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Sulfate donor based supramolecular coordination complexes [{ fac-Re(CO)}(μ-SO)(L ){ fac-Re(CO)}] (1-3) were obtained using ditopic N donors (L ; n = 1-3), NaHSO, and Re(CO) in a one-pot, multicomponent, coordination-driven self-assembly approach, in which SO becomes oxidized to SO during the reaction and acts as a building framework. Complexes 1-3 were characterized using IR, ESI-TOF-MS, and H NMR spectroscopy. The structures of complexes 1-3 were confirmed using single-crystal X-ray diffraction analysis. The transformation of the dinuclear heteroleptic triple-stranded helicate to the dinuclear homoleptic double-stranded mesocate [{Re(CO)Cl}(L )] (L = L, L, L; 4a-6a) was achieved by the addition of BaCl. The direct treatment of Re(CO)X (X = Cl, Br) with L/L/L yielded the dinuclear homoleptic double-stranded helicates [{Re(CO)X} (L )] (4b-6b and 7-9).
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http://dx.doi.org/10.1021/acs.inorgchem.8b01343 | DOI Listing |
Dalton Trans
July 2025
Eduard-Zintl-Institut für Anorganische und Physikalische Chemie, Technische Universität Darmstadt, Peter-Grünberg-Str. 12, 64287 Darmstadt, Germany.
The co-condensation of atomic metal vapors of iron, nickel and cobalt with toluene, followed by a direct reaction with isonitriles, between -30 °C and -78 °C, yields stable homoleptic metal isonitrile complexes. Complexes of Fe, Ni, and Co with DippNC (Dipp = 2,6-(CH(CH))CH) and 4-fluorophenylisonitrile (4-FPI) are obtained in high yields using this method. This method offers an efficient and straightforward approach compared to previously reported syntheses.
View Article and Find Full Text PDFACS Omega
June 2025
Department of Chemistry, Hiroshima University, Higashi-Hiroshima, Hiroshima 739-8526, Japan.
A series of dinuclear iridium pentahydride complexes bearing chiral BINAP ligands were synthesized and characterized. The complexes can be synthesized in good yields through the hydrogenation of mononuclear precursors obtained from the reaction of [Ir-(cod)]-BF with -BINAP and -BINAP. New heteroleptic dinuclear iridium complexes containing -BINAP and -BINAP at each iridium center could be synthesized using the proposed protocol in addition to the corresponding homoleptic dinuclear complexes.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
Institut für Anorganische Chemie, Freie Universität Berlin, Fabeckstraße 34-36, D-14195 Berlin, Germany.
Herein, we report the solvent-dependent reactivity of Fe(CO) toward AsF in either anhydrous HF or liquid SO. The reaction of Fe(CO) with the superacid HF/AsF leads to the protonation of the iron center and allows for the first-time structural characterization of [FeH(CO)] in the solid state, representing one of the most acidic transition metal hydride complexes to ever be isolated and structurally characterized. In the aprotic but oxidation-stable solvent SO, Fe(CO) is oxidized and dimerized to [Fe(CO)], which is isoelectronic with well-known Mn(CO).
View Article and Find Full Text PDFDalton Trans
November 2024
School of Chemistry, University of Leicester, University Road, Leicester, LE1 7RH, UK.
A diprotic bis(β-thioketoimine) ligand precursor featuring a flexible 4,4'-methylbis(aniline) linker, H2, was synthesised treatment of the corresponding bis(β-ketoimine) with Lawesson's reagent. Lithiation of H2 and coordination with one equivalent of d-block metal(II) chlorides MCl(THF) (M = Fe, Co and Zn) yielded a corresponding series of homoleptic dinuclear complexes, [M(μ-2)]. X-ray diffraction analysis reveals a tetrahedral geometry for the two metals and a double-stranded helicate structure arising from inter-strand face-face π-stacking.
View Article and Find Full Text PDFChem Commun (Camb)
October 2024
Institute of Inorganic Chemistry, RWTH Aachen University, Landoltweg 1, 52056 Aachen, Germany.