Binary silicon-hydrogen compounds
Silanes are saturated chemical compounds with the empirical formula Template:Chem2. They are hydrosilanes, a class of compounds that includes compounds with Template:Chem2 and other Template:Chem2 bonds. All contain tetrahedral silicon and terminal hydrides. They only have Template:Chem2 and Template:Chem2 single bonds. The bond lengths are 146.0 pm for a Template:Chem2 bond and 233 pm for a Template:Chem2 bond. The structures of the silanes are analogues of the alkanes, starting with silane, Template:Chem2, the analogue of methane, continuing with disilane Template:Chem2, the analogue of ethane, etc. They are mainly of theoretical or academic interest.[1]
Inventory
The simplest isomer of a silane is the one in which the silicon atoms are arranged in a single chain with no branches. This isomer is sometimes called the n-isomer (n for "normal", although it is not necessarily the most common). However the chain of silicon atoms may also be branched at one or more silicon atoms. The number of possible isomers increases rapidly with the number of silicon atoms. The members of the series (in terms of number of silicon atoms) follow:
- silane, Template:Chem2, 1 silicon atom and 4 hydrogen atoms, analogous to methane
- disilane, Template:Chem2 or Template:Chem2, 2 silicon atoms and 6 hydrogen atoms, analogous to ethane
- trisilane, Template:Chem2 or Template:Chem2, 3 silicon atoms and 8 hydrogen atoms, analogous to propane
- tetrasilane, Template:Chem2 or Template:Chem2, 4 silicon atoms and 10 hydrogen atoms, analogous to butane (one isomer: isotetrasilane, analogous to isobutane)
- pentasilane, Template:Chem2 or Template:Chem2, 5 silicon atoms and 12 hydrogen atoms, analogous to pentane (two isomers: isopentasilane Template:Chem2 and neopentasilane Template:Chem2, analogous to isopentane and neopentane, respectively)
- hexasilane Template:Chem2 or Template:Chem2, 6 silicon atoms and 14 hydrogen atoms, analogous to hexane
Silanes are named by adding the suffix -silane to the appropriate numerical multiplier prefix. Hence, disilane, Template:Chem2; trisilane Template:Chem2; tetrasilane Template:Chem2; pentasilane Template:Chem2; etc. The prefix is generally Greek, with the exceptions of nonasilane which has a Latin prefix, and undecasilane and tridecasilane which have mixed-language prefixes. Solid phase polymeric silicon hydrides called polysilicon hydrides are also known. When hydrogen in a linear polysilene polysilicon hydride is replaced with alkyl or aryl side-groups, the term polysilane is used.
3-Silylhexasilane, Template:Chem2, is the simplest chiral binary noncyclic silicon hydride.
Cyclosilanes also exist. They are structurally analogous to the cycloalkanes, with the formula Template:Chem2, n > 2.
| Silane | Formula | Melting point [°C] | Boiling point [°C] | Density [g cm−3] (at 25 °C) | Appearance |
|---|---|---|---|---|---|
| Silane | Template:Chem2 | −185 | −112 | Colorless gas | |
| Disilane | Template:Chem2 | −132 | −14 | Colorless gas | |
| Trisilane | Template:Chem2 | −117 | 53 | 0.743 | Colorless liquid |
| Template:Ill | Template:Chem2 | ||||
| Template:Ill | Template:Chem2 | −90 | 108 | 0.793 | Colorless liquid |
| Template:Ill | Template:Chem2 | −72.8 | 153 | 0.827 | Colorless liquid |
| Cyclopentasilane | Template:Chem2 | −10.5Template:Clarify | 194Template:Clarify | 0.963 | Colorless liquid |
| Template:Ill | Template:Chem2 | −44.7 | 193.6 | 0.847 | Colorless liquid |
Production
Early work was conducted by Alfred Stock and Carl Somiesky.[2] Although monosilane and disilane were already known, Stock and Somiesky discovered, beginning in 1916, the next four members of the Template:Chem2 series, up to n = 6. They also documented the formation of solid phase polymeric silicon hydrides.[3] One of their synthesis methods involved the hydrolysis of metal silicides. This method produces a mixture of silanes, which required separation on a high vacuum line.[4][5][6]
The silanes (Template:Chem2) are less thermally stable than alkanes (Template:Chem2). They tend to undergo dehydrogenation, yielding hydrogen and polysilanes. For this reason, the isolation of silanes higher than heptasilane has proved difficult.[7]
The Schlesinger process is used to prepare silanes by the reaction of perchlorosilanes with lithium aluminium hydride.
Applications
Script error: No such module "Labelled list hatnote". The single but significant application for Template:Chem2 is in the microelectronics industry. By metal organic chemical vapor deposition, silane is converted to silicon by thermal decomposition:
Hazards
Silane is explosive when mixed with air (1 – 98% Template:Chem2Template:Clarify). Other lower silanes can also form explosive mixtures with air. The lighter liquid silanes are highly flammable; this risk increases with the length of the silicon chain.
Considerations for detection/risk control:
- Silane is slightly denser than air, while disilane and trisilane are denser than air, thus there is a possibility of pooling at ground levels/pits.
Nomenclature
Script error: No such module "Labelled list hatnote". The IUPAC nomenclature (systematic way of naming compounds) for silanes is based on identifying hydrosilicon chains. Unbranched, saturated hydrosilicon chains are named systematically with a Greek numerical prefix denoting the number of silicons and the suffix "-silane".
IUPAC naming conventions can be used to produce a systematic name.
The key steps in the naming of more complicated branched silanes are as follows:
- Identify the longest continuous chain of silicon atoms
- Name this longest root chain using standard naming rules
- Name each side chain by changing the suffix of the name of the silane from "-ane" to "-anyl", except for "silane" which becomes "silyl"
- Number the root chain so that the sum of the numbers assigned to each side group will be as low as possible
- Number and name the side chains before the name of the root chain
The nomenclature parallels that of alkyl radicals.
Silanes can also be named like any other inorganic compound; in this naming system, silane is named silicon tetrahydride. However, with longer silanes, this becomes cumbersome.
See also
- Organosilicon compounds, compounds containing carbon–silicon bonds
- Hydrosilanes, a larger class of compounds with the formula Template:Chem2 (m ≠ 0)
References
Template:Hydrides by group Template:Authority control
- ↑ a b Script error: No such module "citation/CS1".
- ↑ E. Wiberg, Alfred Stock and the Renaissance of Inorganic Chemistry," Pure Appl. Chem., Vol. 49 (1977) pp. 691-700.
- ↑ J. W. Mellor, "A Comprehensive Treatise on Inorganic and Theoretical Chemistry," Vol. VI, Longman, Green and Co. (1947) pp. 223 - 227.
- ↑ Hydrides of Boron and Silicon. Ithaca (USA) 1933.
- ↑ Script error: No such module "Citation/CS1".
- ↑ Script error: No such module "citation/CS1".
- ↑ W. W. Porterfield "Inorganic Chemistry: A Unified Approach," Academic Press (1993) p. 219.