Reaction of the PNNP ligand system ,'-bis[(2-diphenylphosphino)phenyl]formamidinate (dpfam) featuring different coordination compartments with [AuCl(tht)], [CuMes], [AgMes], or [AuCF(tht)] (tht = tetrahydrothiophene) resulted in tetranuclear homo- and heterometallic coinage metal complexes, as well as a hexanuclear gold complex. All of them feature a metal string conformation. Photophysical investigation revealed a significant dependence of the photoluminescence properties on the metal composition. Below 100 K, the PL efficiency of three compounds approaches nearly 100%.
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http://dx.doi.org/10.1039/d1cc06034a | DOI Listing |
Inorg Chem
March 2024
Department of Chemistry, Southern University of Science and Technology (SUSTech), Shenzhen 518055, China.
Treatment of Co(OTf)·6HO, Li[(pzTp)Fe(CN)], and HPMoO·HO in protic solvents afforded two structurally related Fe-Co cyanometallate complexes: [{(pzTp)Fe(CN)}Co(MeOH)][PMoO]·HO·11MeOH (, pzTp = tetra(pyrazolyl)borate) and {[(pzTp)Fe(CN)]Co(MeOH)(HO)}[HPMoO]·3 MeOH·6.5HO (). Complex consists of a cyanide-bridged hexanuclear [FeCo] cage, characterized by the fused conjunction of two mutually perpendicular trigonal bipyramids (TBPs, [FeCo] and [CoFe]), while complex showcases an intricate cyanide-bridged Fe-Co tape comprising a central chain backbone of vertex-sharing [FeCo] TBPs alongside peripheral [FeCo] squares.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
June 2022
Institut für Anorganische Chemie und Strukturchemie, Lehrstuhl II: Material-, und Strukturforschung, Heinrich-Heine-Universität Düsseldorf, D-40225, Düsseldorf, Germany.
The reaction of ytterbium metal with ammonium tri-fluoro-acetate in liquid ammonia resulted in a green substance comprising a substantial amount of ytterbium(II) tri-fluoro-acetate that is a useful precursor for the oxidative synthesis of the new ytterbium(III) compound, [(NH) (HO) ][YbF(OCCF)(HO)]·4HO ( = 1/4), in aqueous tri-fluoro-acetic acid. This mixed ammonium/oxonium crystalline solid is the first example of a substance containing an -hexa-nuclear ytterbium(III) complex with μ-face-capping fluorido ligands. The main structural features of its [YbF] core are non-bonding Yb⋯Yb distances and Yb-F bond lengths of 3.
View Article and Find Full Text PDFActa Crystallogr C Struct Chem
September 2022
School of Chemistry and Chemical Engineering, Shaanxi Key Laboratory of Chemical Reaction Engineering, Laboratory of New Energy and New Function Materials, Yan'an University, Yan'an 716000, People's Republic of China.
The employment of the new Schiff base ligand 2-[(4-chloro-2-hydroxybenzylideneamino)methyl]phenol (HL) bearing ON donors for the preparation of a novel Co cluster is reported. The hexanuclear cobalt complex, namely, di-μ-acetatotetrakis{μ-2-[(4-chloro-2-oxidobenzylideneamino)methyl]phenolato}tetra-μ-methanolato-tetracobalt(II)dicobalt(III), [CoCo(CHClNO)(CHCOO)(CHO)], was obtained using Co(CHCOO)·4HO and HL as starting materials in MeOH under solvothermal conditions. The six metal ions are linked together by the μ-O atoms of four deprotonated MeOH molecules, two CHCOO units and six phenolate O atoms of four L ligands to form a defect disk-shaped topology.
View Article and Find Full Text PDFChem Commun (Camb)
December 2021
Institute of Inorganic Chemistry, Karlsruhe Institute of Technology (KIT), Engesserstr. 15, Karlsruhe 76131, Germany.
Reaction of the PNNP ligand system ,'-bis[(2-diphenylphosphino)phenyl]formamidinate (dpfam) featuring different coordination compartments with [AuCl(tht)], [CuMes], [AgMes], or [AuCF(tht)] (tht = tetrahydrothiophene) resulted in tetranuclear homo- and heterometallic coinage metal complexes, as well as a hexanuclear gold complex. All of them feature a metal string conformation. Photophysical investigation revealed a significant dependence of the photoluminescence properties on the metal composition.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
July 2021
Département de Chimie, Faculté des Sciences et Techniques, Université Cheik Anta Diop, Dakar, Senegal.
The title mol-ecular structure, namely, di-aqua-tris-(μ-1,3-bis-{[1-(2-oxidophen-yl)ethyl-idene]amino}-propan-2-olato)-μ-hydroxido-dinitrato-hexa-copper(II) ethanol tris-olvate, [Cu(CHNO)(NO)(OH)(HO)]·3CHOH, corres-ponds to a non-symmetric hexa-nuclear copper complex. The complex exhibits one core in which three Cu metal centres are mutually inter-connected, two by two, three phenolato oxygen anions acting in a μ-mode. These three copper cations are inter-connected in a μ-mode by one hydroxyl group.
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