Cyclobis(diethy1ene glycol carbonate), (DEGC),, was synthesized by polycondensation of diethylene glycol with diethyl carbonate followed by thermal depolymerization of the crude polycarbonate in vacuo. BuSnCl,-initiated polymerizations of (DEGC)2 in chlorobenzene at 100 "C gave poor results. Therefo
Polymers of carbonic acid. XVII. Polymerization of cyclobis(tetramethylene carbonate) by means of BuSnCl3 and Sn(II) 2-ethylhexanoate
โ Scribed by Hans R. Kricheldorf; Andreas Mahler
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 577 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0887-624X
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โฆ Synopsis
Dimeric cyclotetramethylenecarbonate (TeMC)2 was polymerized in bulk at 185OC. Either nBuSnC1, or Sn(II)2-ethylhexanoate (SnOct2) were used as catalysts. SnOct, proved to be somewhat less reactive, but high yields (up to 93%) and high viscosities (qinh up to 0.85 dL/g) were obtained with both catalysts. Viscosity-average molecular weights (M,) in the range of 50-75 X lo3 were determined. The isolated crystalline poly(tetramethy1ene carbonate)s were characterized by IR, 'Hand "C-NMR spectra, DSC measurements and WAXD powder pattern. CH20H and octoate end groups were detected by means of 'H-NMR spectroscopy when SnOct2 was used as initiator, but ether groups were absent. DSC measurements revealed that poly(tetramethy1ene carbonate) is a slowly crystallizing polymer with a degree of crystallinity below 50% and a melting temperature in the range of 64-69ยฐC depending on the molecular weight. Thermogravimetric analyses proved that polyTeMC decomposes completely between 240 and 34OoC without leaving a residue. COP and tetrahydrofuran were the main degradation products. 0 1996 John Wiley & Sons, Inc.
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