Structure-InducedReversing Basicity of α‑AnionicFischer Carbenes

Group VI metal carbenes and their α-anionic complexes play an important role in organic synthesis, yet structural characterizations and thermodynamic studies for reactive α-anions remain challenging. This work investigated the molecular structures and thermodynamics of α-anionic Fischer carbenes and their conjugated acids. The results clarify the negative charge localized on the M(CO)<sub>5</sub> moiety and the CX (X = C, N, or O) double bond in all anionic structures. The conjugation between the π-donating group and the M(CO)<sub>5</sub> moiety significantly lowers the energy of neutral complexes, resulting in a reversing acidity between α-methyl, amino, and hydroxyl groups. This study deepens our understanding of the molecular structure, electronic structure, and thermodynamic property of Fischer carbenes.

Publication Details

Journal
Figshare
Published
2025-02-03
DOI
https://doi.org/10.1021/acs.inorgchem.4c03621.s001
Primary Topic
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
Type
article
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Structure-InducedReversing Basicity of α‑AnionicFischer Carbenes

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N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
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Structure-InducedReversing Basicity of α‑AnionicFischer Carbenes

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Abstract

Group VI metal carbenes and their α-anionic complexes play an important role in organic synthesis, yet structural characterizations and thermodynamic studies for reactive α-anions remain challenging. This work investigated the molecular structures and thermodynamics of α-anionic Fischer carbenes and their conjugated acids. The results clarify the negative charge localized on the M(CO)<sub>5</sub> moiety and the CX (X = C, N, or O) double bond in all anionic structures. The conjugation between the π-donating group and the M(CO)<sub>5</sub> moiety significantly lowers the energy of neutral complexes, resulting in a reversing acidity between α-methyl, amino, and hydroxyl groups. This study deepens our understanding of the molecular structure, electronic structure, and thermodynamic property of Fischer carbenes.

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Openalex Percentile: Top 69%
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
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