Repozytorium

Single crystal EPR spectroscopy, magnetic studies and catalytic activity of a self-assembled [2 x 2] CuII4 cluster obtained from a carbohydrazone based ligand.

Autorzy

Rahman Bikas

Hassan Hosseini-Monfared

Pavlo Aleshkevych

Ritta Szymczak

Miłosz Siczek

Tadeusz Lis

Rok wydania

2015

Czasopismo

Polyhedron

Numer woluminu

88

Strony

48-56

DOI

10.1016/j.poly.2014.11.038

Kolekcja

Naukowa

Język

Angielski

Typ publikacji

Artykuł

Streszczenie

A new tetranuclear [2 × 2] cluster of Cu(II) with a symmetric carbohydrazone based ligand, [Cu4L4](NO3)4·1.6(H2O) (1), {where HL donates bis-[(E)-N’-(1-(pyridin-2-yl)ethylidene)]carbohydrazide} was synthesized and characterized by spectroscopic methods and X-ray analysis. The EPR spectra were performed on single crystals of complex 1 at various temperatures and allowed the identification and separation of two types of magnetic objects contributing to magnetism: single atoms of Cu(II) and a tetranuclear Cu4 cluster. The main values of the g-factor and hyperfine structure were determined for single ions of Cu(II). The copper atoms in the tetramer are coupled antiferromagnetically with an isotropic antiferromagnetic exchange J = 215 K (149.4 cm−1). A small anisotropic exchange of the order of 0.06 K (0.04 cm−1) is responsible for the initial zero-field splitting of the energy levels in the tetramer spectrum. Magnetic measurements of complex 1 confirmed the existence of a strong antiferromagnetic exchange coupling between four Cu(II) ions. Complex 1 showed high potential for the catalytic and selective oxidation of cis-cyclooctene with aqueous H2O2.

Słowa kluczowe

Single crystal EPR, magnetic studies, Catalytic epoxidation, [2×2] CuII4 cluster, Exchange coupling

Adres publiczny

http://dx.doi.org/10.1016/j.poly.2014.11.038

Strona internetowa wydawcy

http://www.elsevier.com

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