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  • 1
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Boron Compounds. 6. Synthesis and Molecular Structure of 1,5-Diethyl-2,3-Diphenyl-1,3,5-Triaza-2-Bora-Cyclooctane-4-One: Comparative CompoundsThe title compound is the first example of a medium sized boron heterocycle with a clearly resolved 1H-n.m.r. spectrum. For its interpretation various compounds containing amine, urea and/or diazabora groups have been synthesized and 1H-n.m.r. spectroscopically examined. There are systematic connections between the chemical shifts of methyl and methylene group respectively and their position relative to nitrogen or to boron.
    Notes: Die Titelverbindung ist der erste Borheterocyclus mittlerer Ringgröße mit gut aufgelöstem 1H-NMR-Spektrum. Zur Interpretation wurden zahlreiche Vergleichsverbindungen mit Amin-, Harnstoff- und/oder Diazaboragruppen hergestellt und systematische Zusammenhänge zwischen den chemischen Verschiebungen von Methyl- bzw. Methylenprotonensignalen und ihrer Stellung zum Stickstoff oder zum Bor gefunden.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Boron-Nitrogen Compounds. LXVIII. Nuclear Magnetic Resonance Studies on 1,3,2-Diazaboracyloalkanes and Phenylborane DerivativesThe 1H chemical shift differences Δδ = δ (NCH2) - δ (NCH3) of 1,3-dimethyl1,3,2-diazaboracycloalkanes as well as the corresponding differences of 13C chemical shifts are dependent upon the ring size. No simple correlation exists between δ11B and δ13C of the boron-bonded phenyl carbon atom of phenylborane derivates, although stereochemical factors appear to influence the absolute values of δ13C. 13C Nuclear resonance measurements permit the observation of conformational isomers of bis(methylamino)phenylborane and N-trimethyl-B-triphenylborazine at low temperatures and confirm the pseudoarmatic nature of the 1,3,2-diazaboroline ring system.
    Notes: Die 1H-chemische Verschiebungsdifferenz Δδ = δ (NCH2) - δ (NCH3) von 1,3-Dimethyl-1,3,2-diazaboracyloalkanen ist ebenso von der Ringgröße abhängig wie die entsprechende Differenz der 13C-chemischen Verschiebungen. Zwischen δ11B und δ13C des borgebundenen Phenylkohlenstoffatoms von Phenylboranderivaten besteht keine direkte Beziehung, doch zeigt sich ein stereochemischer Effekt auf die Absolutwerte von δ13C. Mit Hilfe 13C-kernmagnetischer Messungen lassen sich Konformationsisomere von Bis(methylamino)phenylboran und N-Trimethyl-B-triphenyl-borazin bei tiefen Temperaturen nachweisen und auch der pseudoaromatische Charakter von 1,3,2-Diazaborolinen bestätigen.
    Additional Material: 6 Tab.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Boron Compounds. 7. Synthesis and Molecular Structure of 1,5-Diethyl-2,3-Diphenyl-1,3,5-Triaza-2-Bora-Cyclooctane-4-One: The Product of Aminoboronation
    Notes: Die gefundenen systematischen Zusammenhänge zwischen der chemischen Verschiebung von Methyl- bzw. Methylenprotonensignalen und der Stellung dieser Gruppen zum Stickstoff oder zum Bor (vgl. 6. Mitteilung, [1]) erlauben Rückschlüsse auf das Protonenresonanzspektrum der Titelsubstanz. Die Molekülstruktur dieser neuen Verbindungsklasse kann somit als erwiesen angesehen werden.On the basis of the observed systematic connections between the chemical shifts of methyl and methylene groups respectively and their positions relative to nitrogen or boron (cf. 6th publication, [1]) the 1H-n.m.r. spectrum of the title compound can be interpreted. This further evidence for the suggested molecular structure of the aminoboronation products will be given.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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