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A double-helical S,C-bridged tetraphenyl- para -phenylenediamine and its persistent radical cation.

Kaho HaradaChika HasegawaTaisuke MatsumotoHiroki SugishitaChitoshi KitamuraShuhei HigashibayashiMasashi HasegawaShuichi SuzukiShin-Ichiro Kato
Published in: Chemical communications (Cambridge, England) (2023)
A structurally constrained, double-helical S,C-bridged tetraphenyl- para -phenylenediamine (TPPD) has been synthesized. The stable radical cation of the S,C-bridged TPPD was generated by chemical oxidation, and the electron spin was found to be delocalized over the entire π-conjugated framework. The excellent conformational stability of the neutral molecule facilitated the separation of its enantiomers.
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