Abstract

Herein, a highly N-rich covalent triazine framework (CTF) is applied as support for a RuIII complex. The bipyridine sites within the CTF provide excellent anchoring points for the [Ru(acac)2(CH3CN)2]PF6 complex. The obtained robust RuIII@bipy-CTF material was applied for the selective tandem aerobic oxidation-Knoevenagel condensation reaction. The presented system shows a high catalytic performance (>80% conversion of alcohols to α, β-unsaturated nitriles) without the use of expensive noble metals. The bipy-CTF not only acts as the catalyst support but also provides the active sites for both aerobic oxidation and Knoevenagel condensation reactions. This work highlights a new perspective for the development of highly efficient and robust heterogeneous catalysts applying CTFs for cascade catalysis.

Highlights

  • The focus in heterogeneous catalysis lies in the development of novel and efficient porous supports with tailor-made functionalities rather than prefabricated materials for targeted liquid phase reactions [4,5]

  • We introduce here an efficient catalytic system for the tandem aerobic oxidationKnoevenagel condensation reaction

  • Our results indicate that the synergistic effects between the N-rich bipy-covalent triazine framework (CTF) and the RuIII complex are beneficial to obtaining a highly active and selective catalyst for tandem catalysis in the absence of any co-oxidant

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Summary

Introduction

The focus in heterogeneous catalysis lies in the development of novel and efficient porous supports with tailor-made functionalities rather than prefabricated materials for targeted liquid phase reactions [4,5]. The recently emerging porous materials, metal–organic frameworks (MOFs) and covalent organic frameworks (COFs) have led to excellent progress in the field [6]. These materials possess a large surface area with regular and accessible pores, and an adjustable skeleton, making them attractive for several purposes of interest [7]. CTFs are formed through a trimerization reaction followed by the subsequent oligomerization of aromatic nitriles [11]

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