| Literature DB >> 26691558 |
Pierre-Thomas Skowron1, Melissa Dumartin2, Emeric Jeamet2, Florent Perret2, Christophe Gourlaouen3, Anne Baudouin2, Bernard Fenet2, Jean-Valère Naubron1, Frédéric Fotiadu1, Laurent Vial4, Julien Leclaire2.
Abstract
A family of p-cyclophanes based on bis- or tetrafunctionalized 1,4-bisthiophenol units linked by disulfide bridges was obtained by self-assembly on a gram scale and without any chromatographic purification. The nature of the functionalities borne by these so-called dyn[4]arenes plays a crucial role on their structural features as well as their molecular recognition abilities. Tuning these functions on demand yields tailored receptors for cations, anions, or zwitterions in organic or aqueous media.Entities:
Year: 2016 PMID: 26691558 DOI: 10.1021/acs.joc.5b02605
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354