Aqueous Solution Properties of Disulfide Linked Gemini and Cleaved Monomeric Thiol Surfactants
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- Asakawa Tsuyoshi
- Division of Material Sciences, Graduate School of Natural Science & Technology, Kanazawa University
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- Shimizu Yasuhiro
- Division of Material Sciences, Graduate School of Natural Science & Technology, Kanazawa University
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- Ozawa Tadahiro
- Division of Material Sciences, Graduate School of Natural Science & Technology, Kanazawa University
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- Ohta Akio
- Division of Material Sciences, Graduate School of Natural Science & Technology, Kanazawa University
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- Miyagishi Shigeyoshi
- Division of Material Sciences, Graduate School of Natural Science & Technology, Kanazawa University
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説明
Monomeric thiol surfactants, [CnH2n+1N(CH3)2CH2CH2SH]Br, were produced by the cleavage of gemini surfactant containing a disulfide bond in the spacer chain, [CnH2n+1N(CH3)2CH2CH2SSCH2CH2N(CH3)2CnH2n+1]2Br. The disulfide bond was completely reduced by the addition of four times moles of dithiothreitol in water at room temperature. The critical micelle concentrations of monomeric surfactants were significantly increased in comparison with original gemini surfactants. The monomeric thiol surfactants were stable in the presence of dithiothreitol, whereas they returned gradually to their original gemini surfactants within several days due to air oxidation in water without dithiothreitol. The micelle formation induced by the disulfide linkage formation was suggested by the fluorescence intensity ratio of pyrene. The time course of decrease in thiol concentration associated with the recovery of gemini surfactants was confirmed by the absorption spectra utilizing the reactions with 4,4’-dithiopyridine.<br>
収録刊行物
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- Journal of Oleo Science
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Journal of Oleo Science 57 (4), 243-249, 2008
公益社団法人 日本油化学会
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詳細情報 詳細情報について
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- CRID
- 1390282679068818816
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- NII論文ID
- 130000055411
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- NII書誌ID
- AA11503337
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- ISSN
- 13473352
- 13458957
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- NDL書誌ID
- 9421025
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- NDL
- Crossref
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