abstract
The gas-phase stabilities of linear, branched and cyclic silicates made of up to five silicon atoms were studied with density functional theory (DFT). The starting geometries for the DFT calculations at the B3LYP/6-311+G(2d,2p) level of theory were obtained from classical molecular dynamics simulations. We have observed that geometric parameters and charges are mainly affected by the degree of deprotonation. Charges on Si atoms are also influenced by their degree of substitution. The enthalpy of deprotonation of the neutral species was found to decrease with the size of the molecule, while the average deprotonation enthalpy of highly charged compounds increased with molecular size. Furthermore, the formation of rings in highly charged silicates is enthalpically preferred to chain growth. These observations result from two competing effects: the easier distribution of negative charge in silicates with low charge density and the strong intramolecular repulsions present in silicates with high charge density. As a consequence, highly charged silicates in the gas phase tend to be as small and as highly condensed as possible, which is in line with experimental observations from solution NMR. (C) 2008 Elsevier Ltd. All rights reserved.
keywords
AB-INITIO CALCULATIONS; SI-29 NMR; CHEMICAL-SHIFTS; MFI ZEOLITE; TPAOH-TEOS-H2O SYSTEM; POPULATION ANALYSIS; POTASSIUM SILICATE; AQUEOUS-SOLUTION; ATOMIC CHARGES; ENERGIES
subject category
Geochemistry & Geophysics
authors
Gomes, JRB; Cordeiro, MNDS; Jorge, M
our authors
