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Fluorescent Probe Solubilization in the Headgroup and Core Regions of Micelles: Fluorescence Lifetime and Orientational Relaxation Measurements
Author(s) -
Stephan Matzinger,
Deborah M. Hussey,
M. D. Fayer
Publication year - 1998
Publication title -
the journal of physical chemistry b
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.864
H-Index - 392
eISSN - 1520-6106
pISSN - 1520-5207
DOI - 10.1021/jp981860t
Subject(s) - chromophore , micelle , chemistry , fluorescence , relaxation (psychology) , fluorescence anisotropy , population , photochemistry , bromide , counterion , analytical chemistry (journal) , chemical physics , aqueous solution , inorganic chemistry , organic chemistry , ion , optics , membrane , psychology , social psychology , physics , demography , sociology , biochemistry
Experimental results demonstrate that the fluorescent probes 2-(N-hexadecylamino)-naphthalene-6-sulfonate (HANS) and 2-(N-decylamino)-naphthalene-6-sulfonate (DANS) are solubilized in two distinct regions, that is, the headgroup and core, within micelles of cetyltrimethylammoniumbromide (CTAB), tetradecyltrimethylammoniumbromide (TTAB), dodecyltrimethylammoniumbromide (DTAB), cetyltrimethylammoniumchloride (CTAC), and tetradecyltrimethylammoniumchloride (TTAC). The fluorescence lifetime decays for both chromophores are biexponential in all the different micelles. The population associated with the shorter lifetime (τ1 ≅ 4−5 ns) is located in the Stern layer, where reduction of the fluorescence lifetime occurs because of quenching induced by the bromide counterions. The second population of chromophores is located in the hydrocarbon core region of the micelle. In this environment the chromophores have a considerably longer lifetime (τ2 ≅ 19−20 ns) because there is no significant quenching by bromide counte...

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