OALib Journal期刊
ISSN: 2333-9721
费用:99美元
|
|
|
含氮杂环类阴离子受体*
, PP. 1207-1216
Keywords: 传感器,阴离子识别,氮杂环,吡咯,吲哚,咪唑,咔唑
Abstract:
含氮杂环类阴离子受体是目前超分子阴离子识别领域研究的热点之一。此类受体具有主体结构丰富、可调节性强、识别范围广、选择性强、灵敏度高等优点。本文综述了以吡咯、吲哚、咪唑、吡唑等含氮杂环为识别基团的阴离子受体的设计原理、识别性能和机理,展望了该领域的发展方向。
References
[1] | [ 6 ] Anslyn E V , Snowden T S. Curr. Opin. Chem. Biol . , 1999 , 3 :740 —746
|
[2] | [ 7 ] Beer P D , Gale P A. Angew. Chem. Int . Ed. , 2001 , 40 : 486 —516
|
[3] | [ 8 ] Martínez-Màìez R , Sacenón F. Chem. Rev. , 2003 , 103 : 4419 —4476
|
[4] | [ 9 ] Chmielewski M J , Jurczak J . Chem. Eur. J . , 2005 , 11 : 6080 —6094
|
[5] | [10 ] Gunnlaugsson T, Glynn M, Tocci GM. Coord. Chem. Rev. , 2006 ,250 : 3094 —3117
|
[6] | [11 ] Suksai C , Tuntulani T. Chem. Soc. Rev. , 2003 , 32 : 192 —202
|
[7] | [12 ] Gale P , García-Garrido S E , Garric J . Chem. Soc. Rev. , 2008 ,37 : 151 —190
|
[8] | [13 ] Llinares J M, Powell D , Bowman-James K. Coord. Chem. Rev. ,2003 , 240 : 57 —75
|
[9] | [14 ] Casnati A , Sansone F , Ungaro R. Acc. Chem. Res. , 2003 , 36 :246 —254
|
[10] | [27 ] Sessler J L , Davis J M. Acc. Chem. Res. , 2001 , 34 : 989 —997
|
[11] | [28 ] Sessler J L , Camiolo S , Gale P A. Coord. Chem. Rev. , 2003 ,240 : 17 —55
|
[12] | [29 ] Gale P A. Chem. Commun. , 2005 , 3761 —3772
|
[13] | [30 ] 郭勇(Guo Y) , 邵士俊(Shao S J ) , 何丽君(He L J ) 等. 化学进展(Prog. Chem. ) , 2003 , 15 (4) : 319 —326
|
[14] | [33 ] Anzenbacher P , Try A C , Sessler J L , et al . J . Am. Chem. Soc. ,2000 , 122 : 10268 —10272
|
[15] | [37 ] Aldakov D , Anzenbacher P. J . Am. Chem. Soc. , 2004 , 126:4752 —4753
|
[16] | [38 ] Maeda H , Kusunose Y. Chem. Eur. J . , 2005 , 11 : 5661 —5666
|
[17] | [42 ] Fujimoto C , Kusunose Y, Maeda H. J . Org. Chem. , 2006 , 71 :2389 —2394
|
[18] | [57 ] Janosik T, Wahlstrêm N , Bergman J . Tetrahedron , 2008 , 64 :9159 —9180
|
[19] | [58 ] Curiel D , Cowley A , Beer P D. Chem. Commun. , 2005 , 236 —238
|
[20] | [67 ] 张有明(Zhang YM) , 崔文辉(Cui W H) , 魏太保(Wei T B) . 有机化学(Chin. J . Org. Chem. ) , 2007 , 27 (7) : 893 —897
|
[21] | [73 ] Niu H T, Yin Z, Su D , et al . Tetrahedron , 2008 , 64 : 6300 —6306
|
[22] | [74 ] Niu H T, Yin Z. Su D , et al . Dalton Trans. , 2008 , 3694 —3700
|
[23] | [75 ] Alhashimy N , Brougham D J , Nolan K, et al . Tetrahedron Lett . ,2007 , 48 : 125 —128
|
[24] | [76 ] Qin D B , Xu F B , Zhang Z Z, et al . Tetrahedron Lett . , 2006 , 47 :5641 —5643
|
[25] | [62 ] Suk J M, Chae M K, Kim N K, et al . Pure Appl . Chem. , 2008 ,80 : 599 —608
|
[26] | [63 ] Kang J , Kim H S , Jang D O. Tetrahedron Lett . , 2005 , 46 : 6079 —6082
|
[27] | [64 ] Singh N , Jang D O. Org. Lett . , 2007 , 9 : 1991 —1994
|
[28] | [65 ] YuM, Lin H K, Zhao G, et al . J . Mol . Recognit . , 2007 , 20 :69 —73
|
[29] | [66 ] Chetia B , Iyer P K. Tetrahedron Lett . , 2008 , 49 : 94 —97
|
[30] | [68 ] 魏太保(Wei T B) , 师海雄(Shi H X) , 张志仁(Zhang Z R) 等.有机化学(Chin. J . Org. Chem. ) , 2007 , 27 (9) : 1116 —1120
|
[31] | [69 ] Yoon J , Kim S K, Singh NJ , et al . Chem. Soc. Rev. , 2006 , 35 :355 —360
|
[32] | [70 ] Xu Z, Kim S , Lee K H , Yoon J . Tetrahedron Lett . , 2007 , 48 :3797 —3800
|
[33] | [71 ] Khatri V K, Upreti S , Pandey P S. Org. Lett . , 2006 , 8 : 1755 —1758
|
[34] | [72 ] Chahar M, Upreti S , Pandey P S. Tetrahedron , 2007 , 63 : 171 —176
|
[35] | [77 ] Hirano J , Miyata H , Zaitsu K, et al . Tetrahedron Lett . , 2007 , 48 :4861 —4864
|
[36] | [78 ] Maeda H , Ito Y, Kusunose Y, et al . Chem. Commun. , 2007 ,1136 —1138
|
[37] | [79 ] Juwarker H , Lenhardt J M, Pham D M, et al . Angew. Chem. Int .Ed. , 2008 , 47 : 3740 —3743
|
[38] | [ 1 ] Sessler J L , Gale P A , Cho W S. Anion Receptor Chemistry.Cambridge : Royal Society of Chemistry , 2006. 1 —22
|
[39] | [ 2 ] Park C H , Simmons H E. J . Am. Chem. Soc. , 1968 , 90 : 2429 —2431
|
[40] | [ 3 ] Graf E , Lehn J M. J . Am. Chem. Soc. , 1976 , 98 : 6403 —6405
|
[41] | [ 4 ] Schmidtchen F P , Berger M. Chem. Rev. , 1997 , 97 : 1609 —1646
|
[42] | [ 5 ] Antonisse MM G, Reinhoudt D N. Chem. Commun. , 1998 , 443 —448
|
[43] | [15 ] Frontera A , Morey J , Oliver A , et al . J . Org. Chem. , 2006 , 71 :7185 —7195
|
[44] | [16 ] Swamy KM K, Lee YJ , Lee H N , et al . J . Org. Chem. , 2006 ,71 : 8626 —8628
|
[45] | [17 ] Zhao YL , Zhang H Y, WangM, et al . J . Org. Chem. , 2006 , 71 :6010 —6019
|
[46] | [18 ] Kang S O , Begum R A , Bowman-James K. Angew. Chem. Int .Ed. , 2006 , 45 : 7882 —7894
|
[47] | [19 ] 吴芳英(Wu F Y) , 温珍昌(Wen Z C) , 江云宝(Jiang YB) . 化学进展(Prog. Chem. ) , 2004 , 16 (5) : 776 —784
|
[48] | [20 ] Zhang Y M, Qin J D , Lin Q , et al . J . Fluorine Chem. , 2006 ,127 : 1222 —1227
|
[49] | [21 ] 张有明(Zhang YM) , 任海鲜(Ren H X) , 魏太保(Wen T B) .高等学校化学学报(Chem. J . Chinese Univ. ) , 2006 , 27 (11) :2079 —2083
|
[50] | [22 ] Zhang YM, Cao C , Wei W, et al . Chin. J . Chem. , 2007 , 25 :709 —713
|
[51] | [23 ] 张有明(Zhang YM) , 徐维霞(Xu WX) , 周艳青(Zhou YQ) 等.化学学报(Acta Chim. Sin. ) , 2006 , 64 (1) :79 —84
|
[52] | [24 ] 张有明(Zhang YM) , 徐维霞(Xu W X) , 李满林(Li M L) 等.无机化学学报(Chin. J . Inorg. Chem. ) , 2005 , 21 (12) :1815 —1820
|
[53] | [25 ] Best M D , Tobey S L , Anslyn E V. Coord. Chem. Rev. , 2003 ,240 : 3 —15
|
[54] | [26 ] Gale P A , Anzenbacher P , Sessler J L. Coord. Chem. Rev. , 2001 ,222 : 57 —102
|
[55] | [31 ] 刘冬美(Liu D M) , 郑松志(Zheng S Z) , 李俊锋(Li J F) 等. 有机化学(Chin. J . Org. Chem. ) , 2008 , 28 (3) : 398 —406
|
[56] | [32 ] Black C B , Andrioletti B , Sessler J L , et al . J . Am. Chem. Soc. ,1999 , 121 : 10438 —10439
|
[57] | [34 ] Sessler J L , Cho D G, Lynch V. J . Am. Chem. Soc. , 2006 , 128 :16518 —16519
|
[58] | [35 ] Mizuno T, Wei W H , Sessler J L , et al . J . Am. Chem. Soc. ,2002 , 124 : 1134 —1135
|
[59] | [36 ] Anzenbacher PJ , Aldakov D. Chem. Commun. , 2003 , 1394 —1395
|
[60] | [39 ] Maeda H , Ito Y. Inorg. Chem. , 2006 , 45 : 8205 —8210
|
[61] | [40 ] Maeda H , Kusunose Y, Mihashi Y, et al . J . Org. Chem. , 2007 ,72 : 2612 —2616
|
[62] | [41 ] Maeda H , Haketa Y, Nakanishi T. J . Am. Chem. Soc. , 2007 ,129 : 13661 —13674
|
[63] | [43 ] Maeda H , Mihashi Y, Haketa Y. Org. Lett . , 2008 , 10 : 3179 —3198
|
[64] | [44 ] Renic’M, Basaric’N , Mlinaric’-Majerski K. Tetrahedron Lett . ,2007 , 48 : 7873 —7877
|
[65] | [45 ] Huggins M T, Musto C , Munro L , et al . Tetrahedron , 2007 , 63 :12994 —12999
|
[66] | [46 ] Miyaji H , Sato W, Sessler J L. Angew. Chem. Int . Ed. , 2000 ,39 : 1777 —1780
|
[67] | [47 ] Anzenbacher P Jr , Nishiyabu R. J . Am. Chem. Soc. , 2005 , 127 :8270 —8271
|
[68] | [48 ] Palacios M A , Nishiyabu R , Marquez M, et al . J . Am. Chem.Soc. , 2007 , 129 : 7538 —7544
|
[69] | [49 ] Sessler J L , Mody TD , Ford D A , et al . Angew. Chem. Int . Ed. ,1992 , 31 : 452 —455
|
[70] | [50 ] Sessler J L , An D , Cho W S , et al . Chem. Commun. , 2005 ,540 —542
|
[71] | [51 ] Starnes S D , Arungundram S , Saunders C H. Tetrahedron Lett . ,2002 , 43 : 7785 —7788
|
[72] | [52 ] He X, Hu S , Shao S J , et al . Org. Lett . , 2006 , 8 : 333 —336
|
[73] | [53 ] Lee J Y, Lee M H , Jeong K S. Supramolecular Chemistry , 2007 ,19 : 257 —263
|
[74] | [54 ] Zieliński T, Dydio P , Jurczak J . Tetrahedron , 2008 , 64 : 568 —574
|
[75] | [55 ] Oi W, Nishiki M, Ito K. Lett . Org. Chem. , 2007 , 4 : 112 —119
|
[76] | [56 ] Pfeffer F M, Lim K F , Sedgwick KJ . Org. Biomol . Chem. , 2007 ,5 : 1795 —1799
|
[77] | [59 ] Kwon T H , Jeong K S. Tetrahedron Lett . , 2006 , 47 : 8539 —8541
|
[78] | [60 ] Wang T, Bai Y, Ma L , Yan X P. Org. Biomol . Chem. , 2008 , 6 :1751 —1755
|
[79] | [61 ] Chang KJ , Moon D , Lah M S , et al . Angew. Chem. Int . Ed. ,2005 , 44 : 7926 —7929
|
Full-Text
|
|
Contact Us
service@oalib.com QQ:3279437679 
WhatsApp +8615387084133
|
|