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dc.contributor.authorLohmann, J.-
dc.date.accessioned2025-02-07T02:16:35Z-
dc.date.available2025-02-07T02:16:35Z-
dc.date.issued1972-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/17303-
dc.description.abstractThe naphthalenedicarboxylic anhydrides (1,2-, 2,3- and 1,8-) do not decompose upon irradiation in a polymer-matrix. Their triplet-states are observed in emission and absorption. The half-lives of the triplet-states are 0.4–1.3 s in a polymer-matrix and 1 to 20 µs in the gas phase. The anhydrides decompose in gas phase upon u.-v. irradiation (λ < 300 nm) primarily to the corresponding dehydronaphthalenes (DHNs). The u.-v. spectra of the DHNs exhibit broad absorptions which are assigned to π—π* transitions. 2,3-DHN dimerizes to the extent of 45 %. The rate constant of the dimerization is k300°C=(4 ± 2)× 1010 l. mol–1 s–1 and is larger than the rate constant of the dimerization of dehydrobenzene (DHB). 1,2-DHN and 1,8-DHN dimerize only to a small extent (< 5 %). This is explained by the thermal instability of the dimers under the given conditions or by the preference for polymerization respectively. 55 % of the 1,8-DHN can be trapped by acetylene. In the reaction of 2,3-DHN with DHB the expected products are formed in approximately statistical proportions whereas in the reactions of 1,8-DHN with DHB or with 2,3-DHN the products are not formed in statistical proportion.en_US
dc.language.isoenen_US
dc.publisherJournal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1972, 68 (5)en_US
dc.subjectChemistryen_US
dc.subjectFlash Photolysisen_US
dc.subjectNaphthalenedicarboxylic Anhydridesen_US
dc.subjectPhotochemical Reactionsen_US
dc.subjectExcited State Dynamicsen_US
dc.subjectJournal of the Chemical Society : Faraday Transaction - Ien_US
dc.titleFlash Photolysis of Naphthalenedicarboxylic Anhydridesen_US
dc.typeArticleen_US
Appears in Collections:Journal Articles (before-1995)

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