0000000000184342

AUTHOR

Rafael Gomez

showing 6 related works from this author

Frontispiece: Hierarchy of Asymmetry at Work: Chain-Dependent Helix-to-Helix Interactions in Supramolecular Polymers

2018

chemistry.chemical_classificationWork (thermodynamics)Hierarchy (mathematics)media_common.quotation_subjectOrganic ChemistryGeneral ChemistryHelicityAsymmetryCatalysisSupramolecular polymersSelf sortingchemistryChain (algebraic topology)Chemical physicsHelixmedia_commonChemistry - A European Journal
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Synergy of Axial and Point Chirality to Construct Helical N -Heterotriangulene-Based Supramolecular Polymers

2018

chemistry.chemical_classificationAtropisomerMaterials science010405 organic chemistryRenewable Energy Sustainability and the EnvironmentEnergy Engineering and Power TechnologyCooperativity010402 general chemistry01 natural sciencesHelicity0104 chemical sciencesBiomaterialsSupramolecular polymerschemistryChemical physicsMaterials ChemistryPoint (geometry)Chirality (chemistry)ChemNanoMat
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Hierarchy of Asymmetry at Work: Chain-Dependent Helix-to-Helix Interactions in Supramolecular Polymers.

2018

A detailed investigation of the hierarchy of asymmetry operating in the self-assembly of achiral (1) and chiral ((S)-2 and (R)-3) 1,3,5-triphenylbenzenetricarboxamides (TPBAs) is reported. The aggregation of these TPBAs is conditioned by the point chirality at the peripheral side chains for (S)-2 and (R)-3. An efficient helix-to-helix interaction that goes further in the organization of fibrillar bundles is experimentally detected and theoretically supported only for the achiral TPBA 1. The effective interdigitation of the achiral aliphatic side chains produces a social self-sorting to form preferentially heterochiral macromolecular aggregates.

chemistry.chemical_classificationHierarchy (mathematics)010405 organic chemistrymedia_common.quotation_subjectOrganic ChemistryGeneral Chemistry010402 general chemistry01 natural sciencesAsymmetryCatalysis0104 chemical sciencesSupramolecular polymersCrystallographyChain (algebraic topology)chemistryHelixSide chainChirality (chemistry)Macromoleculemedia_commonChemistry (Weinheim an der Bergstrasse, Germany)
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Blue-emitting pyrene-based aggregates.

2015

The self-assembling features and gel formation of two pyrene imidazoles are presented. The supramolecular aggregation of these synthesised molecules results in an unusual blue-monomeric emission, which is rationalized by a combined experimental and theoretical investigation.

Metals and AlloysSupramolecular chemistrymacromolecular substancesGeneral ChemistryPhotochemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundMonomerchemistryPolymerizationMaterials ChemistryCeramics and CompositesBlue emittingPyreneChemical communications (Cambridge, England)
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Impact of Molecular Size and Shape on the Supramolecular Co‐Assembly of Chiral Tricarboxamides: A Comparative Study

2020

We report herein a comparative investigation of the chiral amplification features of a series of three families of C 3 -symmetric tricarboxamides: 1,3,5-triphenylbenzenetricarboxamides (TPBAs), benzenetricarboxamides (BTAs) and oligo(phenylene ethynylene) tricarboxamides (OPE-TAs). As previously observed for BTAs and OPE-TAs, a similar dichroic response is obtained for TPBAs decorated with three, two or only one chiral side chain bearing stereogenic centers, thus confirming the efficient transfer of point chirality to the supramolecular helical aggregates. Unlike BTAs and OPE-TAs, the chiral amplification ability of TPBAs in majority rules experiments shows a negligible dependence on the nu…

chemistry.chemical_classificationSteric effects010405 organic chemistryChemistryOrganic ChemistrySupramolecular chemistryGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesStereocenterSupramolecular polymersCrystallographyPhenyleneSide chainMoleculeChirality (chemistry)Chemistry – A European Journal
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Design, synthesis and photovoltaic properties of [60]fullerene based molecular materials

2005

Abstract The possibility to use new organic semiconductor materials, in place of silicon wafers, in the fabrication of photovoltaic devices on substrates offer the prospect of lower manufacturing costs, particularly for large area applications. Thus, one of the most promising areas in fullerene research involves its potential application, mixed with conjugated polymers, in mimicking photosynthesis and in the related solar energy conversion. The tendency to phase segregation in blends of C60 derivatives and conjugated polymers has to be optimized to improve both charge photogeneration and transport in photovoltaic devices. In order to optimize device performances, a great deal of work has be…

chemistry.chemical_classificationFullereneFabricationMaterials scienceOrganic solar cellPhotovoltaic systemphotovoltaic devicesBioengineeringNanotechnologyPolymerSettore CHIM/06 - Chimica OrganicaConjugated systemBiomaterialsOrganic semiconductorchemistryMechanics of Materialsfullerene derivativesWafer
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