首页 | 本学科首页   官方微博 | 高级检索  
     检索      


Investigation of main group promoted carbon dioxide reduction
Authors:Brena L Thompson  Zachariah M Heiden
Institution:Department of Chemistry, Washington State University, Pullman, WA 99164, USA
Abstract: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 tBu3P and B(C6F5)3 resulted in converting the sequestered CO2 molecule to CO. Reduction of the CO2 adduct of tBu3P and B(C6F5)3 with both electrons and protons resulted in only proton reduction.
Keywords:Carbon dioxide  Frustrated Lewis pairs  Reduction  Hydride  Formate
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号