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An n-type semiconducting diazaporphyrin-based hydrogen-bonded organic framework.
Sakurai, Takahiro; Tanabe, Tappei; Iguchi, Hiroaki; Li, Zhuowei; Matsuda, Wakana; Tsutsui, Yusuke; Seki, Shu; Matsuda, Ryotaro; Shinokubo, Hiroshi.
Afiliação
  • Sakurai T; Department of Molecular and Macromolecular Chemistry, Graduate School of Engineering, Integrated Research Consortium on Chemical Science (IRCCS), Nagoya University Furo-cho, Chikusa-ku Nagoya 464-8603 Japan hshino@chembio.nagoya-u.ac.jp.
  • Tanabe T; Department of Material Chemistry, Graduate School of Engineering, Integrated Research Consortium on Chemical Science (IRCCS), Nagoya University Furo-cho, Chikusa-ku Nagoya 464-8603 Japan ryotaro.matsuda@chembio.nagoya-u.ac.jp.
  • Iguchi H; Department of Material Chemistry, Graduate School of Engineering, Integrated Research Consortium on Chemical Science (IRCCS), Nagoya University Furo-cho, Chikusa-ku Nagoya 464-8603 Japan ryotaro.matsuda@chembio.nagoya-u.ac.jp.
  • Li Z; Department of Molecular Engineering, Graduate School of Engineering, Kyoto University Nishikyo-ku Kyoto 615-8510 Japan seki@moleng.kyoto-u.ac.jp.
  • Matsuda W; Department of Molecular Engineering, Graduate School of Engineering, Kyoto University Nishikyo-ku Kyoto 615-8510 Japan seki@moleng.kyoto-u.ac.jp.
  • Tsutsui Y; Department of Molecular Engineering, Graduate School of Engineering, Kyoto University Nishikyo-ku Kyoto 615-8510 Japan seki@moleng.kyoto-u.ac.jp.
  • Seki S; Department of Molecular Engineering, Graduate School of Engineering, Kyoto University Nishikyo-ku Kyoto 615-8510 Japan seki@moleng.kyoto-u.ac.jp.
  • Matsuda R; Department of Material Chemistry, Graduate School of Engineering, Integrated Research Consortium on Chemical Science (IRCCS), Nagoya University Furo-cho, Chikusa-ku Nagoya 464-8603 Japan ryotaro.matsuda@chembio.nagoya-u.ac.jp.
  • Shinokubo H; Department of Molecular and Macromolecular Chemistry, Graduate School of Engineering, Integrated Research Consortium on Chemical Science (IRCCS), Nagoya University Furo-cho, Chikusa-ku Nagoya 464-8603 Japan hshino@chembio.nagoya-u.ac.jp.
Chem Sci ; 15(32): 12922-12927, 2024 Aug 14.
Article em En | MEDLINE | ID: mdl-39148781
ABSTRACT
Significant effort has been devoted to the development of materials that combine high electrical conductivity and permanent porosity. This paper discloses a diazaporphyrin-based hydrogen-bonded organic framework (HOF) with porosity and n-type semiconductivity. A 5,15-diazaporphyrin Ni(ii) complex with carboxyphenyl groups at the meso positions afforded a HOF due to hydrogen-bonding interactions between the carboxy groups and meso-nitrogen atoms. The thermal and chemical stabilities of the HOF were examined using powder X-ray diffraction analysis, and the charge-carrier mobility was determined to be 2.0 × 10-7 m2 V-1 s-1 using the flash-photolysis time-resolved microwave conductivity (FP-TRMC) method. An analogous diazaporphyrin, which does not form a HOF, exhibited mobility that was 20 times lower. The results presented herein highlight the crucial role of hydrogen-bonding networks in achieving conductive pathways that can tolerate thermal perturbation.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chem Sci Ano de publicação: 2024 Tipo de documento: Article País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chem Sci Ano de publicação: 2024 Tipo de documento: Article País de publicação: Reino Unido