Controlled ionochromism with polythiophenes bearing crown ether side chains

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Angela Boldea, Isabelle Lévesque and Mario Leclerc


Abstract

Regioregular poly(3-alkoxy-4-methylthiophene)s bearing crown ethers of different sizes (12-crown-4), PT12C4; and (15-crown-5) PT15C5) have been synthesized and their thermochromic and ionochromic behaviors investigated. These polythiophene derivatives exhibit a highly conjugated form in the solid state at room temperature (absorption maximum around 550 nm) and a less conjugated form upon heating (absorption maximum around 425 nm). In acetone or ethyl acetate ionochromic responses have been observed upon addition of some alkali metal cations. Initially, the absorption maximum is located around 425 nm (yellow) but moves to 550 nm (violet). These results indicate the formation of planar (highly conjugated) polymeric assemblies upon the addition of alkali metal cations. PT12C4 is more sensitive to sodium salts while PT15C5 gives more intense ionochromic effects with potassium salts. These effects can be explained by a more stable 2:1 complexation between a given crown ether and an appropriate alkali metal cation.


References

  1. W. J. Feast, J. Tsibouklis, K. L. Pouwer, L. Groenendaal and E. W. Meijer, Polymer, 1997, 37, 5017 CrossRef CAS.
  2. G. Schopf and G. Kossmehl, Adv. Polym. Sci., 1997, 1, 129.
  3. Handbook of Conducting Polymers, eds. T. A. Skotheim, J. R. Reynolds and R. L. Elsenbaumer, Marcel Dekker, NY, 2nd edn., 1997 Search PubMed.
  4. M. Leclerc and K. Faïd, Adv. Mater., 1997, 9, 1087 CrossRef.
  5. M. Ranger, D. Rondeau and M. Leclerc, Macromolecules, 1997, 30, 7686 CrossRef CAS.
  6. R. L. Elsenbaumer, K. Y. Jen and O. Oboodi, Synth. Met., 1986, 15, 169 CrossRef CAS.
  7. M. A. Sato, S. Takeda and K. Kaeriyama, J. Chem. Soc., Chem. Commun., 1986, 873 RSC.
  8. R. Sugimoto, S. Takeda, H. B. Gu and Y. Yoshino, Chem. Express, 1986, 1, 635 Search PubMed.
  9. S. Hotta, S. D. D. V. Rughooputh, A. J. Heeger and F. Wudl, Macromolecules, 1987, 20, 212 CrossRef CAS.
  10. M. R. Bryce, A. Chissel, P. Kathirgamanathan, D. Parker and N. M. R. Smith, J. Chem. Soc., Chem. Commun., 1987, 466 RSC.
  11. J. Roncali, R. Garreau, A. Yassar, P. Marque, F. Garnier and M. Lemaire, J. Phys. Chem., 1987, 91, 6706 CrossRef CAS.
  12. M. Leclerc, F. Martinez and G. Wegner, Makromol. Chem., 1989, 190, 3105 CAS.
  13. M. Feldhues, G. Kampf, H. Litterer, T. Mecklenburg and P. Wegener, Synth. Met., 1989, 28, C487 CAS.
  14. M. Leclerc and G. Daoust, J. Chem. Soc., Chem. Commun., 1990, 273 RSC.
  15. G. Daoust and M. Leclerc, Macromolecules, 1991, 24, 455 CrossRef CAS.
  16. S. Hotta, M. Soga and N. Sonoda, Synth. Met., 1988, 26, 267 CAS.
  17. K. Faïd, R. Cloutier and M. Leclerc, Macromolecules, 1993, 26, 2501 CrossRef CAS.
  18. G. Heywang and F. Jonas, Adv. Mater., 1992, 4, 116 CAS.
  19. J. L. Brédas, G. B. Street, B. Thémans and J. M. André, J. Chem. Phys., 1985, 83, 1323 CrossRef CAS.
  20. B. Thémans, W. R. Salaneck and J. L. Brédas, Synth. Met., 1989, 28, C359 CAS.
  21. S. D. D. V. Rughooputh, S. Hotta, A. J. Heeger and F. Wudl, J. Polym. Sci., Polym. Phys. Ed., 1987, 25, 1071 Search PubMed.
  22. O. Inganäs, W. R. Salaneck, J. E. Osterholm and J. Laakso, Synth. Met., 1988, 22, 395 CrossRef CAS.
  23. K. Tashiro, K. Ono, Y. Minagawa, M. Kobayashi, T. Kawai and K. Yoshino, J. Polym. Sci., Polym. Phys. Ed., 1991, 29, 1223 Search PubMed.
  24. G. Zerbi, B. Chierichetti and O. Inganäs, J. Chem. Phys., 1991, 94, 4646 CrossRef CAS.
  25. C. Roux and M. Leclerc, Macromolecules, 1992, 25, 2141 CrossRef CAS.
  26. K. Faïd, M. Fréchette, M. Ranger, L. Mazerolle, I. Lévesque, M. Leclerc, T. A. Chen and R. D. Rieke, Chem. Mater., 1995, 7, 1390 CrossRef.
  27. C. Roux, J. Y. Bergeron and M. Leclerc, Makromol. Chem., 1993, 194, 869 CAS.
  28. N. DiCésare, M. Belletête, G. Durocher and M. Leclerc, Chem. Phys. Lett., 1997, 275, 533 CrossRef.
  29. M. Leclerc, M. Fréchette, J. Y. Bergeron, M. Ranger, I. Lévesque and K. Faid, Macromol. Chem. Phys., 1996, 197, 2077 CrossRef CAS.
  30. F. Raymond, N. DiCésare, M. Belletête, G. Durocher and M. Leclerc, Adv. Mater., 1998, 10, 599 CrossRef CAS.
  31. R. Hanna and M. Leclerc, Chem. Mater., 1996, 8, 1512 CrossRef CAS.
  32. N. DiCésare, M. Belletête, C. Marrano, M. Leclerc and G. Durocher, J. Phys. Chem. A., 1999, 103, 795 CrossRef CAS.
  33. N. DiCésare, M. Belletête, M. Leclerc and G. Durocher, J. Phys. Chem. A, 1999, 103, 803 CrossRef CAS.
  34. K. Yoshino, S. Nakajima, M. Onoda and R. Sugimoto, Synth. Met., 1989, 28, C419 CrossRef CAS.
  35. I. Lévesque and M. Leclerc, Macromolecules, 1997, 30, 4347 CrossRef CAS.
  36. R. D. McCullough and S. P. Williams, J. Am. Chem. Soc., 1993, 115, 11608 CrossRef CAS.
  37. M. J. Marsella and T. M. Swager, J. Am. Chem. Soc., 1993, 115, 12214 CrossRef CAS.
  38. M. J. Marsella, R. J. Newland, P. J. Caroll and T. M. Swager, J. Am. Chem. Soc., 1995, 117, 9842 CrossRef CAS.
  39. I. Lévesque and M. Leclerc, Chem. Mater., 1996, 8, 2843 CrossRef CAS.
  40. K. Faïd and M. Leclerc, J. Am. Chem. Soc., 1998, 120, 5274 CrossRef.
  41. C. J. Pedersen, J. Am. Chem. Soc., 1967, 89, 2495 CrossRef CAS; C. J. Pedersen, J. Am. Chem. Soc., 1967, 89, 7017 CrossRef CAS; C. J. Pedersen, J. Am. Chem. Soc., 1970, 92, 391 CrossRef CAS.
  42. P. Bäuerle and S. Scheib, (a)Adv. Mater., 1993, 5, 848; (b)Acta Polym., 1995, 46, 124 Search PubMed.
  43. W. Johnstone and M. M. Rose, Tetrahedron, 1979, 35, 2169 CrossRef CAS.
  44. M. Fréchette, M. Belletête, J. Y. Bergeron, G. Durocher and M. Leclerc, Macromol. Chem. Phys., 1997, 198, 1709 CAS.
  45. T. Miyazaki, S. Yanagida, A. Itoh and M. Okahara, Bull. Chem. Soc. Jpn., 1982, 55, 2005 CAS.
  46. Y. Nakatsuji, T. Nakamura, M. Okahara, D. M. Dishong and G. W. Gokel, J. Org. Chem., 1983, 48, 1237 CrossRef CAS.
  47. M. S. Islam, R. A. Pethrick, D. Pugh and M. J. Wilson, J. Chem. Soc., Faraday Trans., 1998, 94, 39 RSC.
  48. B. Wang and M. R. Wasielewski, J. Am. Chem. Soc., 1997, 119, 12 CrossRef.