Abstract

Mononuclear and dinuclear silver(I) complexes bearing 1,8-naphthyridine (napy) were prepared. The crystal structures of [Ag(napy-κ N) 2](PF 6) ( 1) and [Ag 2(μ-napy) 2](PF 6) 2 · 3CH 3CN ( 2 · 3CH 3CN) were determined by X-ray diffraction studies. In complex 1, intermolecular π–π interaction of napy ligands between neighboring molecules forms left-handed hexagonal columns in the solid state. On the other hand, two napy ligands bridging two Ag ions in the dinuclear complex 2 shape a face-to-face π–π stacking with those of the neighboring molecule to form the dimeric unit. Besides, two of four napy ligands, which are located in a diagonal position in the dimeric unit, build intermolecular back-to-back π–π stackings with those of the adjacent dimeric unit, and a ladder-like stairway structure is generated in the solid state. Irrespective of such characteristic structures of 1 and 2 in the solid state, both complexes show very rapid dynamic behavior in solutions. No conversion between 1 and 2 took place even in the presence of excess amounts of Ag + or napy in solutions.

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