Wu Hongwei, Chen Yayun, Rao Caihui, Liu Chuanxiang*. Anion Receptors Based on CH Donor Group[J]. Progress in Chemistry, 2016, 28(10): 1501-1514.
[1] Bianchi E, Bowman-James K, García-España E. Superamolecular Chemistry of Anions, New York:Wiley-VCH, 1997. [2] 刘育(Liu Y),尤成才(You C C),张衡益(Zhang H Y).超分子化学——合成受体的分子识别与组装(Supramolecular Chemistry, Molecular Recognition and Assembly of Synthetic Receptors).天津:南开大学出版社(Tianjin:Nankai University Press), 2003. [3] Xie Y, Morimoto T, Furuta H. Angew. Chem. Int. Ed.,2006, 45:6907. [4] Amendola V, Fabbrizzi L, Mosca L. Chem. Soc. Rev., 2010, 39:3889. [5] Li A, Wang J, Wang F, Jiang Y. Chem. Soc. Rev., 2010, 39:3729. [6] Wang Q, Xie Y, Ding Y, Li X, Zhu W. Chem. Commun., 2010, 46:3669. [7] Cai J, Sessler J L. Chem. Soc. Rev., 2014, 43:305. [8] 吴芳英(Wu F Y), 温珍昌(Wen Z Z), 江云宝(Jiang Y B). 化学进展(Progress in Chemistry), 2004, 16(5):776. [9] 林奇(Lin Q), 魏太保(Wei T B), 姚虹(Yao H), 张有明(Zhang Y M). 化学进展(Progress in Chemistry), 2009, 21(6):1207. [10] Cai J, Sessler J L. Chem. Soc. Rev., 2014, 43:6198. [11] Farnham W B, Roe D C, Dixon D A, Calabrese J C, Harlow R L. J. Am. Chem. Soc., 1990, 112:7707. [12] Zhu S S, Staats H, Brandhorst K, Grunenberg J, Gruppi F, Dalcanale E, Lützen A, Rissanen K, Schalley C A. Angew.Chem. Int. Ed., 2008, 47:788. [13] Bedford R B, Betham M, Butts C P, Coles S J, Hursthouse M B, Scully P N, Tucker J H R, Wilkie J, Willener Y. Chem. Commun., 2008, 2429. [14] Pandian T S, Cho S J, Kang J. J. Org. Chem., 2013, 78:12121. [15] García H M, Morales D, Pérez J, Puerto M, Río I. Chem. Eur. J., 2014, 20:5821. [16] Sabater P, Zapata F, Caballero A, Fernándze I, Arellano C R, Molina P. J. Org. Chem., 2016, 81:3790. [17] Hay B P,Gutowski M, Dixon D A, Garza J, Vargas R, Moyer B A. J. Am. Chem. Soc., 2004, 126:7925. [18] Vargas R, Garza J, Dixon D A, Hay B P. J. Am. Chem. Soc., 2000, 122:4750. [19] Graul S T, Squires R R. J. Am. Chem. Soc., 1990, 112:2517. [20] Davico G E, Bierbaum V M, DePuy C H, Ellison G B, Squires R R. J. Am. Chem. Soc., 1995, 117:2590. [21] Berryman O B, Sather A C, Hay B P, Meisner J S, Johnson D W. J. Am. Chem. Soc., 2008, 130:10895. [22] Amendola V, Bergamaschi G, Boiocchi M, Fabbrizzi L, Milani M. Chem. Eur. J., 2010, 16:4368. [23] Tresca B W, Zakharov L N, Carroll C N, Johnson D W, Haley M M. Chem. Commun., 2013, 49:7240. [24] Lee S, Chen C H, Flood A H. Nat. Chem., 2013, 5:704. [25] Tresca B W, Hansen R J, Chau C V, Hay B P, Zakharov L N, Haley M M, Johnson D W. J. Am. Chem. Soc., 2015, 137:14959. [26] Xu L, Li Y, Li Y. Asian J. Org. Chem., 2014, 3:582. [27] Li Y, Flood A H. Angew. Chem. Int. Ed., 2008, 47:2649. [28] Li Y, Pink M, Karty JA, Flood A H. J. Am. Chem. Soc., 2008, 130:17293. [29] Lee S, Hua Y, Park H, Flood A H. Org. Lett., 2010, 12:2100. [30] McDonald K P, Ramabhadran R O, Lee S, Raghavachari K, Flood A H. Org. Lett., 2011, 13:6260. [31] Ramabhadran R O, Liu Y, Hua Y, Ciardi M, Flood A H, Raghavachari K. J. Am. Chem. Soc., 2014, 136:5078. [32] Meudtner R M, Hecht S. Angew. Chem. Int. Ed., 2008, 47:4926. [33] Fisher M G, Gale P A, Hiscock J R, Hursthouse M B, Light M E, Schmidtchen F P, Tong C C. Chem. Commun., 2009, 3017. [34] Sessler J L, Cai J, Gong H Y, Yang X, Arambula J F, Hay B P. J. Am. Chem. Soc., 2010, 132:14058. [35] Cao Q Y, Pradhan T, Kim S, Kim J S. Org. Lett., 2011, 13:4386. [36] Xu L, Li Y, Yu Y, Liu T, Cheng S, Liu H, Li Y. Org. Biomol. Chem., 2012, 10:4375. [37] Li Y J, Xu L, Yang W L, Liu H B, Lai S W, Che C M, Li Y L. Chem. Eur. J., 2012, 18:4782. [38] Cao L, Jiang R, Zhu Y, Wang X, Li Y, Li Y. Eur. J. Org. Chem., 2014, 2687. [39] Kwon J Y, Singh N J, Kim H N, Kim S K, Kim S K, Yoon J Y. Am. Chem. Soc., 2004, 126:8892. [40] Chellappan K, Singh N J, Hwang I C, Lee J W, Kim K S. Angew. Chem. Int. Ed., 2005, 44:2899. [41] Zhou H, Zhao Y, Gao G, Li S, Lan J, You J. J. Am. Chem. Soc., 2013, 135:14908. [42] Zhuo J B, Lin C X, Wan Q, Xie L L, Yuan Y F. J. Organomet. Chem., 2015, 791:289. [43] Pandian T S, Kang J. Tetra. Let., 2015, 56:4191. [44] Kumar A, Pandey P S. Org. Lett., 2008, 10:165. [45] Schulze B, Friebe C, Hager M D, Günther W, Köhn U, Jahn B O, Görls H, Schubert S. Org. Lett., 2010, 12:2710. [46] Cai J, Hay B P, Young N J, Yang X, Sessler J L. Chem. Sci., 2013, 4:1560. [47] Zaapata F, Gonzale L, Caballero A, Alkorta I, Elguero J, Molina P. Chem. Eur. J., 2015, 21:9797. [48] González L, Zapata F, Caballero A, Molina P, Arellano C R, Alkorta I, Elguero J. Chem. Eur. J., 2016, 22:7533. [49] Chen J, Liu C, Zhang J, Ding W, Zhou M, Wu F. Chem. Commun., 2013, 49:10814. [50] Li B, Zhang C, Liu C, Chen J, Wang X, Liu Z, Yi F. RSC Adv., 2014, 4:46016. [51] Zhou M, Chen J, Liu C, Fu H, Zheng N, Zhang C, Chen Y, Cheng J.Chem. Commun., 2014, 50:14748. [52] Zhang C, Liu C, Li B, Chen J, Zhang H, Hu Z, Yi F. New J. Chem., 2015, 51:8173. [53] Liu C, Wang X, Wu H, Chen Y. Dyes and Pigments, 2016, 133:255. |
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