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• W2017458752 abstract "The article describes the synthesis, structure and magnetic investigations of a series of metal-organic framework compounds formed with Mn+2 and Ni+2 ions. The structures, determined using the single crystal X-ray diffraction, indicated that the structures possess two- and three-dimensional structures with magnetically active dimers, tetramers, chains, two-dimensional layers connected by polycarboxylic acids. These compounds provide good examples for the investigations of magnetic behaviour. Magnetic studies have been carried out using SQUID magnetometer in the range of 2–300 K and the behaviour indicates a predominant anti-ferromagnetic interactions, which appears to differ based on the M-O-C-O-M and/or the M-O-M (M = metal ions) linkages. Thus, compounds with carboxylate (Mn-O-C-O-Mn) connected ones, [C3N2H5][Mn(H2O)“C6H3(COO)3”], I, [“Mn(H2O)3”“C12H8O(COO)2”]·H2O, II, [“Mn(H2O)”“C12H8O(COO)2”], III, show simple anti-ferromagnetic behaviour. The compounds with Mn-O/OH-Mn connected dimer and tetramer units in [NaMn“C6H3(COO)3”], IV, [Mn2(µ3-OH) (H2O)2“C6H3(COO)3”]·2H2O, V, show canted-antiferromagnetic and anti-ferromagnetic behaviour, respectively. The presence of infinite one-dimensional -Ni-OH-Ni- chains in the compound, [Ni2(H2O)(µ3-OH)2(C8H5NO4], VI, gives rise to ferromagnet-like behaviour at low temperatures. The compounds, [Mn3“C6H3(COO)3”2], VII and [“Mn(OH)”2“C12H8O(COO)2”], VIII, have two-dimensional infinite -Mn-O/OH-Mn- layers with triangular magnetic lattices, which resemble the Kagome and brucite-like layer. The magnetic studies indicated canted-antiferromagnetic behaviour in both the cases. Variable temperature EPR and theoretical magnetic modelling studies have been carried out on selected compounds to probe the nature of the magnetic species and their interactions with them." @default.
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• W2017458752 date "2010-01-01" @default.
• W2017458752 modified "2023-09-23" @default.
• W2017458752 title "Magnetic behaviour in metal-organic frameworks—Some recent examples" @default.
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• W2017458752 doi "https://doi.org/10.1007/s12039-010-0001-3" @default.
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