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Spectroscopy, Electrochemistry and Photochemistry of Phenylazonaphthalene Dyes

Bullivant, Chad Quentin (2010) Spectroscopy, Electrochemistry and Photochemistry of Phenylazonaphthalene Dyes. PhD thesis, University of York.

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The spectroscopy, electrochemistry and photochemistry of seven 2-(4-R-phenylazo)naphthalene-4,8-disulfonate dyes (R-Span dyes), were studied to report on their structure and reactivity in water. The dyes differ in their structure by only the R substituent attached to the phenyl ring, representing a range of electron-donating and electron-withdrawing substituents; most studies were carried out on OH-Span. A combination of UV/Visible, NMR, Raman and IR spectroscopy together with DFT calculations has shown that the dyes are planar in their stable trans-isomer form. The spectra were found to be sensitive to the R substituent and generally they show good correlations with Hammett σp substituent constants. The structures of OH-Span (pKa = 7.98) and NH2-Span (pKa = 2.88) are pH dependent, and none of the dyes show aggregation at ≤ 3 * 10^-2 mol dm^-3. Spectroelectrochemistry and controlled potential electrolysis studies showed that OH-Span undergoes an irreversible four electron reduction process, where detailed product analysis showed that naphthyl and phenyl fragments of the dye are produced due to azo bond scission; similar results were observed for the other R-Span dyes. Dyes containing electron-donating R substituents are more resistant to reduction, whereas dyes containing electron-withdrawing R substituents are more resistant to oxidation. The stability of the R-Span dyes was assessed by reaction with photoinitiator generated 2-hydroxy-2-propyl radicals to study reductive fading. Time-resolved studies were carried out on OH-Span:photoinitiator solutions and rate constants for electron transfer to produce the dye radical anion and subsequent disproportionation were found to be 6.00 * 10^9 and 5.00 * 10^8 dm^3 mol^-1 s^-1, respectively. The detailed product analysis identified the naphthyl fragment of the dye, which was also observed for other R-Span dyes, indicating that the reduction mechanism occurs via disproportionation resulting in azo bond scission. The R-Span dyes show trans to cis photoisomerisation, and NH2-, OH-, OMe- and NHAc-Span showed complete cis to trans thermal back reactions within ca. 30 ms, 35 μs, 11 days and 1 day, respectively.

Item Type: Thesis (PhD)
Academic Units: The University of York > Chemistry (York)
Identification Number/EthosID: uk.bl.ethos.533497
Depositing User: Mr Chad Quentin Bullivant
Date Deposited: 20 Sep 2010 11:33
Last Modified: 08 Sep 2016 12:19
URI: http://etheses.whiterose.ac.uk/id/eprint/1018

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