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Boronate- and borinate-based π-systems for blue thermally activated delayed fluorescence materials
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/adfm.201802031openalex-snapshot
High‐Performance Dibenzoheteraborin‐Based Thermally Activated Delayed Fluorescence Emitters: Molecular Architectonics for Concurrently Achieving Narrowband Emission and Efficient Triplet–Singlet Spin Conversion
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Ultrapure Blue Thermally Activated Delayed Fluorescence Molecules: Efficient HOMO–LUMO Separation by the Multiple Resonance Effect
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Versatile Molecular Functionalization for Inhibiting Concentration Quenching of Thermally Activated Delayed Fluorescence
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Controlling Singlet–Triplet Energy Splitting for Deep‐Blue Thermally Activated Delayed Fluorescence Emitters
inferredcites →https://doi.org/10.1002/anie.201508270openalex-snapshot
Triarylboron‐Based Fluorescent Organic Light‐Emitting Diodes with External Quantum Efficiencies Exceeding 20 %
inferredcites →https://doi.org/10.1002/anie.201609459openalex-snapshot
Controlling Singlet–Triplet Energy Splitting for Deep‐Blue Thermally Activated Delayed Fluorescence Emitters
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Multiscale Charge Injection and Transport Properties in Self‐Assembled Monolayers of Biphenyl Thiols with Varying Torsion Angles
inferredcites →https://doi.org/10.1002/chem.201602753openalex-snapshot
Synthesis of Boronate‐Based Benzo[fg]tetracene and Benzo[hi]hexacene via Demethylative Direct Borylation
inferredcites →https://doi.org/10.1002/cphc.201600662openalex-snapshot
The Importance of Vibronic Coupling for Efficient Reverse Intersystem Crossing in Thermally Activated Delayed Fluorescence Molecules
inferredcites →https://doi.org/10.1016/j.tet.2016.01.054openalex-snapshot
10,9-Oxaboraphenanthrenes as luminescent fluorophores
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Thermally Activated Delayed Fluorescence from Azasiline Based Intramolecular Charge-Transfer Emitter (DTPDDA) and a Highly Efficient Blue Light Emitting Diode
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Isobenzofuranone- and Chromone-Based Blue Delayed Fluorescence Emitters with Low Efficiency Roll-Off in Organic Light-Emitting Diodes
inferredcites →https://doi.org/10.1021/acs.jctc.5b00431openalex-snapshot
Reliable Prediction with Tuned Range-Separated Functionals of the Singlet–Triplet Gap in Organic Emitters for Thermally Activated Delayed Fluorescence
inferredcites →https://doi.org/10.1021/acs.jpcc.5b03530openalex-snapshot
On Predicting the Excited-State Properties of Thermally Activated Delayed Fluorescence Emitters
inferredcites →https://doi.org/10.1021/acsami.7b05615openalex-snapshot
Rigidity-Induced Delayed Fluorescence by Ortho Donor-Appended Triarylboron Compounds: Record-High Efficiency in Pure Blue Fluorescent Organic Light-Emitting Diodes
inferredcites →https://doi.org/10.1021/jacs.6b01674openalex-snapshot
Two-Step Synthesis of Boron-Fused Double Helicenes
inferredcites →https://doi.org/10.1021/jacs.6b04092openalex-snapshot
Synthesis of Stable Nanographenes with OBO-Doped Zigzag Edges Based on Tandem Demethylation-Electrophilic Borylation
inferredcites →https://doi.org/10.1021/jacs.6b08664openalex-snapshot
Synthesis, Structure, and Chiroptical Properties of a Double [7]Heterohelicene
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Up-Conversion Intersystem Crossing Rates in Organic Emitters for Thermally Activated Delayed Fluorescence: Impact of the Nature of Singlet vs Triplet Excited States
inferredcites →https://doi.org/10.1021/jacs.7b03848openalex-snapshot
New Molecular Design Concurrently Providing Superior Pure Blue, Thermally Activated Delayed Fluorescence and Optical Out-Coupling Efficiencies
inferredcites →https://doi.org/10.1021/jo049343wopenalex-snapshot
10-Hydroxy-10,9-boroxarophenanthrenes: Versatile Synthetic Intermediates to 3,4-Benzocoumarins and Triaryls
inferredcites →https://doi.org/10.1021/ol5031734openalex-snapshot
Boron-Selective Biaryl Coupling Approach to Versatile Dibenzoxaborins and Application to Concise Synthesis of Defucogilvocarcin M
inferredcites →https://doi.org/10.1038/nmat4154openalex-snapshot
Highly efficient blue electroluminescence based on thermally activated delayed fluorescence
inferredcites →https://doi.org/10.1038/nphoton.2014.12openalex-snapshot
Efficient blue organic light-emitting diodes employing thermally activated delayed fluorescence
inferredcites →https://doi.org/10.1038/s41566-018-0112-9openalex-snapshot
Diboron compound-based organic light-emitting diodes with high efficiency and reduced efficiency roll-off
inferredcites →https://doi.org/10.1039/c5cc00307eopenalex-snapshot
High efficiency pure blue thermally activated delayed fluorescence molecules having 10H-phenoxaborin and acridan units
inferredcites →https://doi.org/10.1039/c5tc01380aopenalex-snapshot
Light blue and green thermally activated delayed fluorescence from 10H-phenoxaborin-derivatives and their application to organic light-emitting diodes
inferredcites →https://doi.org/10.1039/c6tc01353hopenalex-snapshot
Boosting reverse intersystem crossing by increasing donors in triarylboron/phenoxazine hybrids: TADF emitters for high-performance solution-processed OLEDs
inferredcites →https://doi.org/10.1039/c6tc02027eopenalex-snapshot
High-performance blue organic light-emitting diodes with 20% external electroluminescence quantum efficiency based on pyrimidine-containing thermally activated delayed fluorescence emitters
inferredcites →https://doi.org/10.1039/c7cc04875kopenalex-snapshot
Enhancing thermally activated delayed fluorescence characteristics by intramolecular B–N coordination in a phenylpyridine-containing donor–acceptor π-system
inferredcites →https://doi.org/10.1246/bcsj.20150399openalex-snapshot
A Phenazaborin-Based High-Efficiency Blue Delayed Fluorescence Material
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/adfm.202204352openalex-snapshot
Highly Efficient Deep‐Blue Organic Light‐Emitting Diodes Based on Rational Molecular Design and Device Engineering
inferred← citeshttps://doi.org/10.1002/adma.202201778openalex-snapshot
Development of Pure Green Thermally Activated Delayed Fluorescence Material by Cyano Substitution
inferred← citeshttps://doi.org/10.1002/adom.202000922openalex-snapshot
Three‐ and Four‐Coordinate, Boron‐Based, Thermally Activated Delayed Fluorescent Emitters
inferred← citeshttps://doi.org/10.1002/agt2.182openalex-snapshot
Versatile boron‐based thermally activated delayed fluorescence materials for organic light‐emitting diodes
inferred← citeshttps://doi.org/10.1002/ange.201903332openalex-snapshot
Four‐Coordinate Boron Emitters with Tridentate Chelating Ligand for Efficient and Stable Thermally Activated Delayed Fluorescence Organic Light‐Emitting Devices
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Carbazole‐Based DABNA Analogues as Highly Efficient Thermally Activated Delayed Fluorescence Materials for Narrowband Organic Light‐Emitting Diodes
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Intensiv farbige Bor‐dotierte Thiazolthiazole durch reduktive Dimerisierung von Borisothiocyanaten
inferred← citeshttps://doi.org/10.1002/anie.201903332openalex-snapshot
Four‐Coordinate Boron Emitters with Tridentate Chelating Ligand for Efficient and Stable Thermally Activated Delayed Fluorescence Organic Light‐Emitting Devices
inferred← citeshttps://doi.org/10.1002/anie.202012891openalex-snapshot
Carbazole‐Based DABNA Analogues as Highly Efficient Thermally Activated Delayed Fluorescence Materials for Narrowband Organic Light‐Emitting Diodes
inferred← citeshttps://doi.org/10.1002/anie.202015508openalex-snapshot
Highly Colored Boron‐Doped Thiazolothiazoles from the Reductive Dimerization of Boron Isothiocyanates
inferred← citeshttps://doi.org/10.1002/cptc.202100219openalex-snapshot
Recent Advances in the Luminescence of Arylboronic Acids and their Heteroatom Condensates
inferred← citeshttps://doi.org/10.1002/cptc.202200026openalex-snapshot
Tribophosphorescence from a Simple Boronic Ester
inferred← citeshttps://doi.org/10.1016/j.cej.2021.129097openalex-snapshot
A novel molecular design featuring the conversion of inefficient TADF emitters into efficient TADF emitters for deep-blue organic light emitting diodes
inferred← citeshttps://doi.org/10.1016/j.dyepig.2019.107849openalex-snapshot
Highly effective nicotinonitrile-derivatives-based thermally activated delayed fluorescence emitter with asymmetric molecular architecture for high-performance organic light-emitting diodes
inferred← citeshttps://doi.org/10.1016/j.dyepig.2021.109192openalex-snapshot
Novel tetracoordinated organoboron emitters for thermally activated delayed fluorescence organic light-emitting diodes
inferred← citeshttps://doi.org/10.1016/j.dyepig.2024.111988openalex-snapshot
PtII(C^N)(N-donor ligand)Cl-type complexes with the four-coordinate organoboron unit and their optoelectronic properties
inferred← citeshttps://doi.org/10.1016/j.optmat.2020.109726openalex-snapshot
Efficient non-doped blue fluorescent OLEDs based on bipolar phenanthroimidazole-triphenylamine derivatives
inferred← citeshttps://doi.org/10.1016/j.orgel.2023.106960openalex-snapshot
Highly reduced efficiency roll-off with 5,9-dioxa-13b-boranaphtho[3,2,1-de]anthracen-containing unit on bipolar host for improved OLEDs device lifespan
inferred← citeshttps://doi.org/10.1021/acs.chemrev.3c00755openalex-snapshot
The Golden Age of Thermally Activated Delayed Fluorescence Materials: Design and Exploitation
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00266openalex-snapshot
Direct Alkylation of Quinoxalinones with Boracene-Based Alkylborate under Visible Light Irradiation
inferred← citeshttps://doi.org/10.1021/acs.jpca.0c11478openalex-snapshot
Molecular Vibration Accelerates Charge Transfer Emission in a Highly Twisted Blue Thermally Activated Delayed Fluorescence Material
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02846openalex-snapshot
6,12-Dihydro-6,12-diboradibenzo[def,mno]chrysene: A Doubly Boron-Doped Polycyclic Aromatic Hydrocarbon for Organic Light Emitting Diodes by a One-Pot Synthesis
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Multiple Resonance Effect-Induced Sky-Blue Thermally Activated Delayed Fluorescence with a Narrow Emission Band
inferred← citeshttps://doi.org/10.1021/acsmaterialslett.9b00433openalex-snapshot
Pentacyclic Ladder-Heteraborin Emitters Exhibiting High-Efficiency Blue Thermally Activated Delayed Fluorescence with an Ultrashort Emission Lifetime
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Developing Biarylhemiboronic Esters for Biaryl Atropisomer Synthesis via Dynamic Kinetic Atroposelective Suzuki–Miyaura Cross-Coupling
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Multiple donor–acceptor design for highly luminescent and stable thermally activated delayed fluorescence emitters
inferred← citeshttps://doi.org/10.1039/c9nj03993gopenalex-snapshot
Positive charge-dependent cell targeted staining and DNA detection
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Aryl–aryl coupling in a polycyclic aromatic hydrocarbon with embedded tetracoordinate boron centre
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Two-channel emission controlled by a conjugation valve for the color switching of thermally activated delayed fluorescence emission
inferred← citeshttps://doi.org/10.1039/d2tc01243jopenalex-snapshot
High-performance three-coordinated organoboron emitters for organic light-emitting diodes
inferred← citeshttps://doi.org/10.1039/d3cc04302aopenalex-snapshot
Heteroatom-boron-heteroatom-doped π-conjugated systems: structures, synthesis and photofunctional properties
inferred← citeshttps://doi.org/10.1039/d3cs00871aopenalex-snapshot
Synthetic progress of organic thermally activated delayed fluorescence emitters via C–H activation and functionalization
inferred← citeshttps://doi.org/10.1039/d3qm00498hopenalex-snapshot
Recent advances and prospects for organoboron-based thermally activated delayed fluorescence emitters
inferred← citeshttps://doi.org/10.1039/d3sc06989copenalex-snapshot
Achieving efficient and stable blue thermally activated delayed fluorescence organic light-emitting diodes based on four-coordinate fluoroboron emitters by simple substitution molecular engineering
inferred← citeshttps://doi.org/10.1039/d3tc02409aopenalex-snapshot
Donor-modified multiple resonance emitters with accelerated reverse intersystem crossing towards high-efficiency and narrowband deep-blue OLEDs
inferred← citeshttps://doi.org/10.1134/s0036024424700560openalex-snapshot
Theoretical Characterization and Design of Triarylborane-Based Thermally Activated Delayed Fluorescent Molecules for Organic Light-Emitting Diodes
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3230300/v1openalex-snapshot
Rational design of star-shaped triarylborane-based thermally activated delayed fluorescent emitters for organic light-emitting diodes
inferred← citeshttps://doi.org/10.31613/ceramist.2019.22.3.01openalex-snapshot
Research Trends of Thermally Activated Delayed Fluorescence Materials for Organic Light-Emitting Diodes
inferred← citeshttps://doi.org/10.3389/fchem.2020.00373openalex-snapshot
Recent Advancement in Boron-Based Efficient and Pure Blue Thermally Activated Delayed Fluorescence Materials for Organic Light-Emitting Diodes
inferred← citeshttps://doi.org/10.3389/fchem.2020.563411openalex-snapshot
OBO-Fused Benzo[fg]tetracene as Acceptor With Potential for Thermally Activated Delayed Fluorescence Emitters
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