<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>Thazhathethil, Shakkeeb</dc:creator>
  <dc:creator>Thuluvanchery, Fazil Salim</dc:creator>
  <dc:creator>Shimizu, Shohei</dc:creator>
  <dc:creator>Scarlat, Iulia</dc:creator>
  <dc:creator>Clough, Jess M.</dc:creator>
  <dc:creator>Weder, Christoph</dc:creator>
  <dc:creator>Sagara, Yoshimitsu</dc:creator>
  <dc:date>2024</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Mechanochromic mechanophores which instantly and reversibly change their photoluminescence color&#13;
are suitable molecular probes for the in situ visualization and detection of forces that arise in polymers.&#13;
Here, we report that the ring size significantly affects the ratiometric photoluminescence of cyclophane&#13;
mechanophores whose working mechanism relies on the dissociation of intramolecular charge-transfer&#13;
(CT) complexes. We compare three cyclophanes, which each feature a 9,10-bis(phenylethynyl)anthracene&#13;
(BPA) group and one pyromellitic diimide (PMDI) in their cycle. These aromatic groups were connected&#13;
with linkers of different lengths. In toluene solutions, all cyclophanes display suppressed BPA emission in&#13;
comparison to a linear BPA model compound, and a red-shifted emission band associated with a&#13;
BPA:PMDI CT complex is observed. The extent of CT formation scales inversely with the length of the&#13;
spacers and is thus largest for the smallest cyclophane. The three cyclophanes were covalently&#13;
incorporated into segmented polyurethane elastomers, which were processed into thin films. In the&#13;
stress-free state, films of the three materials all display roughly equal monomer and CT emission intensity.&#13;
Upon uniaxial deformation, this ratio changes in favor of the monomer emission. The changes were very&#13;
pronounced for the polymer containing the largest cyclophane, and very small in the material containing&#13;
the smallest mechanophore. Thus, the data show clearly that the mechanoresponse of cyclophane&#13;
mechanophores strongly depends on the ring size, which dictates to what extent the chromophores can&#13;
interact in the absence and presence of an applied force.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/333516</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/333516/files/d4tc00244j.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>https://pubs.rsc.org/en/content/articlelanding/2024/tc/d4tc00244j</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1039/d4tc00244j</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/issn/2050-7526</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>Rights reserved</dc:rights>
  <dc:source>Journal of Materials Chemistry C. - Royal Society of Chemistry (RSC). - 2024, vol. 12, no. 17, p. 6170-6176</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">mechanochemistry</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">supramolecular mechanophore</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">fluorescence</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">polymers</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">force sensing</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/54</dc:subject>
  <dc:title xmlns:ns6="xml" ns6:lang="en">Ring-size dependent ratiometric photoluminescence of cyclophane mechanophores</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
