Repozytorium

Ferromagnetic exchange coupling in phosphonato-bridged dinuclear copper (II) compound with monoethyl (pyridyn-2-ylmethyl)phosphonate ligand (2-mpmpe): Cu2(2-mpmpe)2(H2O)2(NO3)2.

Autorzy

Bogumiła Żurowska

Anna Brzuszkiewicz

Justyn Ochocki

Rok wydania

2008

Czasopismo

Polyhedron

Numer woluminu

27

Strony

1721-1728

DOI

10.1016/j.poly.2008.02.003

Kolekcja

Naukowa

Język

Angielski

Typ publikacji

Artykuł

Streszczenie

The interaction of diethyl (pyridyn-2-ylmethyl)phosphonate (2-pmpe) with Cu(NO3)2 · 6H2O leads to a partial hydrolysis of the starting ligand and formation of the compound of the formula Cu2(2-mpmpe)2(H2O)2(NO3)2, where 2-mpmpe = monoethyl (pyridyn-2-ylmethyl)phosphonate. The crystal and molecular structure of a copper(II) compound was determined by single X-ray diffraction method. Its structure consists of five-coordinated in distorted square planar geometry (CuNO4 chromophore) copper(II) ions doubly bridged by OPO from phosphonate. The Cu⋯Cu distance is 4.69 Å. The crystal packing is determined by the interdinuclear hydrogen bond system, which leads to a three-dimensional (3D) H-bonds network. The compound was characterized by infrared, ligand field, EPR spectroscopy, and magnetic studies. The magnetic properties of the title compound investigated over the 1.8–300 K, revealed the occurrence of a weak ferromagnetic coupling through phosphonate bridge (J = 1.86 cm−1) and interdimer superexchange coupling through H-bond network (zJ′ = −0.17 cm−1). Spectroscopic and magnetic properties are presented in the light of crystal structure.

Słowa kluczowe

Copper(II) compound, Phosphonato-bridge, Crystal structure, Spectroscopy, Magnetism

Adres publiczny

https://doi.org/10.1016/j.poly.2008.02.003

Strona internetowa wydawcy

http://www.elsevier.com

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