Abstract

Endohedral metallofullerenes (EMFs) have attracted special interest as new spherical molecules because they have unusual physical and chemical properties that are imparted by the encapsulated metal atoms.[1] Among the fullerenes in general, paramagnetic EMFs have garnered much attention because of their unique electronic and magnetic properties, quite different from the closely related non-paramagnetic endofullerenes. La@C82 has extensively been investigated as a prototype paramagnetic fullerene because it is the first endohedral metallofullerene which was reported the successful isolation for the first time. [2] Moreover, it was demonstrated that a family of lanthanum containing fullerenes were produced and that extraction with toluene yielded abundantly La@C82. La@C82 has an electronic structure which is best described as [La]3+[C82]3- with an open-shell electronic character that is a consequence of transferring three electrons from lanthanum to C82 (Scheme).[3] The resulting electron spin imposes a unique chemical reactivity comparable to that of a radical character.[4] The latter is believed to induce magnetism[5] and enhance electron conductivity.[6] In this regard, our group has investigated and revealed unprecedented molecular properties of La@C82. In this talk, I will present its unique radical reactivity,[4] photo-induced intramolecular electron transfer,[7] and the SAM demonstrating electrochemical switching[5] based on La@C82.

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