Supramolecular Materials

A special issue of Chemistry (ISSN 2624-8549). This special issue belongs to the section "Supramolecular Chemistry".

Deadline for manuscript submissions: closed (15 November 2021) | Viewed by 4053

Special Issue Editors


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Guest Editor
1. Department of Chemistry, Faraday Building, Lancaster University, Lancaster LA1 4YB, UK
2. Materials Science Institute, Faraday Building, Lancaster University, Lancaster LA1 4YB, UK
Interests: polymer synthesis; supramolecular materials; biomaterials; stimuli-responsive materials; drug delivery; tissue engineering; sustainability
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Guest Editor
School of Chemistry, University of Glasgow, Glasgow G12 8QQ, UK
Interests: supramolecular; organic electronics; self-assembly; electrochromic; SANS; rheology; gels
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

Nature employs a combination of supramolecular interactions (e.g., electrostatic, hydrophobic, π–π, cation/anion–π, van der Waals forces, hydrogen-bonding and metal coordination) to generate hierarchically ordered structures with remarkable stimuli-responsive properties. The same structure-directing forces can, in principle, be employed for the realization of manufactured assemblies with similar or perhaps even greater utility. In this Special Issue of the Chemistry devoted to "Supramolecular Materials", we warmly invite submissions related to the synthesis, characterization and technical/biomedical applications of supramolecular entities.

You may choose our Joint Special Issue in International Journal of Molecular Sciences.

Dr. John G. Hardy
Dr. Emily R. Draper
Guest Editors

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Keywords

  • supramolecular interactions
  • self-assembly
  • host-guest systems
  • template effects
  • dynamic covalent chemistry
  • supramolecular polymers
  • supracolloidal chemistry
  • supramolecular materials
  • supramolecular optoelectronics
  • supramolecular theranostics

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Research

24 pages, 7792 KiB  
Article
Synthesis and Self-Assembling Properties of Peracetylated β-1-Triazolyl Alkyl D-Glucosides and D-Galactosides
by Pooja Sharma, Anji Chen, Dan Wang and Guijun Wang
Chemistry 2021, 3(3), 935-958; https://doi.org/10.3390/chemistry3030068 - 28 Aug 2021
Cited by 8 | Viewed by 3058
Abstract
Carbohydrate-based low-molecular-weight gelators (LMWGs) are useful classes of compounds due to their numerous applications. Among sugar-based LMWGs, certain peracetylated sugar beta-triazole derivatives were found to be effective organogelators and showed interesting self-assembling properties. To further understand the structural influence towards molecular assemblies and [...] Read more.
Carbohydrate-based low-molecular-weight gelators (LMWGs) are useful classes of compounds due to their numerous applications. Among sugar-based LMWGs, certain peracetylated sugar beta-triazole derivatives were found to be effective organogelators and showed interesting self-assembling properties. To further understand the structural influence towards molecular assemblies and obtain new functional materials with interesting properties, we designed and synthesized a library of tetraacetyl beta-1-triazolyl alkyl-D-glucosides and D-galactosides, in which a two or three carbon spacer is inserted between the anomeric position and the triazole moiety. A series of 16 glucose derivatives and 14 galactose derivatives were synthesized and analyzed. The self-assembling properties of these new triazole containing glycoconjugates in different solvents were analyzed. Several glucose derivatives were found to be effective LMWGs, with compound 7a forming gels in a variety of organic solvents as well as in the presence of metal ions in aqueous solutions. The organogels formed by several compounds were characterized using optical microscopy, atomic force microscopy (AFM) and UV-vis spectroscopy, etc. The co-gels formed by compound 7a with the Fmoc derivative 7i showed interesting fluorescence enhancement upon gelation. Several gelators were also characterized using powder X-ray diffraction and FT-IR spectroscopy. The potential applications of these sugar-based gelators for drug delivery and dye removal were also studied. Full article
(This article belongs to the Special Issue Supramolecular Materials)
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