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  • 1
    ISSN: 0009-2940
    Schlagwort(e): Silanes, tetra-1-alkynyl- ; Germanes, tetra-1-alkynyl- ; 1,1-Ethyloboration, intermolecular ; 1,1-Vinyloboration, intramolecular ; Spirosilanes ; Spirogermanes ; Protodeborylation ; Transition metals, η41-complexes of ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Organosubstituted 1,1′-Spirobisiloles and 1,1′-Spirobigermoles by Fourfold Organoboration of Tetra-1-alkynylsilanes and -germanes[1]Si(C≡CR)4 [R=Me (A), R=Ph (B), R=SiMe3 (C)] and Ge(C≡CR)4 [R=Me (D), R=Ph (E)] react with Et3B by twofold intermolecular ethyloboration and twofold intramolecular vinyloboration to form the organo-substituted 5-sila(germa)spiro[4.4]nonatetraenes , R=Me: 1a, R=Ph: 1b; M=Ge, R=Me: 2d, R=Ph: 2e] via the mono-and bisethyloboration compounds 3 or 4 (e.g. 3b, 4c) with different rates: Ge 〉 Si; Me 〉 Ph. For comparison, compounds Sn(C≡CR)4 [R=Me (F), R=Ph (G)] react with Et3B in the absence of a solvent to mixtures of various spirotin compounds (5f, 5g, 6f, 8f, 9g, 10g, 11g) of which only 9g (R=Ph) corresponds to the spirosilanes and -germanes. This is the result of effective competition between intramolecular and intermolecular organoboration in the case of the tetra-1-alkynyltin compounds. The protodeborylation of 1a, b and 2d, e with MeCO2H leads to 12a, b and 13d, e, respectively. 12a isomerises by UV irradiation to allyl isomers 12a′. From 12a with 2 equiv. of maleic anhydride the 1:2 addition compound 14a is obtained, the autaddition of 12a, d leads to 15a, d. Spiro compound 12a reacts with (OC)5Fe or CpCo(C2H4)2 to give the cyclodiastereomeric η41-complexes [(OC)3Fe]2-12a (16a1-a4; X-ray structure analysis of meso- 16a1), (OC)3Fe-12a (17a) and (CpCo)2-12a (18a1-a4). - All products were characterized by multinuclear NMR, including measurements of the coupling constants 1J(13C13C), 2J(29Si29Si), nJ(29Si13C) and nJ(119Sn13C).
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 2221-2226 
    ISSN: 0009-2940
    Schlagwort(e): Silanes, alkynyl[(trimethylstannyl)ethynyl]- ; 1,1-Ethyloboration, intermolecular ; 1,1-Vinyloboration, intramolecular ; Siloles ; Protodeborylation ; Protodestannylation ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The synthesis of alkynyl[(trimethylstannyl)ethynyl]dimethylsilanes 4 [alkynyl R1 - C≡C: R1 = Bu (b), tBu (c), iPent (d), Ph (e), SiMe3 (f)] is reported. The intermolecular 1,1-ethyloboration of 4 with triethylborane takes place selectively at the Sn - C≡ bond to give first the alkenyl(alkynyl)dimethylsilanes 5 and 6. There exists an equilibrium between 5 and 6, and compound 6 has the suitable stereochemistry for the final intramolecular 1,1-vinyloboration to form the 4-(diethylboryl)-2-(trimethylstannyl)siloles 7. Protodeborylation of 7 with water gives the 2-(trimethylstannyl)siloles 8, and protodeborylation and protodestannylation with an excess of acetylacetone affords the siloles 9. Multinuclear NMR (1H-, 11B-, 13C-, 29Si-, and 119Sn-) serves for monitoring the reactions and for the characterization of the products.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    ISSN: 0749-1581
    Schlagwort(e): Determination of coupling signs ; Multinuclear two-dimensional NMR ; Pseudo-triple-resonance experiments ; Solid-state ; 119Sn CP/MAS NMR ; Cyclopentadienyltin(II) compounds ; Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Absolute coupling signs of 1J(119Sn, 13C) (〈O) and 2J(119Sn, 1H) (〈O) in (n5-C5H5)2Sn (1) and 1J(119Sn, 13C) (〈O)2J(119Sn, 13C) (〈O) and 3J(119Sn, 1H) (〉O) in (n5-C5Me5)2Sn (2) were determined using advanced direct and indirect two-dimensional methods. These are based on Ψ-BIRD techniques and z-filtering, leading to pseudotriple-resonance experiments of the type 1H{119Sn(13C)} and 13C{1H(119Sn)}, respectively. A mixed n5-cyclopentadienyltin(II) amide was prepared and characterized by 1H, 13C, 29Si and 119Sn NMR in solution in the presence of its symmetrical redistribution products 1 and [(Me3Si)2N]2Sn. Solid-state 119Sn CP/MAS NMR spectra of 1 shows the presence of two tin sites (in accord with the x-ray analysis) with a 62.2 ppm difference in 119Sn chemical shifts, the mean value being in close agreement with the solution-state δ119Sn value. The symmetries of the shielding tensor for the two tin sites are different and there appears to be a correlation between this property and the ring centroid - Sn - ring centroid angle α. 13C CP/MAS NMR proved insensitive to the structural differences between the two types of molecules of 1 in the unit cell.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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