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首页> 外文期刊>e-Polymers >Silica supported Schiff-base cobaltIII complex-Lewis base system: a highly selective catalyst for alternating copolymerization of CO2 and propylene oxide
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Silica supported Schiff-base cobaltIII complex-Lewis base system: a highly selective catalyst for alternating copolymerization of CO2 and propylene oxide

机译:二氧化硅负载的席夫碱钴III络合物-刘易斯碱体系:一种高选择性催化剂,用于二氧化碳和环氧丙烷的交替共聚

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摘要

An binary catalyst system of a silica supported Schiff-base cobalt complex SalenCoIII (OAC)-MCM-41 (Salen = 3-[N,N-bis-2-(3,5-di-tert-butylsalicylidenamino) ethyl] amine) was developed to generate the copolymerization of CO2 and propylene oxide in presence of (4-dimethylamino)-pyridine (DMAP). The influence of the molar ratio of catalyst components, the operating temperature, reaction time, and CO2 pressure on the yield as well as the molecular weight of polycarbonate was systematically investigated. The high selectivity of polycarbonate over cyclic carbonate at 40 °C was maintained after a longer reaction time to attain quantitative formation of the alternating copolymer. High molecular weight of 67 000 were achieved at an appropriate combination of all variables.
机译:二氧化硅负载的席夫碱钴配合物SalenCoIII(OAC)-MCM-41的二元催化剂体系(Salen = 3- [N,N-双-2-(3,5-二叔丁基水杨醛基氨基)乙基]胺)在(4-二甲基氨基)-吡啶(DMAP)的存在下开发了用于产生CO 2和环氧丙烷的共聚的聚合物。系统地研究了催化剂组分的摩尔比,操作温度,反应时间,CO2压力对聚碳酸酯收率和分子量的影响。较长的反应时间后,在40°C的条件下,聚碳酸酯相对于环状碳酸酯具有较高的选择性,从而可以定量形成交替共聚物。在所有变量的适当组合下,可获得67 000的高分子量。

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