Enhancing the Antiaromaticity of s-Indacenes Through Heterocycle Fusion
| dc.contributor.advisor | Hendon, Christopher | |
| dc.contributor.author | Warren, Gabrielle | |
| dc.date.accessioned | 2024-03-25T17:21:55Z | |
| dc.date.available | 2024-03-25T17:21:55Z | |
| dc.date.issued | 2024-03-25 | |
| dc.description.abstract | Antiaromaticity, while associated with instability, imparts beneficial properties such as decreased HOMO-LUMO energy gaps. Compounds containing antiaromatic subunits are not only of fundamental interest, but of interest as components in organic electronics. Since antiaromatic compounds are generally unstable, various strategies for isolating these compounds, such as annulation of aromatic subunits, have been developed. While this strategy stabilizes the antiaromatic subunit, it generally decreases the degree of antiaromaticity. Thus, methods to stabilize yet maintain or increase the degree of antiaromaticity are desirable. Recently, we found that fusion of aromatic heterocycles to s-indacene, a known antiaromatic molecule, yields isolable compounds with increased antiaromaticity in the s-indacene core. In this dissertation I will discuss the background of s-indacene and an overview of tuning the antiaromaticity of s-indacene, how fusion of naphthothiophene units increases the antiaromaticity of s-indacene and the development a computational understanding for the effect of heterocycle fusion on s-indacene.Chapter I is an overview of the literature about s-indacene followed by a discussion of the methods used to tune the antiaromaticity of s-indacene by the Haley group. Chapter II describes the synthesis of four naphthothiophene-fused s-indacenes, one of which increased the antiaromaticity of the s-indacene core above unsubstituted s-indacene. Chapter III extends the work of Chapter II further developing the synthesis of naphthothiophene-fused s-indacenes, varying the aryl substituents, and providing a detailed comparison of the properties of all isomers. Finally, Chapter IV explores fourteen different benzoheterocycle-fused s-indacenes through a variety of computational techniques to understand the effect of the heteroatom on the antiaromaticity of the s-indacene core. This dissertation includes previously published and unpublished co-authored material. | en_US |
| dc.identifier.uri | https://hdl.handle.net/1794/29278 | |
| dc.language.iso | en_US | |
| dc.publisher | University of Oregon | |
| dc.rights | All Rights Reserved. | |
| dc.title | Enhancing the Antiaromaticity of s-Indacenes Through Heterocycle Fusion | |
| dc.type | Electronic Thesis or Dissertation | |
| thesis.degree.discipline | Department of Chemistry and Biochemistry | |
| thesis.degree.grantor | University of Oregon | |
| thesis.degree.level | doctoral | |
| thesis.degree.name | Ph.D. |
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