Hierarchical Self-Assembly of Supramolecular Helical Fibres from Amphiphilic C3-Symmetrical Functional Tris(tetrathiafulvalenes)

TitreHierarchical Self-Assembly of Supramolecular Helical Fibres from Amphiphilic C3-Symmetrical Functional Tris(tetrathiafulvalenes)
Type de publicationArticle de revue
AuteurPop, Flavia , Melan, Caroline , Danila, Ion, Linares, Mathieu, Beljonne, David, Amabilino, David-B., Avarvari, Narcis
EditeurWiley-VCH Verlag
TypeArticle scientifique dans une revue à comité de lecture
Année2014
LangueAnglais
DateOct-12-2015
Numéro52
Volume20
Titre de la revueChemistry - A European Journal
ISSN0947-6539
Résumé en anglais

The preparation and self-assembly of the enantiomers of a series of C3-symmetric compounds incorporating three tetrathiafulvalene (TTF) residues is reported. The chiral citronellyl and dihydrocitronellyl alkyl chains lead to helical one dimensional stacks in solution. Molecular mechanics and dynamics simulations combined with experimental and theoretical circular dichroism support the observed helicity in solution. These stacks self-assemble to give fibres that have morphologies that depend on the nature of the chiral alkyl group and the medium in which the compounds aggregate. An inversion of macroscopic helical morphology of the citronellyl compound is observed when compared to analogous 2-methylbutyl chains, which is presumably a result of the stereogenic centre being further away from the core of the molecule. This composition still allows both morphologies to be observed, whereas an achiral compound shows no helicity. The morphology of the fibres also depends on the flexibility at the chain ends of the amphiphilic components, as there is not such an apparently persistent helical morphology for the dihydrocitronellyl derivative as for that prepared from citronellyl chains.

URL de la noticehttp://okina.univ-angers.fr/publications/ua10827
DOI10.1002/chem.201404753
Lien vers le document

http://doi.wiley.com/10.1002/chem.201404753

Titre abrégéChem. Eur. J.