Highly conductive new aniline copolymers containing butylthio substituent

Macromolecules

Volumn 34, Issue 3, 2001, Pages 587-591

  Han, Chien Chung ^a   Hong, Shih Ping ^a   Yang, Ku Feng ^a   Bai, Meng Yi ^a   Lu, Chia Hui ^a   Huang, Chao Sheng ^a  

^a NATIONAL TSING HUA UNIVERSITY   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

COPOLYMERIZATION; COPOLYMERS; ELECTRIC CONDUCTIVITY OF SOLIDS; PLASTIC FILMS; SUBSTITUTION REACTIONS;

POLYANILINE;

CONDUCTIVE PLASTICS;

EID: 0035119475     PISSN: 00249297     EISSN: None     Source Type: Journal    
DOI: 10.1021/ma001664w     Document Type: Article

References (42)

1. (a) Handbook of Organic Conductive Molecules and Polymers; Nalwa, H. S., Ed.; John Wiley & Sons: Chichester, 1997; Vols. 1-4.
2. (b) Handbook of Conducting Polymers; Skotheim, T. A., Ed.; Marcel Dekker: New York, 1986; Vols. 1 and 2.
3. (c) Genies, E. M.; Boyle, A.; Lapkowski, M.; Tsintavis, C. Synth. Met. 1990, 36, 139.
4. (a) Wei, Y.; Focke, W. W.; Wnek, G. E.; Ray, A.; MacDiarmid, A. G. J. Phys. Chem. 1989, 93, 495.
5. (b) Conklin, J. A.; Huang, S. C.; Huang, S. M.; Wen, T.; Kaner, R. B. Macromolecules 1995, 28, 6522.
6. (c) Bidan, G.; Genies, E. M.; Penneau, J. F. J. Electroanal. Chem. 1989, 271, 59.
7. (d) Bodalia, R.; Stern, R.; Batich, C.; Duran, R. J. Polym. Sci., Polym. Chem. 1993, 31, 2123.
8. (e) Genies, E. M.; Noel, P. J. Electroanal. Chem. 1991, 310, 89.
9. (f) Chevalier, J.-W.; Bergeron, J.-Y.; Dao, L. H. Macromolecules 1992, 25, 3325.
10. (g) Cattarin, S.; Doubova, L.; Mengoli, G.; Zotti, G. Electrochim. Acta 1988, 33, 1077.
11. (h) Leclerc, M.; Guay, J.; Dao, L. H. Macromolecules 1989, 22, 649.
12. (i) Shenlong, W.; Fosong, W.; Xiaohui, G. Synth. Met. 1986, 16, 99.
13. (a) D'Aprano, G.; Leclerc, M.; Zotti, G.; Schiavon, G. Chem. Mater. 1995, 7, 33.
14. (b) Mattoso, L. H. C.; MacDiarmid, A. G.; Epstein, A. J. Synth. Met. 1994, 68, 1.
15. (c) Dhawan, S. K.; Trivedi, D. C. Synth. Met. 1993, 60, 67.
16. (d) MacInnis, D., Jr.; Funt, B. L. Synth. Met. 1988, 25, 235.
17. (e) Gupta, M. C.; Umare, S. S. Macromolecules 1992, 25, 138.
18. (f) Lacroix, J. C.; Garcia, P.; Audiere, J. P.; Clement, R.; Kahn, O. Synth. Met. 1991, 44, 117.
19. Angelopoulos, M.; Asturias, G. E.; Ermer, S. P.; Ray, A.; Scherr, E. M.; MacDiarmid, A. G. Mol. Cryst. Liq. Cryst. 1988, 160, 151.
20. (a) Wei, Y.; Hariharan, R.; Patel, S. Macromolecules 1990, 23, 758.
21. (b) Dhawan, S. K.; Trivedi, D. C. Synth. Met. 1993, 60, 63.
22. (c) Langer, J. J. Synth. Met. 1990, 35, 295.
23. (d) Langer, J. J. Synth. Met. 1990, 35, 301.
24. (e) Bergeron, J.-Y.; Dao, L. H. Macromolecules 1992, 25, 3332.
25. (a) Pandey, S. S.; Annapoorni, S.; Malhotra, B. D. Macromolecules 1993, 26, 3190.
26. (b) Prevost, V.; Petit, A.; Pla, F. Synth. Met. 1999, 104, 79.
27. Han, C. C.; Jeng, R. C. Chem. Commun. 1997, 553.
28. Han, C. C.; Hseih, W. D.; Yeh, J. Y.; Hong, S. P. Chem. Mater. 1999, 11, 480.
29. Wudl, F.; Angus, R. O., Jr.; Allemand, P. M.; Vachon, D. J.; Norwak, M.; Liu, Z. X.; Heeger, A. J. J. Am. Chem. Soc. 1987, 109, 3677.
30. Socrates, G. Infrared Characteristic Group Frequencies. Tables and Charts, 2nd ed.; John Wiley & Sons: New York, 1994.
31. (a) Beamson, G.; Briggs, D. High-Resolution XPS of Organic Polymers; John Wiley & Sons: New York, 1992.
32. (b) Handbook of X-ray Photoelectron Spectroscopy; Chastain, J., Ed.; Perkin-Elmer Corp.: Eden Prairie, MN, and the references therein.
33. Asturias, G. E.; MacDiarmid, A. G.; McCall, R. P.; Epstein, A. J. Synth. Met. 1989, 29, E157.
34. Wieder, H. H. Laboratory Notes on Electrical and Galvanomagnetic Measurements; Elsevier Scientific Publishing Co.: Amsterdam, 1979.
35. (a) Cao, Y.; Smith, P.; Heeger, A. J. Synth. Met. 1982, 48, 91.
36. (b) MacDiarmid, A. G.; Epstein, A. J. Synth. Met. 1994, 65, 103.
37. Hjertberg, T.; Sandberg, M. Synth. Met. 1989, 29, E257.
38. D'Aprano, G.; Leclerc, M.; Zotti, G. J. Electroanal. Chem. 1993, 351, 145.
39. (a) Yue, J.; Wang, Z. H.; Cromack, K. R.; Epstein, A. J.; MacDiarmid, A. G. J. Am. Chem. Soc, 1991, 113, 2665.
40. (b) Chan, H. S. O.; Neuendorf, A. J.; Ng, S. C.; Wong, P. M. L.; Young, D. J. Chem. Commun. 1998, 1327.
41. 3/2 line was reported to be 163.66 eV for poly(phenylene sulfide) and 163.50 eV for poly(ethylene sulfide); 164.4 eV for phenyl disulfide and 164.1 eV for butyl disulfide; 163.1 eV for thiophenol, 161-163 eV for alkanethiols, and 168.23 eV for poly(sodium 4-styrenesulfonate) (ref 11).
42. C 120.25, 120.38, 124.35, 125.04, 125.08, 125.29, 136.39, 137.7, 149.8, 149.83, 157.84, and 157.9, complicated by the presence of both E and Z forms (ref 15).