一氧化碳
化学
钯
催化作用
乙烯
一氧化碳
丙烯
高分子化学
磷化氢
甲醇
烯烃纤维
齿合度
有机化学
共聚物
聚合物
晶体结构
作者
E. Drent,J. A. M. van Broekhoven,Michael J. Doyle
标识
DOI:10.1016/0022-328x(91)80176-k
摘要
A class of highly efficient homogeneous palladium catalyst systems has been developed for the production of perfectly alternating copolymers of carbon monoxide with ethylene. Mixtures of carbon monoxide, ethylene and propene are converted into the corresponding alternating carbon monoxide/olefin terpolymers in which C3 units randomly replace ethylene units along the chain. The essential features of the new catalyst systems are that they are formed by the combination of an equimolar quantity of a suitable bidentate phosphine ligand with a palladium(II) species in which the counter anions are weakly coordinating. For a series of diphenylphosphinoalkanes of general formula Ph2P(CH2)mPPh2 the most efficient catalyst system for the production of high-molecular-weight polyketones is that with m = 3. High rates with conversions of more than one million molecules of carbon monoxide and ethylene per palladium center are obtained. In methanol, the majority of the polymer chains produced are polyketo-esters of general formula H(CH2CH2CO)nOMe; analyses of methanol-soluble oligomer fractions shows that diesters MeOCO(CH2CH2CO)nOMe and diketones H(CH2CH2CO)nCH2CH3 are also formed. Two interlinked catalytic cycles are invoked to account for the formation of polyketones with keto-ester, diester and diketone end groups.
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