Pi-Expanded Coumarins with Switchable Propeller Geometries

dc.contributor.authorHintz, Heather A.
dc.contributor.authorSortedahl, Nicholas J.
dc.contributor.authorDahl, Bart J.
dc.date.accessioned2017-03-09T18:19:33Z
dc.date.available2017-03-09T18:19:33Z
dc.date.issued2017-03-09T18:19:33Z
dc.descriptionColor poster with text and images.en
dc.description.abstractThe focus of this project is analyzing planar conjugated molecules as molecular geometric switches. Our mission is to synthesize and study different classes of pi-expanded oligocoumarins with Crankshaft and Propeller architectures. The aryl-aryl torsional angle of the oligopheny subunits is controlled by lactone bridging groups to force planar conjugation. The lactone bridges could be reversibly cleaved and re-formed by changes in pH to form an open and closed conformation. Planar compounds with extended pi-conjugation suffer from poor solubility due to strong pi-stacking interactions. The synthesis with various solubilizing groups and switching studies of these compounds could lead to applications in areas such as organic electronics, molecular machines, light-harvesting materials, drug administration and sensors.en
dc.description.sponsorshipUniversity of Wisconsin--Eau Claire Office of Research and Sponsored Programsen
dc.identifier.urihttp://digital.library.wisc.edu/1793/76135
dc.language.isoen_USen
dc.relation.ispartofseriesUSGZE AS589;
dc.subjectLactonesen
dc.subjectMolecular structureen
dc.subjectPostersen
dc.titlePi-Expanded Coumarins with Switchable Propeller Geometriesen
dc.typePresentationen

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