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17 O solid state NMR as a valuable tool for deciphering reaction mechanisms in mechanochemistry: the case study on the 17 O-enrichment of hydrated Ca-pyrophosphate biominerals.

Ieva GoldbergaNicholai D JensenChristèle CombesFrédéric Mentink-VigierXiaoling WangIvan HungZhehong GanJulien TréboscThomas-Xavier MétroChristian BonhommeChristel GervaisDanielle Laurencin
Published in: Faraday discussions (2022)
The possibility of enriching in 17 O the water molecules within hydrated biominerals belonging to the Ca-pyrophosphate family was investigated, using liquid assisted grinding (LAG) in the presence of 17 O-labelled water. Two phases with different hydration levels, namely triclinic calcium pyrophosphate dihydrate (Ca 2 P 2 O 7 ·2H 2 O, denoted t -CPPD) and monoclinic calcium pyrophosphate tetrahydrate (Ca 2 P 2 O 7 ·4H 2 O, denoted m -CPPT β) were enriched in 17 O using a "post-enrichment" strategy, in which the non-labelled precursors were ground under gentle milling conditions in the presence of stoichiometric quantities of 17 O-enriched water (introduced here in very small volumes ∼10 μL). Using high-resolution 17 O solid-state NMR (ssNMR) analyses at multiple magnetic fields, and dynamic nuclear polarisation (DNP)-enhanced 17 O NMR, it was possible to show that the labelled water molecules are mainly located at the core of the crystal structures, but that they can enter the lattice in different ways, namely by dissolution/recrystallisation or by diffusion. Overall, this work sheds light on the importance of high-resolution 17 O NMR to help decipher the different roles that water can play as a liquid-assisted grinding agent and as a reagent for 17 O-isotopic enrichment.
Keyphrases
  • solid state
  • high resolution
  • magnetic resonance
  • mass spectrometry
  • ionic liquid
  • tandem mass spectrometry