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Synthese und Kristallstruktur des Holmium(III)‐chlorid‐oxotellurats(IV) HoClTeO3
Authors:Steffen F Meier  Thomas Schleid
Abstract:Synthesis and Crystal Structure of the Holmium(III) Chloride Oxotellurate(IV) HoClTeO3 Orange coloured, rod—shaped single crystals of the holmium( III) chloride oxotellurate(IV) HoClTeO3 (orthorhombic, Pnma; a = 730.25(5), b = 696.54(5), c = 905.18(7) pm; Z = 4) are obtained during attempts to synthesize holmium(III) oxochlorotellurates(IV) by reaction of holmium oxychloride (HoOCl) and tellurium dioxide (TeO2; 1:1—2molar ratio, 800 °C, 40 d) in evacuated silica tubes. The crystal structure contains sevenfold coordinated Ho 3+ cations surrounded by five oxide and two chloride anions forming a pentagonal bipyramid. Interconnection of the Ho(O1)(O2)4Cl2] polyhedra occurs via two edges made of four equatorial oxygen atoms (O2) under formation of urn:x-wiley:00442313:media:ZAAC526:tex2gif-stack-1{Ho(O1)urn:x-wiley:00442313:media:ZAAC526:tex2gif-inf-8(O2)4/2Cl2/1]5‐} chains running parallel 010]. These arrange as hexagonal closest packing of rods and are linked to each other by Cl anions to a three—dimensional urn:x-wiley:00442313:media:ZAAC526:tex2gif-stack-2{Ho(O1)1/1(O2)4/2Cl2/2]4‐} network. All Te4+ cations are embedded therein and exhibit ψ1—tetrahedral coordination figures as discrete anionic Te(O1)(O2)2]2‐ pyramids due to the stereochemical activity of the non—binding electron pairs („lone pairs”︁). They stabilize the urn:x-wiley:00442313:media:ZAAC526:tex2gif-stack-3{HoO3Cl]4‐} network via covalent bonds to one axial (O1) and two equatorial oxygen atoms (O2) of each HoO5Cl2] polyhedron.
Keywords:Holmium  Tellurium  Oxotellurates(IV)  Crystal Structure
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