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Observation of unusual molecular diffusion behaviour below the lower critical solution temperature of water/2-butoxyethanol mixtures by using fluorescence correlation spectroscopy.

作者信息

Toyouchi Shuichi, Kajimoto Shinji, Barzan Daniel, Kiel Alexander, Enderlein Jörg, Fukumura Hiroshi, Herten Dirk-Peter

机构信息

Department of Chemistry, Graduate School of Science, Tohoku University, Sendai, Miyagi, 980-8578 (Japan); Cellnetworks Cluster and Institute for Physical Chemistry, Heidelberg University, 69120 Heidelberg (Germany).

出版信息

Chemphyschem. 2014 Dec 1;15(17):3832-8. doi: 10.1002/cphc.201402308. Epub 2014 Sep 11.

DOI:10.1002/cphc.201402308
PMID:25212489
Abstract

The effect of solute affinity on solute diffusion in binary liquids well below the lower critical solution temperature (LCST) was studied by using fluorescence correlation spectroscopy. We measured the hydrodynamic radii of a hydrophobic and an amphiphilic fluorescent dye under systematic variation of the relative molar fractions of water/2-butoxyethanol and, for comparison, of water/methanol mixtures, which do not show phase separation. We found that the apparent hydrodynamic radius of the hydrophobic dye almost doubled in water/2-butoxyethanol, whereas it remained largely unchanged for the amphiphilic dye and in water/methanol mixtures. Our results indicate that the translational diffusion of solutes is influenced by transient local solution structures, even at temperatures well below the LCST. We conclude that, even far below LCST, different solutes can experience different environments in binary liquid mixtures depending on both the solute and solvent properties, all of which impact their reactivity.

摘要

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