The cationic complexes of Mn(III) with the 5-Hal-sal323 (Hal = Cl, Br) ligands and a paramagnetic doubly charged counterion [ReCl] have been synthesized: [Mn(5-Cl-sal323)][ReCl] () and [Mn(5-Br-sal323)][ReCl] (). Their crystal structures and magnetic properties have been studied. These isostructural two-component ionic compounds show a thermally induced spin transition at high temperature associated with the cationic subsystem and a field-induced slow magnetic relaxation of magnetization at cryogenic temperature, associated with the anionic subsystem.
View Article and Find Full Text PDFThree tetraphenylborates of mononuclear Mn(III) cation complexes with hexadentate ligands, the products of the reaction between a N,N'-bis(3-aminopropyl)ethylenediamine and salicylaldehydes with the different haloid substitutions at the 5 or 3,5 positions, have been synthesized: [Mn(5-F-sal-N-1,5,8,12)]BPh (1), [Mn(3,5-diCl-sal-N-1,5,8,12)]BPh (2) and [Mn(3,5-Br,Cl-sal-N-1,5,8,12)]BPh (3). Their crystal structure, dielectric constant (ϵ) and magnetic properties have been studied. Ligand substituents have a dramatic effect on the structure and magnetic properties of the complexes.
View Article and Find Full Text PDFWe present herein the synthesis, crystal structure, and electric and magnetic properties of the spin-crossover salt [Mn(5-Cl-sal-N-1,5,8,12)]TCNQ ⋅2 CH CN (I), where 5-Cl-sal-N-1,5,8,12=N,N'-bis(3-(2-oxy-5-chlorobenzylideneamino)propyl)-ethylenediamine, containing distinct conductive and magnetic blocks along with acetonitrile solvent molecules. The Mn complex with a Schiff-base ligand, [Mn(5-Cl-sal-N-1,5,8,12)] , acts as the magnetic unit, and the π-electron acceptor 7,7,8,8-tetracyanoquinodimethane (TCNQ ) is the conducting unit. The title compound (I) exhibits semiconducting behavior with room temperature conductivity σ ≈1×10 ohm cm and activation energy Δ ≈0.
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