Chiral bis(amino acid)- and bis(amino alcohol)-oxalamide gelators. Gelation properties, self-assembly motifs and chirality effects.
about
Chiral hexa- and nonamethylene-bridged bis(L-Leu-oxalamide) gelators: the first oxalamide gels containing aggregates with a chiral morphology.Exploiting molecular self-assembly: from urea-based organocatalysts to multifunctional supramolecular gels.Oxalyl retro-peptide gelators. Synthesis, gelation properties and stereochemical effects.Multistimuli-responsive supramolecular organogels formed by low-molecular-weight peptides bearing side-chain azobenzene moieties.Chirality-Mediated Mechanical and Structural Properties of Oligopeptide Hydrogels.Coordination polymer gels with important environmental and biological applications.Dehydroacetic Acid Derivatives Bearing Amide or Urea Moieties as Effective Anion Receptors.Synthesis and Applications of (ONO Pincer)Ruthenium-Complex-Bound Norvalines.Catalytic dephosphorylation of adenosine monophosphate (AMP) to form supramolecular nanofibers/hydrogels.A synthetic amino acid residue containing a new oligopeptide-based photosensitive fluorescent organogel.Stoichiometry-Controlled Inversion of Supramolecular Chirality in Nanostructures Co-assembled with Bipyridines.The Metal Effect on Self-Assembling of Oxalamide Gelators Explored by Mass Spectrometry and DFT Calculations.Ultrasonication-enhanced gelation properties of a versatile amphiphilic formamidine-based gelator exhibiting both organogelation and hydrogelation abilities.Synthesis, characterization and in vitro biocompatibility assessment of a novel tripeptide hydrogelator, as a promising scaffold for tissue engineering applications.Self-assembled fibrillar networks of a multifaceted chiral squaramide: supramolecular multistimuli-responsive alcogels.Inversion of the Supramolecular Chirality of Nanofibrous Structures through Co-Assembly with Achiral Molecules.Solid state structure and solution thermodynamics of three-centered hydrogen bonds (O∙∙∙H∙∙∙O) using N-(2-benzoyl-phenyl) oxalyl derivatives as model compounds.Pyrene-containing peptide-based fluorescent organogels: inclusion of graphene into the organogel.Catalytic Oxidative Carbonylation of Amino Moieties to Ureas, Oxamides, 2-Oxazolidinones, and BenzoxazolonesSupramolecular Ionic-Liquid Gels with High Ionic ConductivityMacrocyclic gelatorsSelf-inclusion of proline-functionalised calix[4]arene leads to hydrogelation
P2860
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P2860
Chiral bis(amino acid)- and bis(amino alcohol)-oxalamide gelators. Gelation properties, self-assembly motifs and chirality effects.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
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2009年学术文章
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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
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2009年學術文章
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2009年學術文章
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name
Chiral bis(amino acid)- and bi ...... motifs and chirality effects.
@en
Chiral bis(amino acid)- and bi ...... motifs and chirality effects.
@nl
type
label
Chiral bis(amino acid)- and bi ...... motifs and chirality effects.
@en
Chiral bis(amino acid)- and bi ...... motifs and chirality effects.
@nl
prefLabel
Chiral bis(amino acid)- and bi ...... motifs and chirality effects.
@en
Chiral bis(amino acid)- and bi ...... motifs and chirality effects.
@nl
P2860
P356
P1476
Chiral bis(amino acid)- and bi ...... motifs and chirality effects.
@en
P2093
Leo Frkanec
Mladen Zinić
P2860
P304
P356
10.1039/B920353M
P407
P577
2009-12-03T00:00:00Z