The New Cesium Praseodymium Thiophosphate Cs3Pr5[PS4]6

Abstract

AbstractTransparent platelet‐shaped green single crystals of the title compound were obtained by the reaction of cesium bromide, praseodymium, sulfur, and red phosphorus in the molar ratio 1:2:8:2 with an excess of CsBr as flux in evacuated silica ampoules at 950 °C for fourteen days. Cs3Pr5[PS4]6 crystallizes monoclinically in the space group C2/c (a = 1627.78(7), b = 1315.09(6), c = 2110.45(9) pm, β = 103.276(5)°; Z = 4). Its crystal structure is different from all the other alkali‐metal containing ortho‐thiophosphates of the lanthanides, since it is not possible to formulate a layer containing the praseodymium centered sulfur polyhedra ([PrS8]13—, d(Pr—S) = 286 — 307 pm) and the isolated [PS4]3— tetrahedra (d(P—S) = 202 — 207 pm, ∢(S—P—S) = 104 — 106°). All these tetrahedra are edge‐sharing with the metal polyhedra to build up a framework instead. The coordination sphere of the half occupied (Cs2)+ cations (CN = 10 + 2) can be described as two six‐membered sulfur rings in chair conformation containing a “cesium‐pair” in the middle. In contrast the (Cs1)+ cations are surrounded in the not unusual configuration of tetracapped trigonal prisms (CN = 10, better 10 + 2 as well).