Chemically programmed self-sorting of gelator networks

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作者
Kyle L. Morris
Lin Chen
Jaclyn Raeburn
Owen R. Sellick
Pepa Cotanda
Alison Paul
Peter C. Griffiths
Stephen M. King
Rachel K. O’Reilly
Louise C. Serpell
Dave J. Adams
机构
[1] School of Life Sciences,Department of Chemistry
[2] Chichester II Building,Department of Chemistry
[3] University of Sussex,undefined
[4] University of Liverpool,undefined
[5] School of Chemistry,undefined
[6] Main building,undefined
[7] Cardiff University,undefined
[8] University of Warwick,undefined
[9] School of Science,undefined
[10] University of Greenwich,undefined
[11] Rutherford Appleton Laboratory,undefined
[12] Science and Technology Facilities Council,undefined
来源
Nature Communications | / 4卷
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摘要
Controlling the order and spatial distribution of self-assembly in multicomponent supramolecular systems could underpin exciting new functional materials, but it is extremely challenging. When a solution of different components self-assembles, the molecules can either coassemble, or self-sort, where a preference for like-like intermolecular interactions results in coexisting, homomolecular assemblies. A challenge is to produce generic and controlled ‘one-pot’ fabrication methods to form separate ordered assemblies from ‘cocktails’ of two or more self-assembling species, which might have relatively similar molecular structures and chemistry. Self-sorting in supramolecular gel phases is hence rare. Here we report the first example of the pH-controlled self-sorting of gelators to form self-assembled networks in water. Uniquely, the order of assembly can be predefined. The assembly of each component is preprogrammed by the pKa of the gelator. This pH-programming method will enable higher level, complex structures to be formed that cannot be accessed by simple thermal gelation.
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