Martínez Sebastián, Junghanns Marius A, Dunaj Tobias, Lichtenberg Crispin
Department of Chemistry, Philipps-University Marburg, 35032 Marburg, Germany.
ACS Catal. 2025 Aug 13;15(17):14976-14982. doi: 10.1021/acscatal.5c02812. eCollection 2025 Sep 5.
Bismuth radical chemistry has attracted increased interest in recent years. Here, we report a series of bismuth-manganese complexes that catalyze the intramolecular redox-neutral coupling of alkyl iodides and alkynes under purely thermal conditions. Computational studies support the design of catalyst candidates, aiming to achieve low Bi-Mn bond homolytic dissociation energies. The radical nature of the cyclization reaction was supported by EPR spectroscopic spin trap experiments. This underexplored mode of thermally induced radical reactivity was applied to construct a variety of cyclic vinyl iodide compounds, including drug derivatives.
近年来,铋自由基化学引起了越来越多的关注。在此,我们报道了一系列铋 - 锰配合物,它们能在纯热条件下催化烷基碘化物和炔烃的分子内氧化还原中性偶联反应。计算研究为催化剂候选物的设计提供了支持,旨在实现低的铋 - 锰键均裂解离能。EPR光谱自旋捕获实验证实了环化反应的自由基性质。这种尚未充分探索的热诱导自由基反应模式被应用于构建多种环状乙烯基碘化合物,包括药物衍生物。