Please use this identifier to cite or link to this item: http://scholarbank.nus.edu.sg/handle/10635/91500
Title: Halogen-induced chemical copolymerization of pyrrole with N-methylpyrrole
Authors: Neoh, K.G. 
Kang, E.T. 
Tan, T.C. 
Tan, K.I.
Issue Date: 5-Dec-1989
Citation: Neoh, K.G., Kang, E.T., Tan, T.C., Tan, K.I. (1989-12-05). Halogen-induced chemical copolymerization of pyrrole with N-methylpyrrole. Journal of Applied Polymer Science 38 (11) : 2009-2017. ScholarBank@NUS Repository.
Abstract: Due to their inherent stability under ambient conditions, conductive polyheterocycles has become a topic of great research interest. Simultaneous chemical copolymerization and oxidation of pyrrole and N-methylpyrrole by bromine and iodine has been carried out. The composition of the copolymers can be effectively controlled by varying the monomer feed ratio. From elemental analysis the copolymer composition and the monomer reactivity ratios have been determined. As the copolymer composition changes, the IR absorption spectra show changes in the intensity of certain bands. In bromine-induced polymerization, the electrical conductivity, thermal stability, and bromine content of the copolymer complex decrease with increase in N-methylpyrrole fraction. X-ray photoelectron spectroscopy data suggest that a fixed fraction of bromine is incorporated as covalent bromide in the copolymer complex. When iodine is used, the halogen content do not show substantial differences among the copolymers but the electrical conductivity and thermal stability of the copolymers also decrease with increase in N-methylpyrrole fraction.
Source Title: Journal of Applied Polymer Science
URI: http://scholarbank.nus.edu.sg/handle/10635/91500
ISSN: 00218995
Appears in Collections:Staff Publications

Show full item record
Files in This Item:
There are no files associated with this item.

SCOPUSTM   
Citations

12
checked on May 18, 2018

WEB OF SCIENCETM
Citations

10
checked on May 21, 2018

Page view(s)

36
checked on Aug 3, 2018

Google ScholarTM

Check


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.