During the electronic excitation of 4-halo-1-acylnaphthalenes in the presence of a-cyanoenamines one could not only observe the typical cycloaddition, but also substitution of the halogen through C-3 of the cyanoenamine in a high degree. The photoreaction of halogenated 1-acetonaphthones as well as 1-methyl naphthoates with a-cyanoenamines resulted as a rule in two substitution products and regioselective in two "head/tail" 1,2-cycloadducts. One exception is 4-chloro-methyl-1-naphthoate with an additional "head/head"-adduct. The main product in all explored reactions is the E-substitutionproduct. The halogen substituent has an influences on the reaction pathway; 4-bromoacylnaphthalenes show much higher yields of substitutionproduct, which is due to the lower dissociation energy of the C-Br bond. As expected the halogenated methylketones show higher reactivity than the methyl ester. The methylketones prefer 1,2-Cycloadducts with donor-anti and the esters with donor-syn orientation. There is every reason to be ieve that the reaction mechanism for the formation of the substitution products is based on an electron transfer from the olefin to the triplet excited aromatic compound.
| Identifer | oai:union.ndltd.org:DUETT/oai:DUETT:duett-12102002-105512 |
| Date | 11 December 2002 |
| Creators | Schmidt, Monika |
| Contributors | Prof. Dr. phil. Dietrich Döpp, Prof. Dr. rer. nat. Michael Tausch |
| Publisher | Gerhard-Mercator-Universitaet Duisburg |
| Source Sets | Dissertations and other Documents of the Gerhard-Mercator-University Duisburg |
| Language | German |
| Detected Language | English |
| Type | text |
| Format | text/html, application/pdf |
| Source | http://www.ub.uni-duisburg.de/ETD-db/theses/available/duett-12102002-105512/ |
| Rights | unrestricted, I hereby certify that, if appropriate, I have obtained and attached hereto a written permission statement from the owner(s) of each third party copyrighted matter to be included in my thesis, dissertation, or project report, allowing distribution as specified below. I certify that the version I submitted is the same as that approved by my advisory committee. Hiermit erteile ich der Universitaet Duisburg das nicht-ausschliessliche Recht unter den unten angegebenen Bedingungen, meine Dissertation, Staatsexamens- oder Diplomarbeit, meinen Forschungs- oder Projektbericht zu veroeffentlichen und zu archivieren. Ich behalte das Urheberrecht und das Recht das Dokument zu veroeffentlichen und in anderen Arbeiten weiterzuverwenden. |
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