Benzoquinonetetracarboxylic dianhydride
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Benzoquinonetetracarboxylic dianhydride
Benzoquinonetetracarboxylic dianhydride molecule Benzoquinonetetracarboxylic dianhydride molecule
Names
Preferred IUPAC name
Identifiers
ChemSpider
Properties
C10O8
Molar mass
248.102 g·mol−1
1H,3H-Benzo[1,2-c:4,5-c′]difuran-1,3,4,5,7,8-hexone
- 32192-32-8 ☒N
3D model (JSmol)
- 32686035 ☒N
PubChem CID
CompTox Dashboard (EPA)
- InChI=1S/C10O8/c11-5-1-2(8(14)17-7(1)13)6(12)4-3(5)9(15)18-10(4)16 ☒NKey: NWWNDTOPIPOVFQ-UHFFFAOYSA-N ☒N
- InChI=1/C10O8/c11-5-1-2(8(14)17-7(1)13)6(12)4-3(5)9(15)18-10(4)16Key: NWWNDTOPIPOVFQ-UHFFFAOYAX
- O=C(C(C(O3)=O)=C1C3=O)C2=C(C(OC2=O)=O)C1=O
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Chemical compound
Benzoquinonetetracarboxylic dianhydride is an organic compound with formula C
10O
8 (an oxide of carbon) which can be seen as the result of removing two molecules of water H
2O from benzoquinonetetracarboxylic acid.[1]
It is a red solid, stable in dry air up to 140 °C and insoluble in ether, carbon tetrachloride, dichloromethane, and carbon disulfide. It reacts with acetone, ethyl acetate, tetrahydrofuran, ethanol, and water. It dissolves in methylated derivatives of benzene to give solutions ranging from orange to violet. When the molecule is exposed to moist air, it quickly turns blue.
The compound was synthesized in 1963 by P. R. Hammond, who claimed it was "one of the strongest π-electron acceptors so far described."[2]
See also
[edit ]- Ethylenetetracarboxylic dianhydride
- Tetrahydroxy-1,4-benzoquinone biscarbonate
- Tetrahydroxy-1,4-benzoquinone bisoxalate
References
[edit ]- ^ PubChem. "3,3',4,4'-Benzophenonetetracarboxylic dianhydride". pubchem.ncbi.nlm.nih.gov. Retrieved 2024年12月19日.
- ^ Hammond, P. R. (1963). "1,4-Benzoquinone Tetracarboxylic Acid Dianhydride, C1008:A Strong Acceptor". Science. 142 (3591): 502. Bibcode:1963Sci...142..502H. doi:10.1126/science.142.3591.502. PMID 17748167. S2CID 9430830.