Ring-opening copolymerization of anhydroalditols with tetrahydrofuran
โ 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
No coin nor oath required. For personal study only.
โฆ 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.
๐ SIMILAR VOLUMES
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%.