Repozytorium

Synthesis and structure of [2 x 2] molecular grid copper(II) and nickel(II) complexes with a new polydentate oxime-containing Schiff base ligand.

Autorzy

Yurii S. Moroz

Kinga Kulon

Matti Haukka

Elżbieta Gumienna-Kontecka

Henryk Kozłowski

Franc Meyer

Igor O. Fritsky

Rok wydania

2008

Czasopismo

Inorganic Chemistry

Numer woluminu

47

Strony

5656-5665

DOI

10.1021/ic702375h

Kolekcja

Naukowa

Język

Angielski

Typ publikacji

Artykuł

Streszczenie

A new polynucleating oxime-containing Schiff base ligand, 2-hydroxyimino-N′-[1-(2-pyridyl)ethylidene]propanohydrazone (Hpop), has been synthesized and fully characterized. pH potentiometric, electrospray ionization mass spectrometric, and spectrophotometric studies of complex formation in H2O/DMSO solution confirmed the preference for polynuclear complexes with 3d metal ions. Single-crystal X-ray diffraction analyses of [Ni4(pop)4(HCOO)4]·7H2O (1), [Cu4(pop-H)4(HCOOH)4]·H2O (2), and [Cu4(pop-H)4(H2O)4]·9H2O (3) indicated the presence of a [2 × 2] molecular grid structure in all three compounds but distinct configurations of the cores: a head-to-tail ligand arrangement with overall S4 symmetry of the grid in the Cu2+ complexes as opposed to a head-to-head ligand arrangement with (noncrystallographic) C2 grid symmetry for the Ni2+ complex. A cryomagnetic study of 3 revealed intramolecular ferromagnetic exchange between copper ions in the grid, while in 1, antiferromagnetic interactions between the metal ions were observed.

Słowa kluczowe

Amides, Ions, Ligands, Metal, Molecules

Adres publiczny

https://doi.org/10.1021/ic702375h

Strona internetowa wydawcy

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

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