Abstract <p>A series of charge transfer cocrystals of anthracene with benzofurazan and benzofuroxans derivatives was obtained. The ratio of components in cocrystals is determined by hydrogen bonding and dipole-dipole interactions in acceptor subsystem. In case of 4,6-dichloro-5-nitrobenzofuroxan and 4-chloro-7-nitrobenzofurazan cocrystals, acceptor-acceptor interactions are stronger than π–π interactions with anthracene, thus resulting in 1 : 2 donor–acceptor ratio in cocrystals. The value of charge transfer in anthracene/4,6-dichloro-5-nitrobenzofuroxan complex was estimated to be about 0.27<i>e</i>. The acceptors and their complexes were characterized by electrochemistry and UV/Vis spectroscopy.</p>

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Acceptor Properties of Substituted Benzofurazan and Benzofuroxans and Their Charge Transfer Cocrystals with Anthracene

  • Kamil A. Ivshin,
  • Kirill E. Metlushka,
  • Anton P. Fedonin,
  • Ruzal G. Zinnatullin,
  • Vera V. Khrizanforova,
  • Artem I. Laskin,
  • Yulia V. Bakhtiyarova,
  • Luiza M. Yusupova,
  • Irina V. Galkina,
  • Yulia H. Budnikova,
  • Olga N. Kataeva

摘要

Abstract

A series of charge transfer cocrystals of anthracene with benzofurazan and benzofuroxans derivatives was obtained. The ratio of components in cocrystals is determined by hydrogen bonding and dipole-dipole interactions in acceptor subsystem. In case of 4,6-dichloro-5-nitrobenzofuroxan and 4-chloro-7-nitrobenzofurazan cocrystals, acceptor-acceptor interactions are stronger than π–π interactions with anthracene, thus resulting in 1 : 2 donor–acceptor ratio in cocrystals. The value of charge transfer in anthracene/4,6-dichloro-5-nitrobenzofuroxan complex was estimated to be about 0.27e. The acceptors and their complexes were characterized by electrochemistry and UV/Vis spectroscopy.