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  • X-ray structural characterization of charge delocalization onto the three equivalent benzenoid rings in hexamethoxytriptycene cation radical.

X-ray structural characterization of charge delocalization onto the three equivalent benzenoid rings in hexamethoxytriptycene cation radical.

Organic letters (2009-05-29)
Vincent J Chebny, Tushar S Navale, Ruchi Shukla, Sergey V Lindeman, Rajendra Rathore
ABSTRACT

Definitive X-ray crystallographic evidence is obtained for a single hole (or a polaron) to be uniformly distributed on the three equivalent 1,2-dimethoxybenzenoid (or veratrole) rings in the hexamethoxytriptycene cation radical. This conclusion is further supported by electrochemical analysis and by the observation of an intense near-IR transition in its electronic spectrum, as well as by comparison of the spectral and electrochemical characteristics with the model compounds containing one and two dimethoxybenzene rings.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
1,2-Dimethoxybenzene, ≥99%, FG
Sigma-Aldrich
1,2-Dimethoxybenzene, ReagentPlus®, 99%