Tris 2 Phenylbenzo D Thiazole Iridium Iii
quinoline thiophene imidazole thiazole

TRIS[2-PHENYLBENZO[D]THIAZOLE]IRIDIUM(III)

Taiy Chemical

Specifications

HS Code

816778

Chemical Formula C36H24N3S3Ir
Molecular Weight 798.91 g/mol
Appearance Solid (usually)
Color Typically a colored solid, exact color may vary
Solubility Soluble in some organic solvents
Melting Point Data may vary depending on purity
Density Data may be limited and vary
Stability Stable under normal conditions, but sensitive to light and air in some cases
Coordination Geometry Octahedral around iridium(III)
Luminescence Properties May exhibit luminescence, relevant for optoelectronic applications
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General Information
Frequently Asked Questions
What is the main application field of TRIS [2 - PHENYLBENZO [D] THIAZOLE] IRIDIA (III)
"TRIS [2-Phenylbenzo [D] thiazole] iridium (III) " This material has a wide range of main application fields. In the field of lighting, due to its unique luminous properties, it can be used to manufacture organic Light Emitting Diode (OLED) lighting equipment. OLED lighting has become a new favorite in the lighting industry due to its advantages of lightness, energy saving and soft light. This compound can precisely control the luminous color and efficiency, providing the possibility to create a variety of lighting scenarios, such as warm home lighting, or bright light in commercial places.
In the display field, it is also a key material. Today, OLED displays are widely used in mobile phones, TVs and other electronic devices, and are very popular because of their high contrast, wide viewing angle and fast response speed. " TRIS [2-Phenylbenzo [D] thiazole] iridium (III) "acts as a luminescent material in it, ensuring that the display screen presents a clear and gorgeous image, greatly improving the display quality.
In the field of scientific research, it is often used as a fluorescent probe. Due to its sensitive fluorescence properties to environmental changes, it can detect specific substances or physicochemical parameters in organisms, and help biomedical research in depth, such as detecting intracellular ion concentrations, pH changes, and helping researchers understand the mysteries of life activities.
Furthermore, it has made a name for itself in the field of photocatalysis. It can absorb light energy to generate highly active electrons, driving various chemical reactions, such as reactions that are difficult to catalyze in organic synthesis, improving reaction efficiency and selectivity, opening up new paths for organic synthetic chemistry, and promising a greener and more efficient synthesis route.
What are the physicochemical properties of TRIS [2 - PHENYLBENZO [D] THIAZOLE] IRIDIA (III)
This compound is called [2-phenylbenzo [d] thiazole] iridium (III), which is a metal-organic complex. Its physical and chemical properties are unique and have attracted much attention in the fields of chemistry and materials science.
In terms of physical properties, it may be a solid under normal conditions, and has a specific crystal structure due to strong intermolecular forces. Melting point or higher, which is attributed to the stable coordination bonds between metals and ligands and the interaction between ligands, requiring more energy to destroy the lattice and cause it to melt.
In terms of solubility, because of its certain hydrophobicity, its solubility in water is low. However, in organic solvents such as dichloromethane and chloroform, due to the principle of similar miscibility, the solubility is better, which provides convenience for their solution processing and related reactions.
Excellent photophysical properties. The ligand structure makes the complex have strong fluorescence emission characteristics. Under suitable excitation light irradiation, the electrons jump to the excited state, and then jump back to the ground state through radiation and emit light. The luminous color varies according to the ligand structure and coordination environment. It is usually in the visible light region, such as green light and orange light. It has great potential for application in optoelectronic devices such as organic Light Emitting Diode (OLED).
Good chemical stability. The coordination bond between the metal-ligand is stable, and it is not easy to decompose at room temperature and pressure. However, in the case of strong oxidizing agents or reducing agents, the ligand or metal central valence state may change, triggering changes in the structure and properties of the complex. Under specific reaction conditions, it can be used as a catalyst to participate in organic reactions, promoting the reaction with the help of metal central activity and ligand electronic effects, showing unique chemical activity.
What is the synthesis method of TRIS [2 - PHENYLBENZO [D] THIAZOLE] IRIDIA (III)
To prepare TRIS [2-phenylbenzo [D] thiazole] iridium (III), the method is as follows:
First, you need to prepare the raw materials, find the 2-phenylbenzo [D] thiazole, and find the compounds containing iridium, such as potassium hexachloroiridium (III) acid, etc., which are all necessary.
Then, in a clean reaction vessel, inject an appropriate amount of organic solvent, such as dichloromethane, N, N-dimethylformamide, etc., as the reaction medium. Pour the prepared 2-phenylbenzo [D] thiazole and the iridium-containing compound into it in an appropriate ratio. This ratio is crucial and must be weighed accurately. Generally speaking, the molar ratio of 2-phenylbenzo [D] thiazole to iridium-containing compounds may be about 3:1, but it can also be fine-tuned depending on the specific situation.
Then, slowly heat up to bring the reaction system to a suitable temperature. This temperature is usually between 80 and 120 ° C, and the temperature can be controlled by oil bath or water bath. At the same time, continuously stir with a magnetic stirrer to allow the reactants to be fully mixed and contacted to accelerate the reaction.
When reacting, pay attention to the progress of the reaction. The consumption of reactants and the generation of products can be monitored regularly by means of thin layer chromatography or high performance liquid chromatography. When the reaction is complete, that is, the reactant is almost exhausted, and the amount of product generated does not increase significantly, the reaction can be terminated.
After the reaction is completed, the reaction solution is cooled to room temperature. Then, the separation and purification steps are carried out. First, most of the organic solvents are removed by vacuum distillation. Then, by column chromatography, silica gel is used as the stationary phase, and a suitable eluent is selected, such as the mixture of petroleum ether and ethyl acetate, to separate the product from the impurities. After elution, collection, concentration, etc., the pure TRIS [2-phenylbenzo [D] thiazole] iridium (III) product can be obtained, and then the residual solvent is removed by vacuum drying to obtain the final product.
TRIS [2 - PHENYLBENZO [D] THIAZOLE] IRIDIA (III) What are the precautions during use
If TRIS [2 - PHENYLBENZO [D] THIAZOLE] IRIDIUM (III) is used, there are several ends that should be paid attention to.
First, the properties of this substance are specific, and the user must know its physicochemical properties in detail. Its chemical structure is unique, stability, solubility, etc. have their own characteristics. Among different solvents, the solubility may vary. If the solution used is used, it must first know its solubility in the solvent used to prevent precipitation, crystallization, etc., causing the experiment or production to fail to meet expectations.
Second, it is related to its reactivity. When this substance participates in the reaction, the reaction conditions are crucial. Temperature, pH, reaction time, etc. can all affect the process and product of the reaction. If the temperature is too high or causes it to decompose, if it is too low, the reaction will be slow or even difficult to occur. And the change of pH, or the change of the charge state of the compound, then affect its reaction performance.
Third, the matter of safety should not be ignored. Although there is no conclusive evidence that it is highly toxic, chemical substances have many latent risks. When operating, use protective equipment, such as gloves, goggles, etc., to avoid contact with the skin and eyes. If it is in a poorly ventilated place, inhaling its dust or volatile gas may also be harmful to health.
Fourth, the method of storage is also exquisite. It should be placed in a cool, dry and dark place to prevent it from deteriorating due to environmental factors. Isolating air and water vapor can ensure its stability and prolong its service life. If it is not stored properly, its performance will change, and it will be difficult to achieve the expected effect.
Where TRIS [2 - PHENYLBENZO [D] THIAZOLE] IRIDIUM (III) is used, it must be paid attention to the properties, reaction, safety, and storage to make the best use of it and avoid all kinds of errors.
What are the advantages of TRIS [2 - PHENYLBENZO [D] THIAZOLE] IRIDIA (III) over other similar compounds
Fu TRIS [2-phenylbenzo [D] thiazole] iridium (III) has outstanding advantages over other similar compounds. The advantage of this compound is its excellent luminous performance. At the end of the luminous efficiency, it far exceeds its peers. Like a luminous pearl shining brightly, it stands out among all luminous materials and can significantly improve the luminous efficiency. It is promising in the fields of lighting and display.
Furthermore, its stability is particularly excellent. Just like the strength of a rock, it can withstand wind and rain without shaking. Under different environmental conditions, such as temperature changes and humidity differences, it can be stable and self-sustaining, maintaining its chemical and physical properties constant. This stability allows it to last for a long time in practical applications and reduce the risk of performance degradation due to environmental factors.
And its spectral modulation characteristics are also a must. Like a palette in the hands of a skilled craftsman, the spectrum can be precisely adjusted according to actual needs to be suitable for various specific scenarios. For example, in the field of medical testing, specific spectra can be modulated according to the needs of detection to achieve the best detection effect; in scientific research experiments, it can also provide suitable spectral conditions according to different experimental purposes.
In summary, TRIS [2-phenylbenzo [D] thiazole] iridium (III) has significant advantages over other similar compounds in terms of luminous efficiency, stability and spectral modulability, making it a rare product in the field of materials.