Synthesis and properties of first well-defined phosphole-containing π-conjugated polymers

Macromolecules

Volumn 36, Issue 8, 2003, Pages 2594-2597

  Morisaki, Yasuhiro ^a   Aiki, Yasuhiro ^a   Chujo, Yoshiki ^a  

^a KYOTO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

FLUORESCENCE EMISSION SPECTRA;

ABSORPTION SPECTROSCOPY; CATALYSTS; CYCLIC VOLTAMMETRY; ELECTRONS; FLUORESCENCE; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PALLADIUM; SYNTHESIS (CHEMICAL);

ORGANIC POLYMERS;

EID: 0037461412     PISSN: 00249297     EISSN: None     Source Type: Journal    
DOI: 10.1021/ma021095n     Document Type: Article

References (36)

1. Skothim, T. A., Elsenbaumer, R. L., Reynolds, J., Eds.; Handbook of Conducting Polymers, 2nd ed.; Marcel Dekker: New York, 1998.
2. For a recent contribution, see: Schön, J. H.; Dodabalapur, A.; Bao, Z.; Kloc, Ch.; Schenker, O.; Batlogg, B. Nature (London) 2001, 410, 189.
3. For a recent review, see: Kraft, A.; Grimsdale, A. C.; Holmes, A. B. Angew. Chem., Int. Ed. 1998, 37, 402.
4. (a) Nehring, J.; Amstutz, H.; Holmes, P. A.; Nevin, A. Appl. Phys. Lett. 1987, 61, 1283.
5. (b) Moll, A.; Siegfried, N.; Heitz, W. Makromol. Chem., Rapid Commun. 1990, 11, 485.
6. (c) Witteler, H.; Lieser, G.; Wegner, G.; Schulze, M. Makromol. Chem., Rapid Commun. 1993, 14, 471.
7. See, for example: (a) Nonlinear Optical Effects in Organic Polymers; Messier, J., Kajzar, F., Prasad, P. N., Ulrich, D. R., Eds.; Kluwer Academic Publishers: Dordrecht, 1989.
8. (b) Introduction to Nonlinear Optical Effects in Molecules and Polymers; Prasad, P. N., Williams, D. J., Eds.; Wiley: New York, 1990.
9. (c) Materials for Nonlinear Optics; Marder, S. R., Sohn, J. E., Stucky, G. D., Eds.; ACS Symposium Series 455; American Chemical Society: Washington, DC, 1991.
10. (d) Molecular Nonlinear Optics: Materials, Physics, and Devices; Zyss, J., Ed.; Academic Press: Boston, MA, 1994.
11. (e) Bredas, J. L.; Adant, C.; Tackx, P.; Persoons, A. Pierce, B. M. Chem. Rev. 1994, 94, 243.
12. For a recent review, see: McQuade, D. T.; Pullen, A. E.; Swager, T. M. Chem. Rev. 2000, 100, 2537.
13. (a) Mao, S. S. H.; Tilley, T. D. Macromolecules 1997, 30, 5566.
14. (b) Bévierre, M.-O.; Mercier, F.; Ricard, L.; Mathey, F. Angew. Chem., Int. Ed. Engl. 1990, 29, 655.
15. (c) Bévierre, M.-O.; Mercier, F.; Ricard, L.; Mathey, F.; Jutand, A.; Amatore, C. New J. Chem. 1991, 15, 545.
16. (d) Deschamps, E.; Ricard, L.; Mathey, F. Angew. Chem., Int. Ed. Engl. 1994, 33, 1158.
17. (e) Hay, C.; Fischmeister, C.; Hissler, M.; Toupet, L.; Réau, R. Angew. Chem., Int. Ed. 2000, 39, 1812.
18. See, for example: (a) Quin, L. D.; Quin, G. S. In Phosphorus Carbon Heterocyclic Chemistry: The Rise of a New Domain; Mathey, F., Ed.; Pergamon: Amsterdam, 2001.
19. (b) Dillon, K. B.; Mathey, F.; Nixon, J. F. Phosphorus: The Carbon Copy; Wiley: Chichester, 1998.
20. (c) Quin, L. D. In Comprehensive Heterocyclic Chemistry; Katritzky, A. R., Ress, C. W., Scriven, E. F. V., Eds.; Elsevier: Oxford, 1996; Vol. 2.
21. (a) Dieck, H. A.; Heck, R. F. J. Organomet. Chem. 1975, 93, 259.
22. (b) Sonogashira, K.; Tohda, Y.; Hagihara, N. Tetrahedron Lett. 1975, 76, 4467.
23. (a) Negishi, E.; Cederbaum, F. E.; Takahashi, T. Tetrahedron Lett. 1986, 27, 2829.
24. (b) Negishi, E.; Takahashi, T. Acc. Chem. Res. 1994, 27, 124.
25. (a) Doherty, S.; Robins, E. G.; Nieuwenhuyzen, M.; Knight, J. G.; Champkin, P. A.; Clegg, W. Organometallics 2002, 21, 1383.
26. (b) Doherty, S.; Knight, J. G.; Robins, E. G.; Scanlan, T. H.; Champkin, P. A.; Clegg, W. J. Am. Chem. Soc. 2001, 123, 5110.
27. (c) Takahashi, T.; Sun, W.-H.; Nakajima, K. Chem. Commun. 1999, 1595.
28. (a) Li, H.; Powell, D. R.; Hayashi, R. K.; West, R. Macromolecules 1998, 37, 52.
29. (b) Moroni, M,; Moigne, J. L. Macromolecules 1994, 27, 562.
30. Lee, S. H.; Nakamura, T.; Tsutsui, T. Org. Lett. 2001, 3, 2005.
31. Hay, C.; Hissler, M.; Fischmeister, C.; Rault-Berthelot, J.; Toupet, L.; Nyulászi, L.; Réau, R. Chem. - Eur. J. 2001, 7, 4222.
32. Recently, we have reported that alternating copolymers having [2.2]paracyclophane and fluorene units showed a blue emission at the lowest wavelength compared with the fluorene-containing polymers reported so far. See: Morisaki, Y.; Chujo, Y. Chem. Lett. 2002, 194 and references cited therein.
33. D = 1.446) were used].
34. Yamamoto, T.; Morikita, T.; Maruyama, T.; Kubota, K.; Katada, M. Macromolecules 1997, 30, 5390.
35. (a) Takahashi, T.; Tsai, F.-Y.; Li, Y. Chem. Lett. 1999, 1173.
36. (b) Jiang, B.; Tilley, T. D. J. Am. Chem. Soc. 1999, 121, 9744.