2,2′-Bipyridyl as a Redox-Active Borylene Abstraction Agent

被引:7
作者
Liu, Siyuan [1 ,2 ]
Legare, Marc-Andre [1 ,2 ]
Seufert, Jens [1 ,2 ]
Prieschl, Dominic [1 ,2 ]
Rempel, Anna [1 ,2 ]
Englert, Lukas [1 ,2 ]
Dellermann, Theresa [1 ,2 ]
Paprocki, Valerie [1 ,2 ]
Stoy, Andreas [1 ,2 ]
Braunschweig, Holger [1 ,2 ]
机构
[1] Julius Maximilians Univ Wurzburg, Inst Inorgan Chem, D-97074 Wurzburg, Germany
[2] Julius Maximilians Univ Wurzburg, Inst Sustainable Chem & Catalysis Boron, D-97074 Wurzburg, Germany
基金
欧洲研究理事会;
关键词
INTRAMOLECULAR STERIC INTERACTIONS; NUCLEOPHILE CARBEN-CHEMIE; SILICON-COMPOUNDS; BORON; REACTIVITY; BOND; COMPLEXES; COORDINATION; GENERATION; DIBORATION;
D O I
10.1021/acs.inorgchem.0c01383
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
2,2'-Bipyridyl is shown to spontaneously abstract a borylene fragment (R-B:) from various hypovalent boron compounds. This process is a redox reaction in which the bipyridine is reduced and becomes a dianionic substituent bound to boron through its two nitrogen atoms. Various transition metal-borylene complexes and diboranes, as a well as a diborene, take part in this reaction. In the latter case, our results show an intriguing example of the homolytic cleavage of a B=B double bond.
引用
收藏
页码:10866 / 10873
页数:8
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