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Organic luminescent radicals with blue-green emission for organic light-emitting diodes

https://doi.org/10.2139/ssrn.5429733
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/adfm.202002916openalex-snapshot
Radiative and Nonradiative Recombinations in Organic Radical Emitters: The Effect of Guest–Host Interactions
inferredcites →https://doi.org/10.1002/anie.201500242openalex-snapshot
Organic Light‐Emitting Diodes Using a Neutral π Radical as Emitter: The Emission from a Doublet
inferredcites →https://doi.org/10.1002/anie.201811314openalex-snapshot
Synthesis and Properties of a Highly Congested Tri(9‐anthryl)methyl Radical
inferredcites →https://doi.org/10.1002/anie.202300772openalex-snapshot
A Highly Stable Organic Luminescent Diradical
inferredcites →https://doi.org/10.1002/wcms.1493openalex-snapshot
Extended tight‐binding quantum chemistry methods
inferredcites →https://doi.org/10.1007/s00339-016-9792-5openalex-snapshot
Effect of the Pauli exclusion principle on the singlet exciton yield in conjugated polymers
inferredcites →https://doi.org/10.1016/j.chempr.2020.09.024openalex-snapshot
Persistent and Stable Organic Radicals: Design, Synthesis, and Applications
inferredcites →https://doi.org/10.1016/j.orgel.2016.08.020openalex-snapshot
Quenching in single emissive white phosphorescent organic light-emitting devices
inferredcites →https://doi.org/10.1016/j.tetlet.2006.02.022openalex-snapshot
[4-(N-Carbazolyl)-2,6-dichlorophenyl]bis(2,4,6-trichlorophenyl)methyl radical an efficient red light-emitting paramagnetic molecule
inferredcites →https://doi.org/10.1021/acs.accounts.6b00240openalex-snapshot
Phosphorescent Platinum(II) Complexes with C ∧ C* Cyclometalated NHC Ligands
inferredcites →https://doi.org/10.1021/acs.jctc.8b01176openalex-snapshot
GFN2-xTB─An Accurate and Broadly Parametrized Self-Consistent Tight-Binding Quantum Chemical Method with Multipole Electrostatics and Density-Dependent Dispersion Contributions
inferredcites →https://doi.org/10.1021/acs.jpcc.8b08574openalex-snapshot
NIR Emission and Acid-Induced Intramolecular Electron Transfer Derived from a SOMO–HOMO Converted Non-Aufbau Electronic Structure
inferredcites →https://doi.org/10.1021/cr9904009openalex-snapshot
Quantum Mechanical Continuum Solvation Models
inferredcites →https://doi.org/10.1021/j100258a017openalex-snapshot
Photophysics of arylmethyl radicals at 77 K. Structure-photoreactivity correlation
inferredcites →https://doi.org/10.1021/ja805751hopenalex-snapshot
Realization of SOMO−HOMO Level Conversion for a TEMPO-Dithiolate Ligand by Coordination to Platinum(II)
inferredcites →https://doi.org/10.1021/jp105589yopenalex-snapshot
Calculations of Electron Transport through Simple π- and σ-Type Radicals
inferredcites →https://doi.org/10.1021/jp310316bopenalex-snapshot
Surface-Supported Hydrocarbon π Radicals Show Kondo Behavior
inferredcites →https://doi.org/10.1038/nature11687openalex-snapshot
Highly efficient organic light-emitting diodes from delayed fluorescence
inferredcites →https://doi.org/10.1038/s41563-019-0433-1openalex-snapshot
High stability and luminescence efficiency in donor–acceptor neutral radicals not following the Aufbau principle
inferredcites →https://doi.org/10.1038/s41563-019-0453-xopenalex-snapshot
Radically more stable
inferredcites →https://doi.org/10.1038/s41563-020-0705-9openalex-snapshot
Understanding the luminescent nature of organic radicals for efficient doublet emitters and pure-red light-emitting diodes
inferredcites →https://doi.org/10.1038/s41586-018-0695-9openalex-snapshot
Efficient radical-based light-emitting diodes with doublet emission
inferredcites →https://doi.org/10.1039/c3cc46271dopenalex-snapshot
A mechanistic investigation of hydrodehalogenation using ESI-MS
inferredcites →https://doi.org/10.1039/c7qm00273dopenalex-snapshot
Multicarbazolyl substituted TTM radicals: red-shift of fluorescence emission with enhanced luminescence efficiency
inferredcites →https://doi.org/10.1039/c8cp01492bopenalex-snapshot
Effects of substituents on luminescent efficiency of stable triaryl methyl radicals
inferredcites →https://doi.org/10.1039/d1ra04638aopenalex-snapshot
Mixed-halide triphenyl methyl radicals for site-selective functionalization and polymerization
inferredcites →https://doi.org/10.1039/d1tc02196fopenalex-snapshot
Perspectives for polychlorinated trityl radicals
inferredcites →https://doi.org/10.1039/d1tc05268copenalex-snapshot
Electro-optical π-radicals: design advances, applications and future perspectives
inferredcites →https://doi.org/10.1039/d2cc00548dopenalex-snapshot
Synthesis, properties and chemical modification of a persistent triisopropylsilylethynyl substituted tri(9-anthryl)methyl radical
inferredcites →https://doi.org/10.1039/d2cc04481aopenalex-snapshot
Photostability of luminescent tris(2,4,6-trichlorophenyl)methyl radical enhanced by terminal modification of carbazole donor
inferredcites →https://doi.org/10.1039/d2cs00772jopenalex-snapshot
Doublet-emissive materials for organic light-emitting diodes: exciton formation and emission processes
inferredcites →https://doi.org/10.1039/d2tc03299fopenalex-snapshot
Efficient pure near-infrared organic light-emitting diodes based on tris(2,4,6-trichlorophenyl)methyl radical derivatives
inferredcites →https://doi.org/10.1039/d3tc03017bopenalex-snapshot
Efficient radical-based near-infrared organic light-emitting diodes with an emission peak exceeding 800 nm
inferredcites →https://doi.org/10.1063/1.1409582openalex-snapshot
Nearly 100% internal phosphorescence efficiency in an organic light-emitting device
inferredcites →https://doi.org/10.1063/5.0047636openalex-snapshot
Efficient light-emitting diodes from organic radicals with doublet emission
inferredcites →https://doi.org/10.1246/cl.2012.674openalex-snapshot
Effects of Alkoxy Substitution on the Optical Properties of 9,10-Anthraquinone and Anthracene: 2,3,6,7-Tetrapropoxy-substituted vs. 2,6-Dipropoxy-substituted Derivatives
inferredcites →https://doi.org/10.31635/ccschem.020.202000210openalex-snapshot
Stable Luminescent Radicals and Radical-Based LEDs with Doublet Emission
inferredcites →https://doi.org/10.3184/007967402103165388openalex-snapshot
Radical Pairs in Solution
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