Facile Synthesis of 1,7-Phenanthroline Derivatives and Evaluation of Their Properties as Hole-Blocking Materials in Organic Light-Emitting Diodes
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[1] Jun‐Chul Choi,et al. One-Pot Synthesis of Triazatriphenylene Using the Povarov Reaction. , 2021, Journal of Organic Chemistry.
[2] C. Adachi,et al. Thermally-activated Delayed Fluorescence for Light-emitting Devices , 2021 .
[3] Xike Gao,et al. Azulene-Pyridine-Fused Heteroaromatics. , 2020, Journal of the American Chemical Society.
[4] Tsubasa Sasaki,et al. Understanding coordination reaction for producing stable electrode with various low work functions , 2020, Nature Communications.
[5] N. Kumagai,et al. TriQuinoline , 2019, Nature Communications.
[6] J. Yao,et al. Excited‐State Modulation for Controlling Fluorescence and Phosphorescence Pathways toward White‐Light Emission , 2019, Advanced Optical Materials.
[7] J. Menéndez,et al. Progress in the Chemistry of Tetrahydroquinolines. , 2019, Chemical reviews.
[8] J. Kido,et al. Review of Molecular Engineering for Horizontal Molecular Orientation in Organic Light-Emitting Devices , 2019, Bulletin of the Chemical Society of Japan.
[9] M. Akhter,et al. Green recipes to quinoline: A review. , 2019, European journal of medicinal chemistry.
[10] A. Gorodetsky,et al. Aza-Diels-Alder Approach to Diquinolineanthracene and Polydiquinolineanthracene Derivatives. , 2018, Organic letters.
[11] D. Gryko,et al. The Tetraarylpyrrolo[3,2-b]pyrroles-From Serendipitous Discovery to Promising Heterocyclic Optoelectronic Materials. , 2017, Accounts of chemical research.
[12] F. Palacios,et al. Study of the Hetero-[4+2]-Cycloaddition Reaction of Aldimines and Alkynes. Synthesis of 1,5-Naphthyridine and Isoindolone Derivatives. , 2017, The Journal of organic chemistry.
[13] G. Hernández-Sosa,et al. A digitally printed optoelectronic nose for the selective trace detection of nitroaromatic explosive vapours using fluorescence quenching , 2017 .
[14] M. Ingleson,et al. Mechanistic Insights into the B(C6F5)3-Initiated Aldehyde–Aniline–Alkyne Reaction To Form Substituted Quinolines , 2017 .
[15] G. Hernández-Sosa,et al. Emissive Polyelectrolytes As Interlayer for Color Tuning and Electron Injection in Solution-Processed Light-Emitting Devices. , 2016, ACS applied materials & interfaces.
[16] A. Gorodetsky,et al. Synthesis of Nitrogen-Containing Rubicene and Tetrabenzopentacene Derivatives. , 2016, Angewandte Chemie.
[17] J. Ziller,et al. An Aza-Diels-Alder Approach to Crowded Benzoquinolines. , 2016, Organic letters.
[18] Tae Whan Kim,et al. Enhancement of out-coupling efficiency due to an organic scattering layer in organic light-emitting devices , 2015 .
[19] U. Bunz. The Larger Linear N-Heteroacenes. , 2015, Accounts of chemical research.
[20] Seungjun Chung,et al. Selectively modulated inkjet printing of highly conductive and transparent foldable polymer electrodes for flexible polymer light-emitting diode applications , 2015 .
[21] J. Ziller,et al. An Aza-Diels–Alder Route to Polyquinolines , 2015 .
[22] J. Kido,et al. Pyridine‐Containing Electron‐Transport Materials for Highly Efficient Blue Phosphorescent OLEDs with Ultralow Operating Voltage and Reduced Efficiency Roll‐Off , 2014 .
[23] C. Adachi,et al. Molecular Design of High-molecular-orientation Electron-transport Materials and Application to Organic Light-emitting Diodes , 2013 .
[24] Samson A Jenekhe,et al. Solution‐Processed Highly Efficient Blue Phosphorescent Polymer Light‐Emitting Diodes Enabled by a New Electron Transport Material , 2010, Advanced materials.
[25] V. Kouznetsov. Recent synthetic developments in a powerful imino Diels–Alder reaction (Povarov reaction): application to the synthesis of N-polyheterocycles and related alkaloids , 2009 .
[26] H. Tokuyama,et al. Auto-tandem catalysis in the synthesis of substituted quinolines from aldimines and electron-rich olefins: cascade Povarov-hydrogen-transfer reaction. , 2008, The Journal of organic chemistry.
[27] Karsten Walzer,et al. Ultrastable and efficient red organic light emitting diodes with doped transport layers , 2006 .
[28] G. Hughes,et al. Electron-transporting materials for organic electroluminescent and electrophosphorescent devices , 2005 .
[29] Abhishek P. Kulkarni,et al. Electron Transport Materials for Organic Light-Emitting Diodes , 2004 .
[30] Maksudul M. Alam,et al. New n-type organic semiconductors: synthesis, single crystal structures, cyclic voltammetry, photophysics, electron transport, and electroluminescence of a series of diphenylanthrazolines. , 2003, Journal of the American Chemical Society.
[31] Wolfgang Kowalsky,et al. Low-voltage organic electroluminescence device with an ultrathin, hybrid structure , 2003 .
[32] Tetsuo Tsutsui,et al. High electron mobility in bathophenanthroline , 2000 .
[33] S. Forrest,et al. VERY HIGH-EFFICIENCY GREEN ORGANIC LIGHT-EMITTING DEVICES BASED ON ELECTROPHOSPHORESCENCE , 1999 .
[34] Ching Wan Tang,et al. Bright-blue electroluminescence from a silyl-substituted ter-(phenylene–vinylene) derivative , 1999 .
[35] H. Bässler,et al. Electric field-induced photoluminescence quenching in thin-film light-emitting diodes based on poly(phenyl-p-phenylene vinylene) , 1995 .
[36] C. R. Smith. SKRAUP'S REACTION APPLIED TO THE PHENYLENEDIAMINES. PREPARATION OF THE PHENANTHROLINES AND RELATED DIPYRIDYLS , 1930 .