Please use this identifier to cite or link to this item: http://digitalrepository.fccollege.edu.pk/handle/123456789/2271
Title: AN EFFICIENT ESTERIFICATION OF PULLULAN USING CARBOXYLIC ACID ANHYDRIDES ACTIVATED WITH IODINE
Authors: Saeed Iqbal, Mohammad
A. HUSSAIN, Muhammad
SHAHWAR, Dure
N. HASSAN, Muhammad
N. TAHIR, Muhammad
SHER, Muhammad
Keywords: Acid anhydrides; Esterification; Acylation; Iodine; NMR spectroscopy; Polysaccharides; Pullulan.
Issue Date: Jan-2010
Publisher: researchgate.net
Citation: Hussain, Muhammad & Shahwar, Dure & Hassan, Muhammad & Tahir, Muhammad & Iqbal, Mohammad & Sher, Muhammad. (2010). An efficient esterification of pullulan using carboxylic acid anhydrides activated with iodine. Collection of Czechoslovak Chemical Communications. 75. 10.1135/cccc2009095.
Abstract: Acylation of alcohols (esterification) with anhydride is an important and routinely utilized transformation in organic synthesis. Iodine is a cheap and one of the most powerful anhydride activating agents for the esterification of alcohols. Therefore, an efficient and cost effective method was developed for the acylation of pullulan polysaccharide by using different acid anhydrides activated with iodine. A series of organo-soluble pullulan esters were successfully synthesized, purified and characterized. Under solvent free conditions, it was feasible to fabricate pullulan nonaacetate and pullulan stearate. Attachment (covalent) of the pendant groups onto polymer backbone was verified by spectroscopic techniques. All of the products were characterized by using thermal analysis, FTIR and 1H NMR spectroscopy.
Description: In present research work, a new and efficient method for the esterification of pullulan was successfully designed, i.e. pullulan was allowed to react with in situ activated acid anhydrides using iodine as a catalyst. Pullulan was successfully esterified with small sized acetic anhydride and long chain stearic anhydride. Pullulan nonaacetate was synthesized with greater efficiency even without using any solvent. As all reactions were carried out at 50 °C for only 3 h hence present method appeared highly efficient, time saving and energy effective. Because iodine is a cheap, commercially available, non degradative to glycosidic linkages and environment friendly reagent, hence this reaction methodology can be adopted on commercial scale for acetylation of pullulan.
URI: http://202.142.177.21/handle/123456789/2271
Appears in Collections:Chemistry Department

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