On the Reactivity of RSnCl and RSiMe3 {R=4-tBu-2,6-[P(O)(OiPr)2]2C6H2} towards BF3•OEt2: Competing Lewis Acidities

被引：4

作者：

Wagner, Michael ^{[1
]}

Lutter, Michael ^{[1
]}

Dietz, Christina ^{[1
]}

Prosenc, Marc H. ^{[2
]}

Jurkschat, Klaus ^{[1
]}

机构：

[1] Tech Univ Dortmund, Lehrstuhl Anorgan Chem 2, D-44221 Dortmund, Germany

[2] Tech Univ Kaiserslautern, Phys Chem, D-67663 Kaiserslautern, Germany

来源：

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY | 2015年 / 12期

关键词：

Ligand design; Lewis acids; Tin; Phosphorus; ORGANOTIN(II) CATION; ADDUCTS; BOND; DONOR; RINGS; RADII; NHC;

D O I：

10.1002/ejic.201500014

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

The reactions of boron trifluoride with the organostannylene RSnCl {R = 4-tBu-2,6-[P(O)(OiPr)(2)](2)C6H2} and the organosilane RSiMe3 provided the corresponding 1:1 and 1:2 complexes, respectively, through the formation of P=OB interactions. In the former reaction, even with excess BF3OEt2, no SnB complexation involving the lone electron pair at the tin(II) center was observed. The experimental results are supported by DFT calculations.

引用

页码：2152 / 2158

页数：7

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