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Chemistry. 2011 Apr 26;17(18):4946-59. doi: 10.1002/chem.201100050. Epub 2011 Apr 4.
2
Anion-binding behavior of hybrid calixpyrroles.杂化杯吡咯的阴离子结合行为
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4
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Anion-induced synthesis and combinatorial selection of polypyrrolic macrocycles.阴离子诱导的聚吡咯大环化合物的合成与组合筛选
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本文引用的文献

1
Uranyl oxo activation and functionalization by metal cation coordination.铀酰氧基的金属阳离子配位活化与功能化
Nat Chem. 2010 Dec;2(12):1056-61. doi: 10.1038/nchem.904. Epub 2010 Nov 23.
2
Positive homotropic allosteric receptors for neutral guests: annulated tetrathiafulvalene-calix[4]pyrroles as colorimetric chemosensors for nitroaromatic explosives.正同变构受体对中性客体:环化四硫富瓦烯-杯[4]吡咯作为比色化学传感器用于检测硝基芳香族爆炸物。
Chemistry. 2010 Jan 18;16(3):848-54. doi: 10.1002/chem.200902924.
3
Cyclo[8]pyrrole: a simple-to-make expanded porphyrin with no meso bridges.环[8]吡咯:一种易于制备的无中位桥连的扩展卟啉。
Angew Chem Int Ed Engl. 2002 Apr 15;41(8):1422-5. doi: 10.1002/1521-3773(20020415)41:8<1422::aid-anie1422>3.0.co;2-o.
4
Molecular recognition of pertechnetate and perrhenate.高锝酸盐和高铼酸盐的分子识别
Chem Soc Rev. 2009 Jun;38(6):1572-86. doi: 10.1039/b806468g. Epub 2009 Mar 6.
5
A macrocyclic approach to transition metal and uranyl Pacman complexes.一种用于过渡金属和铀酰“吃豆人”配合物的大环方法。
Chem Commun (Camb). 2009 Jun 14(22):3154-65. doi: 10.1039/b904189c. Epub 2009 Apr 27.
6
Rational materials design of sorbent coatings for explosives: applications with chemical sensors.用于爆炸物的吸附剂涂层的合理材料设计:在化学传感器中的应用
Talanta. 2001 May 10;54(3):469-85. doi: 10.1016/s0039-9140(00)00545-2.
7
Uranyl-specific binding at a functionalised interface: a chemophotonic fibre optic sensor platform.功能化界面上的铀酰特异性结合:一种化学光子光纤传感器平台。
Analyst. 2008 May;133(5):616-20. doi: 10.1039/b714625f. Epub 2008 Feb 20.
8
Immobilization of a hexaphyrin(1.0.1.0.0.0) derivative onto a tentagel-amino resin and its use in uranyl cation detection.将一种六卟啉(1.0.1.0.0.0)衍生物固定在tentagel-氨基树脂上及其在铀酰阳离子检测中的应用。
Dalton Trans. 2008 Mar 28(12):1538-40. doi: 10.1039/b718627d. Epub 2008 Feb 7.
9
Cryptand-like porphyrinoid assembled with three dipyrrylpyridine chains: synthesis, structure, and homotropic positive allosteric binding of carboxylic acids.由三条二吡咯吡啶链组装而成的类穴状卟啉:羧酸的合成、结构及同向正变构结合
J Am Chem Soc. 2008 Feb 27;130(8):2404-5. doi: 10.1021/ja710424n. Epub 2008 Feb 5.
10
Reduction and selective oxo group silylation of the uranyl dication.铀酰二价阳离子的还原及选择性氧代基团硅烷化反应
Nature. 2008 Jan 17;451(7176):315-7. doi: 10.1038/nature06467.

寡吡咯大环化合物:潜在危险物质的受体和化学传感器。

Oligopyrrole macrocycles: receptors and chemosensors for potentially hazardous materials.

机构信息

Department of Chemistry and Biochemistry, University of Texas at Austin, 1 University Station A5300, Austin, TX 78712-0165, USA.

出版信息

Chemistry. 2011 Apr 26;17(18):4946-59. doi: 10.1002/chem.201100050. Epub 2011 Apr 4.

DOI:10.1002/chem.201100050
PMID:21465591
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3133723/
Abstract

Oligopyrroles represent a diverse class of molecular receptors that have been utilized in a growing number of applications. Recently, these systems have attracted interest as receptors and chemosensors for hazardous materials, including harmful anionic species, high-valent actinide cations, and nitroaromatic explosives. These versatile molecular receptors have been used to develop rudimentary colorimetric and fluorimetric assays for hazardous materials.

摘要

寡吡咯是一类具有广泛应用前景的分子受体,近年来,它们作为有害阴离子物种、高价锕系阳离子和硝基芳香族爆炸物等有害物质的受体和化学传感器引起了人们的兴趣。这些多功能的分子受体已被用于开发用于有害物质的基本比色法和荧光法测定。

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