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Abstract
Four new Pd(II) coordination complexes using 2-(3-methyl-5-phenyl-1H-pyrazol-1-yl)ethanol (L) with different counter-anions have been prepared to examine their effect on the coordination mode of the ligand as well as on the self-assembly of the supramolecular structure. Reaction of trans-[PdCl2(L)2] (R) with AgCF3SO3 gives the ionic complex [Pd(L)2](CF3SO3)2 (1). When AgNO3 is used, [Pd(NO3)(L)2](NO3) (2) and [Pd(L)2](NO3)2 (3) are obtained in the ratio 70 : 30, respectively, where the nitrate ion is present in- and/or outside the coordination sphere. Reaction of R with Ag2SO4 in the presence of (NH4)2C2O4 yields [Pd(C2O4)(L)2] (4). These new complexes have been characterized by elemental analyzes, conductivity measurements, mass spectrometry, IR, 1H and 13C{1H} NMR spectroscopies, and X-ray diffraction, whenever possible. The denticity varies from N-monodentate to NO-bidentate, depending on the conditions, showing the versatility of L. Finally, the results of X-ray diffraction analyzes of 1 reveal that CF3SO3− plays a fundamental role in self-assembly, generating a 2-D supramolecular layer with different inter- and intra-molecular interactions. The easy preparation and the high efficiency of this ligand make it a promising alternative to improve established systems.