Peripheral Modifications of <i>meso</i>‐Hydroxyporphyrins: Formation of π‐Electronic Anions and Ion‐Pairing Assemblies

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  • Yoshifumi Sasano
    Department of Applied Chemistry, College of Life Sciences Ritsumeikan University Kusatsu 525-8577 Japan
  • Yohei Haketa
    Department of Applied Chemistry, College of Life Sciences Ritsumeikan University Kusatsu 525-8577 Japan
  • Hiroki Tanaka
    Department of Applied Chemistry, College of Life Sciences Ritsumeikan University Kusatsu 525-8577 Japan
  • Nobuhiro Yasuda
    Research and Utilization Division Japan Synchrotron Radiation Research Institute Sayo 679-5198 Japan
  • Ichiro Hisaki
    Green Nanotechnology Research Center, Research Institute for Electronic Science Hokkaido University Sapporo 001-0020 Japan
  • Hiromitsu Maeda
    Department of Applied Chemistry, College of Life Sciences Ritsumeikan University Kusatsu 525-8577 Japan

書誌事項

公開日
2019-04-25
資源種別
journal article
権利情報
  • http://onlinelibrary.wiley.com/termsAndConditions#vor
DOI
  • 10.1002/chem.201901095
公開者
Wiley

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説明

<jats:title>Abstract</jats:title><jats:p>Phenyl groups were introduced at the β‐positions proximal to the <jats:italic>meso</jats:italic>‐hydroxy moiety in hydroxyporphyrin Ni<jats:sup>II</jats:sup> complexes by oxidized BINAP Pd<jats:sup>II</jats:sup> complexes. Ion‐pairing assemblies of deprotonated π‐electronic anions, anionic site of which was stabilized by the introduced phenyl moieties with a bulky cation, were formed. They showed charge‐by‐charge assemblies, assembly modes of which were modulated by the anionic building units.</jats:p>

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