The Reaction of Cobalt Hydrocarbonyls Substituted by Tertiary Phosphines with an Olefin

Masato Tanaka, Yoshihisa Watanabe, T. Mitsudo, Y. Takegami
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Abstract

The carbonylation reaction of ethyl vinyl ether with various cobalt hydrocarbonyls, HCo(CO)4, HCo(CO)3PR3, HCo(CO)3P(OR)3, and HCo(CO)2[P(OR)3]2 was studied. Almost all of the cobalt hydrocarbonyls react with ethyl vinyl ether to form the branched chain acyl complexes, CH3CH(OC2H5)COCo(CO)4-nLn (L; CO, PR3 and P(OR)3), regardless of the character of the ligands at 0∼25°C, while HCo(CO)2[P(OEt)3]2 does not react even at 65°C. The order of the reactivities is parallel to that of the electron-accepting character of the ligand. The addition of an excess of the ligand retards the reaction. The activation parameters of the reaction of HCo(CO)3PPh3 with ethyl vinyl ether were estimated to be ΔH≠=9.88kcal/mol, ΔS≠=-41.0e.u.
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叔膦取代钴羰基与烯烃的反应
研究了乙基乙烯醚与多种钴羰基、HCo(CO)4、HCo(CO)3PR3、HCo(CO)3P(OR)3、HCo(CO)2[P(OR)3]2的羰基化反应。几乎所有的钴羰基与乙基乙烯醚反应生成支链酰基配合物CH3CH(OC2H5)COCo(CO)4-nLn (L;CO, PR3和P(OR)3)在0 ~ 25°C时,与配体的性质无关,而HCo(CO)2[P(OEt)3]2即使在65°C时也不发生反应。反应的顺序与配体的电子接受性的顺序平行。过量配体的加入延缓了反应。HCo(CO)3PPh3与乙基乙烯醚反应的活化参数为ΔH≠=9.88kcal/mol, ΔS≠=-41.0e.u。
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