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Ring-opening copolymerization of anhydroalditols with tetrahydrofuran

โœ Scribed by Joachim Thiem; Wilhelm A. Strietholt


Publisher
John Wiley and Sons
Year
1995
Tongue
English
Weight
386 KB
Volume
196
Category
Article
ISSN
1022-1352

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โœฆ Synopsis


By ring-opening copolymerization of 1,4-anhydr0-2,3-di-O-ethyl-~-erythritol (cis-3,4-diethoxyoxolane, 1) or 1,4:2,5:3,6-trianhydro-~-mannitol (3) with tetrahydrofuran carbohydratecontaining copolyether polyols were obtained. Using trifluoromethanesulfonic acid as catalyst the molecular weights were in a range from M , = 13OOO up to 25000 with about 10% of carbohydrate constituent. The novel copolyethers were studied by polymer analytical procedures, their structures 4 and 5 tentatively assigned and compared to the homopolymerization products of the monomers. The present procedure features an approach to novel partially functionalized high molecular weight copolymer polyols based on carbohydrate-derived materials.


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d at room temperature under an inert gas atmosphee. The color of the reaction mixture changes from yellow to red-brown. The crude product is filtered off and recrystallized from CH,0H/CH2C12; yield ca. 51%.