Catalytic Conversion of CO2 to Formate with Renewable Hydrogen Donors: An Ambient-Pressure and H2-Independent Strategy

被引:56
作者
Kumar, Abhishek [1 ]
Semwal, Shrivats [1 ]
Choudhury, Joyanta [1 ]
机构
[1] Indian Inst Sci Educ & Res Bhopal, Dept Chem, Organometall & Smart Mat Lab, Bhopal 462066, India
关键词
carbon dioxide; formic acid; iridium; transfer hydrogenation; glycerol; FORMIC-ACID; HOMOGENEOUS CATALYSTS; STORAGE; DEHYDROGENATION; METHANOL; TEMPERATURE; HYDRICITY; ALCOHOLS; GLYCEROL; ENERGY;
D O I
10.1021/acscatal.8b04430
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
Catalytic conversion of CO, via "transfer hydrogenation" using renewable non-H-2 compounds (such as biomass derived (poly) alcohols) to produce valuable energy-relevant chemicals, is a promising alternative strategy to the traditionally employed "hydrogenation" of CO2 with gaseous H-2. However, the CO2-transfer hydrogenation has been explored exceptionally less, and limited but encouraging success has been achieved in recent time by applying high pressure (up to 50 atm) of CO2 gas. For safe and simple operation, ambient-pressure protocols are desirable, and toward this end, suitable catalysts are required. Aiming to this goal, herein we report an efficient Ir-aNHC catalyst (aNHC = an abnormal NHC ligand) to achieve ambient-pressure CO2-transfer hydrogenation catalysis for generating formate salt (HCO2-) at the turnover (TOF) value of 90 h(-1) in 12 h of reaction at 150 degrees C using glycerol as hydrogen source.
引用
收藏
页码:2164 / 2168
页数:9
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