Deprotonation-induced aromaticity enhancement and new conjugated networks in meso-hexakis(pentafluorophenyl)[26]hexaphyrin

Won Young Cha, Jong Min Lim, Min Chul Yoon, Young Mo Sung, Byung Sun Lee, Sho Katsumata, Masaaki Suzuki, Hirotaka Mori, Yoshiya Ikawa, Hiroyuki Furuta, Atsuhiro Osuka, Dongho Kim

    研究成果: Contribution to journalArticle査読

    26 被引用数 (Scopus)

    抄録

    meso-Hexakis(pentafluorophenyl)-substituted neutral hexaphyrin with a 26π-electronic circuit can be regarded as a real homolog of porphyrin with an 18π-electronic circuit with respect to a quite flat molecular structure and strong aromaticity. We have investigated additional aromaticity enhancement of meso-hexakis(pentafluorophenyl)[26]hexaphyrin(1.1.1.1.1.1) by deprotonation of the inner N-H groups in the macrocyclic molecular cavity to try to induce further structural planarization. Deprotonated mono- and dianions of [26]hexaphyrin display sharp B-like bands, remarkably strong fluorescence, and long-lived singlet and triplet excited-states, which indicate enhanced aromaticity. Structural, spectroscopic, and computational studies have revealed that deprotonation induces structural deformations, which lead to a change in the main conjugated π-electronic circuit and cause enhanced aromaticity. Circuit tuning: Deprotonation causes significant structural deformations, which give rise to different and more effective π-conjugated circuits that have been found to be responsible for enhanced aromaticity (see figure). This work highlights the potential of the deprotonation strategy for tuning the electronic properties of expanded porphyrins.

    本文言語英語
    ページ(範囲)15838-15844
    ページ数7
    ジャーナルChemistry - A European Journal
    18
    49
    DOI
    出版ステータス出版済み - 12 3 2012

    All Science Journal Classification (ASJC) codes

    • 触媒
    • 有機化学

    フィンガープリント

    「Deprotonation-induced aromaticity enhancement and new conjugated networks in meso-hexakis(pentafluorophenyl)[26]hexaphyrin」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

    引用スタイル