| Autor: |
Goldberga I; ICGM, Univ Montpellier, CNRS, ENSCM, 34293 Montpellier, France., Hung I; National High Magnetic Laboratory (NHMFL), Tallahassee, Florida 32310, United States., Sarou-Kanian V; CNRS, CEMHTI UPR3079, Université d'Orléans, 45071 Orléans, France., Gervais C; LCMCP, UMR 7574, Sorbonne Université, CNRS, 75005 Paris, France., Gan Z; National High Magnetic Laboratory (NHMFL), Tallahassee, Florida 32310, United States., Novák-Špačková J; ICGM, Univ Montpellier, CNRS, ENSCM, 34293 Montpellier, France., Métro TX; ICGM, Univ Montpellier, CNRS, ENSCM, 34293 Montpellier, France., Leroy C; ICGM, Univ Montpellier, CNRS, ENSCM, 34293 Montpellier, France., Berthomieu D; ICGM, Univ Montpellier, CNRS, ENSCM, 34293 Montpellier, France., van der Lee A; IEM, Univ Montpellier, CNRS, ENSCM, 34095 Montpellier, France., Bonhomme C; LCMCP, UMR 7574, Sorbonne Université, CNRS, 75005 Paris, France., Laurencin D; ICGM, Univ Montpellier, CNRS, ENSCM, 34293 Montpellier, France. |
| Abstrakt: |
Oxalate ligands are found in many classes of materials, including energy storage materials and biominerals. Determining their local environments at the atomic scale is thus paramount to establishing the structure and properties of numerous phases. Here, we show that high-resolution 17 O solid-state NMR is a valuable asset for investigating the structure of crystalline oxalate systems. First, an efficient 17 O-enrichment procedure of oxalate ligands is demonstrated using mechanochemistry. Then, 17 O-enriched oxalates were used for the synthesis of the biologically relevant calcium oxalate monohydrate (COM) phase, enabling the analysis of its structure and heat-induced phase transitions by high-resolution 17 O NMR. Studies of the low-temperature COM form (LT-COM), using magnetic fields from 9.4 to 35.2 T, as well as 13 C- 17 O MQ/D-RINEPT and 17 O{ 1 H} MQ/REDOR experiments, enabled the 8 inequivalent oxygen sites of the oxalates to be resolved, and tentatively assigned. The structural changes upon heat treatment of COM were also followed by high-resolution 17 O NMR, providing new insight into the structures of the high-temperature form (HT-COM) and anhydrous calcium oxalate α-phase (α-COA), including the presence of structural disorder in the latter case. Overall, this work highlights the ease associated with 17 O-enrichment of oxalate oxygens, and how it enables high-resolution solid-state NMR, for "NMR crystallography" investigations. |
