1,2,3- versus 1,2-Indeno Ring Fusions Influence Structure Property and Chirality of Corannulene Bowls
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Updated: Feb 12, 2026

1,3,5-Triphenylbenzene and Corannulene as Electron Receptors for Lithium Solvated Electron Solutions
Published on: October 10, 2016
Shi Liu1, Loïc M Roch1,2, Oliver Allemann1,2
1Health Science Platform , Tianjin University , 92 Weijin Road , Nankai District, Tianjin 300072 , PR China.
Abstract:
Annulated corannulenes 3-5 form via distinct synthetic pathways: (i) Pd-catalyzed sp3 CH insertion, (ii) Pd-catalyzed aryl coupling, and (iii) silyl cation-promoted C-F activation/CH insertion. Crystal structure, redox, and photophysical studies elucidate the differing influence of 1,2,3- versus 1,2-indeno ring fusions. Mono and dianions of 3-5 are characterized. Resolution of 4 gives enantiopure forms, allowing assessment of the bowl-inversion barrier.
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