Aqueous Solution Properties of Disulfide-Linked Fluorinated Gemini and Cleaved Monomeric Thiol Surfactants
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- Asakawa Tsuyoshi
- School of Chemistry, College of Science and Engineering, Kanazawa University
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- Ozawa Tadahiro
- School of Chemistry, College of Science and Engineering, Kanazawa University
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- Ohta Akio
- School of Chemistry, College of Science and Engineering, Kanazawa University
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We prepared a fluorinated gemini surfactant containing a disulfide bond in its spacer chain, [C8F17 (CH2)3N(CH3)2CH2CH2SSCH2CH2N(CH3)2(CH2)3C8F17]2Cl, and its analogue with a hexamethylene spacer. Monomeric thiol surfactant, [C8F17(CH2)3N(CH3)2CH2CH2SH]Cl, was readily produced by the cleavage of the gemini surfactant using dithiothreitol in water. The critical micelle concentration was determined using surface tension, conductivity, and fluorescence probe methods. The critical micelle concentration of the monomeric surfactant was significantly larger than that of the gemini surfactant. The surface tension of aqueous solution for the cleaved monomeric thiol surfactant returned gradually to the original value through the formation of the disulfide bond via air oxidation.
収録刊行物
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- Journal of Oleo Science
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Journal of Oleo Science 60 (9), 469-474, 2011
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
- 1390001204093545216
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- NII論文ID
- 130001008603
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- NII書誌ID
- AA11503337
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- ISSN
- 13473352
- 13458957
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- NDL書誌ID
- 11201839
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- PubMed
- 21852746
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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
- PubMed
- CiNii Articles
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- 使用不可