Abstract
A novel porous metal–organic framework, Mn9(btt)2(HCOO)12·0.7DMF·0.9H2O, was synthesized solvothermally in mixed H2O–DMF. Its structure was characterized by single-crystal X-ray diffraction techniques, which reveal that it is constructed by cross-linking Mn2+ ions with 1,3,5-benzenetristetrazolates and formates, which formed in situ from the hydrolysis of dimethylformamide, to form a 3D framework with parallel hexagonal channels. Although the Mn2+ ions at 4f Wyckoff sites are 75% occupied, the framework remains robust and porous upon evacuation of solvent molecules, with 264 m2g−1 BET surface area and hydrogen adsorption capacity of ca. 0.9 wt% at 77 K and 1 atm. Photoluminescence studies exhibit a blue band with λmax = 418 nm.
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