<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>Pomarico E</dc:creator>
  <dc:creator>Pospíšil P</dc:creator>
  <dc:creator>Bouduban MEF</dc:creator>
  <dc:creator>Vestfrid J</dc:creator>
  <dc:creator>Gross Z</dc:creator>
  <dc:creator>Záliš S</dc:creator>
  <dc:creator>Chergui M</dc:creator>
  <dc:creator>Vlček A</dc:creator>
  <dc:date>2018</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Excited-state dynamics and electronic structures of Al and Ga corrole complexes were studied as a function of the number of β-pyrrole iodine substituents. Using spectrally broad-band femtosecond-resolved fluorescence upconversion, we determined the kinetics of the Soret fluorescence decay, the concomitant rise and subsequent decay of the Q-band fluorescence, as well as of the accompanying vibrational relaxation. Iodination was found to accelerate all involved processes. The time constant of the internal conversion from the Soret to the Q states decreases from 320-540 to 70-185 fs upon iodination. Vibrational relaxation then occurs with about 15 and 0.36-1.4 ps lifetime for iodine-free and iodinated complexes, respectively. Intersystem crossing to the lowest triplet is accelerated up to 200 times from nanoseconds to 15-24 ps; its rate correlates with the iodine p(π) participation in the corrole π-system and the spin-orbit coupling (SOC) strength. TDDFT calculations with explicit SOC show that iodination introduces a manifold of low-lying singlet and triplet iodine → corrole charge-transfer (CT) states. These states affect the photophysics by (i) providing a relaxation cascade for the Soret → Q internal conversion and cooling and (ii) opening new SOC pathways whereby CT triplet character is admixed into both Q singlet excited states. In addition, SOC between the higher Q singlet and the Soret triplet is enhanced as the iodine participation in frontier corrole π-orbitals increases. Our observations that iodination of the chromophore periphery affects the whole photocycle by changing the electronic structure, spin-orbit coupling, and the density of states rationalize the "heavy-atom effect" and have implications for controlling excited-state dynamics in a range of triplet photosensitizers.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://sonar.ch/global/documents/166623</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1021/acs.jpca.8b05311</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/30141941</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:source>The journal of physical chemistry. A. - 2018</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Physical and Theoretical Chemistry</dc:subject>
  <dc:title xmlns:ns2="xml" ns2:lang="en">Photophysical Heavy-Atom Effect in Iodinated Metallocorroles: Spin-Orbit Coupling and Density of States.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
