Pd–Fe3O4@C hybrid nanoparticles: preparation, characterization, and their high catalytic activity toward Suzuki coupling reactions

2012 ◽  
Vol 22 (42) ◽  
pp. 22750 ◽  
Author(s):  
Ren Li ◽  
Peng Zhang ◽  
Yiming Huang ◽  
Ping Zhang ◽  
Hao Zhong ◽  
...  
2019 ◽  
Vol 7 (21) ◽  
pp. 13142-13148 ◽  
Author(s):  
Liang-Liang Yang ◽  
Hong-Juan Wang ◽  
Juan Wang ◽  
Yu Li ◽  
Wen Zhang ◽  
...  

A new graphdiyne-based carbon material was synthesized as an ideal substrate for electroless deposition and stabilization of sub-nanometric Pd catalysts, which showed extremely high catalytic activities for the reduction of nitroarenes and Suzuki coupling reactions.


2017 ◽  
Vol 5 (21) ◽  
pp. 10150-10153 ◽  
Author(s):  
Lini Yang ◽  
Qi Zhan ◽  
Zhenni Wang ◽  
Qiang Chen ◽  
Jing Tong ◽  
...  

Au octahedra have been encapsulated into Pd nanoframes to further enhance the catalytic activity of Pd nanoframes toward Suzuki coupling reactions.


2014 ◽  
Vol 16 (23) ◽  
pp. 11178-11181 ◽  
Author(s):  
Hua Yuan ◽  
Hongyang Liu ◽  
Bingsen Zhang ◽  
Liyun Zhang ◽  
Haihua Wang ◽  
...  

A Pd/CNT-SiC monolith prepared by a simple two-step method exhibits robust catalytic activity and recycling ability in Suzuki coupling reactions.


Synlett ◽  
2018 ◽  
Vol 29 (06) ◽  
pp. 717-722 ◽  
Author(s):  
Teruyuki Kondo ◽  
Ryosuke Taniguchi ◽  
Yu Kimura

Ru3(CO)12-catalyzed divergent ring-opening coupling reactions of a cyclopropenone with methyl acrylate (an electron-deficient alkene) are developed. Under an argon atmosphere, a decarbonylative linear codimer is obtained, while cyclopentenones are obtained under carbon monoxide (20 atm) without decarbonylation. While ruthenium complexes show no catalytic activity for the ring-opening cocyclization of cyclopropenones with ethylene (20 atm) or bicyclo[2.2.1]hept-2-ene (2-norbornene), rhodium complexes, especially [RhCl(η4-1,5-cod)]2, show high catalytic activity for the desired cocyclization reactions to give the corresponding cyclopentenones in high yields and selectivities. In addition, [RhCl(η4-1,5-cod)]2 realizes the catalytic ring-opening co­cyclization of cyclopropenones with internal alkynes to give the corresponding cyclopentadienones. In all these reactions, ruthena- or rhodacyclobutenones are considered to be key intermediates, generated by strain-driven oxidative addition of a cyclopropenone C–C bond to an ­active ruthenium or rhodium species.


2015 ◽  
Vol 3 (3) ◽  
pp. 1272-1278 ◽  
Author(s):  
Shujun Xu ◽  
Kunpeng Song ◽  
Tao Li ◽  
Bien Tan

Microporous polymers were synthesised using external cross-linked N-heterocyclic carbene and benzene. These materials can serve as ligands to bind metal ions and demonstrated high catalytic activity for efficient Suzuki–Miyaura coupling reactions.


2018 ◽  
Vol 10 (3) ◽  
pp. 373-377 ◽  
Author(s):  
Farah Qazi ◽  
Zakir Hussain ◽  
Soneela Asghar ◽  
Ghayoor Abbas ◽  
Muhammad Riaz

Synthesis of nanoparticles through green methods is considered to be more eco-friendly and facile as compared to conventional physical and chemical methods. In this work, an environmental friendly method to synthesize palladium nanoparticles (Pd-NPs) by using a fruit extract has been reported. This extract obtained from Malus domestica (apple); acted as a source of reducing agent and functioned as a capping agent as well. The Pd-NPs were monitored and characterized by ultraviolet-visible (UV-Vis) spectroscopy; powder X-rays diffraction (XRD), scanning electron microscopy (SEM) and Fourier-transform infra-red (FT-IR) spectroscopy. FT-IR spectra revealed the presence of abundant amounts of ascorbic acid in the fruit extract which is assumed to reduce the Palladium chloride to Pd-NPs. XRD results confirmed the crystalline nature of Pd-NPs (JCPDS: No. 05-0681, space group: Fm3m (225)). These nanoparticles were further investigated for their catalytic activity towards the Suzuki coupling reactions where by employing only 2 mol% of the catalyst loading these Pd-NPs demonstrated excellent catalytic activity. Progress and completion of reactions were monitored by gas chromatography (GC) while products formed were characterized by gas chromatography-mass spectrometry (GC-MS), FT-IR as well as from their melting points data. Pd-NPs showed excellent catalytic activity; thereby suggesting their potential and scope for various other catalytic transformations.


Small ◽  
2020 ◽  
Vol 16 (43) ◽  
pp. 2001782
Author(s):  
Xueqin Tao ◽  
Ran Long ◽  
Di Wu ◽  
Yangguang Hu ◽  
Ganhua Qiu ◽  
...  

Synthesis ◽  
2017 ◽  
Vol 49 (18) ◽  
pp. 4372-4382 ◽  
Author(s):  
Mohammed Waheed ◽  
Naseem Ahmed

2-Hydroxyindan-1-ones have been efficiently synthesized and successfully applied as ligands in Pd-catalyzed Ullmann type, Suzuki–Miyaura, and Mizoroki–Heck cross-coupling reactions with aryl tosylates and aryl halides. The ligands are air- and moisture-stable and have shown high catalytic activity with Pd(OAc)2 in these cross-coupling reactions. The system tolerates a variety of functional groups in the product and can be re-used at least three times with maximum efficiency.


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