| 초록 |
The palladium-catalyzed Suzuki-Miyaura coupling reaction is one of the most important organic transformations for the construction of carbon-carbon bonds. Its widespread use in the synthesis of natural products, pharmaceuticals, agrochemicals, and polymers is a testament to its broad impact on the chemical science. In this aspect, porous organic polymer (POP) have a great potential of palladium immoilized, because their porous structures contain organic functionalities. In this study, POP synthesized by urea reaction because the urea functional group has many sites that can immobilize palladium. The experimental was characterized by FT-IR, XPS, BET, SEM, GC Acknowledgments This study was supported by the National Research Foundation of Korea (grant no.: NRF-2015R1A4A1042434). |
