Neue Pnictide im CaAl2Si2-Typ und dessen Existenzgebiet/New Pnictides with the CaAl2Si2 Type Structure and the Stability Range of this Type

Five new compounds were synthesized by heating mixtures of the elements at 600 - 1000 °C and investigated by powder and single crystal X-ray methods. EuMg (a = 4.280(1), c = 7.164(3) Å), EuMg As (a = 4.393(1), c = 7.321(1) Å),EuMg Sb (a = 4.695(1), c = 7.724(2) Å), YbMg Sb (a = 4.650(1), c = 7.540(2...

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Veröffentlicht in:Zeitschrift für Naturforschung. B, A journal of chemical sciences A journal of chemical sciences, 2002-11, Vol.57 (11), p.1270-1276
Hauptverfasser: Wartenberg, Franziska, Kranenberg, Christian, Pocha, Regina, Johrendt, Dirk, Mewis, Albrecht, Hoffmann, Rolf-Dieter, Mosel, Bernd D., Pöttgen, Rainer
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Sprache:eng
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Zusammenfassung:Five new compounds were synthesized by heating mixtures of the elements at 600 - 1000 °C and investigated by powder and single crystal X-ray methods. EuMg (a = 4.280(1), c = 7.164(3) Å), EuMg As (a = 4.393(1), c = 7.321(1) Å),EuMg Sb (a = 4.695(1), c = 7.724(2) Å), YbMg Sb (a = 4.650(1), c = 7.540(2) Å), and SrLiAlSb (a = 4.584(3), c = 7.697(9) Å) crystallize with the CaAl Si type structure (P3̄m1; Z = 1). The magnetic susceptibility of EuMg Sb shows Curie-Weiss behavior with an experimental magnetic moment of 7.48(2) μ /Eu atom and a Weiss constant θ = 3.2(1) K. EuMg Sb is ordered antiferromagnetically at 8.2(3) K. Magnetisation measurements at 4.5 K show a linear increase and a saturation for a magnetic moment of 5.9(1) μ /Eu at 5.5 T, indicating an almost parallel spin alignment with increasing field strength. 151Eu Mössbauer spectra at 78 K show an isomer shift of -11.69(5) mm/s, compatible with divalent europium. At 4.2 K we observe full hyperfine field splitting with 23 T. The Sb spectrum at 4.2 K shows a transferred hyperfine field of 8(2) T at an isomer shift of -7.9(3) mm/s. From the band structure of EuMg Sb we draw the conclusion, that analogous compounds of trivalent rare-earth metals with CaAl Si type structure should not exist due to electronic reasons.
ISSN:0932-0776
1865-7117
DOI:10.1515/znb-2002-1112