Carbon monoxide insertion reactions. VI. Mechanisms of the reactions of methylmanganese pentacarbonyl and acetylmanganese pentacarbonyl with triphenylphosphine
Carbon monoxide insertion reactions. VI. Mechanisms of the reactions of methylmanganese pentacarbonyl and acetylmanganese pentacarbonyl with triphenylphosphine
复制标题
一氧化碳插入反应。
DOI:
10.1021/ic50060a037
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发表时间:
1968
影响因子:
4.6
通讯作者:
F. Calderazzo
中科院分区:
文献类型:
--
作者:
K. Noack;M. Ruch;F. Calderazzo
(CeH6) 3 (I). The cis and trans isomers, which givetwo distinct acetyl proton peaks in nmr spectra, have been separated by chromatography on silica and the infrared spectra of enriched chromatographic fractions were measured. The number of infrared C-0 stretching vibrations is that expected for local Cs and Civ symmetries for the cis and the trans isomers, respec-kl tively. The cis isomer is the initial product of the reaction. The rate of isomerization cis trans follows a first-order kinetic equation with k\= 2.5 X 10-4sec-1 at 30 in acetone. A dissociative intermolecular mechanism involving {CH3-COMnfCOh} is proposed for the isomerization. This is confirmed by the finding that an isomeric mixture of CH3COMn-(CO) 4P (C6H6) 3 exchanges the phosphine ligand with P (C6D5) 3. The infrared study of the reaction between CHWCOMn-(CO) s and triphenylphosphine has shown that the final product is the isomeric mixture of CH313COMn (CO) 4P (C6H5) 3 with retention of 13C labeling at the acetyl position. A dissociative mechanism is proposed for this reaction.