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      Efficient, selective and sustainable catalysis of carbon dioxide

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          Abstract

          The efficient and selective conversion of CO 2 as a sustainable C 1 resource into valuable chemicals and energy-related products through catalysis is reviewed.

          Abstract

          Performing CO 2 conversion in a cost-effective and environmentally benign manner would be promising and remains challenging due to its thermodynamic stability and kinetic inertness. Herein, we would like to summarise significant advances in organic synthesis using CO 2 with high catalytic efficiency and excellent selectivity towards the target product mainly during the last five years (2012–2016). Achieving an efficient and selective CO 2 conversion depends on the development of metal catalysts (especially functional metal complex catalysis) including main-group metal, typical transition metal and lanthanide series metal as well as organocatalysts e.g. N-heterocyclic carbenes, N-heterocyclic olefins, task-specific ionic liquids, superbases and frustrated Lewis pairs that are able to effectively activate CO 2 and/or the substrate on the basis of the mechanistic understanding at the molecular level. This review just covers typical catalytic transformation of CO 2, for instance, carboxylation, amidation, hydrogenation, and representative green processes like solvent-less, halogen-free that use CO 2 as an ideal carbon-neutral source to prepare valuable compounds with improved atom economy and enhanced sustainability of chemical processes through green catalysis. In particular, in situ catalytic CO 2 conversion, i.e. the combination of carbon capture and subsequent conversion, a recent breakthrough in the CO 2 chemistry field, is also discussed.

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          Most cited references172

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          Transformation of carbon dioxide.

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            An overview of N-heterocyclic carbenes.

            The successful isolation and characterization of an N-heterocyclic carbene in 1991 opened up a new class of organic compounds for investigation. From these beginnings as academic curiosities, N-heterocyclic carbenes today rank among the most powerful tools in organic chemistry, with numerous applications in commercially important processes. Here we provide a concise overview of N-heterocyclic carbenes in modern chemistry, summarizing their general properties and uses and highlighting how these features are being exploited in a selection of pioneering recent studies.
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              Frustrated Lewis Pairs: Metal-free Hydrogen Activation and More

              Sterically encumbered Lewis acid and Lewis base combinations do not undergo the ubiquitous neutralization reaction to form "classical" Lewis acid/Lewis base adducts. Rather, both the unquenched Lewis acidity and basicity of such sterically "frustrated Lewis pairs (FLPs)" is available to carry out unusual reactions. Typical examples of frustrated Lewis pairs are inter- or intramolecular combinations of bulky phosphines or amines with strongly electrophilic RB(C(6)F(5))(2) components. Many examples of such frustrated Lewis pairs are able to cleave dihydrogen heterolytically. The resulting H(+)/H(-) pairs (stabilized for example, in the form of the respective phosphonium cation/hydridoborate anion salts) serve as active metal-free catalysts for the hydrogenation of, for example, bulky imines, enamines, or enol ethers. Frustrated Lewis pairs also react with alkenes, aldehydes, and a variety of other small molecules, including carbon dioxide, in cooperative three-component reactions, offering new strategies for synthetic chemistry.
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                Author and article information

                Journal
                GRCHFJ
                Green Chemistry
                Green Chem.
                Royal Society of Chemistry (RSC)
                1463-9262
                1463-9270
                2017
                2017
                : 19
                : 16
                : 3707-3728
                Affiliations
                [1 ]State Key Laboratory and Institute of Elemento-Organic Chemistry
                [2 ]Collaborative Innovation Centre of Chemical Science and Engineering
                [3 ]Nankai University
                [4 ]Tianjin 300071
                [5 ]P. R. China
                Article
                10.1039/C7GC00199A
                7bb8d4e4-a3b2-4fae-bef8-3c5da2403827
                © 2017
                History

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