Unprecedented protocol, consisting in reduction of Buckminsterfullerene with Na=K alloy and successive stirring in presence of O2, affords polyhydroxylated fullerenols which are highly water soluble, from strongly basic to medium acidic conditions. The products have been characterized by means of cross polarization magic angle spinning (CPMAS) NMR, 1H-NMR, electron, FT-IR, Raman and mass spectroscopies. Possible paths of reaction and the role of molecular oxygen in fullerene cage-oxidation are discussed.

HIGHLY WATER SOLUBLE C60 DERIVATIVES: A NEW SYNTHESIS

DIANA, Eliano
2003-01-01

Abstract

Unprecedented protocol, consisting in reduction of Buckminsterfullerene with Na=K alloy and successive stirring in presence of O2, affords polyhydroxylated fullerenols which are highly water soluble, from strongly basic to medium acidic conditions. The products have been characterized by means of cross polarization magic angle spinning (CPMAS) NMR, 1H-NMR, electron, FT-IR, Raman and mass spectroscopies. Possible paths of reaction and the role of molecular oxygen in fullerene cage-oxidation are discussed.
2003
11
35
46
Fullerene, Water solubility, Solid state spectroscopies.
A. Arrais; E. Diana
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/112005
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