Molecular Recognition and Scavenging of Arsenate from Aqueous Solution Using Dimetallic Receptors
A series of copper(II), nickel(II) and zinc(II) dimetallic complexes were prepared and their affinities towards arsenate investigated. Indicator displacement assays (IDAs) were carried out to establish the complexes with best affinities towards arsenate. A di‐zinc complex (3) was selected and its ar...
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Published in: | Chemistry : a European journal Vol. 20; no. 51; pp. 17168 - 17177 |
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Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Weinheim
WILEY-VCH Verlag
15-12-2014
WILEY‐VCH Verlag Wiley Subscription Services, Inc |
Subjects: | |
Online Access: | Get full text |
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Summary: | A series of copper(II), nickel(II) and zinc(II) dimetallic complexes were prepared and their affinities towards arsenate investigated. Indicator displacement assays (IDAs) were carried out to establish the complexes with best affinities towards arsenate. A di‐zinc complex (3) was selected and its arsenate‐binding abilities investigated by isothermal titration calorimetry (ITC). The X‐ray crystal structure of this metallo‐receptor bound to arsenate is also reported, which allowed us to establish the binding mode between 3 and this oxyanion. Immobilising 3 onto HypoGel resin yielded a novel adsorbent (Zn–HypoGel) with high affinity for arsenate. Adsorption of arsenate from competitive solutions and natural groundwater was greater than that of the commercially used iron oxide Bayoxide E33. Zn–HypoGel could be efficiently and simply regenerated by washing with sodium acetate solution.
An arsenate “sponge”: The arsenate‐binding ability of a series of metallo‐receptors is reported. From these, a di‐zinc complex has been shown to have very good affinity for arsenate in aqueous media and has been successfully attached to polymer beads. The resulting functionalized solid material has been successfully employed to remove arsenate from contaminated water to levels well below those currently allowed by legislation. |
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Bibliography: | EPSRC ArticleID:CHEM201404723 Funded Access NERC - No. NE/I527929/1 ark:/67375/WNG-322TPQ2X-4 istex:803870997CDD166B3693A7458FD335653841D4F6 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Supporting information for this article is available on the WWW under http://dx.doi.org/10.1002/chem.201404723. |
ISSN: | 0947-6539 1521-3765 |
DOI: | 10.1002/chem.201404723 |