| Literature DB >> 22282352 |
Daniel M Wood1, Barnaby W Greenland, Aaron L Acton, Francisco Rodríguez-Llansola, Claire A Murray, Christine J Cardin, Juan F Miravet, Beatriu Escuder, Ian W Hamley, Wayne Hayes.
Abstract
A focused library of potential hydrogelators each containing two substituted aromatic residues separated by a urea or thiourea linkage have been synthesised and characterized. Six of these novel compounds are highly efficient hydrogelators, forming gels in aqueous solution at low concentrations (0.03-0.60 wt%). Gels were formed through a pH switching methodology, by acidification of a basic solution (pH 14 to ≈ 4) either by addition of HCl or via the slow hydrolysis of glucono-δ-lactone. Frequently, gelation was accompanied by a dramatic switch in the absorption spectra of the gelators, resulting in a significant change in colour, typically from a vibrant orange to pale yellow. Each of the gels was capable of sequestering significant quantities of the aromatic cationic dye, methylene blue, from aqueous solution (up to 1.02 g of dye per gram of dry gelator). Cryo-transmission electron microscopy of two of the gels revealed an extensive network of high aspect ratio fibers. The structure of the fibers altered dramatically upon addition of 20 wt% of the dye, resulting in aggregation and significant shortening of the fibrils. This study demonstrates the feasibility for these novel gels finding application as inexpensive and effective water purification platforms.Entities:
Year: 2012 PMID: 22282352 DOI: 10.1002/chem.201102137
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236