Abstract
The binding of a series of phosphate anions to coordinatively unsaturated macrocyclic complexes of Yb, Tm, and Eu was studied by 1H-NMR, emission and circularly polarized luminescence (CPL) spectroscopy. Each ternary adduct was distinguished by its spectral profile. With O-phosphorylated amino acids and peptides, chemoselective ligation of the phosphate moiety was favored by Eu over chelation involving the terminal amino group, which was competitive for Tm and Yb. A preference for binding O-phosphono-L-tyrosine sites was found with various Eu complexes, and was signalled by ratiometric changes in metal-based emission and CPL spectra.
| Original language | English |
|---|---|
| Pages (from-to) | 391-405 |
| Number of pages | 15 |
| Journal | Helvetica Chimica Acta |
| Volume | 88 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - Mar 2005 |
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