Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
권호 표지
DOI QR코드

DOI QR Code

Red Fluorescent 4-(Dicyanomethylene)-2-norbonenyl-6-(1,1,7,7-tetramethyljulolidyl-9-enyl)-4H-pyran (DCJNB) for Organic Light-Emitting Diodes (OLEDs)

  • Received : 2010.12.17
  • Accepted : 2011.02.19
  • Published : 2011.04.20
Download PDF
⟨ Previous Next ⟩

Abstract

Keywords

References

  1. Tang, C. W.; VanSlyke, S. A. Appl. Phys. Lett. 1987, 51, 913. https://doi.org/10.1063/1.98799
  2. Organic Light-Emitting Materials and Devices; Li, Z., Meng, H. Eds.; Taylor & Francis: Boca Raton, U. S. A. 2007; p 295.
  3. Lee, K. H.; Kwon, Y. S.; Kang, L. K.; Kim, G. Y.; Seo, J. H.; Kim, Y. K.; Yoon, S. S. Synth. Met. 2009, 159, 2603. https://doi.org/10.1016/j.synthmet.2009.09.018
  4. Kwon, Y. S.; Lee, K. H.; Kim, G. Y.; Seo, J. H.; Kim, Y. K.; Yoon, S. S. J. Nanosci. Nanotechnol. 2009, 9, 7056.
  5. Kim, S. O.; Lee, K. H.; Kang, S.; Lee, J. Y.; Seo, J. H.; Kim, Y. K.; Yoon, S. S. Bull. Korean Chem. Soc. 2010, 31, 389. https://doi.org/10.5012/bkcs.2010.31.02.389
  6. Lee, K. H.; Seo, J. H.; Kim, Y. K.; Yoon, S. S. J. Nanosci. Nanotechnol. 2009, 9, 7099.
  7. Chen, C. Chem. Mater. 2004, 16, 4389. https://doi.org/10.1021/cm049679m
  8. Lee, K. H.; Kim, S. M.; Kim, J. Y.; Kim, Y. K.; Yoon, S. S. Bull. Korean. Chem. Soc. 2010, 31, 2884. https://doi.org/10.5012/bkcs.2010.31.10.2884
  9. Lee, K. H.; Park, M. H.; Kim, S. M.; Kim, Y. K.; Yoon, S. S. Jpn. J. Appl. Phys. 2010, 49, 08JG02. https://doi.org/10.1143/JJAP.49.08JG02
  10. Chen, C. H.; Tang, C. W.; Shi, J., Klubek, K. P. Thin Solid Films 2000, 363, 327. https://doi.org/10.1016/S0040-6090(99)01010-X
  11. Tang, C. W.; Van Slyke, S. A.; Chen, C. H. J. Appl. Phys. 1989, 65, 3610. https://doi.org/10.1063/1.343409
  12. Thomas, K. J. R.; Lin, J. T.; Tao, Y.; Chuen, C. Adv. Func. Mater. 2004, 14, 822. https://doi.org/10.1002/adfm.200490017
  13. Picciolo, L. C.; Murata, H.; Kafati, Z. H. Appl. Phys. Lett. 2001, 78, 2378. https://doi.org/10.1063/1.1362259
  14. Fang, J.; Ma, D. Appl. Phys. Lett. 2003, 83, 4041. https://doi.org/10.1063/1.1626022
  15. Zhao, P.; Tang, H.; Zhang, Q.; Pi, Y.; Xu, M.; Sun, R.; Zhu, W. Dyes and Pigments 2009, 82, 316. https://doi.org/10.1016/j.dyepig.2009.01.016
  16. Yao, Y.-S.; Zhou, Q.-X.; Wang, X.-S.; Wang, Y.; Zhang, B.-W. Adv. Func. Mater. 2007, 17, 93. https://doi.org/10.1002/adfm.200600055
  17. Kim, B.-O.; Kim, C.-S.; Han H.; Kim S.-M.; Kim, J.-Y.; Cho, K.-S.; Jung, S.-Y.; Yun, S. S.; Kwon, H.-J.; Cho, Y.-J.; Kim, Y. K.; Kim, S.-M. WO 121274 (2005).
  18. Jones, G. Org. React. 1967, 15, 204.
  19. Chen, C. H.; Tang, C. W.; Shi, J. US 5935720 (1999).
  20. Chen, C. H.; Tang, C. W.; Shi, J.; Klubek, K. P. Macromol. Symp. 1998, 125, 49. https://doi.org/10.1002/masy.19981250103
  21. Kido, J.; Hayase, H.; Hongawa, K. Appl. Phys. Lett. 1994, 65, 2124. https://doi.org/10.1063/1.112810
  22. Lee, K. H.; Park, M. H.; Kim, J. Y.; Kim, S. M.; Seo, B. M.; Seo, J. H.; Kim, Y. K.; Yoon, S. S. J. Nanosci. Nanotechnol. 2011, 11, 1484. https://doi.org/10.1166/jnn.2011.3363
  23. Seo, J. H.; Park, J. S.; Kim, J. H.; Lee, K. H.; Kim, J. Y.; Yoon, S. S.; Kim, Y. K. Mol. Cryst. Liq. Cryst. 2010, 520, 83. https://doi.org/10.1080/15421401003609756
  24. Kim, S. O.; Lee, K. H.; Kang, S.; Lee, J. Y.; Seo, J. H.; Kim, Y. K.; Yoon, S. S. Bull. Korean Chem. Soc. 2010, 31, 389. https://doi.org/10.5012/bkcs.2010.31.02.389
  25. Lee, K. H.; Kang, L. K.; Lee, J. Y.; Kang, S.; Jeon, S. O.; Yook, K. S.; Lee, J. Y.; Yoon, S. S. Adv. Func. Mater. 2010, 20, 1345. https://doi.org/10.1002/adfm.200901895

Cited by

  1. ChemInform Abstract: Red Fluorescent 4-(Dicyanomethylene)-2-norbornenyl-6- (1,1,7,7-tetramethyljulolidyl-9-enyl)-4H-pyran (DCJNB) for Organic Light-Emitting Diodes (OLEDs). vol.42, pp.38, 2011, https://doi.org/10.1002/chin.201138148
  2. Dicyanomethylene-4H-pyran chromophores for OLED emitters, logic gates and optical chemosensors vol.48, pp.49, 2012, https://doi.org/10.1039/c2cc31581e
  3. Highly Efficient Red Organic Light-Emitting Diodes Using Methylcyclohexylpyran-Containing Emitters vol.32, pp.12, 2011, https://doi.org/10.5012/bkcs.2011.32.12.4419
  4. Donor-Acceptor-Donor Type Red Fluorescent Emitters Containing Adamandane-substituted Julolidines for OLEDs vol.32, pp.8, 2011, https://doi.org/10.5012/bkcs.2011.32.8.2787
  5. Synthesis of Donor-Aromatic-Donor Type π-conjugated Materials and their Application to Red Fluorescent Organic Light-Emitting Diodes vol.563, pp.1, 2011, https://doi.org/10.1080/15421406.2012.689155
  6. Red Fluorescent Organic Light-Emitting Diodes (OLEDs) using 4-(1,3-Indanedione-2-yl)-2-(adaman-1-yl)-6-(10-aza-2,3,4,5,6,7-hexahydronaphtio[1,8-gh]chromen-10(1H)-one-9-enyl)-4H-pyran vol.568, pp.1, 2012, https://doi.org/10.1080/15421406.2012.706551
  7. Synthesis and Electroluminescent Properties of Red Fluorescent 2-(6,8-di-tert-butyl-2-(4-((3,5-di-tert-butylphenyl)(4-(trimethylsilyl)phenyl)amino)styryl)-4H-chromen-4-ylidene)malononitrile (DCCTBPA) vol.568, pp.1, 2011, https://doi.org/10.1080/15421406.2012.706556
  8. Red Fluorescent DCM Derivatives with the Bulky-substituents on Pyran and Julolidine Moieties for Organic Light-Emitting Diodes (OLEDs) vol.33, pp.10, 2011, https://doi.org/10.5012/bkcs.2012.33.10.3433
  9. Synthesis and Electroluminescent Properties of Julolidine-π-Juloidine Type Materials with the Bulky Adamantane Groups vol.33, pp.11, 2011, https://doi.org/10.5012/bkcs.2012.33.11.3883
  10. Red Fluorescent Donor-π-Acceptor Type Materials based on Chromene Moiety for Organic Light-Emitting Diodes vol.35, pp.6, 2011, https://doi.org/10.5012/bkcs.2014.35.6.1670
  11. Solvent-induced Stokes’ shift in DCJTB: Experimental and theoretical results vol.1192, pp.None, 2011, https://doi.org/10.1016/j.molstruc.2019.04.117
  12. Preparation and characterization of Ca-modified Co/Al2O3 and its catalytic application in the one-pot synthesis of 4H-pyrans vol.46, pp.6, 2011, https://doi.org/10.1007/s11164-020-04139-2