Alkali and Alkaline Earth Metal Derivatives of Disila-Bridged Podands: Coordination Chemistry and Structural Diversity.

Within this study, the synthesis and coordination chemistry of open-chain ligands bearing disila-units is presented. Instead of basic 1:1 complexes, structural diversity was discovered in the variety of ligand and salt. Stable complexes of alkali and alkaline earth metal complexes were obtained by equimolar reactions of different salts with the disila-bridged podands 8,9-disila-EO5 (1) and 11,12-disila-EO7 (2) (EO5 = pentaethylene glycol; EO7 = heptaethylene glycol). The respective alkaline earth metal complexes of the type [Ca(8,9-disila-EO5)(OTf)] (3), [Sr(8,9-disila-EO5)I] (5), [Sr(11,12-disila-EO7)I]I (6), and [Ba(11,12-disila-EO7)OTf] (7) (OTf = CFSO) were characterized via single-crystal X-ray diffraction analyses. Within the reaction of the alkali metal salt NaPF with 1, the sodium ion acts as a template during the complexation process. Under elimination of one molecule of diethylene glycol, the dinuclear species [Na(8,9,17,18-tetrasila-EO8)(PF)]·EO2 (4) (EO8 = octaethylen glycol, EO2 = diethylene glycol) is obtained, in which the sodium cations are 7-fold coordinated within a disilane-bearing framework. The reaction of 2 with CsOTf failed, leading to recrystallization of anhydrous CsOTf. By means of DFT calculations it was shown that the disila-bearing ligands are burdened with negative hyperconjugation interactions between the silicon and the oxygen atoms, but the coordination by sufficiently hard cations can easily overcompensate the competing polarization. In contrast, soft Lewis acids barely share interactions with silicon-bonded oxygen atoms. All findings are consistent with observations made in solution according to Si NMR spectroscopical studies.