1,2-Dioxin
Appearance
![]() | |||
| |||
Names | |||
---|---|---|---|
Systematic IUPAC name
1,2-Dioxine[1] | |||
Identifiers | |||
3D model (JSmol)
|
|||
ChemSpider | |||
PubChem CID
|
|||
CompTox Dashboard (EPA)
|
|||
| |||
| |||
Properties | |||
C4H4O2 | |||
Molar mass | 84.074 g·mol−1 | ||
Related compounds | |||
Related compounds
|
Dibenzodioxin | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
1,2-Dioxin is a heterocyclic, organic, antiaromatic compound with the chemical formula C4H4O2. It is an isomeric form of 1,4-dioxin (or p-dioxin).
Due to its peroxide-like characteristics, 1,2-dioxin is very unstable and has not been isolated. Even substituted derivatives are very labile, e.g. 1,4-diphenyl-2,3-benzodioxin.[2] Indeed, in 1990, 3,6-bis(p-tolyl)-1,2-dioxin was wrongly accounted as the first stable derivative.[3] It was subsequently shown that the initial compound was not a derivative of 1,2-dioxin, but a thermodynamically more stable dione.[4]
-
The isomers 1,2-dioxin (left) and 1,4-dioxin (right)
-
Structure of the transient 1,4-diphenyl- 2,3-benzodioxin
-
Dioxin (1) and dione form (2)
References
- ^ "CID 15559065 - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 12 February 2002. Identification and Related Records. Retrieved 7 October 2011.
- ^ Smith, Jimmie P.; Schrock, Alan K.; Schuster, Gary B. (1982). "Chemiluminescence of organic peroxides. Thermal generation of an o-xylylene peroxide". Journal of the American Chemical Society. 104 (4): 1041. doi:10.1021/ja00368a021..
- ^ Shine, Henry J.; Zhao, Da Chuan (1990). "Electron transfer to excited doublet states. Photoirradiation of 10-methylphenothiazine cation radical perchlorate in solutions of phenylacetylene and p-tolylacetylene in acetonitrile". The Journal of Organic Chemistry. 55 (13): 4086. doi:10.1021/jo00300a026..
- ^ Block, Eric; Shan, Zhixing; Glass, Richard S.; Fabian, Jürgen (2003). "Revised Structure of a Purported 1,2-Dioxin: A Combined Experimental and Theoretical Study". The Journal of Organic Chemistry. 68 (10): 4108. doi:10.1021/jo034305i. PMID 12737603.