Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/adma.200901614 | DOI Listing |
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 PDFRSC Adv
October 2024
Department of Chemistry, Sultan Qaboos University P. O. Box 36, Al Khod 123 Oman
A monochromatic red emitting nonacoordinate organoeuropium complex with the formula [Eu(hfaa)(Ph-TerPyr)] (Eu-1) incorporating hexafluoroacetylacetone (hfaa) primary ligands and a tridentate 4'-phenyl-2,2':6',2''-terpyridine (Ph-TerPyr) ancillary ligand has been synthesized. The complex was characterized by analytical and spectroscopic methods, and its structure was established by single crystal X-ray diffraction (SC-XRD) analysis at low temperature, which explicitly confirms that the coordination sphere is composed of a EuON core. Under the UV excitation, Eu-1 displayed typical red emission in solution with a long-excited state lifetime ( = 1048.
View Article and Find Full Text PDFChem Asian J
December 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.
The search for new metal-organic compounds as candidates for quantum information processing technologies is in the spotlight. Several metal ions and organic linkers have been used to obtain such compounds. Herein, we describe the synthesis, crystal structures, and cryomagnetic properties of two air-stable isostructural neodymium(III) and europium(III) one-dimensional (1D) coordination polymers of formula [Nd(Hmpa)(DMSO)] (1) and [Eu(Hmpa)(DMSO)] (2) [Hmpa=N-(4-methylphenyl)oxamate, and DMSO=dimethylsulfoxide].
View Article and Find Full Text PDFInorg Chem
September 2024
Department of Fundamental Chemistry, Institute of Chemistry, University of São Paulo, São Paulo 05508-000, Brazil.
Luminescent trivalent lanthanide (Ln) complexes are compounds of technological interest due to their unique photophysical properties, particularly anionic complexes, given their higher stability and emission quantum yields. However, structural studies on the cation-anion interaction in these complexes and the relation of such to luminescence are still lacking. Herein, the cation-anion interactions in two luminescent anionic tetrakis(2-thenoyltrifluoroacetonato)europate(III) complexes with alkylimidazolium cations, specifically 1-ethyl-3-methylimidazolium and 1-butyl-3-methylimidazolium are investigated.
View Article and Find Full Text PDFBiomacromolecules
September 2024
Institute of Polymer Science and Engineering, National Taiwan University, Taipei 10617, Taiwan.
Lanthanide-containing luminescent hydrogels have shown potential for sensing and imaging applications. Nonetheless, integrating lanthanide ions or complexes into the polymer matrix often results in the poor stability and mechanical strength of the hydrogels. This work presents an innovative approach to fabricating luminescent hydrogels with three dynamic cross-links: imine bond, boronate ester bond, and metal-ligand coordination.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!