The direct synthesis of symmetrical disulfides and diselenides by metal–organic framework MOF-199 as an efficient heterogenous catalyst

RSC Advances ◽  
2015 ◽  
Vol 5 (106) ◽  
pp. 87564-87570 ◽  
Author(s):  
Mohammad Soleiman-Beigi ◽  
Issa Yavari ◽  
Fatemeh Sadeghizadeh

The MOF-199 was used as an efficient heterogeneous catalyst for the one-pot synthesis of organic disulfides/diselenides from aryl halides and elemental S/Se in polyethylene glycol (PEG) with good to excellent yields.

ChemCatChem ◽  
2017 ◽  
Vol 9 (11) ◽  
pp. 1992-2000 ◽  
Author(s):  
Davood Azarifar ◽  
Ramin Ghorbani-Vaghei ◽  
Saba Daliran ◽  
Ali Reza Oveisi

2017 ◽  
Vol 41 (15) ◽  
pp. 7108-7115 ◽  
Author(s):  
Hong-Yan Zhang ◽  
Xiao-Peng Hao ◽  
Li-Ping Mo ◽  
Sha-Sha Liu ◽  
Wen-Bo Zhang ◽  
...  

A novel magnetic metal–organic framework, NiFe2O4@MOF-5, was prepared and demonstrated to be a highly efficient catalyst for the one-pot three-component reaction of aldehyde, indole, and kojic acid.


Nanomaterials ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 845
Author(s):  
Faranak Manteghi ◽  
Fatemeh Zakeri ◽  
Owen James Guy ◽  
Zari Tehrani

A chromium-containing metal-organic framework (MOF), MIL-101 (Chromium(III) benzene-1,4-dicarboxylate), was used to catalyze the one pot, three component synthesis of some 2,4,5-trisubstituted imidazoles under solvent-free conditions. The advantages of using this heterogeneous catalyst include short reaction time, high yields, easy and quick isolation of catalyst and products, low amount of catalyst needed, and that the addition of solvent, salt, and additives are not needed. This catalyst is highly efficient and can be recovered at least 5 times with a slight loss of efficiency. The structure of the metal-organic frameworks (MOF) was confirmed by X-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM). Fourier transform infrared spectroscopy (FTIR) and proton nuclear magnetic resonance (HNMR) were performed to confirm some of the synthesized products. Experimental data indicated that the optimum amount of catalyst was 5 mg for benzil (1 mmol), 4-chlorobenzaldehyde (1 mmol), and ammonium acetate (2.5 mmol), and the synthetic route to the various imidazoles is performed in 10 min by 95% yield, an acceptable result rivalling those of other catalysts.


2019 ◽  
Author(s):  
Nikola Cindro ◽  
Martina Tireli ◽  
Tomislav Mrla ◽  
Krunoslav Uzarevic

Milling under controlled and variable heating programs introduces a new level of mechanochemical reactivity beyond what can be achieved by conventional mechanochemical or solution procedures. The methodology is demonstrated on three different systems: C–C bond forming Knoevenagel condensation, selective C–N bond formation for amide/urea synthesis, and solid-state formation of an archetypal open metal-organic framework, MOF-74. In all cases, the application of specific heating regimes enabled significant acceleration of milling reactions and increased overall energy efficiency, use of much milder milling conditions, and unprecedented product selectivity, best demonstrated on the one-pot selective synthesis of four complex products containing combinations of amide, amine or urea functionalities from the same and simple acyl azide and diamine reactants. Principal control over this enhanced reactivity and selectivity stemmed from the application of specific heating regimes to mechanochemical processing accomplished by a new, in-house developed mechanochemical reactor. As even the moderate increase in temperature strongly affects the selectivity and the rate of mechanochemical reactions, the results presented are in line with recent challenges of the accepted theories of mechanochemical reactivity.


2018 ◽  
Vol 47 (27) ◽  
pp. 9096-9102 ◽  
Author(s):  
Xi Wang ◽  
Dandan Lou ◽  
Xiangcheng Lu ◽  
Jianbin Wu ◽  
Ying Mu ◽  
...  

We enhance the proton conductivity of a lanthanide MOF compared to commercial Nafion by the one-pot loading of tetraethylene glycol.


Author(s):  
Nikola Cindro ◽  
Martina Tireli ◽  
Tomislav Mrla ◽  
Krunoslav Uzarevic

Milling under controlled and variable heating programs introduces a new level of mechanochemical reactivity beyond what can be achieved by conventional mechanochemical or solution procedures. The methodology is demonstrated on three different systems: C–C bond forming Knoevenagel condensation, selective C–N bond formation for amide/urea synthesis, and solid-state formation of an archetypal open metal-organic framework, MOF-74. In all cases, the application of specific heating regimes enabled significant acceleration of milling reactions and increased overall energy efficiency, use of much milder milling conditions, and unprecedented product selectivity, best demonstrated on the one-pot selective synthesis of four complex products containing combinations of amide, amine or urea functionalities from the same and simple acyl azide and diamine reactants. Principal control over this enhanced reactivity and selectivity stemmed from the application of specific heating regimes to mechanochemical processing accomplished by a new, in-house developed mechanochemical reactor. As even the moderate increase in temperature strongly affects the selectivity and the rate of mechanochemical reactions, the results presented are in line with recent challenges of the accepted theories of mechanochemical reactivity.


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