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Updated: May 29, 2025

Facet-to-facet Linking of Shape-anisotropic Colloidal Cadmium Chalcogenide Nanostructures
Published on: August 10, 2017
The cadmium oxidotellurates(IV) Cd5(TeO3)4(NO3)2 and Cd4Te5O14
1TU Wien, Institute for Chemical Technologies and Analytics, Division of Structural Chemistry, Getreidemarkt 9/E164-05-1, 1060 Vienna, Austria.
Abstract:
Monoclinic single crystals of Cd5(TeO3)4(NO3)2 (space group P21/c), penta-cadmium tetra-kis-[oxidotellurate(IV)] dinitrate, and of Cd4Te5O14 (space group C2/c), tetra-cadmium penta-oxidotellurate(IV), were obtained under the same hydro-thermal conditions. Whereas the crystal structure of Cd5(TeO3)4(NO3)2 is distinctively layered, that of Cd4Te5O14 exhibits a tri-periodic framework. In Cd5(TeO3)4(NO3)2, the three CdII atoms have coordination numbers (CN) of 7, 6 and 6. The two types of [CdO6] and the [CdO7] polyhedra [bond lengths range from 2.179 (3) to 2.658 (2) Å] share corners and edges, resulting in layers extending parallel to (100). Both TeIV atoms are coordinated by three oxygen atoms in a trigonal-pyramidal shape. The oxygen atoms of the isolated [TeO3] groups [bond lengths range from 1.847 (3) to 1.886 (3) Å] all are part of the cadmium-oxygen layer. The electron lone pairs ψ of the TeIV atoms are directed away from the layer on both sides. The available inter-layer space is co-occupied by the nitrate group, which is directly connected with two of its O atoms to the layer whereas the third O atom is solely bonded to the N atom and points towards the adjacent layer. In Cd4Te5O14, all three unique CdII atoms are coordinated by six oxygen atoms, considering Cd-O distances from 2.235 (2) to 2.539 (2) Å. By edge- and corner-sharing, the distorted [CdO6] polyhedra form an open framework that is partially filled with three different stereochemically active TeIV atoms. All of them exhibit a CN of 4, with Te-O bonds in a range from 1.859 (2) to 2.476 (2) Å. The corresponding [TeO4] units are linked to each other by corner- and edge-sharing, forming infinite helical 1 ∞[Te10O28] chains extending parallel to [203]. The connectivity in the chains can be described as (⋯-⋄-⋄=⋄-⋄-⋄-⋄-⋄=⋄-⋄-⋄-⋯) where '⋄' denotes a [TeO4] unit, '-' a linkage via corners and '=' a linkage via edges. Such a structural motif is unprecedented in the crystal chemistry of oxidotellurate(IV) compounds.
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