New one-pot method for the synthesis of pyrrolidinofullerenes

New one-pot method for the synthesis of pyrrolidinofullerenes

The reaction of fullerene C 60 with isocyanoacetates and EtMgBr in the presence of stoichiometric amounts of Ti(Oi-Pr) 4 was studied for the first time. Unlike esters and nitriles of carboxylic acids and isonitriles, isocyanoacetates were found to react with C 60 under the developed conditions to gi...

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Veröffentlicht in:RSC advances 2016-01, Vol.6 (85), p.81847-81851
Hauptverfasser: Tuktarov, A. R, Shakirova, Z. R, Budnikova, Yu. G, Salikhov, R. B, Dzhemilev, U. M
Format: Artikel
Sprache:eng
Schlagworte:
Buckminsterfullerene
Carboxylic acids
Derivatives
Esters
Fullerenes
Nitriles
Reduction
Synthesis
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Beschreibung
Zusammenfassung:The reaction of fullerene C 60 with isocyanoacetates and EtMgBr in the presence of stoichiometric amounts of Ti(Oi-Pr) 4 was studied for the first time. Unlike esters and nitriles of carboxylic acids and isonitriles, isocyanoacetates were found to react with C 60 under the developed conditions to give N -unsubstituted pyrrolidinofullerenes. The electrochemical reduction of the C 60 derivatives we synthesized was found to proceed less easily than that of C 60 but more easily than that of unsubstituted pyrrolidinofullerenes. The reaction of fullerene C 60 with isocyanoacetates and EtMgBr in the presence of stoichiometric amounts of Ti(Oi-Pr) 4 was studied for the first time.
ISSN:2046-2069
2046-2069
DOI:10.1039/c6ra15519g