中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
A Highly Efficient Chiral-Bridged Diphosphine Ligand Modified Cationic Palladium(II) Catalyst System for Asymmetric Alternating Copolymerization of Proipene and Carbon Monoxide

文献类型:期刊论文

作者Wang LL(王来来); Wang LL(王来来)
刊名Synlett
出版日期2009
期号16页码:2696-2700
关键词palladium chiral-bridged biphenyl diphosphine propene and CO asymmetric alternating copolymerization chiral polyketone
ISSN号0936-5214
通讯作者王来来
中文摘要A highly efficient chiral-bridged biphenyl diphosphine ligand [(Rax)-BuP] modified cationic palladium(II) catalyst system for the synthesis of optically active polyketone by stereoselective alternating copolymerization of propene and carbon monoxide is reported for the first time. The results show that [Pd(MeCN)4][OTf]2 is an excellent catalyst precursor in a mixed solvent of MeNO2–MeOH. The highest catalytic activity was found to be 221 g polymer/(g Pd·h). A chiral polyketone with molecular weight Mn = 2.9 × 104, polydispersity = 1.4, and molar optical rotation = +37° was afforded under optimized reaction conditions.
学科主题金属有机与超分子催化
收录类别SCI
资助信息the National Natural Science Foundation of China (Nos. 20343005;20473107;20673130;20773147);the Hong Kong PolyU Joint Supervision Scheme (A-PH78)
语种英语
公开日期2012-09-21
源URL[http://210.77.64.217/handle/362003/565]  
专题兰州化学物理研究所_OSSO国家重点实验室
通讯作者Wang LL(王来来); Wang LL(王来来)
推荐引用方式
GB/T 7714
Wang LL,Wang LL. A Highly Efficient Chiral-Bridged Diphosphine Ligand Modified Cationic Palladium(II) Catalyst System for Asymmetric Alternating Copolymerization of Proipene and Carbon Monoxide[J]. Synlett,2009(16):2696-2700.
APA 王来来,&王来来.(2009).A Highly Efficient Chiral-Bridged Diphosphine Ligand Modified Cationic Palladium(II) Catalyst System for Asymmetric Alternating Copolymerization of Proipene and Carbon Monoxide.Synlett(16),2696-2700.
MLA 王来来,et al."A Highly Efficient Chiral-Bridged Diphosphine Ligand Modified Cationic Palladium(II) Catalyst System for Asymmetric Alternating Copolymerization of Proipene and Carbon Monoxide".Synlett .16(2009):2696-2700.

入库方式: OAI收割

来源:兰州化学物理研究所

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