The luminescence properties of two types of heterotrimetallic aluminum-lanthanide-sodium 12-metallacrown-4 compounds are presented here, LnNa(ben)[12-MC-4] (LnAl4Na) and {LnNa[12-MC-4]}(iph) (Ln2Al8Na2), where Ln = Gd, Tb, Er, and Yb, MC is metallacrown, ben is benzoate, shi is salicylhydroximate, and iph is isophthalate. The aluminum-lanthanide-sodium metallacrowns formed with benzoate are discrete monomers while, upon replacement of the benzoate with the dicarboxylate isophthalate, two individual metallacrowns can be joined to form a dimer. In the solid state, the terbium version of each structure type displays emission in the visible region, and the erbium and ytterbium complexes emit in the near-infrared. The luminescence lifetimes () and quantum yields have been collected under ligand excitation (LLn) for both LnAl4Na monomers and Ln2Al8Na2 dimers. Several of these values tend to be shorter (luminescence lifetimes) and smaller (quantum yields) than the corresponding values recorded for the structurally similar gallium-lanthanide monomer and dimer 12-MC-4 molecules. However, the quantum yield value recorded for the visible emitting Tb2Al8Na2 dimer, 43.9%, is the highest value observed in the solid state to date for a Tb based metallacrown.
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http://dx.doi.org/10.1039/d1dt04277g | DOI Listing |
Dalton Trans
April 2022
Centre de Biophysique Moléculaire, CNRS UPR 4301, 45071 Orléans Cedex 2, France.
The luminescence properties of two types of heterotrimetallic aluminum-lanthanide-sodium 12-metallacrown-4 compounds are presented here, LnNa(ben)[12-MC-4] (LnAl4Na) and {LnNa[12-MC-4]}(iph) (Ln2Al8Na2), where Ln = Gd, Tb, Er, and Yb, MC is metallacrown, ben is benzoate, shi is salicylhydroximate, and iph is isophthalate. The aluminum-lanthanide-sodium metallacrowns formed with benzoate are discrete monomers while, upon replacement of the benzoate with the dicarboxylate isophthalate, two individual metallacrowns can be joined to form a dimer. In the solid state, the terbium version of each structure type displays emission in the visible region, and the erbium and ytterbium complexes emit in the near-infrared.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
November 2020
Department of Chemistry and Biochemistry, Shippensburg University, 1871 Old Main Dr., Shippensburg, PA 17257, USA.
The synthesis and crystal structure of the title compound [systematic name: di-μ-acetato-tetra-kis-(μ-,2-dioxido-benzene-1-carboximidato)hexa-methano-ltetra-manganese(III)nickel(II) methanol disolvate monohydrate], [MnNi(CHNO)(CHO)(CHO)]·2CHO·HO or Ni(OAc)[12-MC-4](CHOH)·2CHOH·HO, where MC is metallacrown, OAc is acetate, and shi is salicyl-hydroximate, are reported. The macrocyclic metallacrown is positioned on an inversion center located on the Ni ion that resides in the central MC cavity. The macrocycle consists of an Mn-N-O repeat unit that recurs four times to generate an overall square-shaped mol-ecule.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
August 2020
Department of Chemistry and Biochemistry, Shippensburg University, Shippensburg, PA 17257, USA.
The syntheses and crystal structures for the compounds tetra-μ-aqua--tetra-kis-{2-[aza-nid-yl-ene(oxido)meth-yl]phenolato}tetra-kis-(μ-3-hy-droxy-benzoato)dys-pro-s-ium(III)-tetra-manganese(III)sodium(I) ,-di-methyl-acetamide deca-solvate, [DyMnNa(CHO)(CHNO)(HO)]·10CHNO or [DyNa(4-OHben){12-MC-4}(HO)]·10DMA, , and tetra-μ-aqua--tetra-kis-{2-[aza-nid-yl-ene(oxido)meth-yl]phenolato}tetra-kis-(μ-3-hy-droxy-benzoato)dys-pros-ium(III)tetra-manganese(III)sodium(I) ,-di-methylformamide tetra-solvate, [DyMnNa(CHO)(CHNO)(HO)]·4CHNO or [DyNa(3-OHben){12-MC-4}(HO)]·4DMF, , and where MC is metallacrown, shi is salicyl-hydroximate, 3-OHben is 3-hy-droxy-benzoate, DMA is ,-di-methyl-acetamide, 4-OHben is 4-hy-droxy-benzoate, and DMF is ,-di-methyl-formamide, are reported. For both and , the macrocyclic metallacrown consists of an [Mn-N-O] ring repeat unit, and the domed metallacrown captures two ions in the central cavity: a Dy ion on the convex side of the metallacrown and an Na ion the concave side. The Mn ions are six-coordinate with an elongated tetra-gonally distorted octa-hedral geometry.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
May 2020
Department of Chemistry and Biochemistry, Shippensburg University, Shippensburg, PA 17257, USA.
The title compound, [Mn(CHNO)(HO)][Cu(CHNO)]·CHNO or -[Mn(HO)(DMF)]{Cu[12-MC-4]}·DMF, where MC is metallacrown, shi is salicyl-hydroximate, and DMF is ,-di-methyl-formamide, crystallizes in the monoclinic space group 2/ Two crystallographically independent metallacrown anions are present in the structure, and both anions exhibit minor main mol-ecule disorder by an approximate (non-crystallographic) 180° rotation with occupancy ratios of 0.9010 (9) to 0.0990 (9) for one anion and 0.
View Article and Find Full Text PDFDalton Trans
November 2019
Institute of Inorganic and Analytical Chemistry, Johannes Gutenberg University Mainz, Duesbergweg 10-14, D-55128 Mainz, Germany.
The reaction of Dy(OCMe)·xHO and Ga(NO)·xHO led to the isolation of (BuN)[GaDy(OH)(shi)] (1). The compound possesses a unique chemical structure enclosing the central magnetic Dy ion between diamagnetic Ga-based metallacrown 12-MC-4 ligands. The double-decker complex exhibits field-induced single-molecule magnet (SMM) behaviour with an effective energy barrier (U) of 39 K (27.
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