Synthesis, crystal structure, infrared and Raman spectra of Sr4Cu3(AsO4)2(AsO3OH)4.3H2O and Ba2Cu4(AsO4)2(AsO3OH)3
Creators
- 1. Institut fuer Mineralogie und Kristallographie, Universitaet Wien, Althanstrasse 14, A-1090 Wien (Austria)
- 2. Laboratory of Crystallography, Faculty of Mining and Geology, Dusina 7, 11000 Belgrade (Serbia)
Description
The two new compounds, Sr4Cu3(AsO4)2(AsO3OH)4.3H2O (1) and Ba2Cu4(AsO4)2(AsO3OH)3(2), were synthesized under hydrothermal conditions. They represent previously unknown structure types and are the first compounds synthesized in the systems SrO/BaO-CuO-As2O5-H2O. Their crystal structures were determined by single-crystal X-ray diffraction [space group C2/c, a=18.536(4) A, b=5.179(1) A, c=24.898(5) A, β=93.67(3)o, V=2344.0(8) A3, Z=4 for 1; space group P42/n, a=7.775(1) A, c=13.698(3) A, V=828.1(2) A3, Z=2 for 2]. The crystal structure of 1 is related to a group of compounds formed by Cu2+-(XO4)3- layers (X=P5+, As5+) linked by M cations (M=alkali, alkaline earth, Pb2+, or Ag+) and partly by hydrogen bonds. In 1, worth mentioning is the very short hydrogen bond length, D...A=2.477(3) A. It is one of the examples of extremely short hydrogen bonds, where the donor and acceptor are crystallographically different. Compound 2 represents a layered structure consisting of Cu2O8 centrosymmetric dimers crosslinked by As1φ4 tetrahedra, where φ is O or OH, which are interconnected by Ba, As2 and hydrogen bonds to form a three-dimensional network. The layers are formed by Cu2O8 centrosymmetric dimers of CuO5 edge-sharing polyhedra, crosslinked by As1O4 tetrahedra. Vibrational spectra (FTIR and Raman) of both compounds are described. The spectroscopic manifestation of the very short hydrogen bond in 1, and ABC-like spectra in 2 were discussed. - Graphical abstract: The two new compounds, Sr4Cu3(AsO4)2(AsO3OH)4.3H2O (1) and Ba2Cu4(AsO4)2(AsO3OH)3(2), were synthesized under hydrothermal conditions. They represent previously unknown structure types and are the first compounds synthesized in the systems SrO/BaO-CuO-As2O5-H2O. Their crystal structures were determined by single-crystal X-ray diffraction [space group C2/c, a=18.536(4) A, b=5.179(1) A, c=24.898(5) A, β=93.67(3)o, V=2344.0(8) A3, Z=4 for 1; space group P42/n, a=7.775(1) A, c=13.698(3) A, V=828.1(2) A3, Z=2 for 2]. Vibrational spectra (FTIR and Raman) of both compounds are described. The spectroscopic manifestation of the very short hydrogen bond, where the donor and acceptor are crystallographically different in 1, and ABC-like spectra in 2 were discussed
Availability note (English)
Available from http://dx.doi.org/10.1016/j.jssc.2008.07.025Additional details
Identifiers
- DOI
- 10.1016/j.jssc.2008.07.025;
- PII
- S0022-4596(08)00404-0;
Publishing Information
- Journal Title
- Journal of Solid State Chemistry
- Journal Volume
- 181
- Journal Issue
- 11
- Journal Page Range
- p. 2889-2898
- ISSN
- 0022-4596
- CODEN
- JSSCBI
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 40082333
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- ABSORPTION SPECTROSCOPY; ARSENATES; ARSENIC IONS; ARSENIC OXIDES; BARIUM OXIDES; COPPER IONS; COPPER OXIDES; CROSS-LINKING; FOURIER TRANSFORMATION; HYDROTHERMAL SYNTHESIS; INFRARED SPECTRA; LAYERS; LEAD IONS; MONOCLINIC LATTICES; MONOCRYSTALS; PHOSPHORUS IONS; RAMAN SPECTRA; RAMAN SPECTROSCOPY; SILVER IONS; SPACE GROUPS; STRONTIUM OXIDES; TETRAGONAL LATTICES; X-RAY DIFFRACTION
- Descriptors DEC
- ALKALINE EARTH METAL COMPOUNDS; ARSENIC COMPOUNDS; BARIUM COMPOUNDS; CHALCOGENIDES; CHARGED PARTICLES; CHEMICAL REACTIONS; COHERENT SCATTERING; COPPER COMPOUNDS; CRYSTAL LATTICES; CRYSTAL STRUCTURE; CRYSTALS; DIFFRACTION; INTEGRAL TRANSFORMATIONS; IONS; LASER SPECTROSCOPY; OXIDES; OXYGEN COMPOUNDS; POLYMERIZATION; SCATTERING; SPECTRA; SPECTROSCOPY; STRONTIUM COMPOUNDS; SYMMETRY GROUPS; SYNTHESIS; TRANSFORMATIONS; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2008 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.