Manganese meso-tetra-4-carboxyphenylporphyrin immobilized on MCM-41 as catalyst for oxidation of olefins with different oxygen donors in stoichiometric conditions

2012 ◽  
Vol 16 (03) ◽  
pp. 260-266 ◽  
Author(s):  
Saeed Rayati ◽  
Saeed Zakavi ◽  
Parisa Jafarzadeh ◽  
Omid Sadeghi ◽  
Mostafa M. Amini

Oxidation of olefins with tert-butyl hydroperoxide (TBHP), tetra-n-butylammonium periodate (TBAP) and potassium peroxomonosulfate (Oxone) in the presence of MCM-41 immobilized meso-tetra-4-carboxyphenylporphyrinatomanganese(III) acetate has been studied. The results of this study show better catalytic performance of the heterogonous catalyst using TBHP as oxidant in comparison with Oxone and TBAP in oxidation of the used olefins with the exception of cyclooctene. However, different order of reactivity of various olefins has been observed in the presence of Oxone and TBHP. In spite of the absence of good electron-withdrawing groups at the periphery of porphyrin ligand, the catalyst was recovered and reused (at least four times) without detectable catalyst leaching or a significant loss of the catalytic efficiency. All results have been obtained in the absence of using excess molar ratios of olefin to the oxidant, commonly employed as a strategy to overcome the instability of metalloporphyrins in oxidative conditions.

2012 ◽  
Vol 482-484 ◽  
pp. 985-988
Author(s):  
Qiu Ying Huang ◽  
Wei Liu ◽  
Wen Hao Ye ◽  
Xiu Cheng Zheng

Ti-SBA-15 mesoporous materials with different Si/Ti molar ratios were synthesized via a hydrothermal process and characterized by using various techniques. The effect of Si/Ti molar ratios in the gels on the structure and catalytic efficiency in epoxidation of cyclohexene was discussed in details. The results showed that all the Ti-SBA-15 materials retained SBA-15 mesoporous structure and exhibited good catalytic activity. Furthermore,the sample prepared with Si/Ti =50 exhibited the best catalytic performance under the reaction conditions.


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.


Author(s):  
Mohsen Nikoorazm ◽  
Maryam Khanmoradi ◽  
Masoumeh Sayadian

Introduction:: MCM-41 was synthesized using the sol-gel method. Then two new transition metal complexes of Nickel (II) and Vanadium (IV), were synthesized by immobilization of adenine (6-aminopurine) into MCM-41 mesoporous. The compounds have been characterized by XRD, TGA, SEM, AAS and FT-IR spectral studies. Using these catalysts provided an efficient and enantioselective procedure for oxidation of sulfides to sulfoxides and oxidative coupling of thiols to their corresponding disulfides using hydrogen peroxide at room temperature. Materials and Methods:: To a solution of sulfide or thiol (1 mmol) and H2O2 (5 mmol), a determined amount of the catalyst was added. The reaction mixture was stirred at room temperature for the specific time under solvent free conditions. The progress of the reaction was monitored by TLC using n-hexane: acetone (8:2). Afterwards, the catalyst was removed from the reaction mixture by centrifugation and, then, washed with dichloromethane in order to give the pure products. Results:: All the products were obtained in excellent yields and short reaction times indicating the high activity of the synthesized catalysts. Besides, the catalysts can be recovered and reused for several runs without significant loss in their catalytic activity. Conclusion:: These catalytic systems furnish the products very quickly with excellent yields and VO-6AP-MCM-41 shows high catalytic activity compared to Ni-6AP-MCM-41.


ACS Omega ◽  
2021 ◽  
Vol 6 (5) ◽  
pp. 3875-3883
Author(s):  
Yixuan Huang ◽  
Guangcai Zhang ◽  
Qinhui Zhang

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Shu Fujita ◽  
Kohei Imagawa ◽  
Sho Yamaguchi ◽  
Jun Yamasaki ◽  
Seiji Yamazoe ◽  
...  

AbstractAlthough transition metal phosphides are well studied as electrocatalysts and hydrotreating catalysts, the application of metal phosphides in organic synthesis is rare, and cooperative catalysis between metal phosphides and supports remains unexplored. Herein, we report that a cerium dioxide-supported nickel phosphide nanoalloy (nano-Ni2P/CeO2) efficiently promoted the C-3 alkylation of oxindoles with alcohols without any additives through the borrowing hydrogen methodology. Oxindoles were alkylated with various alcohols to provide the corresponding C-3 alkylated oxindoles in high yields. This is the first catalytic system for the C-3 alkylation of oxindoles with alcohols using a non-precious metal-based heterogeneous catalyst. The catalytic activity of nano-Ni2P/CeO2 was comparable to that reported for precious metal-based catalysts. Moreover, nano-Ni2P/CeO2 was easily recoverable and reusable without any significant loss of activity. Control experiments revealed that the Ni2P nanoalloy and the CeO2 support functioned cooperatively, leading to a high catalytic performance.


Author(s):  
Wei Deng ◽  
Biao Gao ◽  
Ziye Jia ◽  
Dongqi Liu ◽  
Limin Guo

Co-Cr bimetallic oxide with different Co/Cr molar ratios were prepared through a layered double hydroxides (LDHs) derived method. Their physicochemical properties together with catalytic performance for chlorinated aromatics (1, 2-dichlorobenzene...


2015 ◽  
Vol 2015 ◽  
pp. 1-6 ◽  
Author(s):  
Aishwarya Singh Chauhan ◽  
Arunesh Kumar ◽  
Nikhat J. Siddiqi ◽  
B. Sharma

Trichoderma spp. have been reported earlier for their excellent capacity of secreting extracellular α-galactosidase. This communication focuses on the optimization of culture conditions for optimal production of enzyme and its characterization. The evaluation of the effects of different enzyme assay parameters such as stability, pH, temperature, substrate concentrations, and incubation time on enzyme activity has been made. The most suitable buffer for enzyme assay was found to be citrate phosphate buffer (50 mM, pH 6.0) for optimal enzyme activity. This enzyme was fairly stable at higher temperature as it exhibited 72% activity at 60°C. The enzyme when incubated at room temperature up to two hours did not show any significant loss in activity. It followed Michaelis-Menten curve and showed direct relationship with varying substrate concentrations. Higher substrate concentration was not inhibitory to enzyme activity. The apparent Michaelis-Menten constant (Km), maximum rate of reaction (Vmax), Kcat, and catalytic efficiency values for this enzyme were calculated from the Lineweaver-Burk double reciprocal plot and were found to be 0.5 mM, 10 mM/s, 1.30 U mg−1, and 2.33 U mg−1 mM−1, respectively. This information would be helpful in understanding the biophysical and biochemical characteristics of extracellular α-galactosidase from other microbial sources.


2012 ◽  
Vol 20 (3) ◽  
pp. 539-546 ◽  
Author(s):  
Xiucheng Zheng ◽  
Beibei Dong ◽  
Chengyuan Yuan ◽  
Ke Zhang ◽  
Xiangyu Wang

2014 ◽  
Vol 692 ◽  
pp. 240-244
Author(s):  
Gong De Wu ◽  
Xiao Li Wang ◽  
Zhi Li Zhai

A series of transition metal alanine-salicylaldehyde Schiff base chromium (III) complexes immobilized on MCM-41 were prepared and characterized by various physico-chemical measurements such as FIIR, XRD, HRTEM, N2 sorption and elemental analysis. The immobilized complexes were effective and stable catalysts for the epoxidation of styrene and cyclohexene with 30% hydrogen peroxide. Moreover, the metal centers were found to play important roles in the catalytic performance of immobilized complex catalysts.


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