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dc.contributor.authorFowler, Michael
dc.contributor.authorHisko, Victoria
dc.contributor.authorHenderson, Jason
dc.contributor.authorCasier, Remi
dc.contributor.authorLi, Lu
dc.contributor.authorThoma, Janine Lydia
dc.contributor.authorDuhamel, Jean
dc.date.accessioned2017-09-25 19:37:54 (GMT)
dc.date.available2017-09-25 19:37:54 (GMT)
dc.date.issued2015-11-10
dc.identifier.urihttp://dx.doi.org/10.1021/acs.langmuir.5b02770
dc.identifier.urihttp://hdl.handle.net/10012/12446
dc.descriptionThis document is the Accepted Manuscript version of a Published Work that appeared in final form in Langmuir, copyright © American Chemical Society after peer review and technical editing by publisher. To access the final edited and published work see http://dx.doi.org/10.1021/acs.langmuir.5b02770en
dc.description.abstractThis study provides experimental evidence that di(1-pyrenylmethyl) ether or DiPyMe, a well-known fluorescent probe employed to determine the microviscosity of surfactant or polymeric micelles, is being hydrolyzed in the presence of water upon UV irradiation. This effect was established from a careful analysis of the fluorescence spectra and decays acquired with aqueous solutions of DiPyMe dissolved in micelles of sodium dodecyl sulfate (SDS). The size of the SDS micelles could be adjusted from an aggregation number (N-agg) of 70 to 172 by increasing the ionic strength of the aqueous solution from 0.0 to 0.5 M NaCl. The hydrolysis of DiPyMe was much reduced in the larger SDS micelles. While the degradation of DiPyMe in aqueous solutions of SDS micelles affected the analysis of the fluorescence spectra, model-free analysis (MFA) of the fluorescence decays of DiPyMe could reliably retrieve the rate constant < k > of excimer formation for DiPyMe. After calibration with mixtures of organic solvents of known macroscopic viscosity, the < k > values obtained for DiPyMe yielded the microviscosity (mu eta) of the SDS micelles as a function of salt concentration. The mu eta was found to increase from 4.0 to 8.8 mPa.s as the salt concentration increased from 0.0 to 0.5 M. This study demonstrated that, regardless of the problem of its hydrolysis that jeopardizes its use in steady-state fluorescence experiments, DiPyMe remains an extremely valuable probe for describing the microviscosity of hydrophobic domains in aqueous solution as long as its decays are analyzed with a model that accounts for the presence of degradation products as the MFA does.en
dc.description.sponsorshipNSERCen
dc.language.isoenen
dc.publisherAmerican Chemical Societyen
dc.subjectIntramolecular Excimer Formationen
dc.subjectSodium Dodecyl-Sulfateen
dc.subjectHydrophobically-Modified Poly(N-Isopropylacrylamides)en
dc.subjectIntra-Molecular Excimeren
dc.subjectFluorescence Spectroscopyen
dc.subjectForming Probeen
dc.subjectLabeled Macromoleculesen
dc.subjectPyrene Fluorescenceen
dc.subjectSolvent Polaritiesen
dc.subjectPhase-Transitionsen
dc.titleDiPyMe in SDS Micelles: Artifacts and Their Implications in the Interpretation of Micellar Propertiesen
dc.typeArticleen
dcterms.bibliographicCitationFowler, M., Hisko, V., Henderson, J., Casier, R., Li, L., Thoma, J. L., & Duhamel, J. (2015). DiPyMe in SDS Micelles: Artifacts and Their Implications in the Interpretation of Micellar Properties. Langmuir, 31(44), 11971–11981. https://doi.org/10.1021/acs.langmuir.5b02770en
uws.contributor.affiliation1Faculty of Scienceen
uws.contributor.affiliation2Chemistryen
uws.typeOfResourceTexten
uws.peerReviewStatusRevieweden
uws.scholarLevelFacultyen


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