Three new amphiphilic compounds i.e., n‐decyl‐3‐methylpyridinium bromide (a), n‐dodecyl‐3‐methylpyridinium bromide (b), and n‐tetradecyl‐3‐methylpyridinium bromide (c), have been synthesized by condensation reaction and characterized by NMR (1H, 13C) and FTIR spectroscopic techniques. The micellization behavior of the compounds has been studied in ethanol employing conductometry and UV/visible spectroscopy. The critical micellization concentration (CMC) values for compound a, b and c was found to be 0.31, 0.29 and 0.27 m mol L−1, respectively. Effect of temperature on the CMC was checked in the range of 298‐318 K. The thermodynamic parameters such as ΔG, ΔH and ΔS of the micellization process of these surfactants were computed. The negative values of ΔG and positive values of ΔH indicated the spontaneous and endothermic nature of the micellization process. Antimicrobial activities of these amphiphiles showed significant activity against different bacterial strains.
The synthesis of new cationic surfactants i.e., n‐hexyl‐3‐methylpyridium bromide (a) and n‐octyl‐3‐methylpyridium bromide (b), and their characterization using multinuclear nuclear magnetic resonance spectroscopy (NMR) (1H, 13C) and Fourier‐transform infrared spectroscopy (FT‐IR) spectroscopic techniques were reported. The micellization behavior of the synthesized surfactants was studied using conductometry and ultraviolet–Visible spectroscopy. The critical micelle concentration (CMC) of compounds a and b was found to be 0.41 and 0.35 m mol L−1, respectively. The effect of temperature on the CMC of these compounds was examined in the range of 298–318 K and thermodynamic parameters (ΔG, ΔH, and ΔS) of the micellization process were calculated. The antibacterial study of the synthesized surfactants revealed their strong activity against different bacterial strains. Moreover, the interaction of drugs i.e., flurbiprofen and ketoprofen, with the synthesized surfactants was investigated for gaining insights into the role of micelles as drug‐delivery devices. Drug–surfactant interactions were also confirmed via a conductometric method.
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