We describe an S(4)-symmetric {Fe(12)} spin cluster [Fe(12)O(4)(OH)(2)(L)(4)(OAc)(8)][Cl](2) {H(4)L = (HOCH(2)CH(2))(2)NCH(2)CH(2)N(CH(2)CH(2)OH)(2)} where the iron(III) centres describe a squashed hexagonal antiprism. The clusters pack into a large cubic cell with circular cavities, lined by weak C-H···O interactions, and a unit cell volume of over 60,000 Å(3) containing large solvent accessible voids. The core of the cluster is stable in solution, as confirmed by electrospray mass spectrometry. The cluster possesses a non-trivial, frustrated S = 0 ground state, due to the presence of multiple competing antiferromagnetic interactions. The finite temperature Lanczos method has been employed to calculate the temperature dependent magnetic properties of an analogous dodecanuclear S(i) = 3/2 model spin system, in order to reduce the very large Hilbert space. Three archetypal models with two independent exchange coupling parameters have been employed that render a low temperature feature possible, as seen in the χ vs. T plot for the {Fe(12)} spin cluster.
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http://dx.doi.org/10.1039/c1dt10910c | DOI Listing |
Natl Sci Rev
April 2024
Jiangsu Collaborative Innovation Center of Biomedical Functional Materials and Jiangsu Key Laboratory of New Power Batteries, School of Chemistry and Materials Science, Nanjing Normal University, Nanjing 210023, China.
Iron-metal clusters are crucial in a variety of critical biological and material systems, including metalloenzymes, catalysts, and magnetic storage devices. However, a synthetic high-nuclear iron cluster has been absent due to the extreme difficulty in stabilizing species with direct iron-iron bonding. In this work, we have synthesized, crystallized, and characterized a (Tp*)WS(Fe@Fe) cluster (Tp* = tris(3,5-dimethyl-1-pyrazolyl)borate(1-)), which features a rare trideca-nuclear, icosahedral [Fe@Fe] cluster core with direct multicenter iron-iron bonding between the interstitial iron (Fe) and peripheral irons (Fe), as well as Fe···Fe ferromagnetic coupling.
View Article and Find Full Text PDFMaterials (Basel)
August 2021
Institute of Physics, Martin-Luther University Halle-Wittenberg, 06120 Halle, Germany.
We have explored the impact of elevated growth and annealing temperatures on the local interfacial structure of thin Fe(12 nm)/Pt(10 nm) spintronic bilayers, epitaxially grown on MgO (100), and their correlation to magnetization reversal and dynamics. Electron-beam evaporation growth and subsequent annealing at 450 °C causes significant roughening of the MgO/Fe interface with irregular steps and multilevel (100) MgO surface terraces. Consequently, threading dislocations emerging at the step edges propagated in the Fe layer and terminated at the Fe/Pt interface, which appears pitted with pits 1.
View Article and Find Full Text PDFInorg Chem
December 2020
Department of Chemistry, University of Florida, Gainesville, Florida 32611-7200, United States.
A program has been initiated to develop Fe/oxo cluster chemistry with the "pseudocarboxylate" ligand dimethylarsinate (MeAsO) for comparison with the well investigated Fe/oxo/carboxylate cluster area. The synthesis and characterization of three polynuclear Fe complexes are reported, [FeO(OCBu)(OAsMe)(HO)]Cl (), Na[FeNaO(OAsMe)(NO)(MeAsOH)(HO)](NO) (), and [Fe(OAsMe)(MeAsOH)(hqn)](NO) (), where hqnH is 8-hydroxyquinoline. The Fe core of is a type never previously encountered in Fe carboxylate chemistry, consisting of two Fe units each of which comprises two {Fe(μ-O)} units bridged by three MeAsO groups and linked into an Fe loop structure by two η:η:μ MeAsO groups, a bridging mode extremely rare with carboxylates.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
November 2018
Division of Chemistry and Biological Chemistry, School of Physical & Mathematical Sciences, Nanyang Technological University, 21 Nanyang Link, Singapore, 637371, Singapore.
To probe the possibility that carbodicarbenes (CDCs) are redox active ligands, all four members of the redox series [Fe(1) ] (n=2-5) were synthesized, where 1 is a neutral tridentate CDC. Through a combination of spectroscopy and DFT calculations, the electronic structure of the pentacation is shown to be [Fe (1 ) ] (S= ). That of [Fe(1) ] is more ambiguous, but it has significant contributions from the open-shell singlet [Fe (1)(1 )] (S=0).
View Article and Find Full Text PDFInorg Chem
July 2018
Institute of Applied Physics, Academiei 5, MD2028 Chisinau , Moldova.
Trinuclear μ-oxo-centered iron(III) isobutyrate clusters readily react with polyalcohol organic ligands under one-pot synthesis conditions. Depending on the ligand, solvent, and temperature, a range of hexa-, dodeca-, and doicosanuclear iron(III) oxo-hydroxo condensation products, isolated as (mdeaH)[FeO(thme)Cl]·0.5(MeCN)·0.
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