4.8 Article

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

期刊

ACS CATALYSIS
卷 9, 期 3, 页码 2164-2168

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.8b04430

关键词

carbon dioxide; formic acid; iridium; transfer hydrogenation; glycerol

资金

  1. DST-SERB [EMR/2016/003002]
  2. IISER Bhopal
  3. UGC

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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.

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