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Chloride Anion Controlled Molecular “Switching”. Binding of 2,5,7-Trinitro-9-dicyanomethylenefluorene-C60 by Tetrathiafulvalene Calix[4]pyrrole and Photophysical Generation of Two Different Charge-Separated States

Abstract :

The binding of the snake-like trinitrodicyanomethylenefluorene-C60 derivative (TNDCF-C60) to the dynamic receptor, tetrathiafulvalene calix[4]pyrrole (TTF-calix[4]pyrrole), may be controlled via the use of a chloride anion as an external trigger. Whereas, in the absence of a chloride anion, the TNDCF ?tail? of the trinitrodicyanomethylenefluorene-C60 substrate binds to the TTF?calix[4]pyrrole in a 2:1 (substrate/receptor) stoichiometry in CH2Cl2 solution, addition of a chloride anion (yellow) leads the TNDCF tail to be displaced in favor of a bound C60 ?head?, a process that leads to the formation of a complex with overall 1:2:2 substrate/receptor/chloride anion stoichiometry. These chemical switching events are reflected in easy-to-visualize color changes, as well as in the production of two different kinds of charge-separated states following selective femtosecond photoexcitation.

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https://hal.univ-angers.fr/hal-03343369
Contributeur : Okina Université d'Angers <>
Soumis le : mardi 14 septembre 2021 - 10:29:48
Dernière modification le : mercredi 15 septembre 2021 - 03:27:15

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Kent Nielsen, Ginka-H. Sarova, Luis Martín-Gomis, Paul-C. Stein, Lionel Sanguinet, et al.. Chloride Anion Controlled Molecular “Switching”. Binding of 2,5,7-Trinitro-9-dicyanomethylenefluorene-C60 by Tetrathiafulvalene Calix[4]pyrrole and Photophysical Generation of Two Different Charge-Separated States. Journal of the American Chemical Society, American Chemical Society, 2008, 130 (2), pp.460 - 462. ⟨10.1021/ja0772243⟩. ⟨hal-03343369⟩

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