Dibora[2]ferrocenophane: A Carbene-Stabilized Diborene in a Strained cis-Configuration

被引:41
作者
Braunschweig, Holger [1 ,2 ]
Krummenacher, Ivo [1 ,2 ]
Lichtenberg, Crispin [1 ,2 ]
Mattock, James D. [3 ]
Schaefer, Marius [1 ,2 ]
Schmidt, Uwe [1 ,2 ]
Schneider, Christoph [1 ,2 ]
Steffenhagen, Thomas [1 ,2 ]
Ullrich, Stefan [1 ,2 ]
Vargas, Alfredo [3 ]
机构
[1] Julius Maximilians Univ Wurzburg, Inst Anorgan Chem, D-97074 Wurzburg, Germany
[2] Julius Maximilians Univ Wurzburg, Inst Sustainable Chem & Catalysis Boron, D-97074 Wurzburg, Germany
[3] Univ Sussex, Sch Life Sci, Dept Chem, Brighton BN1 9QJ, Sussex, England
基金
欧洲研究理事会;
关键词
boron; density functional calculations; diborenes; metallocenes; strained molecules; MAIN-GROUP ELEMENTS; BORON MULTIPLE BONDS; METALLOCENE CATALYSTS; OLEFIN POLYMERIZATION; CRYSTAL-STRUCTURE; PAIR; POLY(FERROCENYLENEVINYLENE); DIBORATION; CHALCOGENS; CHEMISTRY;
D O I
10.1002/anie.201609601
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Unsaturated bridges that link the two cyclopentadienyl ligands together in strained ansa metallocenes are rare and limited to carbon-carbon double bonds. The synthesis and isolation of a strained ferrocenophane containing an unsaturated two-boron bridge, isoelectronic with a C=C double bond, was achieved by reduction of a carbene-stabilized 1,1'-bis(dihaloboryl) ferrocene. A combination of spectroscopic and electrochemical measurements as well as density functional theory (DFT) calculations was used to assess the influence of the unprecedented strained cis configuration on the optical and electrochemical properties of the carbene-stabilized diborene unit. Initial reactivity studies show that the dibora[2] ferrocenophane is prone to boron-boron double bond cleavage reactions.
引用
收藏
页码:889 / 892
页数:4
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