Self-Organizing Properties of Monosubstituted Sucrose Fatty Acid Esters: The Effects of Chain Length and Unsaturation
✍ Scribed by Valérie Molinier; Paul J. J. Kouwer; Juliette Fitremann; Alain Bouchu; Grahame Mackenzie; Yves Queneau; John W. Goodby
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 745 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0947-6539
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✦ Synopsis
Abstract
Three families of mono‐substituted sucrose fatty acid esters were prepared by enzymatic and classical synthetic procedures, and their self‐assembly and self‐organizational properties were investigated by thermal polarised light microscopy, differential scanning calorimetry and X‐ray diffraction. The properties were evaluated as a function of the fatty acid chain length. For the lower homologues of the series columnar liquid‐crystalline stacking structures were found, whereas for the higher homologues, lamellar phases predominated. A model for the columnar stacking arrangement, consisting of a unique arrangement of the molecules which could lead to the creation of multiple internal ion channels between the hydrophobic interior and the hydrophilic exterior of the columns, is suggested.
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Kinetic data are reporled for the halogenation of the first five members of the fatty acid series. The influence of substitution of electron withdrawing and electron releasing group in the methyl radical of acetic acid was studied in solution. The mechanism of the reaction has been discussed. Uber
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