English
新闻公告
More
化学进展 2009, Vol. 21 Issue (6): 1207-1216 前一篇   后一篇

• 综述与评论 •

含氮杂环类阴离子受体*

林奇;魏太保;姚虹;张有明**   

  1. (西北师范大学 化学化工学院 甘肃省高分子材料重点实验室 兰州 730070)
  • 收稿日期:2008-07-18 修回日期:2008-08-31 出版日期:2009-06-24 发布日期:2009-06-16
  • 通讯作者: 张有明 E-mail:zhangnwnu@126.com
  • 基金资助:

    国家自然科学基金

Azo-Heterocycle Based Anion Receptors

Lin Qi;  |Wei Taibao;  |Yao Hong;  |Zhang Youming**   

  1. (College of Chemistry and Chemical Engineering, Key Laboratory of Polymer Materials of Gansu Province, Northwest Normal University, Lanzhou 730070, China)
  • Received:2008-07-18 Revised:2008-08-31 Online:2009-06-24 Published:2009-06-16
  • Contact: Zhang Youming E-mail:zhangnwnu@126.com

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。

The development of azo-heterocycle based anion receptors is a very important field for the supramolecular chemistry. These kinds of anion receptors possess a great deal of merits such as various host structures, wide adaptability, high selectivity and sensitivity. This review summarizes the main design principles, anion recognition abilities and recognition mechanism of the azo-heterocycle based receptors which having pyrrole, indole, imidazole and carbazole as recognition groups.

Contents
1 Introduction
2 Pyrrole based anion receptors
2.1 Uncyclic pyrrole derivatives based anion receptors
2.2 Cyclic pyrrole derivatives based anion receptors
3 Indole based anion receptors
3.1 Indole based anion receptors
3.2 Indolocarbazole based anion receptors
4 Imidazole based anion receptors
5 Other azo-heterocycle based anion receptors
6 Prospect

中图分类号: 

()

[ 1 ]  Sessler J L , Gale P A , Cho W S. Anion Receptor Chemistry.Cambridge : Royal Society of Chemistry , 2006. 1 —22
[ 2 ]  Park C H , Simmons H E. J . Am. Chem. Soc. , 1968 , 90 : 2429 —2431
[ 3 ]  Graf E , Lehn J M. J . Am. Chem. Soc. , 1976 , 98 : 6403 —6405
[ 4 ]  Schmidtchen F P , Berger M. Chem. Rev. , 1997 , 97 : 1609 —1646
[ 5 ]  Antonisse MM G, Reinhoudt D N. Chem. Commun. , 1998 , 443 —448
[ 6 ]  Anslyn E V , Snowden T S. Curr. Opin. Chem. Biol . , 1999 , 3 :740 —746
[ 7 ]  Beer P D , Gale P A. Angew. Chem. Int . Ed. , 2001 , 40 : 486 —516
[ 8 ]  Martínez-Màìez R , Sacenón F. Chem. Rev. , 2003 , 103 : 4419 —4476
[ 9 ]  Chmielewski M J , Jurczak J . Chem. Eur. J . , 2005 , 11 : 6080 —6094
[10 ]  Gunnlaugsson T, Glynn M, Tocci GM. Coord. Chem. Rev. , 2006 ,250 : 3094 —3117
[11 ]  Suksai C , Tuntulani T. Chem. Soc. Rev. , 2003 , 32 : 192 —202
[12 ]  Gale P , García-Garrido S E , Garric J . Chem. Soc. Rev. , 2008 ,37 : 151 —190
[13 ]  Llinares J M, Powell D , Bowman-James K. Coord. Chem. Rev. ,2003 , 240 : 57 —75
[14 ]  Casnati A , Sansone F , Ungaro R. Acc. Chem. Res. , 2003 , 36 :246 —254
[15 ]  Frontera A , Morey J , Oliver A , et al . J . Org. Chem. , 2006 , 71 :7185 —7195
[16 ]  Swamy KM K, Lee YJ , Lee H N , et al . J . Org. Chem. , 2006 ,71 : 8626 —8628
[17 ]  Zhao YL , Zhang H Y, WangM, et al . J . Org. Chem. , 2006 , 71 :6010 —6019
[18 ]  Kang S O , Begum R A , Bowman-James K. Angew. Chem. Int .Ed. , 2006 , 45 : 7882 —7894
[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
[20 ]  Zhang Y M, Qin J D , Lin Q , et al . J . Fluorine Chem. , 2006 ,127 : 1222 —1227
[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
[22 ]  Zhang YM, Cao C , Wei W, et al . Chin. J . Chem. , 2007 , 25 :709 —713
[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
[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
[25 ]  Best M D , Tobey S L , Anslyn E V. Coord. Chem. Rev. , 2003 ,240 : 3 —15
[26 ]  Gale P A , Anzenbacher P , Sessler J L. Coord. Chem. Rev. , 2001 ,222 : 57 —102
[27 ]  Sessler J L , Davis J M. Acc. Chem. Res. , 2001 , 34 : 989 —997
[28 ]  Sessler J L , Camiolo S , Gale P A. Coord. Chem. Rev. , 2003 ,240 : 17 —55
[29 ]  Gale P A. Chem. Commun. , 2005 , 3761 —3772
[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
[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
[32 ]  Black C B , Andrioletti B , Sessler J L , et al . J . Am. Chem. Soc. ,1999 , 121 : 10438 —10439
[33 ]  Anzenbacher P , Try A C , Sessler J L , et al . J . Am. Chem. Soc. ,2000 , 122 : 10268 —10272
[34 ]  Sessler J L , Cho D G, Lynch V. J . Am. Chem. Soc. , 2006 , 128 :16518 —16519
[35 ]  Mizuno T, Wei W H , Sessler J L , et al . J . Am. Chem. Soc. ,2002 , 124 : 1134 —1135
[36 ]  Anzenbacher PJ , Aldakov D. Chem. Commun. , 2003 , 1394 —1395
[37 ]  Aldakov D , Anzenbacher P. J . Am. Chem. Soc. , 2004 , 126:4752 —4753
[38 ]  Maeda H , Kusunose Y. Chem. Eur. J . , 2005 , 11 : 5661 —5666
[39 ]  Maeda H , Ito Y. Inorg. Chem. , 2006 , 45 : 8205 —8210
[40 ]  Maeda H , Kusunose Y, Mihashi Y, et al . J . Org. Chem. , 2007 ,72 : 2612 —2616
[41 ]  Maeda H , Haketa Y, Nakanishi T. J . Am. Chem. Soc. , 2007 ,129 : 13661 —13674
[42 ]  Fujimoto C , Kusunose Y, Maeda H. J . Org. Chem. , 2006 , 71 :2389 —2394
[43 ]  Maeda H , Mihashi Y, Haketa Y. Org. Lett . , 2008 , 10 : 3179 —3198
[44 ]  Renic’M, Basaric’N , Mlinaric’-Majerski K. Tetrahedron Lett . ,2007 , 48 : 7873 —7877
[45 ]  Huggins M T, Musto C , Munro L , et al . Tetrahedron , 2007 , 63 :12994 —12999
[46 ]  Miyaji H , Sato W, Sessler J L. Angew. Chem. Int . Ed. , 2000 ,39 : 1777 —1780
[47 ]  Anzenbacher P Jr , Nishiyabu R. J . Am. Chem. Soc. , 2005 , 127 :8270 —8271
[48 ]  Palacios M A , Nishiyabu R , Marquez M, et al . J . Am. Chem.Soc. , 2007 , 129 : 7538 —7544
[49 ]  Sessler J L , Mody TD , Ford D A , et al . Angew. Chem. Int . Ed. ,1992 , 31 : 452 —455
[50 ]  Sessler J L , An D , Cho W S , et al . Chem. Commun. , 2005 ,540 —542
[51 ]  Starnes S D , Arungundram S , Saunders C H. Tetrahedron Lett . ,2002 , 43 : 7785 —7788
[52 ]  He X, Hu S , Shao S J , et al . Org. Lett . , 2006 , 8 : 333 —336
[53 ]  Lee J Y, Lee M H , Jeong K S. Supramolecular Chemistry , 2007 ,19 : 257 —263
[54 ]  Zieliński T, Dydio P , Jurczak J . Tetrahedron , 2008 , 64 : 568 —574
[55 ]  Oi W, Nishiki M, Ito K. Lett . Org. Chem. , 2007 , 4 : 112 —119
[56 ]  Pfeffer F M, Lim K F , Sedgwick KJ . Org. Biomol . Chem. , 2007 ,5 : 1795 —1799
[57 ]  Janosik T, Wahlstrêm N , Bergman J . Tetrahedron , 2008 , 64 :9159 —9180
[58 ]  Curiel D , Cowley A , Beer P D. Chem. Commun. , 2005 , 236 —238
[59 ]  Kwon T H , Jeong K S. Tetrahedron Lett . , 2006 , 47 : 8539 —8541
[60 ]  Wang T, Bai Y, Ma L , Yan X P. Org. Biomol . Chem. , 2008 , 6 :1751 —1755
[61 ]  Chang KJ , Moon D , Lah M S , et al . Angew. Chem. Int . Ed. ,2005 , 44 : 7926 —7929
[62 ]  Suk J M, Chae M K, Kim N K, et al . Pure Appl . Chem. , 2008 ,80 : 599 —608
[63 ]  Kang J , Kim H S , Jang D O. Tetrahedron Lett . , 2005 , 46 : 6079 —6082
[64 ]  Singh N , Jang D O. Org. Lett . , 2007 , 9 : 1991 —1994
[65 ]  YuM, Lin H K, Zhao G, et al . J . Mol . Recognit . , 2007 , 20 :69 —73
[66 ]  Chetia B , Iyer P K. Tetrahedron Lett . , 2008 , 49 : 94 —97
[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
[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
[69 ]  Yoon J , Kim S K, Singh NJ , et al . Chem. Soc. Rev. , 2006 , 35 :355 —360
[70 ]  Xu Z, Kim S , Lee K H , Yoon J . Tetrahedron Lett . , 2007 , 48 :3797 —3800
[71 ]  Khatri V K, Upreti S , Pandey P S. Org. Lett . , 2006 , 8 : 1755 —1758
[72 ]  Chahar M, Upreti S , Pandey P S. Tetrahedron , 2007 , 63 : 171 —176
[73 ]  Niu H T, Yin Z, Su D , et al . Tetrahedron , 2008 , 64 : 6300 —6306
[74 ]  Niu H T, Yin Z. Su D , et al . Dalton Trans. , 2008 , 3694 —3700
[75 ]  Alhashimy N , Brougham D J , Nolan K, et al . Tetrahedron Lett . ,2007 , 48 : 125 —128
[76 ]  Qin D B , Xu F B , Zhang Z Z, et al . Tetrahedron Lett . , 2006 , 47 :5641 —5643
[77 ]  Hirano J , Miyata H , Zaitsu K, et al . Tetrahedron Lett . , 2007 , 48 :4861 —4864
[78 ]  Maeda H , Ito Y, Kusunose Y, et al . Chem. Commun. , 2007 ,1136 —1138
[79 ]  Juwarker H , Lenhardt J M, Pham D M, et al . Angew. Chem. Int .Ed. , 2008 , 47 : 3740 —3743

[1] 陈戈慧, 马楠, 于帅兵, 王娇, 孔金明, 张学记. 可卡因免疫及适配体生物传感器[J]. 化学进展, 2023, 35(5): 757-770.
[2] 鲍艳, 许佳琛, 郭茹月, 马建中. 基于微纳结构的高灵敏度柔性压力传感器[J]. 化学进展, 2023, 35(5): 709-720.
[3] 赵京龙, 沈文锋, 吕大伍, 尹嘉琦, 梁彤祥, 宋伟杰. 基于人体呼气检测应用的气体传感器[J]. 化学进展, 2023, 35(2): 302-317.
[4] 钟衍裕, 王正运, 刘宏芳. 抗坏血酸电化学传感研究进展[J]. 化学进展, 2023, 35(2): 219-232.
[5] 卢继洋, 汪田田, 李湘湘, 邬福明, 杨辉, 胡文平. 电喷印刷柔性传感器[J]. 化学进展, 2022, 34(9): 1982-1995.
[6] 乔瑶雨, 张学辉, 赵晓竹, 李超, 何乃普. 石墨烯/金属-有机框架复合材料制备及其应用[J]. 化学进展, 2022, 34(5): 1181-1190.
[7] 姜鸿基, 王美丽, 卢志炜, 叶尚辉, 董晓臣. 石墨烯基人工智能柔性传感器[J]. 化学进展, 2022, 34(5): 1166-1180.
[8] 林瑜, 谭学才, 吴叶宇, 韦富存, 吴佳雯, 欧盼盼. 二维纳米材料g-C3N4在电化学发光中的应用研究[J]. 化学进展, 2022, 34(4): 898-908.
[9] 孙义民, 李厚燊, 陈振宇, 王东, 王展鹏, 肖菲. MXene在电化学传感器中的应用[J]. 化学进展, 2022, 34(2): 259-271.
[10] 孙华悦, 向宪昕, 颜廷义, 曲丽君, 张光耀, 张学记. 基于智能纤维和纺织品的可穿戴生物传感器[J]. 化学进展, 2022, 34(12): 2604-2618.
[11] 彭倩, 张晶晶, 房新月, 倪杰, 宋春元. 基于表面增强拉曼光谱技术的心肌生物标志物检测[J]. 化学进展, 2022, 34(12): 2573-2587.
[12] 龚筑轲, 许辉. 晶态咔唑基有机室温磷光材料[J]. 化学进展, 2022, 34(11): 2432-2461.
[13] 赵静, 王子娅, 莫黎昕, 孟祥有, 李路海, 彭争春. 微结构化柔性压力传感器的性能增强机制、实现方法与应用优势[J]. 化学进展, 2022, 34(10): 2202-2221.
[14] 侯慧鹏, 梁阿新, 汤波, 刘宗坤, 罗爱芹. 光子晶体生化传感器的构建及应用[J]. 化学进展, 2021, 33(7): 1126-1137.
[15] 廖金花, 高佳俊, 王宇超, 孙巍. 微结构化弹性体介电层的制备方法与应用[J]. 化学进展, 2021, 33(6): 975-987.
阅读次数
全文


摘要

含氮杂环类阴离子受体*