Platforms for Stable Carbon-Centered Radicals

被引:142
作者
Kato, Kenichi [1 ]
Osuka, Atsuhiro [1 ]
机构
[1] Kyoto Univ, Grad Sch Sci, Dept Chem, Sakyo Ku, Oiwake Cho, Kyoto 6068502, Japan
关键词
electronic structure; fused-ring systems; magnetic properties; materials science; radicals; ELECTRON-SPIN-RESONANCE; ORGANIC-MOLECULES; CRYSTAL-STRUCTURE; CHEMISTRY; DIMER; FLUORESCENCE; REACTIVITY; ESR; SUBSTITUENTS; DISSOCIATION;
D O I
10.1002/anie.201900307
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Organic radicals can potentially play important roles in functional materials owing to an unpaired electron, but they are usually highly reactive and difficult to use. Therefore, stabilization of organic radicals is important. Among organic radicals, carbon-centered radicals are promising because of their trivalent nature, which enables structural diversity and elaborate designs, but they are also less stable because of the reactivities towards carbon-carbon bond formation and atmospheric oxygen. Recently, stable carbon-centered radicals across diverse molecular platforms have been increasingly explored. This Minireview highlights these newly explored, stable carbon-centered radicals, with a focus on porphyrinoid-stabilized radicals because of their remarkable spin delocalization abilities.
引用
收藏
页码:8978 / 8986
页数:9
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