about
A switchable self-assembling and disassembling chiral system based on a porphyrin-substituted phenylalanine-phenylalanine motifEnantioselective complexation of chiral propylene oxide by an enantiopure water-soluble cryptophane.Influence of the chemical structure of water-soluble cryptophanes on their overall chiroptical and binding properties.High affinity of water-soluble cryptophanes for cesium cations.Toward a molecular understanding of the detection of amyloid proteins with flexible conjugated oligothiophenes.A Palette of Fluorescent Thiophene-Based Ligands for the Identification of Protein Aggregates.Expression of chirality in molecular layers at surfaces: insights from modelling.Modelling charge transport of discotic liquid-crystalline triindoles: the role of peripheral substitution.Designing NHC-Copper(I) Dipyridylamine Complexes for Blue Light-Emitting Electrochemical Cells.Tuning the supramolecular chirality of one- and two-dimensional aggregates with the number of stereogenic centers in the component porphyrins.Orthohalogen substituents dramatically enhance hydrogen bonding of aromatic ureas in solution.Structure and dynamics of a bisurea-based supramolecular polymer in n-dodecane.Dynamics of molecular self-ordering in tetraphenyl porphyrin monolayers on metallic substrates.The nature of resonance in allyl ions and radical.Lewis-based valence bond scheme: application to the allyl cation.Role of the Bridging Group in Bis-Pyridyl Ligands: Enhancing Both the Photo- and Electroluminescent Features of Cationic (IPr)CuI Complexes.Study of the cold charge transfer state separation at the TQ1/PC71 BM interface.Origin of DNA-Induced Circular Dichroism in a Minor-Groove Binder.Effect of Polarization on the Mobility of C60: A Kinetic Monte Carlo Study.On the photo-induced charge-carrier generation within monolayers of self-assembled organic donor-acceptor dyads.Chirality in dynamic supramolecular nanotubes induced by a chiral solvent.Hybrid Complex Polarization Propagator/Molecular Mechanics Method for Heterogeneous Environments.Consequences of conformational flexibility in hydrogen-bond-driven self-assembly processes.Binding sites for luminescent amyloid biomarkers from non-biased molecular dynamics simulations.Binding Modes and Selectivity of Ruthenium Complexes to Human Telomeric DNA G-QuadruplexesOptical properties of wine pigments: theoretical guidelines with new methodological perspectivesElucidating DNA binding of dithienylethenes from molecular dynamics and dichroism spectraBottom-Up Hierarchical Self-Assembly of Chiral Porphyrins through Coordination and Hydrogen BondsElectronic and vibrational circular dichroism spectroscopies for the understanding of chiral organization in porphyrin aggregatesHierarchical Chiral Expression from the Nano- to Mesoscale in Synthetic Supramolecular Helical Fibers of a NonamphiphilicC3-Symmetrical π-Functional MoleculeChiral Expression at the Solid−Liquid Interface: A Joint Experimental and Theoretical Study of the Self-Assembly of Chiral Porphyrins on GraphiteConformational Effects Induced by Guest Encapsulation in an Enantiopure Water-Soluble CryptophaneKinetic Monte Carlo simulations of organic ferroelectricsSuppressing depolarization by tail substitution in an organic supramolecular ferroelectricAdsorption and conformation of porphyrins on metallic surfacesQuantifying resonance through a Lewis valence bond approach: application to haloallyl and carbonyl cationsValence bond approach of metal-ligand bonding in the Dewar-Chatt-Duncanson modelEngineering the cavity of self-assembled dynamic nanotubesTwo-leg molecular ladders formed by hierarchical self-assembly of an organic radicalComplex polarization propagator approach in the restricted open-shell, self-consistent field approximation: the near K-edge X-ray absorption fine structure spectra of allyl and copper phthalocyanine
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Q27330000-EE1333A5-9184-4359-97A9-61EDABFF5E25Q33863998-D1B4AC89-784F-4F2A-905F-826AEBC5A15BQ33986447-D65E46F8-D569-453F-8685-19CDB1A6F5D4Q34108576-62A17B15-E47F-4305-AF74-750EF073DB95Q34440035-319EF476-B927-4EA2-B1C3-67274C6B0622Q36270755-D3BF4644-318A-4B3A-8149-CEEAD406DA5EQ37423896-7E811127-FB3C-41AE-9E53-EB66A10C8F38Q38608389-682972D4-89AD-4BE2-B1A6-3314BAD226ADQ38862547-C515E120-183A-463C-AF70-812971F1374BQ43013222-8B481F73-14A6-4469-B437-A86094203C4CQ45278846-5D610F5C-42AA-4C2A-8F4A-321D19F03F8EQ45909279-92E26489-E0E1-4EDD-933E-020A7E11125CQ45966810-D3515C92-02F5-482A-A376-2A566336EF0CQ46260142-FAB02727-34D4-4958-9963-193B3C466ACEQ46946057-07A1F8F2-A1DD-40D9-AC1D-62254287A6D8Q47716155-983CFD2C-A7C5-45B5-8EFF-5767ADF33467Q48104490-06574417-D769-4B77-93DB-50DAB348A8A5Q48259930-98A4B3DB-8EC5-4E2B-9D5E-9A011DE79EA6Q48696283-AF1B5F8E-CDF7-40B7-8BC6-5B3D2D0B49F0Q53056295-C6CAA2E9-5D54-4C88-AB6A-CECAB72BCB0AQ53062009-1F76D8F0-DEEE-4152-9587-62235B1F1A23Q53114834-067C5010-B2F9-4B09-873F-2AFD2F6453B8Q53215758-24045FE0-3375-4C68-9704-03309BC3F55EQ53273737-FC48FE3B-3178-415D-B24F-AD750C713DE6Q57813184-8109E150-3C97-4AC1-84B6-CC79855E346AQ57954799-38BD26A3-C2E8-40B9-BEB0-DB59B2267B91Q58090828-44CFE151-2082-4A8A-9E21-F1F8E57DD229Q60338434-5467CEED-3A3A-41A5-9A12-8C22D4249A52Q60338524-99E4B764-D1A8-4518-BA6D-ACA834E32897Q60338582-AAD047A6-9F84-41A0-A365-C4AF845CD8EAQ60338675-BDEE5879-AF52-4DCE-8836-945BAD18EFDFQ60734346-1D0F45E2-C95C-4E68-AD2D-D1922E54F059Q62514162-F4DFF882-53C1-462F-B9DB-8156336F0496Q62514164-655CB8C0-F393-4BE6-900F-7669392193CCQ63972791-5C2B33E1-E637-48CB-B532-BF7EC2F9BCD5Q79845306-CC119444-D7C3-46AF-9A04-DDE342322C69Q80109778-D3E55A9F-DF62-4B93-A6D6-C3561B02A3CEQ83385871-D65E43A8-D6DA-4C33-8189-C5666E1EEA19Q83636467-4B5ACB9B-93CE-4F7C-982B-AFE4BEDB5A2BQ84546142-19A8982F-F296-4830-9679-9A54C0B0B282
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description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Mathieu Linares
@ast
Mathieu Linares
@en
Mathieu Linares
@es
Mathieu Linares
@nl
type
label
Mathieu Linares
@ast
Mathieu Linares
@en
Mathieu Linares
@es
Mathieu Linares
@nl
prefLabel
Mathieu Linares
@ast
Mathieu Linares
@en
Mathieu Linares
@es
Mathieu Linares
@nl
P106
P1153
23485951500
P31
P496
0000-0002-9720-5429