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tetracyanomethane
Sign in to saveAlso known as methanetetracarbonitrile, 2,2-dicyanomalononitrile, carbon tetracyanide, C(CN)4, neopentanetetranitrile, C5N4
Tetracyanomethane or carbon tetracyanide is an organic compound with the chemical formula . It is a percyanoalkane. It is a molecular carbon nitride. The structure can be considered as methane with all hydrogen atoms replaced by cyanide groups. It was first made by Erwin Mayer in 1969.
Chemical data
- Formula
- C5N4
- Molecular weight
- 116.08 g/mol
- IUPAC name
- methanetetracarbonitrile
- SMILES
- C(#N)C(C#N)(C#N)C#N
- InChIKey
- XKGUKYPCHPHAJL-UHFFFAOYSA-N
- XLogP
- -0.4
- Polar surface area
- 95.2 Ų
- H-bond donors
- 0
- H-bond acceptors
- 4
- Formal charge
- 0
via PubChem
Wikidata facts
- Subclass of
- acyclic compound
- Mass
- 116.01229599999999
Show 3 more facts
- canonical SMILES
- C(#N)C(C#N)(C#N)C#N
- chemical formula
- C₅N₄
- Commons category
- Tetracyanomethane
Sources (2)
via Wikidata · CC0
~2 min read
Encyclopedic overview
5 sectionsContents
- Properties
- Production
- Reactions
- See also
- References
Tetracyanomethane or carbon tetracyanide is an organic compound with the chemical formula . It is a percyanoalkane. It is a molecular carbon nitride. The structure can be considered as methane with all hydrogen atoms replaced by cyanide groups. It was first made by Erwin Mayer in 1969.
==Properties== Tetracyanomethane is a solid at room temperature. It decomposes over 160 °C without melting, and although it can be in a dilute vapour, no liquid form is known. The molecules of tetracyanomethane have a tetrahedral symmetry (3m or Td). The molecule has C-C distance of 1.484 Å and C-N distance of 1.161 Å in the gas form. In the solid the C≡N bond shortens to 1.147 Å. The C-C bond has a force constant of 4.86×105 dyn/cm which is slightly greater than the C-Cl bond in carbon tetrachloride, but a fair bit weaker than in the tricyanomethanide ion. At pressures over 7 GPa tetracyanomethane starts to polymerize to form a disorganised covalent network solid. At higher pressure the white colour yellows and darkens to black. Over 20 GPa the polymerization is total.
Excerpted from Wikipedia’s “tetracyanomethane” article, available under the CC BY-SA 4.0 licence.