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Article Dans Une Revue Beilstein Journal of Organic Chemistry Année : 2014

Synthesis and characterization of a new photoinduced switchable β-cyclodextrin dimer

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This paper reports an efficient preparation of bridged bis-β-CD AZO-CDim 1 bearing azobenzene as a linker and exhibiting high solubility in water. The photoisomerization properties were studied by UV–vis and HPLC and supported by ab initio calculations. The cis/trans ratio of AZO-CDim 1 is 7:93 without irradiation and 37:63 after 120 min of irradiation at 365 nm; the reaction is reversible after irradiation at 254 nm. The photoinduced, switchable binding behavior of AZO-CDim 1 was evaluated by ITC, NMR and molecular modeling in the presence of a ditopic adamantyl guest. The results indicate that AZO-CDim 1 can form two different inclusion complexes with an adamantyl dimer depending on its photoinduced isomers. Both cavities of cis-AZO-CDim 1 are complexed simultaneously by two adamantyl units of the guest forming a 1:1 complex while trans-AZO-CDim 1 seems to lead to the formation of supramolecular polymers with an n:n stoichiometry.

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hal-01307688 , version 1 (26-04-2016)

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Florian Hamon, Claire Blaszkiewicz, Marie Buchotte, Estelle Banaszak-Léonard, Hervé Bricout, et al.. Synthesis and characterization of a new photoinduced switchable β-cyclodextrin dimer. Beilstein Journal of Organic Chemistry, 2014, 10, pp.2874-2885. ⟨10.3762/bjoc.10.304⟩. ⟨hal-01307688⟩
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