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Synthesis and Characterization of New Push-Pull Chromophores Containing BF2-Azopyrrole Derivatives

고혜민
대한화학회|2016.02|대한화학회지 (Journal of the Korean Chemical Society)|제60권 제1호|pp. 21-27|DOI http://dx.doi.org/10.5012/jkcs.2016.60.1.21

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참고문헌

키워드

Organic solar cellAsymmetric BF2-azopyrrole molecules
주제분류화학

초록

Novel push-pull chromophores containing 5’-(4-(bis(9,9-dimethyl-9H-fluoren-2-yl)aniline (bisDMFA) as a donor and phenylazo-methylpyrrolyl-boron difluoride (PhAPy-BF2) as an acceptor were designed and synthesized by the Knoevenagel condensation reaction for organic solar cells. Various electron withdrawing moieties were effectively introduced using 2,4-dimethyl-1H-pyrrole to afford new asymmetric BF2-azopyrrole molecules that were characterized by UV-vis spectroscopy and cyclic voltammetry measurements.

Abstract

Novel push-pull chromophores containing 5’-(4-(bis(9,9-dimethyl-9H-fluoren-2-yl)aniline (bisDMFA) as a donor and phenylazo-methylpyrrolyl-boron difluoride (PhAPy-BF2) as an acceptor were designed and synthesized by the Knoevenagel condensation reaction for organic solar cells. Various electron withdrawing moieties were effectively introduced using 2,4-dimethyl-1H-pyrrole to afford new asymmetric BF2-azopyrrole molecules that were characterized by UV-vis spectroscopy and cyclic voltammetry measurements.

참고문헌 (53)

  1. Robertson, N., , Angew. Chem, 118, pp.2398~ (2006)
  2. Robertson, N., , Angew. Chem. Int. Ed, 45, pp.2338~ (2006)
  3. Nielsen, T. D., , Sol. Energy Mater. Sol. Cells, 94, pp.1553~ (2010)
  4. Krebs, F. C., , ACS Appl. Mater. Interfaces, 2, pp.877~ (2010)
  5. Chen, L. M., , Adv. Mater, 21, pp.1434~ (2009)
  6. Krebs, F. C., , Nanoscale, 2, pp.873~ (2010)
  7. Bund-gaard, E., , Macromolecules, 43, pp.8115~ (2010)
  8. Krebs, F. C., , J. Mater. Chem, 20, pp.8994~ (2010)
  9. Krebs, F. C., , Mater. Chem, 19, pp.5442~ (2009)
  10. Kippelen, B., , Energy Environ. Sci, 2, pp.251~ (2009)
  11. Krebs, F. C., , Energy Environ. Sci, 3, pp.512~ (2010)
  12. Walker, B., , Chem. Mater, 23, pp.470~ (2011)
  13. Roncali, J., , Acc. Chem. Res, 42, pp.1719~ (2009)
  14. Lloyd, M. T., , Mater. Today, 10, pp.34~ (2007)
  15. Li, W., , Chem. Mater, 21, pp.5327~ (2009)
  16. Lloyd, M. T., , J. Am. Chem. Soc, 129, pp.9144~ (2007)
  17. Marrocchi, A., , Chem. Commun, 45, pp.1380~ (2009)
  18. Bruckstummer, H., , Mater. Chem, 20, pp.240~ (2010)
  19. Kronen-berg, N. M., , Chem. Commun, 44, pp.6489~ (2008)
  20. Ma, C. Q., , Adv. Funct. Mater, 18, pp.3323~ (2008)
  21. Silvestri, F., , J. Am. Chem. Soc, 130, pp.17640~ (2008)
  22. Mayerhoffer, U., , Angew. Chem. Int. Ed, 48, pp.8776~ (2009)
  23. Lincker, F., , Adv. Funct. Mater, 18, pp.3444~ (2008)
  24. Velusamy, M., , Org. Lett, 11, pp.4898~ (2009)
  25. Xue, L. L., , J. Phys. Chem. C, 113, pp.12911~ (2009)
  26. Mikroyan-nidis, J. A., , Org. Electron, 10, pp.1320~ (2009)
  27. Liu, Y., , J. Mater. Chem, 20, pp.2464~ (2010)
  28. Zhang, W., , J. Mater. Chem, 20, pp.2182~ (2010)
  29. Yang, Y., , J. Phys. Chem. C, 114, pp.3701~ (2010)
  30. Zhao, X., , J. Chem. Mater, 22, pp.2325~ (2010)
  31. Tamayo, A. B., , J. Phys. Chem. C, 112, pp.11545~ (2008)
  32. Tamayo, A. B., , Appl. Phys. Lett, 94, pp.103301~ (2009)
  33. Walker, B., , Adv. Funct. Mater, 19, pp.3063~ (2009)
  34. Domercq, B., , J. Phys. Chem. B, 108, pp.8647~ (2004)
  35. Sun, Y., , J. Mater. Chem, 16, pp.4499~ (2006)
  36. Mikroyannidis, J. A., , J. Mater. Chem, 20, pp.6464~ (2010)
  37. Mikroyannidis, J. A., , J. Phys. Chem. C, 114, pp.1520~ (2010)
  38. Mikroyannidisa, J. A., , J. Power Sources, 195, pp.5391~ (2010)
  39. Rousseau, T., , Roncali, J. Chem. Commun, 45, pp.1673~ (2009)
  40. Benstead, M., , Tetrahedron, 2011(67), pp.3573~ (2011)
  41. Kim, B., , J. Chem. Commun, 46, pp.4148~ (2010)
  42. Kılıcoglu, T., , Microelectron. Eng, 88, pp.150~ (2011)
  43. Collado, D., , Chem. Eur. J, 17, pp.498~ (2011)
  44. Zhao, H., , Tetrahedron Lett, 54, pp.6019~ (2013)
  45. Tsujimoto, K., , Tetrahedron Lett, 54, pp.1251~ (2013)
  46. Law, K. Y, , Chem. Rev, 93, pp.449~ (1993)
  47. Ko, H. M., , Mater. Chem, 21, pp.7248~ (2011)
  48. Kim, S., , J. Am. Chem. Soc, 128, pp.16701~ (2006)
  49. Kim, S., , Tetrahedron, 63, pp.9206~ (2007)
  50. Rousseau, T., , Chem. Commun, 46, pp.5082~ (2010)
  51. Ziessel, R., , Chem. Eur. J, 15, pp.1359~ (2009)
  52. Blom, P. W. M., , Phys. Rev. B, 55, pp.R656~ (1997)
  53. Blom, P. W. M., , Adv. Mater, 19, pp.1551~ (2007)

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