Palladium Supported on Oleic Acid-coated Magnetic Nanoparticle as an Efficient Catalyst for Heck Coupling Reaction in Aqueous Media

2014 ◽  
Vol 11 (10) ◽  
pp. 707-712 ◽  
Author(s):  
Ezzat Rafiee ◽  
Ali Ataei ◽  
Mohammad Joshaghani
2015 ◽  
Vol 70 (3) ◽  
pp. 171-176 ◽  
Author(s):  
Shahrzad Abdolmohammadi ◽  
Maryam Afsharpour

AbstractA green, efficient and simple protocol was developed for the synthesis of dihydropyrimido[4,5-d]pyrimidinetrione derivatives via a coupling reaction of 6-aminouracils, aromatic aldehydes and urea in aqueous media in the presence of nano-crystalline CuI at room temperature. The products were obtained in high yields. CuI nanoparticles can be recycled three times without significant loss of catalytic activity.


2014 ◽  
Vol 409 ◽  
pp. 302-309 ◽  
Author(s):  
Ezzat Rafiee ◽  
Ali Ataei ◽  
Shirin Nadri ◽  
Mohammad Joshaghani ◽  
Sara Eavani

2021 ◽  
Vol 11 (11) ◽  
pp. 4822
Author(s):  
Hamed M. Alshammari ◽  
Obaid F. Aldosari ◽  
Mohammad Hayal Alotaibi ◽  
Raja L. Alotaibi ◽  
Mosaed S. Alhumaimess ◽  
...  

Palladium-based carbon catalysts (Pd/C) can be potentially applied as an efficient catalyst for Suzuki–Miyaura and Mizoroki–Heck coupling reactions. Herein, a variety of catalysts of palladium on activated carbon were prepared by varying the content of ‘Pd’ via an in situ reduction method, using hydrogen as a reducing agent. The as-prepared catalysts (0.5 wt % Pd/C, 1 wt % Pd/C, 2 wt % Pd/C and 3 wt % Pd/C) were characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX) and Brunauer–Emmett–Teller (BET) analyses. The catalysts were tested as a coupling catalyst for Suzuki–Miyaura coupling reactions involving aryl halides and phenyl boronic acid. The optimization of the catalyst by varying the palladium content on the activated carbon yielded Pd/C catalysts with very high catalytic activity for Suzuki reactions of aryl halides and a Mizoroki–Heck cross-coupling reaction of 4-bromoanisol and acrylic acid in an aqueous medium. A high ‘Pd’ content and uniform ‘Pd’ impregnation significantly affected the activity of the catalysts. The catalytic activity of 3% Pd/C was found to make it a more efficient catalyst when compared with the other synthesized Pd/C catalysts. Furthermore, the catalyst reusability was also tested for Suzuki reactions by repeatedly performing the same reaction using the recovered catalyst. The 3% Pd/C catalyst displayed better reusability even after several reactions.


RSC Advances ◽  
2016 ◽  
Vol 6 (61) ◽  
pp. 56028-56034 ◽  
Author(s):  
Li Wu ◽  
Bin Yuan ◽  
Mengmeng Liu ◽  
Hongfei Huo ◽  
Yu Long ◽  
...  

A Pd0/Fe3O4-DA/DMG catalyst exhibited excellent catalytic activity toward the Suzuki, Heck and Kumada cross coupling reaction with a high yield. It is an especially efficient catalyst for Suzuki and Heck coupling in water.


Molecules ◽  
2010 ◽  
Vol 15 (2) ◽  
pp. 649-659 ◽  
Author(s):  
Sedat Yaşar ◽  
Emine Özge Özcan ◽  
Nevin Gürbüz ◽  
Bekir Çetinkaya ◽  
İsmail Özdemir

2017 ◽  
Vol 13 ◽  
pp. 1717-1727 ◽  
Author(s):  
Carolina S García ◽  
Paula M Uberman ◽  
Sandra E Martín

Aqueous Mizoroki–Heck coupling reactions under microwave irradiation (MW) were carried out with a colloidal Pd nanocatalyst stabilized with poly(N-vinylpyrrolidone) (PVP). Many stilbenes and novel heterostilbenes were achieved in good to excellent yields starting from aryl bromides and different olefins. The reaction was carried out in a short reaction time and with low catalyst loading, leading to high turnover frequency (TOFs of the order of 100 h−1). The advantages like operational simplicity, high robustness, efficiency and turnover frequency, the utilization of aqueous media and simple product work-up make this protocol a great option for stilbene syntheses by Mizoroki–Heck reaction.


2018 ◽  
Vol 54 (52) ◽  
pp. 7155-7158 ◽  
Author(s):  
Babak Karimi ◽  
Hossein Barzegar ◽  
Hojatollah Vali

An ionic liquid derived highly nitrogen-rich mesoporous carbon supported Au–Pd alloy was found to be an efficient and recyclable catalyst for the Ullmann coupling reaction of various aryl chlorides at room temperature.


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