Weil Matthias, Veyer Théo
Institute for Chemical Technologies and Analytics, Division of Structural Chemistry, TU Wien, Getreidemarkt 9/164-SC, A-1060 Vienna, Austria.
IUT Bordeaux 1, 15 Rue Naudet, 33175 Gradignan, France.
Acta Crystallogr E Crystallogr Commun. 2018 Oct 12;74(Pt 11):1561-1564. doi: 10.1107/S2056989018014214. eCollection 2018 Nov 1.
Phase-formation studies in the system CdO-TeO using a CsCl/NaCl melt at comparatively low temperatures revealed that tricadmium orthotellurate(VI), CdTeO, is dimorphic. The new modification of CdTeO is denoted as the β-form and adopts the rhombohedral MgTeO structure type with one Cd and two O sites in general positions, and two Te sites with site symmetry each. In comparison with the previously reported monoclinic cryolite-type α-form that was prepared at higher temperatures, β-CdTeO has a much lower density and most likely represents a metastable modification. Whereas the [TeO] octa-hedra in both polymorphs are very similar and show only minor deviations from ideal values, the polyhedra around the Cd sites are different, with a distorted [CdO] octa-hedron in both modifications but an additional [CdO] polyhedron with a [4 + 4] coordination in the α-form.
在相对较低温度下使用CsCl/NaCl熔体对CdO-TeO体系进行的相形成研究表明,原碲酸镉(VI),CdTeO,具有二态性。CdTeO的新变体被标记为β型,采用菱面体MgTeO结构类型,其中一个Cd和两个O位点处于一般位置,两个Te位点各自具有位点对称性。与先前报道的在较高温度下制备的单斜冰晶石型α型相比,β-CdTeO密度低得多,很可能代表一种亚稳变体。虽然两种多晶型物中的[TeO]八面体非常相似,与理想值仅有微小偏差,但Cd位点周围的多面体不同,两种变体中[CdO]八面体均发生扭曲,但α型中还有一个具有[4 + 4]配位的额外[CdO]多面体。