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The effect of pyridinecarboxylate chelating groups on the stability and electronic relaxation of gadolinium complexes

Chatterton, Nicholas; Gateau, Christelle; Mazzanti, Marinella; Pécaut, Jacques; Borel, Alain; Helm, Lothar and Merbach, André (2005). The effect of pyridinecarboxylate chelating groups on the stability and electronic relaxation of gadolinium complexes. Dalton Transactions(6) pp. 1129–1135.

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DOI (Digital Object Identifier) Link: https://doi.org/10.1039/b416150e
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Abstract

The ligand N,N′-bis[(6-carboxy-2-pyridylmethyl]ethylenediamine-N,N′-diacetic acid (H4bpeda) was synthesised using an improved procedure which requires a reduced number of steps and leads to a higher yield with respect to the published procedure. It was obtained in three steps from diethylpyridine-2,6-dicarboxylate and commercially available ethylenediamine-N,N′-diacetic acid with a total yield of [similar]20%. The crystal structure of the hexa-protonated form of the ligand which was determined by X-ray diffraction shows that the four carboxylates and the two amines are protonated. The crystal structure of the polynuclear complex [Gd(bpeda)(H2O)2]3[Gd(H2O)6]2Cl3 (2), isolated by slow evaporation of a 1 ∶ 1 mixture of GdCl3 and H4bpeda at pH ~ 1, was determined by X-ray diffraction. In complex 2 three [Gd(bpeda)(H2O)2] units, containing a Gd(III) ion ten-coordinated by the octadentate bpeda and two water molecules, are connected in a pentametallic structure by two hexa-aquo Gd3+ cations through four carboxylato bridges. The protonation constants (pKa1 = 2.9(1), pKa2 = 3.5(1), pKa3 = 5.2(2), and pKa4 = 8.5(1)) and the stability constants of the complexes formed between Gd(III) and Ca(II) ions and H4bpeda (log βGdL = 15.1(3); log βCaL = 9.4(1)) were determined by potentiometric titration. The unexpected decrease in the stability of the gadolinium complex and of the calcium complex of the octadentate ligand bpeda4− with respect to the hexadentate ligand edta4− has been interpreted in terms of an overall lower contribution to stability of the metal-nitrogen interactions. The EPR spectra display very broad lines (apparent ΔHpp ~800–1200 G at X-band and 90–110 G at Q-band depending on the temperature), indicating a rapid transverse electron spin relaxation. At X-band, Gd(bpeda) is among the fastest relaxing Gd3+ complexes to date suggesting that the presence of pyridinecarboxylate chelating groups in itself does not lead to slow electron relaxation.

Item Type: Journal Item
Copyright Holders: 2005 The Royal Society of Chemistry
ISSN: 1477-9234
Academic Unit/School: Faculty of Science, Technology, Engineering and Mathematics (STEM) > Life, Health and Chemical Sciences
Faculty of Science, Technology, Engineering and Mathematics (STEM)
Item ID: 43978
Depositing User: Nicholas Chatterton
Date Deposited: 13 Aug 2015 10:38
Last Modified: 27 Jun 2020 07:30
URI: http://oro.open.ac.uk/id/eprint/43978
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