We investigate a family of dinuclear dysprosium metallocene single-molecule magnets (SMMs) bridged by methyl and halogen groups [Cp' Dy(μ-X)] (Cp'=cyclopentadienyltrimethylsilane anion; 1: X=CH ; 2: X=Cl ; 3: X=Br ; 4: X=I ). For the first time, the magnetic easy axes of dysprosium metallocene SMMs are experimentally determined, confirming that the orientation of them are perpendicular to the equatorial plane which is made up of dysprosium and bridging atoms. The orientation of the magnetic easy axis for 1 deviates from the normal direction (by 10.3°) due to the stronger equatorial interactions between Dy and methyl groups. Moreover, its magnetic axes show a temperature-dependent shifting, which is caused by the competition between exchange interactions and Zeeman interactions. Studies of fluorescence and specific heat as well as ab initio calculations reveal the significant influences of the bridging ligands on their low-lying exchange-based energy levels and, consequently, low-temperature magnetic properties.
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http://dx.doi.org/10.1002/anie.202004537 | DOI Listing |
ACS Omega
December 2024
School of Chemistry, Chemical Engineering and Life Science, Wuhan University of Technology, 122 Luoshi Road, Wuhan 430070, Hubei, P. R. China.
Design and synthesis of high-performance single-molecule magnets (SMMs) have long been a research focus. Inspired by the best dysprosium(III) metallocene SMMs and dysprosium(III) bis(methanediide) SMMs, we assumed dysprosium SMMs, which had electrical neutrality by combining the two types of ligands. As the Dy center is coordinated by one (substituted-)cyclopentadienyl (Cp) ligand and one methanediide ({C(PPhNSiMe)}) ligand on the axial sites, this ideal structure with linear C-Dy-Cp would strengthen the magnetic anisotropy and exhibit excellent SMM properties.
View Article and Find Full Text PDFThe generation of noncovalent intermolecular interactions represents a powerful method to control molecular vibrations and rotations. Combining these with the axial ligand field enforced by the metallocene ligand scaffold provides a dual-pronged approach in controlling the magnetic-relaxation pathways for dysprosium-based single-molecule magnets (SMMs). Here, we present the first implementation of 2,3,4,5-tetraiodopyrrole (TIPH) in its anionic form [TIP] as a ligand in three isostructural rare-earth metal complexes Cp*RE(TIP) (1-RE, RE = Y, Gd, and Dy; Cp* = pentamethylcylopentadienyl), where the TIP ligand binds through the nitrogen and one iodine atom κ(N,I) to the metal centre.
View Article and Find Full Text PDFJ Am Chem Soc
September 2023
Department of Chemistry, School of Life Sciences, University of Sussex, Brighton BN1 9QJ, U.K.
High-yield syntheses of the lanthanide dinitrogen complexes [(CpM)(μ-1,2-N)] (, M = Gd, Tb, Dy; Cp = 1,2,4-CBuH), in which the [N] ligands solely adopt the rare end-on or 1,2-bridging mode, are reported. The bulk of the -butyl substituents and the smaller radii of gadolinium, terbium, and dysprosium preclude formation of the side-on dinitrogen bonding mode on steric grounds. Elongation of the nitrogen-nitrogen bond relative to N is observed in , and their Raman spectra show a major absorption consistent with N═N double bonds.
View Article and Find Full Text PDFDalton Trans
October 2023
Department of Chemistry, Indian Institute of Technology Madras, Chennai, India.
The present work describes the dynamic magnetic properties of the complex [(Cp)DyIII2ClK]·3.5(CH) (1), synthesized by employing a tri-aryl-substituted cyclopentadienyl ligand (Cp), [4,4'-(4-phenylcyclopenta-1,3-diene-1,2-diyl)bis(methylbenzene) = CpH]. Each Dy(III)-metallocene weakly couples KCl, displaying slow relaxation of magnetization below 14.
View Article and Find Full Text PDFInorg Chem
June 2023
Department of Chemistry, School of Life Sciences, University of Sussex, Brighton BN1 9QJ, U.K.
The structure and magnetic properties of the bimetallic borohydride-bridged dysprosocenium compound [{(η-Cp)(η-Cp)Dy}(μ:κ:κ-BH)][B(CF)] ([][B(CF)]) are reported along with the solution-phase dynamics of the isostructural yttrium and lutetium analogues (Cp is 1,2,4-tri(-butyl)cyclopentadienyl, Cp is tetramethyl(-butyl)cyclopentadienyl). The synthesis of [][B(CF)] was accomplished in the 2:1 stoichiometric reactions of [(η-Cp)(η-Cp)Dy(BH)] () with [CPh][B(CF)], with the metallocenes obtained from reactions of the half-sandwich complexes [(η-Cp)M(BH)(THF)] () (M = Y, Dy, Lu) with NaCp. Crystallographic studies show significant lengthening of the M···B distance on moving through the series , , and , with essentially linear {M···B···M} bridges in .
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