Thiourea as a "Polar Hydrophobic" Hydrogen-Bonding Motif: Application to Highly Durable All-Underwater Adhesion

被引:8
|
作者
Kikkawa, Kohei [1 ]
Sumiya, Yosuke [2 ,3 ]
Okazawa, Kazuki [2 ,4 ]
Yoshizawa, Kazunari [2 ,5 ]
Itoh, Yoshimitsu [1 ,6 ]
Aida, Takuzo [1 ,7 ]
机构
[1] Univ Tokyo, Sch Engn, Dept Chem & Biotechnol, Bunkyo Ku, Tokyo 1138656, Japan
[2] Kyushu Univ, Inst Mat Chem & Engn, Nishi Ku, Fukuoka 8190395, Japan
[3] Yamaguchi Univ, Dept Appl Chem, Tokiwadai 2-16-1, Ube 7558611, Japan
[4] Univ Tsukuba, Ctr Computat Sci, Tsukuba 3058577, Japan
[5] Kyoto Univ, Fukui Inst Fundamental Chem, 34-4 Takano Nishihiraki Cho,Sankyo Ku, Kyoto 6068103, Japan
[6] Japan Sci & Technol Agcy JST, Precursory Res Embryon Sci & Technol PRESTO, Kawaguchi, Saitama 3320012, Japan
[7] RIKEN Ctr Emergent Matter Sci, Wako, Saitama 3510198, Japan
关键词
POLYMER;
D O I
10.1021/jacs.4c07515
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Here, we report that, in contrast to urea, thiourea functions as a "polar hydrophobic" hydrogen-bonding motif. Although thiourea is more acidic than urea, thiourea exchanges its N-H protons with water at a rate that is 160 times slower than that for urea at 70 degrees C. This suggests that thiourea is much less hydrated than urea in an aqueous environment. What led us to this interesting principle was the serendipitous finding that self-healable poly(ether thiourea) adhered strongly to wet glass surfaces. This discovery enabled us to develop an exceptionally durable all-underwater adhesive that can maintain large adhesive strength for over a year even in seawater, simply by mechanically mixing three water-insoluble liquid components on target surfaces. Because thiourea is hydrophobic, its hydrogen-bonding networks within the adhesive structure and at the adhesive-target interface are presumed to be dehydrated. For comparison, a reference adhesive using urea as a representative "polar hydrophilic" hydrogen-bonding motif was durable for less than 4 days in water. Highly durable all-underwater adhesives are needed in various fields of marine engineering and biomedical sciences, but their development has been a major challenge because a hydration layer that spontaneously forms in water always inhibits adhesion.
引用
收藏
页码:21168 / 21175
页数:8
相关论文
共 10 条
  • [1] Cooperative Tridentate Hydrogen-Bonding Interactions Enable Strong Underwater Adhesion
    Lamberty, Zachary D.
    Tran, Ngon T.
    van Engers, Christian D.
    Karnal, Preetika
    Knorr Jr, Daniel B.
    Frechette, Joelle
    ACS APPLIED MATERIALS & INTERFACES, 2023, 15 (29) : 35720 - 35731
  • [2] A highly directional fourfold hydrogen-bonding motif for supramolecular structures through self-assembly of fullerodendrimers
    Hahn, U
    González, JJ
    Huerta, E
    Segura, M
    Eckert, JF
    Cardinali, F
    de Mendoza, J
    Nierengarten, JF
    CHEMISTRY-A EUROPEAN JOURNAL, 2005, 11 (22) : 6666 - 6672
  • [3] Application of MOSCED and UNIFAC to screen hydrophobic solvents for extraction of hydrogen-bonding organics from aqueous solution
    Frank, Timothy C.
    Anderson, John J.
    Olson, James D.
    Eckert, Charles A.
    INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2007, 46 (13) : 4621 - 4625
  • [4] HYDROGEN-BONDING IN POLAR LIQUID SOLUTIONS .5. THEORY OF DIPOLE CORRELATION FOR CHAIN-ASSOCIATED SOLVENTS CONTAINING HYDROGEN-BONDING SOLUTES - APPLICATION TO 1-OCTANOL
    PAN, KC
    GRUNWALD, E
    JOURNAL OF PHYSICAL CHEMISTRY, 1976, 80 (27): : 2941 - 2944
  • [5] Highly Enantioselective Direct Michael Addition of Nitroalkanes to Nitroalkenes Catalyzed by Amine-Thiourea Bearing Multiple Hydrogen-Bonding Donors
    Dong, Xiu-Qin
    Teng, Huai-Long
    Wang, Chun-Jiang
    ORGANIC LETTERS, 2009, 11 (06) : 1265 - 1268
  • [6] Highly anti-selective asymmetric nitro-mannich reactions catalyzed by bifunctional amine-thiourea-bearing multiple hydrogen-bonding donors
    Wang, Chun-Jiang
    Dong, Xiu-Qin
    Zhang, Zhi-Hai
    Xue, Zhi-Yong
    Teng, Huai-Long
    Journal of the American Chemical Society, 2008, 130 (27): : 8606 - 8607
  • [7] Highly anti-selective asymmetric nitro-Mannich reactions catalyzed by bifunctional amine-thiourea-bearing multiple hydrogen-bonding donors
    Wang, Chun-Jiang
    Dong, Xiu-Qin
    Zhang, Zhi-Hai
    Xue, Zhi-Yong
    Teng, Huai-Long
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (27) : 8606 - +
  • [8] Rapid neutron-diffraction data collection for hydrogen-bonding studies: application of the Laue diffractometer (LADI) to the case study zinc (tris)thiourea sulfate
    Cole, JM
    McIntyre, GJ
    Lehmann, MS
    Myles, DAA
    Wilkinson, C
    Howard, JAK
    ACTA CRYSTALLOGRAPHICA SECTION A, 2001, 57 : 429 - 434
  • [9] Multiple Hydrogen-Bonding Bifunctional Thiourea-Catalyzed Asymmetric Dearomative [4+2] Annulation of 3-Nitroindoles: Highly Enantioselective Access to Hydrocarbazole Skeletons
    Yue, Deng-Feng
    Zhao, Jian-Riang
    Chen, Xiao-Zhen
    Zhou, Yan
    Zhang, Xiao-Mei
    Xu, Xiao-Ying
    Yuan, Wei-Cheng
    ORGANIC LETTERS, 2017, 19 (17) : 4508 - 4511
  • [10] Highly Enantioselective Michael Addition of 3-Aryloxindoles to Phenyl Vinyl Sulfone Catalyzed by Cinchona Alkaloid-Derived Bifunctional Amine-Thiourea Catalysts Bearing Sulfonamide as Multiple Hydrogen-Bonding Donors
    Zhao, Mei-Xin
    Tang, Wen-Hao
    Chen, Ming-Xiao
    Wei, Deng-Ke
    Dai, Tong-Lei
    Shi, Min
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2011, 2011 (30) : 6078 - 6084