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Rare-Earth-Containing Magnetic Liquid Crystals

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TLDR
In this paper, rare earth-containing metallomesogens with 4-alkoxy-N-alkyl-2-hydroxybenzaldimine ligands are reported and the stoichiometry of the complexes is [Ln(LH)(3)(NO3)(3)], where Ln is the trivalent rare earth ion;(Y, La, and Pr to Lu, except Pm) and LH is the Schiff base.
Abstract
Rare-earth-containing metallomesogens with 4-alkoxy-N-alkyl-2-hydroxybenzaldimine ligands are reported. The stoichiometry of the complexes is [Ln(LH)(3)(NO3)(3)], where Ln is the trivalent rare-earth ion;(Y, La, and Pr to Lu, except Pm) and LH is the Schiff base. The Schiff base ligands are in the zwitterionic form and coordinate through the phenolic oxygen only. The three nitrate groups coordinate in a bidentate fashion. The X-ray single-crystal structures of the nonmesogenic homologous complexes [Ln(LH)(3)(NO3)(3)]where Ln = Nd(III), Tb(III), and Dy(III) and LH = CH3OC6H3(2-OH)CH=NC4H9, are described. Although the Schiff base Ligands do not exhibit a mesophase, the metal complexes do (SmA phase). The mesogenic rare-earth complexes were studied by NMR, IR, EPR, magnetic susceptibility measurements, X-ray diffraction,and molecular modeling. The metal complexes in the mesophase have a very large magnetic anisotropy, so that these magnetic liquid crystals can easily be aligned by an external magnetic field.

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Taking advantage of luminescent lanthanide ions

TL;DR: This critical review has been tailored for a broad audience of chemists, biochemists and materials scientists; the basics of lanthanide photophysics are highlighted together with the synthetic strategies used to insert these ions into mono- and polymetallic molecular edifices.
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Lanthanide-containing molecular and supramolecular polymetallic functional assemblies.

TL;DR: Detailed studies of lanthanide solvates with water or acetonitrile suggest that trivalent lanthanides display a tendency to adopt nine-coordinate tricapped trigonal prismatic (TTP) arrangements around the metal ion in the solid state.
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Thermal, pressure and light switchable spin-crossover materials

TL;DR: The different approaches currently being explored in order to achieve multifunctionality in SCO materials are discussed.
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Ionic Liquid Crystals: Versatile Materials.

TL;DR: The discussion is focused on low molar mass and dendrimeric thermotropic ionic mesogens, as well as selected metal-containing compounds (metallomesogens), but some references to polymeric and/or lyotropic ionIC liquid crystals and particularly to ionic liquids will also be provided.
References
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Journal ArticleDOI

Nuclear magnetic resonance shifts in solution due to lanthanide ions

TL;DR: In this paper, the pseudocontact contribution to the NMR shifts for lanthanide complexes in solution is derived from the anisotropy in the susceptibility, provided that the molecular geometry is independent of temperature and of the lanthanides ion, the shift should vary as T−2 and in a predicted way from ion to ion.
Journal ArticleDOI

Metallomesogens: Metal Complexes in Organized Fluid Phases

TL;DR: Metallomesogens, metal complexes of organic ligands which exhibit liquid crystalline (mesomorphic) character, combine the variety and range of metal-based coordination chemistry with the extraordinary physical properties exhibited by liquid crystals as discussed by the authors.
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