In this investigation, we report the synthesis of biodiesel using benzimidazolium-based brønsted acid ionic liquid (BBAIL) catalyst under the influence of ultrasonication. The prepared BBAIL catalyst was characterized by Fourier transform infrared and NMR spectroscopy techniques, and its acidity was determined by the Hammett method with 4-nitroaniline as the indicator. Ultrasonicator horn (22 kHz, 500 W) was used in this work with an on-off cycle of 50-20 s at 70% amplitude. The highest biodiesel yield of 96% was achieved by ultrasonication when 1:10 molar ratio of castor oil to methyl alcohol was used at 50 °C temperature with 9 mol % of the catalyst in just 90 min, which is about 10 times lesser than the process without ultrasonication. At similar conditions, 96% biodiesel yield was obtained in 14 h without ultrasonication. In summary, ultrasonication proved to be an efficient way to improve biodiesel synthesis in less time and BBAIL showed excellent activity toward the conversion of glycerides to synthesize biodiesel. Other important highlights are easy separation of the catalyst and recyclability up to three cycles with small decrease in its activity.
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http://dx.doi.org/10.1021/acsomega.8b02021 | DOI Listing |
J Agric Food Chem
October 2024
Department of Chemistry, Indian Institute of Technology Ropar, Rupnagar 140001, Punjab, India.
The unregulated use of pesticides, industrial discharge of heavy metals, waste, and agricultural runoff may contaminate surface water and groundwater, consequently threatening ecosystems and human health. Thus, the sensitive detection and degradation of pesticides are essential for safety. In this context, herein, we have developed benzimidazolium-based fluorescent surfactant assemblies and , which exhibit aggregation-induced emission enhancement in an aqueous medium.
View Article and Find Full Text PDFChem Commun (Camb)
August 2024
Department of Chemistry, University of Kashmir, Srinagar-190006, J&K, India.
We present the synthesis of a novel benzimidazolium-based surface active ionic liquid (SAIL), 3-dodecyl-1-3λ-benzo[]imidazole chloride, a SAIL with excellent surface activity and self-aggregation tendency whose aqueous micellar solutions offer exceptional solubilizing capacity and electrocatalytic performance for efficient electrocarboxylation of halocarbons.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
June 2024
Department of Nuclear Medicine, Division of Life Sciences and Medicine, the, First Affiliated Hospital of USTC, CAS Key Laboratory of Urban Pollutant Conversion, Anhui Province Key Laboratory of Biomass Clean Energy, Department of Chemistry, University of Science and Technology of China, Hefei, 230026, Anhui, China.
Cascade radical cyclization constitutes an atom- and step-economic route for rapid assembly of polycyclic molecular skeletons. Although an array of redox-active metal catalysts has recently shown robust applications in enabling various catalytic cascade radical processes, the use of free organic radical as the catalyst, which is capable of triggering strategically distinct cascades, has rarely been developed. Here, we disclosed that the benzimidazolium-based N-heterocyclic carbene (NHC)-boryl radical is capable of catalyzing cascade cyclization reactions in both intra- and intermolecular pathways, assembling [5,5] fused bicyclic and [6,6,6] fused tricyclic molecules, respectively.
View Article and Find Full Text PDFR Soc Open Sci
February 2024
Chemistry Department, Faculty of Applied Sciences, Al-Leith University College, Umm Al-Qura University, Makkah 24831, Saudi Arabia.
Owing to the broad applications of quaternary ammonium salts (QAS), we present the synthesis of benzimidazolium-based analogues with variation in the alkyl and alkoxy group at N-1 and N-3 positions. All the compounds were characterized by spectroscopic techniques and found stable to air and moisture both in the solid and solution state. Moreover, molecular structures were established through single-crystal X-ray diffraction studies.
View Article and Find Full Text PDFJ Org Chem
December 2022
Department of Chemistry and Biochemistry, University of Windsor, 401 Sunset Ave., Windsor, ON N9B 3P4, Canada.
Mono- and (bis)benzimidazoliums were evaluated both experimentally and computationally for their potential as pseudopolyrotaxane axle building blocks. Their aggregation and photophysical behavior, along with their potential to form a [2]pseudorotaxane with dibenzyl-24-crown-8, was studied through the synergistic application of 1D/2D and diffusion-ordered NMR spectroscopy, mass spectrometry, ultraviolet-visible and fluorescence spectroscopy, and time-dependent density functional theory. Their photophysical behavior was measured and modeled as a function of protonation state, solvent, and concentration.
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