Shimizu, Seishi orcid.org/0000-0002-7853-1683 and Matubayasi, Nobuyuki
(2016)
The origin of cooperative solubilisation by hydrotropes.
Physical Chemistry Chemical Physics.
25621 - 25628.
ISSN 1463-9084
Abstract
The signature of hydrotropic solubilisation is the sigmoidal solubility curve; when plotted against hydrotrope concentration, solubility increases suddenly after the minimum hydrotrope concentration (MHC), and reaches a plateau at higher hydrotrope concentrations. This sigmoidal curve is characteristic of cooperative phenomena, yet the true molecular basis of hydrotropic cooperativity has long remained unclear. Here we develop a theory, derived from the first principles of statistical thermodynamics using partially-open ensembles, to identify the origin of hydrophobic cooperativity. Our theory bears a close resemblance to the cooperative binding model used for protein-ligand binding. The cause of cooperativity is the enhancement of hydrotrope m-body interaction induced by the presence of the solute; m can be estimated from experimental solubility data.
Metadata
Item Type: | Article |
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Authors/Creators: |
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Copyright, Publisher and Additional Information: | © Royal Society of Chemistry 2016. This is an author-produced version of the published paper. Uploaded in accordance with the publisher’s self-archiving policy. Further copying may not be permitted; contact the publisher for details.*Author's post-print on institutional repository after 12 months from acceptance* |
Dates: |
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Institution: | The University of York |
Academic Units: | The University of York > Faculty of Sciences (York) > Chemistry (York) |
Depositing User: | Pure (York) |
Date Deposited: | 07 Sep 2016 09:46 |
Last Modified: | 16 Oct 2024 13:12 |
Published Version: | https://doi.org/10.1039/C6CP04823D |
Status: | Published |
Refereed: | Yes |
Identification Number: | 10.1039/C6CP04823D |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:104451 |
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Filename: 2016_pccp_MHC_revision.docx
Description: 2016 pccp MHC revision