<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Peterhans, Lisa</dc:creator>
  <dc:creator>Alloa, Elisa</dc:creator>
  <dc:creator>Sheima, Yauhen</dc:creator>
  <dc:creator>Vannay, Laurent</dc:creator>
  <dc:creator>Leclerc, Mario</dc:creator>
  <dc:creator>Corminboeuf, Clémence</dc:creator>
  <dc:creator>Hayes, Sophia C.</dc:creator>
  <dc:creator>Banerji, Natalie</dc:creator>
  <dc:date>2017-11-01</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">We report here the photophysical properties of a water-soluble conjugated  polythiophene with cationic side-chains. When dissolved in aqueous buffer solution  (PBS, phosphate buffered saline), there is ordering of the polymer chains due to the  presence of the salts, in contrast to pure water, where a random-coil conformation is  adopted at room temperature. The ordering leads to a pronounced colour change of  the solution (the absorption maximum shifts from 400 nm to 525 nm). Combining  resonance Raman spectroscopy with density functional theory computations, we show  a significant backbone planarization in the ordered phase. Moreover, the ratio of  ordered phase to random-coil phase in PBS solution, as well as the extent of  intermolecular interactions in the ordered phase, can be tuned by varying the  temperature. Femtosecond transient absorption spectroscopy reveals that the excited- state behaviour of the polyelectrolyte is strongly affected by the degree of ordering.  While triplet state formation is favoured in the random-coil chains, the ordered chains  show a weak yield of polarons, related to interchain interactions. The investigated  polyelectrolyte has been previously used as a biological DNA sensor, based on optical  transduction when the conformation of the polyelectrolyte changes during assembly  with the biomolecule. Therefore, our results, by correlating the photophysical  properties of the polyelectrolyte to backbone and intermolecular conformation in a  biologically relevant buffer, provide a significant step forward in understanding the  mechanism of the biological sensing.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/306178</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/306178/files/pet_sit.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/306178/files/pet_sit_sm.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1039/C7CP02734F</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Physical Chemistry Chemical Physics. - 2017, vol. 19, no. 42, p. 28853–28866</dc:source>
  <dc:subject>info:eu-repo/classification/udc/54</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Salt-induced thermochromism of a conjugated polyelectrolyte</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
