JAHN-TELLER-ORDERING IN COMPOUNDS A2[MnF3(SO4)](A = K, Rb, NH4, Cs)

Werner Massa, Ute Jacobs, Jürgen Pebler

Fachbereich Chemie der Philipps-Universität, D-35032 Marburg, Germany
E-mail: massa@ps1515.chemie.uni-marburg.de

Keywords: manganese(III), fluorosulfatomanganates(III), crystal structures, Jahn-Teller ordering, phase transition, magnetism

Compounds A2[MnF3(SO4)], first described by Edwards [1] and Battacharjie [2] attracted our attention because the published orthorhombic structure of the K compound [1] showed the compressed octahedral geometry for the [MnF4O2] units, unusual for the Jahn-Teller ion Mn3+. We found for all four title compounds (for K below 310 K) isotypic monoclinic structures (space group P21/c, see Table) with chain anions built from [MnF4O2] units alternatingly elongated

Cs2[MnF3(SO4)]

298 K

(NH4)2[MnF3(SO4)]

298 K

Rb2[MnF3(SO4)]

213 K

K2[MnF3(SO4)]

190 K

a = 736,54(4) pm a = 729,91(3) pm a = 727,1(1) pm a = 722,3(1) pm
b = 1161,10(6) pm b = 1115,66(8) pm b = 1109,1(1) pm b = 1074,4(1) pm
c = 921,05(4) pm c = 881,25(5) pm c = 877,6(1) pm c = 844,3(1) pm
= 92,30(1)° = 91,512(4)° = 92,26(1)° = 91,68(1)°
R = 0,0292 R = 0.0248 R = 0.0334 R = 0.0473

along the bridging F-Mn-F axis or along the O-Mn-O axis to the bridging sulfato ligand (antiferrodistortive Jahn-Teller-ordering). According to this ordering scheme, 1D antiferromagnetic properties were detected with reduced exchange energies and inverse dependence of the bridge angle. The K compound undergoes at 310 K a reversible phase transition, probably of 2nd order to an orthorhombic supergroup Pnca. In this phase by a 2D dynamical Jahn-Teller effect the seemingly compressed octahedral geometry appears corresponding to Edwards structure determination.

  1. A.J.Edwards, J. Chem. Soc. A (1971) 3074
  2. M.N.Battacharjee, M.K.Chaudhuri, Polyhedron 3 (1984) 599