化学
对苯二酚
光化学
催化作用
卤化物
氧化还原
卤素
卤键
可见光谱
光催化
电子转移
光催化
组合化学
有机化学
烷基
物理
光电子学
作者
Tarannum Tasnim,Calvin Ryan,Miranda L. Christensen,Christopher J. Fennell,Spencer P. Pitre
出处
期刊:Organic Letters
[American Chemical Society]
日期:2021-12-16
卷期号:24 (1): 446-450
被引量:37
标识
DOI:10.1021/acs.orglett.1c04139
摘要
Exploiting charge-transfer complexes in visible light-promoted single-electron redox reactions is a promising route for opening novel synthetic pathways, and catalytic approaches to complex formation are critical for facilitating this chemistry. This report describes the use of a substituted hydroquinone catalyst to promote radical perfluoroalkylation reactions. Mechanistic studies indicate that the reaction is initiated through formation of a visible light-absorbing halogen bonding complex between the hydroquinone catalyst and the perfluoroalkyl halide radical precursor.
科研通智能强力驱动
Strongly Powered by AbleSci AI