Two novel polymeric Mg formates [(Fmd)Mg(HCOO)3]‘ (1) and [(Gua)Mg(HCOO)3]‘ (2) containing the formamidinium [Fmd+, (NH2–CH+–NH2)] and guanidinium [Gua+, C+(NH2)3] cations have been prepared under solvothermal conditions. 1 and 2 are isostructural; they crystallize in the orthorhombic space group Pnna. Their 3D scaffolds consists of Mg ions in an octahedral coordination environment bridged by formate ligands. The overall framework charge is negative, and the cations are located in the centre of the lattice cavities, forming extensive N–H…O hydrogen bonding with the surrounding cage. Both compounds have been characterized through single-crystal and powder X-ray diffraction, 1D and 2D solid-state NMR (1H, 13C and 15N), IR spectroscopy and TG-MS analysis. Their chemical reactivity towards ion exchange and ability as CO2 storage materials has been finally examined.

Amine-templated polymeric Mg formates: crystalline scaffolds exhibiting extensive hydrogen bonding / Rossin A; Chierotti M R; Giambastiani G; Gobetto R; Peruzzini M. - In: CRYSTENGCOMM. - ISSN 1466-8033. - STAMPA. - 14:(2012), pp. 4454-4460. [10.1039/c2ce25048a]

Amine-templated polymeric Mg formates: crystalline scaffolds exhibiting extensive hydrogen bonding

Giambastiani G;
2012

Abstract

Two novel polymeric Mg formates [(Fmd)Mg(HCOO)3]‘ (1) and [(Gua)Mg(HCOO)3]‘ (2) containing the formamidinium [Fmd+, (NH2–CH+–NH2)] and guanidinium [Gua+, C+(NH2)3] cations have been prepared under solvothermal conditions. 1 and 2 are isostructural; they crystallize in the orthorhombic space group Pnna. Their 3D scaffolds consists of Mg ions in an octahedral coordination environment bridged by formate ligands. The overall framework charge is negative, and the cations are located in the centre of the lattice cavities, forming extensive N–H…O hydrogen bonding with the surrounding cage. Both compounds have been characterized through single-crystal and powder X-ray diffraction, 1D and 2D solid-state NMR (1H, 13C and 15N), IR spectroscopy and TG-MS analysis. Their chemical reactivity towards ion exchange and ability as CO2 storage materials has been finally examined.
2012
14
4454
4460
Rossin A; Chierotti M R; Giambastiani G; Gobetto R; Peruzzini M
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1352169
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