Cyclopentadienone can be generated by the
photolysis or
pyrolysis of various substances (e.g.
1,2-benzoquinone[4]), and then isolated in an
argon matrix at 10 K (−263 °C). It dimerizes readily upon thawing the matrix at 38 K (−235 °C).[5][6]
^Ogliaruso, Michael A.; Romanelli, Michael G.; Becker, Ernest I. (1965). "Chemistry of Cyclopentadienones". Chemical Reviews. 65: 261–367.
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^Quintard, A.; Rodriguez, J. (2014). "Iron Cyclopentadienone Complexes: Discovery, Properties, and Catalytic Reactivity". Angewandte Chemie International Edition. 53: 4044–4055.
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10.1002/anie.201310788.
^Casey, Charles P.; Guan, Hairong (2007). "An Efficient and Chemoselective Iron Catalyst for the Hydrogenation of Ketones". Journal of the American Chemical Society. 129 (18): 5816–5817.
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10.1021/ja071159f.
PMID17439131.
^Brown, Roger F. C. (2012). Pyrolytic Methods in Organic Chemistry: Application of Flow and Flash Vacuum Techniques. Elsevier. p. 173.
ISBN978-0-323-15417-8.
^Maier, Günther; Franz, Lothar Hermann; Hartan, Hans-Georg; Lanz, Klaus; Reisenauer, Hans Peter (1985). "Kleine Ringe. 54. Cyclopentadienon" [Small rings. 54. Cyclopentadienone]. Chemische Berichte (in German). 118 (8): 3196–3204.
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10.1002/cber.19851180819.
^Horspool, William M.; Lenci, Francesco. CRC Handbook of Organic Photochemistry and Photobiology. Vol. 1–2 (2nd ed.). p. 12-8.
ISBN978-0-203-49590-2.