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Assembly of Five Coordination Polymers Based on Furan-2,5-dicarboxylic acid and 4,4′-Azobispyridine: Synthesis, Structures and Luminescence Properties

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Abstract

Five coordination polymers (CPs) {[Zn4(FDA)4(H2O)12]}n (1) {[M(FDA)(azopy)·DMF]}n (2) [M = Zn (2a), Co (2b) and Cd (2c)] and {[Zn(FDA)(azopy)]·CH3CN·0.5DMF}n (3) have been harvested from furan-2,5-dicarboxylic acid (H2FDA) and 4,4′-azobispyridine (azopy), and structurally characterized by infrared spectra, elemental analysis, thermogravimentric analysis, powder X-ray diffraction and single-crystal X-ray diffraction. CP 1 shows an interesting one-dimension chain structure. CP 2a and CP 2b are isostructural and demonstrate two-dimensional 4-connected sql topological structures where FDA2− connected the nearest Zn(II) ions to generate a one-dimension chain and the chains could be further linked by azopy. CP 2c significantly differs from CP 2a and CP 2b in coordination number as well as in the coordination mode of carboxylate groups. However CP 2c can generate the same two-dimensional sql structure as well. While CP 3 is an interesting pillared-layer three-dimensional two-fold interpenetrating framework with a pcu alpha-Po primitive cubic topology. The luminescence properties of CP 1, CP 2a, CP 2c and CP 3 are investigated.

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References

  1. S.R. Batten, S.M. Neville, D.R. Turner, Coordination Polymers Design, Analysis and Application (Royal Society of Chemistry, Cambridge, 2009), www.rsc.org

  2. M. O’Keeffe, O.M. Yaghi, Chem. Rev. 112, 675–702 (2012)

    PubMed  Google Scholar 

  3. Z.J. Lin, M.C. Hong, R. Cao, Chem. Soc. Rev. 43, 5867–5895 (2014)

    CAS  PubMed  Google Scholar 

  4. S. Kitagawa, Chem. Soc. Rev. 43, 5415–5418 (2014)

    PubMed  Google Scholar 

  5. F. Luo, C.S. Yan, L.L. Dang, R. Krishna, W. Zhou, H. Wu, X.L. Dong, Y. Han, T.L. Hu, M. O’Keeffe, L.L. Wang, M.B. Luo, R.B. Lin, B.L. Chen, J. Am. Chem. Soc. 138, 5678–5684 (2016)

    CAS  PubMed  Google Scholar 

  6. J. Duan, M. Higuchi, R. Krishna, T. Kiyonaga, Y. Tsutsumi, Y. Sato, Y. Kubota, M. Takata, S. Kitagawa, Chem. Sci. 5, 660–666 (2014)

    CAS  Google Scholar 

  7. F. Moro, D. Kaminski, F. Tuna, G.F.S. Whitehead, G.A. Timco, D. Collison, R.E.P. Winpenny, A. Ardavan, E.J.L. Mclnnes, Chem. Commun. 50, 91–93 (2014)

    CAS  Google Scholar 

  8. S.W. Zhang, P. Cheng, ChemPlusChem 81, 811–816 (2016)

    CAS  Google Scholar 

  9. J.Y. Zou, W. Shi, N. Xu, L.L. Li, J.K. Tang, H.L. Gao, J.Z. Cui, P. Cheng, Chem. Commun. 49, 8226–8228 (2013)

    CAS  Google Scholar 

  10. S.W. Zhang, H. Li, E.Y. Duan, Z.S. Han, L.L. Li, J.K. Tang, W. Shi, P. Cheng, Inorg. Chem. 55, 1202–1207 (2016)

    CAS  PubMed  Google Scholar 

  11. Z.L. Wu, J. Dong, W.Y. Ni, B.W. Zhang, J.Z. Cui, B. Zhao, Inorg. Chem. 54, 5266–5272 (2015)

    CAS  PubMed  Google Scholar 

  12. Y. Xie, S.G. Ning, Y. Zhang, Z.L. Tang, S.W. Zhang, R.R. Tang, Dyes Pigm. 150, 36–43 (2018)

    CAS  Google Scholar 

  13. Y. Wang, P. Xu, Q. Xie, Q.Q. Ma, Y.H. Meng, Z.W. Wang, S.W. Zhang, X.H. Zhao, J. Chen, Z.L. Wang, Chem. Eur. J. 22, 10459–10474 (2016)

    CAS  PubMed  Google Scholar 

  14. G. Maurin, C. Serre, A. Cooper, G. Férey, Chem. Soc. Rev. 46, 3104–3107 (2017)

    CAS  PubMed  Google Scholar 

  15. Z. Ju, S. Yan, D. Yuan, Chem. Mater. 28, 2000–2010 (2016)

    CAS  Google Scholar 

  16. X.X. Zhao, S.W. Zhang, J.Q. Yan, L.D. Li, G.J. Wu, W. Shi, G.M. Yang, N.J. Guan, P. Cheng, Inorg. Chem. 57, 5030–5037 (2018)

    CAS  PubMed  Google Scholar 

  17. J.Y. Zou, W. Shi, H.L. Gao, J.Z. Cui, P. Cheng, Inorg. Chem. Front. 1, 242–248 (2014)

    CAS  Google Scholar 

  18. W.P. Chen, P.Q. Liao, Y. Yu, Z. Zheng, X.M. Chen, Y.Z. Zheng, Angew. Chem. Int. Ed. 55, 9375–9379 (2016)

    CAS  Google Scholar 

  19. S.W. Zhang, W. Shi, P. Cheng, Coord. Chem. Rev. 352, 108–150 (2017)

    CAS  Google Scholar 

  20. S. Horike, S. Kitagawa, Nat. Mater. 16, 1054–1055 (2017)

    CAS  PubMed  Google Scholar 

  21. Z. Hasan, S.H. Jhung, J. Hazard. Mater. 283, 329–339 (2015)

    CAS  PubMed  Google Scholar 

  22. Q.G. Zhai, X.H. Bu, C.Y. Mao, X. Zhao, L. Daemen, Y.Q. Chen, A.J. Ramirez-Cuesta, C.Y. Mao, Nat. Commun. 7, 1–9 (2016)

    Google Scholar 

  23. S.G. Ning, H.J. Chen, S.W. Zhang, P. Cheng, Polyhedron 155, 457–463 (2018)

    CAS  Google Scholar 

  24. Y.L. Wu, G.P. Yang, Y.Q. Zhao, W.P. Wu, B. Liu, Y.Y. Wang, Dalton Trans. 44, 3271–3277 (2015)

    CAS  PubMed  Google Scholar 

  25. F.L. Hu, F.L. Jiang, J. Zheng, M.Y. Wu, J.D. Pang, M.C. Hong, Inorg. Chem. 54, 6081–6083 (2015)

    CAS  PubMed  Google Scholar 

  26. Y. Wei, R. Sa, Q. Li, K. Wu, Dalton Trans. 44, 3067–3074 (2015)

    CAS  PubMed  Google Scholar 

  27. Z.L. Tang, H.J. Chen, Y. Zhang, B.S. Zheng, S.W. Zhang, P. Cheng, Cryst. Growth Des. 19, 1172–1182 (2019)

    CAS  Google Scholar 

  28. Q.F. Sun, S. Sato, M. Fujita, Angew. Chem. Int. Ed. 53, 13510–13513 (2014)

    CAS  Google Scholar 

  29. L. Li, J.Y. Zou, S.Y. You, H.M. Cui, G.P. Zeng, J.Z. Cui, Dalton Trans. 46, 16432–16438 (2017)

    CAS  PubMed  Google Scholar 

  30. H. Wang, J. Xu, D.S. Zhang, Q. Chen, R.M. Wen, Z. Cheng, X.H. Bu, Angew. Chem. Int. Ed. 54, 1–6 (2015)

    Google Scholar 

  31. K. Liu, H.H. Li, X.J. Zhang, W. Shi, P. Cheng, Inorg. Chem. 54, 10231–10244 (2015)

    Google Scholar 

  32. B. Bhattacharya, R. Dey, P. Pachfule, R. Banerjee, D. Ghoshal, Cryst. Growth Des. 13, 731–739 (2012)

    Google Scholar 

  33. J.Y. Zou, H.L. Gao, W. Shi, J.Z. Cui, P. Cheng, CrystEngComm 15, 2682–2687 (2013)

    CAS  Google Scholar 

  34. O.V. Dolomanov, L.J. Bourhis, R.J. Gildea, J.A.K. Howard, H. Puschmann, J. Appl. Crystallogr. 42, 339–341 (2009)

    CAS  Google Scholar 

  35. G.M. Sheldrick, Acta Crystallogr. A 71, 3–8 (2015)

    Google Scholar 

  36. G.M. Sheldrick, Acta Crystallogr. C 71, 3–8 (2015)

    Google Scholar 

  37. V.A. Blatov, A.P. Shevchenko, D.M. Proserpio, Cryst. Growth Des. 14, 3576–3586 (2014). http://topospro.com

  38. M. O’Keeffe, O.M. Yaghi, S. Ramsden, Reticular Chemistry Structure Resource (2007). Database available at http://rcsr.anu.edu.au/

  39. J.A. Foster, S. Henke, A. Schneemann, R.A. Fischer, A.K. Cheetham, Chem. Commun. 52, 10474–10477 (2016)

    CAS  Google Scholar 

  40. L. Wei, Q. Wei, Z.E. Lin, Q. Meng, H. He, B.F. Yang, G.Y. Yang, Angew. Chem. Int. Ed. 53, 7188–7191 (2014)

    CAS  Google Scholar 

  41. X.L. Zhao, W.Y. Sun, CrystEngComm 16, 3247–3258 (2014)

    CAS  Google Scholar 

  42. A.L. Spek, PLATON. J. Appl. Crystallogr. 36, 7–13 (2003)

    CAS  Google Scholar 

  43. S. Parshamoni, J. Telangae, S. Konar, Dalton Trans. 44, 20926–20935 (2015)

    CAS  PubMed  Google Scholar 

  44. W.H. Fang, L. Zhang, J. Zhang, Chem. Commun. 53, 3949–3951 (2017)

    CAS  Google Scholar 

  45. B.K. Tripuramallu, S. Goswami, I. Goldberg, Cryst. Growth Des. 18, 230–241 (2017)

    Google Scholar 

  46. J.Y. Zou, L. Li, S.Y. You, H.M. Cui, Y.W. Liu, K.H. Chen, Y.H. Chen, J.Z. Cui, S.W. Zhang, Dyes Pigment. 159, 429–438 (2018)

    CAS  Google Scholar 

  47. R.P. Ye, X. Zhang, J.Q. Zhai, Y.Y. Zhang, Y.G. Yao, J. Zhang, CrystEngComm 17, 9155–9166 (2015)

    CAS  Google Scholar 

  48. J.A. Hua, Y. Zhao, Y.S. Kang, Y. Lu, W.Y. Sun, Dalton Trans. 44, 11524–11532 (2015)

    CAS  PubMed  Google Scholar 

  49. Z.Q. Shi, Z.J. Guo, H.G. Zheng, Chem. Commun. 51, 8300–8303 (2015)

    CAS  Google Scholar 

  50. J.Y. Zou, L. Li, S.Y. You, K.H. Chen, X.N. Dong, Y.H. Chen, J.Z. Cui, Cryst. Growth Des. 18, 3997–4003 (2018)

    CAS  Google Scholar 

  51. Y. Hu, M. Ding, X.Q. Liu, L.B. Sun, H.L. Jiang, Chem. Commun. 52, 5734–5737 (2016)

    CAS  Google Scholar 

Download references

Acknowledgements

Financial supports from the National Natural Science Foundation of China (Nos. 21561014 and 21562023), the Key Research Project of Jiangxi Province (No. 20171BBF60074) and the Key Research Project of Jiangxi Academy of Sciences (No. 2018-YZD2-11) are greatly acknowledged.

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Appendix A: Supplementary Data

Appendix A: Supplementary Data

CCDC 1843748 for 1, 1843749 for 2a, 1843752 for 2b, 1843750 for 2c, and 1843754 for 3 contain the supplementary crystallographic data of this paper. These data can be obtained free of charge via http://www.ccdc.cam.ac.uk/conts/retrieving.html, or from the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, UK; fax: (+44) 1223-336-033; or e-mail: deposit@ccdc.cam.ac.uk.

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You, SY., Li, L., Zou, JY. et al. Assembly of Five Coordination Polymers Based on Furan-2,5-dicarboxylic acid and 4,4′-Azobispyridine: Synthesis, Structures and Luminescence Properties. J Inorg Organomet Polym 30, 410–416 (2020). https://doi.org/10.1007/s10904-019-01199-9

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