2023
DOI: 10.1016/j.molstruc.2022.134322
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Novel branched liquid crystal oligomers containing azo and Schiff base groups

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Cited by 7 publications
(2 citation statements)
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“…The absorption peak located at 1598–1628 cm –1 stems from the N–H vibration. The peak at 1631 cm –1 corresponded to the CN bond generated by the Schiff base reaction between the primary amine group (−NH 2 ) grafted on the surface of nanosilica and the aldehyde group (−CHO) of dodecanal. In the FT-IR spectrum, amphiphilic SiO 2 Janus nanoparticle samples exhibited CN bonds that were not present in the amino-modified silica sample, indicating that the hydrophobic alkyl chain had been successfully grafted onto SiO 2 –NH 2 nanoparticles.…”
Section: Resultsmentioning
confidence: 99%
“…The absorption peak located at 1598–1628 cm –1 stems from the N–H vibration. The peak at 1631 cm –1 corresponded to the CN bond generated by the Schiff base reaction between the primary amine group (−NH 2 ) grafted on the surface of nanosilica and the aldehyde group (−CHO) of dodecanal. In the FT-IR spectrum, amphiphilic SiO 2 Janus nanoparticle samples exhibited CN bonds that were not present in the amino-modified silica sample, indicating that the hydrophobic alkyl chain had been successfully grafted onto SiO 2 –NH 2 nanoparticles.…”
Section: Resultsmentioning
confidence: 99%
“…When cholesteryl mono-, bis-or tripodal molecules were performed with branched azobenzenes, it was shown that the liquid crystal phase behavior was closely related to the number of mesogenic units and the rigidity and flexibility of the structure. Indeed, the mesophase ranges were widened as the chain length increased in the same series, or when de degree of branching increased [87]. Halogenated (and especially fluorinated) compounds (LC3 series, Figure 5) can exhibit smectic A phase, even with high chain length [88].…”
Section: Liquid Crystalsmentioning
confidence: 99%