Methylsilane

Last updated
Methylsilane
Methylsilane.svg
Methylsilane-3D-balls.png
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.012.362 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 213-598-5
PubChem CID
  • InChI=1S/CH6Si/c1-2/h1-2H3
    Key: UIUXUFNYAYAMOE-UHFFFAOYSA-N
  • C[SiH3]
Properties
CH6Si
Molar mass 46.14 g/mol
AppearanceColorless gas [1]
Density 0.628 g cm−3
Melting point −157 °C (−251 °F; 116 K)
Boiling point −57 °C (−71 °F; 216 K)
Hazards
GHS labelling:
GHS-pictogram-flamme.svg GHS-pictogram-bottle.svg GHS-pictogram-exclam.svg
Danger
H220, H280, H312, H315, H319, H332, H335, H336
P210, P261, P264, P271, P280, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P332+P313, P337+P313, P362, P363, P377, P381, P403, P403+P233, P405, P410+P403, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Methylsilane is the organosilicon compound with the formula CH3SiH3. It is a colorless gas that ignites in air. It can be prepared by reduction of methyltrichlorosilane with lithium aluminium hydride. [2] It has been investigated as a precursor to silicon carbide. [3]

Methylsilane has been the subject of extensive theoretical analysis. [4]

Related Research Articles

Cyclopropene is an organic compound with the formula C3H4. It is the simplest cycloalkene. Because the ring is highly strained, cyclopropene is difficult to prepare and highly reactive. This colorless gas has been the subject for many fundamental studies of bonding and reactivity. It does not occur naturally, but derivatives are known in some fatty acids. Derivatives of cyclopropene are used commercially to control ripening of some fruit.

<span class="mw-page-title-main">Silylene</span> Chemical compound

Silylene is a chemical compound with the formula SiH2. It is the silicon analog of methylene, the simplest carbene. Silylene is a stable molecule as a gas but rapidly reacts in a bimolecular manner when condensed. Unlike carbenes, which can exist in the singlet or triplet state, silylene (and all of its derivatives) are singlets.

The bond-dissociation energy is one measure of the strength of a chemical bond A−B. It can be defined as the standard enthalpy change when A−B is cleaved by homolysis to give fragments A and B, which are usually radical species. The enthalpy change is temperature-dependent, and the bond-dissociation energy is often defined to be the enthalpy change of the homolysis at 0 K, although the enthalpy change at 298 K is also a frequently encountered parameter.

<span class="mw-page-title-main">Europium(III) chloride</span> Chemical compound

Europium(III) chloride is an inorganic compound with the formula EuCl3. The anhydrous compound is a yellow solid. Being hygroscopic it rapidly absorbs water to form a white crystalline hexahydrate, EuCl3·6H2O, which is colourless. The compound is used in research.

<span class="mw-page-title-main">Sulfur monoxide</span> Chemical compound

Sulfur monoxide is an inorganic compound with formula SO. It is only found as a dilute gas phase. When concentrated or condensed, it converts to S2O2 (disulfur dioxide). It has been detected in space but is rarely encountered intact otherwise.

<span class="mw-page-title-main">Trimethylsilyl</span>

A trimethylsilyl group (abbreviated TMS) is a functional group in organic chemistry. This group consists of three methyl groups bonded to a silicon atom [−Si(CH3)3], which is in turn bonded to the rest of a molecule. This structural group is characterized by chemical inertness and a large molecular volume, which makes it useful in a number of applications.

<span class="mw-page-title-main">Fluoroantimonic acid</span> Chemical compound

Fluoroantimonic acid is a mixture of hydrogen fluoride and antimony penta­fluoride, containing various cations and anions. This substance is a superacid that can be over a billion times stronger than 100% pure sulfuric acid in terms of its protonating ability measured by Hammett function. It even protonates some hydro­carbons to afford pentacoordinate carbo­cations. Fluoro­antimonic acid is corrosive. For example, it cannot be contained directly in glass carboys, as it attacks glass, but can be stored in containers lined with PTFE (Teflon).

<span class="mw-page-title-main">Organosilicon chemistry</span> Organometallic compound containing carbon–silicon bonds

Organosilicon compounds are organometallic compounds containing carbon–silicon bonds. Organosilicon chemistry is the corresponding science of their preparation and properties. Most organosilicon compounds are similar to the ordinary organic compounds, being colourless, flammable, hydrophobic, and stable to air. Silicon carbide is an inorganic compound.

<span class="mw-page-title-main">Xenon difluoride</span> Chemical compound

Xenon difluoride is a powerful fluorinating agent with the chemical formula XeF
2
, and one of the most stable xenon compounds. Like most covalent inorganic fluorides it is moisture-sensitive. It decomposes on contact with water vapor, but is otherwise stable in storage. Xenon difluoride is a dense, colourless crystalline solid.

<span class="mw-page-title-main">Lithium bis(trimethylsilyl)amide</span> Chemical compound

Lithium bis(trimethylsilyl)amide is a lithiated organosilicon compound with the formula LiN(Si 3)2. It is commonly abbreviated as LiHMDS or Li(HMDS) and is primarily used as a strong non-nucleophilic base and as a ligand. Like many lithium reagents, it has a tendency to aggregate and will form a cyclic trimer in the absence of coordinating species.

<span class="mw-page-title-main">Plumbane</span> Chemical compound

Plumbane, PbH4, is a metal hydride and group 14 hydride composed of lead and hydrogen. Plumbane is not well characterized or well known, and it is thermodynamically unstable with respect to the loss of a hydrogen atom. Derivatives of plumbane include lead tetrafluoride, PbF4, and tetraethyllead, (CH3CH2)4Pb.

Trimethylsilanol (TMS) is an organosilicon compound with the formula (CH3)3SiOH. The Si centre bears three methyl groups and one hydroxyl group. It is a colourless volatile liquid.

<span class="mw-page-title-main">Tetramethyltin</span> Chemical compound

Tetramethyltin is an organometallic compound with the formula (CH3)4Sn. This liquid, one of the simplest organotin compounds, is useful for transition-metal mediated conversion of acid chlorides to methyl ketones and aryl halides to aryl methyl ketones. It is volatile and toxic, so care should be taken when using it in the laboratory.

Zinc hydride is an inorganic compound with the chemical formula ZnH2. It is a white, odourless solid which slowly decomposes into its elements at room temperature; despite this it is the most stable of the binary first row transition metal hydrides. A variety of coordination compounds containing Zn–H bonds are used as reducing agents, however ZnH2 itself has no common applications.

<span class="mw-page-title-main">Indium trihydride</span> Chemical compound

Indium trihydride is an inorganic compound with the chemical formula (InH
3
). It has been observed in matrix isolation and laser ablation experiments. Gas phase stability has been predicted. The infrared spectrum was obtained in the gas phase by laser ablation of indium in presence of hydrogen gas InH3 is of no practical importance.

<span class="mw-page-title-main">Metal bis(trimethylsilyl)amides</span>

Metal bis(trimethylsilyl)amides are coordination complexes composed of a cationic metal with anionic bis(trimethylsilyl)amide ligands and are part of a broader category of metal amides.

Scandium compounds are compounds containing the element scandium. The chemistry of scandium is almost completely dominated by the trivalent ion, Sc3+, due to its electron configuration, [Ar] 3d14s2. The radii of M3+ ions in the table below indicate that the chemical properties of scandium ions have more in common with yttrium ions than with aluminium ions. In part because of this similarity, scandium is often classified as a lanthanide-like element.

Chlorotrifluorosilane is an inorganic gaseous compound with formula SiClF3 composed of silicon, fluorine and chlorine. It is a silane that substitutes hydrogen with fluorine and chlorine atoms.

Argon compounds, the chemical compounds that contain the element argon, are rarely encountered due to the inertness of the argon atom. However, compounds of argon have been detected in inert gas matrix isolation, cold gases, and plasmas, and molecular ions containing argon have been made and also detected in space. One solid interstitial compound of argon, Ar1C60 is stable at room temperature. Ar1C60 was discovered by the CSIRO.

<span class="mw-page-title-main">Stannylene</span>

Stannylenes (R2Sn:) are a class of organotin(II) compounds that are analogues of carbene. Unlike carbene, which usually has a triplet ground state, stannylenes have a singlet ground state since valence orbitals of tin (Sn) have less tendency to form hybrid orbitals and thus the electrons in 5s orbital are still paired up. Free stannylenes are stabilized by steric protection. Adducts with Lewis bases are also known.

References

  1. MSDS from Matheson Tri-Gas
  2. Tannenbaum, Stanley; Kaye, Samuel; Lewenz, George F. (1953). "Synthesis and Properties of Some Alkylsilanes". Journal of the American Chemical Society. 75 (15): 3753–3757. doi:10.1021/ja01111a043.
  3. Hurwitz, F. I.; Kacik, T. A.; Bu, Xin-Ya; Masnovi, J.; Heimann, P. J.; Beyene, K. (1995). "Pyrolytic conversion of methyl- and vinylsilane polymers to Si-C ceramics". Journal of Materials Science. 30 (12): 3130–3136. doi:10.1007/BF01209227. S2CID   97973689.
  4. Nguyen, Kiet A.; Gordon, Mark S.; Raghavachari, Krishnan (1994). "Mechanisms and Energetics of the Reaction of Si+ with CH3-SiH3". The Journal of Physical Chemistry. 98 (27): 6704. doi:10.1021/j100078a010.