摘要:
Six tin complexes of the type (O, N, N, O) Sn and (O, N, N, O) SnCl2 ((LSn)-Sn-1, (LSn)-Sn-2, (LSn)-Sn-3, (LSnCl2)-Sn-1, (LSnCl2)-Sn-2, L3SnCl2) with di-anionic salen type tetradentate O, N, N, O chelators were synthesized and characterized by H-1, C-13, (11)9Sn NMR spectroscopy, single-crystal X-ray diffraction, and elemental analysis ((LSn)-Sn-1, (LSn)-Sn-2, (LSnCl2)-Sn-1, (LSnCl2)-Sn-2, (LSnCl2)-Sn-3) or Sn-119 solid state NMR spectroscopy and elemental analysis (L3Sn). The length of the oligomethylene bridge of the ligands (L-1)(2)-, (L-2)(2)-and (L-3)(2)-(which are the anions of di-, tri- and tetramethylene-a,.-N, N'-bis(2-hydroxyacetophenoneimine, respectively) was found to have significant influence on the configuration of the tin coordination sphere. In detail, the Sn atom in (LSn)-Sn-1 occupies the apex of a (O, N, N, O) square pyramid, whereas (LSn)-Sn-2 resembles a see-saw setup of the tin coordination sphere, and (LSn)-Sn-3 appears to be of oligomeric nature concluded from its distinctly lower solubility and different Sn-119 NMR shift. In the monomolecular Sn(IV) compounds the Cl atoms are trans-disposed in (LSnCl2)-Sn-1, and cis-arrangements of the Cl atoms in combination with a mer-fac-arrangements of the (O, N, N, O) ligands are found in (LSnCl2)-Sn-2 and (LSnCl2)-Sn-3.