Cobalt-Catalyzed C(sp2)-H Borylation with an Air-Stable, Readily Prepared Terpyridine Cobalt(II) Bis(acetate) Precatalyst

被引:65
|
作者
Leonard, Nadia G. [1 ]
Bezdek, Mate J. [1 ]
Chirik, Paul J. [1 ]
机构
[1] Princeton Univ, Dept Chem, Princeton, NJ 08544 USA
基金
美国国家科学基金会;
关键词
C-H BORYLATION; ALKENE HYDROBORATION; ROOM-TEMPERATURE; BOND FUNCTIONALIZATION; ELECTRONIC-STRUCTURES; COUPLING REACTION; TERTIARY SILANES; COMPLEXES; ARENES; LIGANDS;
D O I
10.1021/acs.organomet.6b00630
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A bench-stable, 4-aryl-substituted terpyridine supported, high-spin cobalt(II) bis(acetate) complex, ((Ar)Tpy)Co-(OAc)(2) ((Ar)Tpy = 4'-(4-N,N'-dimethylaminopheny1)-2,2':6',2 ''-terpyridine), is active for the C(sp(2))-H borylation of arenes and heteroarenes with B(2)Pin(2) (Pin = pinacolato). Optimization of the catalytic borylation reaction revealed improved performance in the presence of LiOMe and turnover numbers of up to 100 have been observed using all air-stable components. EPR specstroscopy identified formation of inactive cobalt species, promoted by excess HBPin. A high-spin cobalt(II) bis[(diacetoxy)-pinacolatoborate-kappa O-3,O,O] compound has been isolated and characterized by X-ray diffraction and is the result of catalyst deactivation.
引用
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页码:142 / 150
页数:9
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