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胺基膦钌卡宾化合物的合成及催化烯烃复分解反应 被引量:2

Synthesis of Aminophosphine Ruthenium Carbene Complex and Its Application in Olefins Metathesis Reaction
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摘要 合成并表征了一类含新型胺基膦配体的Grubbs二代型钌卡宾烯烃复分解催化剂[RuCl2(H2IMes)·(R1HNPR22)(=CHPh)],采用核磁共振波谱和单晶X射线衍射确定了催化剂的结构.在室温条件下,以N,N-二烯丙基-对甲苯磺酰胺的关环复分解反应(RCM)为模型,考察了不同胺基膦配体对钌卡宾催化反应速率的影响.结果表明,G2⁃1表现出最佳的催化活性.通过底物研究发现,G2⁃1催化剂(摩尔分数,1%)对双端烯及多端烯的RCM反应具有较好的活性和官能团适应性,产物收率均>95%;G2⁃1催化剂同样适用于同(异)端烯底物的交叉复分解反应(CM),其催化苯乙烯与3-苯氧基丙烯的CM反应时产物收率高达92%. A series of Grubbs ruthenium carbene catalysts featuring an aminophosphine ligand[RuCl2·(H2IMes)(R1HNPR22)(=CHPh)]was synthesized and characterized by means of nuclear magnetic resonance spectrometry and single crystal X-ray diffraction.Under the ambient conditions,these ruthenium complexes were tested as catalyst for the ring-closing metathesis(RCM)reaction of N,N-diallyl-p-toluenesulfonamide,and complex G2⁃1 was found to have the best catalytic activity.With the catalyst loading in the range of 0.1%—2.0%(molar fraction),G2⁃1 was compatible with the RCM reaction of various diene and polyene,and had high catalytic activity(>95%yield of product).G2⁃1 could also be used as catalyst for cross metathesis(CM)reaction of different terminal olefin substrates,up to 92%yield was achieved in the CM reaction of styrene and 3-phenoxypropene.
作者 王晋宇 柳春丽 陈延辉 WANG Jinyu;LIU Chunli;CHEN Yanhui(Tianjin Key Laboratory of Brine Chemical Engineering and Resource Eco-utilization,College of Chemical Engineering and Materials Science,Tianjin University of Science&Technology,Tianjin 300457,China)
出处 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2020年第12期2766-2773,共8页 Chemical Journal of Chinese Universities
基金 国家自然科学基金(批准号:21371131)资助.
关键词 胺基膦配体 钌卡宾配合物 关环复分解 交叉复分解 Aminophosphine Ruthenium carbene complex Ring-closing metathesis Cross metathesis
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  • 1TrnkaT. M., GrubbsR. H.. Ace. Chem. Res.[J],2001, 34:18--29.
  • 2Buchowicz W. , Holerca M. N. , Percec V.. Macromolecules[ J], 2001, 34:3842--3848.
  • 3Chemtob A. , H6roguez V. , Gnanou Y.. J. Polym. Sci. Part A: Polym. Chem. [J], 2004, 42:1154--1163.
  • 4Quemener D. , Chemtob A. , H roguez V. , et al.. Polymer[J], 2005, 46:1067--1075.
  • 5Gallivan J. P. , Jordan J. P. , Grubbs R. H.. Tetrahedron Lett. [J] , 2005, 46:2577--2580.
  • 6Breitenkamp K. , Emrick T.. J. Polym. Sci. Part A: Polym. Chem. [J] , 2005, 43:5715--5721.
  • 7Hong S. H., Grubbs R. H.. J. Am. Chem. Soc. [J], 2006, 128:3508--3509.
  • 8Samanta D. , Kratz K. , Zhang X. F. , et al.. Macromolecules[J] , 2008, 41:530--532.
  • 9Audic N. , Clavier H. , Mauduit M. , et al.. J. Am. Chem. Soc. [J], 2003, 125:9248--9249.
  • 10Kubisa P.. J. Polym. Sci. , Part A: Polym . Chem. [J] , 2005, 43:4675--4683.

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