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Folding-induced exciton coupling in homo- and heterodimers of merocyanine dyes
David Bialas1, Eva Kirchner, Frank Würthner
1Universität Würzburg, Institut für Organische Chemie & Center for Nanosystems Chemistry, Am Hubland, 97074 Würzburg, Germany. wuerthner@chemie.uni-wuerzburg.de.
Abstract:
Two identical or different merocyanine dyes were tethered by a rigid diphenylacetylene spacer unit that enables the folding of the two dyes into co-facially π-stacked structures in solvents of low polarity. Whilst the solvent-dependent absorption spectra of homodimers of identical dyes are easily interpreted as H-aggregates by exciton theory, the spectra of the heterodimers constitute a novel and more interesting case.
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