4.7 Article

Di-Pyridine-Containing Macrocyclic Triamide Fe(II) and Ni(II) Complexes as ParaCEST Agents

Journal

INORGANIC CHEMISTRY
Volume 61, Issue 42, Pages 16650-16663

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.2c02242

Keywords

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Funding

  1. SERB, India [CRG/2020/004334]
  2. UGC, Delhi
  3. IIT Bhubanes
  4. Italian Ministry for Education and Research (MIUR)

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Fe(II) and Ni(II) paraCEST contrast agents containing di-pyridine macrocyclic ligand were synthesized and characterized. Their structures were determined by crystallography, and their CEST contrast effects were studied at body temperature. The protonation constants and thermodynamic stability constants were determined as well.
Fe(II) and Ni(II) paraCEST contrast agents containing the di-pyridine macrocyclic ligand 2,2',2 ''- (3,7,10-triaza-1,5 (2,6)-dipyridinacyclound e caphane-3,7,10-triyl)triacetamide (DETA) are reported here. Both [Fe(DETA)](2+) and [Ni-(DETA)](2+) complexes were structurally characterized. Crystallographic data revealed the seven-coordinated distorted pentagonal bipyramidal geometry of the [Fe(DETA)]center dot(BF4)(2)center dot MeCN complex with five coordinated nitrogen atoms from the macrocyclic ring and two coordinated oxygen atoms from two amide pendant arms. The [Ni(DETA)]center dot Cl-2 center dot 2H(2)O complex was six-coordinated in nature with a distorted octahedral geometry. Four coordinated nitrogen atoms were from the macrocyclic ring, and two coordinated oxygen atoms were from two amide pendant arms. [Fe(DETA)](2+) exhibited well-resolved sharp proton resonances, whereas very broad proton resonances were observed in the case of [Ni(DETA)](2+) due to the long electronic relaxation times. The CEST peaks for the [Fe(DETA)](2+) complex showed one highly downfield-shifted and intense peak at 84 ppm with another shifted but less intense peak at 28 ppm with good CEST contrast efficiency at body temperature, whereas [Ni(DETA)](2+) showed only one highly shifted intense peak at 78 ppm from the bulk water protons. Potentiometric titrations were performed to determine the protonation constants of the ligand and the thermodynamic stability constant of the [M(DETA)](2+) (M = Fe, Co, Ni, Cu, Zn) species at 25.0 degrees C and I = 0.15 mol-L-1 NaClO4. Metal exchange studies confirmed the stability of the complexes in acidic medium in the presence of physiologically relevant anions and an equimolar concentration of Zn(II) ions.

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