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Rb6LiPr11Cl16[SeO3]12: Ein chloridisch derivatisiertes Rubidium‐Lithium‐Praseodym(III)‐Oxoselenat(IV)
Authors:Christian Lipp  Thomas Schleid
Abstract:Rb6LiPr11Cl16SeO3]12: A Chloride‐Derivatized Rubidium Lithium Praseodymium(III) Oxoselenate(IV) Transparent green square platelets with often truncated edges and corners of Rb6LiPr11Cl16SeO3]12 were obtained by the reaction of elemental praseodymium, praseodymium(III,IV) oxide and selenium dioxide with an eutectic LiCl–RbCl flux at 500 °C in evacuated silica ampoules. A single crystal of the moisture and air insensitive compound was characterized by X‐ray diffraction single‐crystal structure analysis. Rb6LiPr11Cl16SeO3]12 crystallizes tetragonally in the space group I4/mcm (no. 140; a = 1590.58(6) pm, c = 2478.97(9) pm, c/a = 1.559; Z = 4). The crystal structure is characterized by two types of layers parallel to the (001) plane following the sequence 121′2′1. Cl? anions form cubes around the Rb+ cations (Rb1 and Rb2; CN = 8; d(Rb+?Cl?) = 331 – 366 pm) within the first layer. One quarter of the possible places for Rb+ cations within this CsCl‐type kind of arrangement is not occupied, however the Cl? anions of these vacancies are connected to Pr3+ cations (Pr4) above and below instead, forming square antiprisms of (Pr4)O4Cl4]9? units (d(Pr4?O) = 247–249 pm; d(Pr4?Cl) = 284–297 pm) that work as links between layer 1 and 2. Central cations of the second layer consist of Li+ and Pr3+. While the Li+ cations are surrounded by eight O2? anions (d(Li?O5) = 251 pm) in the shape of cubes again, the Pr3+ cations are likewisely coordinated by eight O2? anions as square antiprisms (for Pr1, d(Pr1?O2) = 242 pm) and by ten O2? anions (for Pr2 and Pr3), respectively. The latter form tetracapped trigonal antiprisms (Pr2, d(Pr2?O) = 251–253 pm and 4 × 262 pm) or bicapped distorted cubes (Pr3, d(Pr3?O) = 245–259 pm and 2 × 279 pm). The non‐binding electron pairs (“lone pairs”) at the two crystallographically different Ψ1‐tetrahedral SeO3]2? anions (d(Se4+?O2?) = 169–173 pm) are directing towards the empty cavities between the layer‐connecting (Pr4)O4Cl4]9? units.
Keywords:Praseodymium  Oxoselenates(IV)  Alkali‐metal chloride derivatives  Crystal structure
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