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- W2024892307 endingPage "1917" @default.
- W2024892307 startingPage "1909" @default.
- W2024892307 abstract "We report the synthesis and conformational studies of TTF-containing molecular tweezers based on a 1,2,4,5-tetramethylbenzene scaffold. In the neutral form the tweezers are expected to adopt the closed conformation, while, upon oxidation, the open conformation should be preferred due to electrostatic repulsion between the oxidized TTF moieties. Cyclic voltammetry studies demonstrate electronic pairing with formation of mixed-valence [TTF]2+ species and opening of the tweezers upon the full oxidation of the TTF groups. Variable-temperature (VT) NMR studies evidence tight intramolecular TTF pairing at low temperature. Molecular modeling studies showed clear preference for an open conformation of tweezers in a fully oxidized state." @default.
- W2024892307 created "2016-06-24" @default.
- W2024892307 creator A5018368779 @default.
- W2024892307 creator A5047519398 @default.
- W2024892307 creator A5061684819 @default.
- W2024892307 date "2008-02-01" @default.
- W2024892307 modified "2023-10-15" @default.
- W2024892307 title "Synthesis of electrochemically responsive TTF-based molecular tweezers: evidence of tight intramolecular TTF pairing in solution" @default.
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- W2024892307 doi "https://doi.org/10.1016/j.tet.2007.11.110" @default.
- W2024892307 hasPublicationYear "2008" @default.
- W2024892307 type Work @default.