Thin films of fullerodendron (C(60)(Gn-COOMe) (n = 0.5, 1.5, 2.5)), which was synthesized from fullerene and anthracenyl poly(amido amine) dendron with methyl ester terminals and different generations (G), were fabricated by the Langmuir-Blodgett (LB) and adsorption techniques. It was characterized by X-ray reflectometry that the LB films possessed well-ordered structure, although the adsorption method led to random orientation of molecules. As to C(60)(G0.5-COOMe) and C(60)(G1.5-COOMe), the LB films took a four-layer structure consisting of a double layer of molecules, and fullerene moieties exist in the interior of the LB films. On the other hand, C(60)(G2.5-COOMe) led to a two-layer structure in which the fullerene moieties were at the air side and the dendron moieties were at the substrate side. With increasing generation of dendron, the monolayer formation ability at the air/water interface as amphiphilic molecule strengthens and the amphiphilic property becomes superior to the fullerene-fullerene attractive interaction that prevents the monolayer formation. Furthermore, in the case of C(60)(G0.5-COOMe) and C(60)(G1.5-COOMe), the reduction peak in cyclic voltammetry of the LB film remained even after UV light irradiation. On the contrary, the peak of the C(60)(G2.5-COOMe) LB film disappeared, indicating that molecular arrangement in the films affects electrochemical properties.
Fullerodendrimer acts as a new catalyst that uses oxygen and light to generate singlet oxygen (1O2). The dendrimer facilitates various types of singlet oxygenation reactions including ene reaction, the Diels–Alder reaction, and oxidation of phenol and sulfide.
Photochemistry O 0160Photooxygenation of Olefins, Phenol, and Sulfide Using Fullerodendrimer as Catalyst. -The title catalyst facilitates various types of singlet oxygenation reactions including ene reaction, Diels-Alder reaction and oxidation of phenol and sulfide. -(TAKAGUCHI*, Y.; YANAGIMOTO, Y.; FUJIMA, S.; TSUBOI, S.; Chem. Lett. 33
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