Nickel(ii) complexes were synthesized using chiral N-thiophosphorylated thioureas as the starting compounds and 4-dimethylaminopyridine as a co-ligand. The reaction with racemic thiourea afforded homochiral complexes due to the distortion of the nickel coordination. The unsaturated coordination sphere of nickel ions results in the formation of supramolecular homochiral 1D chains in the crystal through steric key—lock interactions between adjacent molecules. Conformational flexibility of the ligands is responsible for disorder of molecules in the crystals and the occurrence of polymorphs.
相似文献The results of a femtosecond optical and magneto-optical spectroscopy study of a thin epitaxial film of a low-temperature magnetically soft Pd0.94Fe0.06 alloy on a ({dy001})-MgO substrate are reported. The photoinduced demagnetization and magnetization recovery times are determined. The latter increases critically at approaching the ferromagnetic ordering temperature TC = 190 K from below. It is shown that the reflectivity dynamics after a photoexcitation pulse evolves from a two-exponential in the paramagnetic phase to a four-component at 80 K < T < TC, simplifying to a three-component at T < 50 K. According to our interpretation, such an evolution, along with the manifestation of an additional increasing component in the magnetic response at 80 K < T < TC, indicates a magnetic and electronic inhomogeneity of the film associated with the distribution of local iron concentrations. The fraction of small-scale inclusions of the paramagnetic phase is estimated as ≈10 vol %.
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