Different geometries of novel cobalt(II) compounds with 2-hydroxy benzophenones and neocuproine: Crystal and molecular structures of [Co(2-hydroxybenzophenone) 2(neoc)],[Co(2-hydroxy-4-methoxybenzophenone)(neoc)Br] and [Co(neoc)Br2]_CH3OH_H2O

 
This item is provided by the institution :
University of Ioannina
Repository :
Repository of UOI Olympias
see the original item page
in the repository's web site and access all digital files if the item*
share



2013 (EN)
Different geometries of novel cobalt(II) compounds with 2-hydroxy benzophenones and neocuproine: Crystal and molecular structures of [Co(2-hydroxybenzophenone) 2(neoc)],[Co(2-hydroxy-4-methoxybenzophenone)(neoc)Br] and [Co(neoc)Br2]_CH3OH_H2O (EN)

M. Lalia-Kantouri, (EN)

Πανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείας (EL)
M. Lalia-Kantouri, (EN)

Ten mixed-ligand Co(II) compounds with 2-hydroxy-benzophenones(ketones) and neocuproine(neoc) were synthesized and characterized by physicochemical and spectral (IR, UV-Vis) data. The cyclic voltammetry study in CH3CN gave all the expected waves for the redox processes of the metal Co(II) and the studied ligands. The X-ray diffraction study of two representative compounds proved the two different geometries, octahedral for [Co(2-hydroxy-benzophenone)2(neoc)] (3) and trigonal bipyramidal for [Co(2-hydroxy-4-methoxybenzophenone)(neoc)Br] (10). Additionally, the precursor compound [Co(neoc)Br2]Β·CH3OHΒ·H2O (11) was proved by (X-ray) to posses tetrahedral geometry. The molecular structure and the possible isomers of the trigonal bipyramidal complex 10 were studied by means of density functional calculations (DFT). The thermal stability was investigated by means of simultaneous TG/DTG-DTA technique in nitrogen atmosphere up to 1000 Β°C, where metallic cobalt was found as the solid residue. (EN)

Cobalt (EN)

Πανεπιστήμιο Ιωαννίνων (EL)
University of Ioannina (EN)

Polyhedron (EN)

2013


Elsevier (EN)



*Institutions are responsible for keeping their URLs functional (digital file, item page in repository site)