Complementary hydrogen bonding interaction-mediated hole injection in organic light-emitting devices
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[1] Junfei Liang,et al. Efficient white polymer light-emitting diodes from single polymer exciplex electroluminescence , 2017 .
[2] Junfei Liang,et al. Recent advances in high performance solution processed WOLEDs for solid-state lighting , 2016 .
[3] Hanxu Ji,et al. Architecture of Conjugated Donor–Acceptor (D–A)‐Type Polymer Films with Cross‐Linked Structures , 2016 .
[4] Duu-Jong Lee,et al. Bio-complementary supramolecular polymers with effective self-healing functionality , 2015 .
[5] Ji-hoon Kim,et al. Progress and perspective of iridium-containing phosphorescent polymers for light-emitting diodes , 2015 .
[6] Yu-Lin Chu,et al. New bioinspired hole injection/transport materials for highly efficient solution-processed phosphorescent organic light-emitting diodes , 2015 .
[7] Robert B. Moore,et al. Nucleobase-functionalized acrylic ABA triblock copolymers and supramolecular blends , 2015 .
[8] F. Huang,et al. Water/alcohol soluble conjugated polymers for the interface engineering of highly efficient polymer light-emitting diodes and polymer solar cells. , 2015, Chemical communications.
[9] Feihe Huang,et al. Supramolecular polymers constructed by orthogonal self-assembly based on host-guest and metal-ligand interactions. , 2015, Chemical Society reviews.
[10] Biwu Ma,et al. Facile Photo‐Crosslinking of Azide‐Containing Hole‐Transporting Polymers for Highly Efficient, Solution‐Processed, Multilayer Organic Light Emitting Devices , 2014 .
[11] Martin Baumgarten,et al. Designing pi-conjugated polymers for organic electronics , 2013 .
[12] U. Jeng,et al. Bioinspired assembly of functional block-copolymer nanotemplates. , 2013, Soft matter.
[13] M. Liang,et al. Nucleobase-grafted polycaprolactones as reversible networks in a novel biocompatible material , 2013 .
[14] A. Ellington,et al. Effect of Complementary Nucleobase Interactions on the Copolymer Composition of RAFT Copolymerizations. , 2013, ACS macro letters.
[15] Chuluo Yang,et al. Blue fluorescent emitters: design tactics and applications in organic light-emitting diodes. , 2013, Chemical Society reviews.
[16] Aihui Liang,et al. Supramolecular Phosphorescent Polymer Iridium Complexes for High-Efficiency Organic Light-Emitting Diodes , 2013 .
[17] Junbiao Peng,et al. A supramolecular large band gap host for phosphorescent organic light-emitting diodes , 2013 .
[18] Ronan Mchale,et al. Nucleobase Containing Synthetic Polymers: Advancing Biomimicry via Controlled Synthesis and Self-Assembly , 2012 .
[19] Yu-Lin Chu,et al. Bioinspired hole-conducting polymers for application in organic light-emitting diodes , 2012 .
[20] Yu-Lin Chu,et al. A New Supramolecular Hole Injection/Transport Material on Conducting Polymer for Application in Light‐Emitting Diodes , 2012, Advanced materials.
[21] E. W. Meijer,et al. Functional Supramolecular Polymers , 2012, Science.
[22] Sebastian Seiffert,et al. Physical chemistry of supramolecular polymer networks. , 2012, Chemical Society reviews.
[23] Antonio Facchetti,et al. π-Conjugated Polymers for Organic Electronics and Photovoltaic Cell Applications† , 2011 .
[24] K. Meerholz,et al. Novel non-conjugated main-chain hole-transporting polymers for organic electronics application. , 2010, Macromolecular rapid communications.
[25] Chih-Chia Cheng,et al. Synthesis and Assembly Behavior of Heteronucleobase-Functionalized Poly(ε-caprolactone) , 2010 .
[26] Chih-Chia Cheng,et al. Biocomplementary interaction behavior in DNA‐like and RNA‐like polymers , 2009 .
[27] Khai Leok Chan,et al. Synthesis of light-emitting conjugated polymers for applications in electroluminescent devices. , 2009, Chemical reviews.
[28] E. W. Meijer,et al. White-light emitting hydrogen-bonded supramolecular copolymers based on pi-conjugated oligomers. , 2009, Journal of the American Chemical Society.
[29] Chih-Feng Huang,et al. A “plug and play” polymer through biocomplementary hydrogen bonding , 2008 .
[30] C. Ha,et al. Polymers for flexible displays: From material selection to device applications , 2008 .
[31] Klaus Meerholz,et al. New crosslinkable hole conductors for blue-phosphorescent organic light-emitting diodes. , 2007, Angewandte Chemie.
[32] Jonathan L Sessler,et al. Molecular recognition via base-pairing. , 2007, Chemical Society reviews.
[33] Yun Chi,et al. Crosslinkable Hole‐Transport Layer on Conducting Polymer for High‐Efficiency White Polymer Light‐Emitting Diodes , 2007 .
[34] Kwanghee Lee,et al. Synthesis of a new cross-linkable perfluorocyclobutane-based hole-transport material. , 2006, Organic letters.
[35] J. V. Hest,et al. Synthesis and assembly behavior of nucleobase‐functionalized block copolymers , 2006 .
[36] Klaus Meerholz,et al. Highly Efficient Polymeric Electrophosphorescent Diodes , 2006 .
[37] A. Jen,et al. Efficient CdSe/CdS quantum dot light-emitting diodes using a thermally polymerized hole transport layer. , 2006, Nano letters.
[38] R. Advíncula,et al. Cross-Linked Polyfluorene Polymer Precursors: Electrodeposition, PLED Device Characterization, and Two-Site Co-deposition with Poly(vinylcarbazole) , 2005 .
[39] Stuart J Rowan,et al. Nucleobases as supramolecular motifs. , 2005, Chemical Society reviews.
[40] Stephen R. Forrest,et al. White Organic Light‐Emitting Devices for Solid‐State Lighting , 2004 .
[41] Frank Nüesch,et al. Water Vapor and Oxygen Degradation Mechanisms in Organic Light Emitting Diodes , 2001 .
[42] V. Rotello,et al. Reversible Side Chain Modification through Noncovalent Interactions. “Plug and Play” Polymers , 2001 .
[43] M.J.A. de Voigt,et al. Stability of the interface between indium-tin-oxide and poly(3,4-ethylenedioxythiophene)/poly(styrenesulfonate) in polymer light-emitting diodes , 2000 .
[44] L. Fielding. Determination of Association Constants (Ka) from Solution NMR Data , 2000 .
[45] J. Reynolds,et al. Poly(3,4‐ethylenedioxythiophene) and Its Derivatives: Past, Present, and Future , 2000 .
[46] Franco Cacialli,et al. Molecular-scale interface engineering for polymer light-emitting diodes , 2000, Nature.
[47] P. Bäuerle,et al. Specific Recognition of Nucleobase-Functionalized Polythiophenes , 1998 .
[48] A. Rich,et al. An infrared study of hydrogen bonding between adenine and uracil derivatives in chloroform solution. , 1967, Journal of the American Chemical Society.