The water-soluble conducting copolymer of poly(aniline-co-o-aminobenzenesulfonic acid) (PAOABSA) was synthesized directly from aniline and o-aminobenzenesulfonic acid and characterized by elemental analysis, FTIR, UV-Vis, X-ray powder diffraction, and XPS. The room-temperature conductivity of the co
Synthesis and characterization of electrically conducting copolymer of aniline and o-bromoaniline using methane sulfonic acid as dopant
✍ Scribed by Bidhan C. Roy; Maya Dutta Gupta; Leena Bhowmik; Jayanta K. Ray
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 190 KB
- Volume
- 86
- Category
- Article
- ISSN
- 0021-8995
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✦ Synopsis
Abstract
Polyaniline (PAN), poly(o‐bromoaniline) (POBA), and poly(aniline‐co‐o‐bromoaniline) (PABA) were synthesized by oxidative coupling. These polymers are protonated by 10–20% methane sulfonic acid (MSA) and 1__M__ HCl. The new polymer bases have greater solubility than that of PAN in common polar organic solvents; PAN–MSA was observed to be the most thermally stable of these polymers. POBA is associated with residual quinoid diimine units as illustrated in the IR and UV‐vis spectra, after reduction with hydrazine dihydrochloride. Both the doping agents cause a downward shift of the quinoid absorption in the IR spectra. MSA‐ and HCl‐doped PAN and PABA polymers exhibit a coil‐like conformation in DMSO, whereas only MSA‐doped PAN and PABA show an “expanded coil‐like” conformation in m‐cresol with a “free carrier tail” above 800 nm in their electronic spectra. XPS spectra indicated the presence of covalent bromine in the POBA and PABA polymers. Bromine retention was greater in the homopolymer as evidenced by the IR studies after aging at 350°C. Compared to HCl, MSA is found to be a more effective dopant, enhancing the conductivity of the copolymers by 10^2^–10^3^ times in magnitude. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 2662–2669, 2002
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## Abstract Free‐radical copolymerizations of 1‐vinyl‐2‐pyrrolidone with 2‐acrylamido‐2‐methyl propane sulfonic acid at different feed ratios were investigated. The copolymers were characterized by ^1^H‐NMR, ^13^C‐NMR, and FTIR. The copolymer composition was determined from the elemental analysis.