Mimicking mineral neogenesis for the clean synthesis of metal-organic materials from mineral feedstocks: coordination polymers, MOFs and metal oxide separation

We present a systematic study of a mild approach for the activation of metal oxides, involving reactivity and self-assembly in the solid state, which enables their solvent-free chemical separation and direct solvent-free and low-energy conversion into coordination polymers and open metal-organic frameworks (MOFs). The approach is inspired by geological biomineralization processes known as mineral weathering, in which long-term exposure of oxide or sulfide minerals to molecules of biological origin leads to their conversion into simple coordination polymers. This proof-of-principle study shows how mineral neogenesis can be mimicked in the laboratory to provide coordination polymers directly from metal oxides without a significant input of either thermal or mechanical energy, or solvents. We show that such aging is accelerated by increased humidity, a mild temperature increase and/or brief mechanical activation, enabling the transformation of a variety of high-melting (800 degrees C-2800 degrees C) transition (Mn-II, Co-II, Ni-II, Cu-II, and Zn) and main group (Mg and Pb-II) oxides at or near room temperature. Accelerated aging reactions are readily scaled to at least 10 grams and can be templated for the synthesis of two-dimensional and three-dimensional anionic frameworks of Zn, Ni(II) and Co(II). Finally, we demonstrate how this biomineralization-inspired approach provides an unprecedented opportunity for solvent-free chemical segregation of base metals, such as Cu, Zn and Pb, in their oxide form under mild conditions.