Investigation of main group promoted carbon dioxide reduction

TETRAHEDRON

卷:75

Article

Thompson, Brena L.¹  Heiden, Zachariah M.¹ 

[1] Washington State Univ, Dept Chem, Pullman, WA 99164 USA

关键词: Carbon dioxide;    Frustrated Lewis pairs;    Reduction;    Hydride;    Formate;   

DOI  :  10.1016/j.tet.2019.02.029

来源: Elsevier

【 摘 要 】

The reduction of carbon dioxide (CO2) is of interest to the chemical industry, as many synthetic materials can be derived from CO2. To help determine the reagents needed for the functionalization of carbon dioxide this experimental and computational study describes the reduction of CO2 to formate and CO with hydride, electron, and proton sources in the presence of sterically bulky Lewis acids and bases. The insertion of carbon dioxide into a main group hydride, generating a main group formate, was computed to be more thermodynamically favorable for more hydridic (reducing) main group hydrides. A ten kcal/mol increase in hydricity (more reducing) of a main group hydride resulted in a 35% increase in the main group hydride's ability to insert CO2 into the main group hydride bond. The resulting main group formate exhibited a hydricity (reducing ability) about 10% less than the respective main group hydride prior to CO2 insertion. Coordination of a second identical Lewis acid to a main group formate complex further reduced the hydricity by about another 20%. The addition of electrons to the CO2 adduct of (Bu3P)-Bu-t and B(C6F5)(3) resulted in converting the sequestered CO2 molecule to CO. Reduction of the CO2 adduct of (Bu3P)-Bu-t and B(C6F5)(3) with both electrons and protons resulted in only proton reduction. (C) 2019 Elsevier Ltd. All rights reserved.

【 授权许可】

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