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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1991-6-10
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pubmed:abstractText |
Monoacyl hydrazides based on 5-methyldehydroluciferin and simpler analogs have been synthesized; they proved to be chemiluminescent on treatment with a strong base in DMSO in the presence of oxygen. The light emitters in these cases appear to be the corresponding carboxylate ions; a pathway involving an oxidative decarboxylation was eliminated as a possibility by consideration of the fluorescence wavelengths of the corresponding oxyluciferins. A reaction mechanism for the luminescence involving the possible intermediacy of an azadioxetane is proposed. The corresponding amides were also synthesized; they proved to be equally chemiluminescent to the hydrazides in the dehydroluciferin series.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0031-8655
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
53
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
125-30
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:1902956-Acylation,
pubmed-meshheading:1902956-Amides,
pubmed-meshheading:1902956-Animals,
pubmed-meshheading:1902956-Beetles,
pubmed-meshheading:1902956-Firefly Luciferin,
pubmed-meshheading:1902956-Hydrazines,
pubmed-meshheading:1902956-Luminescence,
pubmed-meshheading:1902956-Structure-Activity Relationship
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pubmed:year |
1991
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pubmed:articleTitle |
The chemiluminescence of amides and monoacyl hydrazides based on firefly dehydroluciferin.
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pubmed:affiliation |
Department of Chemistry, Johns Hopkins University, Baltimore, MD 21218.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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