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Measuring the Spin-Lattice Relaxation Magnetic Field Dependence of Hyperpolarized [1-13C]pyruvate
Published on: September 13, 2019
Trinuclear rare earth pyridyl-β-diketonate complexes: developing new methods towards finding lost toroidal spin
Patrick Mangundu1, Kate E Tanner1, Andrew Bloomfield2
1School of Natural Sciences - Chemistry, University of Tasmania, Hobart, Tasmania, Australia. rebecca.fuller@utas.edu.au.
Researchers synthesized rare earth triangles to study toroic molecules. Inelastic neutron scattering (INS) experiments provided evidence for toroic properties, offering a new method to validate such complexes.
Area of Science:
- Coordination Chemistry
- Inorganic Chemistry
- Magnetochemistry
Background:
- Rare earth (RE) triangles are investigated for their potential as single molecular toroics (SMTs).
- Understanding low-energy excitations in these molecules is crucial for developing molecular magnetic materials.
Purpose of the Study:
- To synthesize novel RE triangles using β-diketonate ligands.
- To investigate the low-energy excitations and toroic properties of these complexes using inelastic neutron scattering (INS).
Main Methods:
- Synthesis of rare earth triangle complexes using β-diketonate ligands.
- Characterization using X-ray diffraction and conventional magnetometry.
- Inelastic neutron scattering (INS) experiments to probe low-energy excitations.
Main Results:
- Several new RE triangle complexes were synthesized, including examples with varying ancillary ligands.
- Conventional magnetometry did not reveal a non-magnetic SMT ground state.
- INS experiments on complexes 1 and a related SMT showed a broad Lorentzian peak close to the calculated energy gap, suggesting toroic properties.
Conclusions:
- The study presents new RE triangle complexes with potential toroic behavior.
- Inelastic neutron scattering (INS) shows promise as a spectroscopic tool for validating complexes with toroic ground states.
- The findings contribute to the understanding of low-energy excitations in molecular toroics.
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