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First synthesis and electronic properties of diphenothiazine dumbbells bridged by heterocycles

According to cyclic voltammetry, symmetrical dumbbell-shaped phenothiazine dyads bridged by heterocycles show intense electronic coupling between the redox-active phenothiazine moieties. Furthermore, the fluorescence of the pyridyl-bridged derivatives can be controlled by pH change giving reversibly...

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Bibliographic Details
Published in:Organic & biomolecular chemistry 2009-01, Vol.7 (3), p.469-475
Main Authors: Franz, Adam W, Popa, Larisa N, Rominger, Frank, Müller, Thomas J J
Format: Article
Language:English
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Summary:According to cyclic voltammetry, symmetrical dumbbell-shaped phenothiazine dyads bridged by heterocycles show intense electronic coupling between the redox-active phenothiazine moieties. Furthermore, the fluorescence of the pyridyl-bridged derivatives can be controlled by pH change giving reversibly switchable redox-active biselectrophore dyads.
ISSN:1477-0520
1477-0539
DOI:10.1039/b814850c