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Preparation of a Corannulene-functionalized Hexahelicene by Copper(I)-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units
Published on: September 18, 2016
Preparation of fullerene-shell dendrimer-core nanoconjugates
Anton W Jensen1, Brijesh S Maru, Xi Zhang
1Department of Chemistry, Central Michigan University, Mount Pleasant, Michigan 48859, USA.
Abstract:
Generation 4 amine-terminated polyamidoamine dendrimer (PAMAM G4) was allowed to react with an excess of buckminsterfullerene (C60) to form a nanoconjugate containing a PAMAM core and C60 shell. The PAMAM-C60 conjugate was characterized by MALDI-TOF, TGA, UV-vis, and IR spectroscopy. Approximately thirty shell fullerenes surround each dendrimer core. The conjugates catalyze photooxidation of thioanisole by generation of singlet oxygen (1O2). The oxidation reactions occur in both organic and aqueous solvents, but the reactivity is enhanced in aqueous solution, possibly due to a nanoreactor effect resulting from diffusion of hydrophobic reactant molecules into dendrimer cavities.

