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Progress in Chemistry 2014, Vol. 26 Issue (05): 706-726 DOI: 10.7536/PC131051 Previous Articles   Next Articles

• Review •

Triply and Quadruply Hydrogen Bonded Systems：Design, Structure and Application

Yang Yong*, Dou Dandan   

  1. Zhejiang Sci-Tech University, Hangzhou 310018, China
  • Received: Revised: Online: Published:
  • Supported by:

    The work was supported by the National Natural Science Foundation of China (No. 91227105), the Natural Science Foundation of Zhejiang Province, China (No. LY12B02021), the Scientific Research Foundation for the Returned Overseas Chinese Scholars (Ministry of Education), Zhejiang Provincial Top Academic Discipline of Applied Chemistry and Eco-Dyeing & Finishing Engineering (No. ZYG2011001), and 521 Talent Program of Zhejiang Sci-Tech University.

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Hydrogen bonding is a kind of noncovalent interaction that holds a very important position in the field of supramolecular chemistry. In the past few years, hydrogen bonding mediated supramolecular polymer has become a hot research topic in supramolecular chemistry. The construction of excellent hydrogen bonding building blocks lies the basis for the area. Among that, triply and quadruply hydrogen bonded systems are widely used for the construction of supramolecular assemblies. In this article, we summarize the progress and applications of triply and quadruply hydrogen bonded systems. We put our emphasis on the design principles of such systems and the factors affecting the stability of each system.

Contents
1 Introduction
2 Triply hydrogen bonded systems and their
applications
2.1 ADA·DAD triply hydrogen bonded systems
2.2 DDA·AAD triply hydrogen bonded systems
2.3 DDD·AAA triply hydrogen bonded systems
3 Quadruply hydrogen bonded systems and their applications
3.1 Quadruply hydrogen bonded systems of separated hydrogen bonding building blocks
3.2 Self-complementary quadruply hydrogen bonded system with DADA·ADAD hydrogen bonding sites
3.3 Self-complementary quadruply hydrogen bonded system with DDAA·AADD hydrogen bonding sites
3.4 Complementary quadruply hydrogen bonded system with DAAD·ADDA hydrogen bonding sites
3.5 Quadruply hydrogen bonded system with AAAA·DDDD hydrogen bonding sites
3.6 Quadruply hydrogen-bonded molecular duplexes free of secondary electrostatic interactions
3.7 Other quadruply hydrogen bonded systems
4 Conclusion and outlook

Key words: hydrogen bonding, triply hydrogen bonded system, quadruply hydrogen bonded system, supramoelcular polymer, supramolecular chemistry

CLC Number: 

[1] Steed J W, Atwood J L. Supramolecular Chemistry. 2nd ed. NY: John Wiley-Sons Ltd., 2008.
[2] Prins L J, Reinhoudt D N, Timmerman P. Angew. Chem. Int. Ed., 2001, 40: 2382.
[3] Jorgensen W L, Pranata J. J. Am. Chem. Soc., 1990, 112: 2008.
[4] Pranata J, Wierschke S G, Jorgensen W L. J. Am. Chem. Soc., 1991, 113: 2810.
[5] Murray T J, Zimmerman S C. J. Am. Chem. Soc., 1992, 114: 4010.
[6] Zimmerman S C, Murray T J. Tetrahedron Lett., 1994, 35: 4077.
[7] Sartorius J, Schneider H J. Chem. Eur. J., 1996, 2: 1446.
[8] Sijbesma R P, Meijer E W. Chem. Commun., 2003, 5.
[9] Zimmerman S C, Corbin P S. in Structure and Bonding (Berlin), 2000, 96: 63.
[10] 黄飞鹤(Huang F H), 翟春熙(Zhai C X), 郑波(Zheng B), 李世军(Li S J). 超分子聚合物(Supramolecular Polymers). 杭州: 浙江大学出版社(Hangzhou: Zhejiang University Press), 2012.
[11] Yan X, Wang F, Zheng B, Huang F. Chem. Soc. Rev., 2012, 41: 6042.
[12] Zheng B, Wang F, Dong S, Huang F. Chem. Soc. Rev., 2012, 41: 1621.
[13] De Greef T F A, Meijer E W. Nature, 2008, 453: 171.
[14] De Greef T F A, Smulders M M J, Wolffs M, Schenning A P H J, Sijbesma R P, Meijer E W. Chem. Rev., 2009, 109: 5687.
[15] Aida T, Meijer E W, Stupp S I. Science, 2012, 335: 813.
[16] Yang S K, Zimmerman S C. Isr. J. Chem., 2013, 53: 511.
[17] Feibush B, Figueroa A, Charles R, Onan K D, Feibush P, Karger B L. J. Am. Chem. Soc., 1986, 108: 3310.
[18] Hamilton A D, van Engen D. J. Am. Chem. Soc., 1987, 109: 5035.
[19] Kyogoku Y, Lord R C, Rich A. Proc. Natl. Acad. Sci. U. S. A., 1967, 57: 250.
[20] Park T K, Schroeder J, Rebek J. J. Am. Chem. Soc., 1991, 113: 5125.
[21] Kelly T R, Bridger G J, Zhao C. J. Am. Chem. Soc., 1990, 112: 8024.
[22] Beijer F H, Sijbesma R P, Vekemans J A J M, Meijer E W, Kooijman H, Spek A L. J. Org. Chem., 1996, 61: 6371.
[23] Fouquey C, Lehn J M, Levelut A M. Adv. Mater., 1990, 2: 254.
[24] Lehn J M. Makromol. Chem. Macromol. Symp., 1993, 69: 1.
[25] Gulik-Krzywicki T, Fouquey C, Lehn J M. Proc. Natl. Acad. Sci. U. S. A., 1993, 90: 163.
[26] Kotera M, Lehn J M, Vigneron J P. J. Chem. Soc. Chem. Commun., 1994, 2: 197.
[27] Kotera M, Lehn J M, Vigneron J P. Tetrahedron, 1995, 51: 1953.
[28] Chang S K, Hamilton A D. J. Am. Chem. Soc., 1988, 110: 1318.
[29] Chang S K, Ungen D V, Hamilton A D. J. Am. Chem. Soc., 1991, 113: 7640.
[30] Kelly T R, Zhao C, Bridger G J. J. Am. Chem. Soc., 1989, 111: 3744.
[31] Hisamatsu Y, Fukumi Y, Shirai N, Ikeda S I, Odashima K. Tetrahedron Lett., 2008, 49: 2005.
[32] McGhee A M, Kilner C, Wilson A J. Chem. Commun., 2008, 344.
[33] Gooch A, McGhee A M, Pellizzaro M L, Lindsay C I, Wilson A J. Org. Lett., 2011, 13: 240.
[34] Gooch A, Barrett S, Fisher J, Lindsay C I, Wilson A J. Org. Biomol. Chem., 2011, 9: 5938.
[35] Murray T J, Zimmerman S C, Kolotuchin S V. Tetrahedron Lett., 1995, 51: 635.
[36] Bell D A, Anslyn E V. Tetrahedron Lett., 1995, 51: 7161.
[37] Djurdjevic S, Leigh D A, McNab H, Parsons S, Teobaldi G, Zerbetto F. J. Am. Chem. Soc., 2007, 129: 476.
[38] Blight B A, Camara-Campos A, Djurdjevic S, Kaller M, Leigh D A, McMillan F M, McNab H, Slawin A M Z. J. Am. Chem. Soc., 2009, 131: 14116.
[39] Wang H B, Mudraboyina B P, Li J X, Wisner J A. Chem. Commun., 2010, 46: 7343.
[40] Wang H B, Mudraboyina B P, Wisner J A. Chem. Eur. J., 2012, 18: 1322.
[41] 齐志奇(Qi Z Q), 邵学斌(Shao X B), 赵新(Zhao X), 李晓强(Li X Q), 王晓钟(Wang X Z), 张未星(Zhang W X), 蒋锡夔(Jiang X K), 黎占亭(Li Z T). 有机化学(Organic Chemistry), 2003, 5: 403.
[42] Ducharme Y, Wuest J D. J. Org. Chem., 1988, 53: 5787.
[43] Wash P L, Maverick E, Chiefari J, Lightner D A. J. Am. Chem. Soc., 1997, 119: 3802.
[44] Griffin R J, Lowe P R. J. Chem. Soc. Perkin Trans. 1, 1992: 1811.
[45] Beijer F H, Kooijman H, Spek A L, Sijbesma R P, Meijer E W. Angew. Chem. Int. Ed., 1998, 37: 75.
[46] Hirschberg J H K K, Brunsveld L, Ramzi A, Vekemans J A J M, Sijbesma R P, Meijer E W. Nature, 2000, 407: 167.
[47] Brunsveld L, Vekemans J A J M, Hirschberg J H K K, Sijbesma R P, Meijer E W. Proc. Natl. Acad. Sci. U. S. A., 2002, 99: 4977.
[48] Yang Y, Yan H J, Chen C F, Wan L J. Org. Lett., 2007, 9: 4991.
[49] Martin A M, Butler R S, Ghiviriga I, Giessert R E, Abboud K A, Castellano R K. Chem. Commun, 2006, 42: 4413.
[50] Li J, Wisner J A, Jennings M C. Org. Lett., 2007, 9: 3267.
[51] Li J, Pandelieva A T, Rowley C N, Woo T K, Wisner J A. Org. Lett., 2012, 14: 5772.
[52] Taylor A, Berryman V E J, Boyd R J. J. Phys. Chem. A, 2012, 116: 7965.
[53] Sijbesma R P, Beijer F H, Brunsveld L, Folmer B J B, Hirschberg J H K K, Meijer E W. Science, 1997, 278: 1601.
[54] Beijer F H, Sijbesma R P, Kooijman H, Spek A L, Meijer E W. J. Am. Chem. Soc., 1998, 120: 6761.
[55] Keizer H M, Sijbesma R P, Meijer E W. Eur. J. Org., 2004, 12: 2553.
[56] Soentjens S H M, Sijbesma R P, van Genderen M H P, Meijer E W. J. Am. Chem. Soc., 2000, 122: 7487.
[57] Ikegami M, Arai T. Chem. Lett., 2001, 7: 694.
[58] Ohshiro I, Ikegami M, Nishimura Y, Arai T. Bull. Chem. Soc. Jpn., 2006, 79: 1950.
[59] Guo D, Sijbesma R P, Zuilhof H. Org. Lett., 2004, 6: 3667.
[60] Wang X Z, Li X Q, Shao X B, Zhao X, Deng P, Jiang X K, Li Z T, Chen Y Q. Chem. Eur. J., 2003, 9: 2904.
[61] Ligthart G B W L, Ohkawa H, Sijbesma R P, Meijer E W. J. Am. Chem. Soc., 2005, 127: 810.
[62] Wang S, Wu L, Zhang L, Tung C. Chin. Sci. Bull., 2006, 51: 129.
[63] Sánchez L, Martín N, Guldi D M. Angew. Chem. Int. Ed., 2005, 44: 5374.
[64] Rispens M T, Sanchez L, Knol J, Hummelen J C. Chem. Commun., 2001, 2: 161.
[65] Gonzalez J J, Gonzalez S, de Mendoza J, Priego E M, Martin N, Luo C P, Guldi D M. Chem. Commun., 2001, 163.
[66] Sánchez L, Rispens M T, Hummelen J C. Angew. Chem. Int. Ed., 2002, 41: 838.
[67] Xu J F, Chen Y Z, Wu D Y, Wu L Z, Tung C H, Yang Q Z. Angew. Chem. Int. Ed., 2013, 52: 9738.
[68] Yan X, Li S, Pollock J B, Cook T R, Chen J, Zhang Y, Ji X, Yu Y, Huang F, Stang P J. Proc. Natl. Acad. Sci. U. S. A., 2013, 110: 15585.
[69] Yan X, Jiang B, Cook T R, Zhang Y, Li J, Yu Y, Huang F, Yang H B, Stang P J. J. Am. Chem. Soc., 2013, 135: 16813.
[70] Corbin P S, Zimmerman S C. J. Am. Chem. Soc., 1998, 120: 9710.
[71] Corbin P S, Lawless L J, Li Z T, Ma Y G, Witmer M J, Zimmerman S C. Proc. Natl. Acad. Sci. U. S. A., 2002, 99: 5099.
[72] Baruah P K, Gonnade R, Phalgune U D, Sanjayan G J. J. Org. Chem., 2005, 70: 6461.
[73] Sun H, Steeb J, Kaifer A E. J. Am. Chem. Soc., 2006, 128: 2820.
[74] Cui L, Gadde S, Shukla A D, Sun H, Mague J T, Kaifer A E. Chem. Commun., 2008, 1446.
[75] Lafitte V G H, Aliev A E, Horton P N, Hursthouse M B, Bala K, Golding P, Hailes H C. J. Am. Chem. Soc., 2006, 128: 6544.
[76] Corbin P S, Zimmerman S C. J. Am. Chem. Soc., 2000, 122: 3779.
[77] Corbin P S, Zimmerman S C, Thiessen P A, Hawryluk N A, Murray T J. J. Am. Chem. Soc., 2001, 123: 10475.
[78] Chien C H, Leung M M, Su J K, Li G H, Liu Y H, Wang Y. J. Org. Chem., 2004, 69: 1866.
[79] Hisamatsu Y, Shirai N, Ikeda S I, Odashima K. Org. Lett., 2009, 11: 4342.
[80] Prabhakaran P, Puranik V G, Sanjayan G J. J. Org. Chem., 2005, 70: 10067.
[81] Mudraboyina B P, Wisner J A. Chem. Eur. J., 2012, 18: 14157.
[82] Ligthart G B W L, Ohkawa H, Sijbesma R P, Meijer E W. J. Org. Chem., 2006, 71: 375.
[83] Anderson C A, Taylor P G, Zeller M A, Zimmerman S C. J. Org. Chem., 2010, 75: 4848
[84] Park T, Zimmerman S C, Nakashima S. J. Am. Chem. Soc., 2005, 127: 6520.
[85] Park T, Todd E M, Nakashima S, Zimmerman S C. J. Am. Chem. Soc., 2005, 127: 18133.
[86] Ong H C, Zimmerman S C. Org. Lett., 2006, 8: 1589.
[87] Kuykendall D W, Anderson C A, Zimmerman S C. Org. Lett., 2009, 11: 61.
[88] Park T, Zimmerman S C. J. Am. Chem. Soc., 2006, 128: 11582.
[89] Park T, Zimmerman S C. J. Am. Chem. Soc., 2006, 128: 13986.
[90] Park T, Zimmerman S C. J. Am. Chem. Soc., 2006, 128: 14236.
[91] Anderson C A, Jones A R, Briggs E M, Novitsky E J, Kuykendall D W, Sottos N R, Zimmerman S C. J. Am. Chem. Soc., 2013, 135: 7288.
[92] Zhang Y, Anderson C A, Zimmerman S C. Org. Lett., 2013, 15: 3506.
[93] Li Y, Park T, Quansah J K, Zimmerman S C. J. Am. Chem. Soc., 2011, 133: 17118.
[94] Lüning U, Kühl C. Tetrahedron Lett., 1998, 39: 5735.
[95] Brammer S, Lüning U, Kühl C. Eur. J. Org. Chem., 2002, 23: 4054.
[96] Lüning U, Kühl C, Uphoff A. Eur. J. Org. Chem., 2002, 23: 4063.
[97] Taubitz J, Lüning U, Grotemeyer J. Chem. Commun., 2004, 2400.
[98] Quinn J R, Zimmerman S C. Org. Lett., 2004, 6: 1649.
[99] Hisamatsu Y, Shirai N, Ikeda S I. Odashima K. Org. Lett., 2010, 12: 1776.
[100] Pellizzaro M L, Barrett S A, Fisher J, Wilson A J. Org. Biomol. Chem., 2012, 10: 4899.
[101] Zhao X, Wang X Z, Jiang X K, Chen Y Q, Li Z T, Chen G J. J. Am. Chem. Soc., 2003, 125: 15128.
[102] Zhou Y X, Zhao X, Li Z T, Chen G J, Liu R Z. Acta Chim. Sin., 2003, 61: 963.
[103] Feng D J, Wang P, Li X Q, Li Z T. Chin. J. Chem., 2006, 24: 1200.
[104] Yang Y, Yang Z Y, Yi Y P, Xiang J F, Chen C F, Wan L J, Shuai Z G. J. Org. Chem., 2007, 72: 4936.
[105] Taubitz J, Lüning U. Aust. J. Chem., 2009, 62: 1550.
[106] Blight B A, Hunter C A, Leigh D A, McNab H, Thomson P I T. Nat. Chem., 2011, 3: 244.
[107] Wilson A. Nat. Chem., 2011, 3: 193.
[108] Leigh D A, Robertson C C, Slawin A M Z, Thomson P I T. J. Am. Chem. Soc., 2013, 135: 9939.
[109] Gong B, Yan Y F, Zeng H Q, Skrzypczak-Jankunn E, Kim Y W, Zhu J, Ickes H. J. Am. Chem. Soc., 1999, 121: 5607.
[110] Yang X W, Martinovic S, Smith R D, Gong B. J. Am. Chem. Soc., 2003, 125: 9932.
[111] Yang X, Gong B. Angew. Chem. Int. Ed., 2005, 44: 1352.
[112] Roland J T, Guan Z. J. Am. Chem. Soc., 2004, 126: 14328.
[113] Zhang P, Chu H Z, Li X H, Feng W, Deng P C, Yuan L, Gong B. Org. Lett., 2011, 13: 54.
[114] Davis A P, Draper S M, Dunne G, Ashton P. Chem. Comm., 1999, 2265.
[115] Schmuck C, Wienand W. J. Am. Chem. Soc., 2003, 125: 452.P, Hailes H C. J. Am. Chem. Soc., 2006, 128: 6544-6545.
[76] Corbin P S, Zimmerman S C. J. Am. Chem. Soc., 2000, 122: 3779-3780
[77] Corbin P S, Zimmerman S C, Thiessen P A, Hawryluk N A, Murray T J. J. Am. Chem. Soc., 2001, 123: 10475-10488
[78] Chien C-H, Leung M-k, Su J-K, Li G-H, Liu Y-H, Wang Y. J. Org. Chem., 2004, 69: 1866-1871
[79] Hisamatsu Y, Shirai N, Ikeda S I, Odashima K. Org. Lett., 2009, 11: 4342-4345
[80] Prabhakaran P, Puranik V G, Sanjayan G J. J. Org. Chem., 2005, 70: 10067-10072
[81] Mudraboyina B P, Wisner J A. Chem. Eur. J., 2012, 18: 14157-14164
[82] Ligthart G B W L, Ohkawa H, Sijbesma R P, Meijer E W. J. Org. Chem., 2006, 71: 375-378
[83] Anderson C A, Taylor P G, Zeller M A, Zimmerman S C. J. Org. Chem., 2010, 75: 4848-4851
[84] Park T, Zimmerman S C, Nakashima S. J. Am. Chem. Soc., 2005, 127: 6520-6521
[85] Park T, Todd E M, Nakashima S, Zimmerman S C. J. Am. Chem. Soc., 2005, 127: 18133-18142
[86] Ong H C, Zimmerman S C. Org. Lett., 2006, 8: 1589-1592
[87] Kuykendall D W, Anderson C A, Zimmerman S C. Org. Lett., 2009, 11: 61-64
[88] Park T, Zimmerman S C. J. Am. Chem. Soc., 2006, 128: 11582-11590
[89] Park T, Zimmerman S C. J. Am. Chem. Soc., 2006, 128: 13986-13987
[90] Park T, Zimmerman S C. J. Am. Chem. Soc., 2006, 128: 14236-14237
[91] Anderson C A, Jones A R, Briggs E M, Novitsky E J, Kuykendall D W, Sottos N R., Zimmerman S C. J. Am. Chem. Soc., 2013, 135: 7288-7295
[92] Zhang Y, Anderson C A, Zimmerman S C. Org. Lett., 2013, 15: 3506-3509
[93] Li Y, Park T, Quansah J K, Zimmerman S C. J. Am. Chem. Soc., 2011, 133: 17118-17121
[94] Lüning U, Kühl C. Tetrahedron Lett., 1998, 39: 5735-5738
[95] Brammer S, Lüning U, Kühl C. Eur. J. Org. Chem., 2002, 23: 4054-4062
[96] Lüning U, Kühl C, Uphoff A. Eur. J. Org. Chem., 2002, 23: 4063-4070
[97] Taubitz J, Lüning U, Grotemeyer J. Chem. Commun., 2004,21: 2400–2401
[98] Quinn J R, Zimmerman S C. Org. Lett., 2004, 6: 1649-1652
[99] Hisamatsu Y, Shirai N, Ikeda S I. Odashima K. Org. Lett., 2010, 12: 1776-1779
[100] Pellizzaro M L, Barrett S A, Fisher J, Wilson A J. Org. Biomol. Chem., 2012, 10: 4899-4906
[101] Zhao X, Wang X Z, Jiang X-K, Chen Y-Q, Li Z T, Chen G-Ju. J. Am. Chem. Soc., 2003, 125: 15128-15139
[102] Zhou Y X, Zhao X, Li Z T, Chen G-J, Liu R-Z. Acta Chim. Sin., 2003, 61: 963-969
[103] Feng D-J, Wang P, Li X-Q, Li Z T. Chin. J. Chem., 2006, 24: 1200-1208
[104] Yang Y, Yang Z-Y, Yi Y-P, Xiang J-F, Chen C-F, Wan L-J, Shuai Z-G. J. Org. Chem., 2007, 72: 4936-4946
[105] Taubitz J, Lüning U. Aust. J. Chem., 2009, 62: 1550-1555
[106] Blight B A, Hunter C A, Leigh D A, McNab H, Thomson P I T. Nature Chem., 2011, 3: 244-248
[107] Wilson A. Nature Chem., 2011, 3: 193-194
[108] Leigh D A, Robertson C C, Slawin A M Z, Thomson P I T. J. Am. Chem. Soc., 2013, 135: 9939-9943
[109] Gong B, Yan Y F, Zeng H Q, Skrzypczak-Jankunn E, Kim, Y W, Zhu J, Ickes H. J. Am. Chem. Soc., 1999, 121: 5607-5608
[110] Yang X W, Martinovic S, Smith R D, Gong B. J. Am. Chem. Soc., 2003, 125: 9932-9933
[111] Yang X, Gong B. Angew. Chem., Int. Ed., 2005, 44: 1352-1356
[112] Roland J T, Guan Z. J. Am. Chem. Soc., 2004, 126: 14328-14329
[113] Zhang P, Chu H-Z, Li X-H, Feng W, Deng P-C,Yuan L, Gong B. Org. Lett., 2011, 13: 54-57
[114] Davis A P, Draper S M, Dunne G, Ashton P. Chem. Comm., 1999, 22: 2265-2266
[115] Schmuck C, Wienand W. J. Am. Chem. Soc., 2003, 125: 452-459

 
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