Search results for "Phthalocyanine"

showing 10 items of 124 documents

Enhanced chemosensing of ammonia based on the novel molecular semiconductor-doped insulator (MSDI) heterojunctions

2011

Abstract A series of new molecular semiconductor-doped insulator (MSDI) heterojunctions as conductimetric transducers to NH3 sensing were fabricated based on a novel semiconducting molecular material, an amphiphilic tris(phthalocyaninato) rare earth triple-decker complex, Eu2[Pc(15C5)4]2[Pc(OC10H21)8], quasi-Langmuir–Shafer (QLS) film, as a top-layer, and vacuum-deposited and cast film of CuPc as well as copper tetra-tert-butyl phthalocyanine (CuTTBPc) QLS film as a sub-layer, named as MSDIs 1, 2 and 3, respectively. MSDIs 1–3 and respective sub-layers prepared from three different methods were characterized by X-ray diffraction, electronic absorption spectra and current–voltage (I–V) measu…

DiffractionMaterials scienceAbsorption spectroscopyDopingMetals and AlloysAnalytical chemistrychemistry.chemical_elementHeterojunctionCondensed Matter PhysicsCopperSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundchemistryMaterials ChemistryPhthalocyanineCrystalliteElectrical and Electronic EngineeringScience technology and societyInstrumentationSensors and Actuators B: Chemical
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Tuning the semiconducting nature of bis(phthalocyaninato) holmium complexes via peripheral substituents

2012

The semiconducting properties of the heteroleptic and homoleptic bis(phthalocyaninato) holmium complexes bearing electron-withdrawing phenoxy substituents at the phthalocyanine periphery, namely Ho(Pc)[Pc(OPh)8] (1) and Ho[Pc(OPh)8]2 (2) [Pc = unsubstituted phthalocyaninate; Pc(OPh)8 = 2,3,9,10,16,17,23,24-octaphenoxyphthalocyaninate] have been investigated comparatively. Using a solution-based Quasi–Langmuir–Shafer (QLS) method, the thin solid films of the two compounds were fabricated. The structure and properties of the thin films were investigated by UV-vis absorption spectra, X-ray diffraction (XRD) and atomic force microscopy (AFM). Experimental results indicated that H-type molecular…

Electron mobilityAbsorption spectroscopyStereochemistrychemistry.chemical_elementGeneral ChemistryConjugated systemConductivitychemistry.chemical_compoundCrystallographychemistryMaterials ChemistryPhthalocyanineThin filmHomolepticHolmiumJournal of Materials Chemistry
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Two-Step Solution-Processed Two-Component Bilayer Phthalocyaninato Copper-Based Heterojunctions with Interesting Ambipolar Organic Transiting and Eth…

2016

International audience; The two-component phthalocyaninato copper-based heterojunctions fabricated from n-type CuPc(COOC8H17)(8) and p-type CuPc(OC8H17)(8) by a facile two-step solution-processing quasi-Langmuir-Shafer method with both n/p- and p/n-bilayer structures are revealed to exhibit typical ambipolar air-stable organic thin-film transistor (OTFT) performance. The p/n-bilayer devices constructed by depositing CuPc(COOC8H17)(8) film on CuPc(OC8H17)(8) sub-layer show superior OTFT performance with hole and electron mobility of 0.11 and 0.02 cm(2) V-1 s(-1), respectively, over the ones with n/p-bilayer heterojunction structure with the hole and electron mobility of 0.03 and 0.016 cm(2) …

Electron mobilityMaterials scienceroom-temperaturematerials designsemiconducting natureairsolution-processability02 engineering and technologythin-film transistorsphthalocyanines010402 general chemistry01 natural sciences[ CHIM ] Chemical Sciencesgas sensorchemistry.chemical_compound[CHIM]Chemical Sciencesorganic heterojunctioncomparative performancesbusiness.industryAmbipolar diffusionMechanical EngineeringBilayerethanol sensorsfield-effect transistorsHeterojunction[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnology0104 chemical sciencesIndium tin oxidechemistryMechanics of MaterialsThin-film transistor[ CHIM.MATE ] Chemical Sciences/Material chemistryPhthalocyanineOptoelectronicsfunctional theory calculationsField-effect transistor0210 nano-technologybusinessambipolar OTFTn-type
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Oxidation of diclofenac in the presence of iron(II) octacarboxyphthalocyanine

2021

Abstract This paper presents the results of the research on the influence of catalytic activity of iron(II) octacarboxyphthalocyanines (FePcOC) on the transformation of diclofenac (DCF) which is the most popular anti-inflammatory analgesic. Diclofenac poses a serious threat to the natural environment. The paper demonstrates that diclofenac, in the presence a monomeric form of iron octacarboxyphthalocyanine and hydroxyl radicals (HO•) (from H2O2), undergoes a transformation into diclofenac-2,5-iminoquinone (DCF-2,5-IQ), causing distinct changes in the UV–Vis absorption spectrum. In the presence of iron octacarboxyphthalocyanine and H2O2, the previously colourless diclofenac solution becomes …

Environmental EngineeringDiclofenacAbsorption spectroscopyIronHealth Toxicology and MutagenesisRadical0208 environmental biotechnology02 engineering and technology010501 environmental sciencesDFT calculations01 natural sciencesHigh-performance liquid chromatographyCatalysischemistry.chemical_compoundDiclofenacmedicineEnvironmental ChemistryFerrous Compounds0105 earth and related environmental sciencesMS analysisHplc analysisChemistryPublic Health Environmental and Occupational HealthMs analysisHydrogen PeroxideGeneral MedicineGeneral ChemistryUV–Vis spectraPollution020801 environmental engineeringTD-DFT spectraMonomerIron octacarboxyphthalocyanineHPLCOxidation-ReductionNuclear chemistrymedicine.drugChemosphere
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Development of Trackable Anticancer Agents Based on Metal Complexes

2016

Abstract The design of trackable anticancer agents is of major interest for the future development of therapeutics based on nonplatinum metal complexes such as Ru(II), Os(II), or Au(I) derivatives, and more particularly for the understanding of the mechanism of action of these metal-based drugs. This review reports the synthesis and the first biological studies of original trackable complexes, in which the metal complex was coupled to an imaging probe, such as a fluorophore (coumarin, borodipyrromethene derivative (BODIPY), porphyrin), or a chelating agent (1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA)) for radioisotopic imaging PET (positron emission tomography) or SPECT …

Fluorophoremedicine.diagnostic_test010405 organic chemistryChemistryStereochemistry010402 general chemistry01 natural sciencesPorphyrinFluorescenceCombinatorial chemistry0104 chemical scienceschemistry.chemical_compoundPositron emission tomographymedicinePhthalocyanineDOTAChelationBODIPY
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Local aromaticity mapping in the vicinity of planar and nonplanar molecules

2019

We report on nucleus-independent magnetic shielding (NICS) scans over the centers of six- and five-membered rings in selected metal phthalocyanines (MPc) and fullerene C60 for more accurate characterization of local aromaticity in these compounds. Detailed tests were conducted on model aromatic molecules including benzene, pyrrole, indole, isoindole, and carbazole and subsequently applied to H2 Pc, ZnPc, Al(OH)Pc, and CuPc. Similar behavior of three selected magnetic probes, Bq, 3 He, and 7 Li+ , approaching perpendicularly the ring centers, was observed. For better visualization of shielding zone over the centers of aromatic rings, we introduced a simple mathematical procedure: the first a…

FullereneNICS010304 chemical physicsCarbazoleChemical shiftAromaticityGeneral Chemistryaromaticity010402 general chemistryRing (chemistry)curve derivatives01 natural sciencesMolecular physics0104 chemical sciencesIonchemistry.chemical_compoundbenzenemetal phthalocyanineschemistrypyrrole0103 physical sciencesMoleculeGeneral Materials ScienceIsoindoleMagnetic Resonance in Chemistry
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2017

The energy levels of the HOMO/LUMO Frontier orbitals and the electronic properties of phthalocyanine macrocycles can be tuned by the introduction of substituents. Starting from tetrafluorophthalonitrile, we studied the substitution of fluorine atoms by (2-thienyl)ethoxy moieties. An optimization of the experimental conditions (nature and stoichiometry of the alcohol and base, temperature) allowed us to obtain the monoalkoxy derivative with a very good yield. It was fully characterized using 19F and 1H NMR spectroscopies, thermal analysis and X-ray diffraction on single crystals. Then, the corresponding zinc phthalocyanine was synthesized, characterized by means of 19F and 1H NMR spectroscop…

General Chemical EngineeringDoping02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesElectron spectroscopy0104 chemical scienceschemistry.chemical_compoundchemistryPolymer chemistryAlkoxy groupPhthalocyanineProton NMR0210 nano-technologyThermal analysisHOMO/LUMODerivative (chemistry)RSC Advances
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Solvent impact on the planarity and aromaticity of free and monohydrated zinc phthalocyanine: a theoretical study

2017

A theoretical investigation on the planarity of molecular structure of zinc phthalocyanine (ZnPc) and its aromaticity has been performed using B3LYP and M06-2X density functionals combined with selected Pople-type basis sets. The effect of the applied calculation method on the optimized structure of ZnPc and ZnPc∙∙∙H2O, both in the gas phase and in the polar solvent, was analyzed. To quantify the aromaticity of the ZnPc and ZnPc∙∙∙H2O complexes, both the geometric and magnetic criteria, i.e., Harmonic Oscillator Model of Aromaticity (HOMA) index and the nucleus-independent chemical shift (NICS) values at the centers or 1 A above the centers of structural subunits, were calculated. The energ…

HOMOLUMONICSmolecular structureplanarity010402 general chemistryRing (chemistry)01 natural sciencesDFTchemistry.chemical_compoundPhysics::Atomic and Molecular ClustersHOMAMoleculeMolecular orbitalPhysics::Chemical PhysicsPhysical and Theoretical ChemistryBenzeneHOMO/LUMOAstrophysics::Galaxy Astrophysics010405 organic chemistryChemistryAromaticityCondensed Matter PhysicsPlanarity testing0104 chemical sciencesSolventzinc phthalocyaninePhysical chemistryStructural Chemistry
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Synthesis and study of new fluorescent probes for optical imaging, Cherenkov imaging and multimodal imaging

2015

The goal of this work was to prepare and study new fluorescent probes, which could give rise to novel optical or Cherenkov imaging agents. The first section of this work describes the synthesis of fluorescent subphthalocyanines and phthalocyanines probes, which possess relevant chemicals groups suitable for optical imaging applications. The optical and physico-chemical properties of the new probes were carefully examined to ensure they comply with the specification of the fluorophores for the desired application. The second part focused on the subsequent development of a few selected probes into real imaging agents. The biovectorisation of subphtalocyanines was achieved upon conjugation of …

Imagerie CherenkovPhthalocyaninesOptical ImagingCherenkov ImagingSubphthalocyaninesTitania nanotubesMultimodal ImagingUSPIO[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryLiposomePhtalocyanines[CHIM.THEO] Chemical Sciences/Theoretical and/or physical chemistryDOTAImagerie optiqueImagerie multimodaleNanotubes d’oxyde de titaneFluorescéineSubphtalocyaninesFluoresceine
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Porphyrin and phthalocyanine photosensitizers designed for targeted photodynamic therapy of colorectal cancer

2020

Colorectal cancer is of particular concern due to its high mortality rate count. Recent investigations on targeted phototherapy involving novel photosensitizers and drug-delivery systems have provided promising results and realistic prospects for a successful medical treatment. New research trends have been focused particularly on development of advanced molecular systems offering effective photoactive species which could be selectively delivered directly into the affected cells. Porphyrins and phthalocyanines have been considered extremely attractive for this purpose due to their molecular versatility, excellent photochemical properties and multifunctional nature. In this review it has bee…

IndolesPorphyrinsCell SurvivalColorectal cancerPhthalocyaninesmedicine.medical_treatmentClinical BiochemistryPharmaceutical ScienceAntineoplastic AgentsPhotodynamic therapyIsoindolesMolecular systems01 natural sciencesBiochemistryPhotodynamic therapyTargeted therapyTargeted therapyMiceStructure-Activity Relationshipchemistry.chemical_compoundCoordination ComplexesCell Line TumorDrug DiscoverymedicineAnimalsHumansMolecular BiologyCell ProliferationPhotosensitizing AgentsDose-Response Relationship DrugMolecular StructureMedical treatment010405 organic chemistryOrganic ChemistryNeoplasms Experimentalmedicine.diseaseColorectal cancerPorphyrin0104 chemical sciencesPhthalocyanine derivatives010404 medicinal & biomolecular chemistryPhotochemotherapychemistryPhthalocyanineCancer researchMolecular MedicineDrug Screening Assays AntitumorColorectal NeoplasmsBioorganic & Medicinal Chemistry
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