A new mesoporous Ce-Mn-LDH-based Co-MOF nano-composite for the green synthesis of tetrazoloquinazolines.

Tannic acid (TA), as a plant polyphenol, has many active sites for chelation with metals, so TA-oligomers (TA-Olig) were used for the first time as ligands on the surface of Ce-Mn-LDH to prepare the layered double hydroxide-based metal-organic framework (Ce-Mn-LDH@CPTMS@TA-Olig@Co-MOF = E) nanocomposite. In this regard, a homogeneous water/ethanol solution was prepared by sol-gel method using polyethylene glycol and ammonia solution, and then TA was converted into a set of oligomers in the presence of formaldehyde. In the next step, Ce-Mn-LDH was prepared in a ratio of 1 : 4 of Ce to Mn, modified with 3-chloropropylmethoxysilane, functionalized by TA-Olig, and then cobalt salt was used to prepare E.

The protocatechuic acid-based deep eutectic solvent-mediated green synthesis of 1,2,4,5-tetrasubstituted imidazoles.

A novel protocatechuic acid-based deep eutectic solvent (ETPPBr/PCA-DES) was prepared by mixing ethyltriphenylphosphonium bromide (ETPPBr) and protocatechuic acid (PCA = 3,4-dihydroxybenzoic acid), and its structure was fully investigated by using the FT-IR, TGA/DTA, densitometer, eutectic point and H NMR techniques. Different molar ratios of ETPPBr to PCA were examined and the eutectic point phase diagram showed that the best ratio for the synthesis of the new DES is the one-to-one ratio of the two starting materials (ETPPBr and PCA). Then, the novel DES was used as a new and capable catalyst for the green synthesis of diverse 1,2,4,5-tetrasubstituted imidazoles a1-a12 from the four-component condensation reaction of phenanthrene-9,10-dione, aromatic amine, aromatic aldehyde, and ammonium acetate with high yields and very short reaction times.