Fluorographene Modified by Grignard Reagents: A Broad Range of Functional Nanomaterials

Vlastimil Mazánek, Alena Libánská, Jiří Šturala, Daniel Bouša, David Sedmidubský, Martin Pumera, Zbyněk Janoušek, Jan Plutnar, Zdeněk Sofer

Research output: Contribution to journalArticlepeer-review

29 Citations (Scopus)


Fluorographene is the youngest stoichiometric derivative of graphene; hence, its reactivity is only poorly explored. Compared to graphene, the significantly higher reactivity of C−F bonds makes this material a suitable platform for a large number of chemical modifications. Fluorographene is also the only member of the halographene family that can be prepared in the stoichiometric composition (C1F1). Herein, the chemical modification of fluorographene with Grignard reagents, which are well known in organic synthesis for the formation of new C−C bonds, is presented. The reaction with alkyl magnesium bromides led to successful modification of fluorographene with ethyl, vinyl, ethynyl and propargyl groups. Chemical characterisation showed the presence of covalently bonded functional groups in a high concentration exceeding one functional group per C6motif. The reactivity of Grignard reagents with fluorographene decreased from ethyl to ethynyl. The terminal carbon–carbon triple bonds were used for click reactions with organic azides leading to the formation of triazole rings. These findings open up a broad spectrum of opportunities for simple and robust modification of graphene by chemical reactions proceeding at room temperature under mild conditions. These results have major application potential in sensing, biomedical and energy-related applications.

Original languageEnglish
Pages (from-to)1956-1964
Number of pages9
JournalChemistry - A European Journal
Issue number8
Publication statusPublished - 2017 Feb 3

Bibliographical note

Publisher Copyright:
© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim

All Science Journal Classification (ASJC) codes

  • Catalysis
  • Organic Chemistry


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