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Updated: Jul 23, 2026

Combining Solid-state and Solution-based Techniques: Synthesis and Reactivity of Chalcogenidoplumbates(II or IV)
Published on: December 29, 2016
Solid-state NMR characterization of the mineral searlesite and its detection in complex synthesis mixtures
C A Fyfe1, J Skibsted, W Schwieger
1Department of Chemistry, University of British Columbia, Vancouver, British Columbia, Canada V6T 1Z1. fyfe@chem.ubc.ca
Abstract:
The mineral searlesite (NaBSi(2)O(5)(OH)(2)) was synthesized and characterized by (1)H, (11)B, (23)Na, and (29)Si magic-angle spinning (MAS) NMR spectroscopy. From these spectra, the (11)B and (23)Na quadrupole coupling parameters and isotropic chemical shifts and the (29)Si chemical shift anisotropies have been precisely determined. These parameters are all consistent with the local environments obtained from the crystal structure for searlesite from X-ray diffraction, and they demonstrate that the synthetic sample has a high degree of both short- and long-range order. Furthermore, these anisotropic parameters are found to provide a unique fingerprinting of searlesite in complex mixtures where the presence of this mineral is not anticipated. This is demonstrated for product mixtures formed in attempts to incorporate boron in the structures of the layer silicates magadiite and kenyaite. These mixtures have been investigated by (11)B, (23)Na, and (29)Si MAS NMR which clearly reveal that the samples are mixtures of searlesite and magadiite/kenyaite and that searlesite production consumes all of the boron in these synthesis mixtures. However, the (29)Si MAS NMR spectra of these mixtures indicate that the presence of boron in the reaction mixtures nevertheless has an important influence on the quality of the magadiite and kenyaite layer silicates produced.
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