Answers are grounded in this paper and cite their sources.
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 1H 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.
No takes yet. Share an insight, caveat, or question.
Wan et al. (2000) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: