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91.
《应用有机金属化学》2017,31(4)
A green method for the synthesis of supported Pd nanoparticles (NPs) using pine needle extract as the reducing agent and the extracted residue of pine needle (RPN) as the carrier is described. The Pd/RPN nanocomposites were characterized using Fourier transform infrared, UV–visible, inductively coupled plasma atomic emission and X‐ray photoelectron spectroscopies, transmission electron microscopy and X‐ray diffraction. The spherical Pd NPs had a mean particle size of 3.25 nm and were evenly distributed on the RPN surface. More importantly, the Pd/RPN nanocomposite, as a heterogeneous catalyst, presented superior catalytic activity for the Suzuki coupling reaction. The yield of the reaction of 4‐bromotoluene with phenylboronic acid catalyzed by Pd0.03/RPN reached 98% with low Pd loading (0.1 mmol%) at room temperature for 30 min. In addition, the catalyst could be easily separated by centrifugation and reused at least six times without significant loss of activity. 相似文献
92.
Dr. Yong Guo Dr. Wengang Li Dr. Jingjing Yan Dr. Basem Moosa Dr. Ma'an Amad Prof. Charles J. Werth Prof. Niveen M. Khashab 《化学:亚洲杂志》2012,7(12):2842-2847
Metal‐free fullerene (C60) was found to be an effective catalyst for the reduction of azo groups in basic aqueous solution under UV irradiation in the presence of NaBH4. Use of NaBH4 by itself is not sufficient to reduce the azo dyes without the assistance of a metal catalyst such as Pd and Ag. Experimental and theoretical results suggest that C60 catalyzes this reaction by using its vacant orbital to accept the electron in the bonding orbital of azo dyes, which leads to the activation of the N?N bond. UV irradiation increases the ability of C60 to interact with electron‐donor moieties in azo dyes. 相似文献
93.
《应用有机金属化学》2017,31(5)
Tungstate salt with imidazolium framework is found to be a recoverable and heterogeneous system favouring the highly selective oxidation of primary benzylic alcohols to corresponding aldehydes with 30% H2O2 as a green oxidant under neutral aqueous reaction conditions. Furthermore, in order to demonstrate the recyclability of the catalyst, it was recovered and efficiently reused in seven succeeding reaction cycles without any significant loss. The use of green solvent, very short reaction time with excellent yields and recyclability of the catalyst make this protocol highly advantageous. 相似文献
94.
Mizoroki–Heck and Suzuki–Miyaura reactions mediated by poly(2‐acrylamido‐2‐methyl‐1‐propanesulfonic acid)‐stabilized magnetically separable palladium catalyst
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The purpose of this work was to synthesize and characterize a new magnetic polymer nanosphere‐supported palladium(II) acetate catalyst for reactions requiring harsh conditions. In this regard, an air‐stable, moisture‐stable and highly efficient heterogenized palladium was synthesized by the coordination of palladium(II) acetate with poly(2‐acrylamido‐2‐methyl‐1‐propanesulfonic acid)‐grafted modified magnetic nanoparticles with a core–shell structure. The structure of the newly developed catalyst was characterized using various techniques. The catalytic activity of the resultant nano‐organometallic catalyst was evaluated in Mizoroki–Heck and Suzuki–Miyaura reactions to afford the corresponding coupling products in good to excellent yields. High selectivity as well as outstanding turnover number (14 143, 4900) and turnover frequency (28 296, 7424) values were recorded for the catalyst in Suzuki–Miyaura and Mizoroki–Heck reactions, respectively. Magnetic separation and recycling of the catalyst for at least six runs became possible without any significant loss of efficiency or any detectable palladium leaching. 相似文献
95.
Mixed valent Pd(0)/Pd(II) nano‐sized aggregates supported onto a chemically robust layered zirconium carboxyphosphonate framework is prepared and its catalytic activity in Suzuki‐Miyaura cross coupling reaction is explored. The exceptionally high catalytic efficacy of the heterogeneous catalyst in Suzuki‐Miyaura cross coupling reaction is signified by remarkably short reaction time 2 minutes and high turnover frequency of 1.3 x 104 hr?1. The catalyst can be recycled several times without significant loss of catalytic efficacy, while spectroscopic, structural and microscopic investigations suggest the integrity of the catalyst even after fifth catalytic cycle. The unique ability of the zirconium carboxyphosphonate framework to interact strongly with palladium in dual Pd(0)/Pd(II) oxidation states has been attributed to this remarkable augmentation of catalytic efficacy. 相似文献
96.
A practical heterogeneous palladium‐catalyzed carbonylative Suzuki coupling of aryl iodides with arylboronic acids under carbon monoxide gas‐free conditions has been developed using a bidentate phosphino‐functionalized magnetic nanoparticle‐immobilized palladium(II) complex as catalyst. Formic acid was utilized as the carbon monoxide source with dicyclohexylcarbodiimide as the activator, and a wide variety of biaryl ketones were generated in moderate to high yields. The new heterogeneous palladium catalyst can be prepared via a simple procedure and can easily be separated from a reaction mixture by simply applying an external magnet and recycled up to 10 times without any loss of activity. 相似文献
97.
For the first time, a novel, straightforward and inexpensive route for immobilization of metals in Schiff base complex form is reported applying 2,4‐toluenediisocyanate as a precursor of primary amine group. A nickel(II) Schiff base complex supported on nano‐TiO2 was designed and synthesized as an effective heterogeneous nanocatalyst for organic reactions, and well characterized using various techniques such as Fourier transform infrared spectroscopy, field emission scanning electron microscopy, transmission electron microscopy, X‐ray diffraction, energy‐dispersive X‐ray analysis and thermogravimetric analysis. The catalytic efficiency of the complex was evaluated in selective oxidation of sulfide to sulfoxide by hydrogen peroxide as an oxidant under solvent‐free conditions at room temperature, which successfully resulted in high yield and high conversion of products. Effective factors including solvent type, oxidant and catalyst amount were also optimized. The catalyst shows outstanding reusability and could be impressively recovered for six consecutive cycles without significant change of its catalytic efficiency. 相似文献
98.
A fast and efficient eco‐friendly two‐step preparation of a palladium‐containing mesoporous carbon catalyst ( C1 ) from green and readily available carbon precursors (phloroglucinol and glyoxal), a porogen template (pluronic F‐127) and PdCl2 is described. Catalyst C1 contains ultra‐small Pd nanoparticles (1.2 nm) uniformly dispersed in the carbon network and shows an outstanding activity for Suzuki‐Miyaura reactions in pure water: extremely low amounts of palladium (10 μequiv. in most cases) are sufficient to afford almost palladium‐free products (containing <0.25 ppm of precious metal without further purification steps). 相似文献
99.
Surface modified SPIONs‐Cr(VI) ions‐immobilized organic‐inorganic hybrid as a magnetically recyclable nanocatalyst for rapid synthesis of polyhydroquinolines under solvent‐free conditions at room temperature
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In this work, a magnetic hybrid dichromate nanocomposite with triphenylphosphine surface modified superparamagnetic iron oxide nanoparticles (SPIONs) as a recyclable nanocatalyst was designed, prepared and characterized by Fourier transform infrared spectroscopy (FT‐IR) spectra, X‐ray diffraction (XRD) pattern analysis, vibrating sample magnetometer (VSM) curves, X‐ray fluorescence (XRF) analysis, thermogravimetric analysis (TGA), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) images and dynamic light scattering (DLS) analysis. Then, it was used in a green and efficient procedure for one‐pot multicomponent synthesis of polyhydroquinoline derivatives by the condensation of aldehydes, dimedone or 1,3‐cyclohexadione, ethyl acetoacetate and ammonium acetate. This protocol includes some new and exceptional advantages such as short reaction times, low catalyst loading, high yields, solvent‐free and room temperature conditions, easy separation and reusability of the catalyst. 相似文献
100.
Fe3O4@SiO2@propyltriethoxysilane@o‐phenylendiamine as an environmentally‐benign functionalized silica‐coated magnetic organometallic nanomaterial has been synthesized and characterized by Fourier transforms infrared (FT‐IR) spectroscopy, scanning electron microscopy (SEM) images and energy dispersive X‐ray (EDX) and vibrating sample magnetometer (VSM) analyses. Then, its catalytic activity was investigated for the one‐pot three‐component condensation reaction between dimedone, malononitrile and various substituted aromatic aldehydes to afford the corresponding 2‐amino‐4H‐chromene derivatives under mild reaction conditions. This nanocatalyst can be easily recovered from the reaction mixture by using a magnet and reused for at least five times without significant decrease in catalytic activity. 相似文献