Source:http://linkedlifedata.com/resource/pubmed/id/14690221
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
2003-12-23
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pubmed:abstractText |
Contrary to what is known about cis-1,2-diphenylcyclopropane and its derivatives, we find that they have triplet energies of ca. 311 kJ mol(-1), do not undergo intersystem crossing upon direct excitation, undergo the less common adiabatic photoisomerization to the corresponding trans isomers, and show emission from excited 1,3-diradical intermediates.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:status |
PubMed-not-MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
1474-905X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
2
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1101-6
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pubmed:year |
2003
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pubmed:articleTitle |
Photoisomerization of 2,3-diphenylcyclopropane-1-carboxylic acid derivatives.
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pubmed:affiliation |
Department of Chemistry, Tulane University, New Orleans, LA 70118, USA.
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pubmed:publicationType |
Journal Article
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