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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 2000 (2000), S. 1061-1063 
    ISSN: 1434-193X
    Keywords: Photochemistry ; Matrix isolation ; Density functional calculations ; Isomerizations ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---Ultraviolet irradiation of matrix-isolated formamide (1) in solid argon with light of wavelength 248 nm leads to the formation of formimidic acid (2). Comparison of the experimental IR spectrum of the photoproduct with the calculated IR spectrum of 2 shows clearly that two rotamers 2a and 2b are formed.Supporting information for this article is available on the WWW under //http://www.wiley-vch.de/contents/jc_2046/2000/99501_s.pdf or from the author.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1998 (1998), S. 1285-1290 
    ISSN: 1434-193X
    Keywords: Matrix isolation ; Silicon π systems ; Silacyclopropenylidenes ; Photochemistry ; Density functional calculations ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Flash pyrolysis of 1,1-diethynyl-2,2,2-trimethyldisilane (16) and triethynylsilane (18) led to the formation of two silylenes of the elemental composition C4H2Si, namely diethynylsilylene (10) and ethynylsilacyclopropenylidene (7), which were isolated in an argon matrix at 10 K. Both compounds could be photoconverted into another isomer, butadiynylsilylene (9). The identification of these reactive intermediates is based on the comparison between the experimental and calculated IR spectra for the parent compounds as well as for their dideuterated and fully 13C-labeled isotopomers.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0947-3440
    Keywords: Matrix isolation ; Photochemistry ; CHNO isomers ; Hydrogen-bonded complexes ; Density functional calculations ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The complex photochemistry of matrix-isolated dihaloformoximes 8a, 8b, and 8c, which are transformed upon irradiation into the new hydrogen-bonded complexes HalCN…HOHal 10a-c′, identified by their IR spectra, has been unveiled. An earlier assignment of the experimental IR absorptions to isofulminic acid HONC (4) must be withdrawn. A competitive reaction to the formation of complexes 10a-c′ produces the hydrogen-bonded complexes HalNCO/HHal 12a-c′, which can be regarded as intermediates on the photochemical pathway to the final product isocyanic acid HNCO (1), and are tentatively identified by their IR absorptions. Our findings are supported by deuteration experiments and theoretical calculations using the density functional method BLYP/6-311G*.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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