Source:http://linkedlifedata.com/resource/pubmed/id/19082147
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
19
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pubmed:dateCreated |
2008-12-16
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pubmed:abstractText |
A spontaneous resolution chiral fluorescent system is prepared by using 2-anthracenecarboxylic acid, and racemic (rac)-1-phenylethylamine or rac-1-cyclohexylethylamine. Although chiral functional organic materials are usually prepared using chiral molecules, in this system, a chiral organic fluorophore, which exhibits fluorescence in the solid state, is prepared from achiral and rac molecules.
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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 |
Oct
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pubmed:issn |
1477-0539
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
7
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pubmed:volume |
6
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
3471-5
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pubmed:meshHeading |
pubmed-meshheading:19082147-Absorption,
pubmed-meshheading:19082147-Amines,
pubmed-meshheading:19082147-Anthracenes,
pubmed-meshheading:19082147-Carboxylic Acids,
pubmed-meshheading:19082147-Circular Dichroism,
pubmed-meshheading:19082147-Crystallography, X-Ray,
pubmed-meshheading:19082147-Fluorescence,
pubmed-meshheading:19082147-Stereoisomerism,
pubmed-meshheading:19082147-Time Factors
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pubmed:year |
2008
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pubmed:articleTitle |
Preparation of a spontaneous resolution chiral fluorescent system using 2-anthracenecarboxylic acid.
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pubmed:affiliation |
Department of Applied Chemistry, Faculty of Science and Engineering, Kinki University, 3-4-1 Kowakae, Higashi-Osaka, Osaka 577-8502, Japan. y-imai@apch.kindai.ac.jp
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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