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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.
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页码:10866 / 10873
页数:8
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