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Updated: Aug 19, 2026

Preparation of a Corannulene-functionalized Hexahelicene by Copper(I)-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units
Published on: September 18, 2016
Supramolecular porphyrin-fullerene via 'two-point' binding strategy: axial-coordination and cation-crown ether
Francis D'Souza1, Raghu Chitta, Suresh Gadde
1Department of Chemistry, Wichita State University, 1845, Fairmount, Wichita, KS 67260-0051, USA.
Abstract:
A highly stable porphyrin-fullerene conjugate with defined distance and orientation, was formed using a newly developed 'two-point' binding strategy involving axial-coordination and cation-crown ether complexation; photochemical studies performed in benzonitrile revealed efficient charge separation and slow charge-recombination in the supramolecular complex.
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