化学
氢酰化
催化作用
铀酰
氢原子
光化学
Atom(片上系统)
氢
有机化学
铑
离子
计算机科学
嵌入式系统
烷基
作者
Lei Chen,Kexin Tan,Zhijian Zheng,Xiao‐Ling Lin,Bangming Ming,Zhibin Zhang,Guo‐Ping Yang
标识
DOI:10.1002/ejoc.202400001
摘要
Abstract The direct C−H to C−N bond conversion at room temperature using heterogeneous visible‐light catalysts is both interesting and challenging. Herein, we disclosed visible‐light‐promoted hydroacylation of azodicarboxylates using uranyl‐organic framework [UO 2 (OH)(cpt)] n ( Ucpt , Hcpt=4‐(4′‐carboxyphenyl)‐1,2,4‐triazole) as an efficient heterogeneous hydrogen atom transfer photocatalyst. In this procedure, diverse benzaldehydes are compatible using dimethyl carbonate (DMC) as a green solvent at room temperature, achieving direct conversion of C−H to C−N bond with excellent yields (up to 99%). The key to excellent catalytic activity lies in the fact that the coordination of the conjugated ligand changes the HOMO energy level of Ucpt , resulting in more active sites and longer‐lived photo excitons. Simultaneously, this heterogeneous photocatalyst can be easily separated and reused for seven successive cycles and maintain high catalytic activity, showing outstanding sustainability and recyclability.
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