Synthesis and Magnetism of Extended Solids Containing Transition-Metal Cations in Square-Planar, MO4 Coordination Sites
Author(s) -
Michael A. Hayward
Publication year - 2019
Publication title -
inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.348
H-Index - 233
eISSN - 1520-510X
pISSN - 0020-1669
DOI - 10.1021/acs.inorgchem.9b00960
Subject(s) - chemistry , transition metal , crystallography , metastability , chalcogenide , coordination complex , halide , paramagnetism , magnetism , metal , ion , planar , square pyramidal molecular geometry , crystal structure , inorganic chemistry , coordination number , square (algebra) , chemical physics , condensed matter physics , catalysis , biochemistry , physics , computer graphics (images) , geometry , mathematics , organic chemistry , computer science
With the exception of systems containing Cu 2+ , complex metal oxides containing paramagnetic transition-metal cations in square-planar coordination are rare. However, by either introducing chalcogenide, pnictide, or halide anions to form mixed-anion systems or by utilizing low-temperature topochemical reduction via anion deintercalation, an extensive range of phases containing square-planar MO 4 units can be prepared. The crystal chemistry of a series of transition-metal A 2 MO 2 X 2 oxyhalide and A 2 MO 2 B 2 X 2 oxychalcogenide and oxypnictide phases is reviewed along with how their magnetic behavior changes as a function of the transition-metal and electron count. As a contrast, these mixed-anion phases are then compared to a series of topochemically reduced, metastable transition-metal oxides that also contain square-planar-coordinated transition metals, to more fully illustrate the magnetic properties of extended frameworks of square-planar MO 4 units.
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