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| ==Preparation== | ==Preparation== | ||
| This compound may be made by the dehydrohalogenation of 1,4-dichloro-2-butyne by potassium hydroxide at low temperature:<ref>{{cite journal | last1 = Verkruijsse | first1 = H. D. | last2 = Brandsma | first2 = L. | title = A Detailed procedure for the preparation of Butadiyne | journal = Synthetic Communications | volume = 21 | pages = 657 | year = 1991 | doi = 10.1080/00397919108020833}}</ref> | This compound may be made by the dehydrohalogenation of 1,4-dichloro-2-butyne by potassium hydroxide at low temperature:<ref>{{cite journal | last1 = Verkruijsse | first1 = H. D. | last2 = Brandsma | first2 = L. | title = A Detailed procedure for the preparation of Butadiyne | journal = Synthetic Communications | volume = 21 | pages = 657 | year = 1991 | doi = 10.1080/00397919108020833 | issue = 5}}</ref> | ||
| : ClCH<sub>2</sub>C≡CCH<sub>2</sub>Cl → HC≡C-C≡CH | : ClCH<sub>2</sub>C≡CCH<sub>2</sub>Cl → HC≡C-C≡CH | ||
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| ==Further reading== | ==Further reading== | ||
| * {{cite journal | last1 =Maretina | first1 =Irina A | last2 =Trofimov | first2 =Boris A | title =Diacetylene: a candidate for industrially important reactions | journal =Russian Chemical Reviews | volume =69 | pages =591 | year =2000 | doi =10.1070/RC2000v069n07ABEH000564}} | * {{cite journal | last1 =Maretina | first1 =Irina A | last2 =Trofimov | first2 =Boris A | title =Diacetylene: a candidate for industrially important reactions | journal =Russian Chemical Reviews | volume =69 | pages =591 | year =2000 | doi =10.1070/RC2000v069n07ABEH000564 | issue =7}} | ||
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Revision as of 02:57, 7 October 2011
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| Names | |
|---|---|
| Other names 1,3-butadiyne, buta-1,3-diyne, biacetylene, butadiyne | |
| Identifiers | |
| CAS Number | |
| 3D model (JSmol) | |
| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.006.641 
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| PubChem CID | |
| CompTox Dashboard (EPA) | |
InChI
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SMILES
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| Properties | |
| Chemical formula | C4H2 |
| Molar mass | 50.060 g·mol |
| Appearance | Gas |
| Melting point | −10 °C (14 °F; 263 K) |
| Boiling point | 10 °C (50 °F; 283 K) |
| Hazards | |
| Occupational safety and health (OHS/OSH): | |
| Main hazards | Highly flammable |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).
 Y verify (what is ?)
Infobox references
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Diacetylene (also known as butadiyne), with the formula C4H2, is a highly unsaturated hydrocarbon that contains three single bonds and two triple bonds. It is the first in the series of polyynes.
Occurrence
Diacetylene has been identified in the atmosphere of Titan and in the protoplanetary nebula CRL 618 by its characteristic vibrational modes. The molecule is most likely to have formed in Titan's atmosphere by a reaction between acetylene and the ethynyl radical C2H, which is produced when acetylene undergoes photolysis. This radical can in turn attack the triple bond in acetylene and react efficiently even at cold temperatures. Diacetylene has also been found on the Moon.
Preparation
This compound may be made by the dehydrohalogenation of 1,4-dichloro-2-butyne by potassium hydroxide at low temperature:
- ClCH2C≡CCH2Cl → HC≡C-C≡CH
The bis(trimethylsilyl)-protected derivative may be prepared by the Hay coupling of (trimethylsilyl)acetylene:
- 2 (tms)C≡CH → (tms)C≡C-C≡CH
See also
References
- "The Multiplying Mystery of Moonwater", March 18, 2010. Retrieved on 2010-03-18.
- Verkruijsse, H. D.; Brandsma, L. (1991). "A Detailed procedure for the preparation of Butadiyne". Synthetic Communications. 21 (5): 657. doi:10.1080/00397919108020833.
- Graham E. Jones, David A. Kendrick, and Andrew B. Holmes (1993). "1,4-Bis(trimethylsilyl)buta-1,3-diyne". Organic Syntheses
{{cite journal}}: CS1 maint: multiple names: authors list (link); Collected Volumes, vol. 8, p. 63.
Further reading
- Maretina, Irina A; Trofimov, Boris A (2000). "Diacetylene: a candidate for industrially important reactions". Russian Chemical Reviews. 69 (7): 591. doi:10.1070/RC2000v069n07ABEH000564.