Аннотация: Magnetochiral dichroism (MΧD) originates in the coupling of local electric fields and magnetic moments in systems where a simultaneous break of space parity and time-reversal symmetries occurs. This magnetoelectric coupling, displayed by chiral magnetic materials, can be exploited to manipulate the magnetic moment of molecular materials at the single molecule level. We demonstrate herein the first experimental observation of X-ray magnetochiral dichroism in enantiopure chiral trigonal single crystals of a chiral mononuclear paramagnetic lanthanide coordination complex, namely, holmium oxydiacetate, at the Ho L3-edge. The observed magnetochiral effect is opposite for the two enantiomers and is rationalised on the basis of a multipolar expansion of the matter–radiation interaction. These results demonstrate that 4f–5d hybridization in chiral lanthanoid coordination complexes is at the origin of magnetochiral dichroism, an effect that could be exploited for addressing of their magnetic moment at the single molecule level.
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Держатели документа:
Univ Copenhagen, Dept Chem, Univ Pk 5, DK-2100 Copenhagen, Denmark.
ESRF European Synchrotron, CS 40220, F-38043 Grenoble 9, France.
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Akademgorodok 50,Bld 38, Krasnoyarsk 660036, Russia.
Univ Penn, Dept Chem, 231 South 34th St, Philadelphia, PA 19014 USA.
Доп.точки доступа:
Mitcov, D.; Platunov, M. S.; Платунов, Михаил Сергеевич; Buch, C. D.; Reinholdt, A.; Dossing, A. R.; Wilhelm, F.; Rogalev, A.; Piligkos, S.; VILLUM FONDEN [13376]; Carlsberg FoundationCarlsberg Foundation [CF18-0613]; Independent Research Fund Denmark [9036-00015B]; Russian Science FoundationRussian Science Foundation (RSF) [19-72-00002]