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Chromophore-Labeled Quinoxaline Derivatives as Efficient Electroluminescent Materials
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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The chemistry of electroluminescent organic materials
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High-efficiency red electroluminescence from a narrow recombination zone confined by an organic double heterostructure
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Organic Electroluminescent Devices
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Spectroscopic (Ft–Ir, Ft–Raman, Uv–Vis–Nir) Investigations, Quantum Chemical Analysis (Pes, Mep, Homo–Lumo, Fmo, Nlo) And Molecular Docking Studies of Quinoxaline
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inferred← citeshttps://doi.org/10.1007/s11164-012-0693-8openalex-snapshot
Nanocrystalline 5 % Fe/ZnO as an efficient catalyst for quinoxaline synthesis
inferred← citeshttps://doi.org/10.1007/s11164-015-2014-5openalex-snapshot
Protic ionic liquids: a lucid, rational tool for synthesis of phthalazinediones, quinoxalines and benzopyrans
inferred← citeshttps://doi.org/10.1007/s11164-015-2377-7openalex-snapshot
Synthesis of quinoxalines and pyrido[2,3-b]pyrazines by Suzuki–Miyaura cross-coupling reaction
inferred← citeshttps://doi.org/10.1007/s11164-016-2437-7openalex-snapshot
A rapid and efficient domino protocol for the synthesis of functionalized benzo[a]pyrano[2,3-c]phenazine and benzo[f]pyrano[2,3-h]quinoxaline derivatives
inferred← citeshttps://doi.org/10.1007/s11164-016-2667-8openalex-snapshot
Silica nanosphere–graphene oxide (SiO2–GO) hybrid catalyzed facile synthesis of functionalized quinoxaline derivatives
inferred← citeshttps://doi.org/10.1007/s11164-020-04258-wopenalex-snapshot
An efficient method for the synthesis of quinoxaline derivatives catalyzed by titanium silicate-1
inferred← citeshttps://doi.org/10.1007/s11164-021-04430-wopenalex-snapshot
Brönsted acid hydrotrope combined catalysis in water: a green approach for the synthesis of indoloquinoxalines and bis-tetronic acids
inferred← citeshttps://doi.org/10.1007/s11164-022-04914-3openalex-snapshot
Ca(IO3)2 nanoparticles: fabrication and application as an eco-friendly and recyclable catalyst for the green synthesis of quinoxalines, pyridopyrazines, and 2,3-dicyano pyrazines
inferred← citeshttps://doi.org/10.1007/s11164-024-05410-6openalex-snapshot
Kinetics, thermodynamics, and optimization studies using response surface methodology in quinoxalines synthesis with efficient heterogeneous catalysts: environmental sustainability metrics assessment
inferred← citeshttps://doi.org/10.1007/s12039-011-0081-8openalex-snapshot
Polyethylene glycol in water: A simple, efficient and green protocol for the synthesis of quinoxalines
inferred← citeshttps://doi.org/10.1007/s12039-015-0973-0openalex-snapshot
Synthesis, photophysical, electrochemical and thermal investigation of Triarylamines based on 9H-Xanthen-9-one: Yellow–green fluorescent materials
inferred← citeshttps://doi.org/10.1007/s12039-017-1235-0openalex-snapshot
Rapid, efficient and eco-friendly procedure for the synthesis of quinoxalines under solvent-free conditions using sulfated polyborate as a recyclable catalyst
inferred← citeshttps://doi.org/10.1007/s12039-022-02074-wopenalex-snapshot
Zinc ferrite as reusable and green catalyst for synthesis of quinoxaline derivatives
inferred← citeshttps://doi.org/10.1007/s13738-016-0868-0openalex-snapshot
Ionic liquid functionalized cellulose as an efficient heterogeneous catalyst for the facile and green synthesis of benzoxazine, pyrazine and quinoxaline derivatives in aqueous media
inferred← citeshttps://doi.org/10.1007/s13738-018-1290-6openalex-snapshot
Synthesis of a polymer-capped palladium nanoparticles and its application as a reusable catalyst in oxidative coupling reaction of α-hydroxyketones and 1,2-diamines for preparation of pyrazines and quinoxalines
inferred← citeshttps://doi.org/10.1016/b978-008044992-0.00703-3openalex-snapshot
Pyrazines and their Benzo Derivatives
inferred← citeshttps://doi.org/10.1016/j.arabjc.2012.06.003openalex-snapshot
Synthesis and physicochemical studies of some new quinolinoxazine pentamethine cyanine dyes
inferred← citeshttps://doi.org/10.1016/j.arabjc.2013.11.021openalex-snapshot
A green protocol for the synthesis of quinoxaline derivatives catalyzed by polymer supported sulphanilic acid
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.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.2009.12.015openalex-snapshot
Synthesis of quinoxaline derivatives catalyzed by PEG-400
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.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.2008.09.020openalex-snapshot
Multifunctional emissive material based on 1-phenyl-1,2,3,4-tetrahydroquinoline
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.2010.03.012openalex-snapshot
The tautomerism, solvatochromism and non-linear optical properties of fluorescent 3-hydroxyquinoxaline-2-carboxalidine-4-aminoantipyrine
inferred← citeshttps://doi.org/10.1016/j.dyepig.2010.06.008openalex-snapshot
The synthesis and spectral characterization of red dyes containing biphenyl or fluorene conjugation and dicyanovinyl acceptors
inferred← citeshttps://doi.org/10.1016/j.dyepig.2013.03.030openalex-snapshot
Luminescent materials incorporating pyrazine or quinoxaline moieties
inferred← citeshttps://doi.org/10.1016/j.dyepig.2018.02.020openalex-snapshot
Synthesis and characterization of quinoxaline derivative for high performance phosphorescent organic light-emitting diodes
inferred← citeshttps://doi.org/10.1016/j.ejmech.2014.06.058openalex-snapshot
Quinoxaline, its derivatives and applications: A State of the Art review
inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2022.111120openalex-snapshot
Recent advances on visible light Thiophene-based photoinitiators of polymerization
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.ijbiomac.2022.12.310openalex-snapshot
Quinoxaline-probe embedded injectable fluorogenic hydrogels: Comparative detection of mesitylene in guar gum and i-carrageenan hydrogels
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.129517openalex-snapshot
Indenoquinoxaline-phenylacrylohydrazide hybrids as promising drug candidates for the treatment of type 2 diabetes: In vitro and in silico evaluation of enzyme inhibition and antioxidant activity
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.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.2006.02.003openalex-snapshot
Highly efficient greenish blue-emitting organic diodes based on pyrene derivatives
inferred← citeshttps://doi.org/10.1016/j.jlumin.2022.119350openalex-snapshot
2,2′,3,3′-Tetrakis(4-bromophenyl)-6,6′-biquinoxaline based novel Donor–Acceptor–Acceptor−Donor (DAAD) Blue−Orange emitting molecules: Opto-electrochemical, AIE and theoretical investigation
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2009.02.016openalex-snapshot
Novel iridium complex with carboxyl pyridyl ligand for dye-sensitized solar cells: High fluorescence intensity, high electron injection efficiency?
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2019.112101openalex-snapshot
A reaction-based fluorescent probe for detecting o-phenylenediamine in water and lateritic soil samples
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.mcat.2021.112046openalex-snapshot
Tungstophosphoric acid/mesoporous silicas as suitable catalysts in quinoxaline synthesis
inferred← citeshttps://doi.org/10.1016/j.molliq.2015.07.069openalex-snapshot
Interaction studies of methyl acetate in aqueous solutions of quinoxaline derivatives: Effect of temperature and concentration
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.2019.111763openalex-snapshot
Molecular 5,8-π-extended quinoxaline derivatives as chromophores for photoluminescence applications
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.2021.132260openalex-snapshot
One-pot synthesis of novel substituted quinoxaline piperazine derivatives and their antimicrobial activities
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.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.orgel.2013.10.019openalex-snapshot
Fluorene derivatives for highly efficient non-doped single-layer blue organic light-emitting diodes
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.reactfunctpolym.2013.03.013openalex-snapshot
Synthesis, characterization and third-order nonlinear optical properties of novel hyperbranched donor–acceptor polyfluorenes based on 1,3,6,8-tertsubstituted carbazole core
inferred← citeshttps://doi.org/10.1016/j.rechem.2025.102148openalex-snapshot
Oxidant-free annulation of α-hydroxy ketones with diamines using aluminum(III) chloride: A supramolecular approach for practical quinoxaline synthesis
inferred← citeshttps://doi.org/10.1016/j.synthmet.2008.09.013openalex-snapshot
Synthesis and characterization of benzothiazole derivatives for blue electroluminescent devices
inferred← citeshttps://doi.org/10.1016/j.talanta.2023.124723openalex-snapshot
Domino protocol for the synthesis of diversely functionalized derivatives of a novel fused pentacyclic antioxidant/anticancer fluorescent scaffold: Pyrazolo[5'',1'':2',3']pyrimido[4',5':5,6][1,4]thiazino[2,3-b]quinoxaline
inferred← citeshttps://doi.org/10.1016/j.tet.2009.11.109openalex-snapshot
Two-photon absorption and effective broadband optical power limiting properties of a multi-branched chromophore containing 2,3-diarylquinoxalinyl moieties as the electron-pulling units
inferred← citeshttps://doi.org/10.1016/j.tet.2010.11.014openalex-snapshot
Synthesis of quinoxaline–benzoxale conjugates and mesomorphic properties
inferred← citeshttps://doi.org/10.1016/j.tet.2010.11.071openalex-snapshot
Fluorene as the π–spacer for new two-photon absorption chromophores
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.2014.02.034openalex-snapshot
2,3-Diarylquinoxaline directed mono ortho-aroylation via cross-dehydrogenative coupling using aromatic aldehydes or alkylbenzenes as aroyl surrogate
inferred← citeshttps://doi.org/10.1016/j.tet.2014.04.009openalex-snapshot
Organic dyes containing indolo[2,3-b]quinoxaline as a donor: synthesis, optical and photovoltaic properties
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.2016.07.076openalex-snapshot
Mesogenic heterocycles derived from quinoxaline Schiff Bases
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.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.2005.08.166openalex-snapshot
Benzo[1,2,5]selenadiazole bridged amines: electro-optical properties
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.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.2009.12.136openalex-snapshot
Highly fluorescent intramolecular dimmers of two pyrenyl-substituted fluorenes bridged by 1,6-hexanyl: synthesis, spectroscopic, and self-organized properties
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.2011.10.074openalex-snapshot
Synthesis of novel twisted carbazole–quinoxaline derivatives with 1,3,5-benzene core: bipolar molecules as hosts for phosphorescent OLEDs
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.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.2015.10.065openalex-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.2018.02.044openalex-snapshot
An expedient regio and diastereoselective synthesis of novel spiropyrrolidinylindenoquinoxalines via 1,3-dipolar cycloaddition reaction
inferred← citeshttps://doi.org/10.1016/j.tsf.2008.02.010openalex-snapshot
Efficient fluorescent red, green, and blue organic light-emitting devices with a blue host of spirobifluorene derivative
inferred← citeshttps://doi.org/10.1016/s1452-3981(23)16251-1openalex-snapshot
Electrochemical Synthesis Of Quinoxalinediones: 1,4-di(2- Pyridylmethyl)-1,2,3,4-Tetrahydroquinoxaline-6,7-Dione
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02087openalex-snapshot
Regioselective Synthesis of Trisubstituted Quinoxalines Mediated by Hypervalent Iodine Reagents
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02581openalex-snapshot
Four- and Five-Component Syntheses and Photophysical Properties of Emission Solvatochromic 3-Aminovinylquinoxalines
inferred← citeshttps://doi.org/10.1021/acs.jpca.3c01732openalex-snapshot
Accelerated Intramolecular Charge Transfer in Tetracyanobutadiene- and Expanded Tetracyanobutadiene-Incorporated Asymmetric Triphenylamine–Quinoxaline Push–Pull Conjugates
inferred← citeshttps://doi.org/10.1021/acs.jpca.3c05077openalex-snapshot
Harnessing Proton-Coupled Electron Transfer for Hydrogenation of Aza-Arenes: Photochemistry of Quinoxaline Derivatives in Methanol
inferred← citeshttps://doi.org/10.1021/acs.jpcb.5c06969openalex-snapshot
Tuning of Quinoxaline-Based Molecules for Aggregation-Induced Emission and Room Temperature Liquid Crystallinity
inferred← citeshttps://doi.org/10.1021/acs.jpcb.8b01004openalex-snapshot
Radical Ions of 3-Styryl-quinoxalin-2-one Derivatives Studied by Pulse Radiolysis in Organic Solvents
inferred← citeshttps://doi.org/10.1021/acs.jpcc.0c05731openalex-snapshot
Novel Triazine-Based Donor–Acceptor Ionic Green Emitters for Nondoped Light-Emitting Electrochemical Cells
inferred← citeshttps://doi.org/10.1021/acs.jpcc.1c04762openalex-snapshot
Novel Thenil-Based Ionic Small Molecules for Nondoped Light-Emitting Electrochemical Cells for Ultrapure Green Emission
inferred← citeshttps://doi.org/10.1021/acs.jpcc.5b07871openalex-snapshot
Phenanthroimidazole Derivative as an Easily Accessible Emitter for Non-Doped Light-Emitting Electrochemical Cells
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c03465openalex-snapshot
Cobalt-Catalyzed Effective Access to Quinoxalines with Insights in Annulation of Terminal Alkynes and o-Phenylenediamines
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00309openalex-snapshot
One-Pot Regiospecific Synthesis of Quinoxalines via a CH2-Extrusion Reaction
inferred← citeshttps://doi.org/10.1021/acsomega.5c09337openalex-snapshot
Mild and Green Methodology for NIS-Mediated Synthesis of Quinoxalines from o -Phenylenediamines and Sulfoxonium Ylides at Room Temperature
inferred← citeshttps://doi.org/10.1021/acsomega.8b01706openalex-snapshot
Aggregation-Induced Emission and White Luminescence from a Combination of π-Conjugated Donor–Acceptor Organic Luminogens
inferred← citeshttps://doi.org/10.1021/acsomega.9b01635openalex-snapshot
Graphitic Carbon Nitride Nanosheets Covalently Functionalized with Biocompatible Vitamin B1: Synthesis, Characterization, and Its Superior Performance for Synthesis of Quinoxalines
inferred← citeshttps://doi.org/10.1021/cm0613760openalex-snapshot
n-Type Conjugated Oligoquinoline and Oligoquinoxaline with Triphenylamine Endgroups: Efficient Ambipolar Light Emitters for Device Applications
inferred← citeshttps://doi.org/10.1021/cm4030414openalex-snapshot
Bipolar Phenanthroimidazole Derivatives Containing Bulky Polyaromatic Hydrocarbons for Nondoped Blue Electroluminescence Devices with High Efficiency and Low Efficiency Roll-Off
inferred← citeshttps://doi.org/10.1021/co500036nopenalex-snapshot
Ugi-Based Approaches to Quinoxaline Libraries
inferred← citeshttps://doi.org/10.1021/cr100428aopenalex-snapshot
Pyrene-Based Materials for Organic Electronics
inferred← citeshttps://doi.org/10.1021/jo100028dopenalex-snapshot
Facile C−H Alkylation in Water: Enabling Defect-Free Materials for Optoelectronic Devices
inferred← citeshttps://doi.org/10.1021/jo1016663openalex-snapshot
Synthesis, Spectra, and Theoretical Investigations of the Triarylamines Based on 6H-Indolo[2,3-b]quinoxaline
inferred← citeshttps://doi.org/10.1021/jo200857popenalex-snapshot
Synthesis and Optical Properties of Acidochromic Amine-Substituted Benzo[a]phenazines
inferred← citeshttps://doi.org/10.1021/jo400594jopenalex-snapshot
Palladium-Catalyzed Chelation-Assisted Aromatic C–H Nitration: Regiospecific Synthesis of Nitroarenes Free from the Effect of the Orientation Rules
inferred← citeshttps://doi.org/10.1021/jo9002147openalex-snapshot
Fluorescence Control on Panchromatic Spectra via C-Alkylation on Arylated Quinoxalines
inferred← citeshttps://doi.org/10.1021/jp104710yopenalex-snapshot
Star-Shaped Donor-π-Acceptor Conjugated Oligomers with 1,3,5-Triazine Cores: Convergent Synthesis and Multifunctional Properties
inferred← citeshttps://doi.org/10.1021/jp500397gopenalex-snapshot
Synthesis, Photophysics, and Reverse Saturable Absorption of Bipyridyl Platinum(II) Bis(acetylide) Complexes Bearing Aromatic Electron-Withdrawing Substituents on the Acetylide Ligands
inferred← citeshttps://doi.org/10.1021/ma800304mopenalex-snapshot
Block Co-oligomers for Organic Electronics and Optoelectronics: Synthesis, Photophysics, Electroluminescence, and Field-Effect Charge Transport of Oligothiophene-b-oligoquinoline-b-oligothiophene Triblock Co-oligomers
inferred← citeshttps://doi.org/10.1021/ol802287kopenalex-snapshot
Turning on Fluorescent Emission from C-Alkylation on Quinoxaline Derivatives
inferred← citeshttps://doi.org/10.1038/s41598-025-15308-xopenalex-snapshot
Magnetic nanohybrids of folic acid as green biocatalysts for the synthesis of heterocyclic compounds
inferred← citeshttps://doi.org/10.1039/b509325bopenalex-snapshot
Hexaphenylphenylene dendronised pyrenylamines for efficient organic light-emitting diodes
inferred← citeshttps://doi.org/10.1039/b510035fopenalex-snapshot
Novel distyrylcarbazole derivatives as hole-transporting blue emitters for electroluminescent devices
inferred← citeshttps://doi.org/10.1039/b510677jopenalex-snapshot
Cerium (iv) ammonium nitrate (CAN) as a catalyst in tap water: A simple, proficient and green approach for the synthesis of quinoxalines
inferred← citeshttps://doi.org/10.1039/b703180gopenalex-snapshot
Luminescence of fluorenes 2,7-conjugatively extended with pyrenylvinylene and pyrenylvinylene-phenylenevinylene
inferred← citeshttps://doi.org/10.1039/c0jm03300fopenalex-snapshot
Bipolar anthracene derivatives containing hole- and electron-transporting moieties for highly efficient blue electroluminescence devices
inferred← citeshttps://doi.org/10.1039/c3ra41038bopenalex-snapshot
Surfactant micelles as microreactors for the synthesis of quinoxalines in water: scope and limitations of surfactant catalysis
inferred← citeshttps://doi.org/10.1039/c4cc07083fopenalex-snapshot
Oxidative tandem nitrosation/cyclization of N-aryl enamines with nitromethane toward 3-(trifluoromethyl)quinoxalines
inferred← citeshttps://doi.org/10.1039/c4gc01316fopenalex-snapshot
Efficient synthesis of quinoxalines from 2-nitroanilines and vicinal diols via a ruthenium-catalyzed hydrogen transfer strategy
inferred← citeshttps://doi.org/10.1039/c4ra08589bopenalex-snapshot
I 2 catalyzed tandem protocol for synthesis of quinoxalines via sp 3 , sp 2 and sp C–H functionalization
inferred← citeshttps://doi.org/10.1039/c4ra08615eopenalex-snapshot
l -Proline mediated synthesis of quinoxalines; evaluation of cytotoxic and antimicrobial activity
inferred← citeshttps://doi.org/10.1039/c4ra15461dopenalex-snapshot
Palladium catalyzed ortho-halogenation of 2-arylbenzothiazole and 2,3-diarylquinoxaline
inferred← citeshttps://doi.org/10.1039/c4tc00684dopenalex-snapshot
A novel ambipolar polymer: from organic thin-film transistors to enhanced air-stable blue light emitting diodes
inferred← citeshttps://doi.org/10.1039/c4tc01753fopenalex-snapshot
Phosphine oxide functionalized pyrenes as efficient blue light emitting multifunctional materials for organic light emitting diodes
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