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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

  • DOI - Digital Object Identifier

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

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    CC - Organic chemistry

  • OECD FORD branch

Result continuities

  • Project

  • 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

  • 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

  • EID of the result in the Scopus database