4 research outputs found

    Bimetallic Fe–Ir and Trimetallic Fe–Ir–Au Carbonyl Clusters Containing Hydride and/or Phosphine Ligands: Syntheses, Structures and DFT Studies

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    The reaction of [HFe4(CO)12(IrCOD)]2− (1) with CO at ambient conditions afforded [HFe4Ir(CO)14]2− (2), that, in turn, reacted with HBF4·Et2O affording [Fe4Ir(CO)15]− (3). 1 reacted with a slight excess of PPh3 resulting in a mixture of [HFe2Ir2(CO)10(PPh3)2]− (ca. 37%) (5) and [H2Fe3Ir(CO)10(PPh3)2]− (ca. 63%) (6). 5 and 6 co-crystallized as their [NEt4][H1+xFe2+xIr2-x(CO)10(PPh3)2]·CH2Cl2 (x = 0.63) salt. The reaction of 1 with Au(PPh3)Cl afforded [Fe3Ir(CO)12(AuPPh3)]2− (7). The related hydride [HFe3Ir(CO)12]2− (9) was prepared from the reaction of [HFe4(CO)12]3− (8) with [Ir(COE)2Cl]2 (COE = cyclo-octene). For sake of comparison, [HFe3Co(CO)12]2− (10) was obtained from 8 and Co2(CO)8. All the new clusters have been fully characterized via IR, 1H,13C{1H} and 31P{1H} NMR spectroscopies and their structures determined by means of single crystal X-ray crystallography. Possible isomers have been investigated by DFT calculations

    Bimetallic Fe–Au Carbonyl Clusters Derived from Collman’s Reagent: Synthesis, Structure and DFT Analysis of Fe(CO)4(AuNHC)2 and [Au3Fe2(CO)8(NHC)2]−

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    The reaction of the Collman's reagent Na2Fe(CO)(4) with two equivalents of Au(NHC)Cl (NHC = IMes, IPr, IBu) in thf results in the bimetallic Fe(CO)(4)(AuNHC)(2) (NHC = IMes, 2; IPr, 3; IBu, 4; IMes = C3N2H2(C6H2Me3)(2); IPr = C3N2H2(C6H (3) (i) Pr-2)(2); IBu = C3N2H2(CMe3)(2)) clusters in good yields. Heating 2 in dmf at 100 A degrees C results in the higher nuclearity cluster [Au3Fe2(CO)(8)(IMes)(2)](-) (5). 2-5 have been fully characterized via IR, H-1 and C-13 NMR spectroscopies and their structures determined by means of single crystal X-ray crystallography. Gas-phase DFT calculations were carried out on 2-5 and the model compound cis-Fe(CO)(4)(AuIDM)(2) (6) (IDM = C3N2H2Me2), in order to better understand the metal-metal and metal-ligand interactions in these compounds without the influence of packing forces

    The Rise of Near-Infrared Emitters: Organic Dyes, Porphyrinoids, and Transition Metal Complexes

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