Abstract
A new "click" ligand, 2,6-bis(1-(pyridin-4-ylmethyl)-1H-1,2,3-triazol-4-yl) pyridine (L) featuring a tridentate 2,6-bis(1,2,3-triazol-4-yl) pyridine (tripy) pocket and two pyridyl (py) units was synthesized in modest yield (42%) using the copper(I) catalyzed azide-alkyne cycloaddition (CuAAC) reaction. The coordination chemistry of the ligand with silver(I) and iron(II) ions was examined using a battery of solution (H-1 and DOSY (diffusion ordered spectroscopy) nuclear magnetic resonance (NMR), infrared and absorption spectroscopies, high-resolution electrospray ionization mass spectrometry (HR-ESI-MS)), and solid state (X-ray crystallography, elemental analysis) techniques. When treated with silver(I) ions, the ligand forms discrete [Ag(L)](+) (X, where X- = BF4-, NO3- or SbF6-) complexes in dimethyl sulfoxide (DMSO) solution but these complexes crystallize as coordination polymers. The addition of [Fe(H2O)(6)](BF4)(2) to an acetonitrile solution of the ligand forms the expected monomeric octahedral [Fe(L)(2)](2+) complex and treatment of the iron(II) complex with AgBF4 generates a heterometallic linear coordination polymer.