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Tough nanocomposite ionogel-based actuator exhibits robust performance.Supramolecular gels with high strength by tuning of calix[4]arene-derived networks.Poly(aryl ether) Dendrons with Monopyrrolotetrathiafulvalene Unit-Based Organogels exhibiting Gel-Induced Enhanced Emission (GIEE).MPTTF-containing tripeptide-based organogels: receptor for 2,4,6-trinitrophenol and multiple stimuli-responsive properties.Supramolecular organic frameworks: engineering periodicity in water through host-guest chemistry.Click chemistry-assisted, bis-cholesteryl-appended, isosorbide-based, dual-responsive organogelators and their self-assemblies.Fe(iii) phytate metallogel as a prototype anhydrous, intermediate temperature proton conductor.Hierarchical heteroaggregation of binary metal-organic gels with tunable porosity and mixed valence metal sites for removal of dyes in water.Adaptable hydrogel networks with reversible linkages for tissue engineering.Synthesis of Fluorescent Gelators and Direct Observation of Gelation with a Fluorescence Microscope.A new class of organogelators based on triphenylmethyl derivatives of primary alcohols: hydrophobic interactions alone can mediate gelation.Biomaterials and emerging anticancer therapeutics: engineering the microenvironment.Supramolecular metal-organic frameworks that display high homogeneous and heterogeneous photocatalytic activity for H2 production.Multistimuli Sensitive Behavior of Novel Bodipy-Involved Pillar[5]arene-Based Fluorescent [2]Rotaxane and Its Supramolecular Gel.Supramolecular gel phase crystallization: orthogonal self-assembly under non-equilibrium conditions.Controlled-release systems for metal-based nanomedicine: encapsulated/self-assembled nanoparticles of anticancer gold(III)/platinum(II) complexes and antimicrobial silver nanoparticles.Supramolecular organogels based on dendrons and dendrimers.Self-healing gels based on constitutional dynamic chemistry and their potential applications.1,3:2,4-Dibenzylidene-D-sorbitol (DBS) and its derivatives--efficient, versatile and industrially-relevant low-molecular-weight gelators with over 100 years of history and a bright future.Multifarious facets of sugar-derived molecular gels: molecular features, mechanisms of self-assembly and emerging applications.Drying Affects the Fiber Network in Low Molecular Weight Hydrogels.Chiral supramolecular organization from a sheet-like achiral gel: a study of chiral photoinduction.Supramolecular gels made from nucleobase, nucleoside and nucleotide analogs.A vegetable oil-based organogel for use in pH-mediated drug delivery.Solid state NMR studies of gels derived from low molecular mass gelators.A supramolecular topical gel derived from a non-steroidal anti-inflammatory drug, fenoprofen, is capable of treating skin inflammation in mice.Fluorous 'ponytails' lead to strong gelators showing thermally induced structure evolution.A Hybrid Supramolecular Polymeric Hydrogel with Rapid Self-Healing Property.Multiple-stimulus-responsive supramolecular gels and regulation of chiral twists: the effect of spacer length.Improving the reactivity of phenylacetylene macrocycles toward topochemical polymerization by side chains modificationSupramolecular motifs in dynamic covalent PEG-hemiaminal organogels.Self-Assembly and Drug Release Capacities of Organogels via Some Amide Compounds with Aromatic Substituent Headgroups.Manipulating three-dimensional gel network entanglement by thin film shearing.A supramolecular gel from a quadruple zwitterion that responds to both acid and base.Rational design of heat-set and specific-ion-responsive supramolecular hydrogels based on the Hofmeister effect.Two-component supramolecular gels derived from amphiphilic shape-persistent cyclo[6]aramides for specific recognition of native arginine.Multi-component hybrid hydrogels - understanding the extent of orthogonal assembly and its impact on controlled release.Gelation-driven selection in dynamic covalent C[double bond, length as m-dash]C/C[double bond, length as m-dash]N exchangeAromatic-Aromatic Interactions Enable α-Helix to β-Sheet Transition of Peptides to Form Supramolecular Hydrogels.Synthesis, Crystal Structure, and Supramolecular Understanding of 1,3,5-Tris(1-phenyl-1H-pyrazol-5-yl)benzenes.
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Characterization of supramolecular gels.
@en
type
label
Characterization of supramolecular gels.
@en
prefLabel
Characterization of supramolecular gels.
@en
P2860
P50
P356
P1476
Characterization of supramolecular gels.
@en
P2860
P304
P356
10.1039/C3CS60080G
P577
2013-08-01T00:00:00Z