106319-02-2Relevant articles and documents
Synthesis of glycoluril-tetrathiafulvalene molecular clips for electron-deficient neutral guests through a straightforward Diels-Alder strategy
Hardouin-Lerouge, Marie,Cotelle, Yoann,Legoupy, Stphanie,Hudhomme, Pitrick
, p. 5341 - 5348 (2014)
An electroactive molecular clip incorporating tetrathiafulvalene (TTF) sidewalls grafted on a glycoluril platform has been synthesized using a straightforward Diels-Alder strategy. This way of attachment to the glycoluril U-shape scaffold afforded a rigidified and closed receptor for which the electron-rich TTF pincers are expected to be at a suitable distance for sandwiching neutral guests through donor-acceptor interactions. The efficient complexation ability of this host architecture toward one molecule of tetracyanoquinodimethane derivative (F4-TCNQ) in solution has been demonstrated using cyclic voltammetry and UV-Visible titration methods.
Glycoluril-tetrathiafulvalene molecular clips: On the influence of electronic and spatial properties for binding neutral accepting guests
Cotelle, Yoann,Hardouin-Lerouge, Marie,Legoupy, Stéphanie,Alévêque, Olivier,Levillain, Eric,Hudhomme, Piétrick
, p. 1023 - 1036 (2015/08/18)
Glycoluril-based molecular clips incorporating tetrathiafulvalene (TTF) sidewalls have been synthesized through different strategies with the aim of investigating the effect of electrochemical and spatial properties for binding neutral accepting guests. W
Novel Concave Building Block for the Synthesis of Organic Hoest.
Smeets, Jan W. H.,Sijbesma, Rint P.,Niele, Frank G. M.,Spek, Anthony L.,Smeets, Wilberth J.J.,Nolte, Roeland J. M.
, p. 928 - 929 (2007/10/02)
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