Influence of copolymer composition on the structure of conducting poly(aniline-co-o-phenylenediamine)

International Journal of Polymer Analysis and Characterization

Volumn 10, Issue 1-2, 2005, Pages 1-13

  Umare, Suresh S ^b   Waware, Umesh S ^b   Ingole, Sudeep ^b   Viswanath, S G ^a  

^a LAXMINARAYAN INSTITUTE OF TECHNOLOGY   (India)

^b VISVESVARAYA NATIONAL INSTITUTE OF TECHNOLOGY   (India)

Author keywords

Conducting copolymers; Conductivity and solubility; Polyaniline and derivatives; Thermal stability

Indexed keywords

EID: 29244436112     PISSN: 1023666X     EISSN: None     Source Type: Journal    
DOI: 10.1080/10236660500345398     Document Type: Article

References (21)

1. Anand, J., S. Palaniappan, and D. N. Sathyanarayana. (1998). Spectral, thermal and electrical properties of poly(o- and m-toludine)-polystyrene blends prepared by emulsion pathway. J. Polym. Sci. Polym. Chem. 36, 2291-2299.
2. MacDiarmid, A. G. and A. J. Epstein. (1991). The polyaniline: A novel class of conducting polymers. Am. Chem. Soc. Poly. Chem. 32, 709-710.
3. Oh, S. Y., K. Akagi, H. Shirakawa, and K. Araya. (1993). Synthesis and properties of liquid-crystalline polyacetylenes with a phenycyclohexyl mesogenic moiety in the side group. Macromolecules 26, 6203-6206.
4. Genies, E. M., A. Boyle, M. Lapkowski, and C. Tsintavis. (1990). Polyaniline: A historical survey. Synth. Met. 36, 139-182.
5. Kaneko, M. and H. Nakamura. (1985). Photoresponse of the liquid junction polyaniline film. J. Chem. Soc. Chem. Commun. 6, 346-347.
6. Sato, M., S. Tanaka, and K. Kaeriyama. (1986). Soluble conducting polythiophenes. J. Chem. Soc. Chem. Commun. 2, 873-874.
7. Li, S., Y. Cao, and Z. Xue. (1987). Soluble polyaniline. Synth. Met. 2, 141-149.
8. Mattoso, L. H. C. and L. F. Malmonge. (1999). Morphology variation as a function of composition for blends of PVDP and a polyaniline derivative. Polymer 40, 513-518.
9. Fan, J., M. Wan, and D. Zhu. (1998). Synthesis and characterization of water-soluble conductivity copolymer poly(aniline-co-o-aminobenzenesulfonic acid). J. Polym. Sci. Polym. Chem. 36, 3013-3019.
10. Gupta, M. C. and S. S. Umare. (1992). Studies on poly(o-methoxyaniline). Macromolecules 25, 138-142.
11. Umare, S. S., M. M. Huque, M. C. Gupta, and S. G. Visvanath. (1996). Studies on substituted derivatives of polyaniline: Effect of polymerization conditions on electrical conductivity. Macromol. Rep. A33, 381-389.
12. Cao, Y., P. Smith, and A. J. Heeger. (1992). Counter-ion induced processibility of conducting polyaniline and of conducting polyblends of polyaniline in bulk polymers. Synth. Met. 48, 91-97.
13. Borkar, A. D., M. C. Gupta, and S. S. Umare. (2001). Electrical and optical properties of conducting copolymer: Poly(aniline-co-N-ethylaniline). Polym. Plast. Technol. Eng. 40, 225-234.
14. Dao, L. H., M. Leclerc, J. Guoy, and J. W. Chevalier. (1989). Synthesis and characterization of substituted polyanilines. Synth. Met. 29, E377-E382.
15. Ye, S., N. T. Do, L. H. Dao, and A. K. Vijh. (1997). Electrochemical preparation and characterization of conducting copolymers: Poly(aniline-co-N- butylaniline). Synth. Met. 88, 65-72.
16. Chen, S. A. and G. W. Hwang. (1995). Water soluble self-acid doped conducting polyaniline: Structure and properties. J. Am. Chem. Soc. 117, 10055-10062.
17. 2O. J. Inorg. Nucl. Chem. 35, 3455-3461.
18. Huang, W. S., B. D. Humphrey, and A. G. MacDiarmid. (1986). Polyaniline: A novel conducting polymer. Morphology & chemistry of its oxidation-reduction in aqueous electrolytes. J. Chem. Soc. Faraday Trans. 82, 2385-2400.
19. Chiang, J. C. and A. G. MacDiarmid. (1986). Polyaniline: Protonic acid doping of the emeraline form to the metallic regime. Synth. Met. 13, 193-205.
20. Ray, A., A. G. MacDiarmid, J. M. Ginder, and A. J. Epstein. (1990). Optical studies of polyanilines: Effect of alkyl ring substitution and solvent environment. Mater. Res. Soc. Symp. Proc. 173, 353-357.
21. Mizoguchi, K. (1990). Spin dynamics in conducting polymers. Makromol. Chem., Macromol. Symp. 37, 53-66.