magnetic amine-functionalized graphene oxide as a novel and recyclable bifunctional nanocatalyst for solvent-free synthesis of pyrano[3,2-c]pyridine derivatives

The new magnetic amine-functionalized graphene oxide (fe3o4-go-nh2) nanocatalyst was prepared through the reaction of 3-aminopropyltriethoxysilane (aptes) with magnetic graphene oxide (fe3o4-go). it was characterized by xrd, tem, sem, ft-ir and edx techniques. the intrinsic carboxylic acids on the edges of fe3o4-go along with the amine groups post grafted to the surface of fe3o4-go led to preparation of an acid-base bifunctional magnetically recyclable nanocatalyst. it proved to be efficient nanocatalyst for solvent-free synthesis of pyrano[3,2-c]pyridine derivatives under mild reaction conditions with good to excellent yields. this heterogeneous catalyst also exhibited higher activities than acid or base functionalized mesoporous silica, magnetic go or basic al2o3 an even higher than some basic homogeneous catalysts such as triethylamine and piperazine. more importantly, due to the loaded iron oxide nanoparticles, this catalyst could be easily recovered from the reaction mixture using an external magnet and reused without significant decrease in activity even after 7 runs.