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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 118 (1985), S. 2548-2551 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: NMR Investigations on Tricyclo[5.3.0.02,8]decane Systems - Unusual Highfield Shift at Sterically Fixed Cycloheptadiene FragmentsThe NMR spectra of tricyclo[5.3.0.02,8]decane (8) and some of its derivatives were investigated. The tricyclo[5.3.0.02,8]deca-3,5-diene (7), which contains a sterically fixed cycloheptadiene subunit, exhibits an unusual highfield shift of the homoallylic carbon atoms C-1 and C-8 in its 13C NMR spectrum. This is in contrast to an unusual downfield shift in compounds with fixed cyclopentene subunit.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 1851-1859 
    ISSN: 0009-2940
    Keywords: Carbonyl oxides ; Quinone oxides ; Dioxiranes ; Substituent effects ; Matrix isolation ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Triplet 4-oxocyclohexadienylidenes 6, matrix-isolated in Ar/ 2% O2 at 10 K, react with triplet O2 on annealing the matrix. Primary reaction products are quinone oxides 4, which have been characterized by IR and UV/Vis spectrometry. They are very photolabile; long-wavelength irradiation converts them into spiro-dioxiranes 5, which in turn yield lactones 10 upon irradiation with visible light. Experimental data have been obtained for quinone oxides 4a-g; additionally, ground-state properties and UV/Vis absorptions of quinone oxides 4a,b and 4e-1 have been calculated by the MINDO-3/UHF and CNDO/S methods. Since the theoretical and experimental maxima of the π → π* transitions are in good agreement, we conclude that our semiempirical calculations give an adequate picture of quinone oxides 4 which may best be described as dipolar diradicals.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 267-269 
    ISSN: 0009-2940
    Keywords: Betaine dye ; Solvatochromism ; Ylide ; Carbene reaction ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of 3,5-di-tert-butyl-4-oxo-2,5-cyclohexadienylidene (3d) with pyridine affords 2,6-di-tert-butyl-4-(2,4,6-tri-tert-butylpyridinio)phenolate (1d)  -  which is not accessible by the classical route via pyrylium salts  -  in reasonable yield. Carbene 3d is generated by thermal decomposition of the corresponding quinone diazide 2d in cyclohexane. Betaine 1d shows the expected large solvatochromism.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 123 (1990), S. 89-90 
    ISSN: 0009-2940
    Keywords: Dioxasilirane/Silylene oxidation/Matrix isolation ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of difluorosilylene and dichlorosilylene with molecular oxygen in Ar matrices has been investigated. Under the reaction conditions the silylenes proved to be of low thermal reactivity, and irradiation in the UV/VIS was necessary to produce difluorodioxasilirane and dichlorodioxasilirane, respectively. The IR spectra have been assigned by isotopic labelling and by comparison with ab initio calculations.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 2813-2815 
    ISSN: 0009-2940
    Keywords: Silene ; Oxidation ; Molecular oxygen ; Matrix isolation ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal oxidation of 1,1,2-trimethylsilene (1) has been investigated in O2-doped argon matrices. The oxidation proceeds rapidly at temperatures below 40 K, and two principal oxidation products have been identified as dimethylvinylsilyl hydroperoxide (6) and dimethylvinyloxysilanol (7). The mechanism leading to these products is discussed.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 2101-2109 
    ISSN: 0009-2940
    Keywords: Quinone diazides ; Matrix isolation ; Electronic structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of p-benzoquinone diazides were investigated by 13C-NMR and IR spectroscopy as well as by semiempirical and abinitio calculations. In addition, X-ray structure analyses of the parent compound and three derivatives were performed. The electronic structure and effects of substituents can be described in terms of diazoketo and diazonium phenolate resonance structures. While alkyl groups as substituents have only a minor influence on quinone diazides, electron-withdrawing substituents lead to a larger participation of the aromatic diazonium phenolate structure. Benzoannellation, on the other hand, leads to a decrease of the interaction between the keto and diazo functional group and to properties more reminiscent of “ordinary” ketones and diazo compounds.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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