Imidazolium supported palladium–chloroglycine complex: recyclable catalyst for Suzuki–Miyaura coupling reactions

1-Glycyl-3-methyl imidazolium chloride–palladium(II) complex [[Gmim]Cl–Pd(II)] was found to be a catalyst for the Suzuki–Miyaura reaction with excellent yields with high turnover number (6.5 × 10²–9.4 × 10²).     

Facile and efficient protocols for C–C and C–N bond formation reactions using a superparamagnetic palladium complex as reusable catalyst

Research on Chemical Intermediates - Facile and efficient protocols for some multicomponent coupling reactions such as the Suzuki reaction and synthesis of polyhydroquinoline and...     

An in situ generated CuI/metformin complex as a novel and efficient catalyst for C–N and C–O cross-coupling reactions

An in situ generated complex of copper(I) and a biguanide, namely metformin, was found to be a highly efficient homogeneous catalyst in N/O-arylation reactions. The O-arylation of substituted phenols with various aryl iodides and bromides was also achieved using this copper catalyst to afford diaryl ethers in good to excellent yields in DMF. This heterogeneous copper catalyst also promotes the N-arylation of imidazole with a variety of aryl halides (Cl, Br, I) in acetonitrile.     

Aluminium–SALEN complex: a new catalyst for the enantioselective Michael reaction

A new heterobimetallic complex prepared from a chiral SALEN ligand and Red-Al® was found to catalyse the Michael reaction between various dialkyl malonates and cycloalkenones to give products in high yields with e.e.s of up to 58%.     

Palladium tetrazole–supported complex as an efficient catalyst for the Heck reaction

Abstract  

A tetrazole-supported polymeric ligand has been synthesized. The palladium complex derived from the polymeric material has been evaluated as a catalyst for the Heck reaction of aryl iodides and bromides with styrene to provide the corresponding products in high yields. The reaction proceeded smoothly in the presence of 1 mol% with respect to Pd of catalyst in DMF at 125 or 140 °C within 1–3 h. Recycling studies showed that the catalyst can be readily recovered and reused for several times without significant loss of catalytic activity.     

Palladiumimmobilized on chitosan nanofibers cross-linked by glutaraldehyde as an efficient catalyst for the Mizoroki–Heck reaction

Nonwoven chitosan (CS) nanofiber mats were successfully prepared by the electrospinning of the mixture of CS and poly(ethylene oxide) (PEO) in acetic acid aqueous solution. The CS/PEO fiber mats were treated with glutaraldehyde aqueous solution to stabilize fibers in solution. The concentration of glutaraldehyde is important for incorporating swelling properties in the cross-linked CS/PEO fiber mats. The cross-linked CS/PEO fibers (CCS/PEO fibers) were then used as supports for palladium catalysts in the Mizoroki–Heck reaction. The results of the study demonstrated that the catalytic activities of Pd catalyst supported on CCS/PEO fiber (Pd-CCS/PEO fiber) were highly dependent on the concentration of glutaraldehyde in the cross-linking process. Density functional theory (DFT) calculations indicated that the Schiff bond formed between CS and glutaraldehyde could reduce the energy needed to form a chelate complex between the CCS/PEO fibers and palladium active species. This in turn could decrease the activation energy of the Mizoroki–Heck reactions which occur in the presence of the Pd-CCS/PEO fiber catalysts. The optimized Pd-CCS/PEO fiber catalyst was very efficient and stable in the Mizoroki–Heck reaction of aromatic iodides with olefins.     

Combination of permanent hydrosilylation and reversible Diels–Alder reactions for self-healing poly(dimethylsiloxane) materials with enhanced ageing properties

Poly (dimethylsiloxane)s (PDMS) are widely used in space applications thanks to their transparency, thermal and UV resistance, inter alia. The prolonged exposure of these materials to the geostationary environment leads to the apparition of cracks and changes in their optical properties, this being detrimental to their function. To enhance their lifespan, self-healing PDMS based on a dual network featuring both permanent and reversible units thanks to hydrosilylation and Diels–Alder reactions were designed. The tunable chemical composition of the networks was characterized by proton Nuclear Magnetic Resonance spectroscopy (¹H NMR) and Fourier-transformed infrared-attenuated total reflection (FTIR-ATR) measurements. The thermal and mechanical behaviors of pristine and healed materials were mainly studied by differential scanning calorimetry, dynamic mechanical analysis, and tensiometry. Ageing under proton irradiations was also performed, simulating part of the radiations encountered in geostationary environment. Ultraviolet-visible-near infrared analyses were carried out to compare the materials optical properties both before and after irradiations. Finally, chemical degradation mechanisms were studied by FTIR-ATR analyses and discussed.     

Pd(0)-Schiff-base@MCM-41 as high-efficient and reusable catalyst for C–C coupling reactions

A Pd-Schiff-base grafted on functionalized mesoporous MCM-41 (Pd(0)-Schiff-base@MCM-41) was prepared using a post-grafting procedure and used as a highly efficient and reusable nanostructural catalyst for the carbon–carbon cross-coupling reactions of various aryl halides (including aryl iodide, bromide and chloride) with sodium tetraphenyl borate, phenylboronic acid and butyl acrylate. This catalyst exhibits interesting reactivity through Heck and Suzuki reactions.     

Pd salen complex@CPGO as a convenient,effective heterogeneous catalyst for Suzuki–Miyaura and Heck–Mizoroki cross-coupling reactions

Research on Chemical Intermediates - A Pd(II) Schiff base complex supported on graphene oxide nanosheets (Pd(II) salen@CPGO) has been synthesized and characterized by FT-IR, ICP-AES, XRD, SEM/EDX...     

Organic–inorganic hybrid porous aerogel: efficient catalyst in transesterification reactions

Hybrid silica-based porous aerogels containing propylsulfonic acid and methyl functionalities were prepared by co-condensation route from the corresponding mercaptopropyltriethoxysilane and methyltriethoxysilane precursors using aqueous ammonia as hydrolyzing agent in the absence of any organic templates. The hybrid aerogel was dried under supercritical CO₂ and characterized by SEM, TEM, ¹³C CP-MAS NMR, ²⁹Si MAS NMR, TG/DTA, and nitrogen adsorption/desorption analyses. The hybrid-silica aerogel containing propylsulfonic acid serves as an efficient heterogeneous acid catalyst in transesterification of fatty acid esters with methanol in a batch reactor.     

Synthesis of platinum complexes containing (+)-bornyl- and (−)-menthylammonium in the outer coordination sphere and their catalytic activity in hydrosilylation reactions

Optically active (+)-bornyl- and (−)-menthylammonium platinates were synthesized starting from H₂[PtCl₆] · 4H₂O and hydrochlorides of the corresponding amines. Catalytic activity of the complexes in the hydrosilylation reactions of 1,3-divinyl-1,1,3,3-tetramethyldisiloxane with 1,1,3,3-tetramethyldisiloxane and acetophenone with diphenylsilane was studied. The addition of the siloxanes leads to a predominant formation of β-adduct. Activity of the catalysts, evaluated on the 50% conversion of the substrate, decreases in the following sequence: (−)-(menthylNH₃)₂[PtCl₆] > (Et₃NH)₂[PtCl₆] > (+)-(bornylNH₃)₂[PtCl₄] > (+)-(bornylNH₃)₂[PtCl₆]. Asymmetric induction is observed in the hydrosilylation of aceto-phenone in the presence of (+)-(bornylNH₃)₂[PtCl _n ] (n = 4, 6); (+)-(bornylNH₃)₂[PtCl₆] showed the highest catalytic activity and selectivity. The hydrosilylation of acetophenone gave 1-phenylethoxy(diphenyl)silane, 1-phenylvinyloxy(diphenyl)silane, and 2-phenylethyl-2-diphenylsiloxy(diphenyl)silane as the products. Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 2, pp. 341–349, February, 2008.     

Organically modified montmorillonite and chitosan–phosphotungstic acid complex nanocomposites as high performance membranes for fuel cell applications

Nanocomposite membranes based on polyelectrolyte complex (PEC) of chitosan/phosphotungstic acid (PWA) and different types of montmorillonite (MMT) were prepared as alternative membranes to Nafion for direct methanol fuel cell (DMFC) applications. Fourier transform infrared spectroscopy (FTIR) revealed an electrostatically fixed PWA within the PEC membranes, which avoids a decrease in proton conductivity at practical condition. Various amounts of pristine as well as organically modified MMT (OMMT) (MMT: Cloisite Na, OMMT: Cloisite 15A, and Cloisite 30B) were introduced to the PEC membranes to decrease in methanol permeability and, thus, enhance efficiency and power density of the cells. X-ray diffraction patterns of the nanocomposite membranes proved that MMT (or OMMT) layers were exfoliated in the membranes at loading weights of lower than 3 wt.%. Moreover, the proton conductivity and the methanol permeability as well as the water uptake behavior of the manufactured nanocomposite membranes were studied. According to the selectivity parameter, ratio of proton conductivity to methanol permeability, the PEC/2 wt.% MMT 30B was identified as the optimum composition. The DMFC performance tests were carried out at 70 °C and 5 M methanol feed and the optimum membrane showed higher maximum power density as well as acceptable durability compared to Nafion 117. The obtained results indicated that owing to the relatively high selectivity and power density, the optimum nanocomposite membrane could be considered as a promising polyelectrolyte membrane (PEM) for DMFC applications.     

Pd–Co bimetallic nanoparticles supported on graphene as a highly active catalyst for Suzuki–Miyaura and Sonogashira cross-coupling reactions

Graphene (G) supported Pd–Co bimetallic nanoparticles (NPs) as a highly active catalyst was prepared by a chemical reduction method and used for coupling reactions. With the characterization of X-ray diffraction, X-ray photoelectron spectroscopy, transmission electron microscopy, and Raman spectrum, the composition of resulting Pd–Co material was identified to be alloy structural. The Pd–Co (1:1)/G exhibited the highest catalytic activity for the Sonogashira-type coupling reactions and also exerted satisfied catalytic activity and recycle stability for Suzuki–Miyaura cross-coupling reactions. This Pd–Co/G material also possessed other advantages such as low-cost, easy recycled from reaction system by a magnet for their magnetic property, and easy experimental handling.     

Formation and structure of chitosan–poly(sodium methacrylate) complex nanoparticles

Interpolyelectrolyte complex (IPEC) dispersions were prepared from chitosan and poly(sodium acrylate), NaPMA, by mixing their solutions, at different carboxyl-to-aminium molar ratios, r_CA. Gyration radius was determined by small angle x-ray scattering (SAXS) and showed that, as r_CA was increased, IPEC dimensions decreased and reached a minimum at r_CA?=?0.75, which was considered the ratio at which IPEC cluster dimensions were minimum, following collapse, phase segregation, nucleation, and growth of larger particles. Pair distance distributions, P(r), became narrower up to r_CA?=?0.75, increasing its width from this point. Relaxation-related parameters from dynamic light scattering (DLS) intensity correlation functions (ICFs) identified three main relaxation processes. The fast process, related to free polyelectrolyte molecules random motion disappeared as r_CA, was increased. The other two relaxation processes also were a function of r_CA and presented marked changes at r_CA?=?0.75. At the same value of r_CA, the energy of activation for the average relaxation rate showed the occurrence of a clear change in the nature of IPEC-related interactions. As hydrodynamic diameter, determined by DLS, was much larger than the gyration radius determined by SAXS, IPEC particles could be described as being composed by a core, rich in segregated, insoluble material, enveloped by IPEC soluble clusters, possibly in the form of water-rich gels.     

Nanocrystalline bioactive TiO2–chitosan impedimetric immunosensor for ochratoxin-A

Fourier transform infrared (FT-IR) and UV-visible spectroscopy were used to optimize TiO₂ concentration in chitosan (CS) to develop a sensitive CS/TiO₂ bioactive electrode. Electrochemical impedance spectroscopy (EIS) used to measure electro-activity of these bioactive electrodes associated with enhance oligosaccharide containing –CO groups from degradation of CS molecules. This matrix has free –NH₂ and –OH functional groups due to higher probability of hydrogen and covalent bonding between –OH group in CS molecules with Ti–O–Ti which supported immobilization of rabbit antibodies (IgGs) and proteins. Ochratoxin A (OTA) was detected and showed a linear response up to 10 ng/mL with CS/TiO₂ bio-electrode. The OTA detection sensitivity of 7.5 mM TiO₂ added CS bioactive electrode was four times higher than only CS.     

Iron(III)–salen complex on a polymer scaffold as heterogeneous catalyst for synthesis of benzimidazoles

Research on Chemical Intermediates - Benzimidazoles are important bioactive compounds with diverse applications in the medicinal, industrial, as well as agrochemical fields. In this study, an...     

Unique copper–salen complex: an efficient catalyst for N-arylations of anilines and imidazoles at room temperature

We have reported here the catalytic activity of a unique Cu–salen type complex in N-arylation of anilines with arylboronic acids in water. The protocol is found to be applicable for a wide range of electronically diversified arylboronic acids and anilines with excellent yields of the isolated product. Further the scope of this protocol has been extended to the synthesis of various N-aryl imidazoles in iso-propanol.     

Solid supported Hayashi–Jørgensen catalyst as an efficient and recyclable organocatalyst for asymmetric Michael addition reactions

A comparison of three different catalytic systems for the efficient, asymmetric synthesis of N-({(3R,4R)-4-[(benzyloxy)methyl]pyrrolidin-3-yl}methyl)-N-(2-methylpropyl)benzenesulfonamide 1 (BZN) is described. The presented strategy is based on the organocatalytic Michael addition of aldehyde 2 to trans-nitroalkene 3, and subsequent reductive cyclization. High yields, enantio-, and diastereoselectivities were achieved in the Michael addition by application of a POSS- or Wang resin-supported Hayashi–Jørgensen catalyst.