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Gelation or molecular recognition; is the bis-(α,β-dihydroxy ester)s motif an omnigelator?

Understanding the gelation of liquids by low molecular weight solutes at low concentrations gives an insight into many molecular recognition phenomena and also offers a simple route to modifying the physical properties of the liquid. Bis-(α,β-dihydroxy ester)s are shown here to gel thermoreversibly...

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Autores principales: Griffiths, Peter C, Knight, David W, Morgan, Ian R, Ford, Amy, Brown, James, Davies, Ben, Heenan, Richard K, King, Stephen M, Dalgliesh, Robert M, Tomkinson, John, Prescott, Stuart, Schweins, Ralf, Paul, Alison
Formato: Texto
Lenguaje:English
Publicado: Beilstein-Institut 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002023/
https://www.ncbi.nlm.nih.gov/pubmed/21160568
http://dx.doi.org/10.3762/bjoc.6.123
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author Griffiths, Peter C
Knight, David W
Morgan, Ian R
Ford, Amy
Brown, James
Davies, Ben
Heenan, Richard K
King, Stephen M
Dalgliesh, Robert M
Tomkinson, John
Prescott, Stuart
Schweins, Ralf
Paul, Alison
author_facet Griffiths, Peter C
Knight, David W
Morgan, Ian R
Ford, Amy
Brown, James
Davies, Ben
Heenan, Richard K
King, Stephen M
Dalgliesh, Robert M
Tomkinson, John
Prescott, Stuart
Schweins, Ralf
Paul, Alison
author_sort Griffiths, Peter C
collection PubMed
description Understanding the gelation of liquids by low molecular weight solutes at low concentrations gives an insight into many molecular recognition phenomena and also offers a simple route to modifying the physical properties of the liquid. Bis-(α,β-dihydroxy ester)s are shown here to gel thermoreversibly a wide range of solvents, raising interesting questions as to the mechanism of gelation. At gelator concentrations of 5–50 mg ml(−1), gels were successfully formed in acetone, ethanol/water mixtures, toluene, cyclohexane and chloroform (the latter, albeit at a higher gelator concentration). A range of neutron techniques – in particular small-angle neutron scattering (SANS) – have been employed to probe the structure of a selection of these gels. The universality of gelation in a range of solvent types suggests the gelation mechanism is a feature of the bis-(α,β-dihydroxy ester) motif, with SANS demonstrating the presence of regular structures in the 30–40 Å range. A correlation between the apparent rodlike character of the structures formed and the polarity of the solvent is evident. Preliminary spin-echo neutron scattering studies (SESANS) indicated the absence of any larger scale structures. Inelastic neutron spectroscopy (INS) studies demonstrated that the solvent is largely unaffected by gelation, but does reveal insights into the thermal history of the samples. Further neutron studies of this kind (particularly SESANS and INS) are warranted, and it is hoped that this work will stimulate others to pursue this line of research.
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spelling pubmed-30020232010-12-15 Gelation or molecular recognition; is the bis-(α,β-dihydroxy ester)s motif an omnigelator? Griffiths, Peter C Knight, David W Morgan, Ian R Ford, Amy Brown, James Davies, Ben Heenan, Richard K King, Stephen M Dalgliesh, Robert M Tomkinson, John Prescott, Stuart Schweins, Ralf Paul, Alison Beilstein J Org Chem Full Research Paper Understanding the gelation of liquids by low molecular weight solutes at low concentrations gives an insight into many molecular recognition phenomena and also offers a simple route to modifying the physical properties of the liquid. Bis-(α,β-dihydroxy ester)s are shown here to gel thermoreversibly a wide range of solvents, raising interesting questions as to the mechanism of gelation. At gelator concentrations of 5–50 mg ml(−1), gels were successfully formed in acetone, ethanol/water mixtures, toluene, cyclohexane and chloroform (the latter, albeit at a higher gelator concentration). A range of neutron techniques – in particular small-angle neutron scattering (SANS) – have been employed to probe the structure of a selection of these gels. The universality of gelation in a range of solvent types suggests the gelation mechanism is a feature of the bis-(α,β-dihydroxy ester) motif, with SANS demonstrating the presence of regular structures in the 30–40 Å range. A correlation between the apparent rodlike character of the structures formed and the polarity of the solvent is evident. Preliminary spin-echo neutron scattering studies (SESANS) indicated the absence of any larger scale structures. Inelastic neutron spectroscopy (INS) studies demonstrated that the solvent is largely unaffected by gelation, but does reveal insights into the thermal history of the samples. Further neutron studies of this kind (particularly SESANS and INS) are warranted, and it is hoped that this work will stimulate others to pursue this line of research. Beilstein-Institut 2010-11-18 /pmc/articles/PMC3002023/ /pubmed/21160568 http://dx.doi.org/10.3762/bjoc.6.123 Text en Copyright © 2010, Griffiths et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Griffiths, Peter C
Knight, David W
Morgan, Ian R
Ford, Amy
Brown, James
Davies, Ben
Heenan, Richard K
King, Stephen M
Dalgliesh, Robert M
Tomkinson, John
Prescott, Stuart
Schweins, Ralf
Paul, Alison
Gelation or molecular recognition; is the bis-(α,β-dihydroxy ester)s motif an omnigelator?
title Gelation or molecular recognition; is the bis-(α,β-dihydroxy ester)s motif an omnigelator?
title_full Gelation or molecular recognition; is the bis-(α,β-dihydroxy ester)s motif an omnigelator?
title_fullStr Gelation or molecular recognition; is the bis-(α,β-dihydroxy ester)s motif an omnigelator?
title_full_unstemmed Gelation or molecular recognition; is the bis-(α,β-dihydroxy ester)s motif an omnigelator?
title_short Gelation or molecular recognition; is the bis-(α,β-dihydroxy ester)s motif an omnigelator?
title_sort gelation or molecular recognition; is the bis-(α,β-dihydroxy ester)s motif an omnigelator?
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002023/
https://www.ncbi.nlm.nih.gov/pubmed/21160568
http://dx.doi.org/10.3762/bjoc.6.123
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