Enhancement in Chemiluminescence by Carbonate for Cobalt(II)-catalyzed Oxidation of Luminol with Hydrogen Peroxide
Chemiluminescence (CL) from the cobalt(II)‐catalyzed oxidation of luminol with hydrogen peroxide was dramatically enhanced by the presence of carbonate. The CL signal increases by several orders of magnitude over a wide range of concentrations of Co(II), luminol, or hydrogen peroxide. A limit of det...
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Veröffentlicht in: | Journal of the Chinese Chemical Society (Taipei) 2005-08, Vol.52 (4), p.657-664 |
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description | Chemiluminescence (CL) from the cobalt(II)‐catalyzed oxidation of luminol with hydrogen peroxide was dramatically enhanced by the presence of carbonate. The CL signal increases by several orders of magnitude over a wide range of concentrations of Co(II), luminol, or hydrogen peroxide. A limit of detection of 10−12 M for Co(II) and luminol and 10−8 M for hydrogen peroxide can be achieved. The CL emission spectrum exhibits a maximum at 425 nm, indicating that the excited 3‐aminophthalate is the emitting species. ESR spin‐trapping experiments revealed a large increase in the production of hydroxyl and carbonate radicals by the presence of carbonate, which is responsible for the enormous CL enhancement. Uric acid, ascorbic acid, acetaminophen, and p‐hydroxyphenyl acetic acid are capable of scavenging the radicals, thereby inhibiting the CL emission. The inhibition of CL intensity can be used to determine these substances at the sub‐micromolar level. |
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The CL signal increases by several orders of magnitude over a wide range of concentrations of Co(II), luminol, or hydrogen peroxide. A limit of detection of 10−12 M for Co(II) and luminol and 10−8 M for hydrogen peroxide can be achieved. The CL emission spectrum exhibits a maximum at 425 nm, indicating that the excited 3‐aminophthalate is the emitting species. ESR spin‐trapping experiments revealed a large increase in the production of hydroxyl and carbonate radicals by the presence of carbonate, which is responsible for the enormous CL enhancement. Uric acid, ascorbic acid, acetaminophen, and p‐hydroxyphenyl acetic acid are capable of scavenging the radicals, thereby inhibiting the CL emission. The inhibition of CL intensity can be used to determine these substances at the sub‐micromolar level.</description><identifier>ISSN: 0009-4536</identifier><identifier>EISSN: 2192-6549</identifier><identifier>DOI: 10.1002/jccs.200500093</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>Carbonate ; Chemiluminescence ; Co(II)-Luminol-H2O2 ; Stopped-flow</subject><ispartof>Journal of the Chinese Chemical Society (Taipei), 2005-08, Vol.52 (4), p.657-664</ispartof><rights>Copyright © 2005 The Chemical Society Located in Taipei & Wiley‐VCH Verlag GmbH & Co. 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The CL signal increases by several orders of magnitude over a wide range of concentrations of Co(II), luminol, or hydrogen peroxide. A limit of detection of 10−12 M for Co(II) and luminol and 10−8 M for hydrogen peroxide can be achieved. The CL emission spectrum exhibits a maximum at 425 nm, indicating that the excited 3‐aminophthalate is the emitting species. ESR spin‐trapping experiments revealed a large increase in the production of hydroxyl and carbonate radicals by the presence of carbonate, which is responsible for the enormous CL enhancement. Uric acid, ascorbic acid, acetaminophen, and p‐hydroxyphenyl acetic acid are capable of scavenging the radicals, thereby inhibiting the CL emission. The inhibition of CL intensity can be used to determine these substances at the sub‐micromolar level.</description><subject>Carbonate</subject><subject>Chemiluminescence</subject><subject>Co(II)-Luminol-H2O2</subject><subject>Stopped-flow</subject><issn>0009-4536</issn><issn>2192-6549</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqF0D1PwzAQBmALgUQprMweYUi5xHE-RgiFFlUFQRGj5dhn6pLGyAlqw6-nVVHFxnTS3fvc8BJyHsIgBIiuFko1gwiAA0DODkgvCvMoSHicH5LedhfEnCXH5KRpFgAxi3jeI35Yz2WtcIl1S21NizkubfW1tDU2CjcHWna0kL50tWyRGudp4UpZtRfj8WWgZCur7hs1fVxbLVvrauoMnWy9q-jKtnM66rR371jTJ_Ruk8JTcmRk1eDZ7-yT17vhrBgFk8f7cXE9CRSLUhZoLYEByDBTsQkNxDoHbgBlFCclzzUDTNBAykKTxlmZQcmyKNNguE4UlyXrk8Hur_KuaTwa8entUvpOhCC2jYltY2Lf2AbkO7CyFXb_pMVDUbz8tcHO2qbF9d5K_yGSlKVcvE3vxc00uX26mz2LmP0Aly-Alg</recordid><startdate>200508</startdate><enddate>200508</enddate><creator>Yeh, Hui-Chun</creator><creator>Hsu, Wen-Tong</creator><creator>Lin, Wann-Yin</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>200508</creationdate><title>Enhancement in Chemiluminescence by Carbonate for Cobalt(II)-catalyzed Oxidation of Luminol with Hydrogen Peroxide</title><author>Yeh, Hui-Chun ; Hsu, Wen-Tong ; Lin, Wann-Yin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3273-dda0300a18c4f1f04d905f0ea246b59d30e6ef0731f748b80b3828d0f5d6c5ab3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Carbonate</topic><topic>Chemiluminescence</topic><topic>Co(II)-Luminol-H2O2</topic><topic>Stopped-flow</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yeh, Hui-Chun</creatorcontrib><creatorcontrib>Hsu, Wen-Tong</creatorcontrib><creatorcontrib>Lin, Wann-Yin</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>Journal of the Chinese Chemical Society (Taipei)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yeh, Hui-Chun</au><au>Hsu, Wen-Tong</au><au>Lin, Wann-Yin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enhancement in Chemiluminescence by Carbonate for Cobalt(II)-catalyzed Oxidation of Luminol with Hydrogen Peroxide</atitle><jtitle>Journal of the Chinese Chemical Society (Taipei)</jtitle><addtitle>Jnl Chinese Chemical Soc</addtitle><date>2005-08</date><risdate>2005</risdate><volume>52</volume><issue>4</issue><spage>657</spage><epage>664</epage><pages>657-664</pages><issn>0009-4536</issn><eissn>2192-6549</eissn><abstract>Chemiluminescence (CL) from the cobalt(II)‐catalyzed oxidation of luminol with hydrogen peroxide was dramatically enhanced by the presence of carbonate. The CL signal increases by several orders of magnitude over a wide range of concentrations of Co(II), luminol, or hydrogen peroxide. A limit of detection of 10−12 M for Co(II) and luminol and 10−8 M for hydrogen peroxide can be achieved. The CL emission spectrum exhibits a maximum at 425 nm, indicating that the excited 3‐aminophthalate is the emitting species. ESR spin‐trapping experiments revealed a large increase in the production of hydroxyl and carbonate radicals by the presence of carbonate, which is responsible for the enormous CL enhancement. Uric acid, ascorbic acid, acetaminophen, and p‐hydroxyphenyl acetic acid are capable of scavenging the radicals, thereby inhibiting the CL emission. The inhibition of CL intensity can be used to determine these substances at the sub‐micromolar level.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/jccs.200500093</doi><tpages>8</tpages></addata></record> |
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subjects | Carbonate Chemiluminescence Co(II)-Luminol-H2O2 Stopped-flow |
title | Enhancement in Chemiluminescence by Carbonate for Cobalt(II)-catalyzed Oxidation of Luminol with Hydrogen Peroxide |
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