Radical addition reactions of fluorinated species Part 6. Regioselectivity of the Addition of Nucleophilic Radicals to Halogenopropenes and Evidence for a Steric Effect of the Chlorine Substituent.
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F67985858%3A_____%2F97%3A27020278" target="_blank" >RIV/67985858:_____/97:27020278 - isvavai.cz</a>
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Radical addition reactions of fluorinated species Part 6. Regioselectivity of the Addition of Nucleophilic Radicals to Halogenopropenes and Evidence for a Steric Effect of the Chlorine Substituent.
Original language description
Nucleophilic radicals derived from alkanols and cyclic ethers (oxolane, 1,3-dioxolane, 2,2-dimethyl-1,3-dioxolane) were employed to test the regioselectivity of addition to 3-chloro-1,1,2,3,3-pentafluoropropene (1), 1,3-dichloro-1,2,3,3-tetrafluoropropene (2), 1,1,3-trichloro-2,3,3-trifluoropropene (3) and 1,3-dichloro-2,3,3-trifluoropropene (4). The regioselectivity was strongly dependent on the number of chlorine atoms at the terminal position and on the character of the additive. Thus the two chlorine atoms in 3 completely reversed the regioselectivity to an anti-Kharasch mode. The relative reaction rates were dramatically decreased with increasing number of terminal chlorine atoms in olefins. 1-3. The allylic chlorine atom in 1 appeared to mimic alonger perfluoroalkyl chain. Experimental results were compared with the shapes of frontier orbitals and electron densities calculated using PM3 and ab initio (3-12G and 6-311 + G**) methods. The transformations of the adducts to chlorofl
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
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Result continuities
Project
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Continuities
Z - Vyzkumny zamer (s odkazem do CEZ)
Others
Publication year
1997
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Journal of Fluorine Chemistry
ISSN
0022-1139
e-ISSN
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Volume of the periodical
86
Issue of the periodical within the volume
2
Country of publishing house
NL - THE KINGDOM OF THE NETHERLANDS
Number of pages
17
Pages from-to
155-171
UT code for WoS article
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EID of the result in the Scopus database
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