Search results for "Molecular logic"

showing 3 items of 3 documents

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
researchProduct

Boolean operations mediated by an ion-pair receptor of a multi-readout molecular logic gate

2013

A heteroditopic BODIPY dye that performs all basic Boolean operations with a cation (K+) and an anion (F-) as inputs and absorption, transmission and fluorescence as outputs is described. The molecular logic gate can also act as a digital comparator between the inputs.

Molecular logic gateMetal-IonsAnalytical chemistryTopologyCatalysisIonchemistry.chemical_compoundComplexDrivenMaterials ChemistryKeypad LockCrown EtherFluorescence EnhancementChemistryMetals and AlloysGeneral ChemistryIon pairsFluorescenceSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsRecognitionTransmission (telecommunications)Ceramics and CompositesDigital comparatorInputsBoolean operations in computer-aided designBODIPY
researchProduct

Synthèse in situ de fluorophores organiques : formation de liaisons covalentes par déclenchement enzymatique et applications en biodétection

2017

Fluorescence imaging is a growing field of biology over the past decades. Intensive works mainly focused on instrumental developments and chemistry of contrast agents (probes), were already done to improve such bioanalytical technique. The main goal of this Ph. D. thesis was to explore various fluorogenic molecular platforms responsive to various (bio)chemical stimuli and capable of releasing organic fluorophores in the biological medium to analyze. This approach named "in-situsynthesis" is based on domino reactions belonging to the repertoire of "covalent chemistry", triggered by the target (bio)analyte. This kind of process should provide advanced fluorogenic probes with high signal-to-no…

Porte logique moléculaireHybride DHX-hémicyanineMolecular logic gateSynthèse in-situ[CHIM.ORGA]Chemical Sciences/Organic chemistryDihydroxanthene-hemicyanine hybridCoumarineMulti-analytes detectionSonde fluorogéniqueCoumarin[CHIM.ORGA] Chemical Sciences/Organic chemistryFluorescenceIn-situ synthesisActivation enzymatiqueBenzophénoxazineDétection "multi-analytes"Fluorogenic probePyroninePro-fluorescencePyroninEnzymatic activation
researchProduct