3102-79-2

Usage

Uses

Used in Protective Coatings Industry:
1H,1H,2H,2H-PERFLUORODECYLMETHYLDICHLOROSILANE is used as a surface modifier for enhancing the durability and resistance of protective coatings. Its hydrophobic and oleophobic properties contribute to the creation of coatings that are resistant to water, oil, and other liquids, thereby prolonging the lifespan and functionality of the coated materials.
Used in Water-Repellent Materials:
In the textile and fabric industry, 1H,1H,2H,2H-PERFLUORODECYLMETHYLDICHLOROSILANE is used as a treatment agent for imparting water-repellent properties to materials. This application is particularly beneficial for outdoor clothing, tents, and other textiles that require resistance to water absorption, ensuring comfort and performance in wet conditions.
Used in Easy-Clean Surfaces:
1H,1H,2H,2H-PERFLUORODECYLMETHYLDICHLOROSILANE is utilized as a component in the formulation of easy-clean surfaces. Its ability to repel liquids makes it an ideal additive for creating surfaces that are easier to clean and maintain, reducing the need for frequent cleaning and the use of harsh chemicals.
Used in Microelectronics:
1H,1H,2H,2H-PERFLUORODECYLMETHYLDICHLOROSILANE is employed in the microelectronics field as a material for creating protective layers and coatings. Its hydrophobic and oleophobic characteristics are advantageous in protecting sensitive electronic components from moisture and other environmental factors, thereby enhancing the reliability and performance of microelectronic devices.

InChI:InChI=1/C11H7Cl2F17Si/c1-31(12,13)3-2-4(14,15)5(16,17)6(18,19)7(20,21)8(22,23)9(24,25)10(26,27)11(28,29)30/h2-3H2,1H3

Upstream product

• 75-54-7 Dichloromethylsilane 
• 21652-58-4 1H,1H,2H-perfluorodecene 

Relevant academic research and scientific papers

Syntheses and Reaction of Metal Organics. XVII. Synthesis of Silane Coupling Agent Having Fluorocarbon Chain and Surface Modification of Glass Plate

Four silane coupling agents, 1H,1H,2H,2H-polyfluoroalkyl(dimethoxy)(methyl)silanes (1H,1H,2H,2H-henicosafluorododecyl(dimethoxy)(methyl)silane, C10F21C2H4Si(CH3)(OCH3)2, 1H,1H,2H,2H-heptadecafluorodecyl(dimethoxy)(methyl)silane, C8F17C2H4Si(CH3)(OCH3)2, 1H,1H,2H,2H-tridecafluorooctyl(dimethoxy)(methyl)silane, C6F13C2H4Si(CH3)(OCH3)2, and 1H,1H,2H,2H-nonafluorohexyl(dimethoxy)(methyl)silane, C4F9C2H4Si(CH3)(OCH3)2), were prepared by the hydrosilylation of dichloro(methyl)silane with the corresponding 1H,1H,2H,2H-polyfluoro-1-alkene in the presence of hydrogen hexachloroplatinate(IV), followed by the reaction with sodium methoxide.The surface modification of glass plate was attempted uisng these products.From measurements of the contact angles θ(deg) of water and oleic acid against a modified glass plate surface, the coupling agents were found to have high modification ability.The oxidation resistance of the modified glass surface was also investigated.

Fluorine-based organic polysilazane or preparation methode thereof

The present invention relates to a fluorine-based organic polysilazane or a method for manufacturing the same. More specifically, the present invention relates to: a polysilazane in which lyphophilic property is removed by introducing a fluorinated alkyl group; and a method for manufacturing the same. In order to achieve the object, the present invention is to manufacture the fluorine-based organic polysilazane by ammonolysis of perfluorodichlorosilane and halosilane under ammonia gas.COPYRIGHT KIPO 2020

Redistribution of dichlorosilanes and dihydridosilanes. Synthesis of chloro hydridosilanes

The redistribution of dichlorosilanes RSi(CH3)Cl2 and dihydridosilanes RSi(CH3)H2, prepared by reduction of the homologues dichlorosilanes, in the presence of a quaternary ammonium salt is presented. The influence of the nature of R (fluoroalkyl chain RFCH2CH2 with RF = CF3, C4F9, C8F17, alkyl chain R = C6H13 or aromatic R = C6H5) and of the temperature on the rate of the reaction is studied. The equilibrium constants and free enthalpies are calculated and discussed taking into account the nature of R. The new products described were characterized from I.R, 1H, 19F and 29Si NMR spectroscopies.