Exciplex formation between pyrene and guanine in highly polar solvents
Literature Information
Publication Date
2004-02-24
DOI
10.1039/B316315F
Impact Factor
6.222
Authors
Takahiro Kawai, Masashi Ikegami, Tatsuo Arai
View Original
Abstract
Guanine derivatives connected to pyrene with methylene spacers exhibited exciplex emission in highly polar solvents such as N,N-dimethylformamide, acetonitrile, and water. The result will open up a novel approach to synthesis of fluorescent nucleic bases.
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Source Journal
Chemical Communications
CiteScore:
8.6
Self-citation Rate:
4.7%
Articles per Year:
2458
ChemComm publishes urgent research which is of outstanding significance and interest to experts in the field, while also appealing to the journal’s broad chemistry readership. Our communication format is ideally suited to short, urgent studies that are of such importance that they require accelerated publication. Our scope covers all topics in chemistry, and research at the interface of chemistry and other disciplines (such as materials science, nanoscience, physics, engineering and biology) where there is a significant novelty in the chemistry aspects. Major topic areas covered include: Analytical Chemistry Catalysis Chemical Biology and medicinal chemistry Computational Chemistry and Machine Learning Energy and sustainable chemistry Environmental Chemistry Green Chemistry Inorganic Chemistry Materials Chemistry Nanoscience Organic Chemistry Physical Chemistry Polymer Chemistry Supramolecular Chemistry
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2-(4,4-Difluorobutyl)-1H-isoindole-1,3(2H)-dione
CAS Number:
1265341-14-7
Molecular Formula:
C12H11F2NO2
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