Implications of CO2 Activation by Frustrated Lewis Pairs in the Catalytic Hydroboration of CO2: A View Using N/Si+ Frustrated Lewis Pairs

被引:106
|
作者
von Wolff, N. [1 ]
Lefevre, G. [1 ]
Berthet, J. -C. [1 ]
Thuery, P. [1 ]
Cantat, T. [1 ]
机构
[1] Univ Paris Saclay, CNRS, NIMBE, CEA, Gif Sur Yvette, France
来源
ACS CATALYSIS | 2016年 / 6卷 / 07期
基金
欧洲研究理事会;
关键词
organocatalysis; CO2; hydroboration; mechanisms; DFT calculations; CARBON-DIOXIDE REDUCTION; B(C6F5)(3)-CATALYZED HYDROSILATION; COORDINATION CHEMISTRY; METHANOL; REACTIVITY; DIHYDROGEN; MECHANISM; ALCOHOLS; CRYSTAL; COMPLEX;
D O I
10.1021/acscatal.6b00421
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A series of base-stabilized silylium species were synthesized and their reactivity toward CO, explored, yielding the characterization of a novel N/Si+ FLP-CO2 adduct. These silicon species are active catalysts in the hydroboration of CO2 to the methoxide level with 9-BBN, catecholborane (catBH), and pinacolborane (pinBH). Both experiments and DFT calculations highlight the role of the FLP-CO2 adduct in the catalysis. Depending on the nature of the hydroborane reductant, two distinct mechanisms have been unveiled. While 9-BBN and catBH are able to reduce an intermediate FLP-CO2 adduct, the hydroboration of CO2 with pinBH follows a different and novel path where the B-H bond is activated by the silicon-based Lewis acid catalyst. In these mechanisms, the formation of a highly stabilized FLP-CO2 adduct is found detrimental to the kinetics of the reaction.
引用
收藏
页码:4526 / 4535
页数:10
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