Non-heme (L)Fe and (L)Fe -O-Fe (L) complexes (L=1,1-di(pyridin-2-yl)-N,N-bis(pyridin-2-ylmethyl)ethan-1-amine) underwent reduction under irradiation to the Fe state with concomitant oxidation of methanol to methanal, without the need for a secondary photosensitizer. Spectroscopic and DFT studies support a mechanism in which irradiation results in charge-transfer excitation of a Fe -μ-O-Fe complex to generate [(L)Fe =O] (observed transiently during irradiation in acetonitrile), and an equivalent of (L)Fe . Under aerobic conditions, irradiation accelerates reoxidation from the Fe to the Fe state with O , thus closing the cycle of methanol oxidation to methanal.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5887871 | PMC |
http://dx.doi.org/10.1002/anie.201712678 | DOI Listing |
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