铋
光催化
光化学
催化作用
激进的
化学
分子内力
电泳剂
电子转移
金属
杂原子
氧化还原
无机化学
立体化学
有机化学
烷基
作者
Dominik Birnthaler,Rok Narobe,Eliseo Lopez Berguno,Christoph Haag,Burkhard Koenig
标识
DOI:10.26434/chemrxiv-2022-45m6f
摘要
Ligand-to-metal charge transfer (LMCT) photocatalysis allows the activation and synthetic utilization of halides and other heteroatoms in metal complexes. The coordination makes photoinduced intramolecular electron transfer processes even at very short excited state lifetimes possible. A screening assay identifying LMCT activity enabled us to expand this catalysis concept to main group elements, such as bismuth. Bismuth (III) complexes generate the elusive bismuth (II) species and electrophilic carboxyl and chlorine radicals upon irradiation. The latter was utilized in C(sp3)–H bond activation and redox neutral trapping in a Giese-type coupling protocol. Combined cyclovoltammetry and UV-vis studies gave insight in the radical behavior of the highly reactive bismuth (II) catalyst fragment.
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