[70]Fullerene-Fused Lactones: Regioselective Synthesis and Electrochemical Derivatization

[70]Fullerene (C₇₀)-fused five-membered-ring lactones were synthesized via manganese(III) acetate (Mn(OAc)₃)- or air-promoted protocols. Under Mn(OAc)₃-promoted conditions, three isomers <b>2a</b>-<b>c</b> were obtained. In contrast, the single isomer <b>2a</b> was regioselectively generated under aerobic conditions, representing a distinctive phenomenon in the exohedral functionalization of C₇₀. The electrochemically generated dianion from lactone <b>2a</b> was further reacted with different electrophiles to regioselectively produce either monoalkylated 1,2-adducts (<b>4a</b>-<b>c</b>) or bisalkylated 2,5-adducts (<b>5a</b>-<b>c</b>). Notably, the unprecedented C₇₀-fused cyclobutanone <b>6a</b> was readily obtained by treatment with an acyl chloride, and its application as a third component achieved an improved power conversion efficiency of 19.0% in organic photovoltaics.