Isomerization Kinetics of Hydroxy-Substituted Azobenzenes Using a Modified Commercial Flash Photolysis Spectrometer
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...
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Veröffentlicht in: | Journal of chemical education 2023-07, Vol.100 (7), p.2762-2769 |
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description | 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. |
doi_str_mv | 10.1021/acs.jchemed.3c00200 |
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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.</description><identifier>ISSN: 0021-9584</identifier><identifier>EISSN: 1938-1328</identifier><identifier>DOI: 10.1021/acs.jchemed.3c00200</identifier><language>eng</language><publisher>Easton: American Chemical Society and Division of Chemical Education, Inc</publisher><subject>Azo compounds ; Enthalpy ; Entropy ; Entropy of activation ; Ethanol ; Flash photolysis ; Isomerization ; Kinetics ; Light sources ; Nanotechnology ; Phenols ; Photolysis ; Physical chemistry ; Science education ; Statistical thermodynamics ; Students ; Substitutes ; Temperature dependence ; Thermodynamics</subject><ispartof>Journal of chemical education, 2023-07, Vol.100 (7), p.2762-2769</ispartof><rights>2023 The Authors. 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Chem. Educ</addtitle><description>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.</description><subject>Azo compounds</subject><subject>Enthalpy</subject><subject>Entropy</subject><subject>Entropy of activation</subject><subject>Ethanol</subject><subject>Flash photolysis</subject><subject>Isomerization</subject><subject>Kinetics</subject><subject>Light sources</subject><subject>Nanotechnology</subject><subject>Phenols</subject><subject>Photolysis</subject><subject>Physical chemistry</subject><subject>Science education</subject><subject>Statistical thermodynamics</subject><subject>Students</subject><subject>Substitutes</subject><subject>Temperature dependence</subject><subject>Thermodynamics</subject><issn>0021-9584</issn><issn>1938-1328</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kMtOAjEUhhujiYg-gZsmrgd6G6ZdEiJCxGiCrJvS6UjJzBTbTuLw9FbBrauTc_7LST4A7jEaYUTwWOkw2uudaUw5ohohgtAFGGBBeYYp4ZdgkG44Ezln1-AmhD1CmOSCD0BYBtcYb48qWtfCZ9uaaHWAroKLvvTuq8_W3TZEG7toSjg9uq1pj6Y1AW6CbT-ggi-utJVN4sw1qUpbVcN5rcIOvu1cdHUfbIDrg9HRp1fR-FtwVak6mLvzHILN_PF9tshWr0_L2XSVKUZ4zCqhC8GrtJAJV3khWJ5TSoxSXJWF0fmWC66MRqUqGME5Y7xQCCNaTphgBaZD8HDqPXj32ZkQ5d51vk0vJeGUFxNWcJ5c9OTS3oXgTSUP3jbK9xIj-UNXJrryTFee6abU-JT6Ff9q_0t8A50KghA</recordid><startdate>20230711</startdate><enddate>20230711</enddate><creator>Sever, Mary</creator><creator>Young, Mark A.</creator><general>American Chemical Society and Division of Chemical Education, Inc</general><general>American Chemical Society</general><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><orcidid>https://orcid.org/0000-0002-7805-9075</orcidid></search><sort><creationdate>20230711</creationdate><title>Isomerization Kinetics of Hydroxy-Substituted Azobenzenes Using a Modified Commercial Flash Photolysis Spectrometer</title><author>Sever, Mary ; Young, Mark A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a428t-f9c798fa42268a579455332eaa8ad7ec5b898aec0da742154487a0103d6494713</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Azo compounds</topic><topic>Enthalpy</topic><topic>Entropy</topic><topic>Entropy of activation</topic><topic>Ethanol</topic><topic>Flash photolysis</topic><topic>Isomerization</topic><topic>Kinetics</topic><topic>Light sources</topic><topic>Nanotechnology</topic><topic>Phenols</topic><topic>Photolysis</topic><topic>Physical chemistry</topic><topic>Science education</topic><topic>Statistical thermodynamics</topic><topic>Students</topic><topic>Substitutes</topic><topic>Temperature dependence</topic><topic>Thermodynamics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sever, Mary</creatorcontrib><creatorcontrib>Young, Mark A.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><jtitle>Journal of chemical education</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sever, Mary</au><au>Young, Mark A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Isomerization Kinetics of Hydroxy-Substituted Azobenzenes Using a Modified Commercial Flash Photolysis Spectrometer</atitle><jtitle>Journal of chemical education</jtitle><addtitle>J. Chem. Educ</addtitle><date>2023-07-11</date><risdate>2023</risdate><volume>100</volume><issue>7</issue><spage>2762</spage><epage>2769</epage><pages>2762-2769</pages><issn>0021-9584</issn><eissn>1938-1328</eissn><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.</abstract><cop>Easton</cop><pub>American Chemical Society and Division of Chemical Education, Inc</pub><doi>10.1021/acs.jchemed.3c00200</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-7805-9075</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Azo compounds Enthalpy Entropy Entropy of activation Ethanol Flash photolysis Isomerization Kinetics Light sources Nanotechnology Phenols Photolysis Physical chemistry Science education Statistical thermodynamics Students Substitutes Temperature dependence Thermodynamics |
title | Isomerization Kinetics of Hydroxy-Substituted Azobenzenes Using a Modified Commercial Flash Photolysis Spectrometer |
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