Theoretical Insight into Non-Covalent Complexes of Closo-Borate Anions [BnHn−1X]y− with Glycine

Non-covalent contacts play a significant role in binding between fragments in supramolecular assemblies. Understanding the non-covalent binding capabilities of closo-borate anions and their derivatives is a significant research challenge, due to their ability to interact with biomolecules. The present work was focused on the theoretical study of non-covalent complexes between glycine and closo-borate anions [BnHn−1X]y− (X = H, NH3, OH, SH, F; n = 10, 12; y = 1, 2). The main binding patterns between glycine and cluster systems were defined, and the effect of the exo-polyhedral substituent on the stability of non-covalent complexes was analysed. Complexes based on ammonium and hydroxy derivatives of closo-borate anions [BnHn−1X]y− (X = NH3, OH; n = 10, 12; y = 1, 2) were the most stable among all the derivatives considered. The findings of this work can be applied to the design of non-covalent complexes of closo-borate systems with biomolecules.