Advanced Search

Journal Navigation

Journal Home

Subscriptions

Archive

Contact Us

Table of Contents

Click here to sign up for SAGE Journal Email Alerts today!

Sign In to gain access to subscriptions and/or personal tools.
High Performance Polymers
This Article
Right arrow Full Text (PDF)
Right arrow References
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Add to Saved Citations
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Request Reprints
Right arrow Add to My Marked Citations
Citing Articles
Right arrow Citing Articles via Google Scholar
Right arrow Citing Articles via Scopus
Google Scholar
Right arrow Articles by Ronova, I. A
Right arrow Articles by Shishkin, O. V
Right arrow Search for Related Content
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

Molecular Design of Rigid-Chain Polyheteroarylenes and the Effect of Substituents at the Central Heterocyclic Fragment on the Polyheteroarylene Equilibrium Rigidity

Inga A Ronova

Igor I Ponomarev

Andrey Yu Kovalevsky

Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, ul. Vavilova 28, Moscow 117813, Russia

Oleg V Shishkin

Alkali Halide Crystal Department, Institute of Single Crystals, National Academy of Sciences of Ukraine, prosp. Lenina 60, Kharkov 310072, Ukraine

Quantum-chemical calculations and calculations by the Monte Carlo method were used for conformational analysis of heterocyclic polymers. The steric effect of various substituents on the equilibrium geometry and conformational dynamics of 1, 4, 5, 8-naphthalenetetracarboxydiimide was studied using the AM1 semiempirical quantum-chemical method. It was shown that addition of bulky groups to the naphthalene moiety of 1, 4, 5, 8-naphthalenetetracarboxydiimide increases conformational rigidity of the imide rings. Using the example of rigid-chain polymers containing the naphthoileneimide ring, it was demonstrated that the introduction of four bulky substituents into the structure of 1, 4, 5, 8-naphthalenetetracarboxydiimide results in a considerable increase in the equilibrium rigidity of the polymer.

High Performance Polymers, Vol. 11, No. 4, 355-365 (1999)
DOI: 10.1088/0954-0083/11/4/301


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?