|
OALib Journal期刊
ISSN: 2333-9721
费用：99美元
|
|
|
|
方酰胺衍生物及其在离子识别中的应用
DOI: 10.7536/PC140705, PP. 1701-1711
Keywords: 方酰胺,氢键,阴离子识别,主-客体识别,超分子化学
Abstract:
方酰胺骨架具有芳香性的四元环状刚性结构，作为双氢键受体和双氢键给体能与许多客体物种结合，是一类重要、理想的氢键给/受体单元，同时该类给/受体的功能化设计为离子识别行为的检测提供了方便。本文综述了近年来方酰胺化合物的结构特性、衍生化方法，及其在超分子中对阴离子、阳离子与两性离子的识别，实现对离子的跨膜传输、分离与萃取、凝胶响应等功能，以及其在有机小分子催化反应中稳定离子型中间体实现对反应底物催化的功能，并展望了方酰胺化合物在离子识别中的发展前景。
| [1] | Amendola V, Fabbrizzi L, Mosca L. Chem. Soc. Rev., 2010, 39(10): 3889.
|
| [2] | Malerich J P, Hagihara K, Rawal V H. J. Am. Chem. Soc., 2008, 130(44): 14416.
|
| [3] | Aleman J, Parra A, Jiang H, Jorgensen K A. Chem. Eur. J., 2011, 17(25): 6890.
|
| [4] | Qui？onero D, Frontera A, Ballester P, Deyà P M. Tetrahedron Lett., 2000, 41(12): 2001.
|
| [5] | Tomàs S, Prohens R, Vega M, Rotger M C, Deyà P M, Ballester P, Costa A. J. Org. Chem., 1996, 61(26): 9394.
|
| [6] | Xu Z, Singh N J, Lim J, Pan J, Kim H N, Park S, Kim K S, Yoon J. J. Am. Chem. Soc., 2009, 131(42): 15528.
|
| [7] | Li S, Jia C, Wu B, Luo Q, Huang X, Yang Z, Li Q S, Yang X J. Angew. Chem. Int. Ed., 2011, 50(25): 5721.
|
| [8] | Prohens R, Martorell G, Ballester P, Costa A. Chem. Commun., 2001, (16): 1456.
|
| [9] | Frontera A, Morey J, Oliver A, Pi？a M N, Qui？onero D, Costa A, Ballester P, Deyà P M, Anslyn E V. J. Org. Chem., 2006, 71(19): 7185.
|
| [10] | Ramalingam V, Domaradzki M E, Jang S, Muthyala R S. Org. Lett., 2008, 10(15): 3315.
|
| [11] | Al-Sayah M H, Branda N R. Thermochim. Acta, 2010, 503: 28.
|
| [12] | Jin C, Zhang M, Deng C, Guan Y, Gong J, Zhu D, Pan Y, Jiang J, Wang L. Tetrahedron Lett., 2013, 54(8): 796.
|
| [13] | Elmes R B, Turner P, Jolliffe K A. Org. Lett., 2013, 15(22): 5638.
|
| [14] | Onaran M B, Comeau A B, Seto C T. J. Org. Chem., 2005, 70(26): 10792.
|
| [15] | Sanna E, Martinez L, Rotger C, Blasco S, Gonzalez J, Garcia-Espana E, Costa A. Org. Lett., 2010, 12(17): 3840.
|
| [16] | Ni M, Guan Y, Wu L, Deng C, Hu X, Jiang J, Lin C, Wang L. Tetrahedron Lett., 2012, 53(47): 6409.
|
| [17] | Frontera A, Orell M, Garau C, Qui？onero D, Molins E, Mata I, Morey J. Org. Lett., 2005, 7(8): 1437.
|
| [18] | Ling J B, Su Y, Zhu H L, Wang G Y, Xu P F. Org. Lett., 2012, 14: 1090.
|
| [19] | Li A F, Wang J H, Wang F, Jiang Y B. Chem. Soc. Rev., 2010, 39(10): 3729.
|
| [20] | Maahs G, Hegenber P. Angew. Chem. Int. Ed., 1966, 5(10): 888.
|
| [21] | Tomas S, Rotger M C, Gonzalez J F, Deya P M, Ballester P, Costa A. Tetrahedron Lett., 1995, 36(14): 2523.
|
| [22] | Storer R I, Aciro C, Jones L H. Chem. Soc. Rev., 2011, 40(5): 2330.
|
| [23] | Ni X, Li X, Wang Z, Cheng J P. Org. Lett., 2014, 16(6): 1786.
|
| [24] | Yang W, Du D M. Org. Lett., 2010, 12(23): 5450.
|
| [25] | Wurm F R, Klok H A. Chem. Soc. Rev., 2013, 42(21): 8220.
|
| [26] | Schmidt A H. Synthesis, 1980: 961.
|
| [27] | Rostami A, Colin A, Li X Y, Chudzinski M G, Lough A J, Taylor M S. J. Org. Chem., 2010, 75(12): 3983.
|
| [28] | Tietze L F, Arlt M, Beller M, Glusenkamp K H, Jahde E, Rajewsky M F. Chem. Ber., 1991, 124(5): 1215.
|
| [29] | Amendola V, Bergamaschi G, Boiocchi M, Fabbrizzi L, Milani M. Chem. Eur. J., 2010, 16(14): 4368.
|
| [30] | Rostami A, Wei C J, Guérin G, Taylor M S. Angew. Chem. Int. Ed., 2011, 50(9): 2059.
|
| [31] | Gaeta C, Talotta C, Della Sala P, Margarucci L, Casapullo A, Neri P. J. Org. Chem., 2014, 79(8): 3704.
|
| [32] | Jin C, Zhang M, Wu L, Guan Y, Pan Y, Jiang J, Lin C, Wang L. Chem. Commun., 2013, 49(20): 2025.
|
| [33] | Davis J T, Gale P A, Okunola O A, Prados P, Iglesias-Sanchez J C, Torroba T, Quesada R. Nat. Chem., 2009, 1(2): 138.
|
| [34] | Busschaert N, Wenzel M, Light M E, Iglesias-Hernandez P, Perez-Tomas R, Gale P A. J. Am. Chem. Soc., 2011, 133(35): 14136.
|
| [35] | Busschaert N, Kirby I L, Young S, Coles S J, Horton P N, Light M E, Gale P A. Angew. Chem. Int. Ed., 2012, 51(18): 4426.
|
| [36] | Lim N C, Morton M D, Jenkins H A, Brückner C. J. Org. Chem., 2003, 68(24): 9233.
|
| [37] | 魏梅莹(Wei M Y), 李少光(Li S G), 贾传东(Jia C D), 吴彪(Wu B). 高等学校化学学报(Chem. Res. Chin. Univ.), 2011, 32(9): 1939.
|
| [38] | Ambrosi G, Formica M, Fusi V, Giorgi L, Macedi E, Micheloni M, Paoli P, Pontellini R, Rossi P. Chem. Eur. J., 2011, 17(5): 1670.
|
| [39] | Lopez C, Sanna E, Carreras L, Vega M, Rotger C, Costa A. Chem. Asian J., 2013, 8: 84.
|
| [40] | Albrecht T, Dickmeiss G, Acosta C F, Rodríguez-Escrich C, Davis R L, J？rgensen K A. J. Am. Chem. Soc., 2012, 134: 2543.
|
| [41] | Su Y, Ling J B, Zhang S, Xu P F. J. Org. Chem., 2013, 78: 11053.
|
| [42] | Yang W, Du D M. Org. Lett., 2010, 12: 5450.
|
| [43] | Zhao B L, Du D M. RSC Advances, 2014, 4: 27346.
|
| [44] | Zhao B L, Du D M. Org. Biomol. Chem., 2014, 12: 1585.
|
Full-Text
|
|
Contact Us
service@oalib.com QQ:3279437679 
WhatsApp +8615387084133
|
|
