Micellar Nanoreactors for Hematin Catalyzed Synthesis of Electrically Conducting Polypyrrole
Enzymatic synthesis of doped polypyrrole (PPy) complexes using oxidoreductases (specifically peroxidases) is very well established “green” methods for producing conducting polypyrrole. The importance of this approach is realized by the numerous potential opportunities of using PPy in biological appl...
Gespeichert in:
Veröffentlicht in: | Langmuir 2012-09, Vol.28 (37), p.13380-13386 |
---|---|
Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 13386 |
---|---|
container_issue | 37 |
container_start_page | 13380 |
container_title | Langmuir |
container_volume | 28 |
creator | Ravichandran, Sethumadhavan Nagarajan, Subhalakshmi Kokil, Akshay Ponrathnam, Timothy Bouldin, Ryan M Bruno, Ferdinando F Samuelson, Lynne Kumar, Jayant Nagarajan, Ramaswamy |
description | Enzymatic synthesis of doped polypyrrole (PPy) complexes using oxidoreductases (specifically peroxidases) is very well established “green” methods for producing conducting polypyrrole. The importance of this approach is realized by the numerous potential opportunities of using PPy in biological applications. However, due to very high costs and low acid stability of these enzymes, there is need for more robust alternate biomimetic catalysts. Hematin, a hydroxyferriprotoporphyrin, has a similar iron catalytic active center like the peroxidases and has previously shown to catalyze polymerization of phenol monomers at pH 12. The insolubility of hematin due to extensive self-aggregation at low pH conditions has prevented its use in the synthesis of conjugated polymers. In this study, we have demonstrated the use of a micellar environment with sodium dodecylbenzenesulfonate (DBSA) for biomimetic synthesis of PPy. The micellar environment helps solubilize hematin, generating nanometer size reactors for the polymerization of pyrrole. The resulting PPy is characterized using UV–visible, Fourier transform infrared, and X-ray photoelectron spectroscopy and reveals the formation of an ordered PPy/DBSA complex with conductivities approaching 0.1 S/cm. |
doi_str_mv | 10.1021/la302494a |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1041141769</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1041141769</sourcerecordid><originalsourceid>FETCH-LOGICAL-a345t-badaa7685670eeb134300e4209a8cae07809de4f17c3c251512af8732b6011e03</originalsourceid><addsrcrecordid>eNpt0E1P20AQgOFVVVRC6KF_oNpLJTgYZj_s9R5RBKQSXxLtrZI1WY9bRxtv2LUP5tdjShouPc3l0YzmZeyLgDMBUpx7VCC11fiBzUQuIctLaT6yGRitMqMLdciOUloDgFXafmKHUloolC1m7Ndt68h7jPwOuxAJXR9i4k2IfEkb7NuOL7BHPz5TzR_Hrv9DqU08NPzSk-tj69D7kS9CVw9u0r_5Q_DjdowxeDpmBw36RJ93c85-Xl3-WCyzm_vr74uLmwyVzvtshTWiKcq8MEC0EkorANISLJYOCUwJtibdCOOUk7nIhcSmNEquChCCQM3ZydvebQxPA6W-2rTp71sdhSFVArQQWpjCTvT0jboYUorUVNvYbjCOE6peY1b7mJP9uls7rDZU7-W_ehP4tgOYpg5NxM616d0VqgRjxbtDl6p1GGI31fjPwRdgdYgy</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1041141769</pqid></control><display><type>article</type><title>Micellar Nanoreactors for Hematin Catalyzed Synthesis of Electrically Conducting Polypyrrole</title><source>MEDLINE</source><source>American Chemical Society Journals</source><creator>Ravichandran, Sethumadhavan ; Nagarajan, Subhalakshmi ; Kokil, Akshay ; Ponrathnam, Timothy ; Bouldin, Ryan M ; Bruno, Ferdinando F ; Samuelson, Lynne ; Kumar, Jayant ; Nagarajan, Ramaswamy</creator><creatorcontrib>Ravichandran, Sethumadhavan ; Nagarajan, Subhalakshmi ; Kokil, Akshay ; Ponrathnam, Timothy ; Bouldin, Ryan M ; Bruno, Ferdinando F ; Samuelson, Lynne ; Kumar, Jayant ; Nagarajan, Ramaswamy</creatorcontrib><description>Enzymatic synthesis of doped polypyrrole (PPy) complexes using oxidoreductases (specifically peroxidases) is very well established “green” methods for producing conducting polypyrrole. The importance of this approach is realized by the numerous potential opportunities of using PPy in biological applications. However, due to very high costs and low acid stability of these enzymes, there is need for more robust alternate biomimetic catalysts. Hematin, a hydroxyferriprotoporphyrin, has a similar iron catalytic active center like the peroxidases and has previously shown to catalyze polymerization of phenol monomers at pH 12. The insolubility of hematin due to extensive self-aggregation at low pH conditions has prevented its use in the synthesis of conjugated polymers. In this study, we have demonstrated the use of a micellar environment with sodium dodecylbenzenesulfonate (DBSA) for biomimetic synthesis of PPy. The micellar environment helps solubilize hematin, generating nanometer size reactors for the polymerization of pyrrole. The resulting PPy is characterized using UV–visible, Fourier transform infrared, and X-ray photoelectron spectroscopy and reveals the formation of an ordered PPy/DBSA complex with conductivities approaching 0.1 S/cm.</description><identifier>ISSN: 0743-7463</identifier><identifier>EISSN: 1520-5827</identifier><identifier>DOI: 10.1021/la302494a</identifier><identifier>PMID: 22906396</identifier><identifier>CODEN: LANGD5</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Catalysis ; Chemistry ; Colloidal state and disperse state ; Electric Conductivity ; Exact sciences and technology ; General and physical chemistry ; Hemin - chemistry ; Hydrogen-Ion Concentration ; Micelles ; Micelles. Thin films ; Molecular Structure ; Nanoparticles - chemistry ; Polymerization ; Polymers - chemical synthesis ; Polymers - chemistry ; Pyrroles - chemical synthesis ; Pyrroles - chemistry ; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</subject><ispartof>Langmuir, 2012-09, Vol.28 (37), p.13380-13386</ispartof><rights>Copyright © 2012 American Chemical Society</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a345t-badaa7685670eeb134300e4209a8cae07809de4f17c3c251512af8732b6011e03</citedby><cites>FETCH-LOGICAL-a345t-badaa7685670eeb134300e4209a8cae07809de4f17c3c251512af8732b6011e03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/la302494a$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/la302494a$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>315,781,785,2766,27081,27929,27930,56743,56793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26380791$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22906396$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ravichandran, Sethumadhavan</creatorcontrib><creatorcontrib>Nagarajan, Subhalakshmi</creatorcontrib><creatorcontrib>Kokil, Akshay</creatorcontrib><creatorcontrib>Ponrathnam, Timothy</creatorcontrib><creatorcontrib>Bouldin, Ryan M</creatorcontrib><creatorcontrib>Bruno, Ferdinando F</creatorcontrib><creatorcontrib>Samuelson, Lynne</creatorcontrib><creatorcontrib>Kumar, Jayant</creatorcontrib><creatorcontrib>Nagarajan, Ramaswamy</creatorcontrib><title>Micellar Nanoreactors for Hematin Catalyzed Synthesis of Electrically Conducting Polypyrrole</title><title>Langmuir</title><addtitle>Langmuir</addtitle><description>Enzymatic synthesis of doped polypyrrole (PPy) complexes using oxidoreductases (specifically peroxidases) is very well established “green” methods for producing conducting polypyrrole. The importance of this approach is realized by the numerous potential opportunities of using PPy in biological applications. However, due to very high costs and low acid stability of these enzymes, there is need for more robust alternate biomimetic catalysts. Hematin, a hydroxyferriprotoporphyrin, has a similar iron catalytic active center like the peroxidases and has previously shown to catalyze polymerization of phenol monomers at pH 12. The insolubility of hematin due to extensive self-aggregation at low pH conditions has prevented its use in the synthesis of conjugated polymers. In this study, we have demonstrated the use of a micellar environment with sodium dodecylbenzenesulfonate (DBSA) for biomimetic synthesis of PPy. The micellar environment helps solubilize hematin, generating nanometer size reactors for the polymerization of pyrrole. The resulting PPy is characterized using UV–visible, Fourier transform infrared, and X-ray photoelectron spectroscopy and reveals the formation of an ordered PPy/DBSA complex with conductivities approaching 0.1 S/cm.</description><subject>Catalysis</subject><subject>Chemistry</subject><subject>Colloidal state and disperse state</subject><subject>Electric Conductivity</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Hemin - chemistry</subject><subject>Hydrogen-Ion Concentration</subject><subject>Micelles</subject><subject>Micelles. Thin films</subject><subject>Molecular Structure</subject><subject>Nanoparticles - chemistry</subject><subject>Polymerization</subject><subject>Polymers - chemical synthesis</subject><subject>Polymers - chemistry</subject><subject>Pyrroles - chemical synthesis</subject><subject>Pyrroles - chemistry</subject><subject>Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</subject><issn>0743-7463</issn><issn>1520-5827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpt0E1P20AQgOFVVVRC6KF_oNpLJTgYZj_s9R5RBKQSXxLtrZI1WY9bRxtv2LUP5tdjShouPc3l0YzmZeyLgDMBUpx7VCC11fiBzUQuIctLaT6yGRitMqMLdciOUloDgFXafmKHUloolC1m7Ndt68h7jPwOuxAJXR9i4k2IfEkb7NuOL7BHPz5TzR_Hrv9DqU08NPzSk-tj69D7kS9CVw9u0r_5Q_DjdowxeDpmBw36RJ93c85-Xl3-WCyzm_vr74uLmwyVzvtshTWiKcq8MEC0EkorANISLJYOCUwJtibdCOOUk7nIhcSmNEquChCCQM3ZydvebQxPA6W-2rTp71sdhSFVArQQWpjCTvT0jboYUorUVNvYbjCOE6peY1b7mJP9uls7rDZU7-W_ehP4tgOYpg5NxM616d0VqgRjxbtDl6p1GGI31fjPwRdgdYgy</recordid><startdate>20120918</startdate><enddate>20120918</enddate><creator>Ravichandran, Sethumadhavan</creator><creator>Nagarajan, Subhalakshmi</creator><creator>Kokil, Akshay</creator><creator>Ponrathnam, Timothy</creator><creator>Bouldin, Ryan M</creator><creator>Bruno, Ferdinando F</creator><creator>Samuelson, Lynne</creator><creator>Kumar, Jayant</creator><creator>Nagarajan, Ramaswamy</creator><general>American Chemical Society</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20120918</creationdate><title>Micellar Nanoreactors for Hematin Catalyzed Synthesis of Electrically Conducting Polypyrrole</title><author>Ravichandran, Sethumadhavan ; Nagarajan, Subhalakshmi ; Kokil, Akshay ; Ponrathnam, Timothy ; Bouldin, Ryan M ; Bruno, Ferdinando F ; Samuelson, Lynne ; Kumar, Jayant ; Nagarajan, Ramaswamy</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a345t-badaa7685670eeb134300e4209a8cae07809de4f17c3c251512af8732b6011e03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Catalysis</topic><topic>Chemistry</topic><topic>Colloidal state and disperse state</topic><topic>Electric Conductivity</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Hemin - chemistry</topic><topic>Hydrogen-Ion Concentration</topic><topic>Micelles</topic><topic>Micelles. Thin films</topic><topic>Molecular Structure</topic><topic>Nanoparticles - chemistry</topic><topic>Polymerization</topic><topic>Polymers - chemical synthesis</topic><topic>Polymers - chemistry</topic><topic>Pyrroles - chemical synthesis</topic><topic>Pyrroles - chemistry</topic><topic>Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ravichandran, Sethumadhavan</creatorcontrib><creatorcontrib>Nagarajan, Subhalakshmi</creatorcontrib><creatorcontrib>Kokil, Akshay</creatorcontrib><creatorcontrib>Ponrathnam, Timothy</creatorcontrib><creatorcontrib>Bouldin, Ryan M</creatorcontrib><creatorcontrib>Bruno, Ferdinando F</creatorcontrib><creatorcontrib>Samuelson, Lynne</creatorcontrib><creatorcontrib>Kumar, Jayant</creatorcontrib><creatorcontrib>Nagarajan, Ramaswamy</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Langmuir</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ravichandran, Sethumadhavan</au><au>Nagarajan, Subhalakshmi</au><au>Kokil, Akshay</au><au>Ponrathnam, Timothy</au><au>Bouldin, Ryan M</au><au>Bruno, Ferdinando F</au><au>Samuelson, Lynne</au><au>Kumar, Jayant</au><au>Nagarajan, Ramaswamy</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Micellar Nanoreactors for Hematin Catalyzed Synthesis of Electrically Conducting Polypyrrole</atitle><jtitle>Langmuir</jtitle><addtitle>Langmuir</addtitle><date>2012-09-18</date><risdate>2012</risdate><volume>28</volume><issue>37</issue><spage>13380</spage><epage>13386</epage><pages>13380-13386</pages><issn>0743-7463</issn><eissn>1520-5827</eissn><coden>LANGD5</coden><abstract>Enzymatic synthesis of doped polypyrrole (PPy) complexes using oxidoreductases (specifically peroxidases) is very well established “green” methods for producing conducting polypyrrole. The importance of this approach is realized by the numerous potential opportunities of using PPy in biological applications. However, due to very high costs and low acid stability of these enzymes, there is need for more robust alternate biomimetic catalysts. Hematin, a hydroxyferriprotoporphyrin, has a similar iron catalytic active center like the peroxidases and has previously shown to catalyze polymerization of phenol monomers at pH 12. The insolubility of hematin due to extensive self-aggregation at low pH conditions has prevented its use in the synthesis of conjugated polymers. In this study, we have demonstrated the use of a micellar environment with sodium dodecylbenzenesulfonate (DBSA) for biomimetic synthesis of PPy. The micellar environment helps solubilize hematin, generating nanometer size reactors for the polymerization of pyrrole. The resulting PPy is characterized using UV–visible, Fourier transform infrared, and X-ray photoelectron spectroscopy and reveals the formation of an ordered PPy/DBSA complex with conductivities approaching 0.1 S/cm.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>22906396</pmid><doi>10.1021/la302494a</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0743-7463 |
ispartof | Langmuir, 2012-09, Vol.28 (37), p.13380-13386 |
issn | 0743-7463 1520-5827 |
language | eng |
recordid | cdi_proquest_miscellaneous_1041141769 |
source | MEDLINE; American Chemical Society Journals |
subjects | Catalysis Chemistry Colloidal state and disperse state Electric Conductivity Exact sciences and technology General and physical chemistry Hemin - chemistry Hydrogen-Ion Concentration Micelles Micelles. Thin films Molecular Structure Nanoparticles - chemistry Polymerization Polymers - chemical synthesis Polymers - chemistry Pyrroles - chemical synthesis Pyrroles - chemistry Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry |
title | Micellar Nanoreactors for Hematin Catalyzed Synthesis of Electrically Conducting Polypyrrole |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-16T06%3A27%3A34IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Micellar%20Nanoreactors%20for%20Hematin%20Catalyzed%20Synthesis%20of%20Electrically%20Conducting%20Polypyrrole&rft.jtitle=Langmuir&rft.au=Ravichandran,%20Sethumadhavan&rft.date=2012-09-18&rft.volume=28&rft.issue=37&rft.spage=13380&rft.epage=13386&rft.pages=13380-13386&rft.issn=0743-7463&rft.eissn=1520-5827&rft.coden=LANGD5&rft_id=info:doi/10.1021/la302494a&rft_dat=%3Cproquest_cross%3E1041141769%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1041141769&rft_id=info:pmid/22906396&rfr_iscdi=true |