PROTONATED DIAMINES AS LINKERS IN THE SUPRAMOLECULAR ASSEMBLIES BASED ON THE [V12B18O60H6] POLYOXOVANADOBORATE ANION
a:2:{s:4:"TEXT";s:233:"P. Hermosilla–Ibanez1,2, J. Costamagna1, A. Vega2,3, V. Paredes–Garcia2,3, M.T. Garland4, E. Le Fur5,6, E. Spodine2,7, D. Venegas–Yazigi1,2";s:4:"TYPE";s:4:"html";}
a:2:{s:4:"TEXT";s:437:"1Universidad de Santiago de Chile, Chile, USACH
diego.venegas@usach.cl
2CEDENNA, Chile
3Universidad Andres Bello, Chile
4Universidad de Chile, Chile
5ENSCR, CNRS, UMR 6226, Rennes, France
6Université Européenne de Bretagne, France
7Farmacéuticas Universidad de Chile, Chile";s:4:"TYPE";s:4:"html";}
Keywords: polyoxometalate, polyoxovanadate, supramolecular, mixed valence, BVO
Subsection: SELF-ASSEMBLY AND SUPRAMOLECULAR ORGANIZATION OF COORDINATION COMPOUNDS
Abstract
Two new polyoxovanadoborates based crystalline lattices are being reported: K5(H3O)2(1,3–diapH2) 2[V12B18O60H6]×10.80H2O (1), and K2(H3O)7(enH2)[V12B18O60H6]×9H2O (2). These structures are characterized by presenting multiple hydrogen bonds between the diprotonated diamines (enH2 and 1,3–diapH2) and hydronium ions, and the oxygen atoms of the [V12B18O60H6] cluster. The crystalline packing and stability of these new polyoxovanadoborates is dominated by the different types of hydrogen interactions present in the lattices ranging from unidirectional to trifurcated ones. The crystallographic data, together with the BVS method, permit to assign a mixed valence ratios for the [V12B18O60H6] anionic cluster for (1) and (2) being 11/1 (VIV/VV) ratio.
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