Abstract
With three trans-dicyanideiron(III) precursors K[Fe(L)(CN)2] as building blocks (L = bpb2−, bpmb2−, bpdmb2−; bpb2− = 1,2-bis(pyridine-2-carboxamido)-4,5-enzenate, bpmb2− = 1,2-bis(pyridine-2-carboxamido)-4-methylbenzenate, bpdmb2− = 1,2-bis(pyridine-2-carboxamido)-4,5-dimethylbenzenate) and two chiral copper(II) compounds Cu[(S,S/R,R-dpen)2](ClO4)2 (S,S/R,R-dpen = S,S/R,R-1,2-diphenylethylenediamine) as assembly segments, three pairs of cyanide-bridged enantiomers, {[(S,S/R,R-dpen)2Cu(μ-CN)Fe(bpb)(CN)]ClO4}2 (1,2), {[(S,S/R,R-dpen)2Cu(μ-CN)Fe(bpmb)(CN)]}ClO4 (3,4), and {[(S,S/R,R-dpen)2Cu(μ-CN)Fe(bpdmb)(CN)]}ClO4 (5,6), have been obtained and characterized by elemental analysis, IR spectroscopy, and X-ray structure determination. Single X-ray diffraction analysis shows their similar binuclear structures, in which the cyanide-containing building blocks acting as a monodentate ligand through one of the two cyanide groups are linked to the five-coordinate Cu(II) ion, for which the four amine N complete the additional coordination positions. Investigation of magnetic properties of 1–6 reveals weak ferromagnetic magnetic exchange between the neighboring Fe(III) and Cu(II) ions through the bridging cyanide.
Graphical abstract
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Disclosure statement
No potential conflict of interest was reported by the authors.