Abstract
Four new coordination polymers, namely [Co3(4,4′-bpy)4(pa)4](NO3)2(4,4′-bpy)(H2O)3.5 (1), [Co(4,4′-bpy)(pa)2(H2O)2](paH)2 (2), [Zn3(4,4′-bpy)4(pa)4](NO3)2(paH)(H2O)2.5 (3), [Cu(4,4′-bpy)0.5(ba)2] (4), as well as one known compound [Cu(pyz)0.5(ba)2] (5) (4,4′-bpy=4,4′-bipyridine; paH=phenylacetic acid; baH=benzoic acid; pyz=pyrazine) have been hydrothermally prepared via metal ion-dependent in situ metal-ligand redox reactions of 2-phenyl-malonic acid (2-phmalH2). Among them, 1, 2 and 3 contain paH and pa as the decarboxylated products of 2-phmalH2, while 4 and 5 contain the redox product baH instead of paH. This results show that the decarboxylation occurs easily to 2-phmalH2 under hydrothermal condition, while an in situ metal/ligand redox reaction undergoes in the presence of copper(II) ion. Compound 1 bearing well isolated, carboxylate-bridged linear trimeric Co3II subunits shows intracluster antiferromagnetic interaction (J=-9 K) and no long-range magnetic ordering down to 2 K.
| Original language | English |
|---|---|
| Pages (from-to) | 9-17 |
| Number of pages | 9 |
| Journal | Journal of Molecular Structure |
| Volume | 796 |
| Issue number | 1-3 |
| DOIs | |
| State | Published - 30 Aug 2006 |
| Externally published | Yes |
Keywords
- Coordination polymer
- Ligand reaction
- Magnetic property
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