4.7 Article

CO2 hydrogenation into formate and methyl formate using Ru molecular catalysts supported on NNN pincer porous organic polymers

期刊

INORGANIC CHEMISTRY FRONTIERS
卷 8, 期 7, 页码 1727-1735

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0qi01123a

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资金

  1. Carbon to X Project through National Research Foundation (NRF) - Ministry of Science ICT [2020M3H7A1098259, 2020M3H7A1098271]
  2. Korea Institute of Science and Technology (KIST)
  3. Chung-Ang University Research Scholarship Grants in 2020
  4. National Research Foundation of Korea [2020M3H7A1098271, 2020M3H7A1098259] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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In this study, NNN pincer incorporated porous organic polymers (POPs) were prepared using a facile knitting method, and Ru-based molecular catalysts supported on the POPs showed high catalytic activity for CO2 hydrogenation. Among them, the heterogeneous Ru/N-Me-3-bpp-POP catalyst exhibited the highest catalytic conversion rates for formate and methyl formate, with good stability over multiple runs.
NNN pincer incorporated porous organic polymers (POPs) were prepared using a facile knitting method of pyridine based ligands via the Friedel-Crafts reaction. Ru-based molecular catalysts supported on the prepared POPs were implemented for catalytic CO2 hydrogenation into formate and methyl formate. In particular, a heterogeneous Ru/N-Me-3-bpp-POP catalyst exhibited the maximum catalytic conversion of CO2 into formate, with a turnover number (TON) of 1877, and into methyl formate with a TON of 2197. In addition, the stability of the Ru/N-Me-3-bpp-POP catalyst was demonstrated over five successive runs with a slight decrease in the catalytic efficiency, which may originate from Ru leaching.

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