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      Single-molecule magnet engineering: building-block approaches

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          Abstract

          This Feature article focuses on the use of building-blocks to direct structure and properties of complexes exhibiting single-molecule magnet behavior.

          Abstract

          Tailoring the specific magnetic properties of any material relies on the topological control of the constituent metal ion building blocks. Although this general approach does not seem to be easily applied to traditional inorganic bulk magnets, coordination chemistry offers a unique tool to delicately tune, for instance, the properties of molecules that behave as “magnets”, the so-called single-molecule magnets (SMMs). Although many interesting SMMs have been prepared by a more or less serendipitous approach, the assembly of predesigned, isolatable molecular entities into higher nuclearity complexes constitutes an elegant and fascinating strategy. This Feature article focuses on the use of building blocks or modules (both terms being used indiscriminately) to direct the structure, and therefore also the magnetic properties, of metal ion complexes exhibiting SMM behaviour.

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          Most cited references273

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          Molecular spintronics using single-molecule magnets.

          A revolution in electronics is in view, with the contemporary evolution of the two novel disciplines of spintronics and molecular electronics. A fundamental link between these two fields can be established using molecular magnetic materials and, in particular, single-molecule magnets. Here, we review the first progress in the resulting field, molecular spintronics, which will enable the manipulation of spin and charges in electronic devices containing one or more molecules. We discuss the advantages over more conventional materials, and the potential applications in information storage and processing. We also outline current challenges in the field, and propose convenient schemes to overcome them.
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            Lanthanide double-decker complexes functioning as magnets at the single-molecular level.

            Double-decker phthalocyanine complexes with Tb3+ or Dy3+ showed slow magnetization relaxation as a single-molecular property. The temperature ranges in which the behavior was observed were far higher than that of the transition-metal-cluster single-molecule magnets (SMMs). The significant temperature rise results from a mechanism in the relaxation process different from that in the transition-metal-cluster SMMs. The effective energy barrier for reversal of the magnetic moment is determined by the ligand field around a lanthanide ion, which gives the lowest degenerate substate a large |Jz| value and large energy separations from the rest of the substates in the ground-state multiplets.
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              Macroscopic quantum tunnelling of magnetization in a single crystal of nanomagnets

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                Author and article information

                Journal
                CHCOFS
                Chem. Commun.
                Chem. Commun.
                Royal Society of Chemistry (RSC)
                1359-7345
                1364-548X
                2014
                2014
                : 50
                : 34
                : 4396-4415
                Affiliations
                [1 ]CNRS
                [2 ]CRPP
                [3 ]UPR 8641
                [4 ]F-33600 Pessac, France
                [5 ]Univ. Bordeaux
                [6 ]Department of Chemistry
                [7 ]University of Copenhagen
                [8 ]Denmark
                Article
                10.1039/C4CC00339J
                1b2a8f70-3618-4388-888d-1d6a37942116
                © 2014
                History

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