Vinylsilane
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| Names | |
|---|---|
| Preferred IUPAC name
Vinylsilane | |
| Systematic IUPAC name
Ethenylsilane[1] | |
| Identifiers | |
7291-09-0  | |
| ChemSpider | 73732  |
| Jmol interactive 3D | Image |
| PubChem | 81714 |
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| Properties | |
| C2H6Si | |
| Molar mass | 58.1545 g mol−1 |
| Appearance | Colorless to tan waxy solid[2] |
| Hydrolysis[2] | |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| verify (what is ?) | |
| Infobox references | |
Vinylsilane, also called vinyl silane or ethenyl silane, is an organic chemical with chemical formula C
2H
6Si or CH2=CH–SiH3. It is a derivative of silane.
Vinylsilane may also refer generically to any vinyl-substituted silane, such as vinyltrimethoxysilane or vinyltriethoxysilane. In this context it can refer to a monomer used for some copolymer plastics such as ethylene-vinyltrimethoxysilane and ethylene-vinyl acetate-vinyltrimethoxysilane. Vinyltrialkoxysilanes are also used as cross-linking agents during the manufacture of cross-linked polyethylene (PEX). The alkoxysilane moiety is reactive toward water, and in the presence of moisture, it forms silicon-oxygen-silicon bonds that cross-link the material to cure it. Moisture-curable polymers are used as electrical insulation in some kinds of cables and for water pipe in under-floor heating installations.
Vinyltrialkoxysilanes are also used as a coupling agents or adhesion promoters for treatment of glass fibers and particulate minerals in order to form stronger bonds with resin and produce fiberglass with better mechanical properties. Amino-functional silanes such as (3-aminopropyl)triethoxysilane and epoxy-functional silanes are used for the same purpose. The silane group attaches to the glass substrate via covalent Si-O-Si bond, while the resin reacts with the vinyl-, amino-, or epoxy- group and binds to it.