Search results for "PORP"

showing 10 items of 567 documents

A Very Low Band Gap Diketopyrrolopyrrole-Porphyrin Conjugated Polymer

2017

International audience; A porphyrin-diketopyrrolopyrrole-containing polymer (poly(porphyrin-diketopyrrolopyrrole) (PPDPP)) shows impressive molar absorption coefficients from lambda=300 to 1000 nm. The photophysical and structural properties of PPDPP have been studied. With PPDPP as the electron donor and [ 6,6]phenyl C-71 butyric acid methyl ester (PC71BM) as the electron acceptor, the bulk heterojunction polymer solar cell showed overall power conversion efficiencies of 4.18 and 6.44% for as-cast and two-step annealing processed PPDPP: PC71BM (1: 2) active layers, respectively. These results are quite impressive for porphyrin-containing polymers, especially when directly included in the p…

Materials scienceBand gapbuilding-blockporphyrinoidsElectron donorthin-film transistors02 engineering and technologyConjugated system010402 general chemistryPhotochemistry[ CHIM ] Chemical Sciences01 natural sciencesPolymer solar cellheterojunction solar-cellschemistry.chemical_compound[CHIM]Chemical Sciencessmall-moleculepolymerschemistry.chemical_classificationsemiconducting polymerscharge transferGeneral ChemistryPolymerChromophoreElectron acceptorside-chains021001 nanoscience & nanotechnologyPorphyrinphotovoltaic properties0104 chemical sciencesphotodynamic therapychemistryorganic photovoltaics0210 nano-technologyabsorptionperformanceconjugationChemPlusChem
researchProduct

Self-organization of porphyrin units induced by magnetic field during sol-gel polymerization

2007

The use of a magnetic field as a controlling factor during the hydrolysis-polycondensation of porphyrin precursors substituted by Si(OR)(3) groups, induces a self-organization of porphyrin moieties due to the stacking of these units in the hybrid material and this study also confirms the effect of the magnetic field in the nano- and micrometric organization during the kinetically controlled polycondensation process.

Materials scienceCondensation polymerpolymerStackingmagnetic field02 engineering and technology010402 general chemistryPhotochemistry01 natural sciencesCatalysischemistry.chemical_compound[ CHIM.ORGA ] Chemical Sciences/Organic chemistryNano-Materials ChemistrySol-gel[CHIM.ORGA]Chemical Sciences/Organic chemistryMetals and AlloysGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistryequipment and supplies021001 nanoscience & nanotechnologyPorphyrinself-organization0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMagnetic fieldchemistryPolymerization[ CHIM.MATE ] Chemical Sciences/Material chemistryCeramics and Compositesporphyrin network0210 nano-technologyHybrid materialhuman activities
researchProduct

Photoinduced Electron Transfer Reactions in a Porphyrin−Viologen Complex:  Observation of S2 to S1 Relaxation and Electron Transfer from the S2 State

1999

Photoinduced Energy Transfer Reactions in a Porphyrin-Viologen Complex: Observation of S2 to S1 Relaxation and Electron Transfer from the S2 state

Materials scienceEnergy transferViologenPhotochemistryPorphyrinPhotoinduced electron transferSurfaces Coatings and Filmschemistry.chemical_compoundElectron transferFörster resonance energy transferchemistryMaterials ChemistrymedicineRelaxation (physics)Physical and Theoretical ChemistryProton-coupled electron transfermedicine.drugThe Journal of Physical Chemistry B
researchProduct

Ultra-thin film sensors based on porphyrin-5-ylphosphonate diesters for selective and sensitive dual-channel optical detection of mercury(II) ions

2020

International audience; Reusable dual-channel optical sensors for Hg2+ ions were prepared by Langmuir-Schaefer (LS) method from amphiphilic (trans-A2)BC-type porphyrins functionalized at meso-positions of the tetrapyrrolic macrocycle by sterically demanding diethoxyphosphoryl and mesityl groups as well as electron donating RO, RS or RNH substituents (R = n-C8H17). These three novel amphiphilic porphyrin derivatives were synthesized in good yields and their floating films at the air⎯water interface were investigated. In these monolayers, porphyrin molecules display a slipped stack-of-card orientation, but their strong π stacking is prohibited by bulky diethoxyphosphoryl and mesityl groups. T…

Materials scienceGeneral Chemical EngineeringHeteroatomSubstituentStacking02 engineering and technology010402 general chemistryPhotochemistry01 natural sciencesAbsorbancechemistry.chemical_compoundMonolayerMolecule[CHIM]Chemical Sciencesdual-channel optical sensorLangmuir monolayersolid thin-film sensorHydrogen bondProcess Chemistry and TechnologyLangmuir-Schaefer filmmercury(II) detection021001 nanoscience & nanotechnologyPorphyrin0104 chemical scienceschemistry13. Climate action0210 nano-technologyporphyrin
researchProduct

Magnesium(II) polyporphine: The first electron-conducting polymer with directly linked unsubstituted porphyrin units obtained by electrooxidation at …

2010

Abstract Electrooxidation of magnesium(II) porphine, a totally unsubstituted porphyrin, in acetonitrile solution under potentiostatic or potentiodynamic regime leads to a polymer film at the electrode surface. Polymer deposition takes place at extremely low potential, several hundred mV less positive even compared to the deposition potential for pyrrole or EDOT (at identical monomer concentrations) in the same solvent. Film thickness can be controlled by the passed deposition charge. This material and its THF-soluble fraction have been characterized by various electrochemical methods as well as by UV–visible and IR spectroscopies, XPS, XRD and MALDI-TOF techniques. This analysis has allowed…

Materials scienceGeneral Chemical EngineeringInorganic chemistry02 engineering and technology010402 general chemistryElectrochemistry01 natural scienceschemistry.chemical_compoundX-ray photoelectron spectroscopy[CHIM.ANAL]Chemical Sciences/Analytical chemistryElectrochemistryElectroactive polymers[CHIM.COOR]Chemical Sciences/Coordination chemistryAcetonitrileComputingMilieux_MISCELLANEOUSchemistry.chemical_classificationConductive polymer[CHIM.ORGA]Chemical Sciences/Organic chemistryPolymer[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyPorphyrin0104 chemical sciencesMonomerchemistry0210 nano-technology
researchProduct

Molecular flattening effect to enhance the conductivity of fused porphyrin tape thin films.

2019

The straightforward synthesis of directly fused porphyrins (porphyrin tapes) from 5,15-diphenyl porphyrinato nickel(II) complexes with different substituents on the phenyl rings is achieved while processing from the gas phase. The porphyrin tapes, exhibiting NIR absorption, are readily obtained in thin film form. The gas phase approach cuts the need for solubilizing groups allowing for the first time the study of their conductivity according to the substituent. 2-Point probe and conductivity AFM measurements evidence that reducing the size of the meso substituents, phenyl < mesityl < di(3,5-tert-butyl)phenyl < di(2,6-dodecyloxy)phenyl, improves the thin film conductivity by several orders o…

Materials scienceGeneral Chemical EngineeringSubstituentStackingGeneral ChemistryConductivityPorphyrinchemistry.chemical_compoundCrystallographyMolecular geometrychemistryIntramolecular forceMoleculeThin filmRSC advances
researchProduct

BODIPY–diketopyrrolopyrrole–porphyrin conjugate small molecules for use in bulk heterojunction solar cells

2018

Two small molecules denoted as BD-pPor and BD-tPor composed of a central BODIPY core surrounded with two DPP and two porphyrin units have been designed and synthesized. In BD-pPor and BD-tPor, porphyrins are linked to the central BODIPY by phenyl and thiophene bridges, respectively. The optical and electrochemical properties were systematically investigated in order to employ them as donors along with PC71BM as an acceptor for solution processed bulk heterojunction organic solar cells. After the optimization of the active layer, the organic solar cells based on BD-pPor and BD-tPor exhibit overall power conversion efficiencies of 6.67% and 8.98% with an energy loss of 0.63 eV and 0.50 eV. Th…

Materials scienceOrganic solar cell02 engineering and technology010402 general chemistryPhotochemistry7. Clean energy01 natural sciencesPolymer solar cellchemistry.chemical_compound[CHIM.ANAL]Chemical Sciences/Analytical chemistryThiopheneGeneral Materials Science[CHIM.COOR]Chemical Sciences/Coordination chemistryHOMO/LUMOComputingMilieux_MISCELLANEOUSRenewable Energy Sustainability and the Environment[CHIM.ORGA]Chemical Sciences/Organic chemistryGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologySmall moleculeAcceptorPorphyrin0104 chemical scienceschemistryBODIPY0210 nano-technology
researchProduct

Porphyrins and BODIPY as Building Blocks for Efficient Donor Materials in Bulk Heterojunction Solar Cells

2017

International audience; Advances in the synthesis and application of highly efficient polymers and small molecules over the last two decades have enabled the rapid advancement in the development of organic solar cells and photovoltaic technology as a promising alternative to conventional solar cells, based on silicon and other inorganic semiconducting materials. Among the different types of organic semiconducting materials, porphyrins and BODIPY-based small molecules and conjugated polymers attract high interest as efficient semiconducting organic materials for dye sensitized solar cells and bulk heterojunction organic solar cells. The highest power conversion efficiency exceeding 9% has be…

Materials scienceOrganic solar cellEnergy Engineering and Power Technologypower-conversion efficiency02 engineering and technologydonor materials010402 general chemistryporphyrins7. Clean energy01 natural sciencesPolymer solar cellbulk heterojunction solar cellsphotoinduced electron-transferchemistry.chemical_compoundBODIPYElectrical and Electronic Engineeringsmall-moleculelow-bandgap polymerbusiness.industryfield-effect transistors[CHIM.MATE]Chemical Sciences/Material chemistryHybrid solar cellpi-conjugated copolymersd-a021001 nanoscience & nanotechnologyAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic Materialsphotovoltaic propertieschemistryopen-circuit voltage[ CHIM.MATE ] Chemical Sciences/Material chemistryOptoelectronicsorganic photovoltaicsBODIPY0210 nano-technologybusiness
researchProduct

Highly soluble multifunctional MnO nanoparticles for simultaneous optical and MRI imaging and cancer treatment using photodynamic therapy

2010

Superparamagnetic MnO nanoparticles were functionalized using a hydrophilic ligand containing protoporphyrin IX as photosensitizer. By virtue of their magnetic properties these nanoparticles may serve as contrast enhancing agents for magnetic resonance imaging (MRI), while the fluorescent target ligand protoporphyrin IX allows simultaneous tumor detection and treatment by photodynamic therapy (PDT). Caki-1 cells were incubated with these nanoparticles. Subsequent exposure to UV light lead to cell apoptosis due to photoactivation of the photosensitizer conjugated to the nanoparticles. This method offers great diagnostic potential for highly proliferative tissues, including tumors. In additio…

Materials scienceProtoporphyrin IXmedicine.medical_treatmentNanoparticlePhotodynamic therapyGeneral ChemistryConjugated systemLigand (biochemistry)PhotochemistryFluorescencechemistry.chemical_compoundchemistryMaterials ChemistryBiophysicsmedicinePhotosensitizerSuperparamagnetismJournal of Materials Chemistry
researchProduct

Metal–organic covalent network chemical vapor deposition for gas separation

2016

The chemical vapor deposition (CVD) polymerization of metalloporphyrin building units is demonstrated to provide an easily up-scalable one-step method toward the deposition of a new class of dense and defect-free metal–organic covalent network (MOCN) layers. The resulting hyper-thin and flexible MOCN layers exhibit outstanding gas-separation performances for multiple gas pairs.

Materials scienceRadical polymerization02 engineering and technologyChemical vapor deposition010402 general chemistry01 natural sciencesMetalPolymer chemistryiPECVDDeposition (phase transition)General Materials ScienceGas separationgas separationmetalloporphyrinsMechanical Engineering021001 nanoscience & nanotechnologymetal–organic covalent networks0104 chemical sciencesChemical engineeringPolymerizationMechanics of Materialsvisual_artNetwork covalent bondingvisual_art.visual_art_medium0210 nano-technologyfree-radical polymerizationAdvanced Materials
researchProduct