A new BiCl3-loaded montmorillonite K10 catalyst has been prepared by solid dispersion method and was characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), and cyclic voltammetry (CV) measurements. BiCl3 loaded K10 (BiCl3-K10) has been used as solid acid catalyst for the synthesis of azine derivatives from benzophenone hydrazone and ketones/aldehydes by ...

Well-dispersed palladium (0) nanoparticles stabilized with phosphonium based ionic liquid were synthesized conveniently and fully characterized. A catalyst system comprising of the Pd(0) nanoparticles and a base was found to be recyclable and efficient for the aminocarbonylation reaction of aryl iodide in ionic liquid media. In the presence of potassium tert-butyloxide, for the relatively stabl...

Recyclable ( -p-cymene)-ruthenium(II) 2-naphthylazo-p-methylphenolate catalyst of formulation [RuCl( -pcymene)(L)] (where L = mono anionic 2-naphthylazo-p-methylphenolate ligand) is shown to be an efficient catalyst for transfer hydrogenation of a wide range of alkyl and aryl ketones in the presence of 2-propanol and KOH.

A novel and green approach for efficient and rapid synthesis of biologically active polyhydroquinoline derivatives via unsymmetric Hantzsch reaction using nanorods Vanadatesulfuric acid (VSA NRs) as a new and recyclable catalyst under solvent-free conditions was reported. The catalyst was characterized by FT-IR, XRD, XRF and TEM analysis. The present method offers several advantages such as sim...

cui nanoparticles as an expedient and recyclable catalyst for the synthesis of n-cyclohexyl-3-aryl-quinoxaline-2-amines in ethanol via a multi-component reaction are established. the products were separated from the catalyst simply by filtration. the catalyst could be recycled and reused for several times without noticeably decreasing the catalytic activity.

Here, we report insights into the new recyclable catalyst 1, (DMAP·saccharin). The DMAP·saccharin-catalysed acylation of alcohols has been successfully carried out more than 8 times. Only 1 mol% of catalyst 1 efficiently promotes acylation with almost equimolar amounts of acid anhydrides, under both base-free and solvent-free conditions.

Cellulose/KI is a very active, selective, stable, and recyclable catalyst for the cycloaddition reactions of CO(2) and epoxides due to the excellent synergetic effect of cellulose and KI. It is found that the hydroxyl groups on the vicinal carbons of cellulose play a key role for the very high efficiency of the catalyst.

The chiral selectivities were altered and high diastereo- and enantio-selectivities of the products were obtained in water medium without adding acid co-catalysts when a primary-tertiary diamine catalyst was immobilized on mesoporous SBA-15 to form a recyclable catalyst for the direct asymmetric aldol reaction of cyclohexanone with p-nitrobenzaldehyde.

Magnetic C-C@Fe3O4 hollow microspheres were prepared by using aerosol-based Fe3O4@C-SiO2 core-shell particles as templates. The magnetic double-shelled microspheres efficiently worked as carriers to load Pt nanoparticles, thus making the catalyst recyclable and reusable.