A detailed analysis of the solvothermal synthesis in DMF of the polymeric magnesium formate H[Mg(HCOO)(3)]superset of NHMe2(infinity) (1) from Mg(ClO4)(2)center dot 6H(2)O revealed that the final crystalline product is formed after an acid-catalyzed DMF hydrolysis, producing formic acid and dimethylamine. The former bridges magnesium(II) centers, creating the 3D scaffold, while the latter is trapped inside the cubic cavities of the polymer, engaging in strong hydrogen bonding with the formate ions of the cage. After thermal activation and guest removal, the material was tested for hydrogen uptake at T = 77K over the 0-80 bar pressure range, and the existence of preferred H-2 adsorption sites was assessed through grand canonical Monte Carlo (GCMC) simulations. No specific low-energy site was found, and the H-2 molecules positions within the framework cavities are mainly dependent on packing effects. Thus, at low H-2 loadings the most populated site is the center of the cubic cavities, even though, at higher pressures, two more "localized" positions have been found by the simulation because of the reduced freedom of movement. The maximum experimental H-2 uptake corresponds to 8.8 mg/g or 13.5 mg/cm(3).
Hydrogen Uptake by H[Mg(HCOO)(3)]superset of NHMe2(infinity) and Determination of Its H-2 Adsorption Sites through Monte Carlo Simulations
J. G. Vitillo
2011-01-01
Abstract
A detailed analysis of the solvothermal synthesis in DMF of the polymeric magnesium formate H[Mg(HCOO)(3)]superset of NHMe2(infinity) (1) from Mg(ClO4)(2)center dot 6H(2)O revealed that the final crystalline product is formed after an acid-catalyzed DMF hydrolysis, producing formic acid and dimethylamine. The former bridges magnesium(II) centers, creating the 3D scaffold, while the latter is trapped inside the cubic cavities of the polymer, engaging in strong hydrogen bonding with the formate ions of the cage. After thermal activation and guest removal, the material was tested for hydrogen uptake at T = 77K over the 0-80 bar pressure range, and the existence of preferred H-2 adsorption sites was assessed through grand canonical Monte Carlo (GCMC) simulations. No specific low-energy site was found, and the H-2 molecules positions within the framework cavities are mainly dependent on packing effects. Thus, at low H-2 loadings the most populated site is the center of the cubic cavities, even though, at higher pressures, two more "localized" positions have been found by the simulation because of the reduced freedom of movement. The maximum experimental H-2 uptake corresponds to 8.8 mg/g or 13.5 mg/cm(3).
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