aDepartment of Chemistry, University of Minnesota Duluth, Duluth, Minnesota, USA bDepartment of Chemistry, University of Alberta, Edmonton, Alberta, Canada
Abstract:
Fullerene C60 reacts with hypervalent iodine reagents (azido-, acetoxy-, sulfonyloxy- and chloroiodanes) under mild conditions with the formation of the appropriate functionalized fullerenes.
Document Type:
Article
Language: English
Citation:
V. V. Zhdankin, K. J. Hanson, A. E. Koposov, E. Blomquist, R. R. Tykwinski, “Functionalization of buckminsterfullerene by hypervalent iodine reagents”, Mendeleev Commun., 11:2 (2001), 51–52
Linking options:
https://www.mathnet.ru/eng/mendc4212
https://www.mathnet.ru/eng/mendc/v11/i2/p51
This publication is cited in the following 13 articles:
Yang-Rong Yao, Olivia Fernandez-Delgado, Luis Echegoyen, Handbook of Carbon-Based Nanomaterials, 2021, 19
Wen-Qiang Zhai, Sheng-Peng Jiang, Ru-Fang Peng, Bo Jin, Guan-Wu Wang, “Facile Access to Novel [60]Fullerenyl Diethers and [60]Fullerene–Sugar Conjugates via Annulation of Diol Moieties”, Org. Lett., 17:8 (2015), 1862
Hongzhang Han, Nicolay V. Tsarevsky, “Employing exchange reactions involving hypervalent iodine compounds for the direct synthesis of azide-containing linear and branched polymers”, Chem. Sci., 5:12 (2014), 4599
Hypervalent Iodine Chemistry, 2013, 145
Robert M. Moriarty, Jerome W. Kosmeder, Viktor V. Zhdankin, Christine Courillon, Emmanuel Lacôte, Max Malacria, Benjamin Darses, Philippe Dauban, Encyclopedia of Reagents for Organic Synthesis, 2012
Igor V. Kuvychko, Alexey V. Streletskii, Natalia B. Shustova, Konrad Seppelt, Thomas Drewello, Alexey A. Popov, Steven H. Strauss, Olga V. Boltalina, “Soluble Chlorofullerenes C60Cl2,4,6,8,10. Synthesis, Purification, Compositional Analysis, Stability, and Experimental/Theoretical Structure Elucidation, Including the X-ray Structure of C1-C60Cl10”, J. Am. Chem. Soc., 132:18 (2010), 6443
Nicolay V. Tsarevsky, “Hypervalent iodine‐mediated direct azidation of polystyrene and consecutive click‐type functionalization”, J. Polym. Sci. A Polym. Chem., 48:4 (2010), 966
Robert M. Moriarty, Jerome W. Kosmeder, Viktor V. Zhdankin, Christine Courillon, Emmanuel Lacôte, Max Malacria, Encyclopedia of Reagents for Organic Synthesis, 2007
Robert M. Moriarty, Jerome W. Kosmeder II, Viktor V. Zhdankin, Encyclopedia of Reagents for Organic Synthesis, 2004
Viktor V. Zhdankin, Peter J. Stang, “Recent Developments in the Chemistry of Polyvalent Iodine Compounds”, Chem. Rev., 102:7 (2002), 2523
Viktor V. Zhdankin, Kari J. Hanson, Alexey E. Koposov, Erin Blomquist, Rik R. Tykwinski, “ChemInform Abstract: Functionalization of Buckminsterfullerene by Hypervalent Iodine Reagents.”, ChemInform, 32:33 (2001)
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