![[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]](kj2024contents.gif)
Acta Cryst. (2006). E62, m2260-m2262 [ doi:10.1107/S1600536806032673 ]
Abstract: For the first time, cocrystallization of two isomorphous silanethiolate complexes has been carried out. (Acetonitrile)bis(tri-tert-butoxysilanethiolato-
2O,S)cobalt(II) and (acetonitrile)bis(tri-tert-butoxysilanethiolato-
2O,S)zinc(II) gave orthorhombic monocrystals of their solid solution with a Co:Zn ratio refined to 0.81 (5):0.19 (5), viz. [Co(C12H27O3SSi)2(C2H3N)]0.81[Zn(C12H27O3SSi)2(C2H3N)]0.19. The product retained the structural characteristics of the substrates, viz. distorted trigonal-bipyramidal arrangement of ligands around the MII atom and crystallographically imposed C2 symmetry with the M-NCMe fragment lying on a twofold rotation axis.
Online 18 August 2006
Copyright © International Union of Crystallography
IUCr Webmaster