Self-assembly of two-component gels: stoichiometric control and component selection.
about
Supramolecular synthons in designing low molecular mass gelling agents: L-amino acid methyl ester cinnamate salts and their anti-solvent-induced instant gelation.Characterization of supramolecular gels.Supramolecular organogels based on dendrons and dendrimers.In situ encapsulating silver nanocrystals into hydrogels. A "green" signaling platform for thiol-containing amino acids or small peptides.Supramolecular design for two-component hydrogels with intrinsic emission in the visible region.Phenylalanine-containing cyclic dipeptides--the lowest molecular weight hydrogelators based on unmodified proteinogenic amino acids.N-Boc-protected 1,2-diphenylethylenediamine-based dendritic organogels with multiple-stimulus-responsive properties.Multi-component hybrid hydrogels - understanding the extent of orthogonal assembly and its impact on controlled release.Stoichiometry-Controlled Inversion of Supramolecular Chirality in Nanostructures Co-assembled with Bipyridines.Supramolecular gels formed from multi-component low molecular weight species.Multicomponent low molecular weight gelators.The effect of self-sorting and co-assembly on the mechanical properties of low molecular weight hydrogels.Redox-sensitive reversible self-assembly of amino acid-naphthalene diimide conjugates.Sulfamide-Lattice Restructuring To Form Dimensionally Controlled Molecular Arrays and Gel-Forming Systems.Strong Fluorescent Smart Organogel as a Dual Sensing Material for Volatile Acid and Organic Amine Vapors.Scaleable two-component gelator from phthalic acid derivatives and primary alkyl amines: acid-base interaction in the cooperative assembly.Selective shrinkage and separation of isomeric naphthoic acids via supramolecular gelation.Multi-stimuli-responsive chiral organogels based on peptide derivatives.Chirality control of self-assembled achiral nanofibers using amines in their solid state.Exploring molecular recognition pathways in one- and two-component gels formed by dendritic lysine-based gelatorsDiffusion across a gel-gel interface - molecular-scale mobility of self-assembled 'solid-like' gel nanofibres in multi-component supramolecular organogelsMulti-component supramolecular gels for the controlled crystallization of drugs: synergistic and antagonistic effectsSelf-organisation effects in dynamic nanoscale gels self-assembled from simple mixtures of commercially available molecular-scale componentsControl of molecular gelation by chemical stimuli
P2860
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P2860
Self-assembly of two-component gels: stoichiometric control and component selection.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh-hant
name
Self-assembly of two-component gels: stoichiometric control and component selection.
@en
Self-assembly of two-component gels: stoichiometric control and component selection.
@nl
type
label
Self-assembly of two-component gels: stoichiometric control and component selection.
@en
Self-assembly of two-component gels: stoichiometric control and component selection.
@nl
prefLabel
Self-assembly of two-component gels: stoichiometric control and component selection.
@en
Self-assembly of two-component gels: stoichiometric control and component selection.
@nl
P2093
P2860
P50
P356
P1476
Self-assembly of two-component gels: stoichiometric control and component selection.
@en
P2093
Andrew R Hirst
Juan F Miravet
Laurence Noirez
P2860
P304
P356
10.1002/CHEM.200801475
P407
P577
2009-01-01T00:00:00Z