For a wide range of trivalent lanthanide ion coordination complexes of tricapped trigonal prism or monocapped square antiprism configurations, the bonds between the central lanthanide ions and the capping ligands are found to violate Badger's rule: they can get weaker as they get shorter. We demonstrate that this observation originates from the screening and repulsion effect of the prism ligands. Both effects enhance as the electric field of the central ion or the softness of the prism ligands increases. Thus, for heavier lanthanides, despite the fact that the capping bond could be shorter, it is more efficient to be weakened by the prism ligands, being inherently labile. This concept of "labile capping bonds phenomenon" is then successfully used to interpret many problems in lanthanide(III) hydration, e.g., why the water exchange rate of a lanthanide(III) complex is much higher in a twisted square antiprism than in square antiprism configuration. Thus, the theory proposed in this paper offers new insights in understanding chemical problems.
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Dalton Trans
December 2024
Dipartimento Scienze Chimiche, Università degli Studi di Catania, and INSTM UdR Catania, Viale Andrea Doria 6, 95125 Catania, Italy.
This work reports the engineering and functional properties of an emerging class of heterobimetallic 3d-4f ionic complexes designed with cobalt and rare-earth (RE) metals. We present a comprehensive examination of the structural, magnetic, optical, and thermal properties of the heterobimetallic ionic complexes with the general formula [Co(hfa)][RE(hfa)tetraglyme] (RE = Dy, Eu, and Y), where the metal centres are coordinated by hexafluoroacetylacetonate (Hhfa = 1,1,1,5,5,5-hexafluoro-2,4-pentanedione), β-diketone and tetraglyme (2,5,8,11,14-pentaoxapentadecane) polyether. Structural analysis reveals an octahedral coordination geometry enveloping the cobalt(II) centre, characterized by inherent symmetry properties consistent across the derivatives, while a capped square-antiprism coordination polyhedron is observed for the RE ions.
View Article and Find Full Text PDFPhys Chem Chem Phys
October 2024
State Key Laboratory for Mineral Deposits Research, School of Earth Science and Engineering, Nanjing University, Nanjing 210023, China.
Ion adsorption-type deposits (IADs) are the dominant sources of rare earth elements (REEs), in which REEs are mainly enriched in clay minerals. However, the adsorption mechanism of REEs in the interlayer region of clay minerals is still poorly understood. In this study, by using molecular dynamics (MD) simulations, we explored the interlayer structures and dynamics of REEs-intercalated montmorillonite.
View Article and Find Full Text PDFDalton Trans
October 2024
State Key Laboratory of High-Efficiency Utilization of Coal and Green Chemical Engineering, College of Chemistry and Chemical Engineering, Ningxia University, Yinchuan 750021, China.
Based on a β-diketonate ligand, a mononuclear Dy(III) complex, [Dy(dmpd)(bpy)] (1) (dmpd = 4,4-dimethyl-1-phenylpentane-1,3-dione, bpy = 2,2'-dipyridyl), of [DyNO] type has been synthesized with a capping nitrogen-containing coligand. Then, a dual capping coligand 2,2'-bipyrimidine (bmp) is introduced to be a bridge to link two β-diketonate-Dy(III) motifs, leading to a new dinuclear Dy(III) complex, [Dy(dmpd)(bmp)] (2). Dy(III) centers in both complexes feature an NO octacoordinated environment with an approximate square-antiprism geometry ().
View Article and Find Full Text PDFActa Crystallogr C Struct Chem
October 2024
College of Chemistry and Materials Science, Anhui Normal University, Wuhu, Anhui 241000, People's Republic of China.
A new three-dimensional (3D) coordination polymer, namely, poly[diaqua[μ-2,2'-(1,3,5,7-tetraoxo-1,2,3,5,6,7-hexahydropyrrolo[3,4-f]isoindole-2,6-diyl)diacetato]barium(II)], [Ba(CHNO)(HO)], (I), has been synthesized by the microwave-irradiated reaction of Ba(NO) with N,N'-bis(glycinyl)pyromellitic diimide {BGPD, namely, 2,2'-(1,3,5,7-tetraoxo-1,2,3,5,6,7-hexahydropyrrolo[3,4-f]isoindole-2,6-diyl)diacetatic acid, HL}. The title compound was structurally characterized by single-crystal X-ray diffraction analysis and powder X-ray diffraction analysis, as well as IR spectroscopy. In the crystal structure of (I), the Ba ion is nine-coordinated by six carboxylate O atoms from five symmetry-related L dianions and one imide O atom, as well as two water O atoms.
View Article and Find Full Text PDFDalton Trans
September 2024
Departamento de Química, Instituto de Ciências Exatas, Universidade Federal de Minas Gerais, Av. Antônio Carlos 6627, Pampulha, Belo Horizonte, Minas Gerais, 31270-901, Brazil.
Developing and investigating advanced multifunctional materials with magnetic properties as candidates for assembling spin qubits for quantum computing is imperative. A new polytopic ligand based on oxamate and aniline was used to promote the synthesis of three neutral homometallic lanthanide-coordinated polymers. New complexes with the formula {Ln(phox)(DMSO)(HO)}, where Ln = Eu (1), Gd (2), and Tb (3) [phox = -(phenyl)oxamate and DMSO = dimethylsulfoxide], were synthesized and well characterized by spectroscopic methods as well as X-ray crystallographic analysis.
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