DFT study on the selective complexation of B12N12 nanocage with alkali metal ions. (4th March 2018)

• Record Type: Journal Article
• Authors: Khavani, Mohammad; Izadyar, Mohammad; Housaindokht, Mohammad Reza
• Is Part Of: Phosphorus, sulfur, and silicon and the related elements. Volume 193:Number 3(2018)
• Page Start: 178
• Page End: 184
• Publication Date: 2018-03-04
• Subjects: Nanocage -- natural bond orbital analysis -- electrostatic interaction -- selective complexation -- alkali metal ion -- molecular topology; Sulfur compounds -- Periodicals; Organosulfur compounds -- Periodicals; Phosphorus compounds -- Periodicals; Organophosphorus compounds -- Periodicals; Silicon compounds -- Periodicals; Organosilicon compounds -- Periodicals; 546
• DOI: 10.1080/10426507.2017.1394301
• Languages: English
• ISSNs: 1042-6507

Abstract

GRAPHICAL ABSTRACT: Quantum chemistry calculations indicate that BN nanocage is a good candidate for selective complex formation with Li + in the presence of different alkali metal ions. ABSTRACT: Density functional theory (DFT) calculations were applied at the M05-2X/6-311++G(d, p) level of the theory to investigate the interaction of the B12 N12 nanocage (BN) and alkali metal ions (Li +, Na +, K +, Rb + and Cs + ) in the gas phase and in water. On the basis of the results, BN nanocage is able to form a selective complex with Li + . Water, as a solvent, reduces the stability of the metal ion-BN complexes in comparison with the gas phase. Natural bond orbital (NBO) and quantum theory of atoms in molecules (QTAIM) analyses, reveal that the electrostatic interaction between the BN and metal ions can be considered as the driving force for complex formation in which the role of water is of significance. Density of states (DOSs) analysis of the BN nanocage structure in the presence of different metal ions showed a noticeable change in the frontier orbitals, especially in the gas phase, and Fermi level shifting toward the lower values.