化学
芴
单重态
芘
共轭体系
光化学
基态
芳基
表征(材料科学)
立体化学
有机化学
纳米技术
激发态
聚合物
原子物理学
材料科学
物理
烷基
作者
Koki Horii,Ryohei Kishi,Masayoshi Nakano,Daisuke Shiomi,Kazunobu Sato,Takeji Takui,Akihito Konishi,Makoto Yasuda
摘要
Bis-periazulene (cyclohepta[def]fluorene), which is an unknown pyrene isomer, was synthesized as kinetically protected forms. Its triaryl derivatives 1c-e exhibited the superimposed electronic structures of peripheral, polarized, and open-shell π-conjugated systems. In contrast to previous theoretical predictions, bis-periazulene derivatives were in the singlet ground state. Changing an aryl group controlled the energy gap between the lowest singlet-triplet states.
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