Search results for "PORP"

showing 10 items of 567 documents

Synthesis, characterization and electrochemistry of bismuth porphyrins: X-ray crystal structure of (OEP)Bi(SO3CF3)

2000

The metalation of several free base porphyrins by the bismuth salts Bi(NO3)3 and Bi(SO3CF3)3 in DMF or pyridine is described. The resulting stable Bi(III) porphyrin complexes are characterized by electrochemistry, 1H NMR and UV-vis spectroscopy. The structure of ( OEP ) Bi ( SO 3 CF 3) was also determined by single-crystal X-ray diffraction and shows that ( OEP ) Bi ( SO 3 CF 3) exists as a dimer which is stabilized by electrostatic interactions in which the two [(OEP)Bi]+ cations are linked via oxygen atoms of two symmetrically related [Formula: see text] anions, leading to a heptacoordinated bismuth center. Electrochemical oxidation of ( OEP ) Bi ( SO 3 CF 3) and ( T p TP ) Bi ( SO3CF3 )…

MetalationDimerInorganic chemistrychemistry.chemical_elementFree baseGeneral ChemistryCrystal structureElectrochemistryPorphyrinBismuthchemistry.chemical_compoundCrystallographychemistryPyridineJournal of Porphyrins and Phthalocyanines
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Facile formation of a meso–meso linked porphyrin dimer catalyzed by a manganese(iv)–oxo porphyrin

2011

A manganese(IV)-oxo porphyrin catalyzes C-C bond formation between zinc porphyrins at the meso-position with a two-electron oxidant to afford the meso-meso linked porphyrin dimer efficiently. The meso-meso linked dimer is formed via formation of the porphyrin radical cation, and the rate-determining step in the catalytic cycle is the formation of a manganese(IV)-oxo porphyrin with a two-electron oxidant.

MetalloporphyrinsDimerchemistry.chemical_elementManganeseZincPhotochemistryCatalysisCatalysischemistry.chemical_compoundPolymer chemistrypolycyclic compoundsMaterials Chemistryheterocyclic compoundsChemistryfungiMetals and AlloysGeneral ChemistryBond formationPorphyrinSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialscarbohydrates (lipids)Manganese CompoundsRadical ionCatalytic cycleCeramics and CompositesDimerizationChemical Communications
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Photophysical properties of a rhodium tetraphenylporphyrin-tin corrole dyad. The first example of a through metal-metal bond energy transfer

2005

The luminescence spectroscopy study and the determination of the photophysical parameters for the M-M'-bonded rhodium meso-tetraphenylporphyrin-tin(2,3,7,13,17,18-hexamethyl-8,12-diethylcorrole) complex, (TPP)Rh-Sn(Me6Et2Cor) 1, was investigated. The emission bands as well as the lifetimes (tau(e)) and the quantum yields (Phi(e); at 77 K using 2MeTHF as solvent) were compared with those of (TPP)RhI 2 (TPP = tetraphenylporphyrin) and (Me6Et2Cor)SnCl 3 (Me6Et2Cor = 2,3,7,13,17,18-hexamethyl-8,12-diethylcorrole) which are the two chemical precursors of 1. The energy diagram has been established from the absorption, fluorescence and phosphorescence spectra. The Rh(TPP) and Sn(Me6Et2Cor) chromop…

MetalloporphyrinsPhotochemistrychemistry.chemical_element010402 general chemistryPhotochemistry7. Clean energy01 natural sciencesBiochemistryRhodiumchemistry.chemical_compoundrhodium porphyrinTetraphenylporphyrinRhodium[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryBond energyCorrole010405 organic chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistryGeneral MedicineAcceptor3. Good health0104 chemical sciencesEnergy TransferchemistryMetalsSpectrophotometryExcited statemetal-metal bond energy transferTinPhosphorescencetin corrole
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Cobalt(IV) corroles as catalysts for the electroreduction of O2: reactions of heterobimetallic dyads containing a face-to-face linked Fe(III) or Mn(I…

2006

Abstract A series of heterobinuclear cofacial porphyrin–corrole dyads containing a Co(IV) corrole linked by one of four different spacers in a face-to-face arrangement with an Fe(III) or Mn(III) porphyrin have been examined as catalysts for the electroreduction of O 2 to H 2 O and/or H 2 O 2 when adsorbed on the surface of a graphite electrode in air-saturated aqueous solutions containing 1 M HClO 4 . The examined compounds are represented as (PCY)M III ClCo IV Cl where P is a porphyrin dianion, C is a corrole trianion and Y is a biphenylene (B), 9,9-dimethylxanthene (X), dibenzofuran (O) or anthracene (A) spacer. The catalytic behavior of the seven investigated dyads in the two heterobimet…

Metalloporphyrinschemistry.chemical_element010402 general chemistryElectrochemistryElectrocatalystPhotochemistryporphyrins01 natural sciencesBiochemistryMedicinal chemistryFerric CompoundsCatalysisCatalysisInorganic Chemistrychemistry.chemical_compoundElectron transfer[ CHIM.CATA ] Chemical Sciences/Catalysiscatalytic dioxygen reductionCorrolecorrolesComputingMilieux_MISCELLANEOUSManganeseBinding Sites010405 organic chemistryCobalt[CHIM.CATA]Chemical Sciences/CatalysisBiphenylenePorphyrin0104 chemical sciencesOxygenchemistryelectrochemistryCobaltOxidation-Reduction
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Dehydrogenation versus Oxygenation in Two-Electron and Four-Electron Reduction of Dioxygen by 9-Alkyl-10-methyl-9,10-dihydroacridines Catalyzed by Mo…

2004

Dehydrogenation of 10-methyl-9,10-dihydroacridine (AcrH(2)) by dioxygen (O(2)) proceeds efficiently, accompanied by the two-electron and four-electron reduction of O(2) to produce H(2)O(2) and H(2)O, which are effectively catalyzed by monomeric cobalt porphyrins and cofacial dicobalt porphyrins in the presence of perchloric acid (HClO(4)) in acetonitrile (MeCN) and benzonitrile (PhCN), respectively. The cobalt porphyrin catalyzed two-electron reduction of O(2) also occurs efficiently by 9-alkyl-10-methyl-9,10-dihydroacridines (AcrHR; R = Me, Et, and CH(2)COOEt) to yield 9-alkyl-10-methylacridinium ion (AcrR+) and H(2)O(2). In the case of R = Bu(t) and CMe(2)COOMe, however, the catalytic two…

Metalloporphyrinschemistry.chemical_elementElectronsReaction intermediatePhotochemistryBiochemistryMedicinal chemistryCatalysisCatalysischemistry.chemical_compoundColloid and Surface ChemistryDehydrogenationPerchloric acidAlkylchemistry.chemical_classificationPerchloratesChemistryCobaltGeneral ChemistryNADPorphyrinKineticsBenzonitrileAcridinesHydrogenationOxidation-ReductionCobaltJournal of the American Chemical Society
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Influence of heme oxygenase 1 modulation on the progression of murine collagen-induced arthritis.

2005

Contains fulltext : 48023.pdf (Publisher’s version ) (Closed access) OBJECTIVE: Heme oxygenase 1 (HO-1) can be induced by inflammatory mediators as an adaptive response. The objective of the present study was to determine the consequences of HO-1 modulation in the murine collagen-induced arthritis (CIA) model. METHODS: DBA/1J mice were treated with an inhibitor of HO-1, tin protoporphyrin IX (SnPP), or with an inducer of HO-1, cobalt protoporphyrin IX (CoPP), from day 22 to day 29 after CIA induction. The clinical evolution of disease was monitored visually. At the end of the experiment, joints were examined for histopathologic changes. Cytokine levels in paws were measured by enzyme-linked…

Metalloporphyrinsmedicine.medical_treatmentImmunologyArthritisProtoporphyrinsInflammationPharmacologyAuto-immunity transplantation and immunotherapy [N4i 4]MiceRheumatologyFibrosismedicinePerception and Action [DCN 1]Immunology and AllergyAnimalsPharmacology (medical)Enzyme InhibitorsChronic inflammation and autoimmunity [UMCN 4.2]biologybusiness.industryMembrane Proteinsmedicine.diseaseCOPPArthritis ExperimentalHeme oxygenaseEnzyme ActivationPathogenesis and modulation of inflammation [N4i 1]Disease Models AnimalCytokineCyclooxygenase 2Mice Inbred DBAProstaglandin-Endoperoxide SynthasesImmunologyChronic DiseaseHeme Oxygenase (Decyclizing)biology.proteinDisease ProgressionTumor necrosis factor alphaJointsCyclooxygenasemedicine.symptombusinessInfection and autoimmunity [NCMLS 1]Heme Oxygenase-1
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The Alzheimer’s disease associated bacterial protease RgpB from P. gingivalis activates the alternative β-secretase meprin β thereby increasing Aβ ge…

2019

AbstractAlzheimer’s disease (AD) is the most common type of dementia and characterized by tau hyperphosphorylation, oxidative stress, reactive microglia and amyloid-β (Aβ) deposits. A recent study revealed that Porphyromonas gingivalis infection is associated with amyloid β generation in Alzheimer’s disease. Increased Aβ levels, tau degradation and neuronal toxicity were observed as a consequence of ginigipain R (RgpB) activity, a cysteine protease constitutively secreted by P. gingivalis. Of note, we previously identified RgpB as a potent activator of the metalloproteinase meprin β. Interestingly, meprin β is an alternative β-secretase of the amyloid precursor protein (APP), which together…

MetalloproteinaseProteasebiologyMicrogliaActivator (genetics)Chemistrymedicine.medical_treatmentHEK 293 cellsbiology.organism_classificationMolecular biologyCysteine proteasemedicine.anatomical_structuremedicineAmyloid precursor proteinbiology.proteinPorphyromonas gingivalis
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Singlet and triplet energy transfer rate acceleration by additions of clusters in supramolecular pigment-organometallic cluster assemblies

2011

Both S(1) and T(1) energy transfer rates (porphyrin → cluster) increase from mono- to di- to tetracarboxylate[tetraphenyl-(zinc)porphyrin] adducts with [Pd(3)(dppm)(3)(CO)](2+) clusters.

Metals and AlloysSupramolecular chemistrychemistry.chemical_elementGeneral ChemistryZincPhotochemistryPorphyrinCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAdductchemistry.chemical_compoundPigmentchemistryvisual_artMaterials ChemistryCeramics and CompositesCluster (physics)visual_art.visual_art_mediumSinglet stateEnergy transfer rateChemical Communications
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The gut microbiota of larvae of Rhynchophorus ferrugineus Oliver (Coleoptera: Curculionidae)

2014

Background: The red palm weevil (RPW) Rhynchophorus ferrugineus Olivier (Coleoptera: Curculionidae) is one of the major pests of palms. The larvae bore into the palm trunk and feed on the palm tender tissues and sap, leading the host tree to death. The gut microbiota of insects plays a remarkable role in the host life and understanding the relationship dynamics between insects and their microbiota may improve the biological control of insect pests. The purpose of this study was to analyse the diversity of the gut microbiota of field-caught RPW larvae sampled in Sicily (Italy). Results: The 16S rRNA gene-based Temporal Thermal Gradient Gel Electrophoresis (TTGE) of the gut microbiota of RPW …

Microbiology (medical)DNA BacterialFirmicutesMolecular Sequence DataPorphyromonadaceaeCarbohydratesGut floraSettore BIO/19 - Microbiologia GeneraleMicrobiologyDNA RibosomalCytosolEnterobacteriaceaeRNA Ribosomal 16SBotanyAnimalsCluster AnalysisSicilyTTGEPhylogenybiologyHost (biology)fungiBacteroidetesEnterobacteriaceae Dysgonomonas TTGE PyrosequencingPyrosequencingSequence Analysis DNAbiology.organism_classificationBiotaDysgonomonasGastrointestinal TractRhynchophorusSettore AGR/11 - Entomologia Generale E ApplicataItalyLarvaWeevilsAnaerobic bacteriaProteobacteriaResearch ArticleBMC Microbiology
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Porphyrin-templated synthetic G-quartet (PorphySQ): a second prototype of G-quartet-based G-quadruplex ligand.

2012

Template-assembled synthetic G-quartet (TASQ) has been reported recently as a G-quadruplex ligand interacting with DNA according to an unprecedented, nature-inspired ‘like likes like’ approach, based on the association between two G-quartets, one being native (quadruplex) and the other one artificial (ligand). Herein, a novel TASQ-based ligand is designed, synthesized and its quadruplex-recognition properties are evaluated in vitro: PorphySQ (for porphyrin-templated synthetic G-quartet) displays enhanced quadruplex recognition properties as compared to the very first reported prototype (DOTASQ, for DOTA-templated synthetic G-quartet), since the porphyrin template insures a more stable intra…

Models Molecular0303 health sciencesPorphyrinsStereochemistryOrganic ChemistryHydrogen Bonding010402 general chemistryG-quadruplexLigands01 natural sciencesBiochemistryPorphyrin0104 chemical sciencesG-Quadruplexes03 medical and health scienceschemistry.chemical_compoundchemistryIntramolecular force[CHIM]Chemical SciencesPhysical and Theoretical ChemistryDNAComputingMilieux_MISCELLANEOUS030304 developmental biologyOrganicbiomolecular chemistry
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