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Updated: Jul 26, 2025

Microwave-assisted Intramolecular Dehydrogenative Diels-Alder Reactions for the Synthesis of Functionalized Naphthalenes/Solvatochromic Dyes
Published on: April 1, 2013
Comparative study of the self-assembly behaviour of 3-chloro-4-hydroxy-phenylazo dyes
Wenke Müller1, Ralf Schweins1, Bernd Nöcker2
1Institut Laue-Langevin, DS/LSS, 71 Avenue des Martyrs, 38000 Grenoble, France. we-mue@gmx.net.
Abstract:
The complexity of intermolecular interactions and the difficulty to predict assembly behaviour solely based on chemical constitution was demonstrated by studying the self-assembly of three one-fold negatively charged 3-chloro-4-hydroxy-phenylazo dyes (Yellow, Blue and Red). Dye self-assembly was investigated using UV/vis- and NMR-spectroscopy, light- and small-angle neutron scattering. Significant differences between the three dyes were observed. While Yellow does not self-assemble, Red assembles into higher-order aggregates and Blue forms well-defined H-aggregate dimers with a dimerization constant of KD = (728 ± 8) L mol-1. Differences between dyes were suggested to emerge from variations in the propensity to form π-π-interactions due to electrostatic repulsion, sterical constraints and hydrogen-bonding interactions.
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