Thorium copper phosphides: More diverse metal-phosphorus and phosphorus-phosphorus interactions than U analogues

Geng Bang Jin*, Christos D. Malliakas, Jian Lin

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

To explore the chemical analogy between thorium and heavier actinides in soft anionic environments, three new thorium phosphides (ThCuP2, β-ThCu2P2, and ThCu5P3) have been prepared through solid-state reactions using CuI as a reaction promoter. The structure of ThCuP2 can be described as a filled UTe2-type with both dimeric P24- and monomeric P3- anions, in which Th is coordinated by eight P atoms in a bicapped trigonal prismatic arrangement and Cu is tetrahedrally coordinated by four P atoms. β-ThCu2P2 contains only P3- anions and is isostructural with BaCu2S2. In this structure, Th is coordinated by seven P atoms in monocapped trigonal prismatic geometry and Cu is tetrahedrally coordinated by four P atoms. ThCu5P3 adopts the YCo5P3-type structure consisting of P3- anions. This structure contains Th atoms coordinated by six P atoms in a trigonal prismatic arrangement and Cu atoms that are either tetrahedrally coordinated by four P atoms or square pyramidally coordinated by five P atoms. Electric resistivity measurements and electronic structure calculations on β-ThCu2P2 indicate a metal. These new compounds may be charge-balanced and formulated as Th4+Cu+(P24-)1/2P3-, Th4+(Cu+)2(P3-)2, and Th4+(Cu+)5(P3-)3, respectively. The structural, bonding, and property relationships between these Th compounds and related actinide and rare-earth phases are discussed. Titled compounds display more diverse ion-ion interactions and different electronic structures from those in UCuP2 and UCu2P2 that were synthesized under similar experimental conditions, suggesting divergence of thorium-phosphide chemistry from uranium-phosphide chemistry.

Original languageEnglish (US)
Pages (from-to)12041-12052
Number of pages12
JournalDalton Transactions
Volume46
Issue number36
DOIs
StatePublished - 2017

Funding

This work was performed at the Argonne National Laboratory operated by UChicago Argonne LLC for the United States Department of Energy under contract number DE-AC02-06CH11357 and was supported by the DOE Office of Basic Energy Sciences, Chemical Sciences, Heavy Elements Chemistry. C. D. M. was supported by the IMSERC at Northwestern University, which has received support from the Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource (NSF NNCI-1542205), the State of Illinois and the International Institute for Nanotechnology (IIN).

ASJC Scopus subject areas

  • Inorganic Chemistry

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