Repozytorium

Cu2+ coordination properties of a 2-pyridine heptaamine tripod: characterization and binding mechanism.

Autorzy

A. S. Ten

N. Humbert

B. Verdejo

J. M. Llinares

M. Elhabiri

Julia Jezierska

C. Soriano

Henryk Kozłowski

A.-M. Albrecht-Gary

Enrique Garcia-Espaňa

Rok wydania

2009

Czasopismo

Inorganic Chemistry

Numer woluminu

48

Strony

8985-8997

DOI

10.1021/ic9010955

Kolekcja

Naukowa

Język

Angielski

Typ publikacji

Artykuł

Streszczenie

The synthesis, protonation, and Cu2+ coordination chemistry of a tripodal heptaamine ligand (L1) functionalized with 2-pyridine fragments at the ends of its three branches are reported. L1 presents six relatively high protonation constants followed by much more reduced constant that as indicated by the UV−vis and NMR data, occur on the pyridine fragments. p[H]-metric, ESI/MS+, EPR and UV−vis data show that L1 is able to form mono-, di-, and trinuclear Cu2+ complexes. Slippage movements and molecular reorganizations have been observed to occur as a function of p[H] in the 1:1 Cu2+ complexes. The kinetic studies showed that the complex formation is fast and proceeds through a dissociative Eigen−Wilkins mechanism. The decomposition of CuL1 upon addition of acid excess occurs with two separate kinetic steps; the rate constant for the fast process does not vary with respect to the H+ concentration whereas a linear dependence on H+ is observed for the slow step.

Adres publiczny

https://doi.org/10.1021/ic9010955

Strona internetowa wydawcy

https://www.acs.org/content/acs/en.html

Podobne publikacje
2002

Pyridine-2,6-dihydroxamic acid, a powerful dihydroxamate ligand for Ni2+ and Cu2+ ions.

Świątek-Kozłowska Jolanta, Gumienna-Kontecka Elżbieta, Dobosz Agnieszka, Golenya Irina A., Fritsky Igor O.

2012

Coordination of Ni2+ and Cu2+ to metal ion binding domains of E.coli SlyD protein.

Witkowska Danuta, Valensin Daniela, Rowińska-Żyrek Magdalena, Karafova Anna, Kamysz Wojciech, Kozłowski Henryk