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Oxocarbono (Spanish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Oxocarbono" in Spanish language version.

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37doi.org
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3google.com.br
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3nih.gov
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2harvard.edu
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2sciencedirect.com
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1iupac.org
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1jstor.org
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1archive.org
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1nasa.gov
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archive.org

  • Bugge (1914), Chemie: En neues Kohenoxyd. Revisión del descubrimiento de Meyer y Steiner del C12O9. Naturwissenschaftliche Wochenschrift, vol. 13/29, núm. 12, 22 de marzo de 1914, p. 188. versión en línea Consultado el 09-07-2009.

doi.org

dx.doi.org

  • William S. Hummers Jr., y Richard E. Offeman (1958), "Preparation of Graphitic Oxide". J. Am. Chem. Soc., 1958, 80 (6), 1339-1339 doi 10.1021/ja01539a017
  • A. W. Snow, H. Haubenstock, N.-L. Yang (1978): "Poly(carbon suboxide). Characterization, Polymerization, and Radical Structure". Macromolecules, 11 (1), pp 77–86. doi 10.1021/ma60061a015
  • Brodie B. C. (1873). «Note on the Synthesis of Marsh-Gas and Formic Acid, and on the Electric Decomposition of Carbonic Oxide». Proceedings of the Royal Society (Londres) 21 (139–147): 245-247. JSTOR 113037. doi:10.1098/rspl.1872.0052. 
  • 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. 
  • 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 y Timothy K. Minton (2009), Hyperthermal O-Atom Exchange Reaction O2 + CO2 through a CO4 Intermediate. J. of the American Chemical Society, vol. 131, núm. 39, pp. 13940–13942. doi 10.1021/ja903944k
  • Corey S. Jamieson, Alexander M. Mebel, Ralf I. Kaiser (2007). «Novel detection of the C2v isomer of carbon tetraoxide (CO4)». Chemical Physics Letters 440 (1–3): 105-109. Bibcode:2007CPL...440..105J. doi:10.1016/j.cplett.2007.04.043. 
  • Jamieson, Corey S.; Mebel, Alexander M., Kaiser, Ralf I. (26 de julio de 2007). «First detection of the C2 symmetric isomer of carbon pentaoxide (CO5) at 10K». Chemical Physics Letters 443 (1-3): 49-54. doi:10.1016/j.cplett.2007.06.009. 
  • Corey S. Jamieson, Alexander M. Mebel and Ralf I. Kaiser (4 de enero de 2008). «First detection of the Cs symmetric isomer of carbon hexaoxide (CO6) at 10 K». Chemical Physics Letters 450 (4-6): 312-317. doi:10.1016/j.cplett.2007.11.052. 
  • 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., 1969, 91 (25), p 7209. doi 10.1021/ja01053a065
  • Richard Bos, Neil W. Barnett, Gail A. Dyson, Kieran F. Lim, Richard A. Russell y 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, vol. 502, núm. 2, 30 de enero de 2004, pp. 141-147. doi 10.1016/j.aca.2003.10.014
  • 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. 
  • Haijun Jiao y Hai-Shun Wu (2003), Are Neutral Oxocarbons Stable? J. Org. Chem., vol. 68, 1475-1479. doi 10.1021/jo026243m
  • 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. 
  • 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». Angewandte Chemie International Edition in English 27 (4): 566-568. doi:10.1002/anie.198805661. 
  • 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. PMID 18834097. doi:10.1021/jp806725s. 
  • 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 y John H. Bowie (mayo de 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 y Caroline Chick Jarrold (2006), Production of C6O6- from Oligomerization of CO on Molybdenum Anions. J. Am. Chem. Soc. vol. 128 núm. 42, pp. 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, vol. 46 núm. 4, pp. 1121–1127. doi 10.1002/hlca.19630460404
  • David Eggerding y 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. 
  • Haiyan Chen, Michel Armand, Matthieu Courty, Meng Jiang, Clare P. Grey, Franck Dolhem, Jean-Marie Tarascon, y 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
  • Schleyer, P. v. R.; Najafian, K.; Kiran, B.; Jiao, H. (2000). «Are Oxocarbon Dianions Aromatic?». J. Org. Chem. 65 (2): 426-431. PMID 10813951. doi:10.1021/jo991267n. 
  • Hammond P. R. (1963). «1,4-Benzoquinone Tetracarboxylic Acid Dianhydride, C10O8: A Strong Acceptor». Science 142 (3591): 502. Bibcode:1963Sci...142..502H. doi:10.1126/science.142.3591.502. 
  • Jürgen Sauer, Barbara Schröder, Richard Wiemer (1967), Eine Studie der Diels-Alder-Reaktion, VI. Kinetischer Nachweis des Moleküls C6O6 (Dianhydrid der Äthylentetracarbonsäure). Chemische Berichte vol. 100 núm. 1, pp. 306-314 doi 10.1002/cber.19671000135
  • H. S. Verter, R. Dominic (1967), A new carbon oxide: synthesis of hexahydroxybenzene tris oxalate. Tetrahedron, vol. 23, núm. 10, pp. 3863-3864 doi 10.1016/S0040-4020(01)97894-9
  • (H. S. Verter, H. Porter, y R. Dominic, 1968), A new carbon oxide: synthesis of tetrahydroxybenzoquinone bisoxalate. Chemical Communications (Londres), p. 973b–974. doi 10.1039/C1968000973b
  • C. Nallaiah (1984), Synthesis of tetrahydroxy-1,4-benzoquinone biscarbonate and hexahydroxybenzene triscarbonate - new organic carbon oxides Tetrahedron, vol. 40, núm. 23, 1984, pp. 4897-4900 doi 10.1016/S0040-4020(01)91324-9
  • Yves Rubin, Carolyn B. Knobler, y Francois Diederich (1990). «Precursors to the cyclo[n]carbons: from 3,4-dialkynyl-3-cyclobutene-1,2-diones and 3,4-dialkynyl-3-cyclobutene-1,2-diols to cyclobutenodehydroannulenes and higher oxides of carbon». J. Am. Chem. Soc. 112 (4): 1607-1617. doi:10.1021/ja00160a047. 
  • Paolo Strazzolini, Alberto Gambi, Angelo G. Giumanini and Hrvoj Vancik (1998). «The reaction between ethanedioyl (oxalyl) dihalides and Ag2C2O4: a route to Staudinger’s elusive ethanedioic (oxalic) acid anhydride». J. Chem. Soc., Perkin Trans. 1 (16): 2553-2558. doi:10.1039/a803430c. 
  • T. Hamura, Y. Ibusuki, H. Uekusa, T. Matsumoto, J. S. Siegel, K. K. Baldridge, K. Suzuki (2006). Dodecamethoxy- and Hexaoxotricyclobutabenzene: Synthesis and Characterization. J. Am. Chem. Soc. 128, 10032–10033. doi 10.1021/ja064063e
  • Holger Butenschön (2007). «A new oxocarbon C12O6 via highly strained benzyne intermediates». Angew Chem Int Ed Engl 46 (22): 4012-4014. PMID 17508349. doi:10.1002/anie.200700926. 
  • B. D. Kybett, G. K. Johnson, C. K. Barker, y J. L. Margrave (1965), "The Heats of Formation and Polymerization of Carbon Suboxide". J. Phys. Chem., 69 (10), 3603–3606. doi 10.1021/j100894a060
  • A. I. Katz, D. Schiferl, y R. L. Mills (1984), New phases and chemical reactions in solid carbon monoxide under pressure. J. Physical Chemistry, vol. 88 núm. 15, 3176–3179. doi 10.1021/j150659a007
  • W. J. Evans, M. J. Lipp, C.-S. Yoo, H. Cynn, J. L. Herberg, R. S. Maxwell, y M. F. Nicol (2006), Pressure-Induced Polymerization of Carbon Monoxide: Disproportionation and Synthesis of an Energetic Lactonic Polymer. Chemistry of Materials, vol. 18, 2520–2531. doi 10.1021/cm0524446

google.com.br

books.google.com.br

  • (en alemán) J. Liebig, F. Wöhler (1830), Ueber die Zusammensetzung der Honigsteinsäure Poggendorfs Annalen der Physik und Chemie, vol. 94, núm. 2, pp.161–164. versión en línea Consultado el 08-07-2009.
  • Leopold Gmelin (1825), Ueber einige merkwürdige, bei der Darstellung des Kaliums nach der Brunner'schen Methode, erhaltene Substanzen. Poggendorfs Annalen der Physik und Chemie, vol. 4, p. 31. versión en línea Consultado el 08-07-2009.
  • Johann Florian Heller (1837), Die Rhodizonsäure, eine aus den Produkten der Kaliumbereitung gewonnene neue Säure, und ihre chemischen Verhältnisse, Justus Liebigs Annalen der Pharmacie, vol. 24, núm. 1, pp. 1–16. versión en línea Consultado el 08-07-2009.

harvard.edu

adsabs.harvard.edu

iupac.org

goldbook.iupac.org

jstor.org

  • Brodie B. C. (1873). «Note on the Synthesis of Marsh-Gas and Formic Acid, and on the Electric Decomposition of Carbonic Oxide». Proceedings of the Royal Society (Londres) 21 (139–147): 245-247. JSTOR 113037. doi:10.1098/rspl.1872.0052. 

nasa.gov

spec.jpl.nasa.gov

  • H. M. Pickett E. A. Cohen B. J. Drouin J. C. Pearson (2003), Submillimeter, Millimeter, and Microwave Spectral Line Catalog. NASA/JPL, versión en línea Consultado el 11-07-2009.

nih.gov

ncbi.nlm.nih.gov

  • 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. PMID 18834097. doi:10.1021/jp806725s. 
  • Schleyer, P. v. R.; Najafian, K.; Kiran, B.; Jiao, H. (2000). «Are Oxocarbon Dianions Aromatic?». J. Org. Chem. 65 (2): 426-431. PMID 10813951. doi:10.1021/jo991267n. 
  • Holger Butenschön (2007). «A new oxocarbon C12O6 via highly strained benzyne intermediates». Angew Chem Int Ed Engl 46 (22): 4012-4014. PMID 17508349. doi:10.1002/anie.200700926. 

sciencedirect.com