Methyltrimethoxysilane
 | |
| Names | |
|---|---|
| IUPAC name
Trimethoxy(methyl)silane | |
| Other names
MTM, Trimethoxymethylsilane | |
| Identifiers | |
| 1185-55-3 | |
| 3D model (Jmol) | Interactive image |
| ChemSpider | 13803 |
| ECHA InfoCard | 100.013.350 |
| PubChem | 14456 |
| |
| |
| Properties | |
| C4H12O3Si | |
| Molar mass | 136.22 g·mol−1 |
| Appearance | Colorless liquid |
| Density | 0.955 g/cm3 |
| Boiling point | 102–104 °C (216–219 °F; 375–377 K) |
| hydrolysis | |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Methyltrimethoxysilane is an organosilicon compound with the formula CH3Si(OCH3)3. It is a colorless, free-flowing liquid. It is a crosslinker in the preparation of polysiloxane polymers.[1][2]
Preparation, structure and reactivity
Methyltrimethoxysilane is usually prepared from methyltrichlorosilane and methanol:
- CH3SiCl3 + 3 CH3OH → CH3Si(OCH3)3 + 3 HCl
Alcoholysis of alkylchlorosilanes typically proceeds via an SN2 mechanism. Inversion of the configuration is favored during nucleophilic attack when displacing good leaving groups, such as chloride.[3] In contrast, displacement of poor leaving groups, such as alkoxide, retention is favored.[4]
Methyltrimethoxysilane is tetrahedral and is often described as sp3 hybridized. It has idealized C3v point symmetry.
Hydrolysis of MTM proceeds both under acidic and basic conditions. Under acid conditions, rates of successive hydrolyses for methyltrimethoxysilane decreases with each step. Under basic condition the opposite is true.[1]
References
- 1 2 Brinker, C.J. (1988). "Hydrolysis and condensation of silicates: Effects on structure". Journal of Non-Crystalline Solids. 100: 31. Bibcode:1988JNCS..100...31B. doi:10.1016/0022-3093(88)90005-1.
- ↑ Kuroda, Kazuyuki; Shimojima, Atsushi; Kawahara, Kazufumi; Wakabayashi, Ryutaro; Tamura, Yasuhiro; Asakura, Yusuke; Kitahara, Masaki (2014). "Utilization of Alkoxysilyl Groups for the Creation of Structurally Controlled Siloxane-Based Nanomaterials". Chemistry of Materials. 26: 211. doi:10.1021/cm4023387.
- ↑ Stephan, Pawlenko (1986). Organosilicon Chemistry. Berlin: Walter de Gruyter. ISBN 9780899252025.
- ↑ Colvin, W. Ernest, Silicon in Organic Synthesis, Butterworth and Co Ltd, 1981.