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Polyoxometalate cluster [V12B18O60H6] functionalized with the copper(II) bis-ethylenediamine complex

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2011
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Brown, Kareen
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Polyoxometalate cluster [V12B18O60H6] functionalized with the copper(II) bis-ethylenediamine complex
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Author
  • Brown, Kareen;
  • Car, Pierre Emmanuel;
  • Vega, Andrés;
  • Venegas Yazigi, Diego;
  • Paredes García, Verónica;
  • Vaz, María G.F.;
  • Allao, Rafael A.;
  • Pivan, Jean-Yves;
  • Le Fur, Eric;
  • Spodine Spiridonova, Evgenia;
Abstract
Three compounds based on the polyoxometalate building block [V12B18O60H6], (Na)10[(H2O)V12- B18O60H6] 18H2O (1), Na8[Cu(en)2]2[V12B18O60H6](NO3)2 14.7H2O (2), Na7[Cu(en)2]2[V12B18O60H6] (NO3) 15.5H2O (3), (en = ethylenediamine), have been hydrothermally synthesized and characterized by single-crystal X-ray diffraction analysis and TGA. Compound 1 consists of polyoxovanadium borate [V12B18O60H6] clusters which are surrounded by sodium countercations in octahedral sites, stabilized by electrostatic interactions with the oxygen atoms of both vanadium and boron centres. However, compounds 2 and 3 correspond to more complicated structures, constructed from the same polyoxometalate clusters, which are interconnected by [Cu(en)2]2+ moieties via the terminal oxygen atoms of the polyoxoanions, generating one-dimensional structures. The functionalization of this polyoxovanadium borate cluster has been obtained by the use of [Cu(en)2]2+ complex ions, thus demonstrating the capacity of the terminal oxygen atoms of the cluster to bind transition metal centres. The structural stability of the [V12B18O60H6] cluster permits the formation of functionalized polyoxometalate clusters, generating various crystalline lattices.
Patrocinador
Authors acknowledge ECOS-CONICYT C08E02 International Project. The authors also thank Financiamiento Basal Program FB0807 and FONDECYT 1080316 for partial financial support. This work was done under the LIA-MIF CNRS 836 Collaborative Program. KBA thanks CONICYT for the 21050162 and AT-24071044 doctoral scholarships, and the University of Chile AVV-5 grant. M.G.F.V. and R.A.A. acknowledge LDRX-UFF, and partial financial support from CAPES, FAPERJ and CNPq.
Identifier
URI: https://repositorio.uchile.cl/handle/2250/121617
DOI: doi:10.1016/j.ica.2010.11.045
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Inorganica Chimica Acta 367 (2011) 21–28
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