作者: Daniel A. Padron , Kevin K. Klausmeyer
关键词: Trifluoromethanesulfonate 、 Stereochemistry 、 Counterion 、 Nuclear magnetic resonance spectroscopy 、 Supramolecular chemistry 、 Pyridine 、 Crystallography 、 Crystal structure 、 Ligand 、 Ion 、 Chemistry
摘要: The coordination properties of the 2-[(diphenylphosphanyl)methyl]pyridine N,P-dioxide ligand towards three different silver(I) salts are described. molecular structures complexes obtained showed a strong dependence on and binding ability counterion. strongly trifluoroacetate ion yielded unique planar silver cluster complex, whereas less triflate BF4– polymeric structures. synthesized were fully characterized by elemental analysis multinuclear NMR spectroscopy techniques. crystal determined single-crystal X-ray crystallography.