A study of the single-crystal-to-single-crystal transformation induced by temperature variation for the chain polymer Cu(II) complex with nitronyl nitroxide showed that an increase in the hydrostatic pressure of up to ∼0.07 GPa completely changes the intracrystalline displacements of molecules relative to one another. This, in turn, significantly affects the interaction energy of the unpaired electrons of the paramagnetic centers and hence the form of the temperature dependence of the magnetic susceptibility . The cooling of crystals under normal conditions causes a rearrangement of the intrachain exchange clusters {>N-•O-Cu(II)-O•-N<} accompanied by a shortening of the distances between the paramagnetic centers. This changes the character of exchange interactions and generates multistage spin transitions. An increase in the hydrostatic pressure leads to a drastic change in the O···O distances between the nitroxyl fragments of adjacent chains, an increase in the antiferromagnetic exchange between them, and complete suppression of spin transitions.
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http://dx.doi.org/10.1021/acs.inorgchem.9b00815 | DOI Listing |
Nano Lett
January 2025
Materials Science and Technology Division, Oak Ridge National Laboratory, 1 Bethel Valley Rd, Oak Ridge, Tennessee 37831, United States.
Thermally driven transitions between ferromagnetic and paramagnetic phases are characterized by critical behavior with divergent susceptibilities, long-range correlations, and spin dynamics that can span kHz to GHz scales as the material approaches the critical temperature , but it has proven technically challenging to probe the relevant length and time scales with most conventional measurement techniques. In this study, we employ scanning nitrogen-vacancy center based magnetometry and relaxometry to reveal the critical behavior of a high- ferromagnetic oxide near its Curie temperature. Cluster analysis of the measured temperature-dependent nanoscale magnetic textures points to a 3D universality class with a correlation length that diverges near .
View Article and Find Full Text PDFACS Mater Au
January 2025
Department of Chemistry, Clemson University, Clemson, South Carolina 29634, United States.
Lanthanide materials with a 4f electron configuration (S) offer an exciting system for realizing multiple addressable spin states for qubit design. While the S ground state of 4f free ions displays an isotropic character, breaking degeneracy of this ground state and excited states can be achieved through local symmetry of the lanthanide and the choice of ligands. This makes Eu attractive as it mirrors Gd in exhibiting the S ground state, capable of seven spin-allowed transitions.
View Article and Find Full Text PDFFood Chem
December 2024
Department of Food and Bioproduct Sciences, University of Saskatchewan, Saskatoon S7N 5A8, Saskatchewan, Canada. Electronic address:
A soluble fraction of faba bean protein was conjugated with tannic acid via the free-radical grafting method using a mixture of ascorbic acid and hydrogen peroxide. Surface plasmon resonance showed a strong bonding between them, while the free amino and thiol group measurements indicated tannic acid's bonding with the amino groups and cysteine residues on the proteins. Structural analysis using intrinsic fluorescence and surface hydrophobicity demonstrated tannic acid's interaction with the aromatic and hydrophobic amino acids of the protein.
View Article and Find Full Text PDFAdv Sci (Weinh)
January 2025
Faculty of Health Sciences, University of Macau, Macau SAR, 999078, China.
Imaging abnormal copper/iron with effective fluorescent tools is essential to comprehensively put insight into many pathological events. However, conventional coordination-based detection is mired in the fluorescence quenching induced by paramagnetic Cu(II)/Fe(III). Moreover, the strong chelating property of the probe will consume dissociative metal ions and inevitably interfere with the physiological microenvironment.
View Article and Find Full Text PDFPhys Chem Chem Phys
January 2025
Magnetic Resonance Center (CERM), University of Florence, via Luigi Sacconi 6, Sesto Fiorentino, 50019, Italy.
The function of biomolecular systems, including biological macromolecules, often crucially depends on their dynamics. Nuclear magnetic resonance (NMR) is one of the most informative methods used to study biomolecules and their internal mobility, with atomic resolution, in near-physiological conditions. NMR relaxation profiles, obtained from the field dependence of the nuclear relaxation rates, in particular, offer the possibility to probe dynamic processes over a wide range of time scales.
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