Tailoring Structural Diversity in Dimethyltin Carboxylates by the pH-Controlled Hydrothermal Approach.

The study presents a rational synthesis of new dimethyltin carboxylates, MeSn(Hbtec) (), MeSn(btec)(), [MeSn(HO)(btec)]·HO (), and [{MeSnOSn(OH)Me}(MeSnOH)(btec)]·HO (), derived from tetratopic 1,2,4,5-benzenetetracarboxylic acid (Hbtec). The method relies upon hydrothermal reaction (130 °C, 72 h) of dimethyltin dichloride and Hbtec under optimized pH (2 < pH < 8) conditions that allow control over dimethyltin speciation in aqueous medium as well as degree of deprotonation of the tetrafuntional carboxylic acid. The formation of a three-dimensional assembly in is assisted by the bridging bidentate (μ) mode of the carboxylate and O-H···O hydrogen bonds involving -COOH groups. The structure represents a unique example of the diorganotin framework derived from a partially deprotonated polyfuntional carboxylic acid. The structure of adopts a three-dimensional motif wherein each pair of μ-carboxylate groups (designated by C1 and C4) of the tetraanionic ligand form different spatial arrangements. For , the formation of one-dimensional motif with eight-coordinated tin atoms is assisted by the anisobidentate character of the carboxylate groups. The structure of includes linear chains comprised of [MeSn(μ-OH)] and the carboxylate ligand which extend to a layered motif with symmetrically substituted ladder-like distannoxanes acting as linkers. The underlying nets of , , and exhibit sqc11, scu(sqc170), and sql topologies, respectively. Notably, these assemblies are extremely robust and show no sign of degradation upon exposure to neutral as well as weakly acidic/basic aqueous medium for 7 days.