Macrocyclic squaramides: anion receptors with high sulfate binding affinity and selectivity in aqueous media

被引:98
|
作者
Qin, Lei [1 ]
Hartley, Anna [1 ]
Turner, Peter [1 ]
Elmes, Robert B. P. [1 ,2 ]
Jolliffe, Katrina A. [1 ]
机构
[1] Univ Sydney, Sch Chem, Sydney, NSW 2006, Australia
[2] Maynooth Univ, Natl Univ Ireland Maynooth, Dept Chem, Maynooth, Kildare, Ireland
关键词
RECOGNITION; CHLORIDE; FLUORESCENT; EXCHANGE; PROTEIN; WATER; ARMS;
D O I
10.1039/c6sc01011c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A number of macrocyclic squaramide-containing receptors (MSQs) have been designed and synthesised and their interaction with a range of inorganic anions was studied in solution by H-1 NMR spectroscopy and ESI-HRMS. The binding data revealed remarkable binding of sulfate in aqueous mixtures from 0.5 to 50% v/v (HO)-O-2/DMSO-d(6). The larger [3]-MSQs were found to better match the size and shape of the sulfate ion than the [2]-MSQs, providing high affinity and selectivity for sulfate while other tetrahedral divalent anions such as selenate, phosphate species and chromate have substantially lower binding affinities. In mixtures of anions mimicking the composition of either nuclear waste or plasma, the [3]-MSQs were still able to bind sulfate ions with high affinity.
引用
收藏
页码:4563 / 4572
页数:10
相关论文
共 50 条
  • [1] Thermodynamics of sulfate anion binding by macrocyclic polyammonium receptors
    Arranz, P
    Bencini, A
    Bianchi, A
    Diaz, P
    García-España, E
    Giorgi, C
    Luis, SV
    Querol, M
    Valtancoli, B
    JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 2001, (09): : 1765 - 1770
  • [2] High affinity sulfate binding in aqueous media by cyclic peptides with thiourea arms
    Dungan, Victoria J.
    Huy Tien Ngo
    Young, Philip G.
    Jolliffe, Katrina A.
    CHEMICAL COMMUNICATIONS, 2013, 49 (03) : 264 - 266
  • [3] High-Affinity Anion Binding by Steroidal Squaramide Receptors
    Edwards, Sophie J.
    Valkenier, Hennie
    Busschaert, Nathalie
    Gale, Philip A.
    Davis, Anthony P.
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2015, 54 (15) : 4592 - 4596
  • [4] Tetrakis(imidazolium) macrocyclic receptors for anion binding
    Wong, WWH
    Vickers, MS
    Cowley, AR
    Paul, RL
    Beer, PD
    ORGANIC & BIOMOLECULAR CHEMISTRY, 2005, 3 (23) : 4201 - 4208
  • [5] The Influence of Binding Site Geometry on Anion-Binding Selectivity: A Case Study of Macrocyclic Receptors Built on the Azulene Skeleton
    Lichosyt, Dawid
    Wasilek, Sylwia
    Dydio, Pawel
    Jurczak, Janusz
    CHEMISTRY-A EUROPEAN JOURNAL, 2018, 24 (45) : 11683 - 11692
  • [6] Benzenebistriazole-strapped calix[4]pyrrole: a neutral anion receptor with CH and NH donor groups that exhibits high sulfate binding affinity and selectivity in aqueous solutions
    He, Ying-Chun
    Yan, Yan-Mei
    Tong, Hong-Bo
    Ren, Zhen-Xing
    Wang, Jun-Hong
    Zhang, Yong-Bin
    Chao, Jian-Bin
    Wang, Meng-Liang
    CHEMICAL COMMUNICATIONS, 2020, 56 (65) : 9364 - 9367
  • [7] Simple squaramide receptors for highly efficient anion binding in aqueous media and transmembrane transport
    Picci, Giacomo
    Kubicki, Maciej
    Garau, Alessandra
    Lippolis, Vito
    Mocci, Rita
    Porcheddu, Andrea
    Quesada, Roberto
    Ricci, Pier Carlo
    Scorciapino, M. Andrea
    Caltagirone, Claudia
    CHEMICAL COMMUNICATIONS, 2020, 56 (75) : 11066 - 11069
  • [8] Pseudo-allosteric regulation of the anion binding affinity of a macrocyclic coordination complex
    Kuwabara, Junpei
    Yoon, Hyo Jae
    Mirkin, Chad A.
    DiPasquale, Antonio G.
    Rheingold, Arnold L.
    CHEMICAL COMMUNICATIONS, 2009, (30) : 4557 - 4559
  • [9] The Presence of Arginine Regulates the Selectivity and Binding Affinity of Lysine Receptors
    Abron, Jessicca
    Pinkin, Nicholas
    Waters, Marcey
    BIOPHYSICAL JOURNAL, 2015, 108 (02) : 235A - 235A
  • [10] Multidentate Anion Receptors for Binding Glyphosate Dianion: Structure and Affinity
    Kadam, Sandip A.
    Haav, Kristjan
    Toom, Lauri
    Pung, Astrid
    Mayeux, Charly
    Leito, Ivo
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2017, 2017 (11) : 1396 - 1406