Name | Trideca-1,1,1,2,2,3,3,4,4,5,5,6,6-fluorohexane |
Molecular Formula | C6F13H5 |
Molecular Weight | 338.09 |
Chemical Formula | C6H3F13 |
Molar Mass | 338.07 g/mol |
Appearance | Colorless liquid (expected, based on similar fluorinated hydrocarbons) |
Boiling Point | Low boiling point (estimated around -10 to 10 °C, due to weak intermolecular forces from fluorine substitution) |
Melting Point | Low melting point (estimated well below 0 °C) |
Density | Higher than water (estimated around 1.6 - 1.8 g/cm³ as fluorinated compounds are usually dense) |
Solubility In Water | Poorly soluble in water as it is a non - polar fluorinated hydrocarbon |
Solubility In Organic Solvents | Soluble in non - polar organic solvents like hexane, toluene |
Vapor Pressure | Relatively high vapor pressure (due to low molecular weight and weak intermolecular forces) |
Chemical Formula | C6H3F13 |
Molecular Weight | 338.07 |
Appearance | Colorless liquid |
Boiling Point | 45 - 46 °C |
Density | 1.627 g/cm³ |
Vapor Pressure | Data may vary with temperature |
Solubility | Insoluble in water, soluble in some organic solvents |
Flash Point | Non - flammable |
Refractive Index | Data may vary, around typical fluorocarbon values |
Stability | Stable under normal conditions |
Chemical Formula | C6H3F13 |
Molecular Weight | 300.07 g/mol |
Appearance | Colorless liquid |
Boiling Point | 56 - 57 °C |
Melting Point | -110 °C |
Density | 1.66 g/cm³ |
Vapor Pressure | 14.5 kPa (20 °C) |
Solubility In Water | Insoluble |
Flash Point | Non - flammable |
Refractive Index | 1.264 (20 °C) |
Trideca - 1, 1, 2, 2, 3, 3, 4, 4, 5, 5, 6, 6 - What is the Chinese name for fluorohexane?
Tridecafluoro-1, 1, 2, 2, 3, 3, 4, 4, 5, 5, 6, 6-fluorohexane, which is a fluorine-containing organic compound. According to its name, "tridecafluoro" indicates that there are thirteen fluorine atoms in the molecule; "1, 1, 2, 2, 3, 3, 4, 5, 5, 6-fluorohexane", where the number combination indicates the substitution of fluorine atoms at specific positions in the parent structure of hexane. Hexane is a straight-chain alkane with six carbon atoms, and these fluorine atoms replace hydrogen atoms in this distribution, so this compound is obtained. Such fluorine-containing organic compounds are used in many fields, such as some special materials, chemical additives, etc., and often play a key role due to their unique chemical properties, such as low surface energy and high chemical stability.
Trideca - 1, 1, 2, 2, 3, 3, 4, 4, 5, 5, 6, 6 - What are the main uses of fluorohexane?
"Tiangong Kaiwu" says: "Each thing has its own use, and each is suitable for its own use." Jin Yan and Trideca - 1, 1, 2, 2, 3, 4, 4, 5, 5, 6, 6 - fluorohexane, which are quite versatile.
This compound has extraordinary uses in the field of materials. Because of its unique fluorine-containing structure, it gives the material excellent water and oil repellent properties. In the textile industry, fabrics treated with this compound can resist water and oil stains, and do not damage the original breathability and softness of the fabric, making clothing durable and suitable for outdoor clothing and high-end home textiles.
In the field of surface treatment, it also shines brightly. It can form an ultra-thin and stable protective film on the surface of the object, reducing surface energy, reducing friction and wear, and improving the anti-fouling self-cleaning ability of the material. Such as glass, ceramics and other building materials after treatment, stains are difficult to adhere, easy to clean, widely used in building exterior and interior decoration materials.
In the field of electronics industry, Trideca - 1, 1, 2, 2, 3, 3, 4, 5, 5, 6, 6 - fluorohexane can be used as a protective coating for electronic components. Its excellent insulation properties and chemical stability can effectively protect electronic components from moisture, dust and chemical erosion, ensure the stable operation of electronic equipment, prolong the service life, and are indispensable in the production of electronic products such as mobile phones and computers. In addition, in some special chemical synthesis reactions, this compound can be used as a catalyst or reaction intermediate to assist in the synthesis of specific compounds and promote technological innovation and product upgrades in the chemical industry.
What are the physical properties of trideca - 1, 1, 2, 2, 3, 3, 4, 4, 5, 5, 6, 6 - fluorohexane?
"Tiangong Kaiwu" is a Chinese science and technology masterpiece, but the book does not contain "Trideca - 1, 1, 2, 2, 3, 3, 4, 4, 5, 5, 6, 6 - fluorohexane". However, according to today's chemical knowledge, its physical properties can be described.
This compound is called trideca-1, 1, 1, 2, 2, 3, 3, 4, 5, 5, 6, 6 - hexane. The introduction of fluorine atoms changes the intermolecular force. First, due to the extremely high electronegativity of fluorine, the surface tension of this compound may be extremely low, and its hydrophobicity is strong. It is like a lotus leaf that is not stained with water, and can become a waterproof and oil-proof material. Second, its boiling point may be affected. The increase of fluorine atoms, although the relative molecular weight increases, causes the intermolecular dispersion force to increase; however, the repulsion effect between fluorine atoms and the influence on the molecular structure, or the boiling point does not simply increase according to the relative molecular Third, the density may be higher than that of ordinary hexane derivatives due to the weight of fluorine atoms. Fourth, in terms of solubility, due to its hydrophobicity, it is difficult to dissolve in polar solvents, and may have a certain solubility in non-polar or weakly polar organic solvents.
Although this substance is not covered in "Tiangong Kaiji", according to the current chemical principles, it can be known that its physical properties are approximate, which can provide ideas for using this substance in materials, chemical industry and other fields.
Is Trideca - 1, 1, 2, 2, 3, 3, 4, 4, 5, 5, 6, 6 - fluorohexane chemically stable?
The chemical properties of this "tridecafluoro-1,1,1,2,2,3,3,4,4,5,5,6,6-fluorohexane" are quite stable under normal conditions. Due to its molecular structure, fluorine atoms are numerous and closely connected to carbon atoms. Fluorine atoms are highly electronegative, and the formed carbon-fluorine bond energy is quite high. It takes a lot of energy to break the bond, so it is not easy to participate in the reaction under normal chemical reaction conditions.
However, it should be noted that although it is stable under common circumstances, it may exhibit different chemical activities under extreme conditions, such as high temperature, high pressure and the presence of specific catalysts. High temperature and high pressure can give molecules enough energy to break the carbon-fluorine bond, and specific catalysts can reduce the activation energy of the reaction and promote it to react with other substances.
Furthermore, this compound contains many fluorine atoms, or has some special physical and chemical properties, such as surface activity, low surface tension, etc. These properties may also indirectly affect its chemical stability and reactivity. In short, although the chemical properties of "tridecafluoro-1,1,2,2,3,4,4,5,5,6,6-fluorohexane" are stable under normal conditions, it may also change under special conditions.
What are the methods for preparing Trideca - 1, 1, 2, 2, 3, 3, 4, 4, 5, 5, 6, 6 - fluorohexane?
There are several methods for preparing tridecafluoro-1, 1, 1, 2, 2, 3, 4, 5, 5, 6, 6-fluorohexane.
First, it can be prepared by the reaction of haloalkanes and fluorine-containing reagents. Take a suitable halohexane and mix it with a fluorinating reagent such as potassium fluoride under specific reaction conditions. This process requires the selection of a suitable solvent, such as dimethyl sulfoxide (DMSO), to facilitate the reaction. The reaction temperature and time also need to be carefully adjusted. Too high or too low temperature, too long or too short time may affect the yield and purity of the product. Generally speaking, under appropriate heating and stirring conditions, after several hours of reaction, halogen atoms can be gradually replaced by fluorine atoms, and then the target product can be formed. < Br >
Second, the addition reaction of olefins and fluorine-containing compounds can be used. An olefin containing six carbon atoms is selected to react with a fluorine-containing addition reagent. For example, under the action of a catalyst, the addition of olefins to trifluoromethylation reagents can introduce fluorine atoms. The key to this method lies in the choice of catalyst, and different catalysts have a great impact on the selectivity and activity of the reaction. Such as transition metal catalysts, with the coordination of suitable ligands, can effectively promote the occurrence of addition reactions, and can precisely control the addition position of fluorine atoms, thereby improving the yield of the target product.
Third, it can also be from the perspective of long chain construction of organic synthesis routes. The shorter carbon chain containing some fluorine atoms is first constructed, and then the carbon chain is gradually increased and the remaining fluorine atoms are introduced through carbon-carbon bond formation reactions, such as coupling reactions. This process involves a multi-step reaction, and each step requires strict control of the reaction conditions to ensure the smooth progress of each step and the purity of the product. Finally, trifluoride-1,1,1,2,2,3,4,5,6,6-fluorohexane is synthesized.