Research graph
References from Conformationally controlled thermally activated delayed fluorescence in a nitro-substituted phenothiazine: a combined spectroscopic and kinetic study. Local targets link to admitted publications; unresolved targets remain external evidence.
Highly efficient organic light-emitting diodes from delayed fluorescence
10.1038/nature11687 · 2012 · External reference
Triplet-singlet emission in fluid solutions. Phosphorescence of eosin
10.1039/tf9615701894 · 1961 · External reference
Thermally activated delayed fluorescence (TADF) path toward efficient electroluminescence in purely organic materials: molecular level insight
10.1021/acs.accounts.8b00174 · 2018 · External reference
The triplet state of organo-transition metal compounds. Triplet harvesting and singlet harvesting for efficient OLEDs
10.1016/j.ccr.2011.01.042 · 2011 · External reference
Design of efficient thermally activated delayed fluorescence materials for pure blue organic light emitting diodes
10.1021/ja306538w · 2012 · External reference
Recent progress of narrowband TADF emitters and their applications in OLEDs
10.1039/d0tc02682d · 2020 · External reference
Improving processability and efficiency of resonant TADF emitters: a design strategy
10.1002/adom.201901627 · 2020 · External reference
Purely organic thermally activated delayed fluorescence materials for organic light-emitting diodes
10.1002/adma.201605444 · 2017 · External reference
Aromatic-imide-based thermally activated delayed fluorescence materials for highly efficient organic light-emitting diodes
10.1002/anie.201704435 · 2017 · External reference
Highly twisted thermally activated delayed fluorescence (TADF) molecules and their applications in organic light-emitting diodes (OLEDs)
2023 · External reference
Thermally activated delayed fluorescence material: an emerging class of metal-free luminophores for biomedical applications
10.1002/advs.202102970 · 2021 · External reference
Indolizine-benzophenone hybrid acceptors enable TADF materials for bioimaging and photodynamic therapy in living cells
10.1016/j.cclet.2025.111721 · 2026 · External reference
Thermally activated delayed fluorescence in aqueous solution: preparation, performance, and biomedical application
2026 · External reference
A three-dimensional ratiometric sensing strategy on unimolecular fluorescence-thermally activated delayed fluorescence dual emission
10.1038/s41467-019-08684-2 · 2019 · External reference
Unresolved reference
1991 · External reference
Photophysics of thermally activated delayed fluorescence molecules
10.1088/2050-6120/aa537e · 2017 · External reference
Unresolved reference
1989 · External reference
Getting the right twist: influence of donor–acceptor dihedral angle on exciton kinetics and singlet–triplet gap in deep blue thermally activated delayed fluorescence emitter
10.1021/acs.jpcc.9b08269 · 2019 · External reference
Tuning the twist angle of thermally activated delayed fluorescence molecules via a dendronization strategy: high-efficiency solution-processed non-doped OLEDs
10.1039/c7tc00119c · 2017 · External reference
Optimal dihedral angle in twisted donor-acceptor organic emitters for maximized thermally activated delayed fluorescence
2022 · External reference
Structure-induced optoelectronic properties of phenothiazine-based materials
10.1039/d0tc03421e · 2020 · External reference
The interplay of conformations and electronic properties in N-aryl phenothiazines
10.1039/d0qo00182a · 2020 · External reference
Regio- and conformational isomerization critical to design of efficient thermally-activated delayed fluorescence emitters
10.1038/ncomms14987 · 2017 · External reference
Control of the dual emission from a thermally activated delayed fluorescence emitter containing phenothiazine units in organic light-emitting diodes
10.1039/c8ra10393c · 2019 · External reference
Novel phenoxazine-benzonitrile and phenothiazine-benzonitrile donor-acceptor molecules with thermally activated delayed fluorescence (TADF)
10.1016/j.dyepig.2019.108114 · 2020 · External reference
Enabling red thermally activated delayed fluorescence by increasing the push–pull strength in naphthalimide-phenothiazine derivatives
10.1039/d3tc01939j · 2023 · External reference
Spin–orbit charge transfer intersystem crossing and thermal activation delayed fluorescence (TADF) studies of compact orthogonal anthraquinone phenothiazine derivatives
10.1039/d3nj03488g · 2023 · External reference
Exploring the theoretical foundations of thermally activated delayed fluorescence (TADF) emission: a comprehensive TD-DFT study on phenothiazine systems
2024 · External reference
Phenothiazine-based TADF emitters with dual conformations for single-molecule white OLEDs
10.1039/d5sc04370k · 2026 · External reference
Thermally activated delayed fluorescence in phenothiazine–phenoxazine–quinoline conjugates and electroluminescence
10.1021/acs.jpcc.5c06119 · 2026 · External reference
Potent strategy towards strongly emissive nitroaromatics through a weakly electron-deficient core
10.1039/d1sc03670j · 2021 · External reference
Making nitronaphthalene fluoresce
10.1021/acs.jpclett.1c02155 · 2021 · External reference
How to make nitroaromatic compounds glow: next-generation large X-shaped, centrosymmetric diketopyrrolopyrroles
10.1002/anie.202005244 · 2020 · External reference
Revisiting the non-fluorescence of nitroaromatics: presumption versus reality
10.1039/d1tc05423f · 2022 · External reference
Nitroaromatics as n-type organic semiconductors for field effect transistors
10.1039/d0cc01236j · 2020 · External reference
Excited state dynamics and photochemistry of nitroaromatic compounds
10.1039/d1cc04999b · 2021 · External reference
Nonadiabatic dynamics simulation predict intersystem crossing in nitroaromatic molecules on a picosecond time scale
10.1002/cptc.201900108 · 2019 · External reference
Relaxation in the triplet manifold of 1-nitronaphthalene observed by transient absorption spectroscopy
10.1021/jp8087397 · 2009 · External reference
On the origin of ultrafast nonradiative transitions in nitro-polycyclic aromatic hydrocarbons: excited-state dynamics in 1-nitronaphthalene
10.1063/1.3272536 · 2009 · External reference
Competition between fluorescence and triplet production ruled by nitro groups in one-arm and two-arm styrylbenzene heteroanalogues
10.1039/d0pp00271b · 2020 · External reference
Fluorescent chromophores containing the nitro group: relatively unexplored emissive properties
10.1002/cplu.202000592 · 2020 · External reference
Heteroatom-mediated performance of dye-sensitized solar cells based on T-shaped molecules
10.1016/j.dyepig.2019.02.055 · 2019 · External reference
Photophysical features of coumarin 120 in reverse micelles
10.1016/j.molstruc.2018.07.019 · 2018 · External reference
Effect of Electron-donating substitution on the triplet state reactivities of 1-nitronaphthalene
10.1016/j.saa.2022.121997 · 2023 · External reference
Transient spectroscopic insights into Nitroindole’s T1 state: elucidating its intermediates and unique photochemical properties
10.1016/j.saa.2024.124555 · 2024 · External reference
Unresolved reference
2016 · External reference
A comprehensive electron wavefunction analysis toolbox for chemists, Multiwfn
10.1063/5.0216272 · 2024 · External reference
Solvatochromic dyes as solvent polarity indicators
10.1021/cr00032a005 · 1994 · External reference
The empirical treatment of solvent-solute interactions: 15 years of π*
10.1021/j100074a003 · 1994 · External reference
Transient IR spectroscopic observation of singlet and triplet states of 2-nitrofluorene: revisiting the photophysics of nitroaromatics
10.1021/acs.jpca.5b09125 · 2016 · External reference
Solvent-dependent dual fluorescence of the push-pull system 2-diethylamino-7-nitrofluorene
10.1039/c8cp00235e · 2018 · External reference
Unresolved reference
2009 · External reference
Free radical studies by resonance Raman spectroscopy: phenothiazine, 10-methylphenothiazine, and phenoxazine radical cations
10.1039/p29810000852 · 1981 · External reference
The influence of structure and conformation on electronic interactions of 4′-nitro-10-phenylphenothiazine
10.1002/jhet.5570210646 · 1984 · External reference