Cooperative effect of anion and mole ratio on the coordination modes of an NO2S3-donor macrocycle.

Abstract

Synthesis of an NO2S3-macrocycle (L) incorporating a pyridine subunit and its anion and/or mole ratio-dependent coordination modes in the formations of mercury(II) complexes is reported. When the mercury(II) salts with different anions (ClO4(-) or Br(-)) were reacted with L, the Hg(ClO4)2 afforded a typical endocyclic complex [HgL](ClO4)2 (1). Meanwhile, the HgBr2 gave an exocyclic complex [HgLBr2] (2) in which the metal ion exists outside the macrocyclic cavity. The observed anion effect on the coordination modes can be explained by the anion coordination ability toward the metal cation. In the mole ratio variation experiments, notably, the use of 1.5 equiv or above of HgBr2 in the same reaction condition gave a unique endo/exocyclic dumbbell-type complex 3, [Hg4L2Br6][Hg2Br6]. However, the formation of the endocyclic Hg(ClO4)2 complex 1 shows no mole ratio dependency. To monitor the observed mole ratio-dependent exocoordination products as well as their reactivities and reversibility, systematic powder X-ray diffraction (PXRD) analysis was also applied. From single crystal X-ray and PXRD analyses, it was found that endocyclic complex 1 is not reactive, but complexes 2 and 3 are reactive and show the reversibility between them in the presence of the corresponding reactants.