The possibility of obtaining volatile polynuclear heterometallic complexes containing lanthanides and transition metals bound by methoxy-β-diketonates was studied. New compounds were prepared by cocrystallization of monometallic complexes from organic solvents. Ln(tmhd) were used as initial monometallic complexes (Ln = La, Pr, Sm, Gd, Tb, Dy, Lu; tmhd = 2,2,6,6-tetramethylheptane-3,5-dionate) in combination with TML in various ratios (TM = Cu, Co, Ni, Mn; L: L = 1,1,1-trifluoro-5,5-dimethoxypentane-2,4-dionate, L = 1,1,1-trifluoro-5,5-dimethoxy-hexane-2,4-dionate, L = 1,1,1-trifluoro-5-methoxy-5-methylhexane-2,4-dionate). Heterometallic complexes of the composition [(LnLtmhd)TM(tmhd)] were isolated for light lanthanides Ln= La, Pr, Sm, Gd, and L= L or L. By single crystal XRD, it has been established that heterometallic compounds containing La, Pr, Cu, Co, and Ni are isostructural linear coordination polymers of alternating mononuclear transition metal complexes and binuclear heteroleptic lanthanide complexes, connected by donor-acceptor interactions between oxygen atoms of the methoxy groups and transition metal atoms. A comparison of powder XRD patterns has shown that all heterometallic complexes obtained are isostructural. Havier lanthanides Ln = Tb, Dy, Lu did not form heterometallics. Instead, homometallic complexes Ln(L) were identified for Ln = Dy, Lu as well as for Ln = La. The thermal properties of the complexes were investigated by TG-DTA and vacuum sublimation tests. The heterometallic complexes were found to be not volatile and decomposed under heating to produce inorganic composites of TM oxides and Ln fluorides. In contrast, Ln(L) is volatile and may be sublimed in a vacuum. Results of magnetic measurements are discussed for several heterometallic and homometallic complexes.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9736739 | PMC |
http://dx.doi.org/10.3390/molecules27238400 | DOI Listing |
Dalton Trans
December 2024
Department of Inorganic and Analytical Chemistry, Budapest University of Technology and Economics, Műegyetem Rkp. 3, 1111 Budapest, Hungary.
Ligands featuring a 1,1'-bis(donor)ferrocene motif can adopt various binding modes. Among them, the κ binding mode, which involves interaction between the iron center of the ferrocene unit and the transition metal is the most unique. Although various examples highlight the interaction itself, the exact quantification of its strength remains uncertain.
View Article and Find Full Text PDFChem Commun (Camb)
December 2024
EaStCHEM School of Chemistry, The University of Edinburgh, David Brewster Road, Edinburgh, EH9 3FJ, UK.
A survey of the literature and the Cambridge Structural Database reveals thirty nine -butylcalix[8]arene-supported transition (3d, limited to V-Cu) and lanthanide metal complexes ranging in nuclearity from one to eighteen, twenty of which are homometallic and nineteen of which are heterometallic. We provide a review of the coordination chemistry of these complexes, including our own work in the area. We also provide our thoughts and perspectives on the common structural themes observed, identify gaps in knowledge and evaluate how that may inform and direct future synthetic efforts.
View Article and Find Full Text PDFDalton Trans
December 2024
School of Materials Science and Engineering, Huazhong University of Science and Technology, Wuhan 430074, China.
Ag/Cu bimetallic clusters have been widely reported, but synthesis of such clusters simple self-assembly of heterometallic ions in air remains challenging due to the susceptibility of Cu ions to oxidation. In this study, protected by the phenylacetylene auxiliary ligand, we utilized [Cu(CHCN)]PF in conjunction with the (PrSAg) polymer to form Ag(I)-Cu(I) oligomer precursors, serving as the starting point for constructing a new [AgCu(PrS)(DPPM)](PF) cluster (DPPM = bis(diphenylphosphino)methane, Ag11-xCux, = 5-9). When the (PrSAg) precursor was replaced by (BuSAg), another cluster [AgCuS(BuS)(CHCN)](CHOH)(HO)(PF) (Ag21Cu4) was obtained.
View Article and Find Full Text PDFDalton 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 PDFAngew Chem Int Ed Engl
January 2025
Univ Brest, UMR CNRS 6521-, Laboratoire CEMCA, F 29200, Brest, France.
Ligands combining two lateral bis-pyridyl-phosphonated-pyclens were synthesized, using a flexible linear pegylated linker (L2) or a bulkier K22 crown-ether (L3). A functionalized pyridyl-phosphonated-pyclen (L1) was also prepared as a mononuclear analogue. Coordination behavior of lanthanide cations was studied via NMR titration with Lu for L1, and UV/Vis and luminescence spectroscopy with Yb for L2/L3.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!