about
Nanospheres with tunable size and chirality from helical polymer-metal complexes.The pattern of distribution of amino groups modulates the structure and dynamics of natural aminoglycosides: implications for RNA recognition.A simple NMR analysis of the protonation equilibrium that accompanies aminoglycoside recognition: dramatic alterations in the neomycin-B protonation state upon binding to a 23-mer RNA aptamer.On the importance of carbohydrate-aromatic interactions for the molecular recognition of oligosaccharides by proteins: NMR studies of the structure and binding affinity of AcAMP2-like peptides with non-natural naphthyl and fluoroaromatic residues.Helical sense selective domains and enantiomeric superhelices generated by Langmuir-Schaefer deposition of an axially racemic chiral helical polymer.Macrocyclic Design Strategies for Small, Stable Parallel β-Sheet Scaffolds.Impact of strand length on the stability of parallel-β-sheet secondary structure.Macrocyclic design strategies for small, stable parallel beta-sheet scaffolds.Reversible assembly of enantiomeric helical polymers: from fibers to gels.Unexpected Chiro-Thermoresponsive Behavior of Helical Poly(phenylacetylene)s Bearing Elastin-Based Side Chains.Diacid linkers that promote parallel beta-sheet secondary structure in water.In tube determination of the absolute configuration of alpha- and beta-hydroxy acids by NMR via chiral BINOL borates.The prediction of the absolute stereochemistry of primary and secondary 1,2-diols by 1H NMR spectroscopy: principles and applications.Nanospheres, nanotubes, toroids, and gels with controlled macroscopic chirality.Simultaneous Adjustment of Size and Helical Sense of Chiral Nanospheres and Nanotubes Derived from an Axially Racemic Poly(phenylacetylene).Chiral Coalition in Helical Sense Enhancement of Copolymers: The Role of the Absolute Configuration of Comonomers.Chiral nanostructure in polymers under different deposition conditions observed using atomic force microscopy of monolayers: poly(phenylacetylene)s as a case study.Multipodal dynamic coordination involving cation-π interactions to control the structure of helical polymers.Predicting the Helical Sense of Poly(phenylacetylene)s from their Electron Circular Dichroism Spectra.The role of the secondary structure of helical poly(phenylacetylene)s in the formation of nanoparticles from polymer-metal complexes (HPMCs).Chiral Nanostructures from Helical Copolymer-Metal Complexes: Tunable Cation-π Interactions and Sergeants and Soldiers Effect.A general route to chiral nanostructures from helical polymers: P/M switch via dynamic metal coordinationArchitecture of Chiral Poly(phenylacetylene)s: From Compressed/Highly Dynamic to Stretched/Quasi-Static HelicesEnantiomeric Nanostructures: Chiral Nanostructures from Helical Copolymer-Metal Complexes: Tunable Cation-π Interactions and Sergeants and Soldiers Effect (Small 2/2016)The leading role of cation–π interactions in polymer chemistry: the control of the helical sense in solutionThe ON/OFF switching by metal ions of the “Sergeants and Soldiers” chiral amplification effect on helical poly(phenylacetylene)sControlled modulation of the helical sense and the elongation of poly(phenylacetylene)s by polar and donor effectsHelical Polymer–Metal Complexes: The Role of Metal Ions on the Helicity and the Supramolecular Architecture of Poly(phenylacetylene)sChiral Amplification and Helical-Sense Tuning by Mono- and Divalent Metals on Dynamic Helical PolymersChiral 1,2-Diols: The Assignment of Their Absolute Configuration by NMR Made EasyThe Stereochemistry of 1,2,3-Triols Revealed by1H NMR Spectroscopy: Principles and ApplicationsChallenging the absence of observable hydrogens in the assignment of absolute configurations by NMR: application to chiral primary alcoholsRelative and Absolute Stereochemistry of Secondary/Secondary Diols: Low-Temperature1H NMR of Their bis-MPA Esters§The1H NMR Method for the Determination of the Absolute Configuration of 1,2,3-prim,sec,sec-Triols‡Absolute configuration of amino alcohols by 1H-NMRDetermining the Absolute Stereochemistry of Secondary/Secondary Diols by1H NMR: Basis and ApplicationsThe Assignment of the Absolute Configuration of 1,2-Diols by Low-Temperature NMR of a Single MPA DerivativePoly(phenylacetylene) Amines: A General Route to Water-Soluble Helical PolyaminesChiral-to-Chiral Communication in Polymers: A Unique Approach To Control Both Helical Sense and Chirality at the PeripherySequential Induction of Chirality in Helical Polymers: From the Stereocenter to the Achiral Solvent
P50
Q34380493-BE90DEE2-BF94-4A6D-8FBC-B51CF77E7786Q38304761-A528C65B-9EAB-4AFD-815F-C49303EA5F54Q38306383-CF763DBB-309C-47D2-8C7A-9C7509C66FA1Q38320004-347ACAC4-110D-475F-84D8-BF737611CBF4Q40082313-76DE471F-1946-456E-8899-1308566BD2F1Q41887602-6F595108-FBAC-4BFF-B0A5-E11D2C291CD6Q42076127-30D05640-4287-4330-9A07-034D44FBE757Q42226664-C35C0FF8-2826-422E-81D1-8F8357CBAD53Q42264305-658E523B-76C9-4564-B7D5-EB0201F1FBEBQ42698104-16D95AF6-F63E-4D9E-8FCF-E1BD2E4DD771Q43119722-C790ABCB-0D73-47F1-9385-D4B42F7016D6Q46358927-7520D74B-931C-418D-9CD1-E7BB2C7AB233Q46607688-A48AD6FD-E909-4EA9-A7D1-2D529BCF7CE5Q46840505-0DC27C4D-28EA-4840-B188-8AFA225465D8Q47266107-C51AE9AE-5083-45FC-9CC5-EDB3C3015836Q47309847-088F95D9-1326-45D5-BB89-70BBD69A94E8Q48053278-7D61FA27-4F79-4B95-B4B5-8C3B562D5DE1Q48115784-3282C4ED-726E-4FC9-963F-6F797BCBAB97Q50060246-2D90CA70-9D26-485E-8A94-F5BD00D2A797Q50237180-32BDC802-71EC-4D32-884C-5C8EE7091691Q53424401-F7BD7C47-3D22-4EAB-9853-02D7B5633384Q57517687-A1FF1664-1E41-4259-B378-114723595B8CQ57517690-0B15F15A-1D51-4173-95C7-847D088CC890Q57517691-45BB7C8D-1695-4152-A6CC-6049C8D24CAEQ57517693-2A456807-6CF7-4B18-9D23-131CE1BE874BQ57517695-D14F51D6-4ACB-4537-9140-BE60A7968ABFQ57517697-27DF4646-F15D-488D-A0AD-C54D235581BBQ57517699-535715FF-E610-45DE-AAAA-98F75A534D1CQ57517701-2D20BAAC-1594-434E-8157-00A2059A2D77Q57517708-5A8CD176-04E9-4928-98F1-93874D2DFCB1Q57517716-2EEA0596-2DF1-45DD-A153-3208C128C553Q57517722-3CB97D3A-7750-42B5-8E5F-6FE51AE97483Q57517726-151B98F0-1D82-4328-BE9A-78CD579E5259Q57517734-32CFF627-8C38-4338-A00D-5A305CC04246Q57517738-54F1D276-4418-402A-A118-632B9C335C93Q57517740-F34D6666-655B-42D5-A0B9-48A05EC62100Q57517744-1859D858-6492-4971-815A-4E86EBD20DEFQ57710567-7D63704C-223E-45D2-9EAB-398EB7D77B55Q57710572-A9895CF3-0D95-438B-8729-CB8D8DDA439FQ57710576-651BFF41-E8B2-4784-8DA8-49A750955699
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Felix Freire
@ast
Felix Freire
@en
Felix Freire
@es
Felix Freire
@nl
Felix Freire
@sl
type
label
Felix Freire
@ast
Felix Freire
@en
Felix Freire
@es
Felix Freire
@nl
Felix Freire
@sl
prefLabel
Felix Freire
@ast
Felix Freire
@en
Felix Freire
@es
Felix Freire
@nl
Felix Freire
@sl
P1053
D-3103-2013
P106
P1153
9632999900
P21
P31
P3829
P496
0000-0002-2672-5830