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      <namePart>Yun, Young Ju</namePart>
   </name>
   <titleInfo>
      <title>Synthesis and Photophysical Characterization of Novel Organic Triplet Donor–Acceptor Dyads for Light-Harvesting/Modulation Application</title>
   </titleInfo>
   <originInfo>
      <dateCreated keyDate="yes">2022</dateCreated>
   </originInfo>
   <note displayLabel="Degree Awarded">Spring 2022</note>
   <typeOfResource authority="aat" valueURI="http://vocab.getty.edu/page/aat/300028029">Dissertation</typeOfResource>
   <name type="corporate">
      <affiliation>Illinois Institute of Technology</affiliation>
   </name>
   <name type="corporate">
      <namePart>CHEM / Chemistry</namePart>
   </name>
  <name authority="wikidata" authorityURI="https://www.wikidata.org" valueURI="https://www.wikidata.org/wiki/Q88840728">
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         <roleTerm type="text" authority="marcrelator" authorityURI="http://id.loc.gov/vocabulary/relators" valueURI="http://id.loc.gov/vocabulary/relators/cre">advisor</roleTerm>
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    <namePart>Ayitou, Anoklase J.-L.</namePart>
   </name>
   <subject>
      <topic>Organic chemistry</topic>
   </subject>
   <subject>
      <topic>Bichromophores</topic>
   </subject>
   <subject>
      <topic>Charge transfer</topic>
   </subject>
   <subject>
      <topic>Donor-Acceptor dyad</topic>
   </subject>
   <subject>
      <topic>Triplet energy transfer (TEnT)</topic>
   </subject>
   <subject>
      <topic>Triplet photochemistry</topic>
   </subject>
   <subject>
      <topic>Triplet-triplet annihilation based photon upconversion (TTA-PUC)</topic>
   </subject>
   <language>
      <languageTerm type="code" authority="rfc3066">en</languageTerm>
   </language>
   <abstract>Donor–acceptor chromophoric systems (D–A) are important scaffolds for several light-harvesting/initiated processes and devices, including light-emitting diodes, photo-catalytic/redox systems, and photovoltaic cells. It has been hypothesized that for efficient photophysical processes (viz. energy/charge-transfer or excited-state interactions); it is ideal to tether the donor and acceptor chromophores into molecular dyads. To this end, I devised and synthesized several dyads by tethering an organic triplet energy donor and various polyaromatic chromophores (e.g., perylene derivatives and anthracene derivatives) onto a conjugated-/non-conjugated-linker (phenylene- and triptycene- linker, respectively). During the 4-5 years of my Ph.D., I synthesized a total of five (5) dyads: o–, p–3, and dyads 3–5. These systems were fully characterized using different spectroscopy tools/techniques. The spectroscopy investigations of the dyads have allowed me to decipher two important energy transfer pathways: through-bond and through-space with the phenylene linker and only through-space energy with the triptycene linker. Furthermore, the investigations led to the discovery that geometrical features such as face-to-face (co-facial) or slip-stacked interactions between the donor and acceptors chromophores might dictate the dynamic/kinetic of light-induced energy transfer in the dyads. Findings from my graduate research project paved the way for developing molecular engineering studies for light-harvesting/modulation applications.Subsequently, I was able to employ the dyads of my interest to achieve intramolecular and intermolecular triplet energy transfer (TEnT) triplet-triplet annihilation-based photon upconversion (TTA-PUC).
</abstract>
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<identifier type="hdl">http://hdl.handle.net/10560/islandora:1024980</identifier></mods>