Halogenated triphenylgallium and - indium in frustrated Lewis pair activations and hydrogenation catalysis

被引:28
作者
Xu, Maotong [1 ]
Possart, Josephine [2 ]
Waked, Alexander E. [1 ]
Roy, Julie [1 ]
Uhl, Werner [2 ]
Stephan, Douglas W. [1 ]
机构
[1] Univ Toronto, Dept Chem, 80 St George St, Toronto, ON M5H 3H6, Canada
[2] Univ Munster, Inst Anorgan & Analyt Chem, Corrensstr 28-30, D-48149 Munster, Germany
来源
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY A-MATHEMATICAL PHYSICAL AND ENGINEERING SCIENCES | 2017年 / 375卷 / 2101期
基金
加拿大自然科学与工程研究理事会;
关键词
gallium; indium; frustrated Lewis pair chemistry; hydrogenation; CO2; REDUCTION; C-H; ASYMMETRIC HYDROGENATION; HYDRIDE ADDUCTS; BOND ACTIVATION; CARBON-DIOXIDE; COMPLEXES; ALUMINUM; BORANE; GALLIUM;
D O I
10.1098/rsta.2017.0014
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The Lewis acids Ga(C6F5)(3), In(C6F5)(3) and Ga(C6Cl5)(3) are prepared and their Lewis acidity has been probed experimentally and computationally. The species Ga(C6F5)(3) and In(C6F5)(3) in conjunction with phosphine donors are shown to heterolytically split H-2 and catalyse the hydrogenation of an imine. In addition, frustrated Lewis pairs (FLPs) derived from Ga(C6F5)(3) and In(C6F5)(3) and phosphines react with diphenyldisulfide to phosphoniumgallates or indates of the form [tBu(3)PSPh][PhSE(C6F5)(3)] and [tBu(3)PSPh][(mu-SPh)(E(C6F5)(3))(2)] (E=Ga, In). The potential of the FLPs based on Ga(C6F5) 3, In(C6F5) 3 and Ga(C6Cl5)(3) and phosphines is also shown in reactions with phenylacetylene to give pure or mixtures of the products [tBu(3)PH][PhCCE(C6X5)(3)] and R3P(Ph)C=C(H) E(C6X5)(3). A number of these species are crystallographically characterized. The implications for the use of these species in FLP chemistry are considered. This article is part of the themed issue 'Frustrated Lewis pair chemistry'.
引用
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页数:12
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