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  • tin  (2)
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  • 1
    ISSN: 1572-8862
    Keywords: Carbonyl ; osmium ; tin ; phosphine ; structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract Pyrolysis a the cluster Os3(µ-H h (CO)10 (SnMe2 H) produced an as yet unidentified purple duster, which upon reaction with PEt2Ph at room temperature, gave essentially a quantitative yield of the cluster Os3(µ-H)3(CO)9(µ3-Sn) Os3(µ-H)(CO)10(PEt2Ph), 4. The X-ray structure of 4 (as the toluene solvate) shows that it consists Or two Os, triangles linked through a µ4-Sn unit, such that one of the Os3 triangle is µ3-bonded to the Sn atom (Os-Sn range 2.689(2)–2.707(2) Å) and the other is bonded via a single covalent bond (Os-Sn = 2.643(2) Å). The phosphine ligand occupies the equatorial site on a second osmium atom a be latter Os3 moiety that is syn to the Sn atom; the unique bridging hydride ligarid is believed to occupy a site that Acis to both the P and Sn atoms. Crystallographic data for compound4. 0.5C7H8: space group,P $$\bar 1$$ ; ca= 11862(4) Å,b = 12.940(4) Å,c = 16.513(5) Å, α=68.96(3),β=80.60(3)°,γ=62.49(2).R=0.029, 4118 observed reflections.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1572-8862
    Keywords: Carbonyl ; osmium ; tin ; lead ; structure
    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 complexes [(OC)4Os(PbMe2)]2 (3) and [(OC)4OsSnBu 2 ′ ]2 (4) have been prepared from be reaction of Na2[Os(CO)4] with Me2PbCl2 and Bu 2 ′ SnCl2, respectively, in THF and their X-ray crystal structures determined. The red derivative,3, was light-sensitive in solution. The reactions or [(OC)4 Os(SnMe2)]2 (2), or its decarbonylated derivative [Os3(CO)7(SnMe2)2]2 (7), with olefins or phosphorus donor ligands have also been investigated, and the structures of two derivatives, viz. [Os2(CO)7(SnMe2)2(C2H4)] (5a) and [Os2(CO)7(SnMe2)2(PMe3)] (6a), have been determined; the noncarbonyl ligand occupies an equatorial site in each case. The X-ray crystal structures of all these compounds, like those of [(OC)4Os(EMe2)]2 (E=Ge (1), Sn (2)) which have been reported previously, show leaning of the axial carbonyl ligands toward the metal tetracycle, i.e., an “umbrella” effect. Crystallographic data for compound3: space group, P21/a;a=13.4404(13) Å,b=10.7494(14) A,c=148967(18) A,β=98.204(9)°,R=0.035, 1983 observed reflections. For compound4: space group,P1;a=9.016(1) Å,b=9.370(1),c=11.334(1) A, α=103.67(1)°,β=100.30(1)°, γ=115.03(1)°, R=0.046, 2026 observed reflections. For compound5a: space group,P1;a=9.2933(11)Å,b=9.7181(3),c=12.2508(15) A, α=89.21(1)°,β=87.61(1)°, γ=86.13(1)°,R=0.038, 2770 observed reflections. For compound6a space groupP1:a=8.7244(9)Å,b=10.9318(6),c=13.2560(13) A, α=87.815(6)°,β=83.655(8)°, γ=82.343(6)°, R=0.030, 3497 observed reflections.
    Type of Medium: Electronic Resource
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