Isolation of a Side-On V(III)-(eta(2)-O-2) through the Intermediacy of a Low-Valent V(II) in a Metal-Organic Framework

We report the isolation of vanadium(II) in a metal-organic framework (MOF) by the reaction of the chloride-capped secondary building unit in the all-vanadium(III) V-MIL-101 (1) with 1, 4-b is (trimethylsilyI)-2,3, 5,6-te tramethyl -1,4- dihydropyraz ine. The reduced material, 2, has a secondary building unit with the formal composition [(VV2III)-V-II], with each metal ion presenting one open coordination site. Subsequent reaction with O-2 yields a side-on eta(2) vanadium-superoxo species, 3. The MOF featuring V(III)-superoxo moieties exhibits a mild enhancement in the isosteric enthalpy of adsorption for methane compared to the parent V-MIL-101. We present this synthetic methodology as a potentially broad way to access low-valent open metal sites within MOFs without causing a loss of crystallinity or porosity. The low-valent sites can serve as isolable intermediates to access species otherwise inaccessible by direct synthesis.