in this paper, fe3o4-chitosan nanoparticles were prepared by the immobilization of chitosan on the surface of fe3o4 nanoparticles. then, the 5-substituted hydantoins were synthesized from the condensation of aldehyde derivatives, ammonium carbonate and zinc cyanide as a well-known cyanating agent by the magnetic fe3o4-chitosan nanoparticles under neat conditions. fe3o4-chitosan nanocatalyst as ...

the magnetically recoverable fe3o4 nanoparticle and the supported brønsted acidic ionic liquid 1-methyl-3-(3-trimethoxysilylpropyl) imidazolium hydrogen sulfate (fe3o4-il-hso4) were synthesized and used as efficient magnetic catalysts for the regioselective thiocyanation of aromatic and heteroaromatic compounds at room temperature in water: ethanol. this procedure provided the target thiocyanat...

a series of fe3o4 supported on mesoporous fdu-12 silica systems were prepared by the hydrothermal conditions. the surface properties of the functionalized catalyst were analyzed by a series of characterization techniques like ftir, xrd, n2 adsorption–desorption and tem. xrd and adsorption–desorption analysis shows that the mesostructure of fdu silica remains intact after fe3o4 modifications, wh...

A magnetically recoverable catalyst consisting of Mn (III) salophen complex was prepared. The synthesized catalyst was characterized by X-ray powder diffraction (XRD), transmission electron microscopy (TEM), vibrating sample magnetometry (VSM), inductively coupled plasma atomic emission spectroscopy (ICP-AES) and Fourier transform infrared (FT-IR). The immobilized catalyst was shown to be an ef...

A magnetically recoverable catalyst consisting of Mn (III) salophen complex was prepared. The synthesized catalyst was characterized by X-ray powder diffraction (XRD), transmission electron microscopy (TEM), vibrating sample magnetometry (VSM), inductively coupled plasma atomic emission spectroscopy (ICP-AES) and Fourier transform infrared (FT-IR). The immobilized catalyst was shown to be an ef...

Chiral amine and polyoxometalate (POM) acids were combined to give highly efficient, stereoselective, and recoverable enamine-based catalysts. Less than 1 mol % of chiral amine loading was sufficient for good catalytic activity, and the catalyst could be recovered and reused 6 times with unchanged enantioselectivity and slightly decreased activity.

An active, recoverable, and recyclable nanocluster catalyst, Au25(SR)18(-), has been developed to catalyze the formation of α,β-unsaturated ketones or aldehydes from propargylic acetates. The catalytic process has been proposed to be initialized by an SN2' addition of OH(-). Moreover, a dramatic solvent effect was observed, for which a rational explanation was provided.

A magnetically recoverable chiral rhodium catalyst exhibited excellent catalytic activity and enantioselectivity in asymmetric transfer hydrogenation of aromatic ketones in aqueous medium, which could be recovered easily via a small magnet and used repetitively ten times without obviously affecting its enantioselectivity.

An efficient and practical synthesis of triaryl and trisindolylmethanes is reported via the bisarylation of aryl aldehydes with activated arenes. The new method features mild solvent-free reaction conditions, in most cases nearly stoichiometric reagent ratios, catalytic amount of the readily available, easily-handled, recoverable and reusable Brønsted acid catalyst o-benzenedisulfonimide.

We have successfully prepared an unsymmetrical analogue of a Katsuki-type salen ligand having a single hydroxyalkyl group at its 6-position, and also its Mn(III) complex; attachment of the complex to a polymer gives a highly enantioselective and recoverable catalyst for epoxidation of 1,2-dihydronaphthalene.