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Flash Photolysis of Naphthalenedicarboxylic Anhydrides

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dc.contributor.author Lohmann, J.
dc.date.accessioned 2025-02-07T02:16:35Z
dc.date.available 2025-02-07T02:16:35Z
dc.date.issued 1972
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/17303
dc.description.abstract The 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.iso en en_US
dc.publisher Journal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1972, 68 (5) en_US
dc.subject Chemistry en_US
dc.subject Flash Photolysis en_US
dc.subject Naphthalenedicarboxylic Anhydrides en_US
dc.subject Photochemical Reactions en_US
dc.subject Excited State Dynamics en_US
dc.subject Journal of the Chemical Society : Faraday Transaction - I en_US
dc.title Flash Photolysis of Naphthalenedicarboxylic Anhydrides en_US
dc.type Article en_US


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