Bulletin of the Korean Chemical Society

  • 제32권4호
  • /
  • Pages.1391-1394
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  • 2011
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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Red Fluorescent 4-(Dicyanomethylene)-2-norbonenyl-6-(1,1,7,7-tetramethyljulolidyl-9-enyl)-4H-pyran (DCJNB) for Organic Light-Emitting Diodes (OLEDs)

  • 투고 : 2010.12.17
  • 심사 : 2011.02.19
  • 발행 : 2011.04.20
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참고문헌

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피인용 문헌

  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