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From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding
Published on: March 24, 2018
Third-generation ionic liquids with N-alkylated 1,4-diazabicyclo[2.2.2]octane cations and pelargonate anions
Anna Turguła1, Konrad Stęsik1, Katarzyna Materna1
1Faculty of Chemical Technology, Poznan University of Technology ul. Berdychowo 4 Poznan 60-965 Poland juliusz.pernak@put.poznan.pl.
Abstract:
Ionic liquids that belong to the third-generation designs due to their intended biological activity are compounds with high potential applications as plant-protection products. The present study describes the synthesis and characterization of novel ionic liquids with cations based on the alkyl derivatives of 1,4-diazabicyclo[2.2.2]octane (DABCO) and an anion derived from naturally occurring pelargonic acid. The developed synthesis method allowed obtaining products with a high yield (≥96%), and the liquids were characterized as high-viscosity liquids at room temperature. This allowed classifying the products as ionic liquids (ILs). The structures of the obtained ILs were confirmed on the basis of their NMR and IR spectra as well as by elemental analysis. All the products exhibited surface activity and were capable of partially wetting a hydrophobic surface. The tested ionic liquids exhibited higher herbicidal activity against winter oilseed rape (Brassica napus L.) and common lambsquarters (Chenopodium album L.) at a lower dose compared to a commercial preparation in greenhouse studies. The studied ionic liquids also exhibited different effects as antifeedants on various insect species. The best results were obtained against beetles belonging to the granary weevil species (Sitophilus granarius L.). The relation between the surface-tension-reduction efficiency pC20 and biological activity was investigated. The herbicidal activity was also correlated with the value of the contact angles for the studied pelargonates. All the obtained results indicate that the designed and synthesized ionic liquids possess double biological functions: herbicidal activity and deterrent activity.
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Halogenation is another class of electrophilic addition reactions where a halogen molecule gets added across a π bond. In alkynes, the presence of two π bonds allows for the addition of two equivalents of halogens (bromine or chlorine). The addition of the first halogen molecule forms a trans-dihaloalkene as the major product and the cis isomer as the minor product. Subsequent addition of the second equivalent yields the tetrahalide.
Alkyl Halides
Alkyl halides are halogen-substituted alkanes wherein one or more hydrogen atoms of an alkane is replaced by a halogen atom such as fluorine, chlorine, bromine, or iodine. The carbon atom in an alkyl halide is bonded to the halogen atom, which is sp3-hybridized and exhibits a tetrahedral shape.
Unlike alkyl halides, compounds in which a halogen atom is bonded to an sp2 -hybridized carbon atom of a carbon-carbon double bond (C=C) are called vinyl halides. Whereas aryl...