0000000000013142

AUTHOR

Julia Buendía

showing 4 related works from this author

Helical supramolecular polymerization of C3-symmetric amides and retroamides: on the origin of cooperativity and handedness.

2016

The cooperative supramolecular polymerization of 1 and 2 yields P- or M-type helical aggregates depending on the absolute configuration (S or R) of the stereogenic centres attached to the side chains. The connectivity of the amide group does not affect the handedness of the helical aggregates, but determines a larger cooperativity for retroamides 1.

010405 organic chemistryStereochemistryMetals and AlloysSupramolecular chemistryAbsolute configurationCooperativityGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsStereocenterchemistry.chemical_compoundCrystallographychemistryPolymerizationAmideMaterials ChemistryCeramics and CompositesSide chainChemical communications (Cambridge, England)
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Supramolecular Polymers: Flexible Chirality in Self-Assembled N -Annulated Perylenedicarboxamides (Small 20/2017)

2017

BiomaterialsSupramolecular polymerschemistry.chemical_classificationCircular dichroismCrystallographyMaterials scienceConvective flowchemistryGeneral Materials ScienceGeneral ChemistryChirality (chemistry)BiotechnologySelf assembledSmall
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Decoding the Consequences of Increasing the Size of Self-Assembling Tricarboxamides on Chiral Amplification

2019

A complete series of experimental and theoretical investigations on the supramolecular polymerization of chiral (1 and 2) and achiral (3) oligo(phenylene ethynylene) tricarboxamides (OPE-TAs) is reported. The performance of seargents-and-soldiers (SaS) and majority rules (MR) experiments has allowed deriving a full set of thermodynamic parameters, including the helix reversal penalty (HRP) and the mismatch penalty (MMP). The results described illustrate the influence exerted by the number of stereogenic centers per monomeric unit and the temperature on the chiral amplification phenomenon. While the HRP decreases upon decreasing the number of chiral side chains, the MMP follows an opposite t…

chemistry.chemical_classificationSteric effectsSupramolecular chemistryGeneral Chemistry010402 general chemistry01 natural sciencesBiochemistryCatalysis0104 chemical sciencesStereocenterSupramolecular polymersCrystallographyColloid and Surface ChemistrychemistryPhenyleneHelixSide chainChirality (chemistry)Journal of the American Chemical Society
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Flexible Chirality in Self-Assembled N-Annulated Perylenedicarboxamides.

2017

N-annulated perylenedicarboxamides 1-3 form supramolecular polymers with a strong tendency to aggregate. The bundles of fibers formed generate a spontaneous anisotropy that conditions the chiroptical features of the described molecules in solution; a strong linear dichroism effect accompanies the circular dichroism (CD) outcome. There is no influence of the point chirality existing at the side chains of 1 and 2, and these molecules present the same chiroptical features as achiral 3. Mechanical rotary stirring increases the CD response and the sign of the dichroic signal changes with the stirring direction. Theoretical calculations indicate that the self-assembly of 1-3 in helical columnar s…

chemistry.chemical_classificationCircular dichroismAtropisomerMaterials science010405 organic chemistryGeneral Chemistry010402 general chemistryLinear dichroism01 natural sciences0104 chemical sciencesBiomaterialsSupramolecular polymersMolecular dynamicschemistryChemical physicsSide chainMoleculeGeneral Materials ScienceChirality (chemistry)BiotechnologySmall (Weinheim an der Bergstrasse, Germany)
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