Citation: Renjie Xue,  Chao Ma,  Jing He,  Xuechao Li,  Yanning Tang,  Lifeng Chi,  Haiming Zhang. Catassembly in the Host-Guest Recognition of 2D Metastable Self-Assembled Networks[J]. Acta Physico-Chimica Sinica, ;2024, 40(9): 230901. doi: 10.3866/PKU.WHXB202309011 shu

Catassembly in the Host-Guest Recognition of 2D Metastable Self-Assembled Networks

  • Corresponding author: Lifeng Chi,  Haiming Zhang, 
  • Received Date: 8 September 2023
    Revised Date: 30 September 2023
    Accepted Date: 9 October 2023

    Fund Project: The project was supported by the National Natural Science Foundation of China (22072103, 51821002, 22161132026), the Collaborative Innovation Center of Suzhou Nano Science & Technology, the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD), the Suzhou Key Laboratory of Surface and Interface Intelligent Matter (SZS2022011), and the “111” Project.

  • Catassembly is a newly developed concept concerning the process of molecular assembly improved by a catalyst-assembler (catassembler). However, it has not been visualized in detail at the molecular level. To achieve the formation of highly complex structures with high efficiency and selectivity, a deeper understanding of catassembly is essential. In this study, we present the scanning tunneling microscopy (STM) characterization of a catassembly process within host-guest assembly. We utilize a metastable self-assembled network of 1,3,5-tris(4-carboxyphenyl)-benzene (BTB) at the liquid-solid interface between 1-octanoic acid and highly oriented pyrolytic graphite (HOPG). Different adsorption behaviors of low-concentration guest molecules (copper phthalocyanine (CuPc), and coronene (COR)) are contrastively analyzed during the host-guest assembly in both single-guest (COR/BTB or CuPc/BTB) and multi-guest molecule (COR&CuPc/BTB) systems. The spontaneous phase transition from a hexagonal to an oblique structure of BTB monolayers (high concentration, approximately 500 μmol∙L−1 in octanoic acid) provides an ideal metastable phase for studying the dynamic assembly process. In the host-guest assembly, the metastable BTB hexagonal phase serves as a host network and can be stabilized by co-assembling guest molecules under a negative bias voltage. However, the stability of the metastable phase varies with different guest molecules. We observe that the BTB metastable phase is more robust with COR guest molecules than with CuPc. In the CuPc/BTB system, we find that low-concentration CuPc (approximately 1.5 μmol∙L−1 in octanoic acid) can hardly co-assemble with BTB, leading to the gradual collapse of the metastable BTB networks into the oblique phase. The different stability of BTB metastable phase in the host-guest assembly is attributed to differences in the kinetics of trapping guest molecules. Guest COR molecules exhibit kinetic advantages over CuPc when assembling with host BTB networks under a negative sample bias. The lower trapping rate of CuPc hinders the formation of co-assembled BTB/CuPc networks. These differences in the dynamic behavior of the guest molecules are further explored in the research of catassembly. In a multi-guest molecule system (COR&CuPc/BTB), COR molecules are preferentially trapped by BTB hexagonal networks and can gradually be replaced by CuPc during continuous scanning. The more energetically stable structure of CuPc/BTB compared to COR/BTB rationalizes the exchange of the guest molecule and the evolution of the assembly phase. The involvement of COR significantly increases both the efficiency and quality of the CuPc/BTB assembly, serving as a catassembler. This observation provides insights into a complete catassembly process at the molecular level, enabling further investigations into the selectivity and efficiency of host-guest phenomena for potential applications in analysis and separation. Additionally, this work serves as a prototype for constructing highly complex 2D assembled monolayers.
  • 加载中
    1. [1]

      (1) Yang, H.; Yuan, B.; Zhang, X.; Scherman, O. A. Acc. Chem. Res. 2014, 47, 2106. doi: 10.1021/ar500105t

    2. [2]

      (2) Li, J. Q.; Qian, Y. X.; Duan, W. B.; Zeng, Q. D. Chin. Chem. Lett. 2019, 30, 292. doi: 10.1016/j.cclet.2018.05.037

    3. [3]

      (3) Teyssandier, J.; Feyter, S.; Mali, K. S. Chem. Commun. 2016, 52, 11465. doi: 10.1039/c6cc05256h

    4. [4]

      (4) De Feyter, S.; Gesquiere, A.; Abdel-Mottaleb, M. M.; Grim, P. C. M.; De Schryver, F. C.; Meiners, C.; Sieffert, M.; Valiyaveettil, S.; Mullen, K. Acc. Chem. Res. 2000, 33, 520. doi: 10.1021/ar970040g

    5. [5]

      (5) De Feyter, S.; Grim, P. C. M.; van Esch, J.; Kellogg, R. M.; Feringa, B. L.; De Schryver, F. C. J. Phys. Chem. B 1998, 102, 8981. doi: 10.1021/jp973177x

    6. [6]

      (6) Xue, J. D.; Deng, K.; Liu, B.; Duan, W. B.; Zeng, Q. D.; Wang, C. RSC Adv. 2015, 5, 39291. doi: 10.1039/c5ra01517k

    7. [7]

      (7) Dai, H. L.; Yi, W. J.; Deng, K.; Wang, H.; Zeng, Q. D. ACS Appl. Mater. Intefaces 2016, 8, 21095. doi: 10.1021/acsami.6b06638

    8. [8]

      (8) Tahara, K.; Kaneko, K.; Katayama, K.; Itano, S.; Nguyen, C. H.; Amorim, D. D. D.; De Feyter, S.; Tobe, Y. Langmuir 2015, 31, 7032. doi: 10.1021/acs.langmuir.5b01507

    9. [9]

      (9) Meng, T.; Lu, Y. B.; Lei, P.; Li, S. J.; Deng, K.; Xiao, X. W.; Ogino, K.; Zeng, Q. D. Langmuir 2022, 38, 3568. doi: 10.1021/acs.langmuir.2c00188

    10. [10]

      (10) Banerjee, K.; Kumar, A.; Canova, F. F.; Kezilebieke, S.; Foster, A. S.; Liljeroth, P. J. Phys. Chem. C 2016, 120, 8772. doi: 10.1021/acs.jpcc.6b01638

    11. [11]

      (11) Yan, L. H.; Kuang, G. W.; Lin, N. Chem. Commun. 2018, 54, 10570. doi: 10.1039/c8cc04491k

    12. [12]

      (12) Steiner, C.; Fromm, L.; Gebhardt, J.; Liu, Y.; Heidenreich, A.; Hammer, N.; Gorling, A.; Kivala, M.; Maier, S. Nanoscale 2021, 13, 9798. doi: 10.1039/d0nr09140e

    13. [13]

      (13) Ciesielski, A.; Palma, C. A.; Bonini, M.; Samori, P. Adv. Mater. 2010, 22, 3506. doi: 10.1002/adma.201001582

    14. [14]

      (14) Yoshimoto, S.; Suto, K.; Tada, A.; Kobayashi, N.; Itaya, K. J. Am. Chem. Soc. 2004, 126, 8020. doi: 10.1021/ja048760n

    15. [15]

      (15) De Feyter, S.; De Schryver, F. C. Chem. Soc. Rev. 2003, 32, 393. doi: 10.1039/b206566p

    16. [16]

      (16) Kudernac, T.; Lei, S. B.; Elemans, J. A. A. W.; De Feyter, S. Chem. Soc. Rev. 2009, 38, 3505. doi: 10.1039/b708902n

    17. [17]

      (17) Mamdouh, W.; Kelly, R. E. A.; Dong, M. D.; Kantorovich, L. N.; Besenbacher, F. J. Am. Chem. Soc. 2008, 130, 695. doi: 10.1021/ja076832f

    18. [18]

      (18) Theobald, J. A.; Oxtoby, N. S.; Phillips, M. A.; Champness, N. R.; Beton, P. H. Nature 2003, 424, 1029. doi: 10.1038/nature01915

    19. [19]

      (19) Ruben, M.; Payer, D.; Landa, A.; Comisso, A.; Gattinoni, C.; Lin, N.; Collin, J. P.; Sauvage, J. P.; De Vita, A.; Kern, K. J. Am. Chem. Soc. 2006, 128, 15644. doi: 10.1021/ja063601k

    20. [20]

      (20) Bellec, A.; Arrigoni, C.; Schull, G.; Douillard, L.; Fiorini-Debuisschert, C.; Mathevet, F.; Kreher, D.; Attias, A. J.; Charra, F. J. Chem. Phys. 2011, 134, 124702. doi: 10.1063/1.3569132

    21. [21]

      (21) Blunt, M. O.; Adisoejoso, J.; Tahara, K.; Katayama, K.; Van der Auweraer, M.; Tobe, Y.; De Feyter, S. J. Am. Chem. Soc. 2013, 135, 12068. doi: 10.1021/ja405585s

    22. [22]

      (22) Gutzler, R.; Sirtl, T.; Dienstmaier, J. F.; Mahata, K.; Heckl, W. M.; Schmittel, M.; Lackinger, M. J. Am. Chem. Soc. 2010, 132, 5084. doi: 10.1021/ja908919r

    23. [23]

      (23) Lei, P.; Zhao, L.; He, L.; Zhao, F. Y.; Xiao, X. W.; Tu, B.; Zeng, Q. D. Appl. Surf. Sci. 2021, 550, 149352. doi: 10.1016/j.apsusc.2021.149352

    24. [24]

      (24) Cometto, F. P.; Kern, K.; Lingenfelder, M. ACS Nano 2015, 9, 5544. doi: 10.1021/acsnano.5b01658

    25. [25]

      (25) Chan, Y.; Khan, S. B.; Mahmood, A.; Saleemi, A. S.; Lian, Z.; Ren, Y.; Zeng, X. M.; Lee, S. L. J. Phys. Chem. C 2020, 124, 815. doi: 10.1021/acs.jpcc.9b10537

    26. [26]

      (26) Cai, Z. F.; Zhan, G. L.; Daukiya, L.; Eyley, S.; Thielemans, W.; Severin, K.; De Feyter, S. J. Am. Chem. Soc. 2019, 141, 11404. doi: 10.1021/jacs.9b05265

    27. [27]

      (27) Lei, S. B.; Tahara, K.; De Schryver, F. C.; Van der Auweraer, M.; Tobe, Y.; De Feyter, S. Angew. Chem. Int. Ed. 2008, 47, 2964. doi: 10.1002/anie.200705322

    28. [28]

      (28) Palma, C. A.; Bjork, J.; Bonini, M.; Dyer, M. S.; Llanes-Pallas, A.; Bonifazi, D.; Persson, M.; Samori, P. J. Am. Chem. Soc. 2009, 131, 13062. doi: 10.1021/ja9032428

    29. [29]

      (29) Velpula, G.; Martin, C.; Daelemans, B.; Hennrich, G.; Van der Auweraer, M.; Mali, K. S.; De Feyter, S. Chem. Sci. 2021, 12, 13167. doi: 10.1039/d1sc02950a

    30. [30]

      (30) Wang, Y.; Lin, H. X.; Chen, L.; Ding, S. Y.; Lei, Z. C.; Liu, D. Y.; Cao, X. Y.; Liang, H. J.; Jiang, Y. B.; Tian, Z. Q. Chem. Soc. Rev. 2014, 43, 399. doi: 10.1039/c3cs60212e

    31. [31]

      (31) Zhang, H. L.; Wang, Y.; Zhang, H.; Liu, X. G.; Lee, A.; Huang, Q. L.; Wang, F.; Chao, J.; Liu, H. J.; Li, J.; et al. Nat. Commun. 2019, 10, 1006. doi: 10.1038/s41467-019-09004-4

    32. [32]

      (32) Nan, Z. A.; Wang, Y.; Chen, Z. X.; Yuan, S. F.; Tian, Z. Q.; Wang, Q. M. Commun. Chem. 2018, 1, 99. doi: 10.1038/s42004-018-0102-3

    33. [33]

      (33) Fang, Y.; Ivasenko, O.; Sanz-Matias, A.; Mali, K. S.; Tahara, K.; Tobe, Y.; De Feyter, S. Nanoscale 2023, 15, 4301. doi: 10.1039/d2nr06400f

    34. [34]

      (34) Steeno, R.; Minoia, A.; Lazzaroni, R.; Mali, K. S.; De Feyter, S. Chem. Commun. 2022, 58, 3138. doi: 10.1039/d1cc07206d

    35. [35]

      (35) Zhan, G.; Cai, Z. F.; Strutynski, K.; Yu, L.; Herrmann, N.; Martinez-Abadia, M.; Melle-Franco, M.; Mateo-Alonso, A.; Feyter, S. Nature 2022, 603, 835. doi: 10.1038/s41586-022-04409-6

    36. [36]

      (36) Mahmood, A.; Zeng, X. M.; Saleemi, A. S.; Cheng, K. Y.; Lee, S. L. Chem. Commun. 2020, 56, 8790. doi: 10.1039/d0cc01670e

    37. [37]

      (37) Wang, J.; Wang, L. M.; Lu, C.; Yan, H. J.; Wang, S. X.; Wang, D. RSC Adv. 2019, 9, 11659. doi: 10.1039/c9ra01493d

    38. [38]

      (38) Li, H.; Xu, X. G.; Shang, J.; Li, J. L.; Hu, X. Q.; Teo, B. K.; Wu, K. J. Phys. Chem. C 2012, 116, 21753. doi: 10.1021/jp303352h

    39. [39]

      (39) Xie, L.; Jiang, H. J.; Li, D. L.; Liu, M. X.; Ding, Y. Q.; Liu, Y. F.; Li, X.; Li, X. C.; Zhang, H. M.; Hou, Z. H.; et al. ACS Nano 2020, 14, 10680. doi: 10.1021/acsnano.0c05227

    40. [40]

      (40) Li, C.; Xu, Z.; Zhang, Y. J.; Li, J.; Xue, N.; Li, R. N.; Zhong, M. J.; Wu, T. H.; Wang, Y. F.; Li, N.; et al. Natl. Sci. Rev. 2023, 10, nwad088. doi: 10.1093/nsr/nwad088

    41. [41]

      (41) Deng, C. F.; Liu, Z. H.; Ma, C.; Zhang, H. M.; Chi, L. F. Langmuir 2020, 36, 5510. doi: 10.1021/acs.langmuir.0c00425

    42. [42]

      (42) Sahare, S.; Ghoderao, P.; Chan, Y.; Lee, S. L. Nanoscale 2023, 15, 1981. doi: 10.1039/d2nr05264d

    43. [43]

      (43) Zhang, X. M.; Zeng, Q. D.; Wang, C. RSC Adv. 2013, 3, 11351. doi: 10.1039/c3ra40473k

    44. [44]

      (44) Cometto, F.; Frank, K.; Stel, B.; Arisnabarreta, N.; Kern, K.; Lingenfelder, M. Chem. Commun. 2017, 53, 11430. doi: 10.1039/c7cc06597c

    45. [45]

      (45) Eder, G.; Kloft, S.; Martsinovich, N.; Mahata, K.; Schmittel, M.; Heckl, W. M.; Lackinger, M. Langmuir 2011, 27, 13563. doi: 10.1021/la203054k

    46. [46]

      (46) Lee, S.; Lin, C.; Cheng, K.; Chen, Y.; Chen, C. J. Phys. Chem. C. 2016, 120, 25505. doi: 10.1021/acs.jpcc.6b09538

    47. [47]

    48. [48]

      (48) Wang, Y.; Miao, X. R.; Deng, W. L.; Brisse, R.; Jousselme, B.; Silly, F. Nanomaterials 2022, 12, 775. doi: 10.3390/nano12050775

  • 加载中
    1. [1]

      Shihui Shi Haoyu Li Shaojie Han Yifan Yao Siqi Liu . Regioselectively Synthesis of Halogenated Arenes via Self-Assembly and Synergistic Catalysis Strategy. University Chemistry, 2024, 39(5): 336-344. doi: 10.3866/PKU.DXHX202312002

    2. [2]

      Peiran ZHAOYuqian LIUCheng HEChunying DUAN . A functionalized Eu3+ metal-organic framework for selective fluorescent detection of pyrene. Chinese Journal of Inorganic Chemistry, 2024, 40(4): 713-724. doi: 10.11862/CJIC.20230355

    3. [3]

      Yunhao Zhang Yinuo Wang Siran Wang Dazhen Xu . Progress in Selective Construction of Functional Aromatics from Nitrogenous Cycloalkanes. University Chemistry, 2024, 39(11): 136-145. doi: 10.3866/PKU.DXHX202401083

    4. [4]

      Xilin Zhao Xingyu Tu Zongxuan Li Rui Dong Bo Jiang Zhiwei Miao . Research Progress in Enantioselective Synthesis of Axial Chiral Compounds. University Chemistry, 2024, 39(11): 158-173. doi: 10.12461/PKU.DXHX202403106

    5. [5]

      Fengqiao Bi Jun Wang Dongmei Yang . Specialized Experimental Design for Chemistry Majors in the Context of “Dual Carbon”: Taking the Assembly and Performance Evaluation of Zinc-Air Fuel Batteries as an Example. University Chemistry, 2024, 39(4): 198-205. doi: 10.3866/PKU.DXHX202311069

    6. [6]

      Jiakun BAITing XULu ZHANGJiang PENGYuqiang LIJunhui JIA . A red-emitting fluorescent probe with a large Stokes shift for selective detection of hypochlorous acid. Chinese Journal of Inorganic Chemistry, 2024, 40(6): 1095-1104. doi: 10.11862/CJIC.20240002

    7. [7]

      Jie ZHAOSen LIUQikang YINXiaoqing LUZhaojie WANG . Theoretical calculation of selective adsorption and separation of CO2 by alkali metal modified naphthalene/naphthalenediyne. Chinese Journal of Inorganic Chemistry, 2024, 40(3): 515-522. doi: 10.11862/CJIC.20230385

    8. [8]

      Junjie Zhang Yue Wang Qiuhan Wu Ruquan Shen Han Liu Xinhua Duan . Preparation and Selective Separation of Lightweight Magnetic Molecularly Imprinted Polymers for Trace Tetracycline Detection in Milk. University Chemistry, 2024, 39(5): 251-257. doi: 10.3866/PKU.DXHX202311084

    9. [9]

      Yinuo Wang Siran Wang Yilong Zhao Dazhen Xu . Selective Synthesis of Diarylmethyl Anilines and Triarylmethanes via Multicomponent Reactions: Introduce a Comprehensive Experiment of Organic Chemistry. University Chemistry, 2024, 39(8): 324-330. doi: 10.3866/PKU.DXHX202401063

    10. [10]

      Qian Huang Zhaowei Li Jianing Zhao Ao Yu . Quantum Chemical Calculations Reveal the Details Below the Experimental Phenomenon. University Chemistry, 2024, 39(3): 395-400. doi: 10.3866/PKU.DXHX202309018

    11. [11]

      Xiaxue Chen Yuxuan Yang Ruolin Yang Yizhu Wang Hongyun Liu . Adjustable Polychromatic Fluorescence: Investigating the Photoluminescent Properties of Copper Nanoclusters. University Chemistry, 2024, 39(9): 328-337. doi: 10.3866/PKU.DXHX202308019

    12. [12]

      Yajun Jian Quanguo Zhai Quan Gu Shengli Gao . Reconstruction and Practice of the Teaching Content of “Carbon Group Elements” in Inorganic Chemistry to Reflect Comprehensive Education Function. University Chemistry, 2024, 39(11): 96-107. doi: 10.12461/PKU.DXHX202403006

    13. [13]

      Lei Shi . Nucleophilicity and Electrophilicity of Radicals. University Chemistry, 2024, 39(11): 131-135. doi: 10.3866/PKU.DXHX202402018

    14. [14]

      Jinlong YANWeina WUYuan WANG . A simple Schiff base probe for the fluorescent turn-on detection of hypochlorite and its biological imaging application. Chinese Journal of Inorganic Chemistry, 2024, 40(9): 1653-1660. doi: 10.11862/CJIC.20240154

    15. [15]

      Donghui PANYuping XUXinyu WANGLizhen WANGJunjie YANDongjian SHIMin YANGMingqing CHEN . Preparation and in vivo tracing of 68Ga-labeled PM2.5 mimetic particles for positron emission tomography imaging. Chinese Journal of Inorganic Chemistry, 2024, 40(4): 669-676. doi: 10.11862/CJIC.20230468

    16. [16]

      Jin Tong Shuyan Yu . Crystal Engineering for Supramolecular Chirality. University Chemistry, 2024, 39(3): 86-93. doi: 10.3866/PKU.DXHX202308113

    17. [17]

      Renxiao Liang Zhe Zhong Zhangling Jin Lijuan Shi Yixia Jia . A Palladium/Chiral Phosphoric Acid Relay Catalysis for the One-Pot Three-Step Synthesis of Chiral Tetrahydroquinoline. University Chemistry, 2024, 39(5): 209-217. doi: 10.3866/PKU.DXHX202311024

    18. [18]

      Xin XIONGQian CHENQuan XIE . First principles study of the photoelectric properties and magnetism of La and Yb doped AlN. Chinese Journal of Inorganic Chemistry, 2024, 40(8): 1519-1527. doi: 10.11862/CJIC.20240064

    19. [19]

      Haiying Wang Andrew C.-H. Sue . How to Visually Identify Homochiral Crystals. University Chemistry, 2024, 39(3): 78-85. doi: 10.3866/PKU.DXHX202309004

    20. [20]

      Yonghui Wang Weilin Chen Yangguang Li . Knowledge Construction of “Solubility of Inorganic Substances” in Elemental Chemistry Teaching. University Chemistry, 2024, 39(4): 261-267. doi: 10.3866/PKU.DXHX202312102

Metrics
  • PDF Downloads(0)
  • Abstract views(470)
  • HTML views(30)

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
Address:Zhongguancun North First Street 2,100190 Beijing, PR China Tel: +86-010-82449177-888
Powered By info@rhhz.net

/

DownLoad:  Full-Size Img  PowerPoint
Return