2014
DOI: 10.1039/c4cc07580c
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The solvent effect in an axially symmetric FeIII4 single-molecule magnet

Abstract: A pair of enantiopure Fe(III)4 SMMs with axial symmetry was synthesized and characterized by magnetization and high-frequency electron paramagnetic resonance methods. The results reveal that the axial symmetry of the structure is broken by the interaction of Fe(III)4 with the disordered solvent molecules.

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Cited by 21 publications
(7 citation statements)
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“…The relative abundance of these conformations can be calculated by assuming statistical distribution based on occupancy factors, so that only a fraction (31%) of the molecules are strictly tetragonal (Table ). This symmetry-lowering may have important consequences in determining the magnetic behavior at low temperature (vide infra). …”
Section: Resultsmentioning
confidence: 99%
“…The relative abundance of these conformations can be calculated by assuming statistical distribution based on occupancy factors, so that only a fraction (31%) of the molecules are strictly tetragonal (Table ). This symmetry-lowering may have important consequences in determining the magnetic behavior at low temperature (vide infra). …”
Section: Resultsmentioning
confidence: 99%
“…All reactions were carried out under aerobic condition. The synthesis procedure of the Schiff base ligands was described in our previous paper. , …”
Section: Methodsmentioning
confidence: 99%
“…Homoleptic tetrairon(III) propellers have formula [Fe 4 L 6 ], where H 2 L is a polydentate ligand containing a chelating pocket for the peripheral ions and an alkoxido or phenoxido bridging group . They normally crystallize as 1:1 mixtures of Λ and Δ propeller isomers (but see ref .…”
Section: Chemistry Of Fe4 and Related Complexesmentioning
confidence: 99%
“…They normally crystallize as 1:1 mixtures of Λ and Δ propeller isomers (but see ref . for an interesting case of spontaneous resolution) and their isolation in enantiopure form requires homochiral H 2 L ligands . Very recently a structurally similar mixed‐valence derivative was reported, with a central Fe 3+ ion linked to three peripheral Fe 2+ centers via phenoxido bridges …”
Section: Chemistry Of Fe4 and Related Complexesmentioning
confidence: 99%