PHOTOHYDRATION REACTION OF 1-(P-NITROPHENYL)-5,5-DIMETHYL-1,3-HEXADIYNE

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dc.contributor.authoreun kyung baekko
dc.contributor.authorsang chul shimko
dc.date.accessioned2013-02-27T19:12:29Z-
dc.date.available2013-02-27T19:12:29Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1995-
dc.identifier.citationJOURNAL OF PHYSICAL ORGANIC CHEMISTRY, v.8, no.11, pp.699 - 705-
dc.identifier.issn0894-3230-
dc.identifier.urihttp://hdl.handle.net/10203/70309-
dc.description.abstractIrradiation of 1-(p-nitrophenyl)-5,5-dimethyl-1,3-hexadiyne (NDHD) in aqueous sulfuric acid yields conjugated allenyl ketones (1 and 2) and beta-dicarbonyl compounds (3 and 4). The products 1 and 2 are primary photoproducts while 3 and 4 are secondary products formed by thermal hydration of the primary photoproducts showing the maximum quantum yield at H-0 = -1.0. A mechanism involving a synchronous addition of hydronium ion (H3O+) to a triplet state of NDHD is proposed.-
dc.languageEnglish-
dc.publisherJOHN WILEY & SONS LTD-
dc.subjectAROMATIC ALKENES-
dc.titlePHOTOHYDRATION REACTION OF 1-(P-NITROPHENYL)-5,5-DIMETHYL-1,3-HEXADIYNE-
dc.typeArticle-
dc.identifier.wosidA1995TJ05000001-
dc.type.rimsART-
dc.citation.volume8-
dc.citation.issue11-
dc.citation.beginningpage699-
dc.citation.endingpage705-
dc.citation.publicationnameJOURNAL OF PHYSICAL ORGANIC CHEMISTRY-
dc.identifier.doi10.1002/poc.610081102-
dc.contributor.nonIdAuthoreun kyung baek-
dc.type.journalArticleArticle-
dc.subject.keywordPlusAROMATIC ALKENES-
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