Abstract

The ternary iron chalcogenides A 9Fe 2X 7 with A  K, Rb, Cs and X  S, Se were synthesized by reaction of alkali carbonates with iron and the respective chalcogen in a stream of hydrogen. The crystal structures of the potassium and rubidium compounds were determined by single-crystal diffractometer data (spacegroup P2 13, Z = 4). The atomic arrangement of the isotypic compounds is characterized by isolated trigonal nearly planar [FeX 3] and tetrahedral [FeX 4] units. The structure corresponds to that of K 9Ni 2O 7. The magnetic susceptibilities of K 9Fe 2S 7 reveal Curie-Weiss behaviour. The moment is due to a high spin state of both Fe 3+ and Fe 2+. Magnetic ordering occurs below 6 K. Mössbauer experiments prove that the Fe 3+ ions must be assigned to the tetrahedral coordination and the Fe 2+ ions to the trigonal planar coordination.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.