The role of molecular mechanics in the prediction of the chain conformation of polymers in the crystalline state: Syndiotactic polymers

✍ Scribed by Roberto Napolitano; Beniamino Pirozzi

• Publisher: John Wiley and Sons
• Year: 1999
• Tongue: English
• Weight: 143 KB
• Volume: 8
• Category: Article
• ISSN: 1022-1344
• DOI: 10.1002/(sici)1521-3919(19990101)8:1<15::aid-mats15>3.0.co;2-x

✦ Synopsis

Molecular mechanics methods have been used in order to find the conformations of various syndiotactic polymers in crystals. Three different classes of polymers have been examined: i) polyolefins, such as poly(propylene), polystyrene, poly(1-butene) and poly(1,2-butadiene); ii) polydienes, such as cis-1,4poly(1,3-pentadiene); iii) alternating copolymers of carbon monoxide with styrene or styrene derivatives. The presence of conformational polymorphism in some of the studied polymers is predicted and explained by maps and minimizations of the conformational energy. The calculated internal parameters and chain axis repeats of all the considered polymers result in very good agreement with X-ray experimental data reported in literature. The role of intramolecular nonbonded interactions in determining the conformations of the polymer chains is thoroughly discussed.