Abstract

AbstractWe report here the physical‐chemical characterization of a highly water‐soluble Gd(III) complex (complex 1) formed with the asymmetric hexadentate ligand H4bedik (2,2′‐((2‐(bis (carboxymethyl)amino)benzyl)azanediyl)diacetic acid). The number of water molecules directly coordinated to the metal, q=2.2, was assessed by measuring luminescence lifetimes of the Tb(III) analogue (complex 2) in H2O and D2O and it further was confirmed by 17O chemical shift measurements on the Gd(III) complex. The complex has moderate thermodynamic stability and remains insensitive to physiological anions [biphosphate (HPO42−), bicarbonate (HCO3−)] and pH variation (in the range 5–10) of the medium as evidenced by negligible changes in longitudinal relaxivity (r1) at 1.41 T, 25 °C. The Gd(III) complex exhibits very fast water exchange, among the fastest reported for Gd(III) chelates, and high relaxivity at high magnetic fields (r1=7.47 mM–1s–1 at 9.4 T, pH ∼ 7 and 25 °C). Interestingly, the very high positive value of the activation entropy indicates a dissociatively activated water exchange for this eight‐coordinate complex.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

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.