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Title: Inorganic-organic hybrid compounds: Synthesis and characterization of three new metal phosphonates with similar characteristic structural features

The phosphonocarboxylic acid H(HO{sub 3}PCH{sub 2}){sub 2}NH-CH{sub 2}C{sub 6}H{sub 4}-COOH (H{sub 5} L ) was synthesized and characterized by NMR- and IR-spectroscopy, thermogravimetric (TG) analysis and single-crystal X-ray diffraction. Reactions of H{sub 5} L with samarium(III) chloride and calcium(II) chloride resulted in three new compounds, Sm[(O{sub 3}PCH{sub 2}){sub 2}NH-CH{sub 2}C{sub 6}H{sub 4}-COOH].H{sub 2}O (1), Ca[H(O{sub 3}PCH{sub 2}){sub 2}NH-CH{sub 2}C{sub 6}H{sub 4}-COOH].H{sub 2}O (2), and Ca[(HO{sub 3}PCH{sub 2}){sub 2}NH-CH{sub 2}C{sub 6}H{sub 4}-COOH]{sub 2}.4H{sub 2}O (3). The single-crystal structure determination of the title compounds reveals that in H{sub 5} L as well as in compounds 1, 2, and 3 zwitterions are present. Within the M-O building units of the metal phosphonates we observed a different degree of dimensionality, depending on the oxidation state of the metal ion and the synthesis conditions. In 1, one-dimensional chains of edge-sharing SmO{sub 8} polyhedra are observed while in 2, isolated units of edge-sharing CaO{sub 6} octahedra and in 3 isolated CaO{sub 6} octahedra are observed. However, looking at the organic part, the rigid phenyl carboxylic acid moieties arrange in a 'zipper-like' fashion and hydrogen bonding plays an important role in the stabilization of the crystal structure. The title compounds were further characterized by IR spectroscopy andmore » TG analysis. Additionally, the thermal stability of 1 was investigated by temperature-dependent X-ray diffraction. -- Graphical abstract: Hydrothermal reactions of the phosphonocarboxylic acid H(HO{sub 3}PCH{sub 2}){sub 2}NH-CH{sub 2}C{sub 6}H{sub 4}-COOH with Sm{sup 3+} and Ca{sup 2+} salts has led to three new inorganic-organic hybrid compounds. All crystal structures contain phosphonate zwitterions and have a layer-like arrangement. The rigid organic groups arrange in a 'zipper-like' fashion and hydrogen bonding plays an important role in the stabilization of the crystal structures.« less
Authors:
 [1] ;  [2] ;  [3]
  1. Institute of Inorganic Chemistry, Christian-Albrechts-University, Otto-Hahn-Platz 6/7, D 24118 Kiel (Germany)
  2. Department of Chemistry and Biochemistry, Ludwig-Maximilians-University, Butenandtstr. 5-13 (E), D 81377 Munich (Germany)
  3. Institute of Inorganic Chemistry, Christian-Albrechts-University, Otto-Hahn-Platz 6/7, D 24118 Kiel (Germany). E-mail: stock@ac.uni-kiel.de
Publication Date:
OSTI Identifier:
20784843
Resource Type:
Journal Article
Resource Relation:
Journal Name: Journal of Solid State Chemistry; Journal Volume: 179; Journal Issue: 1; Other Information: DOI: 10.1016/j.jssc.2005.10.008; PII: S0022-4596(05)00468-8; Copyright (c) 2005 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved; Country of input: International Atomic Energy Agency (IAEA)
Country of Publication:
United States
Language:
English
Subject:
37 INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; CALCIUM COMPOUNDS; CALCIUM IONS; CHLORIDES; CRYSTAL STRUCTURE; INFRARED SPECTRA; NUCLEAR MAGNETIC RESONANCE; PHOSPHONATES; SAMARIUM COMPOUNDS; SAMARIUM IONS; SYNTHESIS; THERMAL GRAVIMETRIC ANALYSIS; X-RAY DIFFRACTION