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dc.contributor.authorShunichi Fukuzumi*
dc.contributor.authorKei Okubo*
dc.date.accessioned2016-08-27T04:08:59Z-
dc.date.available2016-08-27T04:08:59Z-
dc.date.issued2016*
dc.identifier.issn1861-4728*
dc.identifier.issn1861-471X*
dc.identifier.otherOAK-16613*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/218097-
dc.description.abstractPhotochlorination of aromatic substrates by hydrogen chloride with 2,3-dichloro-5,6-cyano-p-benzoquinone (DDQ) occurs efficiently to produce the corresponding monochlorinated products selectively under visible-light irradiation. The yields for the chlorination of phenol were 70% and 18% for p- and o-chlorophenol, respectively, without formation of further chlorinated products. The photoinduced chlorination is initiated by electron transfer from Cl- to the triplet excited state of DDQ. The radical intermediates involved in the photochemical reaction have been detected by time-resolved transient absorption measurements.*
dc.languageEnglish*
dc.publisherWILEY-V C H VERLAG GMBH*
dc.subjectchlorination*
dc.subjectlaser flash photolysis*
dc.subjectphotoinduced electron transfer*
dc.subjectquinone*
dc.subjectradical*
dc.titleAromatic Monochlorination Photosensitized by DDQ with Hydrogen Chloride under Visible-Light Irradiation*
dc.typeArticle*
dc.relation.issue7*
dc.relation.volume11*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage996*
dc.relation.lastpage999*
dc.relation.journaltitleCHEMISTRY-AN ASIAN JOURNAL*
dc.identifier.doi10.1002/asia.201600083*
dc.identifier.wosidWOS:000373920600007*
dc.identifier.scopusid2-s2.0-84960193854*
dc.author.googleOhkubo, Kei*
dc.author.googleFujimoto, Atsushi*
dc.author.googleFukuzumi, Shunichi*
dc.contributor.scopusidShunichi Fukuzumi(35430038100;58409757400)*
dc.contributor.scopusidKei Okubo(7101788990)*
dc.date.modifydate20240401081001*
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자연과학대학 > 화학·나노과학전공 > Journal papers
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