0000000000365467

AUTHOR

Eduard B. Rusanov

0000-0002-7678-0985

showing 2 related works from this author

Ferromagnetism and Chirality in Two-Dimensional Cyanide-Bridged Bimetallic Compounds

2002

The combination of hexacyanoferrate(III) anions, [Fe(CN)(6)](3)(-), with nickel(II) complexes derived from the chiral ligand trans-cyclohexane-1,2-diamine (trans-chxn) affords the enantiopure layered compounds [Ni(trans-(1S,2S)-chxn)(2)](3)[Fe(CN)(6)](2).2H(2)O (1) and [Ni(trans-(1R,2R)-chxn)(2)](3)[Fe(CN)(6)](2).2H(2)O (2). These chiral systems behave as ferromagnets (T(c) = 13.8 K) with a relatively high coercive field (H(c) = 0.17 T) at 2 K. They also exhibit an unusual magnetic behavior at low temperatures that has been attributed to the dynamics of the magnetic domains in the ordered phase.

StereochemistryCyanideChiral ligandchemistry.chemical_elementCoercivityInorganic ChemistryNickelCrystallographychemistry.chemical_compoundEnantiopure drugFerromagnetismchemistryPhysical and Theoretical ChemistryChirality (chemistry)Bimetallic stripInorganic Chemistry
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Synthesis, crystal structures and electronic properties of imidazoline nitroxide radicals bearing active groups in electropolymerisation

2003

Thiophene-, phenylthiophene-, and indole-based nitronyl nitroxide (NN) and imino nitroxide (IN) radicals have been synthesised and their electrochemical and magnetic properties have been studied. Cyclic voltammetry measurements show that NN radicals (1–3) exhibit a one-electron quasi-reversible oxidation process that results in the formation of the corresponding nitrosonium cations. This behaviour pushes the oxidation potential of the other redox-active moiety to very high values. The oxidation of the thiophene subunit occurs at 2.35 V, whereas the oxidation of the phenylthiophene and indole moieties takes place at 1.65 and 1.39 V, respectively. Oxidation of IN radicals (4–5) is irreversibl…

Nitroxide mediated radical polymerizationChemistryStereochemistryHydrogen bondRadicalGeneral ChemistryCrystal structureTriclinic crystal systemMagnetic susceptibilityCatalysisCrystallographychemistry.chemical_compoundMaterials ChemistryThiopheneMonoclinic crystal systemNew Journal of Chemistry
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