0000000000441387

AUTHOR

Francisco Bosca

0000-0002-8479-0841

showing 5 related works from this author

Diastereomeric Differentiation in the Quenching of Excited States by Hydrogen Donors

2003

chemistry.chemical_classificationKetoneQuenching (fluorescence)HydrogenInorganic chemistryDiastereomerHydrogen transferchemistry.chemical_elementGeneral ChemistryPhotochemistryCatalysischemistryExcited stateLaser chemistryAngewandte Chemie International Edition
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Electronic and Functional Scope of Boronic Acid Derived Salicylidenehydrazone (BASHY) Complexes as Fluorescent Dyes

2017

[EN] A series of boronic acid derived salicylidenehydrazone (BASHY) complexes was prepared and photophysically characterized. The dye platform can be modified by (a) electronic tuning along the cyanine-type axis via modification of the donor-acceptor pair and (b) functional tuning via the boronic acid residue. On the one hand, approach (a) allows the control of photophysical parameters such as Stokes shift, emission color, and two-photon absorption (2PA) cross section. The resulting dyes show emission light-up behavior in nonpolar media and are characterized by high fluorescence quantum yields (ca. 0.5-0.7) and brightness (ca. 35000-40000 M-1 cm(-1)). Moreover, the 2PA cross sections reach …

BrightnessDesignFluorophores010402 general chemistryPhotochemistry01 natural sciencessymbols.namesakechemistry.chemical_compoundResidue (chemistry)ChromophoreMolecular logicStokes shiftMoietyPROYECTOS DE INGENIERIABodipy dyes2-Photon absorptionEnhancement010405 organic chemistryChemistryOrganic ChemistryChromophoreFluorescence0104 chemical sciences3. Good healthsymbolsSurface modificationProbesHighly fluorescentDerivativesBoronic acidThe Journal of Organic Chemistry
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Analysis of mebendazole binding to its target biomolecule by laser flash photolysis

2016

[EN] Mebendazole (MBZ) and related anticancer benzimidazoles act binding the beta-subunit of Tubulin (TU) before dimerization with alpha-TU with subsequent blocking microtubule formation. Laser flash photolysis (LFP) is a new tool to investigate drug-albumin interactions and to determine binding parameters such as affinity constant or population of binding sites. The aim of this study was to evaluate the interactions between the nonfluorescent mebendazole (MBZ) and its target biomolecule TU using this technique. Before analyzing the MBZ@TU complex it was needed to determine the photophysical properties of MBZ triplet excited state ((3)MBZ*) in different media. Hence, 3MBZ* showed a transien…

PopulationBiophysicsBinding constantElectron donor010402 general chemistryPhotochemistry01 natural sciencesAnticancer drugschemistry.chemical_compoundQUIMICA ORGANICAMebendazole triplet excited stateTubulinUltrafast laser spectroscopyRadiology Nuclear Medicine and imagingeducationchemistry.chemical_classificationeducation.field_of_studyRadiationPhotolysisRadiological and Ultrasound Technology010405 organic chemistryPhosphorescenceLasersPhotodissociationTemperatureLaser flash photolysisElectron acceptorBinding constant0104 chemical sciencesMebendazolechemistryExcited stateFlash photolysisThermodynamicsSpectrophotometry UltravioletProtein Binding
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Oxidative decarboxylation of naproxen.

1992

The decarboxylation of naproxen (1H) and its salt (1-) was achieved by means of chemical [Ce(IV) or S2O8(2-)] and electrochemical oxidation. The product patterns were compatible with mechanisms involving single-electron transfer from the pi-system or the carboxylate moiety. The results are discussed in connection with the involvement of electron-transfer processes in the reported phototoxicity of naproxen.

NaproxenChemistryDecarboxylationPharmaceutical ScienceElectrochemistryOxidantsMedicinal chemistrychemistry.chemical_compoundNaproxenmedicineElectrochemistrySolventsOrganic chemistryMoietyChemical stabilityCarboxylatePhototoxicityOxidation-ReductionOxidative decarboxylationmedicine.drugJournal of pharmaceutical sciences
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Regio- and stereo-selectivity in the intramolecular quenching of the excited benzoylthiophene chromophore by tryptophan

2000

Laser flash photolysis studies on the photobehaviour of a series of bichromophoric derivatives bearing benzoylthiophene and tryptophan groups have shown that the efficiency of the intramolecular quenching process depends on both the stereochemistry of the chiral centers and the relative ketone versus tryptophan orientation. Perez Prieto, Julia, Julia.Perez@uv.es

KetoneUNESCO::QUÍMICAStereo-selectivityPhotochemistry:QUÍMICA [UNESCO]CatalysisTrytophanStereochemistryMaterials ChemistryRegio-selectivitychemistry.chemical_classificationQuenching (fluorescence)UNESCO::QUÍMICA::Química analíticaMetals and AlloysTryptophanGeneral ChemistryChromophoreRegio-selectivity ; Stereo-selectivity ; Benzoylthiophene chromophore ; Stereochemistry ; TrytophanSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBenzoylthiophene chromophorechemistryExcited stateIntramolecular force:QUÍMICA::Química analítica [UNESCO]Ceramics and CompositesFlash photolysisSelectivityChemical Communications
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