The binding of a series of phosphate anions to coordinatively unsaturated macrocyclic complexes of Yb, Tm, and Eu was studied by 1 H‐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.
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Atkinson et al. (2005) studied this question.
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