0000000000268232

AUTHOR

Tomás Torres

showing 9 related works from this author

Dual-Mode Chiral Self-Assembly of Cone-Shaped Subphthalocyanine Aromatics

2020

This document is the Accepted Manuscript version of a Published Work that appeared in final form in Journal of the American Chemical Society, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/jacs.0c07291

SubphthalocyanineChemistryThermodynamic equilibriumDimerStackingSupramolecular chemistryPorphyrinoidsSelf-assemblyQuímicaGeneral Chemistry010402 general chemistry01 natural sciencesBiochemistryCatalysis0104 chemical scienceschemistry.chemical_compoundColloid and Surface ChemistryEnantiopure drugPolymerizationChemical physicsLiquid crystalSupramolecular PolymersSelf-assembly
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Physicochemical characterization of octakis(alkyloxy)-substituted Zn(ii)-phthalocyanines non-covalently incorporated into an organogel and their rema…

2007

A series of octakis(alkyloxy)-substituted Zn(II)-phthalocyanines were efficiently incorporated into an organogel made of (1R,2R)-trans-1,2-bis(dodecanoylamino)cyclohexane by means of multiple cooperative non-covalent interactions, and SEM revealed the formation of unique brush-like nanostructures.

NanostructureCyclohexaneChemistryMetals and AlloysGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCharacterization (materials science)chemistry.chemical_compoundCovalent bondPolymer chemistryMaterials ChemistryCeramics and CompositesNanoscopic scaleChem. Commun.
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Subphthalocyanines as narrow band red-light emitting materials

2007

A series of new light emitting subphthalocyanines, lower homologues of phthalocyanines, were synthesized having color points covering the red-orange region of the visible spectrum. Additionally, they were found to be of potential use as narrow band emitters for red-light emitting diodes.

Chemistrybusiness.industryOrganic ChemistryPhotochemistryBiochemistryFluorescencelaw.inventionNarrow bandlawDrug DiscoveryOptoelectronicsRed lightbusinessDiodeVisible spectrumLight-emitting diodeTetrahedron Letters
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Incorporation of a tricationic subphthalocyanine in an organic photovoltaic device

2013

A new tricationic subphthalocyanine was synthesized and employed as light-harvesting and donor material in an ionic solid state organic photovoltaic cell. The incorporation of ionic dyes in organic photovoltaics aims to take advantage of ionic movement in order to enhance the charge transport properties of these materials. In this preliminary study, we report the results obtained in the fabrication of a partially solution-processed device with a cationic dye, where an effiency of 0.5% was reached.

FabricationOrganic solar cellChemical engineeringChemistryPhotovoltaic systemCationic polymerizationSolid-stateIonic bondingOrganic chemistryGeneral Chemistry
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A Columnar Liquid Crystal with Permanent Polar Order

2015

et al.

Materials scienceElectric fieldsCondensed matter physicsCrystalline materialsPolar orderSubphthalocyaninesGeneral ChemistryQuímicaPolarization (waves)Liquid crystalline materialsCondensed Matter::Soft Condensed MatterCondensed Matter::Materials ScienceDipoleCrystallographyLiquid crystalElectric fieldMaterials ChemistryMoleculePolarSelf assembly Columnar liquid crystalsLiquid Crystalline MaterialsColumnar phase
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Influence of Peripheral Substitution on the Magnetic Behavior of Single-Ion Magnets Based on Homo- and Heteroleptic TbIIIBis(phthalocyaninate)

2013

A series of homoleptic ([Tb(III)(Pc)(2) ]) and heteroleptic ([Tb(III)(Pc)(Pc')]) Tb(III) bis(phthalocyaninate) complexes that contain different peripheral substitution patterns (i.e., tert-butyl or tert-butylphenoxy groups) have been synthesized in their neutral radical forms and then reduced into their corresponding anionic forms as stable tetramethylammonium/tetrabutylammonium salts. All of these compounds were spectroscopically characterized and their magnetic susceptibility properties were investigated. As a general trend, the radical forms exhibited larger energy barriers for spin reversal than their corresponding reduced compounds. Remarkably, heteroleptic complexes that contain elect…

TetramethylammoniumSingle ion010405 organic chemistryStereochemistryOrganic Chemistrychemistry.chemical_elementTerbiumGeneral Chemistry010402 general chemistryRing (chemistry)01 natural sciencesMagnetic susceptibilityCatalysis0104 chemical sciencesIonchemistry.chemical_compoundCrystallographychemistryMagnetHomolepticChemistry - A European Journal
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State selective electron injection in non-aggregated titanium phthalocyanine sensitised nanocrystalline TiO2 films

2004

We describe a novel titanium phthalocyanine that shows no aggregation when anchored to nanocrystalline TiO2 films through its axial carboxylated ligand without the use of co-adsorbents; state selective electron injection into the TiO2 is demonstrated, resulting in efficient photocurrent generation in dye sensitised photoelectrochemical solar cells. Palomares Gil, Emilio J, epagil@alumni.uv.es

Solar cellsMaterials scienceState selectiveUNESCO::QUÍMICAchemistry.chemical_elementNanotechnologyPhotochemistry:QUÍMICA [UNESCO]Catalysischemistry.chemical_compoundElectron injectionMaterials ChemistryUNESCO::QUÍMICA::Química orgánicaElectron injectionPhotocurrentTitaniumLigand:QUÍMICA::Química orgánica [UNESCO]Metals and AlloysGeneral ChemistryNanocrystalline materialSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryTiO2 filmsCeramics and CompositesPhthalocyanineElectron injection ; Titanium ; TiO2 films ; Solar cellsTitanium
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Non-Centrosymmetric Homochiral Supramolecular Polymers of Tetrahedral Subphthalocyanine Molecules

2015

This is the peer reviewed version of the following article: Angewandte Chemie - International Edition 54.8 (2015): 2543-2547, which has been published in final form at http://dx.doi.org/10.1002/anie.201411272. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving

chemistry.chemical_classificationCircular dichroismMaterials scienceSubphthalocyanineSupramolecular chemistryStackingPorphyrinoidsGeneral MedicineGeneral ChemistrySelf-assemblyQuímicaCatalysisSupramolecular polymersCrystallographychemistryPolymerizationPolymer chemistryMoleculeSelf-assemblyChirality (chemistry)Homochiral aggregatesSupramolecular polymerization
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A Highly Sensitive Hybrid Colorimetric and Fluorometric Molecular Probe for Cyanide Sensing Based on a Subphthalocyanine Dye

2006

A highly sensitive, selective colorimetric and fluorometric molecular probe based on a subphthalocyanine dye has been developed for cyanide-anion determination in aqueous solution. It has also been shown that a carboxysubphthalocyanine derivative can be covalently anchored to transparent mesoporous nanocrystalline high-surface-area metal oxide films to detect low concentrations of cyanide anion in pure water with no interference from other anionic or cationic species.

Conductive polymerAqueous solutionChemistryCyanideCationic polymerizationOxideCondensed Matter PhysicsPhotochemistryElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundCovalent bondElectrochemistryMesoporous materialMolecular probeAdvanced Functional Materials
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