Nitrosyl Linkage Isomers: NO Coupling to N 2 O at a Mononuclear Site

Linkage isomers of reduced metal-nitrosyl complexes serve as key species in nitric oxide (NO) reduction at monometallic sites to produce nitrous oxide (N O), a potent greenhouse gas. While factors leading to extremely rare side-on nitrosyls are unclear, we describe a pair of nickel-nitrosyl linkage...

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Veröffentlicht in:Journal of the American Chemical Society 2019-01, Vol.141 (4), p.1415-1419
Hauptverfasser: Kundu, Subrata, Phu, Phan N, Ghosh, Pokhraj, Kozimor, Stosh A, Bertke, Jeffery A, Stieber, S Chantal E, Warren, Timothy H
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Sprache:eng
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Zusammenfassung:Linkage isomers of reduced metal-nitrosyl complexes serve as key species in nitric oxide (NO) reduction at monometallic sites to produce nitrous oxide (N O), 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 N O. This report outlines a stepwise molecular mechanism of NO reduction to form N O at a mononuclear metal site that provides insight into the related biological reduction of NO to N O.
ISSN:0002-7863
1520-5126
DOI:10.1021/jacs.8b09769