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.
Cite
CITATION STYLE
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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