Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.510614
Title: Anion-tuning of supramolecular gel properties
Author: Lloyd, Gareth Owen
ISNI:       0000 0001 2388 5217
Awarding Body: Durham University
Current Institution: Durham University
Date of Award: 2010
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Abstract:
Low molecular weight gelators (LMWGs) are a class of compounds that has garnered great interest from material, synthetic, supramolecular and biological chemists. Anion tuning of these supramolecular gels is a burgeoning field of study. Two classes of compounds, chiral bisureas and urea derivatised pyrazoles are studied. The synthesized chiral bisurea compounds act as gelators in a variety of solvents. Addition of anions in the form of tetrabutyl ammonium salts was found to afford break up of the gels. Studies reveal that the rheological characteristics of these materials can be tuned using the simple addition of sub-stoichiometric amounts of anion. Variation in the length of the alkyl chain of the spacer separating the chiral and bisurea moieties affects the gel formation of a series of related compounds. Compounds with even numbered spaced alkyl chains were found to gel, whereas the odd numbered spaced alkyl chain compounds did not. Crystal growth within the gel matrix influences the crystallization processes and the use of anion induced break down of the LMWGs allows for easy recovery of the grown crystals. Drug compounds, bound upon gelation of a solution containing the drugs, were found to be released in a controlled manner from the gel matrix. Urea functionalised pyrazoles were synthesized. Crystallographic determination of the hydrogen bonding of the compounds as well as the coordination chemistry of these compounds was obtained. Anion binding studies, in addition to the crystallographic results, reveal that the urea or thiourea groups form an intramolecular hydrogen bond with the pyrazole group resulting in an anti conformation. This prevents formation of gels except in one case. The gelation of 1-(3-methyl-1H-pyrazol-5-yl)-3-(3-nitrophenyl)urea in acidic water overcomes this problem by protonation of the pyrazole group resulting in a syn conformation of the urea group. Anion tuning of the gel properties is revealed where nitrate and chloride result in precipitation of gels and the rheological characteristics can be tuned by changing the anion’s identity.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.510614  DOI: Not available
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