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[(18-冠-6)K][(N≡C)Cu-SiMePh],一种硅烷基氰基铜酸钾,作为与硅硼烷进行硅烷化反应的催化剂模型:合成、结构及催化性能

[(18-C-6)K][(N≡C)Cu-SiMePh], a Potassium Silylcyanocuprate as a Catalyst Model for Silylation Reactions with Silylboranes: Syntheses, Structures, and Catalytic Properties.

作者信息

Plotzitzka Jacqueline, Kleeberg Christian

机构信息

Institut für Anorganische und Analytische Chemie, Technische Universität Carolo-Wilhelmina zu Braunschweig , Hagenring 30, 38106 Braunschweig, Germany.

出版信息

Inorg Chem. 2017 Jun 5;56(11):6671-6680. doi: 10.1021/acs.inorgchem.7b00749. Epub 2017 May 16.

Abstract

Cu-catalyzed silylation reactions involving silylboranes (in particular, pinB-SiMePh (1)) as silyl sources have recently gained considerable attention. One of the most efficient and versatile and yet simplest catalyst systems consists of CuCN/NaOMe; however, nothing is known about the catalytically relevant species. Using an NHC-based model catalyst, copper silyl complexes of the type [(NHC)Cu-SiMePh] have been established to be crucial species in these catalytic processes. The well-defined and spectroscopically and structurally characterized complex [(18-C-6)K][NC-Cu-OtBu] (2), as a model for the catalytic system, CuCN/NaOMe, shows comparable catalytic activity toward established, exemplary substrates (aldehydes, imines, α,β-unsaturated carbonyls) and in extension allows the efficient silylation of ketones. In addition, a number of peculiarities of the catalytic reaction are readily rationalized on the basis of the mechanistic insight already established using [(NHC)Cu-SiMePh] as a model catalyst. Analogously to the NHC model system, the reaction of 2 with the silylborane 1 furnishes the silylcyanocuprate [(18-C-6)K][NC-Cu-SiMePh] (3) as a potential crucial intermediate in these silylation reactions also suggesting mechanistic similarities between (NHC)Cu- and CuCN/NaOMe-based catalyst systems. Moreover, 3 and [(NHC)Cu-SiMePh] complexes also share structurally distinctive features. In the solid state 3 either exists as a linear, two-coordinated copper complex or, depending on the conditions of crystallization, forms binuclear μ-silyl bridged dimers exhibiting very short Cu···Cu distances. Both structural motifs are also known for [(NHC)Cu-SiR] complexes. These findings give an initial insight into the versatile structural chemistry of certain silylcyanocuprates; in particular, the finding of dinuclear silylcuprates gives rise to the question whether these dimeric species are of mechanistic relevance for the catalytic processes. However, all peculiarities of the investigated catalytic reaction can readily be rationalized on the basis of the mechanistic details established using (NHC)Cu model complexes.

摘要

涉及硅硼烷(特别是频哪醇硼酸酯 - 二甲基苯基硅烷(1))作为硅源的铜催化硅烷化反应最近受到了广泛关注。最有效、通用且简单的催化剂体系之一是由氰化铜/甲醇钠组成;然而,对于催化活性相关物种却知之甚少。使用基于氮杂环卡宾(NHC)的模型催化剂,已确定[(NHC)Cu - SiMePh]类型的铜硅配合物是这些催化过程中的关键物种。结构明确且经光谱和结构表征的配合物[(18 - C - 6)K][NC - Cu - OtBu](2),作为催化体系CuCN/NaOMe的模型,对既定的典型底物(醛、亚胺、α,β - 不饱和羰基化合物)表现出相当的催化活性,并且进一步实现了酮的高效硅烷化。此外,基于已使用[(NHC)Cu - SiMePh]作为模型催化剂建立的机理认识,催化反应的许多特性很容易得到合理解释。与NHC模型体系类似,2与硅硼烷1的反应生成了硅氰基铜酸盐[(18 - C - 6)K][NC - Cu - SiMePh](3),它可能是这些硅烷化反应中的关键中间体,这也表明基于(NHC)Cu和基于CuCN/NaOMe的催化剂体系之间存在机理相似性。此外,3和[(NHC)Cu - SiMePh]配合物在结构上也有独特的特征。在固态下,3要么以线性、双配位的铜配合物形式存在,要么根据结晶条件,形成具有非常短的Cu···Cu距离的双核μ - 硅桥联二聚体。这两种结构模式在[(NHC)Cu - SiR]配合物中也有报道。这些发现初步揭示了某些硅氰基铜酸盐丰富的结构化学;特别是,双核硅铜酸盐的发现引发了一个问题,即这些二聚体物种对于催化过程是否具有机理相关性。然而,基于使用(NHC)Cu模型配合物建立的机理细节,所研究的催化反应的所有特性都很容易得到合理解释。

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