Resonances in the 75.5 MHz 13C-NMR spectrum of poly(styrene oxide) (PSO) and of block and statistical copolymers of styrene oxide (SO) and ethylene oxide (EO) have been assigned with the aid of DEFT subspectral editing. Both primary and secondary hydroxyl end-groups have been identified in PSO. A si
Analysis of the 1H and 13C NMR spectra of poly(t-butyl-ethylene oxide) and of block and statistical copolymers of t-butyl-ethylene oxide and ethylene oxide
β Scribed by Frank Heatley; Ga-Er Yu; Jane Lawrance; Colin Booth
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 557 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0014-3057
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β¦ Synopsis
Resonances in the 500 MHz ~H and 75.5 MHz t3C NMR spectra of poly(t-butyl-ethylene oxide) and of block and statistical copolymers of t-butyl-ethylene oxide and ethylene oxide prepared using an anionic initiator have been assigned with the aid of 2-dimensional COSY spectra and DEPT subspectral editing. Monomer placement occurs almost entirely by head-to-tail addition, and in the homopolymers, isotactic enchainment is approximately twice as favourable as syndiotactic, t3C chemical shifts have been rationalised by a simple substituent increment scheme.
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A two-stage stable system of isotactic polypropylene-poly(ethylene oxide) blend, in which poly(ethylene oxide) can be permanent either in molten or in crystallized states in the temperature range from 280 to 327 K, was described. The behavior of that blend was explained in terms of fractionated crys