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Neue Sulfobutyl‐haltige Bis(dimethinmerocyanin)‐Farbstoffe mit isolierten Chromophoren im Molekül und deren Aggregationsverhalten in wässeriger Lösung
Author(s) -
Kussler Manfred,
Balli Heinz
Publication year - 1989
Publication title -
helvetica chimica acta
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.74
H-Index - 82
eISSN - 1522-2675
pISSN - 0018-019X
DOI - 10.1002/hlca.19890720403
Subject(s) - chromophore , chemistry , absorption (acoustics) , crystallography , absorption band , molecule , photochemistry , organic chemistry , physics , optics
Novel Bis(dimethinemerocyanine) Dyes with Isolated Chromophores in the Molecule Containing the Sulfobutyl Group and their Aggregation Tendency in Aqueous Solution The bis(dimethinemerocyanine) dyes 7a – c with Chromophores separated by a polymethylene chain as ‘isolator’ are synthesized in good yield. Their aggregation tendency in organic solvents, organic solvents/H 2 O mixtures, and in H 2 O is investigated. In organic solvents, the dyes 7a – b show a splitted absorption band, due to interaction of the two Chromophores of the dye. In H 2 O, 7a exhibits an intense absorption band at 496 nm (ϵ = 224 300 1·mol −1 ·cm −1 ) with a small width \documentclass{article}\pagestyle{empty}\begin{document}$ (\tilde v_{{\raise0.7ex\hbox{$1$} \!\mathord{\left/ {\vphantom {1 2}}\right.\kern-\nulldelimiterspace} \!\lower0.7ex\hbox{$2$}}} = 1000\;{\rm cm}^{ - 1}) $\end{document} and shoulders at 552 and 580 nm. In presence of starch, this absorption band shifts to 617 nm, probably due to J‐aggregation. The dye 7b shows the same spectral behaviour as 7a . In contrast, 7c exhibits an absorption band without splitting in organic solvents; the interaction of the Chromophores has disappeared. In H 2 O and in H 2 O containing starch, 7c shows a wide absorption band, due to interaction of the Chromophores of the dye.

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