Abstract
Stable lanthanide complexes have been devised in which the emission intensity or lifetime is a sensitive function of pH, pO2 or halide concentration following excitation in the range 350-380 nm. The pH-dependent systems report the pKa of the excited singlet or triplet of an integral phenanthridine chromophore. Modulation of the emission may occur via ligand or metal-centred processes: quenching of the singlet or triplet phenanthridine excited state occurs by halide and oxygen respectively; in complexes with chiral heptadentate ligands displacement of bound water molecules by lactate, phosphate and hydrogencarbonate leads to enhancements in the emission intensity and lifetime and pronounced changes in emission polarisation.
| Original language | English |
|---|---|
| Pages (from-to) | 109-130 |
| Number of pages | 22 |
| Journal | Coordination Chemistry Reviews |
| Volume | 205 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 1 Aug 2000 |
User-Defined Keywords
- Hydrogencarbonate
- Lanthanides
- Luminescence
- pH
- Sensors