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    <subfield code="a">Sever, Mary  </subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Isomerization Kinetics of Hydroxy-Substituted Azobenzenes Using a Modified Commercial Flash Photolysis Spectrometer (Journal Article)</subfield>
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    <subfield code="a">Washington DC </subfield>
    <subfield code="b">:American Chemical Society </subfield>
    <subfield code="c">,2023</subfield>
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    <subfield code="a">2762-2769p.</subfield>
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  <datafield tag="440" ind1=" " ind2=" ">
    <subfield code="a">Journal of Chemical Society </subfield>
    <subfield code="v">, Volume 100: Number 7, July 2023 </subfield>
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    <subfield code="a">***______{For Hard Copy, Please visit Library.}________***   </subfield>
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    <subfield code="a">Abstract: A laboratory experiment that exposes students to fundamental concepts in kinetics and statistical thermodynamics to study systems of great current interest in nanotechnology by employing a foundational technique in physical chemistry is described. A modified commercial flash photolysis spectrometer was used to study photoinduced isomerization reactions on the millisecond time scale for several hydroxy-substituted azobenzene compounds. The temperature-dependent transient decays were analyzed with an Eyring plot to yield the enthalpy and entropy of activation of the reverse isomerization process. The specific compounds studied were 4-phenylazophenol, 4-methyl-2-(phenylazo)phenol, and 2,4-dihydroxyazobenzene in ethanol solvent. Instrumental modifications include substitution of a UV-LED for the probe light source and use of a thin polyimide film heater adhered to the side of the sample cuvette to control temperature. Collection of experimental data and the subsequent plotting and analysis are easily accomplished by upper-division chemistry students and the results are consistently good, comparing well with literature values.</subfield>
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    <subfield code="a">Azobenzene| Isomerization| Kinetic parameters| Mass spectrometers| physical chemistry| kinetics| photochemistry| nanotechnology</subfield>
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    <subfield code="a">Young, Mark A. </subfield>
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    <subfield code="u">https://doi.org/10.1021/acs.jchemed.3c00200</subfield>
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    <subfield code="d">2023-11-20</subfield>
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    <subfield code="r">2023-11-20 00:00:00</subfield>
    <subfield code="w">2023-11-20</subfield>
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    <subfield code="c">44973</subfield>
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