Reactions and catalytic applications of a PNCNP pincer palladium hydride complex

被引:4
|
作者
Chang, Jiarui [1 ]
Ding, Man [1 ]
Mao, Jia-Xue [1 ]
Zhang, Jie [1 ]
Chen, Xuenian [1 ,2 ]
机构
[1] Henan Normal Univ, Collaborat Innovat Ctr Henan Prov Green Mfg Fine C, Sch Chem & Chem Engn,Minist Educ, Henan Key Lab Boron Chem & Adv Energy Mat,KeyLab G, Xinxiang 453007, Henan, Peoples R China
[2] Zhengzhou Univ, Coll Chem & Mol Engn, Zhengzhou 450001, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
BETA-HYDROGEN ELIMINATION; NITRILE HYDRATION; REDUCTIVE ELIMINATION; SELECTIVE HYDRATION; NICKEL-COMPLEXES; CARBON-DIOXIDE; REACTIVITY; IRIDIUM; AMIDES; BOND;
D O I
10.1039/d2dt03131k
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A palladium(ii) hydride complex supported by a benzene-based PNCNP pincer ligand, [2,6-((Bu2PNH)-Bu-t)(2)C6H3]PdH (1), has been synthesized via two different routes: the reaction of the corresponding chloride complex with LiAlH4 and the reaction of the corresponding nitrate complex with KOCH3. Complex 1 exhibits strong deprotonating ability and versatile catalytic activity. Acetamide can be readily deprotonated by complex 1 to form the corresponding acetamido complex, [2,6-((Bu2PNH)-Bu-t)(2)C6H3]PdNHC(O)CH3, in high yield. Complex 1 is an active catalyst for both the dehydrogenation of methanol to formaldehyde under mild conditions and direct hydration of nitriles to primary amides. Particularly, the direct hydration of nitriles to primary amides catalysed by complex 1 represents the most efficient palladium catalytic system for this type of reaction. A wide range of nitriles have been successfully hydrated to primary amides with 100% selectivity and good to excellent isolated yields. The possible reaction mechanisms are discussed.
引用
收藏
页码:17602 / 17608
页数:7
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