Monolithic Covalent Organic Framework Aerogels through Framework Crystallization Induced Self-assembly: Heading towards Framework Materials Synthesis over All Length Scales

Wei Zhao Tian-Pin Wang Jia-Li Wu Ru-Ping Pan Xiang-Yang Liu Xi-Kui Liu

Citation:  Wei Zhao, Tian-Pin Wang, Jia-Li Wu, Ru-Ping Pan, Xiang-Yang Liu, Xi-Kui Liu. Monolithic Covalent Organic Framework Aerogels through Framework Crystallization Induced Self-assembly: Heading towards Framework Materials Synthesis over All Length Scales[J]. Chinese Journal of Polymer Science, 2019, 37(11): 1045-1052. doi: 10.1007/s10118-019-2313-1 shu

Monolithic Covalent Organic Framework Aerogels through Framework Crystallization Induced Self-assembly: Heading towards Framework Materials Synthesis over All Length Scales

English


    1. [1]

      Côté, A. P.; Benin, A. I.; Ockwig, N. W.; O'Keeffe, M.; Matzger, A. J.; Yaghi, O. M. Porous, crystalline, covalent organic frameworks. Science 2005, 310, 1166-1170. doi: 10.1126/science.1120411

    2. [2]

      Oh, H.; Kalidindi, S. B.; Um, Y.; Bureekaew, S.; Schmid, R. A cryogenically flexible covalent organic framework for efficient hydrogen isotope separation by quantum sieving. Angew. Chem. Int. Ed. 2013, 52, 13219-13222. doi: 10.1002/anie.201307443

    3. [3]

      Ding, S. Y.; Wang, W. Covalent organic frameworks (COFs): From design to applications. Chem. Soc. Rev., 2013, 42, 548-568 doi: 10.1039/C2CS35072F

    4. [4]

      Qian, H. L.; Yang, C. X.; Yan, X. P. Bottom-up synthesis of chiral covalent organic frameworks and their bound capillaries for chiral separation. Nat. Commun. 2016, 7, 12104-12111. doi: 10.1038/ncomms12104

    5. [5]

      Xu, H.; Chen, X.; Gao, J.; Lin, J. B.; Addicoat, M.; Irle, S.; Jiang, D. L. Catalytic covalent organic frameworks via pore surface engineering. Chem. Commun. 2014, 50, 1292-1294. doi: 10.1039/C3CC48813F

    6. [6]

      Furukawa, H.; Yaghi, O. M. Storage of hydrogen, methane, and carbon dioxide in highly porous covalent organic frameworks for clean energy applications. J. Am. Chem. Soc. 2009, 131, 8875-8883. doi: 10.1021/ja9015765

    7. [7]

      Deblase, C. R.; Silberstein, K. E.; Truong, T. T.; A, H. A.; Dichtel, W. R. Β. β-Ketoenamine-linked covalent organic frameworks capable of pseudocapacitive energy storage. J. Am. Chem. Soc. 2013, 135, 16821-16824. doi: 10.1021/ja409421d

    8. [8]

      Peng, Y.; Zhao, M.; Chen, B.; Zhang, Z.; Huang, Y.; Dai, F.; Lai, Z.; Cui, X.; Tan, C.; Zhang, H. Hybridization of MOFs and COFs: A new strategy for construction of MOF@COF core-shell hybrid materials. Adv. Mater. 2018, 30, 1705454 doi: 10.1002/adma.v30.3

    9. [9]

      Gole, B.; Stepanenko, V.; Rager, S.; Grgne, M.; Medina, D. D.; Bein, T.; Wgrthner, F.; Beuerle, F. Microtubular self‐assembly of covalent organic frameworks. Angew. Chem. Int. Ed. 2018, 57, 846 –850 doi: 10.1002/anie.201708526

    10. [10]

      Halder, A.; Kandambeth, S.; Biswal, B. P.; Kaur, G.; Roy, N. C.; Addicoat, M.; Salunke, J. K.; Banerjee, S.; Vanka, K.; Heine, T.; Verma, S.; Banerjee, R. Decoding the morphological diversity in two dimensional crystalline porous polymers by core planarity modulation. Angew. Chem. Int. Ed. 2016, 55, 7806 –7810. doi: 10.1002/anie.201600087

    11. [11]

      Kandambeth, S.; Venkatesh, V.; Shinde, D. B.; Kumari, S.; Halder, A.; Verma, S.; Banerjee, R. Self-templated chemically stable hollow spherical covalent organic framework. Nat. Comm. 2015, DOI: 10.1038/ncomms7786

    12. [12]

      Tan, J.; Namuangruk, S.; Kong, W.; Kungwan, N.; Guo, J.; Wang, C. Manipulation of amorphous‐to‐crystalline transformation: Towards the construction of covalent organic framework hybrid microspheres with NIR photothermal conversion ability. Angew. Chem. Int. Ed. 2016, 55, 13979 –13984 doi: 10.1002/anie.v55.45

    13. [13]

      Sun, B.; Liu, J.; Cao, A.; Song, W.; Wang, D. Interfacial synthesis of ordered and stable covalent organic frameworks on amino-functionalized carbon nanotubes with enhanced electrochemical performance. Chem. Commun., 2017, 53, 6303--6306 doi: 10.1039/C7CC01902E

    14. [14]

      Ma, T.; Kapustin, E. A.; Yin, S.; Liang, L.; Zhou. Z.; Niu, J.; Li, L.; Wang, Y.; Su, J.; Li, J.; Wang, X.; Wang, W.; Wang, W.; Sun, J.; Yaghi, O. M. Single-crystal X-ray diffraction structures of covalent organic frameworks. Science, 2018, 361, 48–52 doi: 10.1126/science.aat7679

    15. [15]

      Evans, A. M.; Parent, L. R.; Flanders, N. C.; Bisbey, R. P.; Vitaku, E.; Kirschner, M. S; Schaller, R. D.; Chen, L. X.; Gianneschi, N. C.; Dichtel, W. R. Seeded growth of single-crystal two-dimensional covalent organic frameworks. Science, 2018, 361, 52–57 doi: 10.1126/science.aar7883

    16. [16]

      Dogru, M.; Handloser, M.; Auras, F.; Kunz, T.; Medina, D. A. A photoconductive thienothiophene‐based covalent organic framework showing charge transfer towards included fullerene. Angew. Chem. Int. Ed. 2013, 125, 2992-2996. doi: 10.1002/ange.201208514

    17. [17]

      Feng, X.; Chen, L.; Honsho, Y.; Saengsawang, O.; Liu, L. L.; Wang, L.; Saeki, A.; Irle, S.; Seki, S.; Dong, Y. P.; Jiang, D. L. An ambipolar conducting covalent organic framework with self‐sorted and periodic electron donor‐acceptor ordering. Adv. Mater. 2012, 24, 3026-3031. doi: 10.1002/adma.v24.22

    18. [18]

      Ding, S. Y.; Gao, J.; Wang, Q.; Zhang, Y.; Song, W. G.; Su, C. Y.; Wang, W. Construction of covalent organic framework for catalysis: Pd/COF-LZU1 in Suzuki-Miyaura coupling reaction. J. Am. Chem. Soc. 2011, 133, 19816-19822. doi: 10.1021/ja206846p

    19. [19]

      Calik, M.; Auras, F.; Salonen, L. M.; Bader, K.; Grill, I.; Handloser, M.; Medina, D. D.; Dogru, M.; Löbermann, F.; Trauner, D.; Hartschuh, A.; Bein, T. Extraction of photogenerated electrons and holes from a covalent organic framework integrated heterojunction. J. Am. Chem. Soc. 2014, 136, 17802-17807. doi: 10.1021/ja509551m

    20. [20]

      Warren, N. J.; Armes, S. P. Polymerization-induced self-assembly of block copolymer nano-objects via RAFT aqueous dispersion polymerization. J. Am. Chem. Soc. 2014, 136, 10174−10185 doi: 10.1021/ja502843f

    21. [21]

      Smith, B. J.; Hwang, N.; Chavez, A. D.; Novotney, J. L.; Dichtel, W. R. Growth rates and water stability of 2D boronate ester covalent organic frameworks. Chem. Commun. 2015, 51, 7532-7535. doi: 10.1039/C5CC00379B

    22. [22]

      Smith, B. J.; Overholts, A. C.; Hwang, N.; Dichtel, W. R. Insight into the crystallization of amorphous imine-linked polymer networks to 2D covalent organic frameworks. Chem. Commun. 2016, 52, 3690-3693. doi: 10.1039/C5CC10221A

    23. [23]

      Smith, B. J.; Dichtel, W. R. Mechanistic studies of two-dimensional covalent organic frameworks rapidly polymerized from initially homogenous conditions. J. Am. Chem. Soc. 2014, 136, 8783-8789. doi: 10.1021/ja5037868

    24. [24]

      Bunck, D. N.; Dichtel, W. R. Internal functionalization of three‐dimensional covalent organic frameworks. Angew. Chem. Int. Ed. 2012, 51, 1885-1889. doi: 10.1002/anie.v51.8

    25. [25]

      Vitaku, E.; Dichtel, W. R. Synthesis of 2D imine-linked covalent organic frameworks through formal transimination reactions. J. Am. Chem. Soc. 2017, 139, 12911−12914. doi: 10.1021/jacs.7b06913

    26. [26]

      Biswal, B. P.; Chandra, S.; Kandambeth, S.; Lukose, B.; Heine, T.; Banerjee, R. Mechanochemical synthesis of chemically stable isoreticular covalent organic frameworks. J. Am. Chem. Soc. 2013, 135, 5328-5331. doi: 10.1021/ja4017842

    27. [27]

      Huang, W.; Jiang, Y.; Li, X.; Li, X. J.; Wang, J. Y.; Wu, Q.; Liu, X. K. Solvothermal synthesis of microporous, crystalline covalent organic framework nanofibers and their colorimetric nanohybrid structures. ACS Appl. Mater. Inter. 2013, 5, 8845-8849. doi: 10.1021/am402649g

    28. [28]

      Xu, H.; Tao, S. S.; Jiang, D. L. Proton conduction in crystalline and porous covalent organic frameworks. Nat. Mater. 2016, 15, 722-726. doi: 10.1038/nmat4611

    29. [29]

      Kandambeth, S.; Mallick, A.; Lukose, B.; Mane, M. V.; Heine, T.; Banerjee, R. Construction of crystalline 2D covalent organic frameworks with remarkable chemical (acid/base) stability via a combined reversible and irreversible route. J. Am. Chem. Soc. 2012, 134, 19524-19527. doi: 10.1021/ja308278w

    30. [30]

      Kuecken, S.; Schmidt, J.; Zhi, L.; Thomas, A. Conversion of amorphous polymer networks to covalent organic frameworks under ionothermal conditions: A facile synthesis route for covalent triazine frameworks. J. Mater. Chem. A 2015, 3, 24422-24427. doi: 10.1039/C5TA07408H

    31. [31]

      Gao, Q.; Bai, L.; Zeng, Y.; Wang, P.; Zhang, X.; Zou, R.; Zhao, Y. Reconstruction of covalent organic frameworks by dynamic equilibrium. Chemistry 2015, 21, 16818-16822. doi: 10.1002/chem.v21.47

    32. [32]

      Iwasawa, N.; Takahagi, H. Boronic esters as a system for crystallization-induced dynamic self-assembly equipped with an " on-off” switch for equilibration. J. Am. Chem. Soc. 2007, 129, 7754-7755. doi: 10.1021/ja072319q

    33. [33]

      Gilroy, J. B.; Gädt, T.; Whittell, G. R.; Chabanne, L.; Mitchels, J. M.; Richardson, R. M.; Winnik, M. A.; Manners, I. Monodisperse cylindrical micelles by crystallization-driven living self-assembly. Nat. Chem. 2010, 2, 566-570. doi: 10.1038/nchem.664

    34. [34]

      Chandra, S.; Kandambeth, S.; Biswal, B. P.; Lukose, B.; Kunjir, S. M.; Chaudhary, M.; Babarao, R.; Heine, T.; Banerjee, R. Chemically stable multilayered covalent organic nanosheets from covalent organic frameworks via mechanical delamination. J. Am. Chem. Soc. 2013, 135, 17853-17861. doi: 10.1021/ja408121p

  • 加载中
计量
  • PDF下载量:  0
  • 文章访问数:  2130
  • HTML全文浏览量:  51
文章相关
  • 发布日期:  2019-11-01
  • 收稿日期:  2019-04-15
  • 修回日期:  2019-05-30
  • 网络出版日期:  2019-09-12
通讯作者: 陈斌, bchen63@163.com
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索

/

返回文章