Pentacarbon dioxide

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Pentacarbon dioxide
Pentacarbon dioxide.svg
Pentacarbon dioxide 3D spacefill.png
Pentacarbon dioxide 3D ball.png
Names
IUPAC name
penta-1,2,3,4-tetraene-1,5-dione
Identifiers
3D model (JSmol)
ChemSpider
PubChem CID
  • InChI=1S/C5O2/c6-4-2-1-3-5-7 Yes check.svgY
    Key: BKMBQDLZBSCFGV-UHFFFAOYSA-N Yes check.svgY
  • InChI=1/C5O2/c6-4-2-1-3-5-7
    Key: BKMBQDLZBSCFGV-UHFFFAOYAJ
  • O=C=C=C=C=C=O
Properties
C5O2
Molar mass 92.05 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
X mark.svgN  verify  (what is  Yes check.svgYX mark.svgN ?)

Pentacarbon dioxide, officially penta-1,2,3,4-tetraene-1,5-dione, is an oxide of carbon (an oxocarbon) with formula C5O2 or O=C=C=C=C=C=O.

The compound was described in 1988 by Günter Maier and others, who obtained it by pyrolysis of 2,4,6-tris(diazo)cyclohexane-1,3,5-trione (C6N6O3). [1] [2] :97 Diazo transfer can produce the latter compound from phloroglucinol. [1] It is stable at room temperature in solution. [1] The pure compound is stable up to −90 °C, at which point it polymerizes. [2] :100

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References

  1. 1 2 3 Maier, G.; Reisenauer, H. P.; Schäfer, U.; Balli, H. (1988). "C5O2 (1,2,3,4-Pentatetraene-1,5-dione), a New Oxide of Carbon". Angewandte Chemie International Edition. 27 (4): 566–568. doi:10.1002/anie.198805661.
  2. 1 2 Eastwood, F. W. (1997). "Gas Phase Pyrolytic Methods for the Preparation of Carbon-Hydrogen and Carbon-Hydrogen-Oxygen Compounds". In Vallée, Y. (ed.). Gas Phase Reactions in Organic Synthesis. CRC Press. ISBN   90-5699-081-0.

See also