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Original Articles

PAH and IUPAC Nomenclature

Pages 161-176 | Received 05 Mar 2014, Accepted 10 Apr 2014, Published online: 26 Jan 2015

REFERENCES

  • Favre, H.A. and W.H. Powell. Nomenclature of Organic Chemistry. (London: Royal Society of Chemistry, 2013).
  • International Union of Pure and Applied Chemistry. IUPAC Nomenclature of Organic Chemistry 1957. (London: Butterworths, 1958).
  • Balaban, A.T. and F. Harary. “Chemical Graphs—V : Enumeration and Proposed Nomenclature of Benzenoid Cata-Condensed Polycyclic Aromatic Hydrocarbons.” Tetrahedron 24 (1968): 2505–2516.
  • Cioslowski, J. and A.M. Turek. “A Novel Compact Nomenclature of the Condensed Benzenoid Hydrocarbons.” Tetrahedron 40 (1984): 2161–2164.
  • Wenchen, H. and H. Wenjie. “A Novel Nomenclature of Polycyclic Aromatic Hydrocarbons without using Graph Centre.” Theoretica Chimica Acta 68 (1985): 301–313.
  • Dias, J. “A Periodic Table for Benzenoid Hydrocarbons,” in Advances in the Theory of Benzenoid Hydrocarbons, ed. I. Gutman and S. Cyvin. (Berlin-Heidelberg: Springer, 1990), 123–143.
  • Tristajstić, N., Ž. Jeričević, J.V. Knop, W.R. Mueller, and K. Szymanski. “Computer Generation of Isomeric Structures.” Pure & Applied Chemistry 55 (1983): 379–390.
  • Knop, J.V., W.R. Müller, K. Szymnsky, and N. Trinajstic. Computer Generation of Certain Classes of Molecules. (Zagreb: SKTH, 1985).
  • Dias, J.R. “A Periodic Table for Polycyclic Aromatic Hydrocarbons. Isomer Enumeration of Fused Polycyclic Aromatic Hydrocarbons. Part I.” Journal of Chemical Information and Computer Sciences 22 (1982): 15–22.
  • Panico, R., W.H. Powell, and J.-C. Richter. A Guide to IUPAC Nomenclature of Organic Compounds (Recommendations 1993). (Oxford: Blackwell Scientific Publications, 1993).
  • Favre, H.A., K.-H. Hellwich, G.P. Moss, W.H. Powell, and J.G. Traynham. “Corrections to ‘A Guide to IUPAC Nomenclature of Organic Compounds’.” Pure & Applied Chemistry 71 (1999): 1327–1330.
  • Moss, G.P. “Nomenclature of Fused and Bridged Fused Ring Systems.” http://www.chem.qmul.ac.uk/iupac/fusedring/ accessed: 12/23/2013 (2013).
  • Acdlabs. “IUPAC Nomenclature of Organic Chemistry.” http://www.acdlabs.com/iupac/nomenclature/ accessed: 12/23/2013 (2013).
  • Fetzer, J.C. Large (C> = 24) Polycyclic Aromatic Hydrocarbons: Chemistry and Analysis. (New York: John Wiley & Sons, Inc., 2000).
  • Hellwinkel, D. Die Systematische Nomenklatur Der Organischen Chemie: Eine Gebrauchsanweisung. (Berlin: Springer, 2007).
  • Dias, J.R. Handbook of Polycyclic Hydrocarbons. (Amsterdam: Elsevier, 1987).
  • Moss, G.P. “Nomenclature of Fused and Bridged Fused Ring Systems.” Pure & Applied Chemistry 70 (1998): 143–216.
  • Ismail, Y., A.L. Lafleur, and R.W. Giese. “Polar Forms of Benzo[a]pyrene May Be Ubiquitous in the Environment.” Environmental Science & Technology. 32 (1998): 2494–2497.
  • Jacob, J. “The Significance of Polycyclic Aromatic Hdyrocarbons as Environmental Carcinogens. 35 Years Research on PAH—A Perspective.” Polycyclic Aromatic Compounds. 28 (2008): 242–272.
  • Jacob, J. “The Significance of Polycyclic Aromatic Hydrocarbons as Environmental Carcinogens.” Pure and Applied Chemistry 68 (1996): 301–308.
  • Clar, E. Polycyclic Hydrocarbons, vol. 2. (London: Academic Press, 1964).
  • Bally, O. and R. Scholl. “Einwirkung von Glycerin und Schwefelsäure auf amidierte und auf stickstofffreie Verbindungen der Anthracen-Reihe: Benzanthron und seine Reduktionsprodukte, nebst Bemerkungen über Namenbildung und Ortsbezeichnung hochgegliederter Ringsysteme der Anthracen-Reihe.” Berichte der deutschen chemischen Gesellschaft. 44 (1911): 1656–1670.
  • Clar, E. Polycyclic Hydrocarbons, vol. 1. (New York: Academic Press, 1964).
  • Stelzner, R. and H. Kuh. “Literatur Register der Organischen Chemie. “Literatur Register der Organischen Chemie 3 (1921): 543.
  • Patterson, A.M. “Proposed International Rules for Numbering Organic Ring Systems.” Journal of the American Chemical Society 47 (1925): 543–561.
  • 33 U.S.C. §1251 -1376 40 C.F.R. 104-149 section 303 (d)
  • Sander, L.C. and S.A. Wise. Polycyclic Aromatic Hydrocarbon Structure Index. (Gaithersburg, MD: NIST, 1997).
  • Harvey, R.G. Polycyclic Aromatic Hydrocarbons. (New York: Wiley-VCH, 1997).
  • Service, C. A. https://scifinder.cas.org/ accessed: 12/23/2013.
  • Reaxsys. www.elsevier.com/reaxys accessed: 12/23/2013.
  • Clar, E. “Vorschläge zur Nomenklatur kondensierter Ringsysteme (Aromatische Kohlenwasserstoffe, XXVI. Mitteil.).” Berichte der Deutschen Chemischen Gesellschaft (A and B Series) 72 (1939): 2137–2139.
  • Dias, J.R. “The Most Stable Class of Benzenoid Hydrocarbons and Their Topological Characteristics − Total Resonant Sextet Benzenoids Revisited.” Journal of Chemical Information and Computer Sciences 39 (1998): 144–150.
  • Blümer, G.P. and M. Zander. “Gruppenspezifische Detektion von Polycyclischen Verbindungen in der Hochdruck-Flüssigkeits-Chromatographie Durch Selektive Fluorescenzlöschung.” Fresenius’ Zeitschrift für analytische Chemie 296 (1979): 409–410.
  • Tucker, S.A., H. Darmodjo, J. William, E. Acree, J.C. Fetzer, and M. Zander. “Spectroscopic Investigation of Fluorescence Quenching Agents. Part II: Effect of Nitromethane on the Fluorescence Emission Behavior of Thirty-Six Alternant Benzenoid Polycyclic Aromatic Hydrocarbons.” Applied Spectroscopy 46 (1992): 1260–1265.
  • Marom, H., S. Pogodin, and I. Agranat. 2007. “Double Fjord Motif in Overcrowded Large Polycyclic Aromatic Hydrocarbons: The Conformational Space of hexabenzo[a,cd,f,j,lm,o]perylene.” Polycyclic Aromatic Compounds; 27 (2007): 295–310.
  • Pullman, A. “Structure Électronique et Activité Cancérogène des Hydrocarbures Aromatiques.” Bulletin de la Société Chimique de France (1954): 595–603.
  • Pullman, A. and B. Pullman. “Electronic Structure and Carcinogenic Activity of Aromatic Molecules.” Advanced Cancer Research 3 (1955): 117–169.
  • Williams, A. “Step by Step to the Synthesis of Olympicene.” (2011); http://www.chemconnector.com/2012/03/14/step-by-step-to-the-synthesis-of-olympicene/ accessed: 12/23/2013.
  • Williams, A. “In Celebration of Chemistry in Sports. Introducing Olympicene.” (2011); http://www.chemconnector.com/2011/08/01/in-celebration-of-chemistry-in-sports-introducing-olympicene/ accessed: 12/23/2013.
  • Williams, A. “The Story of Olympicene from Concept to Completion.” (2012); http://www.chemconnector.com/2012/05/27/the-story-of-olympicene-from-concept-to-completion/ accessed: 12/23/2013.
  • Valentine, A.J. S. and D.A. Mazziotti. “Theoretical Prediction of the Structures and Energies of Olympicene and its Isomers.” The Journal of Physical Chemistry A 117 (2013): 9746–9752.
  • Yildirim, H., T. Greber, and A. Kara. “Trends in Adsorption Characteristics of Benzene on Transition Metal Surfaces: Role of Surface Chemistry and van der Waals Interactions.” The Journal of Physical Chemistry C 117 (2013): 20572–20583.
  • Yildirim, H. and A. Kara. “Effect of van der Waals Interactions on the Adsorption of Olympicene Radical on Cu(111): Characteristics of Weak Physisorption versus Strong Chemisorption.” The Journal of Physical Chemistry C 117 (2013): 2893–2902.

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