| Literature DB >> 30599509 |
Subrata Kundu1,2, Phan N Phu3, Pokhraj Ghosh1, Stosh A Kozimor4, Jeffery A Bertke1, S Chantal E Stieber3,4, Timothy H Warren1.
Abstract
Linkage isomers of reduced metal-nitrosyl complexes serve as key species in nitric oxide (NO) reduction at monometallic sites to produce nitrous oxide (N2O), a potent greenhouse gas. While factors leading to extremely rare side-on nitrosyls are unclear, we describe a pair of nickel-nitrosyl linkage isomers through controlled tuning of noncovalent interactions between the nitrosyl ligands and differently encapsulated potassium cations. Furthermore, these reduced metal-nitrosyl species with N-centered spin density undergo radical coupling with free NO and provide a N-N coupled cis-hyponitrite intermediate whose protonation triggers the release of N2O. This report outlines a stepwise molecular mechanism of NO reduction to form N2O at a mononuclear metal site that provides insight into the related biological reduction of NO to N2O.Entities:
Mesh:
Substances:
Year: 2019 PMID: 30599509 PMCID: PMC6686187 DOI: 10.1021/jacs.8b09769
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419