Using sulfate-functionalized Hf-based metal-organic frameworks as a heterogeneous catalyst for solvent-free synthesis of pyrimido[1,2–a]benzimidazoles via one-pot three-component reaction

Author(s):  
Minh-Huy Dinh Dang ◽  
Linh Ho Thuy Nguyen ◽  
Trang Thi Thu Nguyen ◽  
Ngoc Xuan Dat Mai ◽  
Phuong Hoang Tran ◽  
...  
2020 ◽  
Vol 49 (45) ◽  
pp. 16238-16244 ◽  
Author(s):  
Zihao Wang ◽  
Zongzhe Li ◽  
Marcus Ng ◽  
Phillip J. Milner

We describe the mechanochemical, solvent-free synthesis of metal–organic frameworks using liquid organic base for the first time.


2012 ◽  
Vol 9 (4) ◽  
pp. 2037-2043 ◽  
Author(s):  
Abolghasem Davoodnia ◽  
Bahareh Razavi ◽  
Niloofar Tavakoli-Hoseini

Silica gel-supported polyphosphoric acid (PPA-SiO2) was found to be highly efficient, eco-friendly and recyclable heterogeneous catalyst for the synthesis of 2,4,6-triarylpyridines through one-pot three-component reaction of acetophenone, aryl aldehydes, and ammonium acetate under solvent-free conditions. This method has several advantages, such as simple procedure with an easy work-up, short reaction times, and high yields. Furthermore, the catalyst could be recycled after a simple work-up, and used at least three times without substantial reduction in its catalytic activity.


Catalysts ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 309 ◽  
Author(s):  
Mingming Zheng ◽  
Yanxiang Wang ◽  
Pingyun Feng

A family of heterometallic metal-organic frameworks (MOFs) (CPM200s) harmoniously coexisting as Lewis acids and base (azo) sites were prepared. Seven CPM200s were employed as multifunctional heterogeneous cascade catalysts for the one-pot deacetalization-Knoevenagel reaction in a solvent-free system. Benefiting from the cooperation between Lewis acids from the open metal sites and base sites from the ligands, the CPM200s showed high activity and selectivity for the tandem reaction. The heterometallic 3D porous framework reported here not only offers a combination of two opposite active sites in the same framework of materials but also increases mass transfer of the substrate, thus maximizing the efficiency and substrate selectivity of the bifunctional catalysts. The CPM200s showed the highest turnover frequency (TOF), outperforming that of the reported MOFs in tandem with the deacetalization-Knoevenagel reaction. A strong correlation between the TOF and charge-to-radius ratio (z/r) of metal ions in the CPM200s was observed for the first time. The bifunctional CPM200s catalysts can be reused five times without significant loss of activity.


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.


2011 ◽  
Vol 8 (4) ◽  
pp. 1895-1899 ◽  
Author(s):  
Zahed Karimi Jaber ◽  
S. Zoleykha Abbasi ◽  
Baharak Pooladian ◽  
Marziyeh Jokar

A simple and efficient method have been described for the synthesis of 12-aryl-8,9,10,12-tetrahydrobenzo[a]xanthen-11-one derivatives employing a one-pot, three-component reaction of aryl aldehydes, 2-naphthol and dimedone in the presence of trichloroacetic acid under solvent-free conditions. Also the condensation of 2-naphthol with alkyl or aryl aldehydes in the presence of trichloroacetic acid under solvent-free media to afford the corresponding 14-aryl or alkyl -14H-dibenzo [a.j]xanthenes in excellent yields and short reaction times is described.


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