2018
NOTA Complexes with Copper(II) and Divalent Metal Ions: Kinetic and Thermodynamic Studies
KUBICEK, Vojtěch, Zuzana BOHMOVA, Romana ŠEVČÍKOVÁ, Jakub VANĚK, Přemysl LUBAL et. al.Základní údaje
Originální název
NOTA Complexes with Copper(II) and Divalent Metal Ions: Kinetic and Thermodynamic Studies
Autoři
KUBICEK, Vojtěch (203 Česká republika), Zuzana BOHMOVA (203 Česká republika), Romana ŠEVČÍKOVÁ (203 Česká republika, domácí), Jakub VANĚK (203 Česká republika, domácí), Přemysl LUBAL (203 Česká republika, garant, domácí), Zuzana POLAKOVA (203 Česká republika), Romana MICHALICOVÁ (203 Česká republika, domácí), Jan KOTEK (203 Česká republika) a Petr HERMANN (203 Česká republika)
Vydání
Inorganic Chemistry, Washington, American Chemical Society, 2018, 0020-1669
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10402 Inorganic and nuclear chemistry
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 4.850
Kód RIV
RIV/00216224:14310/18:00103745
Organizační jednotka
Přírodovědecká fakulta
UT WoS
000428219500016
Klíčová slova anglicky
MACROCYCLIC CHELATORS; BIFUNCTIONAL CHELATOR; TRIAZACYCLONONANE-TRIACETIC ACID; FORMATION AND DISSOCIATION KINETICS
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 23. 4. 2024 12:29, Mgr. Michal Petr
Anotace
V originále
H(3)nota derivatives are among the most studied macrocyclic ligands and are widely used for metal ion binding in biology and medicine. Despite more than 40 years of chemical research on H(3)nota, the comprehensive study of its solution chemistry has been overlooked. Thus, the coordination behavior of H(3)nota with several divalent metal ions was studied in detail with respect to its application as a chelator for copper radioisotopes in medical imaging and therapy. In the solid-state structure of the free ligand in zwitterionic form, one proton is bound in the macrocyclic cavity through a strong intramolecular hydrogen-bond system supporting the high basicity of the ring amine groups (log K-a = 13.17). The high stability of the [Cu(nota)](-) complex (log K-ML = 23.33) results in quantitative complex formation, even at pH <1.5. The ligand is moderately selective for Cu(II) over other metal ions (e.g., log K-ML(Zn) = 22.32 and log K-ML(Ni) = 19.24). This ligand forms a more stable complex with Mg(II) than with Ca(II) and forms surprisingly stable complexes with alkali-metal ions (stability order Li(I) > Na(I) > K(I)). Thus, H(3)nota shows high selectivity for small metal ions. The [Cu(nota)](-) complex is hexacoordinated at neutral pH, and the equatorial N2O2 interaction is strengthened by complex protonation. Detailed kinetic studies showed that the Cu(II) complex is formed quickly (millisecond time scale at c(Cu) approximate to 0.1 mM) through an out-of-cage intermediate. Conversely, conductivity measurements revealed that the Zn(II) complex is formed much more slowly than the Cu(II) complex. The Cu(II) complex has medium kinetic inertness (tau(1/2) 46 s; pH 0, 25 degrees C) and is less resistant to acid-assisted decomplexation than Cu(II) complexes with H(4)dota and H(4)teta. Surprisingly, [Cu(nota)](-) decomplexation is decelerated in the presence of Zn(II) ions due to the formation of a stable dinuclear complex. In conclusion, H(3)nota is a good carrier of copper radionuclides because the [Cu(nota)](-) complex is predominantly formed over complexes with common impurities in radiochemical formulations, Zn(II) and Ni(II), for thermodynamic and, primarily, for kinetic reasons. Furthermore, the in vivo stability of the [Cu(nota)](-) complex may be increased due to the formation of dinuclear complexes when it interacts with biometals.
Návaznosti
LQ1601, projekt VaV |
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MUNI/A/1237/2016, interní kód MU |
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