Recent advances in metal-free catalysts for the synthesis of cyclic carbonates from CO2 and epoxides

doi:10.1016/S1872-2067(15)61085-3

Abstract

Abstract:

The aim of “green chemistry” and “atom economy” is to utilize carbon dioxide and replace harmful reactants such as CO and phosgene for the production of cyclic carbonates. In this paper, metal-free catalysts including organic bases, ionic liquids, supported catalysts, organic copolymers and carbon materials for the synthesis of cyclic carbonates by the cycloaddition of carbon dioxide to epoxides are reviewed. Recent advances in the design of the catalysts and the understanding of the reaction mechanism are summarized and discussed. The synergistic effects of organic bases and hydrogen bond donors, organic bases and nucleophilic anions, hydrogen bond donors and nucleophilic anions and active components and supports are highlighted. The challenge is to develop metal-free catalysts suitable for carbon dioxide capture and fixation. The ultimate goal is to synthesize cyclic carbonates in a flow reactor directly using carbon dioxide from industrial flue gas at ambient temperature and atmospheric pressure. By using synergetic effects, a multi-functional approach can meet the design strategy of metal-free catalysts for carbon dioxide adsorption and activation as well as epoxide ring opening.

Key words: Cycloaddition, Carbon dioxide, Epoxide, Cyclic carbonate, Metal-free catalyst, Synergy

Dong-Hui Lan, Na Fan, Ying Wang, Xian Gao, Ping Zhang, Lang Chen, Chak-Tong Au, Shuang-Feng Yin. Recent advances in metal-free catalysts for the synthesis of cyclic carbonates from CO₂ and epoxides[J]. Chinese Journal of Catalysis, 2016, 37(6): 826-845.

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References

[1] R. Monastersky, Nature, 2013, 497, 13-14.
[2] M. Liu, J. B. Wu, X. D. Zhu, H. L. He, W. X. Jia, W. N. Xiang, Atmo. Environ., 2015, 114, 75-82.
[3] E. V. Kondratenko, G. Mul, J. Baltrusaitis, G. O. Larrazábal, J. Pérez-Ramírez, Energy Environ. Sci., 2013, 6, 3112-3135.
[4] A. A. Lacis, G. A. Schmidt, D. Rind, R. A. Ruedy, Science, 2010, 330, 356-359.
[5] S. Mathesius, M. Hofmann, K. Caldeira, H. J. Schellnhuber, Nat. Clim. Change, 2015, 5, 1107-1113.
[6] W. H. Wang, Y. Himeda, J. T. Muckerman, G. F. Manbeck, E. Fujita, Chem. Rev., 2015, 115, 12936-12937.
[7] M. Aresta, A. Dibenedetto, A. Angelini, Chem. Rev., 2014, 114, 1709-1742.
[8] C. C. Chong, R. Kinjo, Angew. Chem. Int. Ed., 2015, 54, 12116- 12120.
[9] T. Sakakura, J. C. Choi, H. Yasuda, Chem. Rev., 2007, 107, 2365-2387.
[10] A. Padwa, S. S. Murphree, RKIVOC, 2006, 6-33.
[11] V. D'Elia, J. D. A. Pelletier, J. M. Basset, ChemCatChem, 2015, 7, 1906-1917.
[12] S. Klaus, M. W. Lehenmeier, C. E. Anderson, B. Rieger, Coordin. Chem. Rev., 2011, 255, 1460-1479.
[13] Z. Z. Yang, L. N. He, J. Gao, A. H. Liu, B. Yu, Energy Environ. Sci., 2012, 5, 6602-6639.
[14] L. N. He, Y. Du, J. Q. Wang, C. X. Miao, J. L. Wang, Z. Z. Yang, A. H. Liu, B. Yu, Y. N. Li, D. L. Kong, J. Gao, X. Y. Du, B. Li, Q. W. Song, R. Ma, Y. N. Zhao, Z. F. Diao, F. Wu, Chemistry of Carbon Dioxide, Science Press, Beijing, 2013, 42-44.
[15] Y. Chen, R. H. Qiu, X. H. Xu, C. T. Au, S. F. Yin, RSC Adv., 2014, 4, 11907-11918.
[16] T. Yano, H. Matsui, T. Koike, H. Ishiguro, H. Fujihara, M. Yoshihara, T. Maeshima, Chem. Commun., 1997, 1129-1130.
[17] T. Ema, K. Fukuhara, T. Sakai, M. Ohbo, F. Q. Bai, J. Y. Hasegawa, Catal. Sci. Technol., 2015, 5, 2314-2321.
[18] J. Ma, J. L. Liu, Z. F. Zhang, B. X. Han, Green Chem., 2012, 14, 2410-2420.
[19] Y. Y. Song, C. Cheng, H. W. Jing, Chem. Eur. J., 2014, 20, 12894-12900.
[20] C. Martín, G. Fiorani, A. W. Kleij, ACS Catal., 2015, 5, 1353-1370.
[21] K. Yamaguchi, K. Ebitani, T. Yoshida, H. Yoshida, K. Kaneda, J. Am. Chem. Soc., 1999, 121, 4526-4527.
[22] V. D'Elia, H. L. Dong, A. J. Rossini, C. M. Widdifield, S. V. C. Vummaleti, Y. Minenkov, A. Poater, E. Abou-Hamad, J. D. A. Pelletier, L. Cavallo, L. Emsley, J. M. Basset, J. Am. Chem. Soc., 2015, 137, 7728-7739
[23] S. N. Talapaneni, O. Buyukcakir, S. H. Je, S. Srinivasan, Y. Seo, K. Polychronopoulou, A. Coskun, Chem. Mater., 2015, 27, 6818-6826.
[24] Z. Zhou, C. He, J. H. Xiu, L. Yang, C. Y. Duan, J. Am. Chem. Soc., 2015, 137, 15066-15069.
[25] D. H. Lan, F. M. Yang, S. L. Luo, C. T. Au, S. F. Yin, Carbon, 2014, 73, 351-360.
[26] G. Fiorani, W. S. Guo, A. W. Kleij, Green Chem., 2015, 17, 1375-1389.
[27] B. H. Xu, J. Q. Wang, J. Sun, Y. Huang, J. P. Zhang, X. P. Zhang, S. J. Zhang, Green Chem., 2014, 17, 108-122.
[28] W. N. R. W. Isahak, Z. A. C. Ramli, M. W. M. Hisham, M. A. Yarmo, Renew. Sust. Energy Rev., 2015, 47, 93-106.
[29] A. C. Kathalikkattil, R. Babu, J. Tharun, R. Roshan, D. W. Park, Catal. Surv. Asia, 2015, 19, 223-235.
[30] J. W. Comerford, I. D. V. Ingram, M. North, X. Wu, Green Chem., 2015, 17, 1966-1987.
[31] C. Martín, G. Fiorani, A. W. Kleij, ACS Catal., 2015, 5, 1353-1370.
[32] X. D. Lang, X. F. Liu, L. N. He, Curr. Org. Chem., 2015, 19, 681-694.
[33] R. M. Izatt, S. R. Izatt, R. L. Bruening, N. E. Izatta, B. A. Moyer, Chem. Soc. Rev., 2014, 43, 2451-2475.
[34] K. M. K. Yu, I. Curcic, J. Gabriel, H. Morganstewart, S. C. Tsang, J. Phys. Chem. A, 2010, 114, 3863-3872.
[35] Y. Kayaki, M. Yamamoto, T. Ikariya, Angew. Chem. Int. Ed., 2009, 48, 4194-4197.
[36] X. H. Zhang, N. Zhao, W. Wei, Y. H. Sun, Catal. Today, 2006, 115, 102-106.
[37] D. J. Heldebrant, P. G. Jessop, C. A. Thomas, C. A. Eckert, C. L. Liotta, J. Org. Chem., 2005, 70, 5335-5338.
[38] A. Barbarini, R. Maggi, A. Mazzacani, G. Mori, G. Sartori, R. Sartorio, Tetrahedron Lett., 2003, 44, 2931-2934.
[39] L. Wang, G. Y. Zhang, K. Kodama, T. Hirose, Green Chem., 2016, 18, 1229-1233.
[40] H. Zhou, W. Z. Zhang, C. H. Liu, J. P. Qu, X. B. Lu, J. Org. Chem., 2008, 73, 8039-8044.
[41] M. J. Ajitha, C. H. Suresh, Tetrahedron Lett., 2011, 52, 5403-5406.
[42] Y. B. Wang, Y. M. Wang, W. Z. Zhang, X. B. Lu, J. Am. Chem. Soc., 2013, 135, 11996-12003.
[43] Y. B. Wang, D. S. Sun, H. Zhou, W. Z. Zhang, X. B. Lu, Green Chem., 2015, 17, 4009-4015.
[44] H. K. He, M. J. Zhong, D. Konkolewicz, K. Yacatto, T. Rappold, G. Sugar, N. E. David, J. Gelb, N. Kotwal, A. Merkle, K. Matyjaszewski, Adv. Funct. Mater., 2013, 23, 4720-4728.
[45] Y. M. Shen, W. L. Duan, M Shi, Adv. Synth. Catal., 2003, 345, 337-340.
[46] J. Sun, W. G. Cheng, Z. F. Yang, J. Q. Wang, T. T. Xu, J. Y. Xin, S. J. Zhang, Green Chem., 2014, 16, 3071-3078.
[47] K. R. Roshan, R. A. Palissery, A. C. Kathalikkattil, R. Babu, G. Mathai, H. S. Lee, D. W. Park, Catal. Sci. Technol., 2016, DOI: 10.1039/C5CY01902H.
[48] J. A. Kozak, J. Wu, X. Su, F. Simeon, T. A. Hatton, T. F. Jamison, J. Am. Chem. Soc., 2013, 135, 18497-18501.
[49] L. Wang, L. Lin, G. Y. Zhang, K. Kodama, M. Yasutake, T. Hirose, Chem. Commun., 2014, 50, 14813-14816.
[50] L. Wang, K. Kodama, T. Hirose, Catal. Sci. Technol., 2016, DOI: 10.1039/C5CY01892G.
[51] Z. Z. Yang, L. N. He, C. X. Miao, S. Chanfreau, Adv. Synth. Catal., 2010, 352, 2233-2240.
[52] S. Foltran, J. Alsarraf, F. Robert, Y. Landais, E. Cloutet, H. Cramail, T. Tassaing, Catal. Sci. Technol., 2013, 3, 1046-1055.
[53] S. Foltran, R. Mereau, T. Tassaing, Catal. Sci. Technol., 2014, 4, 1585-1597.
[54] K. R. Roshan, T. Jose, D. Kim, K. A. Cherian, D. W. Park, Catal. Sci. Technol., 2014, 4, 963-970.
[55] M. Petkovic, K. R. Seddon, L. P. N. Rebelo, C. S. Pereira, Chem. Soc. Rev., 2011, 40, 1383-1403.
[56] X. P. Zhang, X. C. Zhang, H. F. Dong, Z. J. Zhao, S. J. Zhang, Y. Huang, Energy Environ. Sci., 2012, 5, 6668-6681.
[57] P. P. Pescarmona, M. Taherimehr, Catal. Sci. Technol., 2012, 2, 2169-2187.
[58] Z. Z. Yang, Y. N. Zhao, L. N. He, RSC Adv., 2011, 1, 545-567.
[59] R. C. Luo, X. T. Zhou, Z. Yang, W. Y. Zhang, H. B. Ji, CIESC J., 2016, 67, 258-276.
[60] A. Mirabaud, J. C. Mulatier, A. Martinez, J. P. Dutasta, V. Dufaud, ACS Catal., 2015, 5, 6748-6752.
[61] A. M. Hardman-Baldwin, A. E. Mattson, ChemSusChem, 2014, 7, 3275-3278.
[62] M. Alves, B. Grignard, S. Gennen, R. Mereau, C. Detrembleur, C. Jerome, T. Tassaing, Catal. Sci. Technol., 2015, 5, 4636-4643.
[63] M. E. Wilhelm, M. H. Anthofer, M. Cokoja, I. I. E. Markovits, W. A. Herrmann, F. E. K?hn, ChemSusChem, 2014, 7, 1357-1360.
[64] S. Sopeña, G. Fiorani, C. Martín, A. W. Kleij, ChemSusChem, 2015, 8, 3248-3254.
[65] D. H. Lan, C. T. Au, S. F. Yin, Curr. Green Chem., 2015, 2, 35-42.
[66] X. F. Liu, Q. W. Song, S. Zhang, L. N. He, Catal. Today, 2016, 263, 69-74.
[67] H. B?ttner, K. Lau, A. Spannenberg, T. Werner, ChemCatChem, 2015, 7, 459-467.
[68] L. Wang, P. Li, X. F. Jin, J. L. Zhang, H. Y. He, S. J. Zhang, J. CO₂ Util., 2015, 10, 113-119.
[69] J. Tharun, G. Mathai, R. Roshan, A. C. Kathalikkattil, K. Bomi, D. W. Park, Phys. Chem. Chem. Phys., 2013, 15, 9029-9033.
[70] M. Galvan, M. Selva, A. Perosa, M. Noè, Asian J. Org. Chem., 2014, 3, 504-513.
[71] T. Werner, H. B?ttner, ChemSusChem, 2014, 7, 3268-3271.
[72] H. B?ttner, J. Steinbauer, T. Werner, ChemSusChem, 2015, 8, 2655-2669.
[73] W. L. Dai, B. Jin, S. L. Luo, X. B. Luo, X. M. Tu, C. T. Au, Appl. Catal. A, 2014, 470, 183-188.
[74] Y. Li, L. Wang, T. F. Huang, J. L. Zhang, H. Q. He, Ind. Eng. Chem. Res., 2015, 54, 8093-8099.
[75] W. L. Dai, B. Jin, S. L. Luo, X. B. Luo, X. M. Tu, C. T. Au, J. Mol. Catal. A, 2013, 378, 326-332.
[76] H. Zhou, G. X. Wang, W. Z. Zhang, X. B. Lu, ACS Catal., 2015, 5, 6773-6779.
[77] M. H. Anthofer, M. E. Wilhelm, M. Cokoja, I. I. E. Markovits, A. Pöthig, J. Mink, W. A. Herrmann, F. E. Kühn, Catal. Sci. Technol., 2014, 4, 1749-1758.
[78] A. L. Girard, N. Simon, M. Zanatta, S. Marmitt, P. Gonçalves, J. Dupont, Green Chem., 2014, 16, 2815-2825.
[79] S. Marmitt, P. F. B. Goncalves, J. Comput. Chem., 2015, 36, 1322-1333.
[80] L Wang, X. F. Jin, P. Li, J. L. Zhang, H. Y. He, S. J. Zhang, Ind. Eng. Chem. Res., 2014, 53, 8426-8435.
[81] M. S. Liu, K. Q. Gao, L. Liang, F. X. Wang, L. Shi, L. Sheng, J. M. Sun, Phys. Chem. Chem. Phys., 2015, 17, 5959-5965.
[82] M. H. Anthofer, M. E. Wilhelm, M. Cokoja, M. Drees, W. A. Herrmann, F. E. K?hn, ChemCatChem, 2015, 7, 94-98.
[83] J. Q. Wang, W. G. Cheng, J. Sun, T. Y. Shi, X. P. Zhang, S. J. Zhang, RSC Adv., 2014, 4, 2360-2367.
[84] L. F. Xiao, D. W. Lv, D. Su, W. Wu, H. F. Li, J. Clean. Prod., 2014, 67, 285-290.
[85] L. Wang, X. F. Jin, Y. Li, P. Li, J. L. Zhang, H. Y. He, S. J. Zhang, Mol. Phys., 2015, 113, 3524-3530.
[86] C. T. Yue, D. Su, X. Zhang, W. Wu, L. F. Xiao, Catal Lett., 2014, 144, 1313-1321.
[87] M. S. Liu, L. Liang, X. Li, X. X. Gao, J. M. Sun, Green Chem., 2016, DOI: 10.1039/C5GC02605A.
[88] J. Tharun, K. R. Roshan, A. C. Kathalikkattil, D. H. Kang, H. M. Ryu, D. W. Park, RSC Adv., 2014, 4, 41266-41270.
[89] B. Chatelet, L. Joucla, J. P. Dutasta, A. Martinez, K. C. Szeto, V. Dufaud, J. Am. Chem. Soc., 2013, 135, 5348-5351.
[90] Z. Q. Zhang, L. C. Xu, W. K. Feng, RSC Adv., 2015, 5, 12382-12386.
[91] B. Chatelet, L. Joucla, J. P. Dutasta, A. Martinez, V. Dufaud, Chem. Eur. J., 2014, 20, 8571-8574.
[92] H. Zhou, Y. M. Wang, W. Z. Zhang, J. P. Qu, X. B. Lu, Green Chem., 2011, 13, 644-650.
[93] F. Adam, M. S. Batagarawa, Appl. Catal. A, 2013, 454, 164-171.
[94] E. A. Prasetyanto, M. B. Ansari, B. H. Min, S. E. Park, Catal. Today, 2010, 158, 252-257.
[95] W. L. Dai, L. Chen, S. F. Yin, S. L. Luo, C. T. Au, Catal. Lett., 2010, 135, 295-304.
[96] W. G. Cheng, X. Chen, J. Sun, J. Q. Wang, S. J. Zhang, Catal. Today, 2013, 200, 117-124.
[97] J. N. Appaturi, F. Adam, Appl. Catal. B, 2013, 136-137, 150-159.
[98] F. Adam, J. N. Appaturi, E. P. Ng, J Mol. Catal. A, 2014, 386, 42-48.
[99] P. Agrigento, S. M. Al-Amsyar, B. Sorée, M. Taherimehr, M. Gruttadauria, C. Aprile, P. P. Pescarmona, Catal. Sci. Technol., 2014, 4, 1598-1607.
[100] C. Kohrt, T. Werner, ChemSusChem, 2015, 8, 2031-2034.
[101] L. A. Bivona, O. Fichera, L. Fusaro, F. Giacalone, M. Buaki-Sogo, M. Gruttadauria, C. Aprile, Catal. Sci. Technol., 2015, 5, 5000-5007.
[102] Y. Y. Zhang, L. Chen, S. F. Yin, S. L. Luo, C. T. Au, Catal. Lett., 2012, 142, 1376-1381.
[103] Q. Y. Deng, G. H. He, Y. Pan, X. H. Ruan, W. J. Zheng, X. M. Yan, RSC Adv., 2016, 6, 2217-2224.
[104] V. B. Saptal, B. M. Bhanage, ChemCatChem, 2016, 8, 244-250.
[105] C. J. Whiteoak, A. H. Henseler, C. Ayats, A. W. Kleij, M. A. Pericàs, Green Chem., 2014, 16, 1552-1559.
[106] A. H. Jadhav, G. M. Thorat, K. Lee, A. C. Lim, H. Kang, J. G. Seo, Catal. Today, 2016, 265, 56-67.
[107] W. L. Dai, L. Chen, S. F. Yin, W. H. Li, Y. Y. Zhang, S. L. Luo, C. T. Au, Catal. Lett., 2010, 137, 74-80.
[108] Y. Y. Zhang, S. F. Yin, S. L. Luo, C. T. Au, Ind. Eng. Chem. Res., 2012, 51, 3951-3957.
[109] W. L. Dai, B. Jin, S. L. Luo, X. B. Luo, X. M. Tu, C. T. Au, Catal. Sci. Technol., 2014, 4, 556-562.
[110] W. Zhang, Q. X. Wang, H. H. Wu, P. Wu, M. Y. He, Green Chem., 2014, 16, 4767-4774.
[111] Y. Zhao, J. S. Tian, X. H. Qi, Z. N. Han, Y. Y. Zhang, L. N. He, J. Mol. Catal. A, 2007, 271, 284-289.
[112] J. X. Chen, B. Jin, W. L. Dai, S. L. Deng, L. R. Cao, Z. J. Cao, S. L. Luo, X. B. Luo, X. M. Tu, C. T. Au, Appl. Catal. A, 2014, 484, 26-32.
[113] J. Sun, J. Q. Wang, W. G. Cheng, J. X. Zhang, X. H. Li, S. J. Zhuang, Y. B. She, Green Chem., 2012, 14, 654-660.
[114] J. Tharun, Y. Hwang, R. Roshan, S. Ahn, A. C. Kathalikkattil, D. W. Park, Catal. Sci. Technol., 2012, 2, 1674-1680.
[115] Y. Xie, Z. F. Zhang, T. Jiang, J. L. He, B. X. Han, T. B. Wu, K. L. Ding, Angew. Chem. Int. Ed., 2007, 46, 7255-7258.
[116] T. Y. Shi, J. Q. Wang, J. Sun, M. H. Wang, W. G. Cheng, S. J. Zhang, RSC Adv., 2013, 3, 3726-3732.
[117] L. N. Han, H. J. Choi, D. K. Kim, S. W. Park, B. Y. Liu, D. W. Park, J. Mol. Catal. A, 2011, 338, 58-64.
[118] A. Dani, E. Groppo, C. Barolo, J. G. Vitillo, S. Bordiga, J. Mater. Chem. A, 2015, 3, 8508-8518.
[119] S. Ghazali-Esfahani, H. B. Song, E. P?unescu, F. D. Bobbink, H. Z. Liu, Z. F. Fei, G. Laurenczy, M. Bagherzadeh, N. Yan, P. J. Dyson, Green Chem., 2013, 15, 1584-1589.
[120] X. C. Wang, Y. Zhou, Z J. Guo, G. J. Chen, J. Li, Y. M. Shi, Y. Q. Liu, J. Wang, Chem. Sci., 2015, 6, 6916-6924.
[121] Y. Leng, D. Lu, P. P. Jiang, C. J. Zhang, J. W. Zhao, W. J. Zhang, Catal. Commun., 2016, 74, 99-103.
[122] Z. Z. Yang, Y. F. Zhao, G. P. Ji, H. Y. Zhang, B. Yu, X. Gao, Z. M. Liu, Green Chem., 2014, 16, 3724-3728.
[123] J. Q. Wang, J. Y. Leong, Y. G. Zhang, Green Chem., 2014, 16, 4515-4519.
[124] J. Q. Wang, J. G. W. Yang, G. S. Yi, Y. G. Zhang, Chem. Commun., 2015, 51, 15708-15711.
[125] J. Roeser, K. Kailasam, A. Thomas, ChemSusChem, 2012, 5, 1793-1799.
[126] X. L. Meng, Y. Nie, J. Sun, W. G. Cheng, J. Q. Wang, H. Y. He, S. J. Zhang, Green Chem., 2014, 16, 2771-2778.
[127] J. H. Yang, D. Yang, P. Tang, D. Ma, Acta Phys. Chim. Sin., 2016, 32, 75-84.
[128] M. B. Ansari, B. H. Min, Y. H. Mo, S. E. Park, Green Chem., 2011, 13, 1416-1421.
[129] Q. Su, J. Sun, J. Q. Wang, Z. F. Yang, W. G. Cheng, S. J. Zhang. Catal. Sci. Technol., 2014, 4, 1556-1562.
[130] Z. J. Huang, F. B. Li, B. F. Chen, T. Lu, Y. Yuan, G. Q. Yuan. Appl. Catal. B, 2013, 136-137, 269-277.
[131] D. H. Lan, H. T. Wang, L. Chen, C. T. Au, S. F. Yin. Carbon, 2016, 100, 81-89.
[132] J. Xu, F. Wu, Q. Jiang, Y. X. Li, Catal. Sci. Technol., 2015, 5, 447-454.
[133] Z. J. Huang, F. B. Li, B. F. Chen, G. Q. Yuan, Catal. Sci. Technol., 2016, DOI: 10.1039/C5CY01805F.
[134] R. C. Luo, X. T. Zhou, Y. X. Fang, H. B. Ji, Carbon, 2015, 82, 1-11.
[135] V. B. Saptal, T. Sasaki, K. Harada, D. Nishio-Hamane, B. M. Bhanage, ChemSusChem, 2016, DOI: 10.1002/cssc.201501438.
[136] D. H. Lan, L. Chen, C. T. Au, S. F. Yin. Carbon, 2015, 93, 22-31.
[137] J. Xu, M. Xu, J. Wu, H. Wu, W. H. Zhang, Y. X. Li, RSC Adv., 2015, 5, 72361-72368.
[138] W. H. Zhang, P. P. He, S. Wu, J. Xu, Y. X. Li, G. Zhang, X. Y. Wei, Appl. Catal. A, 2016, 509, 111-117.
[139] M. P. Liu, Y. P. Luo, L. Xu, L. Sun, H. B. Du, Dalton Trans., 2016, 45, 2369-2373.
[140] S. Baj, T. Krawczyk, K. Jasiak, A. Siewniak, M. Pawlyta, Appl. Catal. A, 2014, 488, 96-102.
[141] Y. L. Zhang, Z. T. Tan, B. L. Liu, D. S. Mao, C. R. Xiong, Catal. Commun., 2015, 68, 73-76.
[142] X. Y. Ma, B. Zou, M. H. Cao, S. L. Chen, C. W. Hu, J. Mater. Chem. A, 2014, 2, 18360-18366.
[143] Y. Li, B. Zou, C. W. Hu, M. H. Cao, Carbon, 2016, 99, 79-89.

Recent advances in metal-free catalysts for the synthesis of cyclic carbonates from CO₂ and epoxides

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[6]	Zhi-Yu Bo, Si-Shun Yan, Tian-Yu Gao, Lei Song, Chuan-Kun Ran, Yi He, Wei Zhang, Guang-Mei Cao, Da-Gang Yu. Visible-light photoredox-catalyzed selective carboxylation of C(sp²)-F bonds in polyfluoroarenes with CO₂ [J]. Chinese Journal of Catalysis, 2022, 43(9): 2388-2394.
[7]	Yu Shang, Yunxuan Ding, Peili Zhang, Mei Wang, Yufei Jia, Yunlong Xu, Yaqing Li, Ke Fan, Licheng Sun. Pyrrolic N or pyridinic N: The active center of N-doped carbon for CO₂ reduction [J]. Chinese Journal of Catalysis, 2022, 43(9): 2405-2413.
[8]	Wanjun Sun, Jiayu Zhu, Meiyu Zhang, Xiangyu Meng, Mengxue Chen, Yu Feng, Xinlong Chen, Yong Ding. Recent advances and perspectives in cobalt-based heterogeneous catalysts for photocatalytic water splitting, CO₂ reduction, and N₂ fixation [J]. Chinese Journal of Catalysis, 2022, 43(9): 2273-2300.
[9]	Zixuan Zhou, Peng Gao. Direct carbon dioxide hydrogenation to produce bulk chemicals and liquid fuels via heterogeneous catalysis [J]. Chinese Journal of Catalysis, 2022, 43(8): 2045-2056.
[10]	Yaping Yi, Chanjuan Xi. Photo-catalyzed sequential dearomatization/carboxylation of benzyl o-halogenated aryl ether with CO₂ leading to spirocyclic carboxylic acids [J]. Chinese Journal of Catalysis, 2022, 43(7): 1652-1656.
[11]	Menghui Chen, Yongting Chen, Zhili Yang, Jin Luo, Jialin Cai, Joey Chung-Yen Jung, Jiujun Zhang, Shengli Chen, Shiming Zhang. Synergy of staggered stacking confinement and microporous defect fixation for high-density atomic Fe^II-N₄ oxygen reduction active sites [J]. Chinese Journal of Catalysis, 2022, 43(7): 1870-1878.
[12]	Lu Wang, Chaorong Qi, Wenfang Xiong, Huanfeng Jiang. Recent advances in fixation of CO₂into organic carbamates through multicomponent reaction strategies [J]. Chinese Journal of Catalysis, 2022, 43(7): 1598-1617.
[13]	Kai Wang, Xiangfeng Lin, Qian Li, Yan Liu, Can Li. The synthesis of tetracyclic coumarins via decarboxylative asymmetric [4+2] cycloadditions enabled by Pd(0)/Cu(I) synergistic catalysis [J]. Chinese Journal of Catalysis, 2022, 43(7): 1812-1817.
[14]	Ke Jing, Ming-Kai Wei, Si-Shun Yan, Li-Li Liao, Ya-Nan Niu, Shu-Ping Luo, Bo Yu, Da-Gang Yu. Visible-light photoredox-catalyzed carboxylation of benzyl halides with CO₂: Mild and transition-metal-free [J]. Chinese Journal of Catalysis, 2022, 43(7): 1667-1673.
[15]	Fenglei Lyu, Wei Hua, Huirong Wu, Hao Sun, Zhao Deng, Yang Peng. Structural and interfacial engineering of well-defined metal-organic ensembles for electrocatalytic carbon dioxide reduction [J]. Chinese Journal of Catalysis, 2022, 43(6): 1417-1432.