NEW TERNARY IRON CHALCOGENIDES A9FE2X7 (A-EQUIVALENT-TO-K, RB, CS X-EQUIVALENT-TO-S, SE) - SYNTHESIS, CRYSTAL-STRUCTURE AND MAGNETIC-PROPERTIES

Citation
W. Bronger et U. Ruschewitz, NEW TERNARY IRON CHALCOGENIDES A9FE2X7 (A-EQUIVALENT-TO-K, RB, CS X-EQUIVALENT-TO-S, SE) - SYNTHESIS, CRYSTAL-STRUCTURE AND MAGNETIC-PROPERTIES, Journal of alloys and compounds, 197(1), 1993, pp. 83-86
Citations number
6
Categorie Soggetti
Chemistry Physical","Metallurgy & Mining","Material Science
ISSN journal
09258388
Volume
197
Issue
1
Year of publication
1993
Pages
83 - 86
Database
ISI
SICI code
0925-8388(1993)197:1<83:NTICA(>2.0.ZU;2-B
Abstract
The ternary iron chalcogenides A9Fe2X7 with A=K, Rb, Cs and X=S, Se we re synthesized by reaction of alkali carbonates with iron and the resp ective chalcogen in a stream of hydrogen. The crystal structures of th e potassium and rubidium compounds were determined by single-crystal d iffractometer data (spacegroup P2(1)3, Z=4). The atomic arrangement of the isotypic compounds is characterized by isolated trigonal nearly p lanar [FeX3] and tetrahedral [FeX4] units. The structure corresponds t o that of K9Ni2O7. The magnetic susceptibilities of K9Fe2S7 reveal Cur ie-Weiss behaviour. The moment is due to a high spin state of both Fe3 + and Fe2+. Magnetic ordering occurs below 6 K. Mossbauer experiments prove that the Fe3+ ions must be assigned to the tetrahedral coordinat ion and the Fe2+ ions to the trigonal planar coordination.