Related Experiment Video
Updated: May 13, 2025

Controlling the Size, Shape and Stability of Supramolecular Polymers in Water
Published on: August 2, 2012
Adsorption and aggregation properties of quaternary-ammonium-salt-based gemini surfactants with a glycinate
Shan Wang1, Hiroki Iwase2, Shin-Ichi Takata3
1Department of Chemistry, Faculty of Science, Nara Women's University, Kitauoyanishi-machi, Nara 630-8506, Japan. yoshimura@cc.nara-wu.ac.jp.
Abstract:
Cationic gemini surfactants have promising bioapplications that are limited by the use of halides as counterions, which pose environmental and human health risks. This can be circumvented by using naturally occurring, highly water-soluble, and nontoxic counterions such as amino acids. In this study, we synthesized novel quaternary-ammonium-salt-based cationic gemini surfactants with glycinate as the counterion [2C(2-O-2) Gly, where n is the alkyl chain length, n = 10, 12, 14]. Their adsorption and aggregation properties were investigated by measuring their electrical conductivity, surface tension, and small-angle neutron scattering and compared with those of the corresponding gemini surfactants with a bromide counterion [2C(2-O-2) Br]. The relationship between the surface tension and concentration of 2C(2-O-2) Gly exhibited a unique behavior with a pronounced minimum near the critical micelle concentration. This suggests that 2C(2-O-2) Gly adsorbs densely at the air/water interface through hydrogen bonding between the amino nitrogen of the counterion and hydrogen atoms of water, as well as between the carboxylate oxygen of the counterion and hydrogen atoms of either the amino group or water. In an aqueous solution, 2C(2-O-2) Gly formed small micelles, whose structure transitioned from spherical to ellipsoidal as the concentration increased.
More Related Videos
06:35Construction and Systematical Symmetric Studies of a Series of Supramolecular Clusters with Binary or Ternary Ammonium Triphenylacetates
Published on: February 15, 2016
09:45Construction of Model Lipid Membranes Incorporating G-protein Coupled Receptors GPCRs
Published on: February 5, 2022
Related Concept Videos
Nomenclature of Secondary and Tertiary Amines
Structure of Amines
Basicity of Aliphatic Amines
To measure the basicity of amines, two conventions are generally used. The first defines Kb as the basicity constant for the deprotonation reaction of water by the amine, as presented in Figure 1. Conventionally, lower Kb indicates...
Colloidal precipitates
Basicity of Heterocyclic Aromatic Amines
Physical Properties of Amines