0000000001314382

AUTHOR

M. Consuelo Cuquerella

showing 7 related works from this author

Photocatalytic coalescence of functionalized gold nanoparticles.

2009

A novel strategy for the synthesis of chromophore-functionalized AuNPs with a narrow size distribution is reported. It consists of increasing the size of preprepared NPs by means of a fast (second scale) and clean (light and an organic photocatalyst) method. The results agree with thiolate ligand liberation from the NP surface promoted by photogenerated radicals. This lets gold cores come together and finally coalesce.

Coalescence (physics)Materials sciencePyrenesLigandNanoparticleMetal NanoparticlesSurfaces and InterfacesChromophoreCondensed Matter PhysicsPhotochemistryPhotochemical ProcessesCatalysisCatalysisBenzophenonesTransition metalColloidal goldElectrochemistryPhotocatalysisGeneral Materials ScienceGoldSpectroscopyLangmuir : the ACS journal of surfaces and colloids
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Triplet stabilization for enhanced drug photorelease from sunscreen-based photocages

2021

[EN] Recently, sunscreen-based drug photocages have been introduced to provide UV protection to photoactive drugs, thus increasing their photosafety. Here, combined experimental and theoretical studies performed on a photocage based on the commercial UVA filter avobenzone (AB) and on the photosensitizing non-steroidal anti-inflammatory drug ketoprofen (KP) are presented unveiling the photophysical processes responsible for the light-triggered release. Particular attention is paid to solvent stabilization of the drug and UV filter excited states, respectively, which leads to a switching between the triplet excited state energies of the AB and KP units. Most notably, we show that the stabiliz…

DrugUltraviolet Raysmedia_common.quotation_subjectUV filter010402 general chemistryPhotochemistry01 natural sciencesBiochemistrychemistry.chemical_compoundQUIMICA ORGANICAHexanesProdrugsPhysical and Theoretical Chemistrymedia_commonPropiophenonesQuenching (fluorescence)PhotolysisPhotosensitizing AgentsEthanol010405 organic chemistryOrganic ChemistryAnti-Inflammatory Agents Non-SteroidalAcceptor0104 chemical sciencesHexaneSolventchemistryModels ChemicalKetoprofenExcited stateSolventsAvobenzoneSunscreening AgentsOrganic and Biomolecular Chemistry
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Building a Functionalizable, Potent Chemiluminescent Agent: A Rational Design Study on 6,8-Substituted Luminol Derivatives.

2021

Luminol is a prominent chemiluminescent (CL) agent, finding applications across numerous fields, including forensics, immunoassays, and imaging. Different substitution patterns on the aromatic ring can enhance or decrease its CL efficiency. We herein report a systematic study on the synthesis and photophysics of all possible 6,8-disubstituted luminol derivatives bearing H, Ph, and/or Me substituents. Their CL responses are monitored at three pH values (8, 10, and 12), thus revealing the architecture with the optimum CL efficiency. The most efficient pattern is used for the synthesis of a strongly CL luminol derivative, bearing a functional group for further, straightforward derivatization. …

Organic ChemistryRational designQuantum chemistryCombinatorial chemistryFluorescenceLuminolAdductlaw.inventionchemistry.chemical_compoundchemistrylawFunctional groupLuminescent MeasurementsLuminolDerivatizationChemiluminescenceThe Journal of organic chemistry
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Characterization of Locally Excited and Charge-Transfer States of the Anticancer Drug Lapatinib by Ultrafast Spectroscopy and Computational Studies

2020

[EN] Lapatinib (LAP) is an anticancer drug, which is metabolized to theN- and O-dealkylated products (N-LAP andO-LAP, respectively). In view of the photosensitizing potential of related drugs, a complete experimental and theoretical study has been performed on LAP,N-LAP andO-LAP, both in solution and upon complexation with human serum albumin (HSA). In organic solvents, coplanar locally excited (LE) emissive states are generated; they rapidly evolve towards twisted intramolecular charge-transfer (ICT) states. By contrast, within HSA only LE states are detected. Accordingly, femtosecond transient absorption reveals a very fast switching (ca. 2 ps) from LE (lambda(max)=550 nm) to ICT states (…

Femtosecond transient absorptionAntineoplastic AgentsSerum Albumin HumanMolecular Dynamics Simulation010402 general chemistryLapatinib01 natural sciencesAnticancer drugsCatalysisFluorescenceQUIMICA ORGANICAComputational chemistrymedicineHumansSpectroscopy010405 organic chemistryChemistryMolecular dynamics simulationsSpectrum AnalysisOrganic Chemistrydigestive oral and skin physiologyCharge (physics)LapatinibGeneral Chemistryequipment and suppliesAnticancer drug0104 chemical sciencesCharacterization (materials science)Excited stateUltrashort pulsehuman activitiesmedicine.drug
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Efficient ultraviolet-light energy dissipation by an aromatic ketone.

2010

Experimental evidence on the efficiency of 2,2'4,4'-tetramethoxybenzil for UV-light energy dissipation is provided. This non-phenolic aromatic ketone has a low energy triplet which quickly decays to the ketone ground state, thus avoiding the generation of undesirable reactive species. El Moncef, Abdelkarim, elmonab@alumni.uv.es ; Cuquerella Alabort, Maria Consuelo, Chelo.Cuquerella@uv.es ; Zaballos Garcia, Elena, Elena.Zaballos@uv.es ; Ramirez de Arellano Sanchez, Maria del Carmen, Carmen.Ramirezdearellano@uv.es ; Stiriba, Salah Eddine, Salah.Stiriba@uv.es ; Perez Prieto, Julia, Julia.Perez@uv.es

Aromatic ketoneKetoneUltraviolet RaysUNESCO::QUÍMICAUV-lightPhotochemistry:QUÍMICA [UNESCO]CatalysisLow energyMaterials ChemistryUltraviolet lightTetramethoxybenzil ; UV-light ; Reactive ; Aromatic KetoneAromatic Ketonechemistry.chemical_classificationMolecular StructureUNESCO::QUÍMICA::Química analíticaMetals and AlloysGeneral ChemistryDissipationKetonesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryReactiveCeramics and Composites:QUÍMICA::Química analítica [UNESCO]TetramethoxybenzilGround stateChemical communications (Cambridge, England)
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Photosensitised Seeding of Thiolate-Stabilised Gold Nanoparticles

2010

PhotochemistrySurface PropertiesChemistryMetal NanoparticlesNanoparticlePhotochemistryAtomic and Molecular Physics and OpticsLaser photolysisColloidal goldPhotocatalysisSeedingGoldSulfhydryl CompoundsParticle SizePhysical and Theoretical ChemistryMetal nanoparticlesChemPhysChem
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CCDC 743200: Experimental Crystal Structure Determination

2010

Related Article: Abdelkarim El Moncef, M. Consuelo Cuquerella, Elena Zaballos, Carmen Ramírez de Arellano, Abdeslem Ben-Tama, Salah-Eddine Stiriba and Julia Pérez-Prieto|2010|Chem.Commun.|46|800|doi:10.1039/B915792A

Space GroupCrystallographyCrystal System12-bis(24-dimethoxyphenyl)ethane-12-dioneCrystal StructureCell ParametersExperimental 3D Coordinates
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