Citation: Li Mingliang, Li Shuo, Wang Guozhi, Guo Xuefeng. Effects of Alkyl-Chain Engineering on the Thermodynamic Properties of Amphiphilic Organic Semiconductors[J]. Acta Physico-Chimica Sinica, ;2020, 36(11): 190803. doi: 10.3866/PKU.WHXB201908036 shu

Effects of Alkyl-Chain Engineering on the Thermodynamic Properties of Amphiphilic Organic Semiconductors

  • Corresponding author: Guo Xuefeng, guoxf@pku.edu.cn
  • Received Date: 29 August 2019
    Revised Date: 12 September 2019
    Accepted Date: 12 September 2019
    Available Online: 17 September 2019

    Fund Project: Natural Science Foundation of Beijing, China Z181100004418003National Natural Science Foundation of China 21727806the National Key R & D Program of China 2017YFA0204901The project was supported by the National Key R & D Program of China (2017YFA0204901), National Natural Science Foundation of China (21727806) and Natural Science Foundation of Beijing, China (Z181100004418003)

  • Due to their special polar structure, amphiphilic molecules are simple to process, low in cost and excellent in material properties. Thus, they can be widely applied in the preparation of functional film materials and bionics related to cell membranes. Therefore, amphiphilic organic semiconductor materials are receiving increasing attention in research and industrial fields. The structure of organic amphiphilic semiconductor molecules usually consists of three functional parts: a hydrophilic group, a hydrophobic group, and a linking group between them. The adjustment of their correlation to achieve the target performance is particularly important and needs experimental discussion regarding synthetic methodologies. In this work, we focused on the engineering of a substituent alkyl-chain, and an amphiphilic functional molecule (benzo[b]benzo[4, 5] thieno[2, 3-d]thiophene, named CnPA-BTBT, n = 3–11) was proposed and synthesized. This molecule links the hydrophobic semiconductor backbone and hydrophilic polar group through alkyl chains of different lengths. Fundamental properties were investigated by nuclear magnetic resonance (NMR) and ultraviolet-visible spectroscopy (UV-Vis) to conform the structure and the band gap properties of the designed organic semiconductor. Thermodynamic features were investigated by thermogravimetric analysis (TGA) and corresponding differential thermal gravity (DTG), which indicate that the functional molecule CnPA-BTBT (n = 3–11) has a great stability in ambient conditions. Moreover, the results show that the binding ability of the amphiphilic molecule to water molecules was regulated by the odd-even alternating effect of the alkyl chain and the intramolecular coupling with BTBT. Furthermore, differential scanning calorimetry (DSC) and polarized optical microscopy (POM) were used to study the material properties in detail. As the length of the alkyl chain increased, the functional molecule CnPA-BTBT (n = 3–11) gradually changed from "hard" species with no thermodynamic changes to a transition one with a pair of thermodynamic peaks, and eventually to a "soft" one as a typical liquid crystal with clear observation of Maltese-cross spherulites. The cooling and freezing points were further studied, and the values and trends of their enthalpy and corresponding temperature fluctuated and alternated due to the volume effect, odd-even alternating effect, flexibility, and other functions of the alkyl chain. Three molecular models were proposed according to the thermodynamic study results, namely the brick-like model, transition model, and liquid crystal model. This work presents in-depth discussion on material structure and corresponding thermodynamic properties, and it is an experimental basis for the design, synthesis, optimization, and screening of target performance materials.
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    1. [1]

      Wang, C.; Dong, H.; Hu, W.; Liu, Y.; Zhu, D. Chem. Rev. 2012, 112, 2208. doi: 10.1021/cr100380z  doi: 10.1021/cr100380z

    2. [2]

      Xu, J.; Wu, H. -C.; Zhu, C.; Ehrlich, A.; Shaw, L.; Nikolka, M.; Wang, S.; Molina-Lopez, F.; Gu, X.; Luo, S.; et al. Nat. Mater. 2019, 18, 594. doi: 10.1038/s41563-019-0340-5  doi: 10.1038/s41563-019-0340-5

    3. [3]

      Lee, M. Y.; Lee, H. R.; Park, C. H.; Han, S. G.; Oh, J. H. Acc. Chem. Res. 2018, 51, 2829. doi: 10.1021/acs.accounts.8b00465  doi: 10.1021/acs.accounts.8b00465

    4. [4]

      Chen, H.; Dong, S.; Bai, M.; Cheng, N.; Wang, H.; Li, M.; Du, H.; Hu, S.; Yang, Y.; Yang, T.; et al. Adv. Mater. 2015, 27, 2113.doi: 10.1002/adma.201405378  doi: 10.1002/adma.201405378

    5. [5]

      Tee, B. C. K.; Chortos, A.; Berndt, A.; Nguyen, A. K.; Tom, A.; McGuire, A.; Lin, Z. C.; Tien, K.; Bae, W. -G.; Wang, H.; et al. Science 2015, 350, 313. doi: 10.1126/science.aaa9306  doi: 10.1126/science.aaa9306

    6. [6]

      Wang, Y.; Chen, Y.; Li, R.; Wang, S.; Su, W.; Ma, P.; Wasielewski, M. R.; Li, X.; Jiang, J. Langmuir 2007, 23, 5836. doi: 10.1021/la063729f  doi: 10.1021/la063729f

    7. [7]

      Garner, L. E.; Park, J.; Dyar, S. M.; Chworos, A.; Sumner, J. J.; Bazan, G. C. J. Am. Chem. Soc. 2010, 132, 10042. doi: 10.1021/ja1016156  doi: 10.1021/ja1016156

    8. [8]

      Yamamoto, S.; Nishina, N.; Matsui, J.; Miyashita, T.; Mitsuishi, M. Langmuir 2018, 34, 10491. doi: 10.1021/acs.langmuir. 8b01694  doi: 10.1021/acs.langmuir.8b01694

    9. [9]

      Bonini, M.; Zalewski, L.; Orgiu, E.; Breiner, T.; Dötz, F.; Kastler, M.; Samorì, P. J. Phys. Chem. C 2011, 115, 9753. doi: 10.1021/jp201556y  doi: 10.1021/jp201556y

    10. [10]

      Khassanov, A.; Steinrück, H. -G.; Schmaltz, T.; Magerl, A.; Halik, M. Acc. Chem. Res. 2015, 48, 1901. doi: 10.1021/acs.accounts.5b00022  doi: 10.1021/acs.accounts.5b00022

    11. [11]

      Lee, J.; Han, A. R.; Kim, J.; Kim, Y.; Oh, J. H.; Yang, C. J. Am. Chem. Soc. 2012, 134, 20713. doi: 10.1021/ja308927g  doi: 10.1021/ja308927g

    12. [12]

      Smits, E. C. P.; Mathijssen, S. G. J.; van Hal, P. A.; Setayesh, S.; Geuns, T. C. T.; Mutsaers, K. A. H. A.; Cantatore, E.; Wondergem, H. J.; Werzer, O.; Resel, R.; et al. Nature 2008, 455, 956. doi: 10.1038/nature07320  doi: 10.1038/nature07320

    13. [13]

      Whitelam, S.; Jack, R. L. Annu. Rev. Phys. Chem. 2015, 66, 143. doi: 10.1146/annurev-physchem-040214-121215  doi: 10.1146/annurev-physchem-040214-121215

    14. [14]

      Inoue, S.; Minemawari, H.; Tsutsumi, J. Y.; Chikamatsu, M.; Yamada, T.; Horiuchi, S.; Tanaka, M.; Kumai, R.; Yoneya, M.; Hasegawa, T. Chem. Mater. 2015, 27, 3809. doi: 10.1021/acs.chemmater.5b00810  doi: 10.1021/acs.chemmater.5b00810

    15. [15]

      Minemawari, H.; Tanaka, M.; Tsuzuki, S.; Inoue, S.; Yamada, T.; Kumai, R.; Shimoi, Y.; Hasegawa, T. Chem. Mater. 2017, 29, 1245. doi: 10.1021/acs.chemmater.6b04628  doi: 10.1021/acs.chemmater.6b04628

    16. [16]

      Dincbas-Renqvist, V.; Lendel, C.; Dogan, J.; Wahlberg, E.; Härd, T. J. Am. Chem. Soc. 2004, 126, 11220. doi: 10.1021/ja047727y  doi: 10.1021/ja047727y

    17. [17]

      North, M. L.; Wilcox, D. E. J. Am. Chem. Soc. 2019, doi: 10.1021/jacs.9b06836  doi: 10.1021/jacs.9b06836

    18. [18]

      Chen, H.; Li, M.; Lu, Z.; Wang, X.; Yang, J.; Wang, Z.; Zhang, F.; Gu, C.; Zhang, W.; Sun, Y.; et al. Nat. Commun. 2019, 10, 3872. doi: 10.1038/s41467-019-11887-2  doi: 10.1038/s41467-019-11887-2

    19. [19]

      Minemawari, H.; Tanaka, M.; Tsuzuki, S.; Inoue, S.; Yamada, T.; Kumai, R.; Shimoi, Y.; Hasegawa, T. Chem. Mater. 2017, 29, 1245. doi: 10.1021/acs.chemmater.6b04628  doi: 10.1021/acs.chemmater.6b04628

    20. [20]

      Inoue, S.; Minemawari, H.; Tsutsumi, J. Y.; Chikamatsu, M.; Yamada, T.; Horiuchi, S.; Tanaka, M.; Kumai, R.; Yoneya, M.; Hasegawa, T. Chem. Mater. 2015, 27, 3809. doi: 10.1021/acs.chemmater.5b00810  doi: 10.1021/acs.chemmater.5b00810

    21. [21]

      Chen, H.; Cheng, N.; Ma, W.; Li, M.; Hu, S.; Gu, L.; Meng, S.; Guo, X. ACS Nano 2016, 10, 436. doi: 10.1021/acsnano.5b05313  doi: 10.1021/acsnano.5b05313

    22. [22]

      Schmaltz, T.; Amin, A. Y.; Khassanov, A.; Meyer-Friedrichsen, T.; Steinrück, H. -G.; Magerl, A.; Segura, J. J.; Voitchovsky, K.; Stellacci, F.; Halik, M. Adv. Mater. 2013, 25, 4511. doi: 10.1002/adma.201301176  doi: 10.1002/adma.201301176

    23. [23]

      Yuan, Y.; Giri, G.; Ayzner, A. L.; Zoombelt, A. P.; Mannsfeld, S. C. B.; Chen, J.; Nordlund, D.; Toney, M. F.; Huang, J.; Bao, Z. Nat. Commun. 2014, 5, 3005. doi: 10.1038/ncomms4005  doi: 10.1038/ncomms4005

    24. [24]

      Izawa, T.; Miyazaki, E.; Takimiya, K. Adv. Mater. 2008, 20, 3388. doi: 10.1002/adma.200800799  doi: 10.1002/adma.200800799

    25. [25]

      Chunbo, Y.; Ying, W.; Yueming, S.; Zuhong, L.; Juzheng, L. Surf. Sci. 1997, 392, L1. doi: 10.1016/S0039-6028(97)00519-0  doi: 10.1016/S0039-6028(97)00519-0

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