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Cycloheptatrienyl trianion: an elusive bridge in the search of exchange coupled dinuclear organolanthanide single-molecule magnets.

ABSTRACT: The preparation of η-cyclopentadienyl (η⁵-C₅R₅), η-arene (η⁶-C₆R₆), and η-cyclooctatetraenyl (η⁸-C₈R₈) bridging motifs are common in organometallic chemistry; however, the synthetic preparation of η-cycloheptatrienyl (η⁷-C₇R₇) bridging motifs has remained a synthetic challenge in 4f chemistry. To this end, we have developed a synthetic route towards a series of rare dinuclear organolanthanide inverse sandwich complexes containing the elusive η⁷-C₇H₇ bridge. Herein, we present the structures and magnetic properties of the lanthanide inverse sandwich complexes [KLn₂(C₇H₇)(N(SiMe₃)₂)₄] (Ln = Gd^III (1), Dy^III (2), Er^III (3)) and [K(THF)₂Er₂(C₇H₇)(N(SiMe₃)₂)₄] (4). These compounds are the first single-molecule magnets (SMMs) to feature this type of bridging motif. Furthermore, η⁷-C₇H₇ was found to efficiently promote ferromagnetic exchange interactions between metal ions. Variable temperature dc magnetic susceptibility measurements and subsequent simulations give significant exchange constants of J = +1.384, +1.798, and +3.149 cm^-1 and dipolar constants of J = -0.603, -0.601, and -0.475 cm^-1 for compounds 2-4, respectively. Frequency dependent ac susceptibility measurements under an applied static field resulted in the observation of dual relaxation processes, and brought forth a greater understanding of the intermolecularly driven process at high frequency. In particular, this type of analysis of compound 3 under 800 Oe elicited an energy barrier of U_eff = 58 K. Ab initio calculations were performed in order to understand the nature of magnetic coupling and the origin of slow relaxation of magnetisation. Through these studies, the effect of the amido ancillary ligands on the magnetic axiality of the lanthanide ions was found to be competitive with the crystal field of the η⁷-C₇H₇ π-electron cloud. Our findings suggest that the tunability of the dipolar and exchange components of the magnetic interactions lie within the dihedral angle imposed by the amido ligands, thus offering potential for the development of new exchange coupled lanthanide systems.

SUBMITTER: Harriman KLM

PROVIDER: S-EPMC5355948 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Project description:The syntheses and properties of four magnetically-supramolecular oligomers of triangular Mn3 units are reported: dimeric [Mn6O2(O2CMe)8(CH3OH)2(pdpd)2] (3) and [Mn6O2(O2CMe)8(py)2(pdpd)2](ClO4)2 (4), and tetrameric [Mn12O4(O2CR)12(pdpd)6](ClO4)4 (R = Me (5), t Bu (6)). They were all obtained employing 3-phenyl-1,5-di(pyridin-2-yl)pentane-1,5-dione dioxime (pdpdH2), either in direct synthesis reactions involving oxidation of MnII salts or in metathesis reactions with the preformed complex [Mn3O(O2CMe)6(py)3](ClO4) (1); complex 6 was then obtained by carboxylate substitution on complex 5. Complexes 3 and 4 contain two [MnIII2MnII(μ3-O)]6+ and [MnIII3(μ3-O)]7+ units, respectively, linked by two pdpd2- groups. Complexes 5 and 6 contain four [MnIII3(μ3-O)]7+ units linked by six pdpd2- groups into a rectangular tetramer [MnIII3]4. Solid-state dc magnetic susceptibility studies showed that the Mn3 subunits in 3 and 4 have a ground-state spin of S = 3/2 and S = 2, respectively, while the Mn3 subunits in 5 and 6 possess an S = 6 ground state. Complexes 5 and 6 exhibit frequency-dependent out-of-phase (χ''M) ac susceptibility signals indicating 5 and 6 to be tetramers of Mn3 single-molecule magnets (SMMs). High-frequency EPR studies of a microcrystalline powder sample of 5·2CH2Cl2 provided precise spin Hamiltonian parameters of D = -0.33 cm-1, |E| = 0.03 cm-1, B04 = -8.0 × 10-5 cm-1, and g = 2.0. Magnetization vs. dc field sweeps on a single crystal of 5·xCH2Cl2 gave hysteresis loops below 1 K that exhibit exchange-biased quantum tunneling of magnetization (QTM) steps with a bias field of 0.19 T. Simulation of the loops determined that each Mn3 unit is exchange-coupled to the two neighbors linked to it by the pdpd2- linkers, with an antiferromagnetic inter-Mn3 exchange interaction of J/kB = -0.011 K (Ĥ = -2Jŝi ·ŝj convention). The work demonstrates a rational approach to synthesizing magnetically-supramolecular aggregates of SMMs as potential multi-qubit systems for quantum computing.

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Cycloheptatrienyl trianion: an elusive bridge in the search of exchange coupled dinuclear organolanthanide single-molecule magnets.

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