Coordination geometry of monomeric, dimeric and polymeric organotin(IV) compounds constructed from 5-bromopyridine-2-carboxylic acid and mono-, di- or tri-organotin precursors

Reactions of mono-, di-, tri-alkyltin chlorides or oxide with 5-bromopyridine-2-carboxylic acid result in five new organotin(IV) compounds, [MeSn(O2CC5NH3Br)Cl2(H2O)]·(C2H5)2O (1), [(n-Bu)Sn(O2CC5NH3Br)Cl2(H2O)]·(C2H5)2O (2), {[(n-Bu)2Sn(O2CC5NH3Br)]2O}2 (3) [(n-Bu)3Sn(O2CC5NH3Br)]n (4) and [Ph3Sn(O2CC5NH3Br)]n (5), which have been characterized by single crystal X-ray diffraction, element analysis, IR, 1H, 13C and 119Sn NMR. Three different coordination modes for the ligand are demonstrated in this group of compounds: (1) bidentate mode with the pyridyl nitrogen atom and carboxyl oxygen atom for mono-alkyltin compounds 1 and 2, in which six-coordinated tin center is also bound with two chlorine ions and one water molecule; (2) compound 3 is a tetranuclear centrosymmetric dimer with a central Sn2O2 four-membered ring. The four tin atoms are linked by two bridging carboxyl groups while the remaining two act as monodentate ligands to the endo- and exo-cyclic tin atoms; (3) for tri-alkyltin compounds 4 and 5, the bidentate bridging carboxylic group coordinates with two different tin atoms through the SnOCO → Sn bond, and the carboxylate bridge propagates 1D polymeric chains, typical for five coordinate tin. However, in compounds 3–5, the pyridyl nitrogen atoms do not participate in the coordination. For triorganotin(IV) polymers 4 and 5, the solution studies show the collapse of the intermolecular interactions observed in the solid state to yield monomeric species.