Polymerization of 3,9-dimethyl-1,5,7,11-tetraoxaspiro [5,5] undecane with dithiols
โ Scribed by Yanming Luo; William J. Bailey
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 594 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0021-8995
No coin nor oath required. For personal study only.
โฆ Synopsis
New polymers containing spiroorthocarbonate units on the main chain were synthesized and characterized. The polymers were prepared by using redox or free-radical catalysts in solution polymerization of 3,9-dimethylene-l,5,7,11-tetraoxaspiro [ 5,5] undecane [or simply called bimethylenespiroorthocarbonate ( BMSOC ) ] and dithiols at lower temperatures.
Their spiroorthocarbonate units could undergo hydrolysis in acidic conditions at room temperature. The structure of polymers was investigated by nuclear magnetic resonance ('Hand 13C-NMR) and Fourier transform infrared (FTIR) spectroscopy. The kind of dithiols had a remarkable effect on properties of the polymers. Block polymers obtained from BMSOC and dithiols could result in a better combination of properties.
๐ SIMILAR VOLUMES
A new spiro ortho carbonate, 3,9-di(p-methoxybenzyl)-1,5,7,11-tetra-oxaspiro(5,5)undecane was prepared by the reaction of 2-methoxybenzyl-1,3-propanediol with di(n-butyl)tin oxide, following with carbon disulยฎde. Its cationic polymerization was carried out in dichloromethane using BF 3 -OEt 2 as cat
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a โFull Textโ option. The original article is trackable v