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Inne
Crystal structure and characterization of manganese(II) carboxylates: 3D metal-organic frameworks.
Autorzy
Rok wydania
2005
Czasopismo
Numer woluminu
5
Strony
1945-1951
DOI
10.1021/cg050169u
Kolekcja
Język
Angielski
Typ publikacji
Artykuł
Three mononuclear manganese (II) complexes with quinoline-2-carboxylate ion (quin-2-c), [Mn(quin-2-c)2(H2O)2]2·Hquin-2-c·2H2O (1), Mn(quin-2-c)2(EtOH)2 (2), and HbimH[Mn(quin-2-c)2Cl] (3) (HbimH+ = benzimidazolium ion), have been obtained by self-assembly and structurally characterized by X-ray diffraction. In all three complexes the quin-2-c ions are bound to manganese in the chelate mode through a ring nitrogen and a monodentate carboxylate group. In complexes 1 and 2 the manganese ions are coordinated in the distorted octahedron with an N2O4 donor set. In the complex anion Mn(quin-2-c)2Cl-, present in the crystal of 3, the manganese ion is five-coordinated by two quin-2-c ligands and the chlorine ion. The solid-state EPR spectra of 1 and 2 are characteristic of the Mn(II) ion in a distorted-octahedral geometry, whereas the spectrum of 3 is more complicated due to the zero-field splitting effect operating at lower symmetry. The EPR spectra of all complexes in frozen ROH are very similar and are characteristic of an octahedral environment around manganese. The systems of strong intermolecular hydrogen bonds form 1D structures in all complexes, which are further engaged in weak C−H···O, π···π and C−H···π interchain interactions, creating the 3D networks. The IR spectra reflect the differences in the hydrogen bond systems in 1−3.
Słowa kluczowe
Noncovalent interactions, Transition metals, Ligands, Molecules, Ions
Adres publiczny
https://doi.org/10.1021/cg050169u
Strona internetowa wydawcy
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