15195-58-1Relevant articles and documents
The Crystal Structure of MnF3 Revisited
Bandemehr, Jascha,Stoll, Christiane,Heymann, Gunter,Ivlev, Sergei I.,Karttunen, Antti J.,Conrad, Matthias,Huppertz, Hubert,Kraus, Florian
, p. 882 - 888 (2020)
We correct the crystal structure of MnF3, of which the space group was reported as monoclinic C2/c (no. 15) with a = 8.9202, b = 5.0472, c = 13.4748 ?, β = 92.64°, V = 606.02 ?3, Z = 12, mS48, T not given, likely 298 K. In the structure model proposed here, we use a unit cell of one third of the former volume. The ruby red crystals of MnF3 were synthesized by a high-pressure/high-temperature method, where MnF4 was used as a starting material. As determined on a single crystal, MnF3 crystallizes in the monoclinic space group I2/a (no. 15) with a = 5.4964(11), b = 5.0084(10), c = 7.2411(14) ?, β = 93.00(3)°, V = 199.06(7) ?3, Z = 4, mS16, T = 183(2) K. The crystal structure of MnF3 is related by a direct group-subgroup transition to the VF3 structure-type. We performed quantum chemical calculations on the crystal structure to allow the assignment of bands of the obtained vibrational spectra.
Mass and FTIR spectroscopic investigations of gaseous manganese tetrafluoride
Nunziante Cesaro,Rau,Chilingarov,Balducci,Sidorov
, p. 179 - 181 (2008/10/08)
Knudsen effusion mass spectrometry has been applied to establish the optimum in situ conditions for the MnF4 synthesis. MnF4 has been generated in the gas phase over the MnF3(s)-TbF4(s) system at 650-780 K in the Knudsen cell. Under the same conditions the supplying gas for the matrix isolation IR spectra was formed. The infrared spectrum of argon-isolated MnF4 molecules has been obtained for the first time. A Td symmetry is suggested for the MnF4 molecule.
Kinetics of Fluorination of Manganese Compounds with Fluorine Gas
Rakov,Ostropikov,Khaustov
, p. 149 - 153 (2008/10/08)
The kinetics of fluorination of MnO2, MnF2, and KMnF3 powders by fluorine in nitrogen carrier gas at atmospheric pressure was studied by gravimetry. The kinetic equations of fluorination were deduced. MnO2 converts to MnF3 markedly more rapidly than MnF2. The volatile product (MnF4) forms above 780 K.