A copper nitride catalyst for the efficient hydroxylation of aryl halides under ligand-free conditions

Author(s):  
Hang Xu ◽  
Sho Yamaguchi ◽  
Takato Mitsudome ◽  
Tomoo Mizugaki

Copper nitride (Cu3N) was used as a heterogeneous catalyst for the hydroxylation of aryl halides under ligand-free conditions. The cubic Cu3N nanoparticles showed high catalytic activity, comparable to those of...

Catalysts ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 656
Author(s):  
Henrietta Kovács ◽  
Krisztina Orosz ◽  
Gábor Papp ◽  
Ferenc Joó ◽  
Henrietta Horváth

Na2[Ir(cod)(emim)(mtppts)] (1) with high catalytic activity in various organic- and aqueous-phase hydrogenation reactions was immobilized on several types of commercially available ion-exchange supports. The resulting heterogeneous catalyst was investigated in batch reactions and in an H-Cube flow reactor in the hydrogenation of phenylacetylene, diphenylacetylene, 1-hexyne, and benzylideneacetone. Under proper conditions, the catalyst was highly selective in the hydrogenation of alkynes to alkenes, and demonstrated excellent selectivity in C=C over C=O hydrogenation; furthermore, it displayed remarkable stability. Activity of 1 in hydrogenation of levulinic acid to γ-valerolactone was also assessed.


RSC Advances ◽  
2016 ◽  
Vol 6 (41) ◽  
pp. 35135-35143 ◽  
Author(s):  
Radoelizo S. Andriamitantsoa ◽  
Jingjing Wang ◽  
Wenjun Dong ◽  
Hongyi Gao ◽  
Ge Wang

The high dispersed –SO3H groups in the framework of MIL-101-Cr–NH–RSO3H ensure high catalytic activity for the condensation of 1,2-diamines with benzil. The catalyst exhibits good stability, general applicability and excellent recycling performance.


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.


RSC Advances ◽  
2015 ◽  
Vol 5 (4) ◽  
pp. 2785-2793 ◽  
Author(s):  
Mahmoud Nasrollahzadeh ◽  
Babak Jaleh ◽  
Parisa Fakhri ◽  
Ali Zahraei ◽  
Esmaeil Ghadery

Various substituted aryl nitrile and 1,2,3-triazole derivatives were prepared by using carbon supported copper nanoparticles (C/Cu NPs) as a heterogeneous catalyst under ligand-free conditions, which provided good to excellent yields.


RSC Advances ◽  
2015 ◽  
Vol 5 (51) ◽  
pp. 40628-40635 ◽  
Author(s):  
Mahmoud Nasrollahzadeh ◽  
S. Mohammad Sajadi ◽  
Mehdi Maham

We report the green synthesis of CuO nanoparticles (CuO NPs) using Tamarix gallica leaf extract and their catalytic activity for N-arylation of nitrogen-containing heterocycles with aryl halides under ligand-free conditions.


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.


2021 ◽  
pp. 174751982110265
Author(s):  
Xinhai Zhang ◽  
Jianhua Qin ◽  
Ruixuan Ma ◽  
Lei Shi

A new copper(II) metal-organic framework is constructed as a sustainable copper heterogeneous catalyst. Cu-DPTCA, with high catalytic activity, can effectively promote the Chan–Lam coupling reaction of arylboronic acids and amines without adding any base or additive.


2018 ◽  
Vol 22 (3) ◽  
pp. 123-128 ◽  
Author(s):  
Yibing Wang ◽  
Jingru Wang ◽  
Bing Wang ◽  
Yingyong Wang ◽  
Guoqiang Jin ◽  
...  

2020 ◽  
Vol 22 (21) ◽  
pp. 7513-7520
Author(s):  
Hong-Rui Tian ◽  
Zhong Zhang ◽  
Shu-Mei Liu ◽  
Tian-Yi Dang ◽  
Zhuo Li ◽  
...  

A POVs-based Cu(i)–MOF was synthesized and utilized as a heterogeneous catalyst for the cyclization of CO2 with propargylic alcohols to obtain value-added α-alkylidene cyclic carbonates, exhibiting high catalytic activity and sustainability.


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