Research Info

Home /Direct Synthesis of Anilines ...
Title Direct Synthesis of Anilines Using Copper Immobilized on Triazine-Aminopyridine -Modified MIL-101(Cr) MOF
Type JournalPaper
Keywords Metal-Organic Frameworks; Cross-Coupling; C-C Coupling; Amines
Abstract A novel metal-organic framework consisting of supported triazine-aminopyridine (MIL-101(Cr)-NH-TA-AP) was fabricated by post-synthetic modifications of MIL-101(Cr)-NH2. Utilizing the excellent chelating ability of triazine-aminopyridine, Cu ions are immobilized over the host matrix (MIL-101(Cr)-NH-TA-AP/Cu). Subsequently the material has been catalytically employed in the cross-coupling of aryl halides with ammonium acetate (NH4OAc), as the amine source in the presence of cesium carbonate (Cs2CO3 ) towards the synthesis of diverse aniline derivatives. Some advantages of the synthesized catalyst are high catalytic activity, mild conditions, high thermal stability, and reusability. Moreover, this porous multifunctional nanomaterial can be used as a new support to immobilize other metals in different catalytic reactions.
Researchers Ramin Ghorbani-Vaghei (Third Researcher), (Second Researcher), . . (First Researcher)