Degree Name

MS (Master of Science)

Program

Chemistry

Date of Award

12-2025

Committee Chair or Co-Chairs

Catherine McCusker

Committee Members

Gregory Bishop, Robert Standaert

Abstract

The release of CO₂ from fossil fuel combustion drives the need for its conversion into more sustainable options like CO and CH₄ via photocatalytic reduction. This process requires a catalyst, sensitizer, and electron donor. Zinc dipyrrin-based complexes are promising photosensitizers, offering an alternative to expensive, rare-metal-based systems. Most first-row transition metal dipyrrin compounds have short excited-state lifetimes due to rapid nonradiative decay, but Zn(II) dipyrrin complexes stand out. With a d¹⁰ configuration, they lack deactivating ligand field states and can access long-lived triplet states through a charge-separated intermediate. A phenyl-substituted Zn(II) dipyrrin complex was synthesized and studied using NMR to understand how aromatic groups affect its photophysics. The synthesis was done to improve triplet formation and excited-state lifetime. TLC and NMR indicated unreacted starting materials, likely due to steric hindrance from bulky phenyl groups or slow reaction kinetics, which limited the overall efficiency of complex formation and resulted in low product yield.

Document Type

Thesis - unrestricted

Copyright

Copyright by the authors.

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