Library

Language
Preferred search index
Number of Hits per Page
Default Sort Criterion
Default Sort Ordering
Size of Search History
Default Email Address
Default Export Format
Default Export Encoding
Facet list arrangement
Maximum number of values per filter
Auto Completion
Feed Format
Maximum Number of Items per Feed
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
    New York, NY [u.a.] : Wiley-Blackwell
    Heteroatom Chemistry 1 (1990), S. 167-173 
    ISSN: 1042-7163
    Keywords: Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: When Cl2NCF2CF2NCl2 is heated with CF2=CFX (X = Cl, F) ClXCFCF2N(Cl)CF2CF2N(Cl)CF2CXClF (X = Cl, 2; F, 3) is formed. Mercury extracts chlorine fluoride from 2 and 3 to form new polyfluorobisazomethines, ClXCFCF2N=CFCF=NCF2CXClF (X = Cl, 4; F, 5). Photolysis of the product obtained from CCl2=NCCl2CCl2N=CCl2 with ClF, CF2ClN(Cl)CF ClCFClN(Cl)CF2Cl (6) gives another bisazomethine, CF2ClN=CFCF=NCF2Cl (7) with concomitant loss of Cl2. At 25°C, in the presence of CsF, 4 and 5 are cyclized to give (X = Cl, 8; F, 9), and 7 forms a bicyclic derivative at 100°C, (1). Addition of chlorine fluoride to 8 and to 1 produces (10) and (14), respectively. Photolysis of 10 results in the loss of CFCl3 to form (11), and 14 loses Cl2 and dimerizes to the hydrazine (15). The further addition of ClF to 11 gives rise to (12) which when photolyzed at 3000 Å forms a second cyclic hydrazine, (13).
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...