Fixation of carbon dioxide and related small molecules by a bifunctional frustrated pyrazolylborane Lewis pair

被引:85
作者
Theuergarten, Eileen [1 ]
Schloesser, Janin [1 ]
Schluens, Danny [1 ]
Freytag, Matthias [1 ]
Daniliuc, Constantin G. [1 ]
Jones, Peter G. [1 ]
Tamm, Matthias [1 ]
机构
[1] Tech Univ Carolo Wilhelmina Braunschweig, Inst Anorgan & Analyt Chem, D-38106 Braunschweig, Germany
关键词
HETEROLYTIC DIHYDROGEN ACTIVATION; FREE CATALYTIC-HYDROGENATION; METAL-FREE; H-2; ACTIVATION; DENSITY FUNCTIONALS; REACTIVITY; CO2; CARBENE; ISOCYANIDE; CLEAVAGE;
D O I
10.1039/c2dt30448a
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The bifunctional frustrated Lewis pair 1-[bis(pentafluorophenyl)boryl]-3,5-di-tert-butyl-1H-pyrazole (1) was employed for small molecule fixation by reaction with carbon dioxide, paraformaldehyde, tert-butyl isocyanate, tert-butyl isothiocyanate, methyl isothiocyanate and benzonitrile, affording the adducts 3-8 as zwitterionic, bicyclic boraheterocycles. Treatment of 1 with tert-butyl isocyanide gave the isocyanide-borane complex 9, whereas the zwitterionic alkynylborate 10 was formed by C-H bond activation of phenylacetylene. The molecular structures of all products 3-10 were established by X-ray diffraction analyses. DFT calculations at the M06-2X/6-311++G(d,p) level of theory revealed that CO2 fixation by 1 and formation of the adduct 3 is strongly exothermic and proceeds with a low energy barrier of approximately 7.3 kcal mol(-1) via an intermediate van der Waals complex.
引用
收藏
页码:9101 / 9110
页数:10
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