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◆ Journal of organometallic chemistry2026-04-01

Valence-localized [Fe2S2]+1 Cluster Supported by a Dinucleating Cyclophane.

Devender Singh, Titto Sunil John, Vincent J Catalano, Arnold L Rheingold, Ricardo García-Serres, Leslie J Murray

原始摘要(英文原文)· Original abstract
[2Fe2S] synthetic model complexes serve as benchmarks for intermediates proposed in enzyme catalysis, and elucidate how structural effects influence the electronic structure of the cluster. Access to [2Fe2S]1+ complexes has been synthetically challenging, with most clusters degrading or aggregating upon reduction. Here, we report an 2Fe2S cluster ligated by a dinucleating bis(β-diketiminate) cyclophane in two oxidation states, with the reduced congener being valence localized based on X-ray diffraction and Mössbauer data.
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Valence-localized [Fe2S2]+1 Cluster Supported by a Dinucleating Cyclophane. — 科研速览 Science Skim