%0 Journal Article
%T A NEW LINDQVIST-TYPE HEXAMOLYBDATE CLUSTER FUNCTIONALIZED WITH THE jt-DONOR LIGAND 4-BROMO-2,6-DIMETHYLPHENYLIMIDO: SPECTROSCOPIC, ELECTROCHEMICAL AND STRUCTURAL STUDIES
%A MARCELA CORT¨¦S
%A MAURICIO FUENTEALBA
%A CAROLINA MANZUR
%A DAVID CARRILLO
%J Journal of the Chilean Chemical Society
%D 2008
%I Sociedad Chilena de Qu¨ªmica
%X A new ionic organic-inorganic hybrid complex of formula ( -Bu4N)2[Mo( 0(18)(NR)]1/2Me2CO, R = -C6H2-2,6-Me2-4-Br, (w-Bu4N)2[l]-i4Me2CO, has been prepared in acetonitrile by reacting tetrabutylammonium a-octamolybdate, ( -Bu4N)4[0t-Mo8O26], with 2,6-dimethyl-4-bromoaniline hydrochloride, 2,6-Me2-4-Br-C6H2NH2HCl, using N,N'-dicyclohexylcarbodiimide, (C6H U)N=C=N(C6H11), as dehydrating agent. This complex, formulated as ( -Bu4N)2[l]1/2Me2CO, contains a C-Br group which can be functionahzed for constructing novel hybrid materials. The complex was fully characterized by IR, UV-Vis, 'H- and "C-NMR spectroscopies, and authenticated by single crystal X-ray diffraction analysis. The asymmetric unit contains two crystallographically independent anions, [l]2", differing by the orientation of the phenyl ring relative to the hexamolybdate skeleton, and one molecule of acetone. Both molecules differ in the angles Mo(l)-N(l)-C(l)= 172.2(6) and Mo(7)-N(2)-C(9)= 175.6(6)¡ã. These angles, near to 180¡ã, indicate the presence of a Mo=N triple bond
%K areneimido-derivative
%K phenylimido-derivative
%K Lindqvist-type hexamolybdate
%K polyoxometalate
%K crystal structure
%K conformational isomers
%U http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072008000100004