scholarly journals A Ru-Complex Tethered to a N-Rich Covalent Triazine Framework for Tandem Aerobic Oxidation-Knoevenagel Condensation Reactions

Molecules ◽  
2021 ◽  
Vol 26 (4) ◽  
pp. 838
Author(s):  
Geert Watson ◽  
Parviz Gohari Derakhshandeh ◽  
Sara Abednatanzi ◽  
Johannes Schmidt ◽  
Karen Leus ◽  
...  

Herein, a highly N-rich covalent triazine framework (CTF) is applied as support for a RuIII complex. The bipyridine sites within the CTF provide excellent anchoring points for the [Ru(acac)2(CH3CN)2]PF6 complex. The obtained robust RuIII@bipy-CTF material was applied for the selective tandem aerobic oxidation-Knoevenagel condensation reaction. The presented system shows a high catalytic performance (>80% conversion of alcohols to α, β-unsaturated nitriles) without the use of expensive noble metals. The bipy-CTF not only acts as the catalyst support but also provides the active sites for both aerobic oxidation and Knoevenagel condensation reactions. This work highlights a new perspective for the development of highly efficient and robust heterogeneous catalysts applying CTFs for cascade catalysis.

Synlett ◽  
2019 ◽  
Vol 30 (06) ◽  
pp. 699-702 ◽  
Author(s):  
Yu Hu ◽  
Nan Yao ◽  
Jin Tan ◽  
Yang Liu

A range of multifunctional magnetic metal–organic framework nanomaterials consisting of various mass ratios of the metal–organic framework MIL-53(Fe) and magnetic SiO2@NiFe2O4 nanoparticles were designed, prepared, characterized, and evaluated as heterogeneous catalysts for the Knoevenagel condensation. The as-fabricated nanomaterials, especially the nanocatalyst MIL-53(Fe)@SiO2@NiFe2O4(1.0), showed good catalytic performance in the Knoevenagel condensation at room temperature as a result of synergistic interaction between the Lewis acid iron sites of MIL-53(Fe) and the active sites of the magnetic SiO2@NiFe2O4 nanoparticles. In addition, the heterogeneous catalyst was readily recovered and a recycling test showed that it could be reused for five times without significant loss of its catalytic activity, making it economical and environmentally friendly.


Catalysts ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 712
Author(s):  
Jiequn Wu ◽  
Weiming Hua ◽  
Yinghong Yue ◽  
Zi Gao

A highly efficient bifunctional catalyst of an s-triazine-based carbon-nitride-supported cobalt oxide is developed for the aerobic oxidation–Knoevenagel condensation tandem reaction of benzyl alcohol and malononitrile, whereby 96.4% benzyl alcohol conversion with nearly 100% selectivity towards benzylmalononitrile can be obtained in 6 h at 80 °C. The excellent catalytic performance derives from the high basicity of carbon nitride and strong redox ability of Co species induced by carbon nitride. The catalyst is also quite stable and can be reused without any regeneration treatment, whose product yield is only an 11.5% reduction after four runs.


2019 ◽  
Vol 43 (40) ◽  
pp. 15871-15878 ◽  
Author(s):  
Liu-Juan Yue ◽  
Ying-Ying Liu ◽  
Guo-Hai Xu ◽  
Jian-Fang Ma

One POM-based Cu(i)-hybrid and one Cd(ii) compound have been achieved by a calix[4]arene ligand. They exhibit efficient catalytic abilities for azide–alkyne cycloaddition and Knoevenagel condensation reactions, respectively.


2019 ◽  
Vol 9 (3) ◽  
pp. 811-821 ◽  
Author(s):  
Zhao-Meng Wang ◽  
Li-Juan Liu ◽  
Bo Xiang ◽  
Yue Wang ◽  
Ya-Jing Lyu ◽  
...  

The catalytic activity decreases as –(SiO)3Mo(OH)(O) > –(SiO)2Mo(O)2 > –(O)4–MoO.


RSC Advances ◽  
2015 ◽  
Vol 5 (99) ◽  
pp. 81415-81428 ◽  
Author(s):  
Wei Jie Ang ◽  
Yong Sheng Chng ◽  
Yulin Lam

Fluorous bispidine-type ligands have been developed to demonstrate its bifunctional property as a ligand and base in copper-catalyzed aerobic oxidation, the Knoevenagel condensation and tandem oxidation/condensation in water under mild conditions.


2019 ◽  
Vol 9 (23) ◽  
pp. 6659-6668 ◽  
Author(s):  
Jie Yang ◽  
Haochen Yu ◽  
Yanbing Wang ◽  
Fuyuan Qi ◽  
Haodong Liu ◽  
...  

Pd/CaMn2O4 provides ideal active sites for oxygen adsorption and desorption, resulting in the promoted charge transfer ability and catalytic activity.


2019 ◽  
Vol 6 (2) ◽  
pp. 106-138 ◽  
Author(s):  
Dipika Pan ◽  
Jhuma Ganguly

Introduction:The popularity of chitosan is increasing among the researchers due to its environment friendly nature, high activity and easy approachability. Chitosan based catalysts are not only the most active and selective in catalytic reaction, but their “green” accessibility also makes them promising in organic catalysis. Chitosan is commonly extracted from chitin by alkaline deacetylation and it is the second abundant biopolymer in nature after cellulose. Chitosan based catalysts are advantageous by means of non-metallic activation as it involves small organic molecules. The robustness, nontoxicity, the lack of metal leaching possibility, inertness towards moisture and oxygen, easy handling and storage are the main advantages of organocatalysts. Traditional drawbacks associated with the metal-based heterogeneous catalysts, like longer reaction times during any synthesis, metal-leaching after every reaction and structural instability of the catalyst for prolonged recycling experiments are also very negligible for chitosan based catalysts. Besides, these catalysts can contribute more in catalysis due to their reusability and these special features increase their demand as the functionalized and profitable catalysts.Objective:The thorough description about the preparation of organocatalysts from chitosan and their uniqueness and novel activities in various famous reactions includes as the main aim of this review. Reusable and recycle nature of chitosan based organocatalysts gain the advantages over traditional and conventional catalyst which is further discussed over here.Methods and Discussions:In this article only those reactions are discussed where chitosan has been used both as support in heterogeneous catalysts or used as a catalyst itself without any co-catalyst for some reactions. Owing to its high biodegradability, nontoxicity, and antimicrobial properties, chitosan is widely-used as a green and sustainable polymeric catalyst in vast number of the reactions. Most of the preparations of catalyst have been achieved by exploring the complexation properties of chitosan with metal ions in heterogeneous molecular catalysis. Organocatalysis with chitosan is primarily discussed for carbon-carbon bond-forming reactions, carbon dioxide fixation through cyclo- addition reaction, condensation reaction and fine chemical synthesis reactions. Furthermore, its application as an enantioselective catalyst is also considered here for the chiral, helical organization of the chitosan skeleton. Moreover, another advantage of this polymeric catalyst is its easy recovery and reusability for several times under solvent-free conditions which is also explored in the current article.Conclusion:Important organocatalyzed reactions with either native chitosan or functionalized chitosan as catalysts have attracted great attention in the recent past. Also, chitosan has been widely used as a very promising support for the immobilization of catalytic metals for many reactions. In this review, various reactions have been discussed which show the potentiality of chitosan as catalyst or catalyst support.


2018 ◽  
Vol 47 (9) ◽  
pp. 3059-3067 ◽  
Author(s):  
Tengfei Li ◽  
Wei Zhang ◽  
Wei Chen ◽  
Haralampos N. Miras ◽  
Yu-Fei Song

In this paper, three solid base catalysts of LDH-IL-Cn (n = 4, 8, 12) were synthesized by adopting an exfoliation/assembly approach. The as-prepared catalyst showed excellent activity and selectivity for the Knoevenagel reaction in aqueous solution.


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