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  • 1
    ISSN: 1572-8862
    Keywords: Cyclopentadiene ; ruthenium ; three-component condensation ; vinylidene
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract The reactions between Ru5(μ 5-C2PPh2)(gm-PPh2(CO)13 (1) and cyclopentadienes afforded the hexanuclear clusters Ru6(μ 6-C)(μ 3-PPh2)2(CO)10(η-C5 R 5) [R 5 = H5 (2), H4Me (3), Me5 (4)] which contain an encapsulated carbide and a face-cappingμ 3-CH group, formed by cleavage of CC and CP bonds of the C2PPh2 moiety in1. In the reaction with cyclopentadiene, the unusual ligand C13H12O, formed by combination of C2, CO and two molecules of C5H6 (or one molecule of dicyclopentadien), was characterized in the complex Ru5(μ 4-PPh) (μ 4-C13H12O)(μ-PPh2(CO)11(η-C5H5) (5). In the reaction with pentamethylcyclopentadiene, the vinylidene complex Ru5(μ 3-CCHPh)(μ 4-PPh)(μ 4-PPh) (μ-PPh2)(CO)9(η-C5Me5) (6) was also formed.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1572-8862
    Keywords: vinylidene ; ruthenium ; dicarbide ; acetylide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract Addition of aqueous HCl to Ru5(μ 3-C=CH2)(μ-SMe)2(μ-PPh2)2(CO)10 afforded the structurally characterized carbyne complex Ru5(μ 3-SMe)(μ 3-CMe)(μ-Cl)(μ-SMe)(μ-PPh2)2(CO)9, formed by addition of H to the vinylidene ligand; a Cl atom bridges an Ru–Ru bond.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-1111
    Keywords: Calix[4]arene ; polyether ; crystal structure ; alkali metal ion binding
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The ligand 5,11,17,23-tetra-t-butyl-25,27-di(phenylmethoxy)-26,28-di(2-methoxy-ethoxy)calix[4]arene,designed as an analogue of some calixcrown speciesin order to evaluate possible origins of their selectivity in alkali metal ion binding, has been synthesised and structurally characterised by X-ray crystallography. The crystals are monoclinic, P21/n, a = 15.940(6), b = 19.388(5), c = 20.020(5) Å,β = 109.10(2) deg., Z = 4, conventional R on |F| being 0.073 for 3454 independent, ’observed‘ (I 〉 3σ(I)) reflections. 1H-NMR studies in 1:1 CD3CN/CDCl3solvent have shown that the ligand exerts a strong preference for the lighteralkali metal ions (Li+ and Na+) contrary to the binding behaviour of knowncalixcrowns. This may reflect interactions restricted to the lower rim donor atoms without concomitant interaction with the calixarene π-electrons, perhaps because the latter interactions are substituted by those with the benzyl group π-electrons.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 543-545 
    ISSN: 1434-1948
    Keywords: Lanthanoid(II) complexes ; Ytterbium ; Thallium ; η2-Pyrazolate complexes ; Diphenylmercury ; Redox transmetallation ; X-ray crystal structure ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ytterbium metal reacts with thallium(I) 3,5-diphenylpyrazolate, or with diphenylmercury and 3,5-diphenylpyrazole (Ph2pzH) in tetrahydrofuran or 1,2-dimethoxyethane (DME) giving, after appropriate isolation, the first lanthanoid(II) pyrazolate complex, [Yb(Ph2pz)2(DME)2]. The molecular structure reveals eight coordinate ytterbium(II) with two cisoid η2-3,5-diphenylpyrazolate and two chelating 1,2-dimethoxyethane ligands.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 751-761 
    ISSN: 1434-1948
    Keywords: Lanthanide(II) complexes ; Ytterbium ; Europium ; Samarium ; Redox transmetallation ; Thallium ; Diphenylmercury ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The complexes [Yb(bind)2(DME)2], [Yb(MePhpz)2(DME)2], [Yb(azin)2(DME)2], and [Eu(Ph2pz)2(DME)2] (bindH = 4,5-dihydro-2H-benz[g]indazole; MePhpzH = 3-methyl-5-phenylpyrazole; azinH = 7-azaindole; Ph2pzH = 3,5-diphenylpyrazole; DME = 1,2-dimethoxyethane) have been prepared by redox transmetallation between ytterbium or europium metal and the corresponding thallium(I) pyrazolate in tetrahydrofuran (THF) in the presence of mercury metal, followed by work up with DME. The thallium reagents were obtained by treatment of the appropriate pyrazole with thallium(I) ethoxide. Both [Yb(Ph2pz)2(DME)2] and [Sm(Ph2pz)2(DME)2] have been prepared by metathesis from LnI2(THF)2 and K(Ph2pz) in THF, whilst the former has also been obtained by redox transmetallation from [Hg(Ph2pz)2] and ytterbium metal and by reaction of 3,5-diphenylpyrazole with Yb(C6F5)2, and the latter from protolysis of [Sm{N(SiMe3)2}2(THF)2] with Ph2pzH, followed in each case by crystallisation of the crude product from DME. Europium(II) 3,5-di-tert-butylpyrazolate was synthesised by a redox transmetallation/ligand exchange reaction between europium metal chunks, diphenylmercury(II), and 3,5-di-tert-butylpyrazole (tBu2pzH) in the presence of mercury metal in THF, and [Eu(tBu2pz)2(DME)2] was isolated on crystallisation of the crude product from DME. The X-ray crystal structures of [Ln(L)2(DME)2] (Ln =Yb, L = bind or azin; Ln = Eu or Sm, L = Ph2pz; Ln = Eu, L = tBu2pz), each of a different crystallographic form, reveal eight-coordinate lanthanoid complexes with two η2-pyrazolate and two chelating DME ligands, but the structures differ in the relationship (cisoid or transoid) between the pyrazolate ligands. Thus cen-Ln-cen (cen = centre of the N-N bond) angles of 106.7° [Yb(bind)2(DME)2] (3a), 141.4° [Yb(azin)2(DME)2] (3c), 142.2° [Eu(Ph2pz)2(DME)2] (4a), 107.4° [Eu(tBu2pz)2(DME)2] (4b), and 102.1° [Sm(Ph2pz)2(DME)2] (5) are observed.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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