惰性
催化作用
铈
表面改性
化学
光催化
金属
配体(生物化学)
光化学
组合化学
无机化学
有机化学
光催化
物理化学
生物化学
受体
作者
Qing An,Liang Chang,Hui Pan,Zhiwei Zuo
标识
DOI:10.1021/acs.accounts.4c00510
摘要
ConspectusChemists have long pursued harnessing light energy and photoexcitation processes for synthetic transformations. Ligand-to-metal charge transfer (LMCT) in high-valent metal complexes often triggers bond homolysis, generating oxidized ligand-centered radicals and reduced metal centers. While photoinduced oxidative activations can be enabled, this process, typically seen as photochemical decomposition, remains underexplored in catalytic applications. To mitigate decomposition during LMCT excitation, we developed a catalytic cycle integrating in situ coordination, LMCT, and ligand homolysis to activate ligated alcohols transiently into alkoxy radicals. This catalytic approach leverages Ce(IV) LMCT excitation and highly reactive alkoxy radical intermediates for selective functionalizations of C(sp
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