Zhao Ling, He Xiaochun, Cui Tianhua, Nie Xufeng, Xu Jiaqi, Zheng Xueli, Jiang Weidong, Yuan Maolin, Chen Hua, Fu Haiyan, Li Ruixiang
Key Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University, 29 Wangjiang Road, Chengdu 610064, P. R. China.
School of Chemistry and Environmental Engineering, Sichuan University of Science & Engineering, Zigong 643000, Sichuan, P. R. China.
J Org Chem. 2022 Apr 1;87(7):4550-4559. doi: 10.1021/acs.joc.1c02828. Epub 2022 Mar 16.
The acceptorless dehydrogenative cross-coupling of primary alcohols to form cross-esters with the liberation of H gas was enabled using a [RuCl(η-CH)(κ-CNP)][PF]Cl complex as the catalyst. This sustainable protocol is applicable to a broad range of primary alcohols, particularly for the sterically demanding ones, featuring good functional group tolerance and high selectivity. The good catalytic performance can be attributed to the nitrogen-phosphine-functionalized N-heterocyclic carbene (CNP) ligand, which adopts a facial coordination mode as well as the facile dissociation of coordinated benzene.
使用[RuCl(η-CH)(κ-CNP)][PF]Cl配合物作为催化剂,实现了伯醇的无受体脱氢交叉偶联反应,以形成交叉酯并释放出氢气。这种可持续的方法适用于多种伯醇,特别是位阻较大的伯醇,具有良好的官能团耐受性和高选择性。良好的催化性能可归因于氮-膦官能化的N-杂环卡宾(CNP)配体,其采用面式配位模式以及配位苯的容易解离。