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Updated: Jul 10, 2026

Using Cyclic Voltammetry, UV-Vis-NIR, and EPR Spectroelectrochemistry to Analyze Organic Compounds
Published on: October 18, 2018
Direct visual evidence for quinoidal charge delocalization in poly-p-phenylene cation radical
Mengtao Sun1, Yong Ding, Hongxing Xu
1Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, PO Box 603-146, Beijing, 100080, PR China. mtsun@aphy.iphy.ac.cn
Abstract:
Recently, X-ray crystallographic evidence of quinoidal charge delocalization in poly-p-phenylene cation radicals was reported [Banerjee, M. et al., J. Am. Chem. Soc. 2007, 129, 8070]. In this paper, direct visual evidence for quinoidal charge delocalization in quaterphylene (QP) is shown with three-dimensional (3D) charge difference densities. It was revealed that the extra positive charge mainly localized on the two center units at the ground state, while the extra positive charge will delocalize to the two outer units upon electronic state transitions by photoexcitation. The 2D plots together with the corresponding charge difference densities were interpreted as large distance-charge oscillations, implying that in the positive species upon excitation a nearly free oscillating motion of a hole occurs. For the QP cation radical, the transition dipole moment of S1 represents mesoscopic dipole antennae.
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