Photochemistry of Nitrogen Heterocycles: Applications in Amine Sensors and Complex Molecule Synthesis
Three ylidenemalononitrile enamines were designed as fast and selective primary amine sensors. These sensors were used as both colorimetric and fluorometric sensors for primary amines in solution. Two of the enamines were coated onto various media and were used to detect prim...
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| Format: | Others |
| Language: | English English |
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Florida State University
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| Online Access: | http://purl.flvc.org/fsu/fd/FSU_2016SP_Chandler_fsu_0071N_13270 |
| Summary: | Three ylidenemalononitrile enamines were designed as fast and selective primary amine sensors. These sensors were used as both
colorimetric and fluorometric sensors for primary amines in solution. Two of the enamines were coated onto various media and were used to
detect primary amine vapors. The enamine derived from acenaphthalene was used as a colorimetric sensor when coated on media. The enamine
derived from 2-phenylacetophenone showed a stronger fluorescent turn-on when coated on media and was used as a fluorescent sensor when
coated on media. Each enamine worked to detect primary amines in complex mixtures without sample preparation. Each sensor was generated in
short reaction sequences that ranged from three to four steps that utilized mild reaction conditions. In addition, each enamine sensor was
synthesized from inexpensive and commercially available starting material. Pyridazine N-oxides were used as photochemical intermediates
for the synthesis of 3,5-disubstituted pyrazoles. These photochemical precursors were synthesized regioselectively following the oxidation
of the commercially available dichloropyridazine. In order to obtain the regioselectivity a Suzuki coupling reaction followed by a
nucleophilic aromatic substitution (SNAr) was completed on the molecule using various boronic acids and pyrrolidine. Followed by
photochemical ring opening the disubstituted pyridazine N-oxide generated a diazo carbonyl intermediate that could then have cyclized into
either a furan or pyrazole. By partitioning between the two mechanisms we were able to selectively synthesize the pyrazole with little to
no furan by product. === A Thesis submitted to the Department of Chemistry in partial fulfillment of the requirements for the
degree of Master of Science. === Spring Semester 2016. === April 15, 2016. === Enamines, Photochemistry, Primary Amine, Pyrazoles, Regioselective, Sensor === Includes bibliographical references. === James H. Frederich, Professor Directing Thesis; Igor Alabugin, Committee Member; Kenneth Hanson,
Committee Member; Michael Shatruk, Committee Member. |
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