Role of Noncovalent Interactions in Vanadium Tellurite Chain Connectivities
journal contributionposted on 20.01.2015, 00:00 by Anahita Nourmahnad, Matthew D. Smith, Matthias Zeller, Gregory M. Ferrence, Joshua Schrier, Alexander J. Norquist
Structural differences in [V2Te2O10]n2n– chain metrics are directly ascribed to variations in noncovalent interactions in a series of organically templated vanadium tellurites, including [C6H17N3][V2Te2O10]·H2O, [C5H16N2][V2Te2O10], and [C4H14N2][V2Te2O10]. The noncovalent interaction (NCI) method was used to locate, quantify, and visualize intermolecular interactions in [C4H14N2][V2Te2O10] and [C5H16N2][V2Te2O10]. Variations in the van der Waals attractions between [1,4-diaminobutaneH2]2+ and [1,5-diaminopentaneH2]2+ result in divergent packing motifs for these cations, which causes a reorganization of N–H···O hydrogen bonding and variances in the [V2Te2O10]n2n– chain metrics. The application of the NCI method to this type of solid-state structure provides a direct method to elucidate the structural effects of weak noncovalent interactions.