Article ID Journal Published Year Pages File Type
1331463 Journal of Solid State Chemistry 2007 8 Pages PDF
Abstract

The new compound Cs4P2Se10 was serendipitously produced in high purity during a high-temperature synthesis done in a nuclear magnetic resonance (NMR) spectrometer. 31P magic angle spinning (MAS) NMR of the products of the synthesis revealed that the dominant phosphorus-containing product had a chemical shift of −52.8 ppm that could not be assigned to any known compound. Deep reddish brown well-formed plate-like crystals were isolated from the NMR reaction ampoule and the structure was solved with X-ray diffraction. Cs4P2Se10 has the triclinic space group P-1 with a=7.3587(11) Å, b=7.4546(11) Å, c=10.1420(15) Å, α=85.938(2)°, β=88.055(2)°, and γ=85.609(2)° and contains the [P2Se10]4− anion. To our knowledge, this is the first compound containing this anion that is composed of two tetrahedral (PSe4) units connected by a diselenide linkage. It was also possible to form a glass by quenching the melt in ice water, and Cs4P2Se10 was recovered upon annealing. The static 31P NMR spectrum at 350 °C contained a single peak with a −35 ppm chemical shift and a ∼7 ppm peak width. This study highlights the potential of solid-state and high-temperature NMR for aiding discovery of new compounds and for probing the species that exist at high temperature.

Graphical abstractThe new compound Cs4P2Se10 was discovered following a high-temperature in situ synthesis in the NMR spectrometer and the structure was determined by single-crystal X-ray diffraction. It contains the new [P2Se10]4− anion.Figure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemistry Inorganic Chemistry
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