钯
化学
配体(生物化学)
齿合度
螯合作用
表面改性
催化作用
惰性
无机化学
药物化学
金属
有机化学
物理化学
生物化学
受体
作者
Hai Sun,Yi Zhang,Ping Chen,Yun‐Dong Wu,Xinhao Zhang,Yong Huang
标识
DOI:10.1002/adsc.201600015
摘要
Abstract The direct functionalization of inert sp 3 CH bonds is limited to a few bond types. Although the activation of sp 3 CH bonds can be accomplished under mild conditions using palladium catalysts, the subsequent functionalization is not trivial due to the high energy required to convert palladium(II) to palladium(IV). We have systematically studied the palladium oxidation using computation‐guided experiments for reactions involving strong chelation control. We find that a mild external ligand could significantly accelerate the oxidation of palladium(II) to palladium(IV) for strong bidentate directing groups. The acceleration is believed to be a result of ligand stabilization of both the palladium(II) and palladium(IV) intermediates. magnified image
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