Addition reaction between piperidine and C-60 to form 1,4-disubstituted C-60 proceeds through van der Waals and dative bond complexes: Theoretical and experimental study

Abstract

A combined computational and experimental study reveals the character of the C-60 complexes with piperidine formed under different reaction conditions. The IR and NMR experiments detect the dative bond complex, which according to NMR, is stable in the oxygen-free environment and transforms to the adduct complex in the presence of 0(2). Computational studies on the character of reaction channels rationalize the experimental observations. They show that the piperidine dimer rather than a single piperidine molecule is required for the complex formation. The calculations reveal significant differences in the dative bond and adduct complexes' character, suggesting a considerable versatility in their electronic properties modulated by the environment. This capability offers new application potential in several fields, such as in energy storage devices.