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1.
Two types of polymer‐supported nanometal catalysts with high catalytic activity and recyclability in water have been developed. One catalyst was composed of linear polystyrene‐stabilized metal nanoparticles (PS‐MtNPs). A palladium catalyst (PS‐PdONPs) was prepared in water by the thermal decomposition of Pd(OAc)2 in the presence of polystyrene. The degree of immobilization of Pd, but not the size of the Pd nanoparticles, was dependent on the molecular weight and cross‐linking of the polystyrene. The PS‐PdONPs exhibited high catalytic activity for Suzuki, Heck, and Sonogashira coupling reactions in water and they could be recycled without loss of activity. Linear polystyrene was also suitable as a stabilizer for in situ generated PdNPs and PtNPs. The second catalyst was a polyion complex that was composed of poly[4‐chloromethylstyrene‐co‐(4‐vinylbenzyl)tributylammonium chloride] and poly(acrylic acid)‐stabilized PdNPs (PIC‐PdNPs). Aggregation and redispersion of PIC‐PdNPs were easily controlled by adjusting the pH value of the solution.  相似文献   

2.
Heterocyclic carbene‐Pd complex was anchored onto the mesoporous silica MCM‐41 which exhibits high catalytic activity in Heck reaction under phosphine free reaction conditions for the reaction of iodo/bromoarenes with olefinic compounds such as butyl acrylate, isopropyl acrylate and styrene. This catalytic system also showed high activity for Sonogashira coupling reaction of various aryl halides under copper, phosphine and solvent‐free reaction conditions. The air and thermally stable catalyst were reused several times without significant loss of its activity. High efficiency of the catalyst along with its recycling ability and the rather low Pd‐loading demonstrated in both Heck and Sonogashira coupling reactions are the merits of the presented catalyst system.  相似文献   

3.
Phosphinated polymer‐incarcerated (PI) Pd catalysts were prepared by immobilization of palladium with phosphinated polymers by using the PI method. The phosphinated PI Pd catalysts showed good catalytic activity without externally added phosphine ligands in the amination of aryl halides for C N bond‐forming reactions, as well as in Suzuki–Miyaura and Sonogashira coupling. No leaching of palladium from the immobilized Pd was observed by fluorescence X‐ray analysis. Furthermore, it was found that immobilization of Pd by the PI process facilitated the suppression of poisoning of the metal by amines. These effects can be ascribed to stabilization of the catalyst by both the phosphine moieties and the benzene rings in the swollen polymer support. The phosphinated PI Pd catalysts could also be recovered by simple filtration and reused several times without leaching of palladium in both the amination and Suzuki–Miyaura coupling reactions.  相似文献   

4.
In this study, a novel heterogeneous palladium catalyst was synthesized by anchoring palladium onto ethylenediaminetetraacetic acid (EDTA)‐coated Fe3O4@SiO2 magnetic nanocomposite and used for the Suzuki and Sonogashira cross‐coupling reactions. The properties of the magnetic catalyst were characterized by FT‐IR, XRD, TEM, FE‐SEM, DLS EDX, XPS, N2 adsorption‐desorption isotherm analysis, TGA, VSM, elemental analysis and the loading level of Pd in catalyst was measured to be 0.51 mmol/g by ICP. The catalyst was used in Suzuki cross‐coupling reactions of various aryl halides, including less reactive chlorobenzenes with phenylboronic acid without any additive or ligand under green conditions. Furthermore, we have reported this recyclable catalytic system for Sonogashira cross‐coupling reactions of various aryl halides (I, Br, Cl) under copper and ligand‐free conditions in the presence of DMF/H2O (1:2/v:v) as a solvent. The magnetic catalyst could also be separated by an external magnet and reused six times without any significant loss of activity.  相似文献   

5.
An interesting silica‐supported iron catalyst was successfully prepared and demonstrated as an efficient heterogeneous catalyst for cross‐coupling reactions of aryl halides. The as‐prepared nanocatalyst was well characterized and found to be highly efficient in Heck reaction under mild and sustainable conditions (water as solvent at 80 °C in short reaction time). Furthermore, the obtained catalyst was used as an efficient, inexpensive and green heterogeneous catalyst for Sonogashira cross‐coupling reactions of various aryl iodides and provided the corresponding products with moderate to good yields. This phosphine, copper and palladium‐free catalyst was simply recovered from the reaction mixture and recycled five times without substantial decrease in its catalytic activity.  相似文献   

6.
In this paper, a highly active, air‐ and moisture‐stable and easily recoverable magnetic nanoparticles tethered mesoionic carbene palladium (II) complex (MNPs‐MIC‐Pd) as nanomagnetic catalyst was successfully synthesized by a simplistic multistep synthesis under aerobic conditions using commercially available inexpensive chemicals for the first time. The synthesized MNPs‐MIC‐Pd nanomagnetic catalyst was in‐depth characterized by numerous physicochemical techniques such as FT‐IR, ICP‐AES, FESEM, EDS, TEM, p‐XRD, XPS, TGA and BET surface area analysis. The prepared MNPs‐MIC‐Pd nanomagnetic catalyst was used to catalyze the Suzuki–Miyaura and Mizoroki–Heck cross‐coupling reactions and exhibited excellent catalytic activity for various substrates under mild reaction conditions. Moreover, MNPs‐MIC‐Pd nanomagnetic catalyst could be easily and rapidly recovered by applying an external magnet. The recovered MNPs‐MIC‐Pd nanomagnetic catalyst exhibited very good catalytic activity up to ten times in Suzuki–Miyaura and five times in Mizoroki–Heck cross‐coupling reactions without considerable loss of its catalytic activity. However, MNPs‐MIC‐Pd nanomagnetic catalyst shows notable advantages such as heterogeneous nature, efficient catalytic activity, mild reaction conditions, easy magnetic work up and recyclability.  相似文献   

7.
We synthesized Ni/Pd core/shell nanoparticles from the consecutive thermal decomposition of metal-surfactant complexes. The nanoparticle catalyst was atom-economically applied for various Sonogashira coupling reactions.  相似文献   

8.
Jana S  Dutta B  Bera R  Koner S 《Inorganic chemistry》2008,47(12):5512-5520
Palladium(0) has been immobilized into the silica-based mesoporous material to develop catalyst Pd(0)-MCM-41, which is found to be highly active in carbon-carbon coupling reactions. [Pd(NH3)4]2+ ions have been incorporated into the mesoporous material during synthesis of MCM-41 and subsequently upon treatments with hydrazine hydrate Pd2+ ions present in mesoporous silica matrix were reduced to Pd(0) almost instantaneously. The catalyst has been characterized by small-angle X-ray diffraction, N2 sorption, and transmission electron microscopy (TEM). TEM and surface area measurements clearly demonstrate that the immobilization of Pd(0) into the mesoporous silica has a significant effect on pore structure of the catalyst. Nevertheless, after immobilization of palladium the meso-porosity of the material is retained, as evidenced in the nitrogen sorption measurement. The TEM micrograph shows that both MCM-41 and Pd(0)-MCM-41 have similar types of external surface morphology; however, Pd(0)-MCM-41 was less ordered. Pd(0)-MCM-41 showed high catalytic activity toward carbon-carbon bond formation reactions like Heck and Sonogashira coupling, as evidenced in high turn-over numbers. In contrast to many other Pd-based catalysts reported so far, Pd(0)-MCM-41 acts as a truly heterogeneous catalyst in C-C coupling reactions. Notably, the new heterogeneous catalyst is found to be efficient in the activation of arylchloride to give impressive conversion in cross coupling (15-45% for Heck and 30% for Sonogashira) reactions under mild conditions.  相似文献   

9.
An efficient heterogeneous Pd catalytic system has been developed, based on immobilization of Pd nanoparticles (PNPs) on a silica‐bonded propylamine–cyanuric–cysteine (SiO2pA–Cyan–Cys) substrate. The synthesized catalyst was characterized by transmission electron microscopy, scanning electron microscopy, FT‐IR, N2 adsorption analysis (BET), TGA and inductively coupled plasma/atomic emission spectroscopy, and catalytic activity of this catalyst was investigated in the Suzuki and Sonogashira cross‐coupling reactions. The catalysts showed excellent performance in these two reactions, including various aryl halide derivatives (except aryl chloride derivatives) with phenylboronic acid and phenylacetylene under green conditions. Moreover, the catalyst was recycled for several runs without any significant loss of catalytic activity. Copyright © 2014 John Wiley & Sons, Ltd.  相似文献   

10.
Screening of different sources of Pd/C shows reagents of highly variable nanoparticle sizes and oxidation states of the metal. Typically, catalysts with higher surface area are viewed as likely to be the more reactive. In this paper a new form of Pd/C, “UC Pd” is described that is shown to contain larger nanoparticles yet it is the most reactive catalyst of those sold commercially for Sonogashira coupling reactions. UC Pd functions efficiently in the absence of a copper co‐catalyst, under very mild and “green” conditions using inexpensive 95 % EtOH at 50 °C. It is also the only form of Pd/C that can be recycled. In side‐by‐side reactions with several commercially available forms of Pd/C, none compete successfully with UC Pd under standardized conditions. Physical data obtained from extensive surface analysis using TEM, XRD, XPS, and CO‐TPD measurements lead to an explanation behind the unique reactivity of this new recyclable form of Pd/C.  相似文献   

11.
Preparation of PVC-supported Pd nanoparticles through the reduction of PdCl2 by a non-toxic and eco-friendly route, employing sodium formate and NaOH in ethanol–water system has been described. The prepared PVC supported Pd nanoparticles were employed as catalyst in the cross coupling reactions, that is, Heck and Sonogashira reactions in water medium to afford the respective products in good to excellent yields.  相似文献   

12.
Cooperation between two different metals plays a crucial role in many synergistic catalytic reactions, such as the Sonogashira C−C cross-coupling reaction, where an interaction between the Pd and Cu centers is proposed in the transmetalation step. Although several heterobimetallic Pd/Cu complexes were proposed as structural models of the active species in Sonogashira coupling, the detailed understanding of the metal–metal cooperation in transmetalation is still lacking in current systems. In this work, we report a stepwise and systematic approach to building heteromultimetallic Pd/Cu assemblies as a tool to study metal–metal cooperativity. We obtained fully characterized Pd/Cu multimetallic assemblies that show reactivity in alkyne activation, formation of catalytically relevant aryl/acetylide species, and C−C elimination, serving as functional models for Sonogashira reaction intermediates. The combined experimental and DFT studies highlight the importance of ligand-controlled coordination geometry, metal–metal distances and dynamics of the multimetallic assembly for transmetalation step.  相似文献   

13.
The baclofen‐MWCNTs‐Pd nanocatalyst was synthesized through covalent grafting of baclofen molecules onto surface‐modified carbon nanotubes and immobilizing Pd nanoparticles by the baclofen ligands. The chemical structure of the produced nanocatalyst was studied by Raman spectroscopy, Fourier transform‐infrared spectroscopy, energy‐dispersive spectroscopy (EDS), elemental mapping and inductively coupled plasma analysis. Also, its surface morphology was determined using the scanning and transmission electron microscopy techniques. Furthermore, the obtained baclofen‐MWCNTs‐Pd nanocatalyst is demonstrated to exhibit very high activity as a heterogeneous phosphine‐free catalyst in Sonogashira cross‐coupling of aryl halides by giving good to excellent yields of different products. In addition, the nanocatalyst can be reused four times without any significant leaching or loss of activity.  相似文献   

14.
Pd(OAc)2‐catalyzed Sonogashira coupling reactions of alkynes and a variety of aryl halides with 1,3‐bis(5‐ferrocenylisoxazoline‐3‐yl)benzene as an efficient non‐phosphorus ligand under copper‐free conditions are presented. The main advantages over previous methodologies include low catalyst loading (0.2 mol% Pd(OAc)2 and 0.4 mol% ferrocenyl bisoxazoline ligand are sufficient for these coupling reactions), less problematic reaction medium (water–dimethylformamide) and more convenient operation (no requirement for nitrogen protection).  相似文献   

15.
A new polystyrene-anchored Pd(II) phenyldithiocarbazate complex is synthesized and characterized. This Pd-complex behaves as an efficient heterogeneous catalyst in the Heck coupling and copper-free Sonogashira coupling reactions under aerobic conditions. Furthermore, the catalyst shows good thermal stability and recyclability.  相似文献   

16.
A variety of unsaturated thioethers have been subjected to cross‐coupling reactions with functionalized zinc reagents in the presence of a transition‐metal catalyst. Three different catalytic systems based on Pd(OAc)2 or [Ni(acac)2] and the ligands S‐Phos or DPE‐Phos gave the best results. N‐Heterocyclic thioethers based on a pyridine, pyrimidine, pyrazine, pyridazine, triazine, benzothiazole, benzoxazole, pyrrole, or quinazoline ring, as well as thiomethylacetylenes, serve as electrophiles in this cross‐coupling reaction. Aryl‐, heteroaryl‐, benzylic, and alkylzinc halides with sensitive functionalities, such as ester, nitrile, or ketone groups react at ambient temperature with unsaturated thioethers using a Ni catalyst. The corresponding Pd‐catalyzed reactions require slightly higher temperatures. Large‐scale cross‐coupling experiments (10–20 mmol) with N‐heterocycles are also reported.  相似文献   

17.
Nanodiamond–graphene core–shell materials have several unique properties compared with purely sp2‐bonded nanocarbons and perform remarkably well as metal‐free catalysts. In this work, we report that palladium nanoparticles supported on nanodiamond–graphene core–shell materials (Pd/ND@G) exhibit superior catalytic activity in CO oxidation compared to Pd NPs supported on an sp2‐bonded onion‐like carbon (Pd/OLC) material. Characterization revealed that the Pd NPs in Pd/ND@G have a special morphology with reduced crystallinity and are more stable towards sintering at high temperature than the Pd NPs in Pd/OLC. The electronic structure of Pd is changed in Pd/ND@G, resulting in weak CO chemisorption on the Pd NPs. Our work indicates that strong metal–support interactions can be achieved on a non‐reducible support, as exemplified for nanocarbon, by carefully tuning the surface structure of the support, thus providing a good example for designing a high‐performance nanostructured catalyst.  相似文献   

18.
Palladium nanoparticle‐incorporated metal–organic framework MIL‐101 (Pd/MIL‐101) was successfully synthesized and characterized using X‐ray diffraction, nitrogen physisorption, X‐ray photoelectron, UV–visible and infrared spectroscopies, and transmission electron microscopy. The characterization techniques confirmed high porosity and high surface area of MIL‐101 and high stability of nano‐size palladium particles. Pd/MIL‐101 nanocomposite was investigated for the Sonogashira cross‐coupling reaction of aryl and heteroaryl bromides with various alkynes under copper‐free conditions. The reusability of the catalyst was tested for up to four cycles without any significant loss in catalytic activity. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

19.
A novel heterogeneous Pd catalyst was synthesized by anchoring Pd(II) onto 4′‐(4‐hydroxyphenyl)‐2,2′:6′,2″‐terpyridine‐coated Fe3O4 (FMNPs@TPy‐Pd). This catalyst has been demonstrated for the first time as a recoverable and reusable heterogeneous nanocatalyst in Suzuki and Heck cross‐coupling reactions. The catalyst is very easy to handle and is environmentally safe and economical. FMNPs@TPy‐Pd was characterized using transmission and scanning electron microscopies, X‐ray diffraction, and Fourier transform infrared and energy‐dispersive X‐ray spectroscopies.  相似文献   

20.
The restriction of decarboxylative cross‐coupling reactions to ortho‐substituted or heterocyclic carboxylate substrates was overcome by holistic optimization of a bimetallic Cu/Pd catalyst system. The combination of a CuI/Me4phen decarboxylation catalyst and a [(MeCN)4Pd](OTf)2/XPhos cross‐coupling catalyst enables the synthesis of biaryls from inexpensive aryl chlorides and potassium benzoates regardless of their substitution pattern.  相似文献   

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