[2 + 1] Cycloaddition reactions of fullerene C60 based on diazo compounds

Abstract

The most common variant of fullerene core functionalization is the [2 + 1] cycloaddition process. Of these, reactions leading to methanofullerenes are the most promising. They are synthesized in two main reactions: nucleophilic cyclopropanation according to the Bingel method and thermal addition of diazo compounds. This present review summarizes the material on the synthesis of monofunctionalized methanofullerenes – analogues of [60]PCBM – based on various diazo compounds. The main cyclopropanating agents for the synthesis of monosubstituted methanofullerenes, the optimal conditions and the mechanism of the [2 + 1] cycloaddition, as well as the practical application of the target products are analyzed.

Keywords

• [2 + 1]-cycloaddition processes
• analogues of [60]pcbm
• diazo compounds
• mechanisms and optimal conditions of cyclopropanation
• methanofullerenes c60