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Usage

Uses

Given the lack of specific applications provided in the materials, the following uses are inferred based on the properties of the constituent elements and similar compounds:
Used in Advanced Materials Industry:
Iridium, bis[2-(2-benzothiazolyl-κN3)phenyl-κC]is used as a component in the development of advanced materials for its potential to contribute to the creation of materials with unique properties, such as high density and corrosion resistance, which are valuable in various industrial applications.
Used in Pharmaceutical Research:
In the pharmaceutical industry, Iridium, bis[2-(2-benzothiazolyl-κN3)phenyl-κC]may be utilized in research for new drug development, leveraging the benzothiazole group's presence, which is known to be a part of various pharmaceutical compounds.
Used in Chemical Science Research:
Iridium,bis[2-(2-benzothiazolyl-κN3)phenyl-κC]could be employed in chemical science research as a subject for studying the effects of combining Iridium with heterocyclic compounds, potentially leading to new insights or discoveries in chemical synthesis and material properties.

Upstream product

• 123-54-6 acetylacetone 

Relevant academic research and scientific papers

Probing the effects of the number and positions of –OCH3 and –CN substituents on color tuning of Ir(III) complex derivatives through a joint computational and experimental study

We performed a joint theoretical and experimental study on sixteen Ir(III) complexes bearing a similar molecular platform of bis(2-phenylbenzothiozolato-N,C2’) iridium(III) (acetylacetonate) by grafting – OCH3 group and/or – CN group on different positions of the C-related arene moiety of the C^N ligand (Cring). Our results reveal that the introduction of – CN renders an overall drop in the FMO energy levels while a reverse increase is observed for – OCH3. The ortho- and para-sites of the C-ring are more effective substitution positions to modulate the HOMO energy level due to the fact that the electronic density of HOMO mainly locates at them while the meta-site would induce a stronger impact on LUMO since the electronic density of LUMO mainly distributes over the position. Utilizing the synergistic effects of the substituents and the substituted positions, a wide color-tuning range from 479 nm to 637 nm was achieved, which covers nearly the whole window of visible spectrum. In particular, the tri-substituted Ir35mo4cn complex (λemmax=637 nm) may be a potential candidate for high efficiency red OLEDs materials due to its greatly enhanced absorption processes, relatively higher3MLCT (%), lower ΔES1–T1, enlarged separation between3MLCT/π–π* and3MC d–d states, and good hole and particle-transporting performances. Finally, six representative complexes were synthesized and their spectra were determined, which confirm the reliability of our computational strategy.

Orange phosphorescent Ir(III) complexes consisting of substituted 2-phenylbenzothiazole for solution-processed organic light-emitting diodes

Orange phosphorescent iridium(III) complexes, (DMBT)2Ir(acac) and (TBT)2Ir(acac), based on either 2-(3,4-dimethylphenyl)benzo[d]thiazole (DMBT) or 2-(4-(trimethylsilyl)phenyl)benzo[d]thiazole (TBT) as the cyclometalated main ligands