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Hydrogen-bond-based magnetic exchange between μ-diethylnicotinamide(aqua)bis(X-salicylato)copper(II) polymeric chains.
Autorzy
Rok wydania
2011
Czasopismo
Zeitschrift für Anorganische und Allgemeine Chemie
Numer woluminu
637
Strony
224-231
DOI
10.1002/zaac.201000301
Kolekcja
Język
Angielski
Typ publikacji
Artykuł
Polymeric salicylatocopper(II) complexes of unusual composition [Cu(X‐sal)2(μ‐denia)(H2O)]n [denia = diethylnicotinamide, and X‐sal = 5‐methylsalicylate (1), 3‐methylsalicylate (2), 4‐methoxysalicylate (3), 3,5‐dichlorosalicylate (4) and 3,5‐dibromosalicylate (5)] were synthesized and characterized. Magnetic measurements were performed in the temperature range 1.8–300 K. The structural unit of all complexes consists of a CuII atom, which is monodentately coordinated by the pair of X‐salicylate anions in trans positions. Water and the diethylnicotinamide ligand occupy the other two basal plane positions of the tetragonal pyramid. The axial positions are occupied by a diethylnicotinamide oxygen atom of neighboring structural units, thus forming a spiral polymeric structure parallel to b axis. Magnetic measurements showed that all complexes 1–5 exhibit a susceptibility maximum at about 6–8 K. The obtained data fit to Bleaney–Bowers equation gave singlet‐triplet energy gaps 2J = –8.60 cm–1 for 1, 2J = –6.57 cm–1 for 2, 2J = –8.57 cm–1 for 3, 2J = –6.82 cm–1 for 4, and 2J = –6.45 cm–1 for 5. The supramolecular structure based on hydrogen bonds [described by supramolecular synthons R22(10) and R22(12)] is the pathway for antiferromagnetic interactions of the magnetically coupled pairs of copper atoms of neighboring chains within the 2D supramolecular layers. The results of the magnetic measurements suggest involvement of the COO groups in the magnetic interaction pathway for all five complexes.
Słowa kluczowe
Coordination polymer, copper, hydrogen bonds, magnetic properties, Supramolecular chemistry
Adres publiczny
https://doi.org/10.1002/zaac.201000301
Strona internetowa wydawcy
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