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Hard magnets with high coercivity, such as Nd2Fe14B and SmCo5 alloys, can maintain magnetisation under a high reverse external magnetic field and have therefore become irreplaceable parts in many practical applications. Molecular magnets are promising alternatives, owing to their precise and designable chemical structures, tuneable functionalities and controllable synthetic methods. Here, we demonstrate that an unusually large coercive field can be achieved in a single-chain magnet. Systematic characterisations, including magnetic susceptibility, heat capacity and neutron diffraction measurements, show that the observed giant coercive field originates from the spin dynamics along the one-dimensional chain of the compound because of the strong exchange coupling between Co(II) centres and radicals.
Our all electron (DFBG) calculations show differences between relativistic and non-relativistic calculations for the structure of the isomers of Og(CO)6
A combinatorial model of molecular conformational space that was previously developped (J. Gabarro-Arpa, Comp. Biol. and Chem. 27, (2003) 153-159), had the drawback that structures could not be properly embedded beacause it lacked explicit rotational
The longitudinal magnetic susceptibility of single crystals of the molecular magnet Mn$_{12}$-acetate obeys a Curie-Weiss law, indicating a transition to a ferromagnetic phase due to dipolar interactions. With increasing magnetic field applied transv
The resolution of any spectroscopic or interferometric experiment is ultimately limited by the total time a particle is interrogated. We here demonstrate the first molecular fountain, a development which permits hitherto unattainably long interrogati
We report characterization and magnetic studies of mixtures of micrometer-size ribbons of Mn$_{12}$ acetate and micrometer-size particles of YBaCuO superconductor. Extremely narrow zero-field spin-tunneling resonance has been observed in the mixtures