Ugljenikov oksid (Serbian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Ugljenikov oksid" in Serbian language version.

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archive.org

  • Bugge (1914), Chemie: En neues Kohenoxyd. Review of Meyer and Steiner's discovery of C12O9. Naturwissenschaftliche Wochenschrift, volume 13/29, issue 12, 22 March 1914, p. 188. Online version accessed on 2009-07-09.

books.google.com

  • J. Liebig, F. Wöhler (1830), Ueber die Zusammensetzung der Honigsteinsäure Poggendorfs Annalen der Physik und Chemie, vol. 94, Issue 2, pp.161–164. Online version accessed on 2009-07-08.
  • 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.

doi.org

  • Hummers, William S.; Offeman, Richard E. (1958). „Preparation of Graphitic Oxide”. Journal of the American Chemical Society. 80 (6): 1339. doi:10.1021/ja01539a017. 
  • Snow, A. W.; Haubenstock, H.; Yang, N.-L. (1978). „Poly(carbon suboxide). Characterization, Polymerization, and Radical Structure”. Macromolecules. 11: 77—86. doi:10.1021/ma60061a015. 
  • C., Brodie B. (1873). „Note on the Synthesis of Marsh-Gas and Formic Acid, and on the Electric Decomposition of Carbonic Oxide”. Proceedings of the Royal Society. 21 (139–147): 245—247. JSTOR 113037. S2CID 96045552. 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. 
  • B., DeMore W.; 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. 
  • Yeung, Laurence Y.; Okumura, Mitchio; Paci, Jeffrey T.; Schatz, George C.; Zhang, Jianming; Minton, Timothy K. (2009). „Hyperthermal O-Atom Exchange Reaction O2 + CO2 through a CO4 Intermediate”. Journal of the American Chemical Society. 131 (39): 13940—13942. PMID 19743846. doi:10.1021/ja903944k. 
  • Jamieson, Corey S.; Mebel, Alexander M.; Kaiser, Ralf I. (2007). „Novel detection of the C-2v 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. 7. 2007). „First detection of the C2 symmetric isomer of carbon pentaoxide (CO5) at 10K”. Chemical Physics Letters. 443 (1–3): 49—54. Bibcode:2007CPL...443...49J. doi:10.1016/j.cplett.2007.06.009. 
  • Jamieson, Corey S.; Mebel, Alexander M.; Kaiser, Ralf I. (4. 1. 2008). „First detection of the Cs symmetric isomer of carbon hexaoxide (CO6) at 10K”. Chemical Physics Letters. 450 (4–6): 312—317. Bibcode:2008CPL...450..312J. doi:10.1016/j.cplett.2007.11.052. 
  • Cordes, Herman F.; Richter, Herbert P.; Heller, Carl A. (1969). „Mass spectrometric evidence for the existence of 1,2-dioxetanedione (Carbon dioxide dimer). Chemiluminescent intermediate”. Journal of the American Chemical Society. 91 (25): 7209. doi:10.1021/ja01053a065. 
  • Bos, Richard; Barnett, Neil W.; Dyson, Gail A.; Lim, Kieran F.; Russell, Richard A.; Watson, Simon P. (2004). „Studies on the mechanism of the peroxyoxalate chemiluminescence reaction”. Analytica Chimica Acta. 502 (2): 141—147. doi:10.1016/j.aca.2003.10.014. 
  • Schröder, Detlef; Heinemann, Christoph; Schwarz, Helmut; Harvey, Jeremy N.; Dua, Suresh; Blanksby, Stephen J.; 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. 
  • Jiao, Haijun; Wu, Hai-Shun (2003). „Are Neutral Oxocarbons Stable?”. The Journal of Organic Chemistry. 68 (4): 1475—1479. PMID 12585891. doi:10.1021/jo026243m. 
  • Shirel Matthew L.; Peter, Pulay (1999). „Stability of Novel Oxo- and Chloro-Substituted Trioxanes”. J. Am. Chem. Soc. 121 (37): 8544—8548. doi:10.1021/ja984451j. 
  • Maier, Günther; Reisenauer, Hans Peter; Schäfer, Ulrich; Balli, Heinz (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.  Непознати параметар |name-list-style= игнорисан (помоћ)
  • Teruhiko, Ogata; Yoshio, Tatamitani (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. 
  • Seitz, Gunther; Imming, Peter (1992). „Oxocarbons and pseudooxocarbons”. Chem. Rev. 92 (6): 1227—1260. doi:10.1021/cr00014a004. 
  • Schröder, Detlef; Schwarz, Helmut; Dua, Suresh; Blanksby, Stephen J.; John H. Bowie (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. 
  • Wyrwas, Richard B.; Jarrold, Caroline Chick (2006). „Production of C6O6- from Oligomerization of CO on Molybdenum Anions”. Journal of the American Chemical Society. 128 (42): 13688—13689. PMID 17044687. doi:10.1021/ja0643927. 
  • Weiss, E.; Büchner, W. (1963). „Zur Kenntnis der sogenannten «Alkalicarbonyle» I die Kristallstruktur des Kalium-acetylendiolats, KOCCOK”. Helvetica Chimica Acta. 46 (4): 1121—1127. doi:10.1002/hlca.19630460404. 
  • Eggerding, David; West, Robert (1976). „Synthesis and properties of deltic acid (Dihydroxycyclopropenone) and the deltate ion”. Journal of the American Chemical Society. 98 (12): 3641—3644. doi:10.1021/ja00428a043. 
  • David, Eggerding; Robert, West (1975). „Synthesis of Dihydroxycyclopropenone (Deltic Acid)”. J. American Chemical Society. 97 (1): 207—208. doi:10.1021/ja00834a047. 
  • Sidney, Cohen; Lacher John R.; Park Joseph D. (1959). „Diketocyclobutanediol”. J. American Chemical Society. 81 (13): 3480. doi:10.1021/ja01522a083. 
  • Chen, Haiyan; Armand, Michel; Courty, Matthieu; Jiang, Meng; Grey, Clare P.; Dolhem, Franck; Tarascon, Jean-Marie; Poizot, Philippe (2009). „Lithium Salt of Tetrahydroxybenzoquinone: Toward the Development of a Sustainable Li-Ion Battery”. Journal of the American Chemical Society. 131 (25): 8984—8988. PMID 19476355. doi:10.1021/ja9024897. 
  • Schleyer, P.; Najafian, K.; Kiran, B.; Jiao, H. (2000). „Are Oxocarbon Dianions Aromatic?”. J. Org. Chem. 65 (2): 426—431. PMID 10813951. doi:10.1021/jo991267n. 
  • R., Hammond P. (1963). „1,4-Benzoquinone Tetracarboxylic Acid Dianhydride, C10O8: A Strong Acceptor”. Science. 142 (3591): 502. Bibcode:1963Sci...142..502H. PMID 17748167. S2CID 9430830. doi:10.1126/science.142.3591.502. 
  • Sauer, Jürgen; Schröder, Barbara; Wiemer, Richard (1967). „Eine Studie der Diels‐Alder‐Reaktion, VI. Kinetischer Nachweis des Moleküls C 6 O 6 (Dianhydrid der Äthylentetracarbonsäure)”. Chemische Berichte. 100: 306—314. doi:10.1002/cber.19671000135. 
  • Verter, H.S.; Dominic, R. (1967). „A new carbon oxide synthesis of hexahydroxybenzene tris oxalate”. Tetrahedron. 23 (10): 3863—3864. doi:10.1016/S0040-4020(01)97894-9. 
  • Verter, H. S.; Potter, H.; Dominic, R. (1968). „A new carbon oxide synthesis of tetrahydroxybenzoquinone bisoxalate”. Chemical Communications (London) (16): 973b. doi:10.1039/C1968000973b. 
  • Nallaiah, C. (1984). „Synthesis of tetrahydroxy-1,4-benzoquinone biscarbonate and hexahydroxybenzene triscarbonate-new organic carbon oxides”. Tetrahedron. 40 (23): 4897—4900. doi:10.1016/S0040-4020(01)91324-9. 
  • Rubin, Yves; Knobler, Carolyn B.; Diederich, Francois (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.  Непознати параметар |name-list-style= игнорисан (помоћ)
  • Strazzolini, Paolo; Gambi, Alberto; Giumanini, Angelo G.; Vancik, Hrvoj (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. 
  • Hamura, Toshiyuki; Ibusuki, Yousuke; Uekusa, Hidehiro; Matsumoto, Takashi; Siegel, Jay S.; Baldridge, Kim K.; Suzuki, Keisuke (2006). „Dodecamethoxy- and Hexaoxotricyclobutabenzene: Synthesis and Characterization”. Journal of the American Chemical Society. 128 (31): 10032—10033. PMID 16881630. 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. 
  • Kybett, B. D.; Johnson, G. K.; Barker, C. K.; Margrave, J. L. (1965). „The Heats of Formation and Polymerization of Carbon Suboxide”. The Journal of Physical Chemistry. 69 (10): 3603—3606. doi:10.1021/j100894a060. 
  • Katz, Allen I.; Schiferl, David; Mills, Robert L. (1984). „New phases and chemical reactions in solid carbon monoxide under pressure”. The Journal of Physical Chemistry. 88 (15): 3176—3179. doi:10.1021/j150659a007. 
  • Evans, W. J.; Lipp, M. J.; Yoo, C.-S.; Cynn, H.; Herberg, J. L.; Maxwell, R. S.; Nicol, M. F. (2006). „Pressure-Induced Polymerization of Carbon Monoxide: Disproportionation and Synthesis of an Energetic Lactonic Polymer”. Chemistry of Materials. 18 (10): 2520—2531. doi:10.1021/cm0524446. 

harvard.edu

adsabs.harvard.edu

iupac.org

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jstor.org

  • C., Brodie B. (1873). „Note on the Synthesis of Marsh-Gas and Formic Acid, and on the Electric Decomposition of Carbonic Oxide”. Proceedings of the Royal Society. 21 (139–147): 245—247. JSTOR 113037. S2CID 96045552. 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, Online version accessed on 2009-07-11.

nih.gov

ncbi.nlm.nih.gov

  • Yeung, Laurence Y.; Okumura, Mitchio; Paci, Jeffrey T.; Schatz, George C.; Zhang, Jianming; Minton, Timothy K. (2009). „Hyperthermal O-Atom Exchange Reaction O2 + CO2 through a CO4 Intermediate”. Journal of the American Chemical Society. 131 (39): 13940—13942. PMID 19743846. doi:10.1021/ja903944k. 
  • Jiao, Haijun; Wu, Hai-Shun (2003). „Are Neutral Oxocarbons Stable?”. The Journal of Organic Chemistry. 68 (4): 1475—1479. PMID 12585891. doi:10.1021/jo026243m. 
  • Teruhiko, Ogata; Yoshio, Tatamitani (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. 
  • Wyrwas, Richard B.; Jarrold, Caroline Chick (2006). „Production of C6O6- from Oligomerization of CO on Molybdenum Anions”. Journal of the American Chemical Society. 128 (42): 13688—13689. PMID 17044687. doi:10.1021/ja0643927. 
  • Chen, Haiyan; Armand, Michel; Courty, Matthieu; Jiang, Meng; Grey, Clare P.; Dolhem, Franck; Tarascon, Jean-Marie; Poizot, Philippe (2009). „Lithium Salt of Tetrahydroxybenzoquinone: Toward the Development of a Sustainable Li-Ion Battery”. Journal of the American Chemical Society. 131 (25): 8984—8988. PMID 19476355. doi:10.1021/ja9024897. 
  • Schleyer, P.; Najafian, K.; Kiran, B.; Jiao, H. (2000). „Are Oxocarbon Dianions Aromatic?”. J. Org. Chem. 65 (2): 426—431. PMID 10813951. doi:10.1021/jo991267n. 
  • R., Hammond P. (1963). „1,4-Benzoquinone Tetracarboxylic Acid Dianhydride, C10O8: A Strong Acceptor”. Science. 142 (3591): 502. Bibcode:1963Sci...142..502H. PMID 17748167. S2CID 9430830. doi:10.1126/science.142.3591.502. 
  • Hamura, Toshiyuki; Ibusuki, Yousuke; Uekusa, Hidehiro; Matsumoto, Takashi; Siegel, Jay S.; Baldridge, Kim K.; Suzuki, Keisuke (2006). „Dodecamethoxy- and Hexaoxotricyclobutabenzene: Synthesis and Characterization”. Journal of the American Chemical Society. 128 (31): 10032—10033. PMID 16881630. 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. 

sciencedirect.com

semanticscholar.org

api.semanticscholar.org

zenodo.org