Kinetics of the Formation of [Ln(DOTAM)]3+ Complexes
- 31 July 2007
- journal article
- research article
- Published by Wiley in European Journal of Inorganic Chemistry
- Vol. 2007 (23) , 3639-3645
- https://doi.org/10.1002/ejic.200700178
Abstract
The kinetics of the formation of lanthanide(III) complexes of the neutral ligand DOTAM differ considerably from those of DOTA and its derivatives, which contain negatively charged pendant groups. Formation of the complexes [Ln(DOTAM)]3+ occurs upon direct encounter of the Ln3+ ions and the fully deprotonated ligand in the pH range 4.7–5.8. The formation of a protonated intermediate, which is characteristic of the complexation of DOTA and its derivatives, was not detected. General base catalysis is not valid in the formation reactions of [Ln(DOTAM)]3+, which also indicates the absence of protonated intermediates. The rates of the proton‐exchange reactions for the ligand species H2DOTAM2+ and HDOTAM+ have been studied by 1H NMR spectroscopy. Proton exchange was found to be a general base‐catalysed process, therefore it cannot play an important role in the formation of these complexes. The second‐order rate constants, kL, which characterize the formation of the complexes [Ln(DOTAM)]3+, are lower than the analogous rate constants reported for the Ln3+ complexes of open‐chain multidentate ligands by three to four orders of magnitude. These low kL values can be interpreted by assuming an early rate‐determining step (probably the second or third Ln3+–amide bond formation) in the reaction sequence that leads to the [Ln(DOTAM)]3+ complex.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)Keywords
This publication has 34 references indexed in Scilit:
- Structural characterisation of a diprotonated ligand lanthanide complex—a key intermediate in lanthanide ion association and complex dissociation pathwaysDalton Transactions, 2006
- PARACEST Agents: Modulating MRI Contrast via Water Proton ExchangeAccounts of Chemical Research, 2003
- Luminescent sensors for pH, pO2, halide and hydroxide ions using phenanthridine as a photosensitiser in macrocyclic europium and terbium complexesJournal of the Chemical Society, Perkin Transactions 2, 1998
- The Amide Oxygen as a Donor Group. Metal Ion Complexing Properties of Tetra-N-acetamide Substituted Cyclen: A Crystallographic, NMR, Molecular Mechanics, and Thermodynamic StudyJournal of the American Chemical Society, 1995
- Lanthanide(III) Tetraamide Macrocyclic Complexes as Synthetic Ribonucleases: Structure and Catalytic Properties of [La(tcmc)(CF3SO3)(EtOH)](CF3SO3)2Angewandte Chemie International Edition in English, 1994
- Equilibrium dynamics in the thallium(III)-chloride system in acidic aqueous solutionJournal of the American Chemical Society, 1989
- Recent developments in solvation and dynamics of the lanthanide(III) ionsPure and Applied Chemistry, 1988
- Nuclear magnetic resonance and potentiometric studies of the protonation scheme of two tetraaza tetraacetic macrocyclesInorganic Chemistry, 1981
- A study of some problems in determining the stoicheiometric proton dissociation constants of complexes by potentiometric titrations using a glass electrodeAnalytica Chimica Acta, 1967
- Ionic Association. III. The Equilibrium between Ion Pairs and Free IonsJournal of the American Chemical Society, 1958