Inorganic Chemistry, University of Oxford, South Parks Road, Oxford, UK OX1 3QR.
Published: April 2009
AI Article Synopsis
Article Abstract
SQUID magnetometry, normally used to characterise the properties of solids, was used to follow a clock reaction in solution, namely the auto-catalytic oxidation of [Co(II)EDTA]2- by H2O2, in real time and it was shown that, in combination with other methods (e.g., magnetic resonance proton relaxation studies and UV-vis absorption analysis), SQUID magnetometry can be a powerful method in elucidating and interpreting the time-profile of chemical reactions so as long as reactants, intermediates and products have suitably large differences in their respective magnetic susceptibilities.
The study focuses on the magnetic properties of the "cartwheel" heptanuclear cluster [FeO(OCBu)(Me-dea)(HO)], utilizing Mössbauer spectroscopy and sub-Kelvin magnetization measurements to provide insights into its spin frustration.
The Fe Mössbauer spectra at temperatures above 150 K revealed a specific ratio of doublets that corresponded to different iron sites within the cluster, confirming a previously proposed spin ground state structure where spins are aligned differently among the central and peripheral sites.
At sub-Kelvin temperatures, the behavior of the cluster changed, showing spin blocking and single-molecule magnet characteristics, along with a defined anisotropy barrier that allows for quantum tunneling at low temperatures.
Department of Neurosurgery, Laboratory for Clinical Medicine, Sanbo Brain Hospital, Capital Medical University, Beijing 100093, People's Republic of China.
Current commercial magnetoencephalography (MEG) systems detect neuro-magnetic signals using superconducting quantum interference devices (SQUIDs), which require liquid helium as cryogen and have many limitations during operation. In contrast, optically pumped magnetometers (OPMs) technology provides a promising alternative to conventional SQUID-MEG. OPMs can operate at room temperature, offering benefits such as flexible deployment and lower costs.
Herein, we report the synthesis and properties of triptycene-based C- and C-symmetric stable triradicals. SQUID magnetometry showed the propeller-shaped triradicals were both an antiferromagnetic equilateral triangle spin system with small spin-spin interactions J/k~-120 K and -106 K, leading to ca. 4/6 coexistence of the doublet/quartet states in thermal equilibrium at room temperature.
A novel heterometallic trinuclear cluster [CuMn(cpdp)(NO)(Cl)] () has been designed and synthesized by employing a molecular library approach that uses CuCl·2HO and Mn(NO)·4HO as inorganic metal salts and Hcpdp as a multifunctional organic scaffold (Hcpdp = ,'-bis[2-carboxybenzomethyl]-,'-bis[2-pyridylmethyl]-1,3-diaminopropan-2-ol). This heterometallic cluster has emerged as an unusual ferromagnetic material and promising electrocatalyst for hydrogen evolution reaction (HER) in the domain of inorganic and materials chemistry. Crystal structure analysis establishes the structural arrangement of , revealing a butterfly-like topology with an unusual seven-coordinated Mn(II) center.
The synthesis of the 1,3,2-dithiazolyl radical () derived from 3,4-dihydro-2H-1,5-benzodioxepine is described. Crystals of were grown by vacuum sublimation and adopt the orthorhombic space group . DC SQUID magnetometry reveals Curie-Weiss behavior for > 20 K ( = 0.
