dc.contributor.author | Hintz, Heather A. | |
dc.contributor.author | Sortedahl, Nicholas J. | |
dc.contributor.author | Dahl, Bart J. | |
dc.date.accessioned | 2017-03-09T18:19:33Z | |
dc.date.available | 2017-03-09T18:19:33Z | |
dc.date.issued | 2017-03-09T18:19:33Z | |
dc.identifier.uri | http://digital.library.wisc.edu/1793/76135 | |
dc.description | Color poster with text and images. | en |
dc.description.abstract | The 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.sponsorship | University of Wisconsin--Eau Claire Office of Research and Sponsored Programs | en |
dc.language.iso | en_US | en |
dc.relation.ispartofseries | USGZE AS589; | |
dc.subject | Lactones | en |
dc.subject | Molecular structure | en |
dc.subject | Posters | en |
dc.title | Pi-Expanded Coumarins with Switchable Propeller Geometries | en |
dc.type | Presentation | en |