Nogami, Emiko Yamazaki, Takashi Kubota, Toshio Yajima, Tomoko Stereochemical Investigation of the Products of the Photoinduced Perfluoroalkylation–Dimerization of Anthracene The photoinduced perfluoroalkylation of anthracene has been shown to provide 9,9′,10,10′-tetrahydro-10,10′-diperfluoroalkyl-9,9′-bianthracenes in over 70% yields, each perfluoroalkyl iodide producing three diastereomers. The structures of all three diastereomers (<i>cis</i>,<i>cis</i>, <i>cis</i>,<i>trans</i>, and <i>trans</i>,<i>trans</i> isomers) have been elucidated by both NMR and X-ray crystallographic analyses. Most notably, an X-ray crystallographic analysis has revealed that the <i>trans</i>,<i>trans</i> diastereomer having the two trifluoromethyl groups in 10,10′-positions adopts a 74° twisted relationship of the two dihydroanthracene rings. Furthermore, each of the two <i>trans</i>,<i>trans</i> isomers <b>2a</b>,<b>b</b> has been shown to exist as a mixture of new types of atropisomers and the energy barrier for the interconversion of the two atropisomers has been estimated to be 12 kcal/mol by variable-temperature NMR analysis. ci;energy barrier;perfluoroalkyl iodide;atropisomer;Stereochemical Investigation;dihydroanthracene rings;diastereomer;isomers;NMR;trifluoromethyl groups;tran;AnthraceneThe photoinduced perfluoroalkylation;analysis 2015-09-18
    https://acs.figshare.com/articles/journal_contribution/Stereochemical_Investigation_of_the_Products_of_the_Photoinduced_Perfluoroalkylation_Dimerization_of_Anthracene/2130205
10.1021/acs.joc.5b01655.s004