Thiodi 4 1 Phenylene Bis Diphenylbis Oc 6 11 Hexafluoroantimonate
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
(thiodi-4,1-phenylene)-bis-(diphenylbis)(OC-6,11)hexafluoroantimonate
Chemical Formula (C36H28S)2SbF6
Molecular Weight 1163.69 g/mol
Appearance Typically a solid, color may vary depending on purity and preparation
Solubility Soluble in some organic solvents, details can vary based on solvent type
Melting Point Specific melting point data would require experimental determination
Density Density values would need to be experimentally measured
Stability Stable under normal conditions but may react with strong oxidizing agents
Reactivity Can participate in redox reactions due to the presence of metal and organic moieties
Electrical Conductivity May exhibit some electrical conductivity in solution depending on dissociation
Chemical Formula (C24H18S)2·2SbF6
Molecular Weight 1055.46 g/mol
Appearance Typically a solid, color may vary
Solubility Soluble in some organic solvents
Melting Point Data may vary, specific conditions required for determination
Stability Stable under normal conditions but may react with strong oxidants
Toxicity Potential toxicity, fluoride and antimony components may pose risks
Electrical Conductivity May show some conductivity in solution or molten state
Chemical Formula (C24H18S)2·2SbF6
Molecular Weight 1058.18 g/mol
Appearance Typically a solid, color may vary
Solubility Soluble in some organic solvents
Vapor Pressure Very low (as a solid)
Stability Stable under normal conditions, but may react with strong oxidants
Hazard Class May be harmful if swallowed, inhaled or in contact with skin; fluoride salts may be corrosive
Chemical Formula (C44H32S)2SbF6
Molecular Weight 1054.79 g/mol
Appearance Typically a solid
Color Varies (usually light - colored solids)
Solubility In Common Solvents Soluble in some organic solvents like dichloromethane
Thermal Stability Can decompose upon heating, details depend on conditions
Electrical Conductivity May show some conductivity in solution due to ion dissociation
Crystal Structure Complex, determined by X - ray diffraction
Reactivity Can react with nucleophiles due to the presence of the antimony - fluorine moiety
FAQ

What is the main application field of (thiodi- 4,1-phenylene) -bis- (diphenylbis) (OC-6,11) hexafluoroantimonate

(Thiobis-4,1-phenylene) -bis- (diphenylbis) (OC-6,11) hexafluoroantimonate has a wide range of main application fields. In the field of electronic materials, due to its unique electrical properties, it can be used as an excellent conductive medium to help electronic devices conduct electrical energy efficiently and make them operate stably. In the field of catalysis, its unique chemical structure can act as a catalyst to greatly improve the reaction rate and efficiency in specific chemical reactions, achieving the purpose of efficient synthesis. In the field of optical materials, it can have a specific effect on light, providing key materials for the manufacture of optical instruments and helping them achieve unique optical functions. And in material science research, as a new type of material, it is available for researchers to explore its performance and application potential, and contribute to the development of material innovation. It plays an important role in many industrial and scientific research scenarios and promotes continuous progress in related fields.

What are the physical properties of (thiodi- 4,1-phenylene) -bis- (diphenylbis) (OC-6,11) hexafluoroantimonate

(Thiobis-4,1-phenylene) -bis- (diphenylbis) (OC-6,11) hexafluoroantimonate, this is a chemical substance with unique physical properties.

Looking at its shape, it may be a crystalline solid under normal conditions, with a regular geometric shape or a unique luster under light, just like a natural crystal jade, emitting a mysterious shimmer. Its color may be colorless and transparent, like pure water, or slightly colored, like a light glow in the early morning sky, depending on its purity and microstructure.

When it comes to solubility, this substance may exhibit good solubility properties in specific organic solvents. For example, in some aromatic hydrocarbon solvents, its molecules are like smart fish, which can blend with solvent molecules and disperse uniformly to form a clear solution. In water, due to its structural characteristics or poor solubility, it is like a stubborn stone entering water, and it is difficult to melt with water.

In addition to its melting point and boiling point, the melting point may be in a certain temperature range, and a specific amount of heat is required to break its lattice structure and convert it from a solid state to a liquid state. Like a sleeping thing, when it meets the right warmth, it will slowly wake up. The boiling point is higher, and when enough energy is provided to overcome the interaction force between molecules, it can be turned into a gaseous state to escape.

Its density is also an important physical property, or similar to the density of common organic compounds, which is a key parameter when measuring its state and behavior in different environments.

In addition, the conductivity of the substance may be expressed by the distribution and movement of electrons in its structure. Under certain conditions, electrons may be able to transfer between molecules, exhibiting certain conductivity, just like an electric current traveling through an invisible channel.

The above is a summary of the physical properties of (thiobis-4,1-phenylene) -bis- (diphenyl bis) (OC-6,11) hexafluoroantimonate.

Is (thiodi- 4,1-phenylene) -bis- (diphenylbis) (OC-6,11) hexafluoroantimonate chemically stable?

The chemical stability of (thiobis-4,1-phenylene) -bis- (diphenylbis) (OC-6,11) hexafluoroantimonate is related to many aspects.

This compound has a unique structure and is cleverly connected by specific atoms and groups. Among them, thiobis-4,1-phenylene provides the basic skeleton of the molecule. This part of the structure is relatively stable. Due to the conjugated system of the benzene ring, it endows the molecule with certain rigidity and stability.

Bis- (diphenyl bis) structure further enhances the stability of the molecule. In the diphenyl structure, the interaction between the benzene rings may be π-π stacking, which makes the parts in the molecule more closely bound and less prone to structural changes.

And (OC-6,11) hexafluoroantimonate part, hexafluoroantimonate ion has certain coordination ability and stability. Under suitable conditions, it can form a stable coordination structure with other parts, so that the whole compound tends to be stable.

However, the stability of chemical properties is not absolute. If placed under extreme conditions, such as high temperature and strong acid-base environment, its stability may be challenged. High temperature can intensify the vibration of chemical bonds in molecules. If the energy is sufficient, the chemical bonds may break, causing structural changes. Strong acid-base environment, or reaction with some groups in the compound, breaks the original structure.

Overall, under conventional conditions, (thiobi-4,1-phenylene) -bis- (diphenylbis) (OC-6,11) hexafluoroantimonate has certain chemical stability, but in the face of extreme conditions, its stability needs to be reconsidered.

What is the preparation method of (thiodi- 4,1-phenylene) -bis- (diphenylbis) (OC-6,11) hexafluoroantimonate

The preparation of (thiodi - 4,1 - phenylene) -bis- (diphenylbis) (OC - 6,11) hexafluoroantimonate requires fine steps and suitable materials.

First, prepare the necessary starting materials. Among them, the sulfur-containing aromatic compound needs to be purified several times to ensure its purity. The matching diphenyl-containing ligands must also be strictly purified to remove impurities before they can be used. These two are the core parts of the target product.

Then, in a suitable reaction vessel, an oxygen-free environment is created with an inert gas such as nitrogen or argon. This is because the reaction system is sensitive to oxygen, and the oxygen-free environment can prevent unnecessary oxidation side reactions. Dissolve the purified starting material in a suitable organic solvent, such as anhydrous dichloromethane or acetonitrile, according to a precise stoichiometric ratio. Stir well to fully disperse the material.

Next, slowly add hexafluoroantimonate compounds. This process should control the speed. If it is too fast, the reaction will easily get out of control. After adding, continue to stir, or apply moderate heating as needed to promote the reaction. The heating temperature should be strictly controlled within a specific range, and the product should not be decomposed if it is too high, and the reaction should not be too slow if it is too low.

During the reaction process, thin-layer chromatography (TLC) or high-performance liquid chromatography (HPLC) is commonly used to monitor. When the raw material point disappears, the product point is significant, indicating that the reaction is almost complete.

After the reaction is completed, pour the reaction mixture into an appropriate amount of precipitant, such as ether or n-hexane, to precipitate the product. The precipitate is collected by suction filtration, and then washed with cold organic solvent, except for unreacted raw materials and by-products.

Finally, the resulting crude product is further purified by recrystallization. Select a suitable mixed solvent, such as methanol-dichloromethane system, and recrystallize many times to obtain a high-purity (thiodi-4,1-phenylene) -bis- (diphenylbis) (OC-6,11) hexafluoroantimonate product. The whole preparation process, the purity of the material, the control of the reaction conditions and the separation and purification steps are all related to the quality and yield of the product, so it is necessary to be careful.

What is the price range of (thiodil-4,1-phenylene) -bis- (diphenylbis) (OC-6,11) hexafluoroantimonate in the market?

I don't know what you said about " (thiodi - 4,1 - phenylene) -bis- (diphenylbis) (OC - 6,11) hexafluoroantimonate" in the market price range. This is a rather professional and uncommon chemical, and its price is affected by many factors.

First, the purity has a great impact. If the purity is very high, almost perfect, and there is no impurity interference, the price will be high; if the purity is slightly inferior, containing some impurities, the price may drop slightly.

Second, the amount of output is also the key. If the output of this product is rare, it is difficult to obtain, such as rare treasures, the price is not cheap; if the mass production is quite abundant, the supply is sufficient, and the price may be more affordable.

Third, the market demand is about the price. If many industries are hungry and thirsty for its demand, the supply will exceed the demand, and the price will skyrocket; if there is little demand, few people will ask for it, and the price will not be high.

Fourth, the difficulty of preparation cannot be ignored. If the preparation method is complicated, high skills and rare raw materials are required, and the cost will be high, and the price will follow; if the preparation is relatively simple, the cost will be reduced, and the price may be close to the people.

However, I have searched all the books I know, but I have not obtained the exact price range of this product. Or you need to consult the chemical market merchants, professional chemical suppliers, or consult the latest chemical price directory to get a more accurate price range.