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   <ref-type name="Journal Article">17</ref-type>
   <contributors>
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     <author></author>
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    </authors>
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   <titles>
    <title></title>
   </titles>
   <dates>
    <year>2022</year>
    <pub-dates>
     <date>2022-01-21</date>
    </pub-dates>
   </dates>
   <doi>10.1016/j.molstruc.2021.132326</doi>
   <abstract>According to the NMR 1Н, 13С and X-ray analysis data molecules of 5,5-bis(bromomethyl)-2-trichloromethyl-1,3-dioxane in the crystalline phase and in solution have a chair conformation with an equatorial trichloromethyl group. The route of conformational transformations for isolated molecule and for a cluster with five chloroform molecules, as well as a transition states and barriers to the internal rotation of the axial and equatorial trichloromethyl group have been established using DFT approximation PBE/3ξ. © 2022 Elsevier B.V.</abstract>
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     <url>https://repo.bashgmu.ru/publication/2162</url>
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     <url>https://repo.bashgmu.ru/files/2337</url>
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