Repozytorium

Coordination chemistry of 2-hydroxymethylbenzimidazole complexes with copper(II) and cadmium(II) ions: similarities and differences.

Autorzy

Barbara Barszcz

Agnieszka Jabłońska-Wawrzycka

Katarzyna Stadnicka

Julia Jezierska

Rok wydania

2008

Czasopismo

Polyhedron

Numer woluminu

27

Strony

3500-3508

DOI

10.1016/j.poly.2008.07.038

Kolekcja

Naukowa

Język

Angielski

Typ publikacji

Artykuł

Streszczenie

The new Cu(II) and Cd(II) complexes of the biologically relevant ligand 2-hydroxymethylbenzimidazole: [CdL2(NO3)2] 1, ([CuL2(NO3)](NO3)(H2O) 2, [CdL3](NO3)2L(EtOH)0.25 3, mer-[CuL3](NO3)2(H2O)(i-PrOH) 4 have been synthesized and characterized by elemental analyses, UV–Vis, IR, Raman, EPR, NMR, X-ray diffraction and magnetic measurements. X-ray studies have confirmed a bidentate fashion of coordination of the 2-CH2OHBIm to the Cd(II) as well to Cu(II) ions. This results in the formulation of a five-membered chelate ring in which both N(imidazole) and O(hydroxymethyl) donors of ligand are involved. A comparison of Cu(II) 4 and Cd(II) 3 model complexes shows that both metals may form complexes which exhibit identical structures (distorted octahedral) forming chromophores of the MN3O3 type. On the contrary, the polyhedra of metal complexes containing two ligands are different. The copper complex 2 is a five-coordinated with tetragonal pyramid as coordination polyhedron (CuN2O3) but cadmium forms an eight-coordinated (CdN2O6) complex 1. Weak C–H⋯π type interactions which were extracted from X-ray data of 1 were confirmed by the 13C NMR method. The IR data indicated that Cd(II) is a considerably better acceptor (Lewis acid) than Cu(II) ion for the N, O-donor ligand. The similarities and differences revealed in the coordination behaviour of Cu(II) and Cd(II) towards N, O-donor ligand should be treated as a test on possibility of the copper(II) ions to be displaced by cadmium(II), for example, in the intracellular sites.

Adres publiczny

https://doi.org/10.1016/j.poly.2008.07.038

Strona internetowa wydawcy

http://www.elsevier.com

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