| Literature DB >> 30786128 |
Philipp Gotico1, Bernard Boitrel2, Régis Guillot3, Marie Sircoglou3, Annamaria Quaranta1, Zakaria Halime3, Winfried Leibl1, Ally Aukauloo1,3.
Abstract
Inspired by nature's orchestra of chemical subtleties to activate and reduce CO2 , we have developed a family of iron porphyrin derivatives in to which we have introduced urea groups functioning as multipoint hydrogen-bonding pillars on the periphery of the porphyrinic ring. This structure closely resembles the hydrogen-bond stabilization scheme of the carbon dioxide (CO2 ) adduct in the carbon monoxide dehydrogenase (CODH). We found that such changes to the second coordination sphere significantly lowered the overpotential for CO2 reduction in this family of molecular catalysts and importantly increased the CO2 binding rate while maintaining high turnover frequency (TOF) and selectivity. Entrapped water molecules within the molecular clefts were found to be the source of protons for the CO2 reduction.Entities:
Keywords: carbon dioxide reduction; hydrogen bonding; iron; porphyrins; urea
Year: 2019 PMID: 30786128 DOI: 10.1002/anie.201814339
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336