Year |
Citation |
Score |
2019 |
Sim YH, Kang SW, Shin DH, Park MY, Kay KY, Park JW. New Pyrene Derivatives Having Rigid Imidazole Moiety for Blue Emitters. Journal of Nanoscience and Nanotechnology. 19: 6206-6211. PMID 31026938 DOI: 10.1166/Jnn.2019.17019 |
0.388 |
|
2019 |
Sim Y, Lee H, Shin D, Park M, Kay KY, Park J. Synthesis and Electroluminescence Property of Pyrene Derivatives Including Dibenzothiophene and Imidazole Moiety. Journal of Nanoscience and Nanotechnology. 19: 4710-4714. PMID 30913774 DOI: 10.1166/Jnn.2019.16693 |
0.42 |
|
2019 |
Sim Y, Kang S, Shin D, Park M, Kay K, Park J. Synthesis and Properties of New Imidazole Derivatives Including Various Chromophore for OLEDs Molecular Crystals and Liquid Crystals. 687: 27-33. DOI: 10.1080/15421406.2019.1648051 |
0.417 |
|
2019 |
Jang J, Sim Y, Kang s, Shin D, Park M, Kay K, Park J. Synthesis and Luminescence Property of Pyrene Derivatives Including Diphenyl-Imidazole Moiety Molecular Crystals and Liquid Crystals. 687: 14-20. DOI: 10.1080/15421406.2019.1648049 |
0.406 |
|
2019 |
Jang J, Kang S, Park M, Kay K, Park J. Synthesis and luminescent property of fluorene-xanthene derivatives for new blue emitters Molecular Crystals and Liquid Crystals. 679: 95-101. DOI: 10.1080/15421406.2019.1597551 |
0.431 |
|
2018 |
Jung H, Lee H, Ryu J, Shin D, Park M, Kay KY, Park J. Synthesis and Electroluminescent Properties of New Dibenzo-Diazocine Derivatives. Journal of Nanoscience and Nanotechnology. 18: 2171-2174. PMID 29448738 DOI: 10.1166/Jnn.2018.14951 |
0.318 |
|
2018 |
Kang S, Lee H, Jung H, Shin D, Park M, Kay KY, Park J. Synthesis and Electroluminescence Properties of New Type Multi-Chromophore Emitting Materials for Organic Light-Emitting Diodes. Journal of Nanoscience and Nanotechnology. 18: 2162-2165. PMID 29448736 DOI: 10.1166/Jnn.2018.14947 |
0.462 |
|
2018 |
Kim T, Kang S, Jung H, Lee H, Shin D, Park M, Kay K, Park J. Synthesis and electroluminescent properties of new diazocine derivatives Molecular Crystals and Liquid Crystals. 662: 102-108. DOI: 10.1080/15421406.2018.1466521 |
0.439 |
|
2018 |
Kang S, Lee H, Jung H, Shin D, Park M, Kay K, Park J. Synthesis and property of diazocine derivatives substituted with imidazole in various positions Molecular Crystals and Liquid Crystals. 662: 96-101. DOI: 10.1080/15421406.2018.1466520 |
0.371 |
|
2017 |
Jung H, Lee H, Kang S, Shin D, Park M, Kay K, Park J. Synthesis and electroluminescent properties of new blue emitters based on dual anthracene and dibenzo-diazocine moieties Molecular Crystals and Liquid Crystals. 659: 140-146. DOI: 10.1080/15421406.2018.1452696 |
0.421 |
|
2017 |
Kang S, Jung H, Lee H, Shin D, Park M, Kay K, Park J. Synthesis and property of diazocine derivatives substituted with imidazole including various chromophores Molecular Crystals and Liquid Crystals. 659: 127-133. DOI: 10.1080/15421406.2018.1450955 |
0.4 |
|
2017 |
Lee H, Kang S, Jung H, Shin D, Park M, Kay K, Park J. Synthesis and electro-optical properties of diazocine derivatives based on different positions of substituted naphthyl group Molecular Crystals and Liquid Crystals. 659: 94-99. DOI: 10.1080/15421406.2018.1450938 |
0.365 |
|
2017 |
Kim T, Kang S, Jung H, Lee H, Shin D, Park M, Kay K, Park J. Synthesis and property of diazocine derivatives substituted with carbazole in meta and para positions Molecular Crystals and Liquid Crystals. 659: 9-14. DOI: 10.1080/15421406.2018.1449787 |
0.363 |
|
2017 |
Jung H, Lee H, Kang S, Shin D, Kay K, Park J. New anthracene derivatives containing coumarin moiety for organic light-emitting diodes Molecular Crystals and Liquid Crystals. 654: 90-95. DOI: 10.1080/15421406.2017.1355708 |
0.334 |
|
2017 |
Lee H, Jung H, Jo M, Shin D, Kay K, Park J. New carbazole derivatives including coumarin moiety for blue emitting materials Molecular Crystals and Liquid Crystals. 654: 34-39. DOI: 10.1080/15421406.2017.1355197 |
0.411 |
|
2017 |
Kang S, Jung H, Lee H, Shin D, Park M, Kay K, Park J. Synthesis and electroluminescence property of new type emitting materials including diazocine for OLEDs Molecular Crystals and Liquid Crystals. 651: 35-41. DOI: 10.1080/15421406.2017.1338490 |
0.366 |
|
2017 |
Ryu J, Jo M, Jung H, Lee H, Shin D, Park M, Kay K, Park J. Synthesis and electroluminescent properties of diazocine derivatives Molecular Crystals and Liquid Crystals. 651: 77-84. DOI: 10.1080/09273948.2017.1338890 |
0.346 |
|
2017 |
Lee H, Kang S, Ann C, Shin D, Park M, Kay K, Park J. New anthracene derivatives including diazocine for blue emitting materials Molecular Crystals and Liquid Crystals. 651: 71-76. DOI: 10.1080/09273948.2017.1338888 |
0.341 |
|
2017 |
Jung H, Kang S, Shin D, Song G, Kay K, Park J. Synthesis and electroluminescent properties of new coumarin derivatives Molecular Crystals and Liquid Crystals. 651: 48-54. DOI: 10.1080/09273948.2017.1338882 |
0.385 |
|
2016 |
El-Khouly ME, El-Kemary MA, El-Refaey A, Kay K, Fukuzumi S. Light harvesting subphthalocyanine–ferrocene dyads: Fast electron transfer process studied by femtosecond laser photolysis Journal of Porphyrins and Phthalocyanines. 20: 1148-1155. DOI: 10.1142/S1088424616500784 |
0.373 |
|
2015 |
Shin H, Kang H, Kim JH, Wang YF, Kim S, Kay KY, Park J. Synthesis and Electroluminescence Property of New Hexaphenyl Benzene Derivatives Including Emitting Core for OLED. Journal of Nanoscience and Nanotechnology. 15: 8289-94. PMID 26726505 DOI: 10.1166/Jnn.2015.11260 |
0.426 |
|
2015 |
Antony MP, Moehl T, Wielopolski M, Moser JE, Nair S, Yu YJ, Kim JH, Kay KY, Jung YS, Yoon KB, Grätzel C, Zakeeruddin SM, Grätzel M. Long-Range π-Conjugation in Phenothiazine-containing Donor-Acceptor Dyes for Application in Dye-Sensitized Solar Cells. Chemsuschem. 8: 3859-68. PMID 26616683 DOI: 10.1002/Cssc.201500931 |
0.405 |
|
2015 |
Kim S, Lee KJ, Lee J, Shin H, Kay KY, Park J. New Amino Methyl Coumarin Derivative for OLED Blue Emitter Molecular Crystals and Liquid Crystals. 620: 139-146. DOI: 10.1080/15421406.2015.1095388 |
0.442 |
|
2015 |
Shin H, Kang H, Kim J, Wang Y, Lee H, Yang G, Lee J, Kim B, Kay K, Park J. Synthesis and Electroluminescence Property of New Hexaphenyl Benzene Derivatives Including Emitting Materials for OLED Molecular Crystals and Liquid Crystals. 618: 38-46. DOI: 10.1080/15421406.2015.1075846 |
0.435 |
|
2014 |
Kim S, Lee SH, Shin H, Kay KY, Park J. New hole transporting materials based on hexaarylbenzene and aromatic amine moiety for organic light-emitting diodes. Journal of Nanoscience and Nanotechnology. 14: 6382-5. PMID 25936121 DOI: 10.1166/Jnn.2014.8291 |
0.37 |
|
2013 |
Kim S, Lee KJ, Kim B, Lee J, Kay KY, Park J. New ambipolar blue emitting materials based on amino coumarin derivatives with high efficiency for organic lightemitting diodes. Journal of Nanoscience and Nanotechnology. 13: 8020-4. PMID 24266184 DOI: 10.1166/Jnn.2013.8151 |
0.439 |
|
2013 |
Shin H, Wang YF, Kim JH, Lee J, Kay KY, Park J. Synthesis and electroluminescence property of new hexaphenylbenzene derivatives including amine group for blue emitters. Nanoscale Research Letters. 8: 421. PMID 24134333 DOI: 10.1186/1556-276X-8-421 |
0.422 |
|
2013 |
El-Khouly ME, Kim J, Kay K, Fukuzumi S. Silicon phthalocyanine-azobenzene-[60]fullerene light harvesting pentad: synthesis, characterization and electron transfer reaction studied by laser flash photolysis Journal of Porphyrins and Phthalocyanines. 17: 1055-1063. DOI: 10.1142/S1088424613501046 |
0.451 |
|
2013 |
Kim S, Lee S, An B, Oh S, Kay K, Park J. New Hole Transporting Materials Based on Tetraphenylbenzene and Aromatic Amine Derivatives for OLEDs Molecular Crystals and Liquid Crystals. 584: 69-77. DOI: 10.1080/15421406.2013.849447 |
0.333 |
|
2013 |
El-Khouly ME, Lee S, Kay K, Fukuzumi S. Synthesis and fast electron-transfer reactions of fullerene–carbazole dendrimers with short linkages New Journal of Chemistry. 37: 3252-3260. DOI: 10.1039/C3Nj00770G |
0.442 |
|
2013 |
Wielopolski M, Kim JH, Jung YS, Yu YJ, Kay KY, Holcombe TW, Zakeeruddin SM, Grätzel M, Moser JE. Position-dependent extension of π-conjugation in D-π-A dye sensitizers and the impact on the charge-transfer properties Journal of Physical Chemistry C. 117: 13805-13815. DOI: 10.1021/Jp402411H |
0.4 |
|
2012 |
El-Khouly ME, Kim J, Kim J, Kay K, Fukuzumi S. Subphthalocyanines as Light-Harvesting Electron Donor and Electron Acceptor in Artificial Photosynthetic Systems Journal of Physical Chemistry C. 116: 19709-19717. DOI: 10.1021/Jp3066103 |
0.346 |
|
2012 |
Kim M, Yu Y, Kim J, Jung Y, Kay K, Ko S, Lee C, Jang I, Kwon Y, Park N. Tuning of spacer groups in organic dyes for efficient inhibition of charge recombination in dye-sensitized solar cells Dyes and Pigments. 95: 134-141. DOI: 10.1016/J.Dyepig.2012.04.002 |
0.343 |
|
2011 |
Supur M, El-Khouly ME, Seok JH, Kay KY, Fukuzumi S. Elongation of lifetime of the charge-separated state of ferrocene-naphthalenediimide-[60]fullerene triad via stepwise electron transfer. The Journal of Physical Chemistry. A. 115: 14430-7. PMID 22112188 DOI: 10.1021/Jp209668W |
0.428 |
|
2010 |
El-Khouly ME, Ju DK, Kay KY, D'Souza F, Fukuzumi S. Supramolecular tetrad of subphthalocyanine-triphenylamine-zinc porphyrin coordinated to fullerene as an "antenna-reaction-center" mimic: formation of a long-lived charge-separated state in nonpolar solvent. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 6193-202. PMID 20411545 DOI: 10.1002/Chem.201000045 |
0.39 |
|
2010 |
El-Khouly ME, Han KJ, Kay KY, Fukuzumi S. Stabilization of the charge-separated States of covalently linked zinc porphyrin-triphenylamine-[60]fullerene. Chemphyschem : a European Journal of Chemical Physics and Physical Chemistry. 11: 1726-34. PMID 20191657 DOI: 10.1002/Cphc.200900885 |
0.411 |
|
2010 |
Supur M, El-Khouly ME, Seok JH, Kim JH, Kay K, Fukuzumi S. Efficient Electron Transfer Processes of the Covalently Linked Perylenediimide−Ferrocene Systems: Femtosecond and Nanosecond Transient Absorption Studies Journal of Physical Chemistry C. 114: 10969-10977. DOI: 10.1021/Jp103094V |
0.395 |
|
2009 |
El-Khouly ME, Kim JH, Kay KY, Choi CS, Ito O, Fukuzumi S. Synthesis and photoinduced intramolecular processes of light-harvesting silicon phthalocyanine-naphthalenediimide-fullerene connected systems. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 5301-10. PMID 19347898 DOI: 10.1002/Chem.200900165 |
0.461 |
|
2009 |
El-Khouly ME, Ryu JB, Kay K, Ito O, Fukuzumi S. Long-Lived Charge Separation in a Dyad of Closely-Linked Subphthalocyanine-Zinc Porphyrin Bearing Multiple Triphenylamines Journal of Physical Chemistry C. 113: 15444-15453. DOI: 10.1021/Jp904310F |
0.36 |
|
2009 |
Seok JH, Park SH, El-Khouly ME, Araki Y, Ito O, Kay K. Photoinduced processes of newly synthesized bisferrocene- and bisfullerene-substituted tetrads with a triphenylamine central block Journal of Organometallic Chemistry. 694: 1818-1825. DOI: 10.1016/J.Jorganchem.2009.01.011 |
0.453 |
|
2008 |
El-Khouly ME, Shim SH, Araki Y, Ito O, Kay KY. Effect of dual fullerenes on lifetimes of charge-separated States of subphthalocyanine-triphenylamine-fullerene molecular systems. The Journal of Physical Chemistry. B. 112: 3910-7. PMID 18335923 DOI: 10.1021/Jp7108658 |
0.422 |
|
2008 |
Kim J, El-Khouly ME, Araki Y, Ito O, Kay K. Photoinduced Processes of Subphthalocyanine-Diazobenzene-Fullerene Triad as an Efficient Excited Energy Transfer System Chemistry Letters. 37: 544-545. DOI: 10.1246/Cl.2008.544 |
0.337 |
|
2007 |
El-Khouly ME, Kang ES, Kay KY, Choi CS, Aaraki Y, Ito O. Silicon-phthalocyanine-cored fullerene dendrimers: synthesis and prolonged charge-separated states with dendrimer generations. Chemistry (Weinheim An Der Bergstrasse, Germany). 13: 2854-63. PMID 17177216 DOI: 10.1002/Chem.200601254 |
0.441 |
|
2007 |
El-Khouly ME, Kim JH, Kwak M, Choi CS, Ito O, Kay K. Photoinduced Charge Separation of the Covalently Linked Fullerene-Triphenylamine-Fullerene Triad. Effect of Dual Fullerenes on Lifetimes of Charge-Separated States Bulletin of the Chemical Society of Japan. 80: 2465-2472. DOI: 10.1246/Bcsj.80.2465 |
0.609 |
|
2007 |
Lee HD, Oh SK, Choi CS, Kay K. A Novel Amphiphilic ReI Complex with Bis(fullerene)‐Substituted Bipyridine Ligands: Synthesis, Electrochemistry, and Langmuir Film European Journal of Inorganic Chemistry. 2007: 503-508. DOI: 10.1002/Ejic.200600875 |
0.362 |
|
2006 |
Kay K, Kim J, Kim S, Park H, Park J. Electroluminescent Properties of Novel Fluorene Derivatives with Aromatic Amine Moieties Molecular Crystals and Liquid Crystals. 444: 121-128. DOI: 10.1080/15421400500365292 |
0.395 |
|
2005 |
Han K, Kay K. Synthesis and Characterization of Novel Red Fluorescent Materials for Organic Electroluminescent Display Journal of the Korean Chemical Society. 49: 233-238. DOI: 10.5012/Jkcs.2005.49.2.233 |
0.328 |
|
2005 |
Han K, Kay K. Synthesis and photoresponsive properties of Cu-phthalocyanine with azobenzene groups Bulletin of the Korean Chemical Society. 26: 1274-1276. DOI: 10.5012/Bkcs.2005.26.8.1274 |
0.407 |
|
2005 |
Kim KN, Choi CS, Kay K. A novel phthalocyanine with two axial fullerene substituents Tetrahedron Letters. 46: 6791-6795. DOI: 10.1016/J.Tetlet.2005.08.038 |
0.392 |
|
2004 |
Han KJ, Kay KY. Synthesis and absorption properties of zinc-phthalocyanineswith photoresponsive azobenzene groups Heterocycles. 63: 2869-2874. DOI: 10.3987/Com-04-10230 |
0.403 |
|
2004 |
Kay K, Kim J, Cho H, Park J. Synthesis and Electroluminescent Properties of Fluorene- And Anthracene-Derivatives Containing Novel Tetraphenylbenzene Moiety Molecular Crystals and Liquid Crystals. 424: 167-172. DOI: 10.1080/15421400490506126 |
0.4 |
|
2002 |
Kay KY, Han KJ, Yu YJ, Park YD. Dendritic fullerenes (C60) with photoresponsive azobenzene groups Tetrahedron Letters. 43: 5053-5056. DOI: 10.1016/S0040-4039(02)00994-2 |
0.323 |
|
2000 |
Kay K, Kim LH, Oh IC. The first methano-bridged diferrocenyl fullerene (C60) Tetrahedron Letters. 41: 1397-1400. DOI: 10.1016/S0040-4039(99)02301-1 |
0.402 |
|
1999 |
Kay KY, Oh IC. The first fullerene(C60)-substituted [2.2](2,7)fluorenophane Tetrahedron Letters. 40: 1709-1712. DOI: 10.1016/S0040-4039(99)00033-7 |
0.405 |
|
1997 |
Kay K, Baek YG. The First Electron‐Donor‐Acceptor Paracyclophanes with Ferrocene NLO‐Phores: Synthesis, Absorption and Electrochemical Properties Chemische Berichte. 130: 581-584. DOI: 10.1002/Cber.19971300508 |
0.357 |
|
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