Computational Study on the Catalytic Role of Pincer Ruthenium(II)-PNN Complex in Directly Synthesizing Amide from Alcohol and Amine: The Origin of Selectivity of Amide over Ester and Imine
Computational Study on the Catalytic Role of Pincer Ruthenium(II)-PNN Complex in Directly Synthesizing Amide from Alcohol and Amine: The Origin of Selectivity of Amide over Ester and Imine
复制标题
钳钌(II)-PNN配合物在醇和胺直接合成酰胺中的催化作用的计算研究:酰胺相对于酯和亚胺选择性的起源
DOI:
10.1021/om200620n
复制
发表时间:
2011-10-10
期刊:
影响因子:
2.8
通讯作者:
Wang, Zhi-Xiang
中科院分区:
文献类型:
--
作者:
Li, Haixia;Wang, Xiaotai;Wang, Zhi-Xiang
Density functional theory calculations have been performed to investigate the mechanism of the reactions of amines with primary alcohols to produce amides, catalyzed by the pincer complex Ru(II)-PNN (PNN = 2-(di-tert-butylphosphinomethyl)-6-diethylaminomethyl)pyridine). The results lead us to propose a catalytic cycle that includes four stages: (stage I) alcohol dehydrogenation to aldehyde, (stage II) coupling of aldehyde with amine to form hemiaminal, (stage III) hemiaminal dehydrogenation to amide, and (stage IV) catalyst regeneration via H2 elimination of the trans Ru dihydride complex produced in the two dehydrogenation stages. Both of the dehydrogenation reactions proceed via the bifunctional double hydrogen transfer mechanism rather than the β-H elimination mechanism. The selectivity of amide over ester is determined by the coupling stage in which the aldehyde∧amine coupling to give hemiaminal is more favorable than aldehyde∧alcohol coupling to give hemiacetal. The competition between dehydrogenatio...