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Sulfonyl-Substituted Heteroleptic Cyclometalated Iridium(III) Complexes as Blue Emitters for Solution-Processable Phosphorescent Organic Light-Emitting Diodes (2016)
Journal Article
Benjamin, H., Zheng, Y., Batsanov, A., Fox, M., Al-Attar, H., Monkman, A., & Bryce, M. (2016). Sulfonyl-Substituted Heteroleptic Cyclometalated Iridium(III) Complexes as Blue Emitters for Solution-Processable Phosphorescent Organic Light-Emitting Diodes. Inorganic Chemistry, 55(17), 8612-8627. https://doi.org/10.1021/acs.inorgchem.6b01179

The synthesis is reported of a series of blue-emitting heteroleptic iridium complexes with phenylpyridine (ppy) ligands substituted with sulfonyl, fluorine, and/or methoxy substituents on the phenyl ring and a picolinate (pic) ancillary ligand. Some... Read More about Sulfonyl-Substituted Heteroleptic Cyclometalated Iridium(III) Complexes as Blue Emitters for Solution-Processable Phosphorescent Organic Light-Emitting Diodes.

Using Guest–Host Interactions To Optimize the Efficiency of TADF OLEDs (2016)
Journal Article
dos Santos, P. L., Ward, J. S., Bryce, M. R., & Monkman, A. P. (2016). Using Guest–Host Interactions To Optimize the Efficiency of TADF OLEDs. Journal of Physical Chemistry Letters, 2016(7), 3341-3346. https://doi.org/10.1021/acs.jpclett.6b01542

We show that the emitter and host combination must be optimized to minimize the reverse intersystem crossing (rISC) barrier and maximize thermally activated delayed fluorescence (TADF). The blue TADF emitter, 2,7-bis(9,9-dimethyl-acridin-10-yl)-9,9-d... Read More about Using Guest–Host Interactions To Optimize the Efficiency of TADF OLEDs.

Pendant Homopolymer and Copolymers as Solution-Processable Thermally Activated Delayed Fluorescence Materials for Organic Light-Emitting Diodes (2016)
Journal Article
Ren, Z., Nobuyasu, R. S., Dias, F. B., Monkman, A. P., Yan, S., & Bryce, M. R. (2016). Pendant Homopolymer and Copolymers as Solution-Processable Thermally Activated Delayed Fluorescence Materials for Organic Light-Emitting Diodes. Macromolecules, 49(15), 5452-5460. https://doi.org/10.1021/acs.macromol.6b01216

Materials that display thermally activated delayed fluorescence (TADF) have recently been identified as the third generation emitters for organic light-emitting diodes (OLEDs). However, there are only a few reported examples of polymeric TADF materia... Read More about Pendant Homopolymer and Copolymers as Solution-Processable Thermally Activated Delayed Fluorescence Materials for Organic Light-Emitting Diodes.

Rational Design of TADF Polymers Using a Donor–Acceptor Monomer with Enhanced TADF Efficiency Induced by the Energy Alignment of Charge Transfer and Local Triplet Excited States (2016)
Journal Article
Nobuyasu, R. S., Ren, Z., Griffiths, G. C., Batsanov, A. S., Data, P., Yan, S., …Dias, F. B. (2016). Rational Design of TADF Polymers Using a Donor–Acceptor Monomer with Enhanced TADF Efficiency Induced by the Energy Alignment of Charge Transfer and Local Triplet Excited States. Advanced Optical Materials, 4(4), 597-607. https://doi.org/10.1002/adom.201500689

The photophysics of thermally activated delayed fluorescence (TADF) in phenothiazine-dibenzothiophene-S,S-dioxide (PTZ-DBTO2) molecule is investigated in detail. First, it is shown that the proximity of local triplet excited states (3LE), e.g., 3D or... Read More about Rational Design of TADF Polymers Using a Donor–Acceptor Monomer with Enhanced TADF Efficiency Induced by the Energy Alignment of Charge Transfer and Local Triplet Excited States.

The interplay of thermally activated delayed fluorescence (TADF) and room temperature organic phosphorescence in sterically-constrained donor–acceptor charge-transfer molecules (2016)
Journal Article
Ward, J. S., Nobuyasu, R. S., Batsanov, A. S., Data, P., Monkman, A. P., Dias, F. B., & Bryce, M. R. (2016). The interplay of thermally activated delayed fluorescence (TADF) and room temperature organic phosphorescence in sterically-constrained donor–acceptor charge-transfer molecules. Chemical Communications, 52(12), 2612-2615. https://doi.org/10.1039/c5cc09645f

A series of phenothiazine–dibenzothiophene-S,S-dioxide charge-transfer molecules have been synthesized. Increasing steric restriction around the donor–acceptor bond significantly alters contributions from TADF and phosphorescence. Bulky substituents... Read More about The interplay of thermally activated delayed fluorescence (TADF) and room temperature organic phosphorescence in sterically-constrained donor–acceptor charge-transfer molecules.