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Tailored homo- and hetero- lanthanide porphyrin dimers: a synthetic strategy for integrating multiple spintronic functionalities into a single molecule.


ABSTRACT: We present the design, synthesis and magnetic properties of molecular magnetic systems that contain all elements necessary for spin-valve control in molecular spintronic devices in a single molecule. We investigate the static and dynamic magnetic properties and quantum spin properties of butadiyne-linked homo- and hetero-nuclear lanthanide-porphyrin dimers. A heterometallated porphyrin dimer containing both TbIII and DyIII centres is created rationally by the stepwise oxidative homocoupling of distinct lanthanide-porphyrin monomers. TbIII and DyIII mononuclear porphyrin complexes, homodimers and heterodimers all exhibit slow magnetic relaxation below 10 kelvin under a static magnetic field. The coherence times for GdIII porphyrin monomers and dimers are found to be in excess of 3.0 ?s at 2 K, allowing distinct magnetic manipulations in low temperature transport experiments.

SUBMITTER: Le Roy JJ 

PROVIDER: S-EPMC6256854 | biostudies-literature | 2018 Dec

REPOSITORIES: biostudies-literature

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Tailored homo- and hetero- lanthanide porphyrin dimers: a synthetic strategy for integrating multiple spintronic functionalities into a single molecule.

Le Roy Jennifer J JJ   Cremers Jonathan J   Thomlinson Isabel A IA   Slota Michael M   Myers William K WK   Horton Peter H PH   Coles Simon J SJ   Anderson Harry L HL   Bogani Lapo L  

Chemical science 20181019 45


We present the design, synthesis and magnetic properties of molecular magnetic systems that contain all elements necessary for spin-valve control in molecular spintronic devices in a single molecule. We investigate the static and dynamic magnetic properties and quantum spin properties of butadiyne-linked homo- and hetero-nuclear lanthanide-porphyrin dimers. A heterometallated porphyrin dimer containing both Tb<sup>III</sup> and Dy<sup>III</sup> centres is created rationally by the stepwise oxida  ...[more]

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