Sponsor
Portland State University. Department of Chemisty
First Advisor
Gary L. Gard
Date of Publication
6-9-1976
Document Type
Thesis
Degree Name
Master of Science (M.S.) in Chemistry
Department
Chemistry
Language
English
Subjects
Pentafluorosulphur bromide, Chemical reactions
DOI
10.15760/etd.2549
Physical Description
1 online resource, digitized manuscript.
Abstract
Addition reactions of pentafluorosulfur bromide with unsaturated substrates were studied and four new compounds containing the pentafluorosulfur group have been prepared.
The mechanism for these reactions seems to involve a radical addition pathway. In reaction with CH2=CFC1, CF3C≡CH and CH3C≡CH the SF5 radical attacks the carbon atoms carrying the most hydrogens. The reaction with CF2=CHCl is interesting, as by analogy with other fluoroolefins, the SF5 primary attack should occur.at the CHCl group, however, SF5CF2CHC1Br was found as the only product for this reaction. The reaction of SF5Br with CF3C≡CH produced two isomers but with CH3C≡CH only one isomer was forrmed.
Analytical data, infrared, nmr .and mass spectra are presented supporting the proposed structures for these new compounds.
Rights
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Persistent Identifier
http://archives.pdx.edu/ds/psu/16151
Recommended Citation
Wang, Qui-Chee Wendy, "The Addition of SF5Br to Unsaturated Systems" (1976). Dissertations and Theses. Paper 2552.
https://doi.org/10.15760/etd.2549