Abstract
N,N-Bis[2-(isonicotinoyloxy)ethyl]-p-toluenesulfonamide (L) as a new ligand was synthesized and characterized. The photoluminescence spectrum of L shows a bright blue emission at 417 nm. The slow diffusion of an organic solution of L into an aqueous solution of AgX (X = BF4- and ClO 4) affords a metallacyclodimer consisting of [Ag(L)] 2X2. Each L acts as a bidentate fashion, and thus connects two Ag(I) ions to form the metallacyclodimer. For [Ag(L)]2(BF 4)2, the BF4- anions are positioned around Ag(I) ion, and for [Ag(L)]2-(ClO4)2, the ClO4 anions are positioned at the metallacyclodimeric ring. The delicate difference between both structures in solid state can be explained by the coordinating ability of anions.
| Original language | English |
|---|---|
| Pages (from-to) | 2157-2160 |
| Number of pages | 4 |
| Journal | Bulletin of the Korean Chemical Society |
| Volume | 29 |
| Issue number | 11 |
| DOIs | |
| State | Published - 2008.11.20 |
Keywords
- Anion effects
- Crystal structures
- Metallacyclodimers
- N,N-bis[2-(isonicotinoyloxy)ethyl]-p-toluenesulfonamide
- Silver(I) complexes
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