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Isomer engineering of dipyrido[3,2- a :3′,4′- c ]phenazine-acceptor-based red thermally activated delayed fluorescent emitters

https://doi.org/10.1039/d2tc00017b
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Organic Long‐Persistent Luminescence from a Thermally Activated Delayed Fluorescence Compound
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Acceptor–Donor–Acceptor‐Type Orange–Red Thermally Activated Delayed Fluorescence Materials Realizing External Quantum Efficiency Over 30% with Low Efficiency Roll‐Off
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Approaching Nearly 40% External Quantum Efficiency in Organic Light Emitting Diodes Utilizing a Green Thermally Activated Delayed Fluorescence Emitter with an Extended Linear Donor–Acceptor–Donor Structure
inferredcites →https://doi.org/10.1002/adom.201800935openalex-snapshot
Optimization on Molecular Restriction for Highly Efficient Thermally Activated Delayed Fluorescence Emitters
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Red Organic Light‐Emitting Diode with External Quantum Efficiency beyond 20% Based on a Novel Thermally Activated Delayed Fluorescence Emitter
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Tetrabenzo[a,c]phenazine Backbone for Highly Efficient Orange–Red Thermally Activated Delayed Fluorescence with Completely Horizontal Molecular Orientation
inferredcites →https://doi.org/10.1002/asia.201901311openalex-snapshot
Molecular Design Strategy of Thermally Activated Delayed Fluorescent Emitters Using CN‐Substituted Imidazopyrazine as a New Electron‐Accepting Unit
inferredcites →https://doi.org/10.1002/chem.201903877openalex-snapshot
CN‐Modified Imidazopyridine as a New Electron Accepting Unit of Thermally Activated Delayed Fluorescent Emitters
inferredcites →https://doi.org/10.1016/j.cej.2021.131510openalex-snapshot
“On-off” switch between red thermally activated delayed fluorescence and conventional fluorescence by isomeric regulation
inferredcites →https://doi.org/10.1016/j.cej.2021.134216openalex-snapshot
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inferredcites →https://doi.org/10.1021/acsami.8b21568openalex-snapshot
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inferredcites →https://doi.org/10.1021/acsami.9b02824openalex-snapshot
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Application of the energy gap law to the decay of charge-transfer excited states
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inferredcites →https://doi.org/10.1039/c8tc01746hopenalex-snapshot
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inferredcites →https://doi.org/10.1039/c9tc02557jopenalex-snapshot
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inferredcites →https://doi.org/10.1039/d0tc01995jopenalex-snapshot
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inferredcites →https://doi.org/10.1039/d0tc04465bopenalex-snapshot
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inferredcites →https://doi.org/10.1039/d1qm00155hopenalex-snapshot
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inferredcites →https://doi.org/10.1039/d1tc01562aopenalex-snapshot
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inferredcites →https://doi.org/10.1063/1.4737006openalex-snapshot
Efficient organic light-emitting diodes through up-conversion from triplet to singlet excited states of exciplexes

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/10.1002/adma.202208602openalex-snapshot
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Synthesis and Photophysical Properties of Bipolar Compound: Triphenylamine/Diazafluorene-Carbazole
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Strategic molecular design of efficient solution- and vacuum-processable deep-red thermally activated delayed fluorescence emitters featuring remarkable color saturation
inferred← citeshttps://doi.org/10.1016/j.cplett.2023.140937openalex-snapshot
Isomer engineering for red thermally activated delayed fluorescence molecules: Luminescence mechanism study and rational molecular design
inferred← citeshttps://doi.org/10.1016/j.dyepig.2024.111981openalex-snapshot
Positional isomeric effect: A simple and feasible strategy for constructing efficient red TADF materials
inferred← citeshttps://doi.org/10.1016/j.dyepig.2026.114190openalex-snapshot
A systematic review of hydrogen bonding in TADF materials: Correlating structure, interactions, and emission behaviour
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.142695openalex-snapshot
Site-specific effects of weak electron-donating/withdrawing groups on the optoelectronic properties of carbonyl/nitrogen MR-TADF emitters
inferred← citeshttps://doi.org/10.1016/j.saa.2025.126856openalex-snapshot
Donor impact on photophysical and electrochemical performance of 1,10-phenanthroline-based thermally-activated delayed fluorescence emitters
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.jpca.4c07345openalex-snapshot
Developing Red and Near-Infrared Delayed Fluorescence Emission in Nitrogen-Substituted Donor–Acceptor Polycyclic Hydrocarbon OLED Emitters: A Theoretical Study
inferred← citeshttps://doi.org/10.1021/acsaom.4c00322openalex-snapshot
“Molecular Designs Featuring Cyanobenzene-Decorated Phenazine Acceptor Units for the Highly Efficient Deep-Red Thermally Activated Delayed Fluorescent Emitters”
inferred← citeshttps://doi.org/10.1021/acsaom.5c00340openalex-snapshot
A Direct Arylation Approach toward Thermally Activated Delayed Fluorescence-Active Benzo[ c ][1,2,5]thiadiazole Emitters for Near-Infrared Solution-Processed OLEDs
inferred← citeshttps://doi.org/10.1039/d2tc02085hopenalex-snapshot
Design strategies and applications of novel functionalized phenazine derivatives: a review
inferred← citeshttps://doi.org/10.1039/d2tc02249dopenalex-snapshot
Rational design of orange-red iridium( iii ) complexes by an isomer engineering strategy for improved performance of white organic light-emitting diodes
inferred← citeshttps://doi.org/10.1039/d2tc03421bopenalex-snapshot
Efficient thermally activated delayed fluorescent emitter based on a spiro-type benzo[ b ]acridine donor and a benzophenone acceptor
inferred← citeshttps://doi.org/10.1039/d2tc03933hopenalex-snapshot
Equilibrating the key parameters of thermally activated delayed fluorescence emitters towards efficient red/near-infrared OLEDs
inferred← citeshttps://doi.org/10.1039/d3tc01632copenalex-snapshot
Asymmetric donor–acceptor–host red thermally activated delayed fluorescent emitter for high-efficiency organic light emitting diodes
inferred← citeshttps://doi.org/10.1039/d3tc02352dopenalex-snapshot
The influence of nitrogen doping of the acceptor in orange-red thermally activated delayed fluorescence emitters and OLEDs
inferred← citeshttps://doi.org/10.1039/d4tc00801dopenalex-snapshot
Pyrazino[2,3- f ][1,10]phenanthroline-based color-tunable thermally activated delayed fluorescence emitters with AIE characteristics for high-efficiency organic light-emitting diodes
inferred← citeshttps://doi.org/10.1039/d4tc00988fopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d4tc01214copenalex-snapshot
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Elucidating the non-radiative losses encountered in intramolecular charge transfer compounds with benzodithiophene-4,8-dione acceptors
inferred← citeshttps://doi.org/10.1039/d5tc02803eopenalex-snapshot
Strategic modification of the quinoxaline acceptor to induce broad-range orange to red thermally activated delayed fluorescence
inferred← citeshttps://doi.org/10.1039/d6cp01669copenalex-snapshot
Recent advancements in phenanthroline-derived TADF materials for efficient organic light-emitting devices
inferred← citeshttps://doi.org/10.26434/chemrxiv-2023-lb4knopenalex-snapshot
Design and Synthesis of Pyrazino[2,3-f][1,10]phenanthroline-Based Color-Tunable Thermally Activated Delayed Fluorescence Emitters: Exploring Novel Molecular Architectures for High-Efficiency Organic Light-Emitting Diodes.
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