Surmounting Alkoxide Trap Strategy: N-Heterocyclic Carbene Chromium(0)-Catalyzed C-Alkylation between Alcohols

被引:22
作者
Su, Peifeng [1 ]
Chen, Zhe [1 ]
Ni, Jinyu [1 ]
Yang, Zhenjie [1 ]
Li, Yinwu [1 ]
Ke, Zhuofeng [1 ]
机构
[1] Sun Yat Sen Univ, Sch Mat Sci & Engn, PCFM Lab, Guangzhou 510006, Peoples R China
关键词
chromium catalysis; metal-alkoxide; oxidationstate; borrowing hydrogen; C-alkylation; RAY PHOTOELECTRON-SPECTROSCOPY; CATALYZED ALPHA-ALKYLATION; TRANSITION-METAL-COMPLEXES; BORROWING HYDROGEN; SECONDARY ALCOHOLS; BOND FORMATION; AROMATIC-AMINES; BETA-ALKYLATION; H ACTIVATION; KETONES;
D O I
10.1021/acscatal.3c03440
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The crucial role of the alkoxide trap problem and the impact of the oxidation state of the chromium center were demonstrated on the catalytic activity due to the d-wall issue. Through the strategy of surmounting the alkoxide trap, a Cr(0) catalyst was presented herein for efficient C-alkylation between alcohols via borrowing hydrogen/hydrogen autotransfer. The synthesized bis-(N-heterocyclic carbene)-Cr(0) system shows an efficient catalytic performance (40 examples, up to 96% yield). Only a catalytic loading of a cheap and readily available base NaOH is effective enough for the reaction. Compared with Cr(III)/Cr(II), Cr(0) can well avoid the d-p p interaction in the key metal-alkoxide intermediate, thus overcoming the thermodynamic sink due to the alkoxide trap problem. It is plausible that the Cr(III) systems need to be reduced to Cr(II) for weakening the alkoxide trap effect and enhancing activity by using reductive strong bases. This surmounting alkoxide trap strategy should be helpful for the development of efficient and nonprecious transition metal catalysts.
引用
收藏
页码:12481 / 12493
页数:13
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