Search results for "Phthalocyanine"

showing 10 items of 124 documents

Effect of quaternary ammonium salts on spectral properties of zinc octacarboxyphthalocyanine

2020

Abstract The paper presents results of the research on the influence of quaternary ammonium salts on UV–vis absorption and emission spectra of zinc octacarboxyphthalocyanine (ZnPcOC). Quaternary ammonium salts which show biological activity play a crucial role. In ZnPcOC solutions with a proper concentration of tetrabutylammonium salts (TBAX), a strong bathochromic shift band (λmax = 760 nm – “R” band) showing red fluorescence appears in time. The presence of tetrabutylammonium salt causes pH increase and, consequently, a gradual dissociation of carboxyl groups in ZnPcOC molecule. It seems that –COO— anions present in the ZnPcOC complex can interact with tetraalkylammonium cations, causing …

010405 organic chemistryChemistryOrganic ChemistryInorganic chemistrySpectral propertieschemistry.chemical_elementZincUV–Vis spectraQuaternary ammonium salts010402 general chemistry01 natural sciencesFluorescenceDissociation (chemistry)Fluorescence0104 chemical sciencesAnalytical ChemistryZinc octacarboxyphthalocyanineInorganic Chemistrychemistry.chemical_compoundPDTBathochromic shiftMoleculeAmmoniumEmission spectrumSpectroscopyJournal of Molecular Structure
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Electronic structure of phthalocyanines : Theoretical investigation of the optical properties of phthalocyanine monomers, dimers, and crystals

1990

We present valence effective Hamiltonian (VEH) calculations on the optical absorptions of a series of phthalocyanine compounds: the metal‐free phthalocyanine molecule, a model system for the lithium phthalocyanine molecule, the metal‐free phthalocyanine dimer, and model systems for the lutetium diphthalocyanine and the lithium phthalocyanine crystal. For these compounds, it is found that the major factor influencing the evolution of the optical transitions is not the electronic structure of the metal but rather the geometric structure: phthalocyanine intraring geometry and, in the dimers and crystals, interring separation and staggering angle. The origin of the so‐called Soret or B absorpti…

Absorption SpectraAbsorption spectroscopyPhthalocyaninesGeneral Physics and AstronomyElectronic structurePhotochemistryCrystalchemistry.chemical_compoundHamiltonian FunctionMoleculePhysical and Theoretical ChemistryDimers:FÍSICA::Química física [UNESCO]Inorganic compoundchemistry.chemical_classificationValence (chemistry)MonomersMolecular CrystalsUNESCO::FÍSICA::Química físicaCrystallographyElectronic StructurechemistryAbsorption bandPhthalocyanineCondensed Matter::Strongly Correlated ElectronsElectronic Structure ; Molecular Crystals ; Dimers ; Monomers ; Absorption Spectra ; Hamiltonian Function ; Phthalocyanines
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Molecular balance forms of indium phthalocyanines in benzene and pyridine solution

2019

Abstract The electronic absorption spectra of In2Pc3, InPc2 and InPcI solid compounds after dissolvation in one of the most commonly used solvents, i.e.: benzene and pyridine have been measured. In benzene, the molecules of the diindium tripledecker phthalocyanine, In2Pc3, undergoes transformation to ionic couples [InPc]+[InPc2]-, whereas when the InPc2 compound is dissolvated, the molecules of the indium sandwiches, InPc2, remain relatively stable in the solvent. When the In2Pc3 compound is dissolvated in py, the inner Pc(2-) ring of diindium tripledecker phthalocyanine molecule undergoes disjunction and rejection. In the results of it in the solution the couple of chromophores, being in t…

Absorption spectroscopy010405 organic chemistryPyridineOrganic ChemistryIonic bondingBenzeneChromophore010402 general chemistry01 natural sciences0104 chemical sciencesAnalytical ChemistryTransformationInorganic ChemistrySolventchemistry.chemical_compoundCrystallographychemistrySpectrum UV–VisPyridinePhthalocyanineMoleculeBenzeneIndium phthalocyaninesSpectroscopyJournal of Molecular Structure
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Interactions of amino acids with aluminum octacarboxyphthalocyanine hydroxide. Experimental and DFT studies

2017

The influence of albumin and amino acids (l-serine, glycine, l-histidine, l-tryptophan, l-cysteine) on the properties of aluminum octacarboxyphthalocyanine hydroxide (Al(OH)PcOC) was investigated in a phosphate buffer (pH 8.0). Particular attention was paid to the spectroscopic properties and photostability of Al(OH)PcOC. The effect of albumin or amino acids on the photodegradation of Al(OH)PcOC was examined in water using red light: 685 nm and daylight irradiation. Analysis of kinetic curves indicated that interaction with those molecules increases the photostability of Al(OH)PcOC. The molecular structure of Al(OH)PcOC complexes (in vacuum and in water) with axially or equatorially coordin…

Absorption spectroscopyInorganic chemistry02 engineering and technologyDFT calculations010402 general chemistryDFT01 natural sciencesPhotodynamic therapyCatalysisInorganic ChemistryAluminum octacarboxyphthalocyanine hydroxidechemistry.chemical_compoundMoleculePhysical and Theoretical ChemistryPhotodegradationchemistry.chemical_classificationamino acidsOriginal PaperChemistryHydrogen bondProteinOrganic Chemistry021001 nanoscience & nanotechnologyAmino acid0104 chemical sciencesComputer Science ApplicationsAmino acidTD-DFT spectraCrystallographyComputational Theory and MathematicsPhthalocyanineHydroxideDensity functional theory0210 nano-technologyJournal of Molecular Modeling
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Spectroscopic and electrochromical properties of metallophthalocyanines in silicate bulks and thin films prepared by the sol–gel method

2000

Abstract Magnesium phthalocyanine (MgPc) and praseodymium bisphthalocyanine (Pr(Pc) 2 ) have been entrapped in bulks and thin films of porous silicate xerogels prepared via the sol–gel method. The electronic absorption data obtained for the complexes immobilized in bulk sol–gel matrices indicate the formation of complex equilibria between their monomeric forms and respective agglomerates. Thin xerogel films doped with metallophthalocyanines and connecting two slides of transparent ITO electrodes display changes in the absorption spectra caused by varying of the applied voltage. These changes appear to be reversible in certain ranges of the applied voltages.

Absorption spectroscopyPraseodymiumOrganic ChemistryInorganic chemistrychemistry.chemical_elementSilicateAnalytical ChemistryInorganic Chemistrychemistry.chemical_compoundchemistryElectrochromismPhthalocyanineThin filmAbsorption (chemistry)SpectroscopySol-gelJournal of Molecular Structure
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Spectral properties and aggregation of ferrooctacarboxyphthalocyanine(II) in aqueous solutions

1996

Spectral properties of ferrooctacarboxyphthalocyanine(II) in aqueous solutions are discussed. A special attention is paid to aggregation in the presence of electrolytes. The influence of many factors (concentration, pH etc.) on forms of its occurence is presented.

AggregationPhthalocyaninesAqueous solutionsSpectral propertiesPolish Journal of Chemistry
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Turning lipophilic phthalocyanines/TiO2 composites into efficient photocatalysts for the conversion of CO2 into formic acid under UV–vis light irradi…

2014

Metal-free, Cu(II)- or Zn(II) tetrakis [4-(2,4-bis-(1,1-dimethylpropyl)phenoxy)]phthalocyanines loaded over TiO2 (anatase) proved to be active in the photoreduction of CO2 to formic acid (HCO2H) in water under UV-vis light. CuPc/TiO2 is catalyst of choice, allowing to reach a maximum yield of HCO2H, unequalled by any other similar catalytic systems. Because of their low environmental impact, low potential cost, and efficient power conversion, these multipurpose materials show promise in the setup of sustainable methods for CO2 valorization. (C) 2014 Elsevier B.V. All rights reserved.

AnataseChemistryFormic acidPhthalocyaninesProcess Chemistry and TechnologyPhthalocyanineLight irradiationPhotochemistryMetallo phthalocyaninesHeterogeneous photocatalysiCatalysisCatalysisHeterogeneous photocatalysischemistry.chemical_compoundUltraviolet visible spectroscopyYield (chemistry)TiO2Settore CHIM/07 - Fondamenti Chimici Delle TecnologieCO2 photo-reductionMetallo phthalocyanineApplied Catalysis A: General
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Hybrid TiO2 @ phthalocyanine catalysts in photooxidation of 4-nitrophenol: Effect of the matrix and sensitizer type

2020

Abstract Microcrystalline and nanocrystalline anatase (TiO2) based hybrid photocatalysts including selected phthalocyanine sensitizers were explored in photooxidation of 4-nitrophenol (4-NP) in water. Composites obtained with the homemade pure nano-anatase displayed a very poor catalytic performance compared to the other ones prepared from the commercial Tioxide-Huntsman (micro) and Evonik P25 (nano) products. In particular, the microcrystalline anatase impregnated with sandwich phthalocyanines of Gd or Yb showed excellent results both in photooxidation of 4-NP and hydroquinone, and proved the only ones which completely removed these two compounds from the system during the same reaction cy…

AnataseGeneral Chemical EngineeringHydroquinoneGeneral Physics and Astronomy02 engineering and technology010402 general chemistry01 natural sciences4-nitrophenolCatalysisChemical kineticsReaction ratechemistry.chemical_compoundMetallophthalocyaninesLanthanideLanthanidesHybrid photocatalystHydroquinoneChemistry4-NitrophenolGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesMicrocrystallineChemical engineeringPhthalocyanineTitanium dioxideMetallophthalocyanine0210 nano-technologyHybrid photocatalystsJournal of Photochemistry and Photobiology A: Chemistry
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Activity of phthalocyanine-sensitized TiO2-anatase in photooxidation of sulfite ions

2015

Abstract Hybrid catalysts based on the TiO2 matrix impregnated with Nd, Eu and Yb diphthalocyanines proved effective in oxidation of sulfite ions under irradiation with light from the UV-visible range. Micro- and nano-crystalline anatase powders were used in preparation of the photocatalysts, which were applied in the form of a suspension in the water phase. The reaction yield was found to depend on the phthalocyanine sensitizer used and the conditions of TiO2 impregnation. The best results were obtained when micro-anatase impregnated with Yb-diphthalocyanine was used.

AnataseMaterials scienceGeneral Chemical EngineeringphotooxidationIndustrial chemistryGeneral ChemistryPhotochemistryIonChemistrychemistry.chemical_compoundchemistrySulfitePhthalocyanineTiO2hybrid photocatalystsanataseQD1-999Biotechnologyphthalocyanine sensitizerPolish Journal of Chemical Technology
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Photocatalytic Degradation of 4-nitrophenol in aqueous suspension by using polycristalline TiO2 samples impregnated with a Cu(II)-phthalocyanine

2002

In this paper, the preparation of polycrystalline TiO2 samples impregnated with a modified Cu(II)-phthalocyanine (TiO2–CuPc) is reported along with an investigation on the photocatalytic behavior of this system compared with bare TiO2 (both in the anatase and rutile form) and with TiO2 samples impregnated with not functionalized commercial phthalocyanine (TiO2–CuPc) or with metal free phthalocyanine (TiO2–Pc). The photocatalytic degradation of 4-nitrophenol (4-NP) was studied as a probe reaction. The presence of modified CuPc showed to be beneficial only for TiO2 (anatase) while the commercial not functionalized CuPc also slightly for both TiO2 (anatase) and TiO2 (rutile). The metal free Pc…

AnataseMaterials scienceTITANIUM-DIOXIDEPHTHALOCYANINE COMPLEXESProcess Chemistry and TechnologyInorganic chemistry4-NitrophenolOXIDATIONMineralization (biology)CatalysisReaction ratechemistry.chemical_compoundchemistryRutilePhthalocyaninePhotocatalysisCrystalliteGeneral Environmental Science
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