![[HTML version]](/e/graphics/htmlborder.gif)
![[PDF version]](/e/graphics/pdfborder.gif)
![[CIF]](/e/graphics/cifborder.gif)
![[3d view]](/e/graphics/3dviewborder.gif)
![[Structure Factors]](/e/graphics/structurefactorsborder.gif)
![[CIF check Report]](/e/graphics/checkcifborder.gif)
![[Buy article online]](/logos/buy.gif)
![[Contents scheme]](lh6297contents.gif)
Acta Cryst. (2004). E60, m1900-m1902 [ doi:10.1107/S1600536804029605 ]
-acetate bridges: di-
-acetato-bis[
-N,N'-bis(salicylidene)-1,4-butanediaminato]tricobalt(II)Abstract: The title linear trinuclear complex, di-
-acetato-1:2
2O,O';2:3
2O,O'-bis{2,2'-[1,4-butanediylbis(nitrilomethylidyne)]diphenolato}-1:2
6O,N,N,O':O,O';2,3
6O,O':O,N,N,O'-tricobalt(II), [Co3(C18H18N2O2)2(C2H3O2)2], was prepared by the reaction of the tetradentate Schiff base ligand bis(salicylidene)-1,4-diaminobutane and Co(CH3COO)2·2H2O in a methanol solution. The central CoII ion, which is located on an inversion center, has a distorted octahedral coordination involving four bridging O atoms from two Schiff base ligands in the equatorial plane and one O atom from each bridging acetate group in the axial positions. The coordination around the terminal CoII ion is irregular square pyramidal, with two O and two N atoms of the ligand in the basal plane and one O atom from an acetate group in the apical position. The acetate bridges linking the central and terminal CoII ions are mutually trans. The closest Co
Co separation is 3.125 (4) Å.
Copyright © International Union of Crystallography
IUCr Webmaster