Formation of fullerenes by pyrolysis of perchlorofulvalene and its derivatives

• Published in: Carbon (New York) 2007, Vol.45 (1), p.117-123
• Main Authors: Amsharov, K.Yu, Jansen, M.
• Format: Article
• Language: English
• Subjects: Cross-disciplinary physics: materials science; rheology; Exact sciences and technology; Fullerenes and related materials; diamonds, graphite; Materials science; Physics; Specific materials
• ISSN: 0008-6223; 1873-3891
• DOI: 10.1016/j.carbon.2006.07.019

In a retro-synthetic approach, [60]fullerene might be accessible by condensing six fulvalene fragments. In order to explore the potential of such a route for direct synthesis of [60]fullerene we have investigated the pyrolysis of perchlorofulvalene (PCF). Low temperature pyrolysis of PCF at 250 °C resulted mainly in the formation of dimers, trimers, tetramers and products of subsequent intramolecular condensation of these oligomers. Increasing the temperature to 300–350 °C leads to the formation of perchlorinated polynuclear aromatic hydrocarbons. Pyrolysis at 400–450 °C gives a cross-linked polymer structure which is the result of intermolecular condensation of the polynuclear aromatic intermediates. Pyrolysis at higher temperatures (>500 °C) mainly leads to graphite. It was found that the two-step pyrolysis of PCF (heating first at 450 °C, after that at 750 °C) yielded a fullerene containing soot via an intermediate polynuclear aromatic net. High temperature rearrangement of the latter gave fullerenes C 60 and C 70. The best results were obtained when a PCF oligomer obtained by Ullmann condensation was used as a precursor. By two-step pyrolysis and further high vacuum sublimation of the soot the fullerenes C 60 and C 70 were obtained in extractable amounts.