C-H bonds are easily the most common type of ordinary chemical bond and studying carbon acidity will help us understand and predict the reactivity of organic compounds. Carbon acidities are ranked using acidity scales. One of the most prominent is the Streitwieser Lithium Indicator (SLI) scale. The term "indicator scale" implies that acids have been measured against one another in sequential fashion. The SLI scale uses lithium ion as the conjugate-base counterion and THF as the solvent. Historically, the SLI scale has emphasized the characterization of weakly-acidic hydrocarbons. Prior to the work of our group, the strongest acid on the SLI scale has a pK value of about 10. Deck and Thornberry extended the scale to ca. pK = 0 by evaluating 23 perfluoroaryl-substituted cyclopentadiene and indene derivatives, using 19F NMR spectroscopy to determine the equilibrium constants of sequential acid-base reactions.
This thesis describes the further extension of the SLI scale to ca. pK = −6. To achieve this result, a set of 11 tetrasubstituted cyclopentadienes were synthesized and their acidities evaluated sequentially with the goal of reaching a low pK value while minimizing the acidity ratio at each incremental step. The four ring substituents were combinations of pentafluorophenyl, perfluoro-4-tolyl, and perfluoro-4-pyridyl, electronegative groups listed in order of increasing electron-withdrawing power. The most acidic compound in the set was 1-pentafluorophenyl-2,3,4-tetrakis(tetrafluoro-4-pyridyl)cyclopentadiene, having pK = −5.99. Trends in the acidities of tetraarylcyclopentadienes are discussed including relative electron-withdrawing power of the three selected substituents, and conformational effects among pairs of regioisomeric cyclopentadiene derivatives. / Master of Science / Carbon acidity refers to the willingness of a carbon-hydrogen bond to release a hydrogen ion. C-H bonds are easily the most common type of ordinary chemical bond, so it makes sense that studying carbon acidity will help us understand and predict the reactivity of organic compounds. For the past several decades, emphasis in this area of research has focused on weak carbon acids, especially the simplest hydrocarbons like benzene and methane. This thesis aims in the opposite direction of synthesizing and measuring stronger and stronger carbon acids until we reach the theoretical limit for a given solvent. Because our research strategy is inherently incremental, compounds were synthesized and their acidities were measured, drawing close to the theoretical limit using tetrahydrofuran as the solvent.
| Identifer | oai:union.ndltd.org:VTETD/oai:vtechworks.lib.vt.edu:10919/110449 |
| Date | 06 June 2022 |
| Creators | Ramsey, Harley Andrew |
| Contributors | Chemistry, Deck, Paul A., Troya, Diego, Tanko, James M. |
| Publisher | Virginia Tech |
| Source Sets | Virginia Tech Theses and Dissertation |
| Language | English |
| Detected Language | English |
| Type | Thesis |
| Format | ETD, application/pdf, application/pdf |
| Rights | In Copyright, http://rightsstatements.org/vocab/InC/1.0/ |
Page generated in 0.1599 seconds