Competitive Di-Μ-Iodobis(P-Cymene)Iodoruthenium(Ii) prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to
sales7@bouling-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@bouling-chem.com
As a leading Di-Μ-Iodobis(P-Cymene)Iodoruthenium(Ii) supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
What is the chemical structure of di-μ-iodobis (p-cymene) iodoruthenium (II)?
Di - μ - iodo bis (p - cymene) iodoruthenium (II) is a chemical substance. Its transformation is interesting. In this compound, ruthenium (II) represents the central atom, with its,
There are also iodine atoms coordinated in the center of ruthenium. The atoms and radicals combine in this way to form the specialization of Di - μ - io dobis (p-cymene) iodoruthenium (II). This makes the compound have both the gold properties of ruthenium, and the properties of p-cymene and iodine atoms. It shows a special activity in the reaction, and the study of chemistry provides the possibility of enrichment.
What are the main application fields of di-μ-iodobis (p-cymene) iodoruthenium (II)
Di-μ-iodobis (p-cymene) iodoruthenium (II) is an important compound in the field of metal-organic chemistry. Its main application fields are quite extensive.
In the field of organic synthesis, this compound often acts as a catalyst. Due to its unique electronic structure and coordination environment, it can effectively catalyze many organic reactions. For example, carbon-carbon bond formation reactions, such as the Suzuki reaction, can promote the coupling of aryl halides and aryl boric acids under mild conditions to form biaryl compounds. This reaction is crucial in many fields such as drug synthesis and materials science, and can help build the skeleton of complex organic molecules.
In the field of materials science, it also has extraordinary functions. It can participate in the preparation of materials with special optoelectronic properties. Through its catalytic action, it can regulate the molecular structure and aggregation state of the material, thereby affecting the conductivity and luminescence properties of the material. For example, in the preparation of organic Light Emitting Diode (OLED) materials, it can help synthesize luminescent materials with specific structures and improve the luminous efficiency and stability of the device.
Furthermore, it has also emerged in the field of biomedical research. Due to its metal center properties, it can interact specifically with biomolecules. Some studies have shown that it may be used as a potential anti-cancer drug. By binding to specific targets in cancer cells, it interferes with the normal physiological activities of cancer cells, thereby inhibiting the growth and proliferation of cancer cells.
Di-μ-iodobis (p-cymene) iodoruthenium (II) has shown significant application potential in the fields of organic synthesis, materials science, and biomedicine, providing powerful tools and approaches for many scientific research and practical applications.
What is the synthesis method of di-μ-iodobis (p-cymene) iodoruthenium (II)
Di - μ - io dobis (p-cymene) iodoruthenium (II) can be prepared according to the following ancient method.
Take an appropriate amount of p-cymene (p-cymene) and place it in a clean reactor. The p-isopropylbenzene needs to be purified by distillation to remove impurities and maintain its purity. Then, measure a certain amount of ruthenium iodide and slowly add it to the kettle. The amount of ruthenium iodide should be accurately weighed according to stoichiometry to achieve the best reaction effect.
Inert gas, such as nitrogen, is introduced into the kettle to drain the air in the kettle to prevent oxidation of the reactants. Then, slowly raise the temperature to make the reaction system reach an appropriate temperature, about 100-150 degrees Celsius. The heating process needs to be slow and stirred continuously to make the reactants fully mixed and promote the reaction to proceed uniformly.
When reacting, pay close attention to the conditions in the kettle to observe the changes in its color, pressure, etc. After several hours of reaction, the reaction in the kettle gradually becomes stable, slightly cold, and drops to about room temperature. Then, the reaction product is moved to a separation device and extracted with an appropriate solvent, such as dichloromethane. After extraction, the product is purified by distillation, recrystallization, etc.
When recrystallizing, select a suitable solvent, such as ethanol-water mixed solvent, control the temperature and solvent ratio, and make the product crystallize and precipitate. Filter the crystals and dry them at low temperature to obtain Di - μ - io dobis (p-cymene) iodoruthenium (II). The whole process requires strict compliance with the operating procedures and attention to detail to obtain a purer product.
How stable is di-μ-iodobis (p-cymene) iodoruthenium (II)?
Di - μ - io dobis (p-cymene) iodoruthenium (II) is also a chemical substance. Its qualitative transformation and the preservation of this substance. In this compound, the atom is more than + 2, and the molecule contains iodine and propylbenzene (p-cymene).
From the molecule, the combination of p-cymene is coordinated with its aromatic daughter cloud atoms to form a certain framework. The iodine atom is also coordinated, which does not affect the daughter cloud density of the central atom, and has a special effect on the molecule. Its qualitative can be determined. First, the weak of the transformation.
Furthermore, the external environment has a large impact on its qualitative stability. Under normal conditions, if it is exposed to dryness, oxidation or the environment of the original material, this compound can maintain its phase stability. However, in case of moisture, water molecules may affect their action and break the coordination, resulting in a decrease in their qualitative. Moreover, the acidic environment may also cause reactions and make the molecule change.
The reduction in the degree of resistance is also due to. At high temperatures, the molecular energy increases, and the coordination vibration increases to a certain extent. Therefore, to preserve this object, it is appropriate to use it in a dry, dry and inert environment, so that it can maintain its quality and be effective in chemical research and related applications.
What is the catalytic performance of di-μ-iodobis (p-cymene) iodoruthenium (II) in the reaction?
Di-μ-iodobis (p-cymene) iodoruthenium (II) is an important metal-organic compound that exhibits unique catalytic properties in many chemical reactions. Its catalytic properties can be discussed from the following aspects.
First of all, this compound often exhibits excellent activity in carbon-carbon bond formation reactions. For example, in cross-coupling reactions, it can effectively promote the formation of stable carbon-carbon bonds between different organic fragments. This is because the central ruthenium atom has a suitable electron cloud density and spatial configuration, which can efficiently coordinate with substrate molecules, thereby reducing the activation energy of the reaction and accelerating the reaction process.
Furthermore, in some reactions involving the formation of carbon-heteroatom bonds, Di-μ-iodobis (p-cymene) iodoruthenium (II) can also play a significant catalytic effect. It can precisely catalyze the reaction between organic molecules and heteroatom-containing reagents, realize the introduction of heteroatom functional groups, and exhibit good selectivity. This selectivity is due to its unique molecular structure, which can accurately identify and locate substrate molecules.
In addition, this compound also has good catalytic activity for some special organic synthesis reactions, such as cyclization reactions. It can induce intra-molecular reactions of substrate molecules to construct various cyclic compounds. Its catalytic activity is not only reflected in the improvement of the reaction rate, but also in the effective control of the structure and stereochemistry of the product.
However, the catalytic performance of this compound is also affected by many factors. Such as reaction temperature, solvent properties, substrate structure and concentration, etc., all have an effect on its catalytic activity and selectivity. Only under suitable reaction conditions can its catalytic advantages be fully realized to achieve efficient and highly selective organic synthesis reactions.