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Towards quantifying the role of hydrogen bonding within amphiphile self-association and resultant aggregate formation

Towards quantifying the role of hydrogen bonding within amphiphile self-association and resultant aggregate formation
Towards quantifying the role of hydrogen bonding within amphiphile self-association and resultant aggregate formation
Herein, we present a series of five tetrabutylammonium (TBA) sulfonate-urea amphiphilic salts. In solution these amphiphilic salts have been shown to form a variety of self-associated species. The proportion and type of which are both solvent and concentration dependent. In DMSO-d(6) a variety of NMR experiments provide evidence towards the formation of mainly dimeric over larger aggregate species. Increasing the percentage of water was shown to increase the concentration of the larger aggregates over dimers in solution. A correlation was established between critical micelle concentration (CMC) values obtained in a 1 : 19 EtOH : H2O mixture, dimeric self-association constants obtained in a DMSO-d(6) -0.5% H2O and the results of simple semi-empirical PM6 computational modelling methods. This approach begins to quantify the role of hydrogen bonding in amphiphile self-association and the effects it imparts on surfactant properties. This consequently provides preliminary evidence that these properties maybe predicted by simple low level computational modelling techniques.
CRITICAL MICELLE CONCENTRATION, DENDRITIC AMPHIPHILES, nmr-spectroscopy, surfactants, recognition, Water, molecules, systems, Models, acids
1478-6524
7620-7630
White, Lisa J.
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Wells, Neil J.
86312185-007b-495b-86da-4e2e5b9b8025
Blackholly, Laura R
c8063cc4-ec80-40e7-bdd6-af1dd40c43c1
Shepherd, Helena J.
70664bbb-30b9-4f37-bc31-a8a0e2dc8894
Wilson, Ben
3698e23f-6697-46c8-a902-b1c2f4dcb797
Bustone, Gianluca P.
bd9fe037-4e31-4426-96de-794c2c1ce133
Runacres, T.
b5c3d215-6096-4157-af32-148f7a7e9f88
Hiscock, Jennifer R.
54da213c-badc-4ddb-b23c-9561367b2f90
White, Lisa J.
bc5cb48e-a465-4ec4-b4e7-77c77bcd47b1
Wells, Neil J.
86312185-007b-495b-86da-4e2e5b9b8025
Blackholly, Laura R
c8063cc4-ec80-40e7-bdd6-af1dd40c43c1
Shepherd, Helena J.
70664bbb-30b9-4f37-bc31-a8a0e2dc8894
Wilson, Ben
3698e23f-6697-46c8-a902-b1c2f4dcb797
Bustone, Gianluca P.
bd9fe037-4e31-4426-96de-794c2c1ce133
Runacres, T.
b5c3d215-6096-4157-af32-148f7a7e9f88
Hiscock, Jennifer R.
54da213c-badc-4ddb-b23c-9561367b2f90

White, Lisa J., Wells, Neil J., Blackholly, Laura R, Shepherd, Helena J., Wilson, Ben, Bustone, Gianluca P., Runacres, T. and Hiscock, Jennifer R. (2017) Towards quantifying the role of hydrogen bonding within amphiphile self-association and resultant aggregate formation. Chemical Science, 8 (11), 7620-7630. (doi:10.1039/c7sc03888g).

Record type: Article

Abstract

Herein, we present a series of five tetrabutylammonium (TBA) sulfonate-urea amphiphilic salts. In solution these amphiphilic salts have been shown to form a variety of self-associated species. The proportion and type of which are both solvent and concentration dependent. In DMSO-d(6) a variety of NMR experiments provide evidence towards the formation of mainly dimeric over larger aggregate species. Increasing the percentage of water was shown to increase the concentration of the larger aggregates over dimers in solution. A correlation was established between critical micelle concentration (CMC) values obtained in a 1 : 19 EtOH : H2O mixture, dimeric self-association constants obtained in a DMSO-d(6) -0.5% H2O and the results of simple semi-empirical PM6 computational modelling methods. This approach begins to quantify the role of hydrogen bonding in amphiphile self-association and the effects it imparts on surfactant properties. This consequently provides preliminary evidence that these properties maybe predicted by simple low level computational modelling techniques.

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Accepted/In Press date: 21 September 2017
e-pub ahead of print date: 26 September 2017
Published date: 1 November 2017
Keywords: CRITICAL MICELLE CONCENTRATION, DENDRITIC AMPHIPHILES, nmr-spectroscopy, surfactants, recognition, Water, molecules, systems, Models, acids

Identifiers

Local EPrints ID: 420885
URI: http://eprints.soton.ac.uk/id/eprint/420885
ISSN: 1478-6524
PURE UUID: 9bd4b2f1-8e96-46ba-ac4e-ef11fc213b2b
ORCID for Neil J. Wells: ORCID iD orcid.org/0000-0002-4607-5791

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Date deposited: 17 May 2018 16:30
Last modified: 16 Mar 2024 02:59

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Contributors

Author: Lisa J. White
Author: Neil J. Wells ORCID iD
Author: Laura R Blackholly
Author: Helena J. Shepherd
Author: Ben Wilson
Author: Gianluca P. Bustone
Author: T. Runacres
Author: Jennifer R. Hiscock

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