Nientiedt André T., Jeitschko Wolfgang
Anorganisch-Chemisches Institut, Universität Münster, Wilhelm-Klemm-Strasse 8, D-48149 Münster, Germany.
Inorg Chem. 1998 Feb 9;37(3):386-389. doi: 10.1021/ic971058q.
The twelve phosphide oxides RZnPO (R = Y, La-Nd, Sm, Gd-Tm) and the nine arsenide oxides (R = Y, La-Nd, Sm, Gd-Dy) have been prepared by reaction of the rare earth elements, ZnO, and phosphorus or arsenic, respectively, in a NaCl/KCl flux. The compounds RZnPO (R = Y, Pr, Nd, Sm, Gd-Tm) crystallize with a new trigonal rhombohedral structure type, determined from single-crystal X-ray diffractometer data of NdZnPO: R&thremacr;m, a = 397.7(1) pm, c = 3097.5(5) pm, Z = 6. The other eleven compounds are isotypic with ZrCuSiAs (P4/nmm, Z = 2). This tetragonal structure was refined from single-crystal X-ray data of LaZnPO (a = 404.0(1) pm, c = 890.8(2) pm) and NdZnAsO (a = 403.0(1) pm, c = 894.9(4) pm). In both structure types rare earth element-oxygen layers alternate with zinc-pnictogen layers. The rare earth element atoms have four oxygen and three (NdZnPO) or four (LaZnPO, NdZnAsO) pnictogen neighbors. The zinc atoms have tetrahedral pnictogen coordination. The arsenide oxides as well as the tetragonal phosphide oxides LaZnPO and CeZnPO are black, while the other (trigonal) phosphide oxides are transparent. The more metallic character of the tetragonal compounds is ascribed to their more delocalized chemical bonding, as is indicated by their higher coordination numbers, which in part also result through significant Zn-Zn bonding.
通过分别使稀土元素、氧化锌与磷或砷在NaCl/KCl助熔剂中反应,制备出了十二种磷氧化物RZnPO(R = Y、La - Nd、Sm、Gd - Tm)和九种砷氧化物(R = Y、La - Nd、Sm、Gd - Dy)。化合物RZnPO(R = Y、Pr、Nd、Sm、Gd - Tm)以一种新的三方菱面体结构类型结晶,该结构由NdZnPO的单晶X射线衍射仪数据确定:R̅m,a = 397.7(1) pm,c = 3097.5(5) pm,Z = 6。其他十一种化合物与ZrCuSiAs同型(P4/nmm,Z = 2)。这种四方结构是根据LaZnPO(a = 404.0(1) pm,c = 890.8(2) pm)和NdZnAsO(a = 403.0(1) pm,c = 894.9(4) pm)的单晶X射线数据精修得到的。在这两种结构类型中,稀土元素 - 氧层与锌 - 氮族元素层交替排列。稀土元素原子有四个氧原子和三个(NdZnPO)或四个(LaZnPO、NdZnAsO)氮族元素邻位原子。锌原子具有四面体氮族元素配位。砷氧化物以及四方磷氧化物LaZnPO和CeZnPO是黑色的,而其他(三方)磷氧化物是透明的。四方化合物更强的金属特性归因于其更离域的化学键,这由它们更高的配位数表明,部分也是由于显著的Zn - Zn键导致的。