Abstract
Complexation of Eu(III) ions with H4dota and its bis(phosphonate)-bearing analogs, H8do3aPBP with phosphinate spacer and H7dotamBP with carboxamide spacer, was studied by UV–Vis spectrophotometry and luminescence life-time measurements. The results show formation of two types of out-of-cage intermediates. The [EuL]oc intermediate is formed under metal ion excess, whereas [EuL2]oc intermediate is formed under ligand excess. At room temperature, their conversion to in-cage complex is comparable but the [EuL2]oc transformation into the in-cage complex is significantly faster at elevated temperatures. Both bis(phosphonate)-bearing ligands show slower complexation rate than H4dota. Comparison of reactivity of H8do3aPBP and H7dotamBP show important role of the spacer connecting the bis(phosphonate) group with the macrocycle. Presence of phosphinate in H8do3aPBP leads to significantly faster (3–4 orders of magnitude) complexation than in case of the amide spacer in H7dotamBP. Both bis(phosphonate)-bearing ligands show nonlinear dependence of the complexation rate on concentration of hydroxide anions due to changes in protonation state of the bis(phosphonate) moiety.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.