ウィキペディア |
 
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オキソカーボン
出典: フリー百科事典『ウィキペディア（Wikipedia）』 (2012/04/08 08:09 UTC 版)
オキソカーボン (oxocarbon) または炭素酸化物 (oxide of carbon) とは炭素と酸素のみの無機化合物である[1][2]。
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- ^ J. Liebig, F. Wöhler (1830). “Ueber die Zusammensetzung der Honigsteinsäure”. Poggendorfs Annalen der Physik und Chemie 94 (2): 161–164.
- ^ Meyer H, Steiner K (1913). “Über ein neues Kohlenoxyd C12O9 (A new carbon oxide C12O9)”. Berichte der Deutschen Chemischen Gesellschaft 46: 813–815. doi:10.1002/cber.191304601105.
- ^ Bugge Chemie: En neues Kohenoxyd. Review of Meyer and Steiner's discovery of C12O9. Naturwissenschaftliche Wochenschrift 1914, 13/29 (12), 188.
- ^ DeMore W. B., Jacobsen C. W. (1969). “Formation of carbon trioxide in the photolysis of ozone in liquid carbon dioxide”. Journal of Physical Chemistry 73 (9): 2935–2938. doi:10.1021/j100843a026.
- ^ Laurence Y. Yeung, Mitchio Okumura, Jeffrey T. Paci, George C. Schatz, Jianming Zhang and Timothy K. Minton (2009). “Hyperthermal O-Atom Exchange Reaction O2 + CO2 through a CO4 Intermediate”. J. Am. Chem. Soc. 131 (39): 13940–13942. doi:10.1021/ja903944k.
- ^ Corey S. Jamieson, Alexander M. Mebel, Ralf I. Kaiser (2007). “Novel detection of the C-2v isomer of carbon tetraoxide (CO4)”. Chem. Phys. Lett. 440 (1–3): 105–109. doi:10.1016/j.cplett.2007.04.043.
- ^ Herman F. Cordes, Herbert P. Richter, Carl A. Heller (1969). “Mass spectrometric evidence for the existence of 1,2-dioxetanedione (carbon dioxide dimer)”. J. Am. Chem. Soc. 91 (25): 7209. doi:10.1021/ja01053a065.
- ^ Richard Bos, Neil W. Barnett, Gail A. Dyson, Kieran F. Lim, Richard A. Russell and Simon P. Watson (2004). “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.
- ^ H. M. Pickett E. A. Cohen B. J. Drouin J. C. Pearson (2003年). “Submillimeter, Millimeter, and Microwave Spectral Line Catalog”. NASA/JPL. 2011年8月29日閲覧。
- ^ a b c Detlef Schröder; Christoph Heinemann, Helmut Schwarz, Jeremy N. Harvey, Suresh Dua, Stephen J. Blanksby, John H. Bowie (1998). “Ethylenedione: An Intrinsically Short-Lived Molecule”. Chemistry - A European Journal 4 (12): 2550–2557. doi:10.1002/(SICI)1521-3765(19981204)4:12<2550::AID-CHEM2550>3.0.CO;2-E.
- ^ a b Errol Lewars(1996), Polymers and oligomers of carbon dioxide: ab initio and semiempirical calculations. Journal of Molecular Structure: THEOCHEM, Volume 363, Number 1, pp. 1–15
- ^ Shirel Matthew L., Pulay Peter (1999). “Stability of Novel Oxo- and Chloro-Substituted Trioxanes”. J. Am. Chem. Soc. 121 (37): 8544–8548. doi:10.1021/ja984451j.
- ^ a b c Haijun Jiao and Hai-Shun Wu (2003). “Are Neutral Oxocarbons Stable?”. J. Org. Chem. 68: 1475-1479. doi:10.1021/jo026243m.
- ^ a b Günter Maier and Hans Peter Reisenauer (2001). “Carbenes in Matrices: Specrospcopy, Structure, and Photochemical Behavior”. In Udo H. Brinker (ed.). Advances in carbene chemistry. Elsevier. pp. 135. ISBN 9780444508928.
- ^ a b W. Kutzelnigg (2002). Einführung in die Theoretische Chemie. Wiley-VCH. ISBN 3-527-30609-9.
- ^ Günther Maier, Hans Peter Reisenauer, Heinz Balli, Willy Brandt, Rudolf Janoschek (1990). “C4O2 (1,2,3-Butatriene-1,4-dione), the First Dioxide of Carbon with an Even Number of C Atoms”. Angew. Chem. Int. Ed. 29 (8): 905–908. doi:10.1002/anie.199009051.
- ^ Günther Maier, Hans Peter Reisenauer, Ulrich Schäfer, and Heinz Balli (1988). “C5O2 (1,2,3,4-Pentatetraene-1,5-dione), a New Oxide of Carbon”. Angew. Chem. Int. Ed. 27 (4): 566–568. doi:10.1002/anie.198805661.
- ^ a b c Frank W. Eastwood (1997). “Gas Phase Pyrolytic Methods for the Preparation of Carbon-Hydrogen and Carbon-Hydrogen-Oxygen Compounds”. In Yannick Vallée. Gas Phase Reactions in Organic Synthesis. CRC Press. ISBN 9789056990817.
- ^ Roman Reusch (2005). Absorptionsspektroskopie von langen Kohlenstoff-Kettenmolekülen und deren Oxide in kryogenen Matrizen (Thesis). Ruprecht-Karls-Universität Heidelberg.
- ^ a b Ogata Teruhiko, Tatamitani Yoshio (2008). “The Simplest Linear-Carbon-Chain Growth by Atomic-Carbon Addition and Ring Opening Reactions”. J. Phys. Chem. A 112 (43): 10713–10715. doi:10.1021/jp806725s. PMID 18834097.
- ^ a b c Gunther Seitz, Peter Imming (1992). “Oxocarbons and pseudooxocarbons”. Chem. Rev. 92 (6): 1227–1260. doi:10.1021/cr00014a004.
- ^ Detlef Schröder,; Helmut Schwarz, Suresh Dua, Stephen J. Blanksby and John H. Bowie (May 1999). “Mass spectrometric studies of the oxocarbons CnOn (n = 3–6)”. International Journal of Mass Spectrometry 188 (1–2): 17–25. doi:10.1016/S1387-3806(98)14208-2.
- ^ Richard B. Wyrwas and Caroline Chick Jarrold (2006), Production of C6O6- from Oligomerization of CO on Molybdenum Anions. J. Am. Chem. Soc. volume 128 issue 42, pages 13688–13689. doi:10.1021/ja0643927
- ^ Werner Büchner, E. Weiss (1963) Zur Kenntnis der sogenannten «Alkalicarbonyle» I Die Kristallstruktur des Kalium-acetylendiolats, KOC≡COK. Helvetica Chimica Acta, Volume 46 Issue 4, Pages 1121–1127. doi:10.1002/hlca.19630460404
- ^ David Eggerding and Robert West (1976), Synthesis and Properties of Deltic Acid (Dihydroxycyclopropenone) and the Deltate Ion J. American Chemical Society, volume 98, p, 3641–3644. doi:10.1021/ja00428a043
- ^ Eggerding David, West Robert (1975). “Synthesis of Dihydroxycyclopropenone (Deltic Acid)”. J. American Chemical Society 97 (1): 207–208. doi:10.1021/ja00834a047.
- ^ Cohen Sidney, Lacher John R., Park Joseph D. (1959). “Diketocyclobutanediol”. J. American Chemical Society 81 (13): 3480. doi:10.1021/ja01522a083.
- ^ Leopold Gmelin (1825), Ueber einige merkwürdige, bei der Darstellung des Kaliums nach der Brunner'schen Methode, erhaltene Substanzen. Poggendorfs Annalen der Physik und Chemie, volume 4, p. 31. Online version accessed on 2009-07-08.
- ^ Johann Florian Heller (1837), Die Rhodizonsäure, eine aus den Produkten der Kaliumbereitung gewonnene neue Säure, und ihre chemischen Verhältnisse, Justus Liebigs Annalen der Pharmacie, volume 24, issue 1, pp. 1–16. Online version accessed on 2009-07-08.
- ^ Carl Löwig (1839), Chemie der organischen Verbindungen. F. Schultess, Zürich.
- ^ Haiyan Chen, Michel Armand, Matthieu Courty, Meng Jiang, Clare P. Grey, Franck Dolhem, Jean-Marie Tarascon, and Philippe Poizot (2009), Lithium Salt of Tetrahydroxybenzoquinone: Toward the Development of a Sustainable Li-Ion Battery J. Am. Chem. Soc., 131 (25), pp. 8984–8988 doi:10.1021/ja9024897
- ^ R. West, J. Niu (1969, Non-benzenoid aromatics. Vol. 1. Edited by J. Snyder. Academic Press New York.
- ^ Schleyer, P. v. R.; Najafian, K.; Kiran, B.; Jiao, H. (2000). “Are Oxocarbon Dianions Aromatic?”. J. Org. Chem. 65 (2): 426–431. doi:10.1021/jo991267n. PMID 10813951.
[続きの解説]
「オキソカーボン」の続きの解説一覧
- 1 オキソカーボンとは
- 2 オキソカーボンの概要
- 3 直線形ニ酸化物
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