Photo-controlled extraction and active transport of amino acids by functional reversed micelles containing spiropyran derivatives |
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Authors: | M. Ino H. Tanaka J. Otsuki K. Araki M. Seno |
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Affiliation: | (1) Institute of Industrial Science, University of Tokyo, 7-22-1, Roppongi, Minato-ku, 106 Tokyo, Japan;(2) Present address: College of Science and Technology, Nihon University, 1-8-14 Kanda-Surugadai, Chiyoda-ku, 101 Tokyo, Japan |
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Abstract: | In a reversed micellarn-decane solution, a spiropyran derivative 3,3-dimethyl-1-octadecyl-6-nitrospiro(2H-benzopyran-2,2-indoline) (PC18) showed normal photochromism, and the reversed micelles provided polar microenvironment increasing stability of a zwitterionic merocyanine (MC) form of PC18. Though the reversed micelles of tetraethyleneglycol dodecylether (TEGDE) alone inn-decane had relatively low ability to extract amino acid from aqueous solutions, the PC18-incorporated TEGDE reversed micelles inn-decane showed good photo-controlled extraction of zwitterionic amino acid under UV-irradiation and release under VIS-irradiation. Extent of the extracted amino acid was higher for tryptophane (Trp) bearing hydrophobic side chain than alanine (Ala), showing amino acid selectivity. Photo-driven active transport of amino acid across a liquid membrane was attained by the PC18-incorporated TEGDE reversed micellar carrier in a water/n-decane/water three-phase system, where one side of an aqueous/organic interface was irradiated by the UV-light and the other side by the VIS-light. When Trp and Ala were present in the aqueous solution, Trp was selectively transported. |
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Keywords: | Reversed micelles spiropyran photochromic transport liquid membrane |
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