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Article Dans Une Revue Helvetica Chimica Acta Année : 2019

Expanding the carbo ‐Benzene Chemical Space for Electron‐Accepting Ability: Trifluorotolyl/Tertiobutyl Substitution Balance

Résumé

With the view to altering the lipophilicity and electron accepting ability of the tetraphenyl-carbo-benzene scaffold, peripheral fluorination of the C18 ring through aromatic linkers was envisaged from the C18Ph6 and o-tBu2C18Ph4 references, by replacement of two Ph substituents with two p-CF3-C6H4 counterparts (FTol). The synthesis relied on a [8+10] macrocyclization involving a common bis(trifluorotolyl)-tetraynedione, followed by reductive aromatization of the resulting [6]pericyclynediols. While p-FTol2C18Ph4 proved to be hardly tractable due to an extremely low solubility, p-FTol2-o-tBu2C18Ph2 could be extensively studied by X-ray crystallography, NMR and UV/Vis spectroscopy, voltammetry, STM imaging of monolayers, and AFM imaging of binary films with P3HT or PC71BM fabricated by spin-coating for organic photovoltaic cells and J−V curve measurement thereof. The electronic and polarity properties are correlated with moderate but consistent electron-withdrawing effects of the CF3 groups, in agreement with the DFT-calculated frontier orbitals and multipole moments. The results provide guidelines for optimization of fluorinated carbo-benzene targets.
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Dates et versions

hal-02330868 , version 1 (24-10-2019)

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Marwa Chammam, Irving Caballero‐quintana, Denisse Barreiro‐argüelles, Olivia Amargós‐reyes, Youssef Aidibi, et al.. Expanding the carbo ‐Benzene Chemical Space for Electron‐Accepting Ability: Trifluorotolyl/Tertiobutyl Substitution Balance. Helvetica Chimica Acta, 2019, 102 (5), pp.e1900049. ⟨10.1002/hlca.201900049⟩. ⟨hal-02330868⟩
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