Polar covalent apex‐base bonding in borapyramidanes probed by solid‐state NMR and DFT calculations

Abstract

AbstractPyramidane molecules have attracted chemists for many decades due to their regular shape, high symmetry and their correspondence in the macroscopic world. Recently, experimental access to a number of examples has been reported, in particular the rarely reported square pyramidal bora[4]pyramidanes. To describe the bonding situation of the nonclassical structure of pyramidanes, we present solid‐state Nuclear Magnetic Resonance (NMR) as a versatile tool for deciphering such bonding properties for three now accessible bora[4]pyramidane and dibora[5]pyramidane molecules. 11B solid‐state NMR spectra indicate that the apical boron nuclei in these compounds are strongly shielded (around −50 ppm vs. BF3‐Et2O complex) and possess quadrupolar coupling constants of less than 0.9 MHz pointing to a rather high local symmetry. 13C−11B spin‐spin coupling constants have been explored as a measure of the bond covalency in the borapyramidanes. While the carbon‐boron bond to the −B(C6F5)2 substituents of the base serves as an example for a classical covalent 2‐center‐2‐electron (2c–2e) sp2‐carbon‐sp2‐boron σ‐bond with 1J(13C‐11B) coupling constants in the order of 75 Hz, those of the boron(apical)‐carbon(basal) bonds in the pyramid are too small to measure. These results suggest that these bonds have a strongly ionic character, which is also supported by quantum‐chemical calculations.