| Literature DB >> 28379689 |
Christina Römelt1, Jinshuai Song1,2, Maxime Tarrago1, Julian A Rees1,3, Maurice van Gastel1, Thomas Weyhermüller1, Serena DeBeer1,4, Eckhard Bill1, Frank Neese1, Shengfa Ye1.
Abstract
Iron porphyrins can act as potent electrocatalysts for CO2 functionalization. The catalytically active species has been proposed to be a formal Fe(0) porphyrin complex, [Fe(TPP)]2- (TPP = tetraphenylporphyrin), generated by two-electron reduction of [FeII(TPP)]. Our combined spectroscopic and computational investigations reveal that the reduction is ligand-centered and that [Fe(TPP)]2- is best formulated as an intermediate-spin Fe(II) center that is antiferromagnetically coupled to a porphyrin diradical anion, yielding an overall singlet ground state. As such, [Fe(TPP)]2- contains two readily accessible electrons, setting the stage for CO2 reduction.Entities:
Year: 2017 PMID: 28379689 DOI: 10.1021/acs.inorgchem.7b00401
Source DB: PubMed Journal: Inorg Chem ISSN: 0020-1669 Impact factor: 5.165