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Pure Appl. Chem., 1994, Vol. 66, No. 10-11, pp. 2091-2094

http://dx.doi.org/10.1351/pac199466102091

The structure and reactivity of C60

H. W. Kroto, R. Taylor and D. R. M. Walton

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  • Indeglia Paul A., Krishna Vijay B., Georgieva Angelina, Bonzongo Jean-Claude J.: Mechanical transformation of fullerene (C60) to aqueous nano-C60 (aqu-nC60) in the presence and absence of light. J Nanopart Res 2013, 15. <http://dx.doi.org/10.1007/s11051-013-2069-4>
  • Ovramenko T., Spillebout F., Bocquet F., Mayne A., Dujardin G., Sonnet Ph., Stauffer L., Ksari Y., Themlin J.-M.: STM imagery and density functional calculations of C60 fullerene adsorption on the 6H-SiC(0001)-3×3 surface. Phys. Rev. B 2013, 87. <http://dx.doi.org/10.1103/PhysRevB.87.155421>
  • McNamara Orla A., Maguire Anita R.: The norcaradiene–cycloheptatriene equilibrium. Tetrahedron 2011, 67, 9. <http://dx.doi.org/10.1016/j.tet.2010.10.030>
  • KROTO H. W., TAYLOR R., WALTON D. R. M.: ChemInform Abstract: The Structure and Reactivity of C60. ChemInform 2010, 26, no. <http://dx.doi.org/10.1002/chin.199507299>
  • Isaacs Lyle, Diederich François, Haldimann Richard F.: Multiple Adducts of C60 by Tether-Directed Remote Functionalization and synthesis of soluble derivatives of new carbon allotropes Cn(60+5). HCA 1997, 80, 317. <http://dx.doi.org/10.1002/hlca.19970800202>
  • Duczek Wolfram, Radeck Wolfgang, Niclas Hans-Joachim, Ramm Matthias, Costisella Burkhard: Diels-Alder Cycloaddition of Substituted Norcaradienes with [60]Fullerene. Tetrahetron Lett 1997, 38, 6651. <http://dx.doi.org/10.1016/S0040-4039(97)01574-8>
  • Nierengarten Jean-François, Gramlich Volker, Cardullo Francesca, Diederich François: Regio- und diastereoselektive Bisfunktionalisierung von C60-Fulleren und enantioselektive Synthese eines C60-Fullerenderivates mit chiralem Additionsmuster. Angew Chem 1996, 108, 2242. <http://dx.doi.org/10.1002/ange.19961081813>
  • Herrmann Andreas, Rüttimann Markus, Thilgen Carlo, Diederich François: Multiple Cyclopropanations of C70. Synthesis and characterization of bis-, tris-, and tetrakis-adducts and chiroptical properties of bis-adducts with chiral addends, including a recommendation for the configurational description of fullerene derivatives with a chiral addition pattern. HCA 1995, 78, 1673. <http://dx.doi.org/10.1002/hlca.19950780705>