4.6 Review

Recent Progress on Ionic Liquid-Mediated CO2 Conversion

Journal

ACTA PHYSICO-CHIMICA SINICA
Volume 37, Issue 5, Pages -

Publisher

PEKING UNIV PRESS
DOI: 10.3866/PKU.WHXB202010022

Keywords

CO2; Ionic liquid; Conversion; Catalysis; Value-added chemicals

Funding

  1. National Natural Science Foundation of China [21890761, 21533011]
  2. Beijing Municipal Science & Technology Commission, China [Z191100007219009]

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Efficient utilization of CO2 is crucial for sustainable development, and recent research efforts have focused on converting CO2 into value-added products. Ionic liquids have shown great potential as catalysts for the selective conversion of CO2 into valuable chemicals under mild conditions.
The efficient utilization of carbon dioxide (CO2) as a C1 feedstock is of great significance for green and sustainable development. Therefore, the efficient chemical conversion of CO2 into value-added products has recently attracted a lot of research attention in recent years. The transformation of CO2 generally requires high-energy substrates, specific catalysts, and harsh reaction conditions due to its high thermodynamic stability and kinetic inertness. Consequently, several efforts have been dedicated toward the development of high-performance catalysts and new reaction routes for CO2 conversion over the last few decades. To date, many routes of convert CO2 into value-added chemicals have been proposed, together with the development of heterogeneous and homogeneous catalysts. Among the advanced catalysts reported to date, ionic liquids (ILs) have been widely investigated and show great potential for the efficient, selective, and economical conversion of CO2 into highly valuable products under mild conditions, even under ambient conditions. Some task-specific ILs have been designed with unique functional groups (e.g., -OH, -SO3H, -NH2, -COOH, and -C N), which can act as the solvent, absorbent, activating agent, catalyst, or cocatalyst to realize the transformation of CO2 under metal-free and mild conditions. In addition, a variety of catalytic systems composed of ILs and metal catalysts have also been reported for the transformation of CO2, in which the combination of the IL and metal catalyst is responsible for CO2 conversion with high efficiency. In this review article, we summarize the recent advances in IL-mediated CO2 transformation into chemicals prepared via C-O, C-N, C-S, C-H, and C-C bond forming processes. ILs that can chemically capture CO2 with high capacity are first introduced, which can activate CO2 via the formation of IL-based carbonates or carbamates, thus realizing the transformation of CO2 under metalfree and mild conditions. Recent progress in IL-mediated CO2 transformations to form carbonates and various kinds of Nand S-containing compounds (e.g., oxazolidinones, ureas, benzimidazolones, formamides, methylamines, benzothiazoles, and other chemicals) as well as CO2 hydrogenation to give formic acid, methane, acetic acid, low-carbon alcohols, and hydrocarbons has been summarized in this review with a focus on the reaction routes, catalytic systems, and reaction mechanism. In these reactions, ILs can simultaneously activate the substrate via strong H-bonding in addition to activating CO2, and the cooperative effects among the ionic and molecular species and metal catalysts accomplish the reactions of CO2 with various kinds of substrates to afford a wide range of value-added chemicals. Finally, the shortcomings and perspectives of ILs are discussed. In short, IL-mediated CO2 transformations provide green and effective routes for the synthesis of high-value chemicals, which may have great potential for a wide range of applications.

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