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dc.creatorKalman, Ferenc K.
dc.creatorNagy, Viktoria
dc.creatorUzal-Varela, Rocio
dc.creatorPerez-Lourido, Paulo
dc.creatorEsteban-Gomez, David
dc.creatorGarda, Zoltan
dc.creatorPota, Kristof
dc.creatorMezei, Roland
dc.creatorPallier, Agnes
dc.creatorToth, Eva
dc.creatorPlatas-Iglesias, Carlos
dc.creatorTircso, Gyula
dc.date.accessioned2021-07-08T14:30:50Z
dc.date.available2021-07-08T14:30:50Z
dc.date.issued2021
dc.identifier.urihttps://doi.org/10.3390/molecules26061524
dc.identifier.urihttps://repository.tcu.edu/handle/116099117/47486
dc.identifier.urihttps://www.mdpi.com/1420-3049/26/6/1524
dc.description.abstractWe report two macrocyclic ligands based on a 1,7-diaza-12-crown-4 platform functionalized with acetate (tO2DO2A(2-)) or piperidineacetamide (tO2DO2AM(Pip)) pendant arms and a detailed characterization of the corresponding Mn(II) complexes. The X-ray structure of [Mn(tO2DO2A)(H2O)]center dot 2H(2)O shows that the metal ion is coordinated by six donor atoms of the macrocyclic ligand and one water molecule, to result in seven-coordination. The Cu(II) analogue presents a distorted octahedral coordination environment. The protonation constants of the ligands and the stability constants of the complexes formed with Mn(II) and other biologically relevant metal ions (Mg(II), Ca(II), Cu(II) and Zn(II)) were determined using potentiometric titrations (I = 0.15 M NaCl, T = 25 degrees C). The conditional stabilities of Mn(II) complexes at pH 7.4 are comparable to those reported for the cyclen-based tDO2A(2-) ligand. The dissociation of the Mn(II) chelates were investigated by evaluating the rate constants of metal exchange reactions with Cu(II) under acidic conditions (I = 0.15 M NaCl, T = 25 degrees C). Dissociation of the [Mn(tO2DO2A)(H2O)] complex occurs through both proton- and metal-assisted pathways, while the [Mn(tO2DO2AM(Pip))(H2O)] analogue dissociates through spontaneous and proton-assisted mechanisms. The Mn(II) complex of tO2DO2A(2-) is remarkably inert with respect to its dissociation, while the amide analogue is significantly more labile. The presence of a water molecule coordinated to Mn(II) imparts relatively high relaxivities to the complexes. The parameters determining this key property were investigated using O-17 NMR (Nuclear Magnetic Resonance) transverse relaxation rates and H-1 nuclear magnetic relaxation dispersion (NMRD) profiles.en_US
dc.language.isoenen_US
dc.publisherMDPI
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceMolecules
dc.subjectmanganeseen_US
dc.subjectmagnetic resonance imagingen_US
dc.subjectstabilityen_US
dc.subjectdissociation kineticsen_US
dc.subjectwater exchangeen_US
dc.subjectcontrast agentsen_US
dc.subjectmacrocyclesen_US
dc.titleExpanding the Ligand Classes Used for Mn(II) Complexation: Oxa-aza Macrocycles Make the Differenceen_US
dc.typeArticleen_US
dc.rights.holder2021 by the authors
dc.rights.licenseCC BY 4.0
local.collegeCollege of Science and Engineering
local.departmentChemistry & Biochemistry
local.personsPota (CHEM)


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