A series of heterometallic complexes of formula [Mn(III)(2)Ln(III)(3)(bdeaH)(3)(bdea)(2)(piv)(8)] x MeCN, where bdeaH(2) = N-butyldiethanolamine, piv = pivalate, and Ln = Y (1), Tb (2), Dy (3), Ho (4), and Er (5), has been prepared. 1-5 are isostructural, with the metal centers forming a novel semicircular Ln(III)-Mn(III)-Ln(III)-Mn(III)-Ln(III) strand. Only 2 and 3 exhibit slow relaxation of the magnetization, suggesting that the highly anisotropic Ln(III) ions (Tb(III) and Dy(III)) are essential for an energy barrier to spin reversal.
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http://dx.doi.org/10.1021/ic9000686 | DOI Listing |
Dalton Trans
November 2024
Department of Chemistry, University of Patras, 26504 Patras, Greece.
A relatively unexplored approach in heterometallic chemistry of transition metals and lanthanides has been developed toward the controlled synthesis of a new family of linear heterotrinuclear Ln(III)-Pd(II)-Ln(III) complexes with the general formula [LnPd(pao)(NO)(MeOH)(HO)]·[Pd(pao)], where Ln = Dy (2), Gd (3), Er (4) and Yb (5). This strategy was based on the diamagnetic 'metalloligand' [Pd(pao)] (1), where pao is the anion of 2-pyridinealdoxime, containing two dangling oximate O-atoms which were to each other and available for binding with oxophilic lanthanide ions. Because of their -configuration, the [Pd(pao)] 'metalloligand' was able to direct the binding of two {Ln(NO)(MeOH)(HO)} units on opposite sites, thus yielding the reported trinuclear {Ln-Pd-Ln} clusters.
View Article and Find Full Text PDFActa Crystallogr C Struct Chem
December 2024
Laboratoire de Cristallographie-Themodynamique, Faculté de Chimie, USTHB, BP 32 El-Alia Bab Ezzouar, Algiers, 16111, Algeria.
Chem Sci
October 2024
Departament de Química Inorgànica i Orgànica, Universitat de Barcelona Diagonal 645 08028 Barcelona Spain
Developing controlled and reproducible molecular assemblies incorporating lanthanide centers is a crucial step for driving forward up- and down-conversion processes. This challenge calls for the development of strategies to facilitate the efficient segregation of different Ln metal ions into distinct positions within the molecule. The unique family of pure [LnLn'Ln] heterometallic coordination compounds previously developed by us represents an ideal platform for studying the desired Ln-to-Ln' energy transfer (ET).
View Article and Find Full Text PDFInorg Chem
October 2024
Key Laboratory of Polyoxometalate and Reticular Material Chemistry of Ministry of Education, Northeast Normal University, Changchun 130024, China.
Incorporating heterometals into titanium-oxygen clusters represents an effective approach to adjusting the band gap and absorption properties. Herein, a family of heterometallic Ti-Cu clusters was synthesized under solvothermal conditions. The unique structural feature of these clusters is the formation of ring clusters with myo-inositol ligands serving as structure-directing ligands.
View Article and Find Full Text PDFDalton Trans
October 2024
Department of Chemistry, University of Cyprus, 1678 Nicosia, Cyprus.
The combined use of 2-(2-pyridyl)-1,3-propane-diol (pypdH) and 2-hydroxymethyl-2-(2-pyridyl)-1,3-propane-diol (pyptH) in Cu/4f chemistry has afforded a new family of isostructural [CuM(pypt)(pypdH)(NO)] [M = Gd (1), Tb (2), Dy (3), and Y (4)] complexes. These compounds are based on an unprecedented three-layered symmetric [CuM(μ-OR)] structural core, formed from the connection of the metal ions by bridging alkoxide arms of the organic ligands. Direct current magnetic susceptibility studies for complexes 1-3 revealed the presence of dominant ferromagnetic exchange interactions, suggesting the existence of large spin ground state values.
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