6533b7dcfe1ef96bd1271f03

RESEARCH PRODUCT

Spin Cross-Over (SCO) Complex Based on Unsymmetrical Functionalized Triazacyclononane Ligand: Structural Characterization and Magnetic Properties

Said YefsahSmail TrikiCarlos J. Gómez-garcíaVéronique PatinecMerzouk HalitMélissa Roger

subject

Crystal structure010402 general chemistryRing (chemistry)01 natural scienceslcsh:Chemistrychemistry.chemical_compoundSpin crossoverPyridineMagnetic propertiesMacrocycle ligands; Iron complex; High spin and Low spin; Spin Cross-Over; Magnetic propertiesMaterials ChemistryMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryIron complex010405 organic chemistryLigand[CHIM.MATE]Chemical Sciences/Material chemistryNuclear magnetic resonance spectroscopy0104 chemical sciencesElectronic Optical and Magnetic MaterialsCrystallographyMonomerchemistrylcsh:QD1-999Chemistry (miscellaneous)Macrocycle ligandsHigh spin and Low spinSpin Cross-Over

description

International audience; The unsymmetrical ligand 1-(2-aminophenyl)-4,7-bis(pyridin-2-ylmethyl)-1,4,7-triazacyclononane (L6) has been prepared and characterized by NMR spectroscopy. The L6 ligand is based on the triazamacrocycle (tacn) ring that is functionalized by two flexible 2-pyridylmethyl and one rigid 2-aminophenyl groups. Reaction of this ligand with Fe(ClO4)2·xH2O led to the complex [Fe(L6)](ClO4)2 (1), which was characterized as the first Fe(II) complex based on the unsymmetrical N-functionalized tacn ligand. The crystal structure revealed a discrete monomeric [FeL6]2+ entity in which the unsymmetrical N-functionalized triazacyclononane molecule (L6) acts as hexadentate ligand. As observed in the few parent examples that are based on the symmetrical N-functionalized tacn ligands, the triazacyclononane ring is facially coordinated and the N-donor atoms of the three functional groups (two pyridine and one aniline groups) are disposed in the same side of the tacn ring, leading to a distorted FeN6 environment. The magnetic studies of 1 revealed the presence of an incomplete spin crossover (SCO) transition above 425 K, whose progress would be prevented by a very exothermic thermal decomposition at ca. 472 K, as shown by thermogravimetric and DSC measurements

10.3390/magnetochemistry5010019http://www.mdpi.com/2312-7481/5/1/19