Synthesis and Investigation of the Effect of Substitution on the Structure, Physical Properties, and Electrochemical Properties of Anthracenodifuran Derivatives

Motonori Watanabe, Yasutaka Doi, Hidehisa Hagiwara, Aleksandar Tsekov Staykov, Shintaro Ida, Taisuke Matsumoto, Teruo Shinmyozu, Tatsumi Ishihara

研究成果: Contribution to journalArticle査読

4 被引用数 (Scopus)

抄録

A series of syn/anti mixtures of anthradifuran (ADF) and substituent compounds were systematically synthesized, and the effect of substitution at the 5,11-positions on the neutral and radical states of ADF was investigated. All compounds were measured and analyzed by absorption and fluorescence spectroscopy, cyclic voltammetry, electrochemical absorption spectroscopy, and DFT calculations. The absorption spectra of 5,11-substituent compounds in their neutral state were red-shifted. In addition, the substituted compounds exhibited increased thermal stability with respect to the parent 1a because of elongation of the conjugation and an increased steric hindrance effect due to the bulky ethynyl substituent groups. The cyclic voltammograms of all of the compounds exhibited irreversible reduction potentials and irreversible oxidation potentials, except in the case of (trimethylsilyl)silylethynyl-substituted ADF. When the materials were subjected to oxidation/reduction potentials, the radical cation and anion species were generated. The absorption spectra of the radical-cation species of the compounds exhibited similar characteristics and similar absorption ranges (550-1400 nm), whereas the spectra of the radical anion species were blue-shifted (550-850 nm) compared than that of the parent 1a•- (550-1100 nm). The DFT computation results suggested that the radical states of lowest energy transitions occurred primarily from to SOMO or from SOMO to.

本文言語英語
ページ(範囲)9159-9166
ページ数8
ジャーナルJournal of Organic Chemistry
80
18
DOI
出版ステータス出版済み - 9 18 2015

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

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