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Synthesis and device characterisation of side-chain polymer electron transport materials for organic semiconductor applications
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Synthesis of ABC-triblock copolymers for light emitting diodes
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The chemistry of electroluminescent organic materials
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Exciplex Electroluminescence from Organic Bilayer Devices Composed of Triphenyldiamine and Quinoxaline Derivatives
inferredcites →https://doi.org/10.1002/apmc.1975.050430109openalex-snapshot
Photoinduzierte Polymerisation von Methylmethacrylat in Gegenwart von niederund hochmolekularen Chinoxalinderivaten
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Poly(4-vinyltriphenylamine): synthesis and application as a hole transport layer in light-emitting diodes
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Recent progress in polymers for electroluminescence: microcavity devices and electron transport polymers
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Light-emitting diodes based on poly(methacrylates) with distyrylbenzene and oxadiazole side chains
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Electron transport in starburst phenylquinoxalines
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Design and Application of Electron-Transporting Organic Materials
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1016/b978-0-12-821263-9.00006-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-823147-0.00001-xopenalex-snapshot
Organic electronics: an overview of key materials, processes, and devices
inferred← citeshttps://doi.org/10.1016/b978-0-443-15225-2.00013-xopenalex-snapshot
Six-membered N,N-heterocycles
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Efficient synthesis of quinoxaline derivatives over ZrO2/M O (M = Al, Ga, In and La) mixed metal oxides supported on MCM-41 mesoporous molecular sieves
inferred← citeshttps://doi.org/10.1016/j.apcata.2010.12.022openalex-snapshot
Easy access to quinoxaline derivatives using alumina as an effective and reusable catalyst under solvent-free conditions
inferred← citeshttps://doi.org/10.1016/j.apsusc.2020.147366openalex-snapshot
Photoelectrical properties and surface examination of luminescent copolymer compounds
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On Water: A practical and efficient synthesis of quinoxaline derivatives catalyzed by CuSO4· 5H2O
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Zn[(l)proline]: A powerful catalyst for the very fast synthesis of quinoxaline derivatives at room temperature
inferred← citeshttps://doi.org/10.1016/j.catcom.2007.07.003openalex-snapshot
A practical and efficient synthesis of quinoxaline derivatives catalyzed by task-specific ionic liquid
inferred← citeshttps://doi.org/10.1016/j.catcom.2007.08.021openalex-snapshot
Ni-nanoparticles: An efficient catalyst for the synthesis of quinoxalines
inferred← citeshttps://doi.org/10.1016/j.catcom.2007.10.024openalex-snapshot
Montmorillonite K-10: An efficient and reusable catalyst for the synthesis of quinoxaline derivatives in water
inferred← citeshttps://doi.org/10.1016/j.catcom.2016.10.026openalex-snapshot
ZnO-loaded mesoporous silica (KIT-6) as an efficient solid catalyst for production of various substituted quinoxalines
inferred← citeshttps://doi.org/10.1016/j.cclet.2009.02.007openalex-snapshot
Catalyst-free and solvent-free method for the synthesis of quinoxalines under microwave irradiation
inferred← citeshttps://doi.org/10.1016/j.cclet.2010.11.002openalex-snapshot
Citric acid: An efficient and green catalyst for rapid one pot synthesis of quinoxaline derivatives at room temperature
inferred← citeshttps://doi.org/10.1016/j.cclet.2010.12.016openalex-snapshot
Nano-TiO2: An eco-friendly alternative for the synthesis of quinoxalines
inferred← citeshttps://doi.org/10.1016/j.cclet.2014.03.003openalex-snapshot
Yb modified NaY zeolite: A recyclable and efficient catalyst for quinoxaline synthesis
inferred← citeshttps://doi.org/10.1016/j.cclet.2014.04.008openalex-snapshot
A highly efficient procedure for the synthesis of quinoxaline derivatives using polyvinylpolypyrrolidone supported triflic acid catalyst (PVPP·OTf)
inferred← citeshttps://doi.org/10.1016/j.cclet.2016.12.035openalex-snapshot
One-pot aqueous-phase synthesis of quinoxalines through oxidative cyclization of deoxybenzoins with 1,2-phenylenediamines catalyzed by a zwtterionic Cu(II)/calix[4]arene complex
inferred← citeshttps://doi.org/10.1016/j.colsurfa.2020.125810openalex-snapshot
Insights into corrosion inhibition mechanism of mild steel in 1 M HCl solution by quinoxaline derivatives: electrochemical, SEM/EDAX, UV-visible, FT-IR and theoretical approaches
inferred← citeshttps://doi.org/10.1016/j.corsci.2009.09.013openalex-snapshot
2,3-Diphenylbenzoquinoxaline: A new corrosion inhibitor for mild steel in sulphuric acid
inferred← citeshttps://doi.org/10.1016/j.cplett.2019.06.062openalex-snapshot
Linear and femtosecond nonlinear optical properties of soluble pyrrolo[1,2-a] quinoxalines
inferred← citeshttps://doi.org/10.1016/j.crci.2009.01.006openalex-snapshot
Green chemistry approaches for the synthesis of quinoxaline derivatives: Comparison of ethanol and water in the presence of the reusable catalyst cellulose sulfuric acid
inferred← citeshttps://doi.org/10.1016/j.crci.2012.12.004openalex-snapshot
Rice husk: A mild, efficient, green and recyclable catalyst for the synthesis of 12-Aryl-8, 9, 10, 12-tetrahydro [a] xanthene-11-ones and quinoxaline derivatives
inferred← citeshttps://doi.org/10.1016/j.crci.2013.02.018openalex-snapshot
ZrOCl2·8H2O in water: An efficient catalyst for rapid one-pot synthesis of pyridopyrazines, pyrazines and 2,3-disubstituted quinoxalines
inferred← citeshttps://doi.org/10.1016/j.crci.2013.11.009openalex-snapshot
Pentafluorophenylammonium triflate: A highly efficient catalyst for the synthesis of quinoxaline derivatives in water
inferred← citeshttps://doi.org/10.1016/j.dyepig.2008.10.018openalex-snapshot
The synthesis and photophysical studies of quinoxaline and pyridopyrazine derivatives
inferred← citeshttps://doi.org/10.1016/j.dyepig.2009.01.010openalex-snapshot
A novel fluorescent bisazomethine dye derived from 3-hydroxyquinoxaline-2-carboxaldehyde and 2,3-diaminomaleonitrile
inferred← citeshttps://doi.org/10.1016/j.dyepig.2009.04.003openalex-snapshot
Tetrahydroquinoxaline based squaraines: Synthesis and photophysical properties
inferred← citeshttps://doi.org/10.1016/j.dyepig.2015.02.006openalex-snapshot
Chemiluminescence properties of luminol related quinoxaline analogs: Experimental and DFT based approach to photophysical properties
inferred← citeshttps://doi.org/10.1016/j.heliyon.2020.e03620openalex-snapshot
Theoretical investigation using DFT of quinoxaline derivatives for electronic and photovoltaic effects
inferred← citeshttps://doi.org/10.1016/j.heliyon.2020.e04986openalex-snapshot
Acenaphtoquinoxaline as a selective fluorescent sensor for Hg (II) detection: experimental and theoretical studies
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e16973openalex-snapshot
Spectroscopic investigation, thermal behavior, catalytic reduction, biological and computational studies of novel four transition metal complexes based on 5-methylthiophene Schiff base type
inferred← citeshttps://doi.org/10.1016/j.inoche.2025.115175openalex-snapshot
Novel synthesis of 2-substituted quinoxaline motifs using copper-nickel ferrite magnetic nanoparticles (Cu0.5Ni0.5Fe2O4 MNPs) as robust heterogenous catalyst
inferred← citeshttps://doi.org/10.1016/j.jare.2016.12.005openalex-snapshot
Bis[(l)prolinate-N,O]Zn: A water-soluble and recycle catalyst for various organic transformations
inferred← citeshttps://doi.org/10.1016/j.jcat.2012.05.002openalex-snapshot
Biomass into chemicals: One-pot two- and three-step synthesis of quinoxalines from biomass-derived glycols and 1,2-dinitrobenzene derivatives using supported gold nanoparticles as catalysts
inferred← citeshttps://doi.org/10.1016/j.jiec.2011.11.048openalex-snapshot
An efficient green synthesis of quinoxaline derivatives using carbon-doped MoO3–TiO2 as a heterogeneous catalyst
inferred← citeshttps://doi.org/10.1016/j.jlumin.2006.03.001openalex-snapshot
Photoluminescence and electroluminescence of a novel green-yellow emitting material–5,6-Bis-[4-(naphthalene-1-yl-phenyl-amino)-phenyl]-pyrazine-2,3-dicarbonitrile
inferred← citeshttps://doi.org/10.1016/j.jlumin.2023.120160openalex-snapshot
2,3-Diphenylquinoxalin-6-yl based dyes: Synthesis and studies of photophysical, aggregation-induced emission enhancement and electrochemical properties
inferred← citeshttps://doi.org/10.1016/j.jphotobiol.2014.07.003openalex-snapshot
Synthesis, spectral, structural analysis and biological evaluation of a new hydrogen-bonded charge-transfer complex: 2,3-Dimethylquinoxalinium-p-toluenesulfonate
inferred← citeshttps://doi.org/10.1016/j.matchemphys.2010.03.037openalex-snapshot
Indeno-1-one [2,3-b]quinoxaline as an effective inhibitor for the corrosion of mild steel in 0.5M H2SO4 solution
inferred← citeshttps://doi.org/10.1016/j.materresbull.2015.10.002openalex-snapshot
Fe 3 O 4 @SiO 2 –imid–PMA n magnetic porous nanosphere as recyclable catalyst for the green synthesis of quinoxaline derivatives at room temperature and study of their antifungal activities
inferred← citeshttps://doi.org/10.1016/j.matpr.2020.04.699openalex-snapshot
Synthesis, characterization, DFT, In-vitro anti-microbial, cytotoxicity evaluation, and DNA binding interactions of transition metal complexes of quinoxaline Schiff base ligand
inferred← citeshttps://doi.org/10.1016/j.matpr.2021.12.395openalex-snapshot
Synthesis, characterization and thermal behavior of 2,2′-dihydroxybiphenyl-formaldehyde-phenylenediamine copolymer
inferred← citeshttps://doi.org/10.1016/j.mcat.2021.112046openalex-snapshot
Tungstophosphoric acid/mesoporous silicas as suitable catalysts in quinoxaline synthesis
inferred← citeshttps://doi.org/10.1016/j.molcata.2013.02.030openalex-snapshot
An efficient and one-pot synthesis of benzimidazoles, benzoxazoles, benzothiazoles and quinoxalines catalyzed via nano-solid acid catalysts
inferred← citeshttps://doi.org/10.1016/j.molcata.2014.07.022openalex-snapshot
Cu doped CdS nanoparticles: A versatile and recoverable catalyst for chemoselective synthesis of indolo[2,3- b ]quinoxaline derivatives under microwave irradiation
inferred← citeshttps://doi.org/10.1016/j.molliq.2015.12.096openalex-snapshot
N-heterocycles as corrosion inhibitors for mild steel in acid medium
inferred← citeshttps://doi.org/10.1016/j.molliq.2017.09.102openalex-snapshot
Effects of solvating media of some phenylquinoxaline derivatives on their photophysical properties. Mixed solvent systems and acidic media
inferred← citeshttps://doi.org/10.1016/j.molliq.2017.10.127openalex-snapshot
Thermodynamics of solution and partition of dioxidine in water and the water/1-octanol biphasic system
inferred← citeshttps://doi.org/10.1016/j.molliq.2021.116539openalex-snapshot
DFT/electronic scale, MD simulation and evaluation of 6-methyl-2-(p-tolyl)-1,4-dihydroquinoxaline as a potential corrosion inhibition
inferred← citeshttps://doi.org/10.1016/j.molstruc.2009.10.035openalex-snapshot
FT-IR, FT-Raman spectra, density functional computations of the vibrational spectra and molecular geometry of 2-hydroxyquinoxaline
inferred← citeshttps://doi.org/10.1016/j.molstruc.2013.09.005openalex-snapshot
Low temperature X-ray molecular structure, tautomerism and spectral properties of 2,3-dihydroxyquinoxaline
inferred← citeshttps://doi.org/10.1016/j.molstruc.2017.12.014openalex-snapshot
Experimental and theoretical characterization of organic salt: 2-((4-bromophenyl)amino) pyrido[1,2- a ] quinoxalin-11-ium bromide monohydrate synthesized via oxidative cyclization
inferred← citeshttps://doi.org/10.1016/j.molstruc.2019.07.005openalex-snapshot
An environmentally benign attribute for the expeditious synthesis of quinoxaline and its derivatives
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.136654openalex-snapshot
Synthesis, structural elucidation, physico-chemical quantum properties and in silico interaction analysis of 2-methyl-3-((4-nitrobenzyl)oxy)quinoxaline
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.137080openalex-snapshot
Synthesis of D−A based violet−red light emitting indolo[2,3-b]quinoxalin-2-yl(phenyl)methanone amine dyes: Opto-electrochemical, AIE, and theoretical properties
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.139602openalex-snapshot
Mesoporous Co-doped-MgO as a new heterogeneous catalyst for the base-free synthesis of Quinoxalines
inferred← citeshttps://doi.org/10.1016/j.optmat.2026.117974openalex-snapshot
CN-anthracene π-conjugated materials: cis/trans isomerization, and structure–property relationships via TD-DFT
inferred← citeshttps://doi.org/10.1016/j.orgel.2003.08.001openalex-snapshot
Development of a new class of hole-transporting and emitting vinyl polymers and their application in organic electroluminescent devices
inferred← citeshttps://doi.org/10.1016/j.orgel.2010.12.006openalex-snapshot
Efficient green OLED devices with an emissive layer comprised of phosphor-doped carbazole/bis-oxadiazole side-chain polymer blends
inferred← citeshttps://doi.org/10.1016/j.physe.2015.10.005openalex-snapshot
Quinoxaline derivatives as corrosion inhibitors for mild steel in hydrochloric acid medium: Electrochemical and quantum chemical studies
inferred← citeshttps://doi.org/10.1016/j.poly.2019.02.032openalex-snapshot
An efficient protocol for the synthesis of spiroindenoquinoxaline derivatives using novel NiFe2O4/Ag3PO4 as a nano magnetically heterogeneous catalyst
inferred← citeshttps://doi.org/10.1016/j.poly.2022.116188openalex-snapshot
Anchoring of a nickel Schiff base complex with mixed ligands on MCM-41 as a heterogeneous catalyst for the synthesis of quinoxaline derivatives by various energies
inferred← citeshttps://doi.org/10.1016/j.polymer.2009.07.034openalex-snapshot
Hole-limiting conductive vinyl copolymers for AlQ3-based OLED applications
inferred← citeshttps://doi.org/10.1016/j.polymer.2015.04.020openalex-snapshot
Polynorbornene copolymer with side-chain triarylborane and iridium(III) groups: An emissive layer material with electron transporting properties for PhOLEDs
inferred← citeshttps://doi.org/10.1016/j.rechem.2023.101211openalex-snapshot
Microwave assisted synthesis of quinoxaline derivatives
inferred← citeshttps://doi.org/10.1016/j.rser.2012.02.021openalex-snapshot
Organic light emitting diodes: Energy saving lighting technology—A review
inferred← citeshttps://doi.org/10.1016/j.synthmet.2005.12.005openalex-snapshot
Synthesis of 2-phenylquinoline-based ambipolar molecules containing multiple 1,3,4-oxadiazole spacer groups
inferred← citeshttps://doi.org/10.1016/j.tet.2012.03.020openalex-snapshot
Et3N-catalyzed oxidative dehydrogenative coupling of α-unsubstituted aldehydes and ketones with aryl diamines leading to quinoxalines using molecular oxygen as oxidant
inferred← citeshttps://doi.org/10.1016/j.tet.2013.09.027openalex-snapshot
Efficient synthesis of quinoxalines with hypervalent iodine as a catalyst
inferred← citeshttps://doi.org/10.1016/j.tet.2015.02.003openalex-snapshot
An efficient iodine–DMSO catalyzed synthesis of quinoxaline derivatives
inferred← citeshttps://doi.org/10.1016/j.tet.2016.08.044openalex-snapshot
Synthesis of arylated and aminated naphthalenes and their synthetic applications for aza-heterocycles
inferred← citeshttps://doi.org/10.1016/j.tet.2017.01.056openalex-snapshot
Metal free synthesis of quinoxalines from alkynes via a cascade process using TsNBr2
inferred← citeshttps://doi.org/10.1016/j.tet.2017.02.014openalex-snapshot
Bromination of quinoxaline and derivatives: Effective synthesis of some new brominated quinoxalines
inferred← citeshttps://doi.org/10.1016/j.tet.2017.06.061openalex-snapshot
A new regiospecific synthesis method of 1 H -pyrazolo[3,4- b ]quinoxalines – Potential materials for organic optoelectronic devices, and a revision of an old scheme
inferred← citeshttps://doi.org/10.1016/j.tet.2025.134456openalex-snapshot
Green and eco-compatible synthesis of quinoxaline molecules using chitosan as a biodegradable catalyst in aqueous hydrotropic medium
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.07.026openalex-snapshot
Molecular iodine: a powerful catalyst for the easy and efficient synthesis of quinoxalines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.06.036openalex-snapshot
An efficient and convenient protocol for the synthesis of quinoxalines and dihydropyrazines via cyclization–oxidation processes using HClO4·SiO2 as a heterogeneous recyclable catalyst
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.06.065openalex-snapshot
Uncatalyzed condensation between aryl-1,2-diamines and diethyl bromomalonate: a one-pot access to substituted ethyl 3-hydroxyquinoxaline-2-carboxylates
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.10.058openalex-snapshot
Gallium(III) triflate-catalyzed synthesis of quinoxaline derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.11.123openalex-snapshot
A novel three-component reaction for the synthesis of N-cyclohexyl-3-aryl-quinoxaline-2-amines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.08.033openalex-snapshot
Biomimetic synthesis of quinoxalines in water
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.01.107openalex-snapshot
A mild and convenient synthesis of quinoxalines via cyclization–oxidation process using DABCO as catalyst
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.05.099openalex-snapshot
One-pot synthesis of quinoxaline-2-carboxylate derivatives using ionic liquid as reusable reaction media
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.11.116openalex-snapshot
A rapid synthesis of quinoxalines starting from ketones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.03.110openalex-snapshot
Quinoxaline synthesis in novel tandem one-pot protocol
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.06.115openalex-snapshot
A novel route to synthesize libraries of quinoxalines via Petasis methodology in two synthetic operations
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.09.141openalex-snapshot
Synthesis of libraries of quinoxalines through eco-friendly tandem oxidation–condensation or condensation reactions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.02.113openalex-snapshot
Ga(ClO4)3-catalyzed synthesis of quinoxalines by cycloaddition of α-hydroxyketones and o-phenylenediamines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.03.097openalex-snapshot
Brönsted acid hydrotrope combined catalyst for environmentally benign synthesis of quinoxalines and pyrido[2,3-b]pyrazines in aqueous medium
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.08.114openalex-snapshot
Reaction mechanism in the mechanochemical synthesis of dibenzophenazine: application of vibronic coupling density analysis
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.01.087openalex-snapshot
One-pot synthesis of 2-substituted quinoxalines using K10-montmorillonite as heterogeneous catalyst
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.08.022openalex-snapshot
Chemoselective synthesis of quinoxalines and benzimidazoles by silica gel catalysis
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.01.138openalex-snapshot
A catalyst free, one pot approach for the synthesis of quinoxaline derivatives via oxidative cyclisation of 1,2-diamines and phenacyl bromides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.04.046openalex-snapshot
Amberlite IR-120H, an efficient and recyclable solid phase catalyst for the synthesis of quinoxalines: a greener approach
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.10.065openalex-snapshot
Graphene oxide (GO) or reduced graphene oxide (rGO): efficient catalysts for one-pot metal-free synthesis of quinoxalines from 2-nitroaniline
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.08.051openalex-snapshot
2-Iodo benzoic acid: An unconventional precursor for the one pot multi-component synthesis of quinoxaline using organo Cu (II) catalyst
inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154820openalex-snapshot
Condensation reactions of dialkoxy-2-phenylchroman-4-ones with 1,2-diamines: A method for the preparation of chromenoquinoxalines
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