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首页> 外文期刊>Bulletin of the Korean Chemical Society >Bis(azido)paIladium(II)Complexes Bearing an(R or S)-(BINAP) Ligand:Synthesis,Structures,and Catalytic Application to Suzuki-Miyaura C-C Coupling Reactions
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Bis(azido)paIladium(II)Complexes Bearing an(R or S)-(BINAP) Ligand:Synthesis,Structures,and Catalytic Application to Suzuki-Miyaura C-C Coupling Reactions

机译:BIS(AZIDO)铜梨体(II)复合物轴承(R或S) - (BINAP)配体:合成,结构和催化应用于Suzuki-Miyaura C-C偶联反应

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摘要

Chiral ligand 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl(BINAP)is widely utilized as an ancillary ligand for late-transition-metal complexes,especially for Ru and Rh metals,in asymmetric organic catalysis.BINAP-Pd(II)complexes in particular have been intensively investigated as catalysts for reactions such as amination and C-C coupling.However,it is worth noting that BESFAP-Pd(II)complexes containing a pseudohalogen ligand have not been reported to exhibit C-C coupling activity,probably because of their poor solubility or low catalytic activity.Our research group has continually investigated the synthesis and catalytic properties of group 10 metal-pseudohalogen complexes.8 As an extension of our investigations into the scope of these complexes,we decided to prepare BINAP-Pd(II)complexes containing an azido ligand as a pseudohalogen group,expecting to find catalytic activity in Suzuki-Miyaura C-C coupling reactions.We report herein the synthesis,structures,and catalytic activity of these complexes.
机译:手性配体2,2'-BIS(二苯基膦基)-1,1'-二苯甲基(Binap)被广泛用作晚期过渡 - 金属配合物的辅助配体,特别是对于不对称的有机催化,特别是Ru和Rh金属。特别是Pd(II)复合物尤其被强烈地研究了用于反应的催化剂,例如胺化和CC偶联。然而,值得注意的是,尚未涉及含有假环核配体的BESFAP-PD(II)络合物以表现CC偶联活性,可能是因为它们的溶解度差或低催化活性。研究组不断调查10族金属-pseudohalogalogers的合成和催化性能.8作为我们对这些配合物的范围的调查的延伸,我们决定制备Binap- Pd(II)含有氮杂吲哚菌属作为假环原族的络合物,期望在铃木 - 宫霉菌CC偶联反应中寻找催化活性。这里的报告是合成,结构和催化活性硒复合物。

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