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 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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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. |
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ISSN: | 0002-7863 1520-5126 |
DOI: | 10.1021/jacs.8b09769 |