Synthesis of a series of aryl tetrazolethiones and investigation of their anion-binding abilities

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dc.contributor.advisor Rayat, Sundeep
dc.contributor.author Sheu, Jerry
dc.date.accessioned 2018-04-30T16:48:41Z
dc.date.available 2018-04-30T16:48:41Z
dc.date.issued 2018-05-05
dc.identifier.uri http://cardinalscholar.bsu.edu/handle/123456789/201145
dc.description Access to thesis permanently restricted to Ball State community only. en_US
dc.description.abstract Anions play a critical role in influencing our life. In biology, chloride ions play an important role in metabolism and regulate acid-base balance in the cells. The transportation of chloride ions across cell membrane occurs through the chloride ion channels. When these channels malfunction, chloride binding molecules are needed to restore the transportation of Cl- across the cell membrane. Similarly, nitrate is a common anion used in fertilizers, and cyanide is employed in polymer production. However, their excessive release in the environment can have dangerous consequences on our health. Thus, anion-binding molecules are needed for monitoring and removal of these harmful anions from our environment. In this thesis, the potential of tetrazolethiones as novel anion binding agents has been investigated. Several tetrazolethione derivatives were synthesized by reacting aryl isothiocyanates with sodium azide under reflux conditions. Some of the required isothiocyanates were commercially obtained, while others were synthesized in our laboratory due to their high cost. To obtain isothiocyanates, substituted anilines were first reacted with N,N-dimethylcarbamoyl chloride, however, this method produced low yields. Alternatively, isothiocyanates were synthesized in good to excellent yields by reacting anilines with carbon disulfide via the formation of thiocarbamates, followed by desulfurylation with di-tert-butyl dicarbonate in the presence of a catalytic amount of DMAP. With aryl isothiocyanates in hand, the phenyl-, -3,5-dimethoxyphenyl-, 4-chlorophenyl-, 4-methoxyphenyl-, and 4-iodophenyl tetrazolethiones as well as the 1,1'-(4-methyl-1,3-phenylene)bistetrazolethione were synthesized by reaction with sodium azide. Next, the ability of two tetrazolethiones (4-chlorophenyl- and 3,5-dimethoxyphenyl tetrazolethiones) to bind to anions, e.g. acetate, bromide, chloride, and nitrate was investigated by using UV and NMR spectroscopy. The results show that tetrazolethiones undergo proton transfer with aceatate anion, while form hydrogen bonded interaction with weakly basic chloride, bromide, nitrate and hydrogen sulfate anions. Among the various anions investigated, tetrazolethiones show selective binding to the chloride anion. Density functional methods were employed to support experimentally calculated association constants. en_US
dc.description.sponsorship Department of Chemistry
dc.description.tableofcontents Anion recognition by artificial receptors -- Synthesis of aryl tetrazolethiones -- Anion binding studies of substituted tetrazolethiones.
dc.subject.lcsh Tetrazoles -- Derivatives.
dc.subject.lcsh Anions -- Receptors.
dc.title Synthesis of a series of aryl tetrazolethiones and investigation of their anion-binding abilities en_US
dc.description.degree Thesis (M.S.) en_US


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  • Master's Theses [5293]
    Master's theses submitted to the Graduate School by Ball State University master's degree candidates in partial fulfillment of degree requirements.

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