## Abstract A novel acetylated anhydroglucose oligomer (AGU‐oligomer), prepared by acid catalyzed transglycosidation of potato starch triacetate and ethylene glycol, was used as a multifunctional coinitiator for the ring‐opening polymerization of ε‐caprolactone (ε‐CL). The polymers were synthesized
Synthesis, characterization, and ring opening polymerization of poly(1,4-cyclohexylenedimethylene terephthalate) cyclic oligomers
✍ Scribed by Xin-Hua Wan; Yi Yang; Hui-Lin Tu; Lan Huang; Samuel Tan; Qi-Feng Zhou; S. Richard Turner
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 103 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0887-624X
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✦ Synopsis
Cyclic oligomers of poly(1,4-cyclohexylenedimethylene terephthalate) (PCT) were prepared by reaction of 1,4-cyclohexanedimethanol (CHDM) with terephthaloyl chloride under diluted conditions and separated from the linear products by silica gel column at a yield of 23.7 wt %. Cyclic dimer, trimer, tetramer, pentamer, and hexamer were further separated by high performance liquid chromatography, and found to constitute 98% of the cyclics mixtures. The structures of PCT cyclics were confirmed by means of mass spectrometry, Fourier transform infrared, and 1 H NMR analysis. A series of experiments were carried out to study the effects of catalysts and cis/trans configuration of isomers of CHDM on the yield of cyclic oligomers. Ring opening polymerization of the cyclic oligomers was carried out by heating the sample mixtures at 310 °C for 30 min in the presence of antimony oxide. Polymerization was confirmed by inherent viscosity changes and infrared spectra of the resulting polyesters.
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