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A synthetic route to ultralight hierarchically micro/mesoporous Al(III)-carboxylate metal-organic aerogelsSupramolecular Hydrogelators and Hydrogels: From Soft Matter to Molecular Biomaterials.Peptide conjugates of a nonsteroidal anti-inflammatory drug as supramolecular gelators: synthesis, characterization, and biological studies.MPTTF-containing tripeptide-based organogels: receptor for 2,4,6-trinitrophenol and multiple stimuli-responsive properties.An Easy Access to Organic Salt-Based Stimuli-Responsive and Multifunctional Supramolecular Hydrogels.Multidrug-Containing, Salt-Based, Injectable Supramolecular Gels for Self-Delivery, Cell Imaging and Other Materials Applications.Supramolecular synthons in designing low molecular mass gelling agents: L-amino acid methyl ester cinnamate salts and their anti-solvent-induced instant gelation.Expanding the gelation properties of valine-based 3,5-diaminobenzoate organogelators with N-alkylurea functionalities.Organo- and hydrogelators based on luminescent monocationic terpyridyl platinum(II) complexes with biphenylacetylide ligands.pH-Tunable hydrogelators for water purification: structural optimisation and evaluation.Molecular hydrogels from bolaform amino acid derivatives: a structure-properties study based on the thermodynamics of gel solubilization.Gel sculpture: moldable, load-bearing and self-healing non-polymeric supramolecular gel derived from a simple organic salt.Supramolecular assemblies by charge-transfer interactions between donor and acceptor chromophores.Synthesis of peptoid based small molecular gelators by a multiple component reaction.Synthesis and characterization of pH responsive D-glucosamine based molecular gelators.An "ingredients" approach to functional self-synthesizing materials: a metal-ion-selective, multi-responsive, self-assembled hydrogel.Hierarchical heteroaggregation of binary metal-organic gels with tunable porosity and mixed valence metal sites for removal of dyes in water.Synthesis of Fluorescent Gelators and Direct Observation of Gelation with a Fluorescence Microscope.Polymer organogelators that make supramolecular organogels through physical cross-linking and self-assembly.What kind of "soft materials" can we design from molecular gels?Coordination polymers: what has been achieved in going from innocent 4,4'-bipyridine to bis-pyridyl ligands having a non-innocent backbone?Coordination polymer gels with important environmental and biological applications.Recent advances in metallogels.Insights into low molecular mass organic gelators: a focus on drug delivery and tissue engineering applications.Supramolecular organogels based on dendrons and dendrimers.Design of nanostructures based on aromatic peptide amphiphiles.Multifarious facets of sugar-derived molecular gels: molecular features, mechanisms of self-assembly and emerging applications.Nanoscale Assemblies of Small Molecules Control the Fate of CellsRationally Developed Organic Salts of Tolfenamic Acid and Its β-Alanine Derivatives for Dual Purposes as an Anti-Inflammatory Topical Gel and Anticancer Agent.Blending gelators to tune gel structure and probe anion-induced disassembly.Metallogels from Coordination Complexes, Organometallic, and Coordination Polymers.A supramolecular topical gel derived from a non-steroidal anti-inflammatory drug, fenoprofen, is capable of treating skin inflammation in mice.Exploiting supramolecular synthons in designing gelators derived from multiple drugs.Gels with sense: supramolecular materials that respond to heat, light and sound.Light driven mesoscale assembly of a coordination polymeric gelator into flowers and stars with distinct properties.Multiple-stimulus-responsive supramolecular gels and regulation of chiral twists: the effect of spacer length.A unique thermo-induced gel-to-gel transition in a pH-sensitive small-molecule hydrogel.Chiral gels derived from secondary ammonium salts of (1R,3S)-(+)-camphoric acid.Triazol-substituted titanocenes by strain-driven 1,3-dipolar cycloadditionsThe conjugation of nonsteroidal anti-inflammatory drugs (NSAID) to small peptides for generating multifunctional supramolecular nanofibers/hydrogels
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 17 October 2008
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Supramolecular gelling agents: can they be designed?
@en
Supramolecular gelling agents: can they be designed?
@nl
type
label
Supramolecular gelling agents: can they be designed?
@en
Supramolecular gelling agents: can they be designed?
@nl
prefLabel
Supramolecular gelling agents: can they be designed?
@en
Supramolecular gelling agents: can they be designed?
@nl
P356
P1476
Supramolecular gelling agents: can they be designed?
@en
P2093
Parthasarathi Dastidar
P304
P356
10.1039/B807346E
P577
2008-10-17T00:00:00Z