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Article Abstract

A structurally constrained, double-helical S,C-bridged tetraphenyl--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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http://dx.doi.org/10.1039/d2cc06144aDOI Listing

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