Structural and metallo selectivity in the assembly of [2 × 2] grid-type metallosupramolecular species: Mechanisms and kinetic control

摘要

An unsymmetrical bis(tridentate) ligand LH in which one binding site can be readily deprotonated forms a kinetically inert [Co(iii)L_2] ~+ complex which can be used as a "corner" species for the "Coupe du Roi" assembly of trans,trans-[Co_2M _2L_4]~(6+) metallogrids (M = Fe(ii), Co(ii), Cu(ii), Zn(ii)). In the mixed Co(iii)/Co(ii) species, the oxidation states appear to be localised. In solution, the ligand LH forms octacationic, homometallic [2 × 2] grids with the individual labile metal ions Fe(ii), Co(ii), Cu(ii), Zn(ii), seemingly as mixtures of all possible isomers arising from the unsymmetrical nature of the ligand. In the solid state, however, [Zn_4L_4](CF_3SO_3)_8· 4CH_3CN crystallises as a single species where the cation has S _4 symmetry. This stereoselectivity in the crystalline lattice is associated with interactions between the cation and triflate anions which can again be analysed in terms of the Coupe du Roi concept.