese complexes, except those with L = amine, were shown to decarbonylate upon heating to yield exclusively cis-CH3Mu(CO)4L. The reaction equilibria are affected by variations in the nucleophilicities and steric requirements of the ligands. A modified methyl-migration mechanism is able to explain the stereochemistry of the products of the decarbonylation reaction. © 1968, American Chemical Society. All rights reserved.
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页码:1806 / +
页数:1
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