Ligand-Dependent Multi-State Reactivity in Cobalt(III)-Catalyzed C-H Activations

被引:25
|
作者
Ma, Pengchen [1 ,2 ]
Chen, Hui [1 ]
机构
[1] Chinese Acad Sci, CAS Key Lab Photochem, CAS Res Educ Ctr Excellence Mol Sci, BNLMS,Inst Chem, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
C-H activation; cobalt-catalyzed; multistate reactivity; two-state reactivity; spin states; ligand effect; COBALT-CATALYZED ANNULATION; TRANSITION-METAL COMPOUNDS; BOND ACTIVATION; EFFICIENT SYNTHESIS; 2-STATE REACTIVITY; ARYL SULFONAMIDES; TERMINAL ALKYNES; BASIS-SETS; DIRECT FUNCTIONALIZATION; HETEROBICYCLIC ALKENES;
D O I
10.1021/acscatal.8b04532
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
Cobalt(III)-promoted C-H activation reactions have witnessed explosive progress in recent few years. However, the roles played by the various spin states of Co(III) center in C-H activation reactivity remain elusive. To resolve this conundrum, herein we go beyond the commonly used DFT methods to explore three typical Co(III)-promoted C-H activation systems. Our high-level coupled cluster modelings demonstrate that multistate reactivity (MSR) involving three spin states operates for C(sp(2))-H and C(sp(3))-H activations with non-Cp-Co(III) type catalyst, while single-state reactivity (SSR) involving only one singlet spin state operates for C(sp(2))-H activation with Cp-Co(III) type catalyst. This ligand-dependent reaction scenario of MSR/SSR reveals the high complexity in mechanisms of Co(III)-promoted C-H activations.
引用
收藏
页码:1962 / 1972
页数:21
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