Recent Advances of Biphenylene: Synthesis, Reactions and Uses

被引:39
|
作者
Takano, Hideaki [1 ]
Ito, Takeharu [1 ]
Kanyiva, Kyalo Stephen [2 ]
Shibata, Takanori [1 ]
机构
[1] Waseda Univ, Sch Adv Sci & Engn, Dept Chem & Biochem, Shinjuku Ku, 3-4-1 Okubo, Tokyo 1698555, Japan
[2] Waseda Univ, Sch Adv Sci & Engn, Global Ctr Sci & Engn, Shinjuku Ku, 3-4-1 Okubo, Tokyo 1698555, Japan
基金
日本学术振兴会;
关键词
Biphenylene; Hydrocarbons; Strained molecules; C-C activation; Metallacycles; C-C BOND; CARBON-CARBON BOND; PORPHYRIN-CORROLE DYADS; SINGLET ENERGY-TRANSFER; OXIDATIVE ADDITION; NICKEL(0) COMPLEXES; AROMATIC-COMPOUNDS; IRIDIUM COMPLEXES; ACTIVATION; CLEAVAGE;
D O I
10.1002/ejoc.201900111
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Biphenylene is an antiaromatic compound that has a strained butadiene skeleton that joins two benzene rings. Various methods for synthesizing the biphenylene core have been developed. In addition, the reactivity of biphenylene has attracted much attention because C-C bonds of biphenylene can be cleaved by various organometallic species. Furthermore, the biphenylene motif not only acts as a spacer in a variety of functional molecules, but also serves as a backbone for catalysts and ligands. This minireview summarizes how to construct the biphenylene structure, how to react biphenylene, and how to use the biphenylene skeleton in functional materials.
引用
收藏
页码:2871 / 2883
页数:13
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