A Pd confined hierarchically conjugated covalent organic polymer for hydrogenation of nitroaromatics: catalysis, kinetics, thermodynamics and mechanism†‡
Abstract
Herein, we propose a fast and scalable synthesis of a triazine based hierarchically conjugated covalent organic polymer under solvent and additive free conditions through a single step process. The synthesized material CCTP (Cyanuric Chloride-Thiourea-Polymer) was thoroughly characterized by various physicochemical techniques. The CCTP exhibited regular sponginess and excellent chemical as well as thermal stability. The solvent and additive free approach for CCTP synthesis provides a sustainable alternative for classical solvothermal methods. The CCTP was immobilized with Pd (0) and subsequently a heterogeneous material Pd@CCTP was obtained, which was used as an efficient catalyst for the hydrogenation of nitroarenes. The rate constant and Ea were measured to be 2.08 × 10−2 s−1 and 15.67 kJ mol−1 respectively and thereafter other thermodynamic parameters like ΔH, ΔS and ΔG for the hydrogenation of p-nitrophenol were also calculated. The obtained results indicate that the catalytic hydrogenation of p-nitrophenol is a non-spontaneous and endothermic process. We have also investigated the effect of surfactants (NH4OH, FA, and N2) on the reaction performance, and consequently NH4OH and FA both slow down the reaction while N2 doesn't affect the reaction medium. Further, we calculated the rate constant for the hydrogenation of 2,4-dinitrophenol and 2,4,6-trinitrophenol. An array of nitroarenes were further reduced to extend the substrate scope at RT; high TOFs were observed. Besides, Pd@CCTP showed excellent reusability in hydrogenation reactions without evident performance falloff.