Improved synthesis of fullerynes by Fisher esterification for modular and efficient construction of fullerene polymers with high fullerene functionality

For the first time, the scope of Fisher esterification has been extended to fullerene derivatives to improve the synthesis of alkyne-functionalized fullerenes (fullerynes) using 1-chloronaphthalene as a solvent and a specially-designed, home-made reactor to promote high yield. The design allows for higher solubility of fullerene derivatives and a continuous azeotropic distillation for the removal of water to drive the reaction to completion with yields >90%. Both fullerynes (Fulleryne01 and Fulleryne02) were found to "click" to polymers, such as azide-functionalized poly(epsilon-caprolactone) (PCL-N(3)), in high efficiency without the need for fractionation. As evidenced by (1)H NMR, (13)C NMR, size exclusion chromatography, and matrix assisted laser desorption ionization time-of-flight (MALDI-TOF) mass spectrometry, the fullerene polymers thus obtained possess well-defined structure, narrow polydispersity (similar to 1.01 by MALDI-TOF mass spectrometry; similar to 1.03 by size exclusion chromatography), and high fullerene functionality (similar to 100%). They can serve as model compounds for the investigations of polymer structures and dynamics. (C) 2011 Elsevier Ltd. All rights reserved.