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Synthesis of Fluorescent Thiophene-derivatized Pentytiptycenes and Their Aggregate Behaviors

  • Song, Jinwoo (Department of Applied Physic, Dankook University)
  • 송진우 (단국대학교 응용물리학과)
  • Received : 2010.03.02
  • Accepted : 2010.03.20
  • Published : 2010.03.31

Abstract

Thiophene-derivatized pentiptycenes were synthesized and characterized by NMR and UV-Vis spectroscopy. Aggregation behavior of thiophene-derivatized pentiptycenes was monitored by the measurement of fluorescence. Fluorescence intensities for the thiophene-derivatized pentiptycenes and thiophene-derivatized pentiptycenes aggregates were compared. There is no shift in the maximum of the emission wavelength. In the range of water fraction between 20% and 40%, the emission intensity of thiophene-derivatized pentiptycene aggregates remains almost identical. Fluorescence efficiency incresaed by about 5 times higher when the thiophene-derivatized pentiptycenes forms the aggregates in solution.

Keywords

References

  1. A. B. Trofimov, J. Schirmer, D. M. P. Holland, A. W. Potts, L. Karlsson, R. Maripuu and K. Siegbahn, "The influence of electron correlation and relativistic effects on the valence shell photoelectron spectrum of iodothiophene", J PHYS B-AT MOL OPT. vol. 35, pp. 5051-5058, 2002. https://doi.org/10.1088/0953-4075/35/24/309
  2. J. P. Czarnik and A. W. Eds. "Chemosensors of Ion and Molecule Recognition Desvergne", Kluwer Academic Publishers: Boston, 1997.
  3. A. P. De Silva, H. Q. N. Gunaratne, T.G unnlaugsson, A. J. M. Huxley, C. P. McCoy, J. T. Rademacher and T. E. Rice, Chem. Rev. "Signaling recognition events with fluorescent sensors and switches", Vol. 97, pp. 1515, 1997.
  4. J. S. Yang and T. M. Swanger. J. AM. Chem. Soc. vol. 120, pp. 1184, 1998.
  5. A. Kraft, A. C. Grimsdale and A. B. Holmes, Angew "Electroluminescent conjugated polymers - Seeing polymers in a new light", Chem., Int. Ed., vol. 37, p. 402, 1998. https://doi.org/10.1002/(SICI)1521-3773(19980302)37:4<402::AID-ANIE402>3.0.CO;2-9
  6. Y. Shirota, J. Mater, Y. Shirota and J. Mater, Chem., "Organic materials for electronic and optoelectronic devices", vol. 10, pp. 1, 2000. https://doi.org/10.1039/a908130e
  7. A. P. H. J. Kilbinger, A. F. M. Biscarini, F. Cavallini, M. Cooper, H. J, Derrick, P. J, Feast, W. J. Lazzaroni, R. Lecle're, P. H. McDonell, L. A, Meijer and E. W. Meskers, J. Am. Chem. Soc. "Supramolecular Organization of [alpha],[alpha]-Disubstituted Sexithiophenes find it", vol. 124, pp. 1269, 2002. https://doi.org/10.1021/ja0113403
  8. R. Azumi, H. Tachibana, H. Sakai, M. Abe, P. Bauerle and M. Matsumoto, Chem. Lett. "Liquid crystalline behavior of $\alpha$-substituted oligothiophenes", p. 1022, 2001.
  9. P. Liu, H. Nakano and Y. Shirota Liq. Cryst. "Synthesis and mesogenic properties of a novel family of oligothiophene derivatives", vol. 28, pp. 581, 2001. https://doi.org/10.1080/02678290010018024
  10. H. Zhang, S. Shiino, A. hishido, A. Kanazawa, O. Tsutsumi and T. Shiono, Adv. Mater. "A Thiophene Liquid Crystal as a Novel -Conjugated Dye for Photo-Manipulation of Molecular Alignment", vol. 12, pp. 1336, 2000. https://doi.org/10.1002/1521-4095(200009)12:18<1336::AID-ADMA1336>3.0.CO;2-A