Citation: Wang Zhitao, Li Hui, Yan Shichen, Fang Qianrong. Synthesis of a Two-dimensional Covalent Organic Framework with the Ability of Conducting Proton along Skeleton[J]. Acta Chimica Sinica, ;2020, 78(1): 63-68. doi: 10.6023/A19110397 shu

Synthesis of a Two-dimensional Covalent Organic Framework with the Ability of Conducting Proton along Skeleton

Wang Zhitao ^a,b ,
Li Hui ^a ,
Yan Shichen ^a ,
Fang Qianrong ^a,,

a.
State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, School of Chemistry, Jilin University, Changchun 130012, China
b.
School of Chemistry, Tonghua Normal College, Tonghua 134002, China

Corresponding author: Fang Qianrong, qrfang@jlu.edu.cn
Received Date: 7 November 2019
Available Online: 10 January 2019
Fund Project: Project supported by the National Natural Science Foundation of China (No. 21571079)the National Natural Science Foundation of China 21571079

Figures(10)

Nitrogen heterocyclic compound like imidazole and triazole are often loaded in porous material for proton conduction. Inspired by this, we employ 5, 5'-diamino-3, 3'-bis(1H-1, 2, 4-triazole) (BTDA) containing triazole fragments in the structure as the construction unit to react with 2, 4, 6-triformylphloroglucinol (TFP) through Schiff-base condensation reaction to synthesize a novel two-dimensional covalent organic framework named TFP-BTDA-COF. The theoretical results were simulated using the Accelrys Material Studios 7.0 software package and compared with the powder X-ray diffraction (PXRD) test data to confirm the crystal structure of TFP-BTDA-COF. The porosity and pore structure of TFP-BTDA-COF were characterized by N₂ adsorption-desorption at 77 K. The condensation reaction was confirmed by Fourier transform infrared spectroscopy (FTIR). Due to the π-π accumulation of the 2D-COF, the N-H bond of the triazole in BTDA connecting unit is periodically and regularly arranged on each layer of the COF to form an ordered array. Under certain humidity conditions, the protons can be transmitted along the array in the one-dimensional pore channel by the intermediary of water molecules. Therefore, the TFP-BTDA-COF has the ability to conduct proton through the skeleton. The proton conductivity of TFP-BTDA-COF is tested by the AC impedance method. The results show that the proton conductivity of the material is gradually enhanced with the increase of the ambient humidity, and the maximum value is 1.4×10^-3 S·cm^-1 at 98% relative humidity. The PXRD of TFP-BTDA-COF in boiling water for 2 h and after 12 h AC impedance test were compared with the original experimental value to evaluate its tolerance under the working conditions of the proton membrane fuel cell. The PXRD diffraction peak intensity did not change obviously compared with that of the original experimental value. The thermogravimetric analysis results show that the thermal stability of TFP-BTDA-COF can reach high to 400℃. The above evidence proves that it has the potential to be used in proton membrane fuel cells.
- covalent organic framework,
- proton conduction,
- crystal structure,
- AC impedance
1. [1]
  Jacobson, M. Z.; Colella, W. G.; Golden, D. M. Science 2005, 308, 1901. doi: 10.1126/science.1109157
2. [2]
  Wang, Y.; Chen, K.; Mishler, J.; Cho, S. C.; Adroher, X. C. Appl. Energy 2011, 88, 981. doi: 10.1016/j.apenergy.2010.09.030
3. [3]
  He, X.-Y.; Gang, M.-Y.; He, G.-W.; Yin, Y.-H.; Cao, L.; Wu, H.; Jiang, Z.-Y. Chin. J. Chem. 2017, 35, 673. doi: 10.1002/cjoc.201600577
4. [4]
  Chen, X.; Yan, H.-J.; Xia, D.-G. Acta Chim. Sinica 2017, 75, 189. doi: 10.3969/j.issn.0253-2409.2017.02.008
5. [5]
  Cui, L.-R.; Zhang, J.; Sun, Y.-Y.; Lu, S.-F.; Xiang, Y. Acta Chim. Sinica 2019, 77, 47. doi: 10.7503/cjcu20180421
6. [6]
  Zhong, G.-Y.; Wang, H.-J.; Yu, H.; Peng, F. Acta Chim. Sinica 2017, 75, 943.
7. [7]
  Zhang, H.-W.; Shen, P.-K. Chem. Rev. 2012, 112, 2780. doi: 10.1021/cr200035s
8. [8]
  Mauritz, K. A.; Moore, R. B. Chem. Rev. 2004, 104, 4535. doi: 10.1021/cr0207123
9. [9]
  Nasef, M. M. Chem. Rev. 2014, 114, 12278. doi: 10.1021/cr4005499
10. [10]
  Shimizu, G. K. H.; Taylor, J. M.; Kim, S. Science 2013, 341, 354. doi: 10.1126/science.1239872
11. [11]
  Yoon, M.; Suh, K.; Natarajan, S.; Kim, K. Angew. Chem., Int. Ed. 2013, 52, 2688. doi: 10.1002/anie.201206410
12. [12]
  Yamada, T.; Otsubo, K.; Makiura, R.; Kitagawa, H. Chem. Soc. Rev. 2013, 42, 6655. doi: 10.1039/c3cs60028a
13. [13]
  Ramaswamy, P.; Wong, N. E.; Shimizu, G. K. H. Chem. Soc. Rev. 2014, 43, 5913. doi: 10.1039/C4CS00093E
14. [14]
  Matoga, D.; Oszajca, M.; Molenda, M. Chem. Commun. 2015, 51, 7637. doi: 10.1039/C5CC01789K
15. [15]
  Tang, Q.; Liu, Y.-W.; Liu, S.-X.; He, D.-F.; Miao, J.; Wang, X.-Q.; Yang, G.-C. J. Am. Chem. Soc. 2014, 136, 12444. doi: 10.1021/ja5069855
16. [16]
  Côté, A. P.; Benin, A. I.; Ockwig, N. W.; O'Keeffe, M.; Matzger, A. J.; Yaghi, O. M. Science 2005, 310, 1166. doi: 10.1126/science.1120411
17. [17]
  Ding, S.-Y.; Wang, W. Chem. Soc. Rev. 2013, 42, 548. doi: 10.1039/C2CS35072F
18. [18]
  Waller, P. J.; Gándara, F.; Yaghi, O. M. Acc. Chem. Res. 2015, 48, 3053. doi: 10.1021/acs.accounts.5b00369
19. [19]
  Chen, Q.-D.; Tang, J.-J.; Fang, Q.-R. Chem. J. Chin. Univ. 2018, 39, 2357. doi: 10.7503/cjcu20180190
20. [20]
  Zheng, C.-N.; Zhu, J.-H.; Yang, C.-Q.; Lu, C.-B.; Chen, Z.-Y.; Zhuang, X.-D. Sci. China Chem. 2019, 62, 1145. doi: 10.1007/s11426-019-9477-y
21. [21]
  Yuan, F.-Y.; Tan, J.; Guo, J. Sci. China Chem. 2018, 61, 143. doi: 10.1007/s11426-017-9162-3
22. [22]
  Huang, N.; Chen, X.; Krishna, R.; Jiang, D.-L. Angew. Chem., Int. Ed. 2015, 54, 2986. doi: 10.1002/anie.201411262
23. [23]
  Dogru, M.; Handloser, M.; Auras, F.; Kunz, T.; Medina, D.; Hartschuh, A.; Knochei, P.; Bein, T. Angew. Chem., Int. Ed. 2013, 52, 2920. doi: 10.1002/anie.201208514
24. [24]
  Cai, P.-W.; Peng, X.-X.; Huang, J.-H.; Jia, J.-C.; Hu, X.; Wen, Z.-H. Sci. China Chem. 2019, 62, 385. doi: 10.1007/s11426-018-9395-1
25. [25]
  Pang, C.-M.; Luo, S.-H.; Hao, Z.-F.; Gao, J.; Huang, Z.-H.; Yu, J.-H.; Yu, S.-M.; Wang, Z.-Y. Chin. J. Org. Chem. 2018, 38, 2606.
26. [26]
  Peng, Z.-K.; Ding, H.-M.; Chen, R.-F.; Gao, C.; Wang, C. Acta Chim. Sinica 2019, 77, 681.
27. [27]
  Chandra, S.; Kundu, T.; Kandambeth, S.; Babarao, R.; Marathe, Y.; Kunjir, S. M.; Banerjee, R. J. Am. Chem. Soc. 2014, 136, 6570. doi: 10.1021/ja502212v
28. [28]
  Xu, H.; Tao, S.-S.; Jiang, D. L. Nat. Mater. 2016, 15, 722. doi: 10.1038/nmat4611
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