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Light-Induced N(2)O Production from a Non-heme Iron–Nitrosyl Dimer
[Image: see text] Two non-heme iron–nitrosyl species, [Fe(2)(N-Et-HPTB)(O(2)CPh)(NO)(2)](BF(4))(2) (1a) and [Fe(2)(N-Et-HPTB)(DMF)(2)(NO)(OH)](BF(4))(3) (2a), are characterized by FTIR and resonance Raman spectroscopy. Binding of NO is reversible in both complexes, which are prone to NO photolysis u...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4160282/ https://www.ncbi.nlm.nih.gov/pubmed/25158917 http://dx.doi.org/10.1021/ja504343t |
Sumario: | [Image: see text] Two non-heme iron–nitrosyl species, [Fe(2)(N-Et-HPTB)(O(2)CPh)(NO)(2)](BF(4))(2) (1a) and [Fe(2)(N-Et-HPTB)(DMF)(2)(NO)(OH)](BF(4))(3) (2a), are characterized by FTIR and resonance Raman spectroscopy. Binding of NO is reversible in both complexes, which are prone to NO photolysis under visible light illumination. Photoproduction of N(2)O occurs in high yield for 1a but not 2a. Low-temperature FTIR photolysis experiments with 1a in acetonitrile do not reveal any intermediate species, but in THF at room temperature, a new {FeNO}(7) species quickly forms under illumination and exhibits a ν(NO) vibration indicative of nitroxyl-like character. This metastable species reacts further under illumination to produce N(2)O. A reaction mechanism is proposed, and implications for NO reduction in flavodiiron proteins are discussed. |
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