1993
DOI: 10.1126/science.262.5132.404
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Production of Perfluoroalkylated Nanospheres from Buckminsterfullerene

Abstract: Perfluoroalkylated nanospheres have been prepared by reaction of fullerenes with a variety of fluoroalkyl radicals. The latter are generated by thermal or photochemical decomposition of fluoroalkyl iodides or fluorodiacyl peroxides. Up to 16 radicals add to C(60) to afford easily isolable fluoroalkylated derivatives. The monosubstituted radical adducts were detected by electron spin resonance in the early stages of the fluoroalkylation reactions. These spheroidal molecules are thermally quite stable, soluble i… Show more

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Cited by 148 publications
(139 citation statements)
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“…We demonstrate this in Fig. 1b, where we simulate the expected fringe visibility for large perfluorinated molecules 26 in a conventional TLI. full-width at half-maximum) can the visibility reach significant values.…”
mentioning
confidence: 58%
“…We demonstrate this in Fig. 1b, where we simulate the expected fringe visibility for large perfluorinated molecules 26 in a conventional TLI. full-width at half-maximum) can the visibility reach significant values.…”
mentioning
confidence: 58%
“…Figure 1 shows an energetically non-relaxed view of the molecule, to illustrate its overall structure and complexity. The molecules [23] were synthesized by one of the authors (P F). The mass of a nanosphere with n=9 side-chains exceeds that of any molecule in all previous slow-beam studies by more than an order of magnitude, and even that of a small protein, such as insulin (m∼5700 amu).…”
Section: A Moleculementioning
confidence: 99%
“…We used an Extrel quadrupole mass spectrometer with electron energy of E kin =40..70 eV which allows to detect molecules with masses up to 9000 amu. We here report on the first on electron impact ionization for detecting those large perflouroalkylated molecules [23]. For the mass spectrum shown in Figure 2 a) the spectrometer was optimzed to the signal of nanospheres with n=7 side-chains (see discussion below).…”
Section: B Beam Machinementioning
confidence: 99%
“…While there is limited literature concerning perfluorinated alkylation of carbon nanomaterials [7], Hirsch and coworkers have derivatized SWNTs with perfluorooctyl groups via UV photolysis of perfluorooctyl iodide [8]. However, the resulting R F -SWNTs showed no solubility enhancement, and product characterization was limited to 19 F nuclear magnetic resonance (NMR).…”
Section: Introductionmentioning
confidence: 99%