Chem. J. Chinese Universities ›› 1997, Vol. 18 ›› Issue (12): 2034.

• Articles • Previous Articles     Next Articles

Electronic Spectra of π Ion-radical Dimer of Porphyrin Derivatives

JIANG Yue-Shun1, YANG Ji-Hua1, WANG De-Jun1, CHEN Yong-Mei1, YANG Wen-Sheng1, BAI Yu-Bai1, LI Tie-Jin1, WANG Yong-Qiang2   

  1. 1. Department of Chemistry, Jilin University, Changchun 130023;
    2. Department of Chemistry, Peking University, Beijing 100871
  • Received:1996-11-19 Online:1997-12-24 Published:1997-12-24

Abstract: The electronic spectra of Kion-radical dimer of porphyrin derivatives were studiedbased on the spectroelectrochemistry of copper (Ⅱ)meso-tetrakis (4-N-methylpyridyl) por-phyrin tetrachloride salt(CuTMPyP) and the fluorescence spectra of partly protonized 5, 10,15-(4-hydroxy phenyl)-20-(4-hexadecyloxy phenyl) porphyrin (P31) LB film.The face-to-face dimer formed through the SOMO'-LUMOinteraction between the electroreducedCuTMPyPanion-radical and the ground state molecule shows Qband at 480 nm and π**band at 820 nm.The face-to-face dimer produced by the SOMO-HOMOinteraction betweenthe protonized P31 cation-radical and the ground state molecule shows the Qband absorptionat the range of 470-515 nm; and the π-π band at 710 nm.These Qbands are blue-shifted.

Key words: Porphyrin derivative, &pi, ion-radical, Dimer-interaction, Spectroelectrochemistry, Fluorescence spectrum

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