CuClSe1.53Te0.47 and CuClSe0.56Te1.44: Structural and vibrational spectroscopic investigations on copper(I) chalcogen chlorides

Nilges, Tom and Zimmerer, Stefan and Kurowski, Daniel and Pfitzner, Arno (2002) CuClSe1.53Te0.47 and CuClSe0.56Te1.44: Structural and vibrational spectroscopic investigations on copper(I) chalcogen chlorides. ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE, 628 (12). pp. 2809-2814. ISSN 0044-2313

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Abstract

CuClSe1.53Te0.47 and CuClSe0.56Te1.44 are obtained from the reaction of CuCl, Se, and Te in stoichiometric amounts. Both copper(l) selenium tellurium chlorides are monoclinic, space group P2(1)/n (no. 14) with lattice constants of a = 7.837(1) A, b = 4.699(1) Angstrom, c = 10.762(2) Angstrom, beta = 104.37(2)degrees, V = 383.9(1) Angstrom(3) (CuClSe0.56Te1.44), and Z = 4. A common feature of these isostructural compounds are heteroatomic strands (1)(infinity)[YY'] (Y, Y' = chalcogen). These strands are running along [010] and are connected to layers by chains (1)(infinity)[CuCl]. Vibrational spectra of CuClSe1.53Te0.47, CuClSe0.56Te1.44, CuXTe2 and CuX'Se-2 (X = Cl, Br, I; X' = Cl, Br) are analysed with respect to the bonding relations of the chalcogen chains. Modes derived from IR and Raman spectra are assigned by correlation with trigonal Se and related copper(I) chalcogen halides. Both, X-ray structural data and an analysis of the chalcogen vibrational modes in IR and Raman spectra, lead to a detailed insight into the ordering phenomena of the chalcogen chains in this type of copper(I) chalcogen halides.

Item Type: Article
Uncontrolled Keywords: CRYSTAL-STRUCTURES; HALIDES; REFINEMENT; CHAINS; SCREWS; SE; copper(I) chalcogen halides; chalcogen chains; crystal structure; IR spectroscopy; Raman spectroscopy
Subjects: 500 Science > 540 Chemistry & allied sciences
Divisions: Chemistry and Pharmacy > Institut für Anorganische Chemie > Chair Prof. Dr. Arno Pfitzner
Depositing User: Dr. Gernot Deinzer
Date Deposited: 27 Aug 2021 04:51
Last Modified: 27 Aug 2021 04:51
URI: https://pred.uni-regensburg.de/id/eprint/39764

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