<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>Antonov, Liudmil</dc:creator>
  <dc:creator>Deneva, Vera</dc:creator>
  <dc:creator>Simeonov, Svilen</dc:creator>
  <dc:creator>Kurteva, Vanya</dc:creator>
  <dc:creator>Crochet, Aurélien</dc:creator>
  <dc:creator>Fromm, Katharina M.</dc:creator>
  <dc:creator>Shivachev, Boris</dc:creator>
  <dc:creator>Nikolova, Rositsa</dc:creator>
  <dc:creator>Savarese, Marika</dc:creator>
  <dc:creator>Adamo, Carlo</dc:creator>
  <dc:date>2015-02-23</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">A series of new tautomeric azonaphthols are synthesized and the possibilities for  molecular switching are investigated using molecular spectroscopy, X-ray analysis  and density functional theory quantum chemical calculations. Two opposite effects  that influence switching are studied: attaching a piperidine sidearm, and adding  substituents to the phenyl ring. On the one hand, the attached piperidine moiety  stabilizes the enol form leading to a controlled shift of the equilibrium upon  protonation. On the other hand, the relative stability of the azonaphthol tautomers  strongly depends on the effects of the substituents on the phenyl ring: electron donors  tend to stabilize the enol tautomer, whereas electron acceptors lead to stabilization of  the keto form. However, these effects do not shift fully the equilibrium towards either of  the tautomers. Nevertheless, the effect of the substituents can be an additional tool to  affect the switching between “on” and “off” states. Electron-withdrawing substituents  stabilize the keto form and impede switching to the off state, whereas electron donors  stabilize the enol form. The effect of the piperidine unit is dominant overall, and with  strongly electron-withdrawing substituents at the phenyl ring, the enol form exists as a  zwitterion.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/304281</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/304281/files/fro_cts.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/304281/files/fro_cts_sm.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1002/cphc.201402691</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>ChemPhysChem. - 2015, vol. 16, no. 3, p. 649–657</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Chemometrics</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Density functional theory</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Molecular switches</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Spectroscopy</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Tautomerism</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/54</dc:subject>
  <dc:title xmlns:ns6="xml" ns6:lang="en">Controlled tautomeric switching in azonaphthols tuned by substituents on the phenyl ring</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
