Synthesis, structure, thermal behavior, thermodynamic, magnetic and luminescent properties of Pr, Sm, Eu, and Gd cymantrenecarboxylates

• Published in: Polyhedron Vol. 43; no. 1; pp. 36 - 46
• Main Authors: Koroteev, P.S., Dobrokhotova, Zh.V., Kiskin, M.A., Lermontov, A.S., Efimov, N.N., Bogomyakov, A.S., Tyurin, A.V., Bykov, M.A., Demina, L.I., Velikodny, Yu.A., Kozyukhin, S.A., Novotortsev, V.M.
• Format: Journal Article
• Language: English
• Published: Elsevier Ltd 13-08-2012
• Subjects: Cymantrenecarboxylate ligands; Lanthanide–manganese complexes; Magnetic properties; Standard thermodynamic functions; Thermal decomposition; X-ray diffraction study; Standard thermodynamic functions; Cymantrenecarboxylate ligands; Lanthanide–manganese complexes; X-ray diffraction study; Thermal decomposition; Magnetic properties
• ISSN: 0277-5387
• DOI: 10.1016/j.poly.2012.05.030

Four novel 3d–4f heterometallic binuclear carboxylate complexes [Ln2(μ-О,η2-OOCCym)2(μ2-OOCCym)2(η2-ООССym)2(py)4]·2py, where Ln=Pr (1), Sm (2), Eu (3), Gd (4) and Cym=(η5-C5H4)Mn(CO)3, were prepared and characterized by X-ray diffraction. Their magnetic, thermodynamic, spectral and luminescent properties were studied and discussed. Thermal decomposition of the complexes in air affords a mixture of LnMn2O5 and Mn2O3. [Display omitted]
► New binuclear lanthanide cymantrenecarboxylate complexes were synthesized. ► Increased antiferromagnetism in Gd cymantrenecarboxylate with pyridine was found. ► Cymantrenecarboxylate ligands significantly suppress Eu3+ luminescence. ► Standard thermodynamic functions for [Nd2(OOCCym)6(THF)4] were calculated. ► Thermolysis of Ln cymantrenecarboxylates under air affords LnMn2O5 and Mn2O3.
New isostructural lanthanide cymantrenecarboxylates [Ln2(μ-О,η2-OOCCym)2(μ2-OOCCym)2(η2-ООССym)2(py)4]·2py, where Ln=Pr (1), Sm (2), Eu (3), Gd (4) and Cym=(η5-C5H4)Mn(CO)3, were synthesized and characterized by X-ray diffraction. The crystals of 1–4 are built of discrete binuclear molecules; the Ln atoms are nine-coordinate. The phases produced by thermal elimination of pyridine from complexes 3 and 4 are identical to the phases formed by elimination of THF from the THF-containing cymantrenecarboxylates prepared earlier. The magnetic properties of complex 4 indicate an enhancement of antiferromagnetic interactions between Gd3+ ions due to the substitution of THF for pyridine; in the product of ligand elimination from 4, ferromagnetic interactions were found. It was shown that the lanthanide cymantrenecarboxylates are virtually nonvolatile. The thermal decomposition of the complexes was studied by differential scanning calorimetry (DSC) and thermogravimetry (TGA). Thermolysis of 1–4 in air affords mixtures of LnMn2O5 and Mn2O3. For the earlier prepared complex [Nd2(μ2-OOCCym)4(OOCCym)2(THF)4] (5), standard thermodynamic functions were calculated from adiabatic calorimetry data. Cymantrenecarboxylate ligands appreciably suppress Eu3+ luminescence and determine the spectral and the fluorescent properties of the lanthanide cymantrenecarboxylates.