Bis(1,3-dithiol-2-ylidene)-Substituted Subtriazachlorin: A Subphthalocyanine Analogue with Redox Properties

Yemei Wang, Shigeki Mori, Hiroyuki Furuta, Soji Shimizu

    Research output: Contribution to journalArticlepeer-review

    4 Citations (Scopus)

    Abstract

    Bis(1,3-dithiol-2-ylidene)-substituted subtriazachlorin was formed because of an unusual reaction of a 1,3-dithiole-2-one-fused subphthalocyanine in a triethylphosphite-mediated tetrathiafulvalene synthesis. In this novel molecule, the bis(1,3-dithiol-2-ylidene)ethane moiety and subtriazachlorin structure are fused, resulting in an electron-donating ability and broad absorption in the near-infrared region.

    Original languageEnglish
    Pages (from-to)10975-10979
    Number of pages5
    JournalAngewandte Chemie - International Edition
    Volume58
    Issue number32
    DOIs
    Publication statusPublished - Aug 5 2019

    All Science Journal Classification (ASJC) codes

    • Catalysis
    • Chemistry(all)

    Fingerprint

    Dive into the research topics of 'Bis(1,3-dithiol-2-ylidene)-Substituted Subtriazachlorin: A Subphthalocyanine Analogue with Redox Properties'. Together they form a unique fingerprint.

    Cite this