Source:http://linkedlifedata.com/resource/pubmed/id/18399913
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2008-9-2
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pubmed:abstractText |
The BF(3)-catalyzed photodimerization of parent coumarin (1), three 6-alkylcoumarins (2-4) and N-methyl-2-quinolone (5) in dichloromethane was studied by time-resolved UV-vis spectroscopy. The lowest triplet state properties in the absence and presence of BF(3) were outlined, in particular the effect of self-quenching which initiates dimerization. The quantum yield of intersystem crossing (Phi(isc)) of 1-4 increases with BF(3) concentration, approaching Phi(isc) = 0.3. Phi(isc) and the relative quantum yield of dimerization go along, thereby favoring an overall triplet mechanism in both the direct and BF(3)-catalyzed photodimerization. The product ratio of 5 changes strongly with the BF(3) concentration from 100%anti-hh for the free quinolone to 100%syn-ht for the 1:1 complex.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Acids,
http://linkedlifedata.com/resource/pubmed/chemical/Boranes,
http://linkedlifedata.com/resource/pubmed/chemical/Coumarins,
http://linkedlifedata.com/resource/pubmed/chemical/Quinolones,
http://linkedlifedata.com/resource/pubmed/chemical/boron trifluoride
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pubmed:status |
MEDLINE
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pubmed:issn |
0031-8655
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
84
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1224-30
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pubmed:meshHeading |
pubmed-meshheading:18399913-Acids,
pubmed-meshheading:18399913-Boranes,
pubmed-meshheading:18399913-Catalysis,
pubmed-meshheading:18399913-Coumarins,
pubmed-meshheading:18399913-Dimerization,
pubmed-meshheading:18399913-Molecular Structure,
pubmed-meshheading:18399913-Photochemistry,
pubmed-meshheading:18399913-Quantum Theory,
pubmed-meshheading:18399913-Quinolones,
pubmed-meshheading:18399913-Ultraviolet Rays
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pubmed:articleTitle |
Lewis-acid-catalyzed photodimerization of coumarins and N-methyl-2-quinolone.
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pubmed:affiliation |
Max-Planck-Institut für Bioanorganische Chemie, Mülheim an der Ruhr, Germany. goerner@mpi-muelheim.mpg.de
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pubmed:publicationType |
Journal Article
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