Sugar-Integrated Gelators of Organic Solvents
Top Cited Papers
- 5 October 2001
- journal article
- concept
- Published by Wiley in Chemistry – A European Journal
- Vol. 7 (20) , 4328-4334
- https://doi.org/10.1002/1521-3765(20011015)7:20<4328::aid-chem4328>3.0.co;2-s
Abstract
Some methyl 4,6‐O‐benzylidene monosaccharides can act as strong low molecular weight gelators for various organic solvents. As they are accessible in a variety of homologues, each with a unique molecular architecture, they can be used for systematic studies of gelation phenomena. Structural details of their hydrogen‐bond‐based fiber network in the gel phase can be resolved by small angle X‐ray scattering (SAXS). Analysis of the molecular arrangement in a single crystal can be a valuable tool for the prediction of gelation ability presupposing that the elongated shape of the gel fibers arises from an anisotropic assembly of the gelator molecules into one‐dimensional aggregates. It is found that some derivatives act as “supergelators”, which can gelate hydrocarbon solvents with 0.03–0.05 wt %. The recent results emerging from these investigations will be outlined in this article.Keywords
This publication has 48 references indexed in Scilit:
- 1H NMR Investigation of the Composition, Structure, and Dynamics of Cholesterol−Stilbene Tethered Dyad OrganogelsLangmuir, 2000
- Cholesterol-based functional tectons as versatile building-blocks for liquid crystals, organic gels and monolayersJournal of Materials Chemistry, 1998
- New sugar-based gelators bearing a p-nitrophenyl chromophore: remarkably large influence of a sugar structure on the gelation abilityJournal of the Chemical Society, Perkin Transactions 2, 1998
- Formation of Organogels by Intermolecular Hydrogen Bonding between Ureylene SegmentChemistry Letters, 1996
- Dual-component cholesterol-based gelators bearing complementary hydrogen-bonding sitesSupramolecular Science, 1996
- Neue Entwicklungen der Molekülchemie für Sol‐Gel‐ProzesseAngewandte Chemie, 1996
- Structures of Organogels Based upon Cholesteryl 4-(2-Anthryloxy)butanoate, a Highly Efficient Luminescing Gelator: Neutron and X-ray Small-Angle Scattering InvestigationsThe Journal of Physical Chemistry, 1995
- Functional organic gels Chirality induction through formation of highly-oriented structureLiquid Crystals, 1995
- Anthraquinone–steroid based gelators of alcohols and alkanesJournal of the Chemical Society, Chemical Communications, 1995
- Utilization of Sugars in Organic Synthesis; Part XXVII. Chemistry of Oxo-Sugars. (2). Regio- and Stereo-Selective Synthesis of Methyl D-Hexopyranosiduloses and Identification of Their Forms Existing in Solutions.CHEMICAL & PHARMACEUTICAL BULLETIN, 1993