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CO2 Capture and in situ Catalytic Transformation

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CO2 Capture and in situ Catalytic Transformation ( co2-capture-and-situ-catalytic-transformation )

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Fu et al. In situ Catalytic Transformation Yadav, M., Linehan, J. C., Karkamkar, A. J., van der Eide, E., and Heldebrant, D. J. (2014). Homogeneous hydrogenation of CO2 to methyl formate utilizing switchable ionic liquids. Inorg. Chem. 53, 9849–9854. doi: 10.1021/ic501378w Yang, Z. Z., and He, L. N. (2014). Efficient CO2 capture by tertiary amine-functionalized ionic liquids through Li+-stabilized zwitterionic adduct formation. Beilstein J. Org. Chem. 10, 1959–1966. doi: 10.3762/bjoc.10.204 Yang, Z. Z., He, L. N., Gao, J., Liu, A. H., and Yu, B. (2012). Carbon dioxide utilization with C–N bond formation: carbon dioxide capture and subsequent conversion. Energy Environ. Sci. 5, 6602–6639. doi: 10.1039/c2ee02774g Yang, Z. Z., He, L. N., Zhao, Y. N., Li, B., and Yu, B. (2011). CO2 capture and activation by superbase/polyethylene glycol and its subsequent conversion. Energy Environ. Sci. 4, 3971–3975. doi: 10.1039/c1ee02156g Yoshida, M., Komatsuzaki, Y., and Ihara, M. (2008). Synthesis of 5- vinylideneoxazolidin-2-ones by DBU-mediated CO2 -fixation reaction of 4-(benzylamino)-2-butynyl carbonates and benzoates. Org. Lett. 10, 2083–2086. doi: 10.1021/ol800663v Yoshida, M., Mizuguchi, T., and Shishido, K. (2012). Synthesis of oxazolidinones by efficient fixation of atmospheric CO2 with propargylic amines by using a silver/1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) Dual-catalyst system. Chem. Eur. J. 18, 15578–15581. doi: 10.1002/chem.201203366 Yu, B., Cheng, B. B., Liu, W. Q., Li, W., Wang, S. S., Cao, J., et al. (2016). Atmospheric pressure of CO2 as protecting reagent and reactant: efficient synthesis of oxazolidin-2-ones with carbamate salts, aldehydes and alkynes. Adv. Synth. Catal. 358, 90–97. doi: 10.1002/adsc.201500921 Zhang, S., Li, Y. N., Zhang, Y. W., He, L. N., Yu, B., Song, Q. W., et al. (2014). Equimolar carbon absorption by potassium phthalimide and in situ catalytic conversion under mild conditions. ChemSusChem 7, 1484–1489. doi: 10.1002/cssc.201400133 Zhang, Y. G., and Lim, D. S. W. (2015). Synergistic carbon dioxide capture and conversion in porous materials. ChemSusChem 8, 2606–2608. doi: 10.1002/cssc.201500745 Zhang, Z. F., Hu, S. Q., Song, J. L., Li, W. J., Yang, G. Y., and Han, B. X. (2009). Hydrogenation of CO2 to formic acid promoted by a diamine-functionalized ionic liquid. ChemSusChem 2, 234–238. doi: 10.1002/cssc.200800252 Zhang, Z. F., Xie, Y., Li, W. J., Hu, S. Q., Song, J. L., Jiang, T., et al. (2008). Hydrogenation of carbon dioxide is promoted by a task-specific ionic liquid. Angew. Chem. Int. Ed. 47, 1127–1129. doi: 10.1002/ange.2007 04487 Zhang, Z. G., Fan, F. J., Xing, H. B., Yang, Q. W., Bao, Z. B., and Ren, Q. L. (2017). Efficient synthesis of cyclic carbonates from atmospheric CO2 using a positive charge delocalized ionic liquid catalyst. ACS Sustain. Chem. Eng. 5, 2841–2846. doi: 10.1021/acssuschemeng.7b00513 Zhao, T., Hu, X., Wu, Y., and Zhang, Z. (2019). Hydrogenation of CO2 to formate with H2: transition metal free catalyst based on a lewis pair. Angew. Chem. Int. Ed. 58, 722–726. doi: 10.1002/anie.201809634 Zhao, Y. F., Wu, Y. Y., Yuan, G. F., Hao, L. D., Gao, X., Yang, Z. Z., et al. (2016). Azole-anion-based aprotic ionic liquids: functional solvents for atmospheric CO2 transformation into various heterocyclic compounds. Chem. Asian J. 11, 2735–2740. doi: 10.1002/asia.201600281 Zhou, H., Wang, G. X., and Lu, X. B. (2017). CO2 Adducts of a-Carbon Alkylated N-Heterocyclic olefins:highly active organocatalysts for CO2 chemical transformation. Asian J. Org. Chem. 6, 1264–1269. doi: 10.1002/ajoc.2017 00152 Zhou, H., Zhang, W. Z., Liu, C. H., Qu, J. P., and Lu, X. B. (2008). CO2 adducts of N-heterocyclic carbenes: thermal stability and catalytic activity toward the coupling of CO2 with epoxides. J. Org. Chem. 73, 8039–8044. doi: 10.1021/jo801457r Conflict of Interest Statement: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. Copyright © 2019 Fu, You, Li and He. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. Frontiers in Chemistry | www.frontiersin.org 15 July 2019 | Volume 7 | Article 525

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