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Elucidation of Dual Magnetic Relaxation Processes in Dinuclear Dysprosium(III) Phthalocyaninato Triple-Decker Single-Molecule Magnets Depending on the Octacoordination Geometry.

Keiichi KatohYu AizawaTakaumi MoritaBrian K BreedloveMasahiro Yamashita
Published in: Chemistry (Weinheim an der Bergstrasse, Germany) (2017)
When applying single-molecule magnets (SMMs) to spintronic devices, control of the quantum tunneling of the magnetization (QTM) as well as a spin-lattice interactions are important. Attempts have been made to use not only coordination geometry but also magnetic interactions between SMMs as an exchange bias. In this manuscript, dinuclear dysprosium(III) (DyIII ) SMMs with the same octacoordination geometry undergo dual magnetic relaxation processes at low temperature. In the dinuclear DyIII phthalocyaninato (Pc2- ) triple-decker type complex [(Pc)Dy(ooPc)Dy(Pc)] (1) (ooPc2- =2,3,9,10,16,17,23,24-octakis(octyloxy)phthalocyaninato) with a square-antiprismatic (SAP) geometry, the ground state is divided by the Zeeman effect, and level intersection occurs when a magnetic field is applied. Due to the ground state properties of 1, since the Zeeman diagram where the levels intersect in an Hdc of 2500 Oe, two kinds of QTM and direct processes occur. However, dinuclear DyIII -Pc systems with C4 geometry, which have a twist angle (ϕ) of less than 45° do not undergo dual magnetic relaxation processes. From magnetic field and temperature dependences, the dual magnetic relaxation processes were clarified.
Keyphrases
  • single molecule
  • molecularly imprinted
  • atomic force microscopy
  • living cells
  • solid phase extraction
  • mass spectrometry