Abstract
The formation of soluble supramolecular 3-D coordination polymers with Nd3+ and La3+ in aqueous solution has been studied for two bifunctional ligands consisting of two pyridine-2,6-dicarboxylate groups connected at the 4-position by O(CH2CH2O)4 and O(CH2CH2O)6 spacers (C4 and C6, respectively). Viscosity measurements were used to monitor the network formation as a function of the ligand concentration, and the ratio between metal ions and ligands. For corresponding conditions C4 solutions with Nd3+ always gave much higher viscosities than C6 solutions with Nd3+. C6 is long, and flexible enough to bind with both chelating groups to only one metal ion (ring formation). This causes the polymers to stop growing, resulting in smaller average sizes of the 3-D polymers. The ring-structures could be demonstrated by 1H NMR spectroscopy using C6 and La3+ at low concentrations.
Original language | English |
---|---|
Pages (from-to) | 2847-2852 |
Number of pages | 6 |
Journal | European journal of inorganic chemistry |
Volume | 2004 |
Issue number | 14 |
DOIs | |
Publication status | Published - 19 Jul 2004 |
Externally published | Yes |
Keywords
- Lanthanides
- NMR spectroscopy
- Self-assembly
- Tridendate ligands
- Viscosity
- n/a OA procedure