Configurational Selectivity Study of Two-dimensional Covalent Organic Frameworks Isomers Containing D2h and C2 Building Blocks

doi:10.1007/s40242-022-2001-5

Abstract

Abstract: The isomerization of covalent organic frameworks(COFs) materials is still a mysterious and attractive topic. Diversified monomer structures are still urgently needed to explore the in-depth mechanism of isomerization in these special COFs. This work provides a new D₂_h monomer for the construction of [D₂_h+C₂] 2D COFs isomers. A new D₂_h monomer adopted here was proven to tend to form a single pore framework structure.

Key words: Covalent organic framework, Isomerization, Kagome, Dynamic covalent bond

ZHENG Xuhan, ZHANG Lin, XIE Chenxiao, WANG Hui, LIU Hui, PAN Qingyan, ZHAO Yingjie. Configurational Selectivity Study of Two-dimensional Covalent Organic Frameworks Isomers Containing D_2h and C₂ Building Blocks[J]. Chemical Research in Chinese Universities, 2022, 38(2): 639-642.

References

[1] Cote A. P., Benin A. I., Ockwig N. W., O'Keeffe M., Matzger A. J., Yaghi O. M., Science, 2005, 18, 310.
[2] Ding S. Y., Wang W., Chem. Soc. Rev., 2013, 42, 548.
[3] Liu H., Kan X. N., Wu C. Y., Pan Q. Y., Li. Z B., Zhao Y. J., Chin. J. Polym. Sci., 2018, 36, 425.
[4] Wu C. Y., Liu Y. M., Liu H., Duan C. H., Pan Q. Y., Zhu J., Hu F., Ma X. Y., Jiu T. G., Li Z. B., Zhao Y. J., J. Am. Chem. Soc., 2018,140, 10016.
[5] Zhao Y. J., Liu H., Wu C. Y., Zhang Z. H., Pan Q. Y., Hu F., Wang R. M., Li P. W., Huang X. W., Li Z. B., Angew. Chem. Int. Ed., 2019, 58, 5376.
[6] Liu H., Ding J. H., Guan X. Y., Chen F. Q., Li C. Y., Zhu L. K., Xue M., Yuan D. Q., Valtchev V., Yan Y. S., Qiu S. L., Fang Q. R., J. Am. Chem. Soc., 2020, 142, 13334.
[7] Nagai A., Guo Z., Feng X., Jin S., Chen X., Ding X., Jiang D., Nat. Commun., 2011, 2, 536.
[8] Neti V. S. P. K., Wu X., Deng S., Echegoyen L.,Polym. Chem., 2013, 4, 4566.
[9] Gao C., Li J., Yin S., Sun J. L., Wang C., Nat. Commun., 2020, 11, 4919.
[10] Liu Y. M., Wu C. Y., Sun Q. Z., Hu F., Pan Q. Y., Sun J., Jin Y. H., Li Z. B., Zhang W., Zhao Y. J., CCS Chem., 2020, 2, 2418.
[11] Wang Y. C., Liu H., Pan Q. Y., Ding N. X., Yang C. M., Zhang Z. H., Jia C. C., Li Z. B., Liu J., Zhao Y. J., ACS Appl. Mater. Interfaces, 2020, 12, 46483.
[12] Ding S. Y., Cao J., Wang Q., Zhang Y., Song W. G., Su C. Y., Wang W., J. Am. Chem. Soc., 2011, 133, 19816.
[13] Fang Q., Gu S., Zheng J., Zhuang Z., Qiu S., Yan Y., Angew. Chem. Int. Ed., 2014, 53, 2878.
[14] Wang Y. C., Liu H., Pan Q. Y., Wu C. Y., Hao W. H., Xu J., Chen R. Z., Liu J., Li Z. B., Zhao Y. J., J. Am. Chem. Soc., 2020, 142, 5958.
[15] Chen R. F., Wang Y., Ma Y., Arindam M., Gao X. Y., Gao L., Qiao L. J., Li X. B., Wu L. Z., Wang C., Nat. Commun., 2021, 12, 1354.
[16] Zhi Y. F., Wang Z. R., Zhang H. L., Zhang Q. C., Small, 2020, 16, 2001070.
[17] Li D. H., Li C. Y., Zhang L. J., Li H., Zhu L. K., Yang D. J., Fang Q. R., Qiu S. L., Yao X. D., J. Am. Chem. Soc., 2020, 142, 8104.
[18] Li H., Pan Q. Y., Ma Y. C., Guan X. Y., Xue M., Fang Q. R., Yan Y. S., Valtchev V., Qiu S. L., J. Am. Chem. Soc., 2016, 138, 14783.
[19] Wan S., Gándara F., Asano A., Furukawa H., Saeki A., Dey S. K., Liao L., Ambrogio M. W, Botros Y. Y., Duan X., Seki S., Stoddart J. F., Yaghi O. M., Chem. Mater., 2011, 23, 4094.
[20] Liao H. P., Ding H. M., Li B. J., Ai X. P., Wang C., J. Mater. Chem. A, 2014, 2, 8854.
[21] Yao C. J., Wu Z., Xie J., Yu F., Guo W., Xu Z. J., Li D. S., Zhang S., Zhang Q., ChemSusChem 2020, 13, 2457.
[22] Li H., Chang J. H., Li S. S., Guan X. Y., Li D. H., Li C. Y., Tang L. X., Xue M., Yan Y. S., Valtchev V., Qiu S. L., Fang Q. R., J. Am. Chem. Soc., 2019, 141, 13324.
[23] Ding H. M., Li Y. H., Hu H., Sun Y. M., Wang J. G., Wang C. X., Wang C., Zhang G. X., Wang B. S., Xu W., Zhang D. Q., Chem. Eur. J., 2014, 20, 14614.
[24] Li Z. L., Li H., Guan X., Tang J. J., Yusran Y., Li Z., Xue M., Fang Q. R., Yan Y. S., Valtchev V., Qiu S. L., J. Am. Chem. Soc., 2017, 139, 17771.
[25] Xie Z., Wang B., Yang Z. F., Yang. X., Yu X., Xing G. L., Zhang Y. H., Chen. L., Angew. Chem. Int. Ed., 2019, 58, 15742.
[26] She P. F., Qin Y. Y., Wang X., Zhang Q. C., Adv. Mater., 2021, 2101175.
[27] Yu F., Liu W. B., Ke S. W., Kurmoo M., Zuo J. L., Zhang Q. C., Nat. Commun., 2020, 11, 5534.
[28] Yu F., Liu W. B., Li B., Tian D., Zuo J. L., Zhang Q. C., Angew. Chem. Int. Ed., 2019, 58, 16101.
[29] Bai L. Y., Phua S. Z. F., Lim W. Q., Jana A., Luo Z., Tham H. P., Zhao L. Z., Gao Q., Zhao Y. L., Chem. Commun., 2016, 52, 4128.
[30] Fang Q. R., Wang J. H., Gu S., Kaspar R. B., Zhuang Z. B., Zheng J., Guo H. X., Qiu S. L., Yan Y. S., J. Am. Chem. Soc., 2015, 137, 8352.
[31] Uribe-Romo F. J., Hunt J. R., Furukawa H., Klöck C., O'Keeffe M., Yaghi O. M., J. Am. Chem. Soc., 2009, 131, 4570.
[32] Meng Y., Luo Y., Shi J. L., Ding H., Lang X., Chen W., Zheng A., Sun J. L., Wang C., Angew. Chem. Int. Ed., 2020, 59, 3624.
[33] Geng K. Y., He T., Liu R. Y., Dalapati S., Tan K. T., Li Z. P., Tao S. S., Gong Y. F., Jiang Q. H., Jiang D. L., Chem. Rev., 2020, 120, 8814.
[34] Ma D. L., Qian C., Qi Q. Y., Zhong Z. R., Jiang G. F., Zhao X., Nano Res., 2021, 14, 381.
[35] Lin G. Q., Ding H. M., Chen R. F., Peng Z. K., Wang B. S., Wang C., J. Am. Chem. Soc., 2017, 25, 8705.
[36] Jiang S. Y., Gan S. X., Zhang X., Li H., Qi Q. Y., Cui F. Z., Lu J., Zhao X., J. Am. Chem. Soc., 2019, 141, 14981.
[37] Han X. H., Qi Q. Y., Zhou Z. B., Zhao X., Chin. J. Chem., 2020, 38, 1676.
[38] Zhang Z. H., Liu H., Sun Q. Z., Shao F., Pan Q. Y., Zhuang T., Zhao Y. J., ChemistryOpen, 2020, 9, 381.
[39] Makal T. A, A. Yakovenko A., Zhou H. C., J. Phys. Chem. Lett., 2011, 2, 1682.
[40] Zhou T. Y., Xu S. Q., Wen Q., Pang Z. F., Zhao X.,J. Am. Chem. Soc., 2014, 136, 15885.
[41] Dong J. Q., Li X., Peh S. B., Yuan Y. D., Wang Y. X., Ji D. X., Peng S. J., Liu G. L., Ying S. M., Yuan D. Q., Jiang J. W., Ramakrishna S., Zhao D., Chem. Mater., 2019, 31, 146.
[42] Mo Y. P., Liu X. H., Wang D., ACS Nano, 2017, 11, 11694.
[43] Liang R. R., Cui F. Z., A R. H., Qi Q. Y., Zhao X., CCS Chem., 2020, 2, 139.
[44] Peng Y. W., Li L. X., Zhu C. Z., Chen B., Zhao M. T., Zhang Z. C., Lai Z. C., Zhang X., Tan C L., Han Y., Zhu Y. H., Zhang H., J. Am. Chem. Soc. 2020, 30, 13162.
[45] Liu X. L., Li J., Gui B., Lin G. Q., Fu Q., Yin S., Liu X. F., Sun J. L., Wang C., J. Am. Chem. Soc., 2021, 143, 2123.
[46] Gao C., Li J., Yin S., Sun J. L., Wang C., J. Am. Chem. Soc., 2020, 142, 3718.
[47] Li Y. S., Chen Q., Xu T. T., Xie Z., Liu J. J., Yu X., Ma S. Q., Qin T. S., Chen L., J. Am. Chem. Soc., 2019, 141, 13822.
[48] Li Y., Guo L., Lv Y., Zhao Z., Ma Y., Chen W., Xing G., Jiang D., Chen L., Angew. Chem. Int. Ed., 2021, 60, 5363.
[49] Troyano. J, Carné-Sánchez A., Pérez-Carvajal J., León-Reina L., Imaz I., Cabeza A., Maspoch D., Angew. Chem. Int. Ed., 2018, 57, 15420.
[50] Krause S., Bon V., Stoeck U., Senkovska I., Többens D. M., Wallacher D., Kaskel S., Angew. Chem. Int. Ed., 2017, 56, 10676.
[51] Huang N., Wang P., Jiang D. L., Nat. Rev. Mater., 2016, 1, 16068.
[52] Dong W. L., Wang L., Ding H. M., Zhao L., Wang D., Wang C., Wan L. J., Langmuir, 2015, 31, 11755.
[53] Pang Z. F., Zhou T. Y., Liang R. R., Qian Q. Y., Zhao X., Chem. Sci., 2017, 8, 3866.
[54] Rabbani M. G., Sekizkardes A. K., Kahveci Z., Reich T. E., Ding R. S., El-Kaderi H. M., Chem. Eur. J., 2013, 19, 3324.
[55] Krishnaraj C., Jena H. S., Bourda L., Laemont A., Pachfule P., Roeser J., Chandran C. V., Borgmans S., Rogge S. M. J., Leus K.., Stevens C. V., Martens J. A., Speybroeck V. V., Breynaert E., Thomas A., Van Der Voort P., J. Am. Chem. Soc., 2020, 142, 20107.
[56] Lyle S. J., Popp T. M. O., Waller P. J., Pei X K., Reimer J. A., Yaghi O. M., J. Am. Chem. Soc., 2019, 141, 11253.
[57] Dalapati S., Jin S. B., Gao J., Xu.Y. H., Nagai A., Jiang D. L., J. Am. Chem. Soc., 2013, 135, 17310.

Configurational Selectivity Study of Two-dimensional Covalent Organic Frameworks Isomers Containing D_2h and C₂ Building Blocks

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