Nanochemistry
Alireza Khorshidi; Shahab Shariati; Masoumeh Aboutalebi; Neda Mardazad
Volume 4, Issue 4, pp. 359-490, Serial No. 13 , October 2016, , Pages 476-482
Abstract
Fe3O4 magnetic nanoparticles were synthesized by co-precipitation of Fe2+ and Fe3+ in aqueous NaOH. Then silica was coated on the obtained nanoparticles and the whole composite was functionalized with chlorosulfonic acid in CH2Cl2. The obtained nanocomposite (Fe3O4@SiO2-SO3H) was characterized by FT-IR, ...
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Fe3O4 magnetic nanoparticles were synthesized by co-precipitation of Fe2+ and Fe3+ in aqueous NaOH. Then silica was coated on the obtained nanoparticles and the whole composite was functionalized with chlorosulfonic acid in CH2Cl2. The obtained nanocomposite (Fe3O4@SiO2-SO3H) was characterized by FT-IR, VSM and XRD techniques and was used as an efficient catalyst in condensation reaction of indoles and aldehydes, and excellent yields of the desired products were obtained. The catalyst was recycled and used for successive runs with no considerable loss of activity. The indole products in their conjugated form were capable of selective sensing of CN- anion in solution.
Organic chemistry
Ahmad Reza Moosavi-Zare; Mahdi Pouraskar-Borazjani; Zahra Naz
Volume 2, Issue 3, pp. 162-231, Serial No. 4 , July 2014, , Pages 168-172
Abstract
1-Carboxymethyl-3-methylimidazolium chloride {[cmmim]Cl} is utilized as a highly efficient and reusable catalyst for the synthesis of bis(indolyl)methanes by the condensation reaction of indole with arylaldehydes under solvent-free conditions at room temperature. In summary, the presented method have ...
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1-Carboxymethyl-3-methylimidazolium chloride {[cmmim]Cl} is utilized as a highly efficient and reusable catalyst for the synthesis of bis(indolyl)methanes by the condensation reaction of indole with arylaldehydes under solvent-free conditions at room temperature. In summary, the presented method have several advantages including simplicity, low cost, generality, efficiency, clean reaction profile, high yield, short reaction time, ease of product isolation, mild reaction conditions, and good agreement with the green chemistry protocols. In this work, all aldehydes, including benzaldehyde and arylaldehydes possessing electron-withdrawing substituents, electron-releasing substituents and halogens on their aromatic ring, afforded the desired bis(indolyl)metanes in high to excellent yields and in short reaction times.