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Please use this identifier to cite or link to this item: http://arks.princeton.edu/ark:/88435/dsp016t053j449
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dc.contributor.advisorMacMillan, David W.-
dc.contributor.authorTsai, Erica Yuh-Ting-
dc.date.accessioned2016-07-28T19:08:33Z-
dc.date.available2016-07-28T19:08:33Z-
dc.date.created2016-04-18-
dc.date.issued2016-07-28-
dc.identifier.urihttp://arks.princeton.edu/ark:/88435/dsp016t053j449-
dc.description.abstractPhotoredox catalysis enables efficient access to broad reactivity under very mild conditions. Synergistic catalysis couples one catalytic mode, ie. photoredox catalysis, with another such as transition metal catalysis or organocatalysis to access greater reaction space. Metallaphotoredox catalysis has been used to achieve and optimize decarboxylative sp2-sp3 bond formation between alkyl carboxylic acids and aryl halides. Of particular interest are iridium(III)-based photocatalysts, due to their high quantum yield and versatility of emission wavelength. While this reaction has been optimized significantly, a current problem exists in which catalytically generated organic radical intermediates deactivate the photocatalyst via the Minisci reaction. By modifying catalyst scaffolds, a catalyst impervious to radical attack could be accessed. Current efforts to synthesize such a catalyst have not been realized; however, future efforts will build upon the knowledge gained thus far in the manipulation of photocatalyst properties.en_US
dc.format.extent93 pagesen_US
dc.language.isoen_USen_US
dc.titleTowards the Discovery of a Novel Radical-Proof, Iridium-Based Photocatalyst for Applications in Synergistic Catalysisen_US
dc.typePrinceton University Senior Theses-
pu.date.classyear2016en_US
pu.departmentChemistryen_US
pu.pdf.coverpageSeniorThesisCoverPage-
Appears in Collections:Chemistry, 1926-2020

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