1,2-Dioxetanedione

The chemical compound 1,2-dioxetanedione, or 1,2-dioxacyclobutane-3,4-dione, often called peroxyacid ester, is an unstable oxide of carbon (an oxocarbon) with formula C₂O₄. It can be viewed as a double ketone of 1,2-dioxetane (1,2-dioxacyclobutane), or a cyclic dimer of carbon dioxide.^[1]

1,2-Dioxetanedione

Names
Preferred IUPAC name 1,2-Dioxetanedione
Other names Peroxyacid ester
Identifiers
CAS Number	26974-08-3 N
3D model (JSmol)	Interactive image
ChemSpider	11535432 Y
PubChem CID	14833747
CompTox Dashboard (EPA)	DTXSID80564519
InChI InChI=1S/C2O4/c3-1-2(4)6-5-1 Y Key: WYNZXNXFHYJUTE-UHFFFAOYSA-N Y InChI=1/C2O4/c3-1-2(4)6-5-1 Key: WYNZXNXFHYJUTE-UHFFFAOYAI
SMILES O=C1OOC1=O
Properties
Chemical formula	C2O4
Molar mass	88.018 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references

In ordinary conditions, it quickly decomposes to carbon dioxide (CO₂) even at 180 K (−93.1 °C), but can be detected by mass spectrometry and other techniques.^[2][3]

1,2-Dioxetanedione is an intermediate in the chemoluminescent reactions used in glowsticks.^[4][5] The decomposition proceeds via a paramagnetic oxalate biradical intermediate.^[6]

It is an intermediate in a reaction (between oxalyl chloride and hydrogen peroxide in ethyl acetate, accumulating in solution at room temperature up to a few micromoles, provided that the activating dye and all traces of metals and other reducing agents are removed from the system, and the reactions are carried out in an inert atmosphere.^[7]

See also

• 1,3-dioxetanedione

References

1. Alfred Hassner (1985): Chemistry of Heterocyclic Compounds: Small Ring Heterocycles, Part 3: Oxiranes, Arene Oxides, Oxaziridines, Dioxetanes, Thietanes, Thietes, Thiazetes, and Others, Volume 42. ISBN 978-0-471-05624-9 ISBN 978-0-470-18720-3 John Wiley & Sons.
2. Herman F. Cordes; Herbert P. Richter; Carl A. Heller (1969). "Mass spectrometric evidence for the existence of 1,2-dioxetanedione (carbon dioxide dimer). Chemiluminescent intermediate". J. Am. Chem. Soc. 91 (25): 7209. doi:10.1021/ja01053a065.
3. J. Stauff; W. Jaeschke; G. Schlögl (1972). "Chemilumineszenz des "Dioxetandions"" [Chemiluminescence of „Dioxetanedione“] (PDF). Z. Naturforsch. B 27 (11): 1434–1435. doi:10.1515/znb-1972-1140. S2CID 94708095.
4. Vacher, Morgane; Fdez. Galván, Ignacio; Ding, Bo-Wen; Schramm, Stefan; Berraud-Pache, Romain; Naumov, Panče; Ferré, Nicolas; Liu, Ya-Jun; Navizet, Isabelle; Roca-Sanjuán, Daniel; Baader, Wilhelm J.; Lindh, Roland (March 2018). "Chemi- and Bioluminescence of Cyclic Peroxides". Chemical Reviews. 118 (15): 6927–6974. doi:10.1021/acs.chemrev.7b00649. PMID 29493234.
5. Richard Bos; Neil W. Barnett; Gail A. Dyson; Kieran F. Lim; Richard A. Russell & Simon P. Watson (2003). "Studies on the mechanism of the peroxyoxalate chemiluminescence reaction: Part 1. Confirmation of 1,2-dioxetanedione as an intermediate using 13C nuclear magnetic resonance spectroscopy". Analytica Chimica Acta. 502 (2): 141–147. doi:10.1016/j.aca.2003.10.014.
6. Richard Bos; Sarah A. Tonkin; Graeme R. Hanson; Christopher M. Hindson; Kieran F. Lim & Neil W. Barnett (2009). "In Search of a Chemiluminescence 1,4-Dioxy Biradical". J. Am. Chem. Soc. 131 (8): 2770–2771. doi:10.1021/ja808401p. PMID 19206238.
7. Luiz F. M. L. Ciscato, Fernando H. Bartoloni, Erick L. Bastos, and Wilhelm J. Baader (2009), Direct Kinetic Observation of the Chemiexcitation Step in Peroxyoxalate Chemiluminescence. Journal of Organic Chemistry, volume 74, 8974–8979. doi:10.1021/jo901402k.

External links

• Media related to 1,2-Dioxetanedione at Wikimedia Commons