Lenka Krešáková , Miroslava Litecká , Itziar Oyarzabal , Róbert Tarasenko , Hryhorii Titikov , Martin Orendáč , Juraj Černák
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引用次数: 0
Abstract
Single crystals of Ce(III) complex {[Ce2(oPDA)3(H2O)2]·2H2O}n (1) with O-donor ligand H2oPDA (o-phenylenediacetic acid) were formed under solvothermal conditions. The crystal structure of 1 is one-dimensional and formed by chains of the Ce(III) ions linked via oPDA2− dianions acting as pentadentate ligands with bridging and chelating functions. The Ce(III) central atom in 1 is nonacoordinated by eight oxygen atoms from four different oPDA2− ligands and one oxygen atom of the aqua ligand yielding O8O donor set. The investigation of the static susceptibility and magnetization suggested Δ/kB = 317 K energy difference between the ground and the first excited doublet. Field induced slow magnetic relaxation was revealed in the investigation of alternating susceptibility. The alternation of the relaxation time with temperature confirmed the coexistence of quantum tunneling and Raman relaxation processes with anomalous coefficients for Raman relaxation.
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