## Abstract We present polarizationโresolved fluorescence measurements of fluorescent molecular rotors 9โ(2โcarboxyโ2โcyanovinyl)julolidine (CCVJ), 9โ(2,2โdicyanovinyl)julolidine (DCVJ), and a __meso__โsubstituted boron dipyrromethene (BODIPYโC~12~). The photophysical properties of these molecules
Fluorescence properties of surface-active styrylcyanine molecular rotors
โ Scribed by M.S.A. Abdel-Mottaleb; A.M.K. Sherief; A.A. Abdel-Azim; M.M. Habashy; L.F.M. Ismail
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- English
- Weight
- 595 KB
- Volume
- 44
- Category
- Article
- ISSN
- 1010-6030
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โฆ Synopsis
This paper reports on some photophysical properties of a newly synthesized styrylcyanine chromogen 1 of electron donor-acceptor type, namely l-cetyl-4-[ 4'-(NJV-dimethylamino)-styryl J -pyridinium bromide. The fluorescence properties of this self-organized surfactant chromogen were studied in non-homogeneous media. Its fluorescence shows a sensitivity to environmental factors which could be exploited profitably as a fluorescence probe in various systems of industrial and biological importance. A remarkable enhancement in its fluorescence efficiency was observed in a rigid ethanol matrix at 77 K and in micellar solutions. Moreover, a considerable edge-excitation red shift was observed in a PMMA matrix at room temperature similar to that found in glassy ethanol. The results provide some information on the free-volume distribution in a PMMA matrix, The changes noted can be rationalized, relative to the shortchain model compound 2, in terms of an enhanced sensitivity of the highly organized and tightly packed molecules 1 to viscosity-torsional reactions between solute and solvent.
๐ SIMILAR VOLUMES
We calculate the time-dependent decay of the surface-plasmon-coupled molecular fluorescence from a SOIU~IOII of drffusmg dye molecules near a metal. Measurements of this slgnal for an ethanol solution of Tb acetylacetonate next to a Ag f&n agree well wwth the calculation when effects due to the non-