Kennesaw State University
Simplified Synthesis of Conjugated Polymers Enabled via 1,4-Dihydropyrrolo[3,2-b]pyrrole
Abstract
dc:description.abstract<p>Conjugated polymers have attracted significant attention as the active layer material in organic electronics, such as organic photovoltaics and light-emitting diodes, partly due to the ability to influence a broad range of properties through structural design motifs. However, high performance conjugated polymers suffer from numerous synthetic steps, generation of toxic waste, and harsh reaction conditions all of which impart additional costs that inhibit their widespread utilization. Therefore, an emphasis on reducing synthetic complexity and utilizing abundant, commercially available starting materials is needed for organic electronics to reach their full potential. Dihydropyrrolo[3,2-b]pyrrole (H<sub>2</sub>DPP) chromophores offer a simple one-pot synthesis to access electron-rich scaffolds for incorporation into a new class of conjugated polymers with tunable optoelectronic properties. Motivated by the simple synthesis, ease of purification, and an overall lower synthetic complexity for accessing monomers, dihalogenated H<sub>2</sub>DPP monomers are synthesized and subsequently polymerized with electron-rich and electron-deficient comonomers. Through the choice of comonomers, H<sub>2</sub>DPP polymers demonstrate facile optical tunability, evident by absorbance and fluorescence across the visible spectrum. Additionally, polymers demonstrate suitable thermal stability for standard processing protocols and motivate exploration of film properties. The synthetic complexity of the resulting polymers also is calculated and H<sub>2</sub>DPP copolymers are quantified to be synthetically simpler compared to many conventional polymers used in solid-state and electrochemical applications. In total, this work shows that the incorporation of H<sub>2</sub>DPP into polymeric materials simplifies the synthesis of conjugated polymers, maintains tailorability through functionality and comonomer choice, and lays the foundation for the continued development of a novel class of organic electronic materials.</p>
Degree
thesis:*- Name thesis:degree_name
- Master of Science in Chemical Sciences (MSCB)
- Level thesis:degree_level
- Thesis
- Discipline thesis:degree_discipline
- Chemistry
- Year dc:date.available
- 2022
Author and committee
dc:creator, dc:contributor.*- Author dc:creator
-
- Bell, Kenneth-John Jack
- Contributors dc:contributor
-
- Graham S. Collier
- Carl Saint-Louis
- Bharat Bharuah
Subjects
dc:subject × 10Identifiers
dc:identifier.*- Repository record dc:identifier
- https://digitalcommons.kennesaw.edu/mscs_etd/48
- OAI identifier oai:identifier
- oai:digitalcommons.kennesaw.edu:mscs_etd-1049