2017
DOI: 10.1039/c6dt04895a
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Novel mononuclear and 1D-polymeric derivatives of lanthanides and (η6-benzoic acid)tricarbonylchromium: synthesis, structure and magnetism

Abstract: Novel derivatives of lanthanides and (η6-benzoic acid)tricarbonylchromium were synthesized and characterized; complexes of Tb, Dy, Er and Yb exhibit SMM behavior.

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Cited by 26 publications
(7 citation statements)
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“…15 kOe, a very smooth augmentation to reach of 3.6 µ B (1) and 2.0 µ B (2) at 50 kOe; no hysteresis was observed. These values are similar to those reported for Tm(III) [12,14] and Yb(III) [30,31] systems, and they confirm that there is an important splitting of the ground J manifold by the ligands [32,33]. For the ground state with a pure M J term, the saturation magnetization is given by M S = 1 2 × J × g J .…”
Section: Magnetic Propertiessupporting
confidence: 86%
“…15 kOe, a very smooth augmentation to reach of 3.6 µ B (1) and 2.0 µ B (2) at 50 kOe; no hysteresis was observed. These values are similar to those reported for Tm(III) [12,14] and Yb(III) [30,31] systems, and they confirm that there is an important splitting of the ground J manifold by the ligands [32,33]. For the ground state with a pure M J term, the saturation magnetization is given by M S = 1 2 × J × g J .…”
Section: Magnetic Propertiessupporting
confidence: 86%
“…In terms of an electrostatic model, the following charge distribution was used: for the NCS – anions, the charge was (–1/3):(–1/3):(–1/3) (N/C/S), bpy and phen were considered as neutral moieties, and the partial charges on the coordinated water molecules were 0:0, +1/8:(–1/4), +1/4:(–1/2), +1/2:(–1) (H/O). As shown previously, the partial charges on electroneutral, as a whole, water molecules may lead to a substantial difference in the magnetization‐reversal barriers. The results of calculations are summarized in Tables S11 and S12.…”
Section: Resultssupporting
confidence: 53%
“…Such a difference, in turn, originates from weaker Coulomb interactions between Cd 2+ and both of acac − ligands comparing with similar Ln 3+ − acac − interactions within {Ln (acac) 3 } moieties. This assumption is supported by the fact that for previously studied similar systems with 1Ln(acac) 3 :1RCOOH molar ratio, [ 19 ] no by‐products with other ratios were formed irrespectively of R composition.…”
Section: Resultsmentioning
confidence: 68%
“…Previously, the efficiency of such an approach, that is, of stepwise acac − to RCOO − substitution, has been demonstrated on a variety of heteroleptic Ln 3+ complexes. Mononuclear, [ 19a,b ] dinuclear [ 19c ] and 1D‐polynuclear Ln carboxylate complexes [ 19d ] derived from corresponding tris ‐acetylacetonates were isolated and studied, and the acac − to RCOO − ratio in resulting complexes always corresponded to the stoichometry of the reaction. If it is possible to expand such an approach for complexes of d ‐elements, for example, Cd 2+ , it will obviously rise new opportunities to control structures and, hence, properties of heteroleptic complexes formed by these elements.…”
Section: Resultsmentioning
confidence: 99%