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A tetradentate Schiff base (teta), obtained from triethylenetetramine and salicylaldehyde, has been covalently bonded to divinylbenzene cross-linked chloromethylated polystyrene. This chelating ligand, abbreviated as PS-teta (PS = polymeric support), reacts with metal chlorides (Cu2+, Co2+, and Ni2+) in methanol to give polymer-bound transition metal complexes, PS-Cu(II)teta/(Cat-1), PS-Ni(II)teta/(Cat-2), and PS-Co(II)teta/(Cat-3), formation of which has been established by various physiochemical methods and spectroscopic techniques. The catalytic potential of these materials has been tested for the oxidation of various alkenes, alkanes, alcohols, and thioethers in the presence of 30% H2O2 as an oxidant. At the same time, these catalysts are very stable and could be reused in oxidation reactions for more than five times without noticeable loss of their catalytic activity.

A polymer-anchored nickel(II)–phenanthroline complex [polyNi(II)–phen] was synthesized and used effectively as a reusable catalyst in various oxidation reactions in the presence of tert-butylhydroperoxide as an oxidant in acetonitrile medium. The catalyst was characterized with elemental analysis, atomic absorption spectrometry (AAS), thermogravimetric analysis, scanning electron microscopy, and spectrometric methods such as diffuse reflectance spectroscopy, ultraviolet–visible spectroscopy, and Fourier transform infrared spectroscopy. The study of the effects of the time, temperature, oxidant, catalyst concentration, molar ratio of substrate to oxidant, and solvent in the oxidation of styrene individually gave the optimized reaction conditions. Under optimized conditions, the catalyst exhibited good conversions for the oxidation reactions of various olefins, alkanes, aromatic alcohols, and thioethers. The catalyst was easily recovered by simple filtration and reused for more than five times with consistent catalytic activity. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012

A novel polystyrene-supported palladium(II) complex, an excellent and recyclable catalyst, was synthesized for Sonogashira reactions. The present complex shows high catalytic activity for Sonogashira cross-coupling reaction of aryl halides with phenylacetylene under phosphine-free and copper-free reaction conditions in aqueous (DMF–H2O) medium. The catalyst could be reused for at least six reaction cycles with almost unchanged catalytic properties.

Polymer supported Cu(II) catalyst was prepared, characterized and employed for the N-arylation and amination reaction of N–H heterocycles with aryl halides as well as arylboronic acids to afford the corresponding coupled products in good to excellent yields. This catalyst can be used several times with consistent catalytic activity. R1 = H, Me, OMe, COMe, NO2; R2 = H, Me, OMe, Cl, F, CF3, NO2.

Immobilization of copper onto polystyrene provided a polymer-supported copper(II) catalyst, which was effective in cross-coupling reactions between N-containing substrates and arylboronic acids using methanol as a solvent in air under base-free conditions. This catalyst was also effective in N-arylation of imidazole with aryl halides in DMSO using K2CO3 as a base under nitrogen atmosphere. The catalyst was characterized by physico-chemical and spectroscopic techniques. The product N-arylimidazoles and N-arylbenzimidazoles were isolated in good to excellent yields. This copper catalyst was air stable and could be recycled with minimal loss of activity.

A new polymer supported Cu(II) Schiff base complex was synthesized. The solid complex was characterized by Fourier transform infrared spectroscopy (FT-IR), UV–vis diffuse reflectance spectroscopy (DRS), thermogravimetric analysis (TGA) and scanning electron microscope (SEM). Its homogeneous analogue was also prepared. The catalytic performances of the copper complex in oxidation reactions were evaluated for both homogeneous and heterogeneous systems. The copper(II) complex was found to be efficient catalyst for the oxidation of alkenes, alkanes and aromatic alcohols in the presence of hydrogen peroxide as oxidant at room temperature. The catalytic investigation revealed that the solid complex performs better than the homogeneous one as an oxidation catalyst. The solids containing the immobilized complex can be recovered from the reaction medium and reused almost five times, maintaining good catalytic activity. Furthermore, the in vitro toxicity of the ligand and complex was tested against the growth of bacterial species, viz., Staphylococcus aureus and Escherichia coli .

A thiosemicarbazone Cu(II) complex anchored to a polystyrene framework has been synthesized and characterized by analytical and spectroscopic techniques. The complex was found to be a highly active catalyst for the oxidation of various organic substrates including alkenes and alcohols using H2O2 as oxidant. The reaction conditions were optimized with respect to temperature, solvent, oxidant, catalyst amount, and substrate to peroxide ratio. The heterogeneous catalyst was reused five times without significant loss of activity. A comparison between the catalytic activities of this polymer-supported Cu(II) complex and its homogeneous analogue was carried out.

Three polymer-anchored metal complexes (Co, Cu, and Pd) were synthesized and characterized. The catalytic performance of these complexes was tested for the oxidation of olefins and aromatic alcohols. These complexes showed excellent catalytic activity and high selectivity. These complexes selectively gave epoxides and aldehydes from olefins and alcohols, respectively. Individually, the effect of various solvents, oxidants, substrate oxidant molar ratios, temperatures, and catalyst amounts for the oxidation of cyclohexene and benzyl alcohol were studied. Under optimized reaction conditions, 96, 81, and 71% conversions of cyclohexene and 86, 79, and 73% conversions of benzyl alcohol were obtained with Co(II), Cu(II), and Pd(II) catalysts, respectively. The catalytic results reveal that these complexes could be recycled more than five times without much loss in activity. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011

Two copper complexes were synthesized from macroporous chloromethylated polystyrene beads. The first one was prepared by sequential attachment of imidazole and copper acetate with chloromethylated polystyrene-divinyl benzene copolymer, and the second one was prepared from 4-vinylpyridine and copper acetate with chloromethylated polystyrene-divinyl benzene copolymer. These catalysts showed excellent catalytic activity in O-arylation reaction of aryl halides with phenol in dimethylsulfoxide using potassium carbonate at 130 °C under open air conditions to give diaryl ethers in high yields. Less reactive aryl bromides and aryl chlorides have also been shown to react with phenols to give good yields of the diaryl ethers. The effects of various parameters such as solvent, catalyst from different copper salt and base on the reaction system were studied. The reaction is applicable to a wide variety of substituted aryl halides and phenols with different steric and electronic properties. These catalysts were recovered by simple filtration, and the reusability experiments showed that these catalysts can be used five times without much loss in the catalytic activity.

Polymer anchored Cu(II) Schiff base complexes have been prepared and characterized by using scanning electron microscope (SEM), elemental analysis, atomic absorption spectroscopy (AAS), thermogravimetric analysis (TGA), spectrometric methods like diffuse reflectance spectra of solid (DRS) and fourier transform infrared spectroscopy (FTIR). These catalysts show excellent catalytic activity in the O-arylation reaction of aryl halides with phenol in acetonitrile using Cs2CO3 at 70°C under an open air condition to give diaryl ethers in high yields. The effects of various parameters such as solvent, catalyst from different copper salt and base on the reaction system have been studied. The reaction is applicable to a wide variety of substituted aryl halides and phenols with different steric and electronic properties. These catalysts are recovered by simple filtration and the reusability experiments show that these catalysts can be used five times without much loss in the catalytic activity.

Immobilisation of copper acetate onto a modified polystyrene provided a polymer-supported copper(II) Schiff base catalyst, which is effective in the O-arylation reaction of phenols with aryl halides to give diaryl ethers in high yields. This catalyst is air-stable and was recycled for five times with minimal loss of activity.

A polymer-anchored Pd(II) Schiff base complex has been synthesized by reacting a polymeric amine with 2-pyridinecarboxaldehyde to get the polymer-anchored Schiff base, which was then reacted with palladium acetate. The catalyst was characterized by physicochemical and spectroscopic methods. It shows excellent catalytic activity in the Sonogashira coupling of phenylacetylene with aryl halides using triethylamine as a base and copper iodide as a co-catalyst in water under open air at 70 °C. We have also studied the effects of base and solvent on the coupling reaction. Sonogashira reactions of phenylacetylene with a variety of functionalized aryl halides were performed under the optimized reaction conditions. This catalyst gives excellent yields without the use of phosphine ligands. Further experiments showed that the catalyst can be used five times without much loss in the catalytic activity.

A new polystyrene-anchored palladium(II) catalyst has been prepared and characterized by conventional spectroscopic methods and elemental analyses. The catalyst was found to be highly effective for...

A novel polystyrene-supported Pd(II) complex is synthesized and applied as heterogenous catalyst for Sonogashira cross-coupling reactions under copper- and phosphine-free conditions.

The new heterogeneous palladium(II) catalyst can be prepared readily from inexpensive and commercially available starting materials.

The copper(II) Schiff base catalyst is air-stable and can be reused for five times with only minimal loss of activity.