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Investigations into Supramolecular Lyotropic Liquid Crystals Based on 1,3,5‐Benzenetricarboxaramides by NMR Spectroscopy

Knoll, Kevin ; Kostner, Tobias ; Lorenz, Christian ; Thiele, Christina M. (2022)
Investigations into Supramolecular Lyotropic Liquid Crystals Based on 1,3,5‐Benzenetricarboxaramides by NMR Spectroscopy.
In: European Journal of Organic Chemistry, 2022 (11)
doi: 10.1002/ejoc.202101490
Artikel, Bibliographie

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Kurzbeschreibung (Abstract)

New supramolecular lyotropic liquid crystals (LLC) based on 1,3,5‐benzenetricarboxamides (BTAs) with n‐alkylaniline sidechains are described. Using NMR spectroscopy, we investigate the effects of different chain lengths along the homologous series and of non‐BTA additives on liquid crystalline behaviour. From this, we attempt to answer two questions: First, how aliphatic chain length and the addition of further aromatic rings affect the self‐assembly process in general and compared to previously reported systems with purely aliphatic sidechains. Second, whether these modifications are suitable to increases the resulting LLC phases’ resilience against disrupting effects of further, non‐BTA additives.

Typ des Eintrags: Artikel
Erschienen: 2022
Autor(en): Knoll, Kevin ; Kostner, Tobias ; Lorenz, Christian ; Thiele, Christina M.
Art des Eintrags: Bibliographie
Titel: Investigations into Supramolecular Lyotropic Liquid Crystals Based on 1,3,5‐Benzenetricarboxaramides by NMR Spectroscopy
Sprache: Englisch
Publikationsjahr: 2022
Ort: Darmstadt
Verlag: Wiley-VCH
Titel der Zeitschrift, Zeitung oder Schriftenreihe: European Journal of Organic Chemistry
Jahrgang/Volume einer Zeitschrift: 2022
(Heft-)Nummer: 11
Kollation: 5 Seiten
DOI: 10.1002/ejoc.202101490
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Kurzbeschreibung (Abstract):

New supramolecular lyotropic liquid crystals (LLC) based on 1,3,5‐benzenetricarboxamides (BTAs) with n‐alkylaniline sidechains are described. Using NMR spectroscopy, we investigate the effects of different chain lengths along the homologous series and of non‐BTA additives on liquid crystalline behaviour. From this, we attempt to answer two questions: First, how aliphatic chain length and the addition of further aromatic rings affect the self‐assembly process in general and compared to previously reported systems with purely aliphatic sidechains. Second, whether these modifications are suitable to increases the resulting LLC phases’ resilience against disrupting effects of further, non‐BTA additives.

Freie Schlagworte: 2H-NMR, BTAs, Lyotropic liquid crystals, Self-assembly, Supramolecular chemistry
Sachgruppe der Dewey Dezimalklassifikatin (DDC): 500 Naturwissenschaften und Mathematik > 540 Chemie
Fachbereich(e)/-gebiet(e): 07 Fachbereich Chemie
07 Fachbereich Chemie > Clemens-Schöpf-Institut
07 Fachbereich Chemie > Clemens-Schöpf-Institut > Fachgebiet Organische Chemie
Hinterlegungsdatum: 02 Aug 2024 12:41
Letzte Änderung: 02 Aug 2024 12:41
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