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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 110 (1977), S. 1086-1094 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Nuclear Magnetic Resonance Studies on Boron Compounds, XII. 1H-, 11B-, 13C-, and 14N-Nuclear Magnetic Resonance Studies on Alkinylboranesπ-Back bonding of the CC-triple bond to boron accounts for δ11 B and δ13C of alkinylboranes (1 - 20, tables 1, 2). δs14 N-data support this interpretation. The diamagnetic anisotropy of the CC-triple bond is responsible for an additional high field shift of δ11B compared with those of alkenylboranes. - The magnitude and sign of the coupling constant 1J(13C11 B) in (C2H5)2 N - B-(C≡CH)2 has been determinded by means of double resonance measurements 1H{11B}. δ1 H of the ethinylic protons depends on anisotropic and mesomeric effects.
    Notes: δ11 B- und δ13C-Werte von Alkinylboranen (1-20, Tab. 1, 2) legen eine π-Rückbindung der CC-Dreifachbindung zum Bor-Atom nahe. δ14 N-Daten stützen diese Interpretation. δ11 B ist infolge des Anisotropieeffektes der benachbarten Dreifachbindung stärker hochfeldverschoben als in Alkenylboranen. - Größe und Vorzeichen der Kopplungskonstante 1J (13C11B) in (C2H5)2N - B(C≡CH)2 wurden mit Hilfe von Doppelresonanzmessungen 1H{11B} bestimmt. δ1 H der Ethinylprotonen wird vom Anisotropieeffekt und vom mesomeren Effekt kontrolliert.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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