6,6-Dibromopenicillanic acid 1,1-Dioxide 분자내 탄소 6-위치 브롬기의 전극촉매 수소화반응과 전극반응기구

The electrochemical reduction of carbon-6-dibromo groups on 6,6-dibromo penicillanic acid 1,1-oxide(DBPA) was investigated by direct current, differential pulse polarography, cyclic voltammetry and controlled potential coulometry. The irreversible two electrons transfer on the reductive debrominatio...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of the Korean Chemical Society 1991, Vol.35 (2), p.165-171
Hauptverfasser: 김일광(Il Kwang Kim), 이영행(Young Haeng Lee), 이채호(Chai Ho Lee)
Format: Artikel
Sprache:kor
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 171
container_issue 2
container_start_page 165
container_title Journal of the Korean Chemical Society
container_volume 35
creator 김일광(Il Kwang Kim)
이영행(Young Haeng Lee)
이채호(Chai Ho Lee)
description The electrochemical reduction of carbon-6-dibromo groups on 6,6-dibromo penicillanic acid 1,1-oxide(DBPA) was investigated by direct current, differential pulse polarography, cyclic voltammetry and controlled potential coulometry. The irreversible two electrons transfer on the reductive debromination of each bromo group proceeded by EC,EC mechanism at the two electrode reduction steps(-0.48, -1.62 volts). The 6-bromo-PA and 6,6-dihydro-PA was synthesized by controlled potential electrolysis. Upon the basis of results on the products analysis and interpretation of polarograms obtained at various pH, electrochemical reaction mechanism was suggested. 6,6-dibromopenicillanic acid 1,1-oxide(DBPA)의 6위치 dibromo기의 전기화학적 환원을 direct current, differential pulse polarography, cyclic voltammetry, 조절전위 전기량법으로 연구하였다. DBPA 환원과정은 2단계-0.48, -1.62 volts)에서 모두 완전비가역으로 2전자씩 이동하는 EC, EC 반응기구로 진행하였다. 조절전위 전기분해를 이용하여 6-bromo-PA와 6,6-dihydro-PA를 단계적으로 합성하였으며, pH 변화에 다른 폴라로그램의 해석과 생성물 분석의 결과를 바탕으로 전기화학적 반응기구도 제안하였다.
format Article
fullrecord <record><control><sourceid>nurimedia_kisti</sourceid><recordid>TN_cdi_kisti_ndsl_JAKO199113464511178</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><nurid>NODE11541823</nurid><sourcerecordid>NODE11541823</sourcerecordid><originalsourceid>FETCH-LOGICAL-k823-7938a59685d6bc91f9088ca93ab465e92fc755e99e779a2c5f3a88e7d03abdb13</originalsourceid><addsrcrecordid>eNpFjstKw0AUhoMoWLTvMBt3DeRkMpmZZWnrtdhN92Fyg6HphUZBtzWIQhcKLiJYURDcdFGwags-UTJ9BwMWXH3_4f_4ORtayTSxpTOCjU2tBAZQ3SQW29bKcSxdg2BMqcFxSRvZFVuvS3fY7_YHQU96MopEASQ86SOoQFH2L6QfoPwrUc93-WiOVleJuh4jW1dPiVqmKF-M89dptpipSYrUS5J9L9X8Nn9_Q-omLczV40M-S9XkPvv4WffrezHLPqe72lYoojgor7mjtfcb7dqh3mwdHNWqTb3DTKxTjpkg3GbEt12PQ8gNxjzBsXAtmwTcDD1KCvKAUi5Mj4RYMBZQ3ygM3wW8o-39zXZkfCadnh9HznH1pAWcA2DLtggAUPbv9c6Hshv4UjiDIojhpXPaqjcAiAXFQ_gXUk-Dqg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>6,6-Dibromopenicillanic acid 1,1-Dioxide 분자내 탄소 6-위치 브롬기의 전극촉매 수소화반응과 전극반응기구</title><source>EZB-FREE-00999 freely available EZB journals</source><creator>김일광(Il Kwang Kim) ; 이영행(Young Haeng Lee) ; 이채호(Chai Ho Lee)</creator><creatorcontrib>김일광(Il Kwang Kim) ; 이영행(Young Haeng Lee) ; 이채호(Chai Ho Lee)</creatorcontrib><description>The electrochemical reduction of carbon-6-dibromo groups on 6,6-dibromo penicillanic acid 1,1-oxide(DBPA) was investigated by direct current, differential pulse polarography, cyclic voltammetry and controlled potential coulometry. The irreversible two electrons transfer on the reductive debromination of each bromo group proceeded by EC,EC mechanism at the two electrode reduction steps(-0.48, -1.62 volts). The 6-bromo-PA and 6,6-dihydro-PA was synthesized by controlled potential electrolysis. Upon the basis of results on the products analysis and interpretation of polarograms obtained at various pH, electrochemical reaction mechanism was suggested. 6,6-dibromopenicillanic acid 1,1-oxide(DBPA)의 6위치 dibromo기의 전기화학적 환원을 direct current, differential pulse polarography, cyclic voltammetry, 조절전위 전기량법으로 연구하였다. DBPA 환원과정은 2단계-0.48, -1.62 volts)에서 모두 완전비가역으로 2전자씩 이동하는 EC, EC 반응기구로 진행하였다. 조절전위 전기분해를 이용하여 6-bromo-PA와 6,6-dihydro-PA를 단계적으로 합성하였으며, pH 변화에 다른 폴라로그램의 해석과 생성물 분석의 결과를 바탕으로 전기화학적 반응기구도 제안하였다.</description><identifier>ISSN: 1017-2548</identifier><identifier>EISSN: 2234-8530</identifier><language>kor</language><publisher>대한화학회</publisher><ispartof>Journal of the Korean Chemical Society, 1991, Vol.35 (2), p.165-171</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,4023</link.rule.ids></links><search><creatorcontrib>김일광(Il Kwang Kim)</creatorcontrib><creatorcontrib>이영행(Young Haeng Lee)</creatorcontrib><creatorcontrib>이채호(Chai Ho Lee)</creatorcontrib><title>6,6-Dibromopenicillanic acid 1,1-Dioxide 분자내 탄소 6-위치 브롬기의 전극촉매 수소화반응과 전극반응기구</title><title>Journal of the Korean Chemical Society</title><addtitle>Journal of the Korean Chemical Society</addtitle><description>The electrochemical reduction of carbon-6-dibromo groups on 6,6-dibromo penicillanic acid 1,1-oxide(DBPA) was investigated by direct current, differential pulse polarography, cyclic voltammetry and controlled potential coulometry. The irreversible two electrons transfer on the reductive debromination of each bromo group proceeded by EC,EC mechanism at the two electrode reduction steps(-0.48, -1.62 volts). The 6-bromo-PA and 6,6-dihydro-PA was synthesized by controlled potential electrolysis. Upon the basis of results on the products analysis and interpretation of polarograms obtained at various pH, electrochemical reaction mechanism was suggested. 6,6-dibromopenicillanic acid 1,1-oxide(DBPA)의 6위치 dibromo기의 전기화학적 환원을 direct current, differential pulse polarography, cyclic voltammetry, 조절전위 전기량법으로 연구하였다. DBPA 환원과정은 2단계-0.48, -1.62 volts)에서 모두 완전비가역으로 2전자씩 이동하는 EC, EC 반응기구로 진행하였다. 조절전위 전기분해를 이용하여 6-bromo-PA와 6,6-dihydro-PA를 단계적으로 합성하였으며, pH 변화에 다른 폴라로그램의 해석과 생성물 분석의 결과를 바탕으로 전기화학적 반응기구도 제안하였다.</description><issn>1017-2548</issn><issn>2234-8530</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>JDI</sourceid><recordid>eNpFjstKw0AUhoMoWLTvMBt3DeRkMpmZZWnrtdhN92Fyg6HphUZBtzWIQhcKLiJYURDcdFGwags-UTJ9BwMWXH3_4f_4ORtayTSxpTOCjU2tBAZQ3SQW29bKcSxdg2BMqcFxSRvZFVuvS3fY7_YHQU96MopEASQ86SOoQFH2L6QfoPwrUc93-WiOVleJuh4jW1dPiVqmKF-M89dptpipSYrUS5J9L9X8Nn9_Q-omLczV40M-S9XkPvv4WffrezHLPqe72lYoojgor7mjtfcb7dqh3mwdHNWqTb3DTKxTjpkg3GbEt12PQ8gNxjzBsXAtmwTcDD1KCvKAUi5Mj4RYMBZQ3ygM3wW8o-39zXZkfCadnh9HznH1pAWcA2DLtggAUPbv9c6Hshv4UjiDIojhpXPaqjcAiAXFQ_gXUk-Dqg</recordid><startdate>1991</startdate><enddate>1991</enddate><creator>김일광(Il Kwang Kim)</creator><creator>이영행(Young Haeng Lee)</creator><creator>이채호(Chai Ho Lee)</creator><general>대한화학회</general><scope>DBRKI</scope><scope>TDB</scope><scope>JDI</scope></search><sort><creationdate>1991</creationdate><title>6,6-Dibromopenicillanic acid 1,1-Dioxide 분자내 탄소 6-위치 브롬기의 전극촉매 수소화반응과 전극반응기구</title><author>김일광(Il Kwang Kim) ; 이영행(Young Haeng Lee) ; 이채호(Chai Ho Lee)</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-k823-7938a59685d6bc91f9088ca93ab465e92fc755e99e779a2c5f3a88e7d03abdb13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>kor</language><creationdate>1991</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>김일광(Il Kwang Kim)</creatorcontrib><creatorcontrib>이영행(Young Haeng Lee)</creatorcontrib><creatorcontrib>이채호(Chai Ho Lee)</creatorcontrib><collection>DBPIA - 디비피아</collection><collection>DBPIA</collection><collection>KoreaScience</collection><jtitle>Journal of the Korean Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>김일광(Il Kwang Kim)</au><au>이영행(Young Haeng Lee)</au><au>이채호(Chai Ho Lee)</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>6,6-Dibromopenicillanic acid 1,1-Dioxide 분자내 탄소 6-위치 브롬기의 전극촉매 수소화반응과 전극반응기구</atitle><jtitle>Journal of the Korean Chemical Society</jtitle><addtitle>Journal of the Korean Chemical Society</addtitle><date>1991</date><risdate>1991</risdate><volume>35</volume><issue>2</issue><spage>165</spage><epage>171</epage><pages>165-171</pages><issn>1017-2548</issn><eissn>2234-8530</eissn><abstract>The electrochemical reduction of carbon-6-dibromo groups on 6,6-dibromo penicillanic acid 1,1-oxide(DBPA) was investigated by direct current, differential pulse polarography, cyclic voltammetry and controlled potential coulometry. The irreversible two electrons transfer on the reductive debromination of each bromo group proceeded by EC,EC mechanism at the two electrode reduction steps(-0.48, -1.62 volts). The 6-bromo-PA and 6,6-dihydro-PA was synthesized by controlled potential electrolysis. Upon the basis of results on the products analysis and interpretation of polarograms obtained at various pH, electrochemical reaction mechanism was suggested. 6,6-dibromopenicillanic acid 1,1-oxide(DBPA)의 6위치 dibromo기의 전기화학적 환원을 direct current, differential pulse polarography, cyclic voltammetry, 조절전위 전기량법으로 연구하였다. DBPA 환원과정은 2단계-0.48, -1.62 volts)에서 모두 완전비가역으로 2전자씩 이동하는 EC, EC 반응기구로 진행하였다. 조절전위 전기분해를 이용하여 6-bromo-PA와 6,6-dihydro-PA를 단계적으로 합성하였으며, pH 변화에 다른 폴라로그램의 해석과 생성물 분석의 결과를 바탕으로 전기화학적 반응기구도 제안하였다.</abstract><pub>대한화학회</pub><tpages>7</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1017-2548
ispartof Journal of the Korean Chemical Society, 1991, Vol.35 (2), p.165-171
issn 1017-2548
2234-8530
language kor
recordid cdi_kisti_ndsl_JAKO199113464511178
source EZB-FREE-00999 freely available EZB journals
title 6,6-Dibromopenicillanic acid 1,1-Dioxide 분자내 탄소 6-위치 브롬기의 전극촉매 수소화반응과 전극반응기구
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T11%3A28%3A23IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-nurimedia_kisti&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=6,6-Dibromopenicillanic%20acid%201,1-Dioxide%20%EB%B6%84%EC%9E%90%EB%82%B4%20%ED%83%84%EC%86%8C%206-%EC%9C%84%EC%B9%98%20%EB%B8%8C%EB%A1%AC%EA%B8%B0%EC%9D%98%20%EC%A0%84%EA%B7%B9%EC%B4%89%EB%A7%A4%20%EC%88%98%EC%86%8C%ED%99%94%EB%B0%98%EC%9D%91%EA%B3%BC%20%EC%A0%84%EA%B7%B9%EB%B0%98%EC%9D%91%EA%B8%B0%EA%B5%AC&rft.jtitle=Journal%20of%20the%20Korean%20Chemical%20Society&rft.au=%EA%B9%80%EC%9D%BC%EA%B4%91(Il%20Kwang%20Kim)&rft.date=1991&rft.volume=35&rft.issue=2&rft.spage=165&rft.epage=171&rft.pages=165-171&rft.issn=1017-2548&rft.eissn=2234-8530&rft_id=info:doi/&rft_dat=%3Cnurimedia_kisti%3ENODE11541823%3C/nurimedia_kisti%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rft_nurid=NODE11541823&rfr_iscdi=true