ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1998 (1998), S. 1291-1295 
    ISSN: 1434-193X
    Keywords: Matrix isolation ; Silicon π systems ; Silacyclopropenylidenes ; Disilacyclobutadienes ; Photochemistry ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Pulsed flash pyrolysis in combination with matrix isolation of three precursor molecules (10, 11, 12) led to the formation of silylsilacyclopropenylidene (1), which was identified by comparison of experimental and calculated (BLYP-6-31G*) IR spectra for both, unlabeled 1 and its perdeuterated isotopomer. Upon irradiation of matrix-isolated silylsilacyclopropenylidene (1) a second C2H4Si2 isomer, namely (silylethynyl)silylene (4) was formed. However, no evidence could be found for the formation of disilatetrahedrane or 1,2- or 1,3-disilacyclobutadiene.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 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
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...