Abstract
With the hetero-binuclear Zn-Nd complex from the ethylene- or phenylene-linkered Salen-type Schiff-base ligand as the building block, further self-assembly of the unsymmetrical exo-dentate IN- (IN- = isonicotinic) anion gave a 2D layer polymeric [ZnL1Nd(IN)(NO3)2]n (1) (H2L1 = N,N′-bis(3-methoxy-salicylidene)ethylene-1,2-diamine) or a discrete binuclear [ZnL2Nd(IN)(NO3)2(DMF] (2) (H2L2 = N,N′-bis(3-methoxy-salicylidene)phenylene-1,2-diamine) complex, respectively. The change of linker flexibility of two Salen-type Schiff-base ligands (H2L1 and H2L2) resulted in the difference of structures and NIR luminescent properties of their mixed-ligands complexes.
| Original language | English |
|---|---|
| Pages (from-to) | 267-271 |
| Number of pages | 5 |
| Journal | Inorganic Chemistry Communications |
| Volume | 12 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - Mar 2009 |
User-Defined Keywords
- Flexibility of linked groups
- NIR luminescence
- Self-assembly
- Unsymmetrical exo-dentate ligand
- Zn-Nd Schiff-base complex
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