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CO2 Capture and Conversion Using a Cobalt(III) Schiff Base Complex as a Catalyst at Ambient Conditions

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EPD Congress 2015

Abstract

CO2 emissions must be reduced by at least 50 % by 2050, and hence the technical solutions to capture and convert CO2 into value-added products should be considered. A Cobalt(III) Schiff base complex (Salen-Co(III)) has been investigated as a catalyst for synthesis of cyclic carbonate from CO2 and epichlorohydrin(ECH) with tetrabutylammonium bromide (TBAB) as co-catalyst. To recover Salen-Co(III) for the next cycling operation, it was immobilized onto zeolite 13X through excessive impregnation method. The immobilized catalyst was characterized using XRD, SEM, BET and ICP-AES techniques. Catalytic tests showed that yield of cyclic carbonate reached 90 % using 0.5 mol % Salen-Co(III) at ambient conditions. The immobilized Salen-Co(III) exhibited better catalytic activity than the homogenous one when used at the first cycle, but the yield decreased by some 20 % after five cycles.

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Reference

  1. A. A. G. Shaikh, and S. Sivaram, “Organic carbonates,” Chemical reviews, 96 (1996), 951–976.

    Article  Google Scholar 

  2. B. Sch. ffner et al., “Organic carbonates as solvents in synthesis and catalysis,” Chemical reviews, 110 (8) (2010), 4554–4581.

    Article  Google Scholar 

  3. N. Kihara, N. Hara, and T. Endo, “Catalytic activity of various salts in the reaction of 2, 3-epoxypropyl phenyl ether and carbon dioxide under atmospheric pressure,” The Journal of Organic Chemistry, 58 (23) (1993), 6198–6202.

    Article  Google Scholar 

  4. P. Ramidi et al., “Synergistic effect of alkali halide and Lewis base on the catalytic synthesis of cyclic carbonate from CO2 and epoxide,” Chemical Physics Letters, 512 (2011), 273–277.

    Article  Google Scholar 

  5. K. Yamaguchi et al., “Mg-Al mixed oxides as highly active acid-base catalysts for cycloaddition of carbon dioxide to epoxides,” Journal of the American Chemical Society, 121 (18) (1999), 4526–4527.

    Article  Google Scholar 

  6. B. M. Bhanage et al., “Synthesis of dimethyl carbonate and glycols from carbon dioxide, epoxides, and methanol using heterogeneous basic metal oxide catalysts with high activity and selectivity,” Applied Catalysis A: General, 219 (1) (2001), 259–266.

    Article  Google Scholar 

  7. V. Caló et al., “Cyclic carbonate formation from carbon dioxide and oxiranes in tetrabutylammonium halides as solvents and catalysts,” Organic letters, 4 (15) (2002), 2561–2563.

    Article  Google Scholar 

  8. J. Q. Wang et al., “Synthesis of cyclic carbonates from epoxides and carbon dioxide over silica-supported quaternary ammonium salts under supercritical conditions,” Journal of Molecular Catalysis A: Chemical, 249 (1) (2006), 143–148.

    Article  Google Scholar 

  9. J. Sun, S. Fujita, and M. Arai, “Development in the green synthesis of cyclic carbonate from carbon dioxide using ionic liquids,” Journal of Organometallic Chemistry, 690 (15) (2005), 3490–3497.

    Article  Google Scholar 

  10. A. L. Girard et al., “Insights on recyclable catalytic system composed of task-specific ionic liquids for the chemical fixation of carbon dioxide,” Green Chemistry, 16 (5) (2014), 2815–2825.

    Article  Google Scholar 

  11. R. L. Paddock, and S. B. T. Nguyen, “Chemical CO2 fixation: Cr (III) salen complexes as highly efficient catalysts for the coupling of CO2 and epoxides,” Journal of the American Chemical Society, 123 (46) (2001), 11498–11499.

    Article  Google Scholar 

  12. C. X. Miao, J. Q. Wang, and L. N. He, “Catalytic processes for chemical conversion of carbon dioxide into cyclic carbonates and polycarbonates,” The Open Organic Chemistry Journal, 2 (2008), 68–82.

    Google Scholar 

  13. T. Chang, L. Jin, and H. Jing, “Bifunctional chiral catalyst for the synthesis of chiral cyclic carbonates from carbon dioxide and epoxides,” ChemCatChem, 1 (3) (2009), 379–383.

    Article  Google Scholar 

  14. A. Ghosh et al., “Cycloaddition of CO2 to epoxides using a highly active Co (III) complex of tetraamidomacrocyclic ligand,” Catalysis letters, 137 (1–2) (2010), 1–7.

    Article  Google Scholar 

  15. P. Ramidi et al., “Synthesis and characterization of Co (III) amidoamine complexes: influence of substituents of the ligand on catalytic cyclic carbonate synthesis from epoxide and carbon dioxide,” Dalton Transactions, 42 (36) (2013), 13151–13160.

    Article  Google Scholar 

  16. J. Meléndez, M. North, and R. Pasquale, “Synthesis of cyclic carbonates from atmospheric pressure carbon dioxide using exceptionally active aluminium (salen) complexes as catalysts,” European journal of inorganic chemistry, 2007 (21) (2007), 3323–3326.

    Article  Google Scholar 

  17. Y. Xie et al., “Capture and conversion of CO2 at ambient conditions by a conjugated microporous polymer,” Nature communications, 2013, 4.

    Google Scholar 

  18. K. Li et al., “Highly efficient catalytic oxidation of cyclohexanol with TBHP over Cr-13X catalysts in a solvent-free system,” Journal of Molecular Catalysis A: Chemical, 387 (2014), 31–37.

    Article  Google Scholar 

  19. A. Mobinikhaledi, M. Zendehdel, and P. Safari, “Effect of substituents and encapsulation on the catalytic activity of copper (II) complexes of two tridentate Schiff base ligands based on thiophene: benzyl alcohol and phenol oxidation reactions,” Transition Metal Chemistry, 39 (2014), 431–442.

    Article  Google Scholar 

  20. J. Q. Guan, and J. Liu, “A Copper(II) Schiff base complex immobilized onto SBA-15 silica for selective oxidation of benzyl alcohol,” Transition Metal Chemistry, 39 (2014), 233–238.

    Article  Google Scholar 

  21. M. North, R. Pasquale, and C. Young, “Synthesis of cyclic carbonates from epoxides and CO2,” Green Chemistry, 12 (9) (2010), 1514–1539.

    Article  Google Scholar 

  22. M. North, P. Villuendas, and C. Young, “Inter-and intramolecular phosphonium salt cocatalysis in cyclic carbonate synthesis catalysed by a bimetallic aluminium (salen) complex,” Tetrahedron Letters, 53 (22) (2012), 2736–2740.

    Article  Google Scholar 

  23. L. Frunza et al., “Host/guest interactions in nanoporous materials I. The embedding of chiral salen manganese (III) complex into mesoporous silicates,” Journal of Molecular Catalysis A: Chemical, 123 (2) (1997), 179–187.

    Article  Google Scholar 

  24. W. M. Ren et al., “Role of the co-catalyst in the asymmetric coupling of racemic epoxides with CO2 using multichiral Co(III) complexes: product selectivity and enantioselectivity,” Chemical Science, 3 (2012), 2094–2102.

    Article  Google Scholar 

  25. M. North, and R. Pasquale, “Mechanism of Cyclic Carbonate Synthesis from Epoxides and CO2,” Angewandte Chemie, 121 (2009), 2990–2992.

    Article  Google Scholar 

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Miao, J., Xue, J., Zhu, J., Liu, K. (2015). CO2 Capture and Conversion Using a Cobalt(III) Schiff Base Complex as a Catalyst at Ambient Conditions. In: Yurko, J.A., et al. EPD Congress 2015. Springer, Cham. https://doi.org/10.1007/978-3-319-48214-9_14

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