Influence of hydrogen bonds and π-π stacking on the self-assembly of aryldipyrrolidones

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Abstract

We report on the self-assembly behaviour in solution and in the solid-state of two newly designed bisdendronized aryldipyrrolidone (BDP and NDP) dyes with two free N-H groups at the lactam positions. Interestingly, while the naphthalene-based NDP self-assembles via π-π-stacking to form conventional columnar liquid-crystalline (LC) assemblies, the smaller benzene-based BDP forms unconventional columnar LC phases with the dyes parallel to the columnar axis, via hydrogen-bonding interactions. This work presents new design principles to modulate hydrogen bonding in dye materials with potential application in optoelectronics.

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Ximenis, P., Rubert, L., Ehmann, H. M. A., & Soberats, B. (2024). Influence of hydrogen bonds and π-π stacking on the self-assembly of aryldipyrrolidones. Organic Chemistry Frontiers, 12(2), 430–436. https://doi.org/10.1039/d4qo01577k

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