Time-Resolved Total-Internal-Reflection Fluorescence Study on Molecular Interactions at Liquid/Liquid Interfaces

  • ISHIZAKA Shoji
    Division of Chemistry, Graduate School of Science, Hokkaido University
  • UEDA Yuichi
    Division of Chemistry, Graduate School of Science, Hokkaido University
  • NISHIJIMA Yoshiaki
    Division of Chemistry, Graduate School of Science, Hokkaido University
  • KITAMURA Noboru
    Division of Chemistry, Graduate School of Science, Hokkaido University

Bibliographic Information

Other Title
  • 時間分解全反射蛍光法による液/液界面における分子間相互作用に関する研究
  • ジカン ブンカイ ゼン ハンシャ ケイコウホウ ニ ヨル エキ エキ カイメン ニ オケル ブンシ カン ソウゴ サヨウ ニ カンスル ケンキュウ

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Description

Molecular interactions proceeding at a water/CCl4 interface were investigated directly by means of time-resolved total-internal-reflection (TIR) fluorescence spectroscopy. The TIR fluorescence decay profiles and fluorescence dynamic anisotropy decays of Riboflavin (RF) in the presence or absence of a N,N -dioctadecyl-[1,3,5]triazine-2,4,6-triamine (DTT) as a guest in the CCl4 phase indicated that molecular recognition mediated by complementary triple hydrogen bonding took place effectively at the water/CCl4 interface. Furthermore, the photoreaction mechanisms of the RF-DTT hydrogen-bonded complex that proceeded at the water/CCl4 interface were considered based on results observed by steady state and dynamic fluorescence measurements of the RF-DTT complex under the TIR conditions. Hybridization of complementary single-stranded DNAs at a water/CCl4 interface was also studied by the fluorescence dynamics of ethidium bromide as a probe for the DNA structure. The structures of double-stranded DNA at the interface were analyzed.<br>

Journal

  • BUNSEKI KAGAKU

    BUNSEKI KAGAKU 54 (5), 339-346, 2005

    The Japan Society for Analytical Chemistry

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