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dc.contributor.author박준우-
dc.date.accessioned2018-06-02T08:14:07Z-
dc.date.available2018-06-02T08:14:07Z-
dc.date.issued1989-
dc.identifier.issn0022-3654-
dc.identifier.otherOAK-17749-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/244002-
dc.description.abstractFormation of inclusion complexes between anionic surfactants, alkanesulfonates (n = 5-8, 10, 12) and alkyl sulfates (n = 8, 10, 12, 14, 16, 18), and β-cyclodextrin was studied by a fluorometric method using 1-anilinonaphthalene-8-sulfonate (1,8-ANS) and 2-anilinonaphthalene-7-sulfonate (2,7-ANS) as probes. The association constants for 1:1 complexes of 1,8-ANS and 2,7-ANS with β-CD were determined as 85 and 1500 M -1, respectively, at 25°C. The first and second association constants of the surfactants with β-CD were calculated from competitive binding data of the surfactants and the ANS's with β-CD. The 2:1 β-CD-surfactant complexes were formed with alkanesulfonates of n ≥ 10 and alkyl sulfates of n ≥ 8. The surfactant-β-CD association was accompanied by a large increase in entropy, and hydrophobic binding appeared to contribute to a great extent to the association. Self-association of 1:1 complexes of surfactants of long hydrocarbon chains was also suggested. © 1989 American Chemical Society.-
dc.languageEnglish-
dc.titleAssociation of anionic surfactants with β-cyclodextrin. Fluorescence-probed studies on the 1:1 and 1:2 complexation-
dc.typeArticle-
dc.relation.issue17-
dc.relation.volume93-
dc.relation.indexSCOPUS-
dc.relation.startpage6454-
dc.relation.lastpage6458-
dc.relation.journaltitleJournal of Physical Chemistry-
dc.identifier.scopusid2-s2.0-33845183041-
dc.author.googlePark J.W.-
dc.author.googleSong H.J.-
dc.contributor.scopusid박준우(35332923800)-
dc.date.modifydate20220119160750-
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자연과학대학 > 화학·나노과학전공 > Journal papers
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