Search results for "PORP"

showing 10 items of 567 documents

Heterobimetallic complexes of cobalt(IV) porphyrin-corrole dyads. Synthesis, physicochemical properties, and X-ray structural characterization.

2005

The synthesis of a novel family of heterobinuclear cofacial biphenylene (B), anthracene (A), 9,9-dimethylxanthene (X), or dibenzofuran (O) bridged porphyrin-corrole complexes, (PCY)MClCoCl, is reported, M being either an iron(III) or manganese(III) ion. Each complex was characterized by electrochemistry, mass spectrometry, UV-vis, IR, and electron spin resonance spectroscopy. Unlike previously examined biscobalt porphyrin-corrole dyads, the cobalt ion of the corrole moiety is present in a high-valence +4 oxidation state, as proven by electrochemistry, spectroelectrochemistry, and an X-ray diffraction study of (PCB)FeClCoCl, which shows the presence of a bound Cl- anion on the cobalt corrole…

Stereochemistrychemistry.chemical_elementBiphenyleneTriclinic crystal systemPorphyrinlaw.inventionInorganic Chemistrychemistry.chemical_compoundCrystallographychemistrylawOxidation stateMoietyPhysical and Theoretical ChemistryCorroleElectron paramagnetic resonanceCobaltInorganic chemistry
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An Octanuclear Metallosupramolecular Cage Designed To Exhibit Spin-Crossover Behavior.

2018

By employing the subcomponent self-assembly approach utilizing 5,10,15,20-tetrakis(4-aminophenyl)porphyrin or its zinc(II) complex, 1H-4-imidazolecarbaldehyde, and either zinc(II) or iron(II) salts, we were able to prepare O-symmetric cages having a confined volume of ca. 1300 Å3 . The use of iron(II) salts yielded coordination cages in the high-spin state at room temperature, manifesting spin-crossover in solution at low temperatures, whereas corresponding zinc(II) salts led to the corresponding diamagnetic analogues. The new cages were characterized by synchrotron X-ray crystallography, high-resolution mass spectrometry, and NMR, Mössbauer, IR, and UV/Vis spectroscopy. The cage structures…

Stereochemistrychemistry.chemical_elementZinc010402 general chemistryMass spectrometry01 natural sciencesCatalysislaw.inventionhost-guest systemschemistry.chemical_compoundspin crossoverlawSpin crossoverMössbauer spectroscopySpectroscopyta116010405 organic chemistryChemistryiron(II) complexesGeneral Chemistryself-assemblymetallosupramolecular chemistryPorphyrinSynchrotron0104 chemical sciencesCrystallographyDiamagnetism
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Catecholato complexes of o-phenylenebis(salicylideneiminato)iron(III) and meso-tetra(parasulphonatephenyl)porphyrinatoferrate(III). A comment on the …

1986

Abstract Formation of catecholato complexes of Fe(saloph) + and Fe(TPPS) 3− in solution is studied. Fe(saloph)(cat) − contains a cat 2− bidentate ligand. Its formation in solution competes efficiently with the hydrolysis and dimerization of Fe(saloph) + to give Fe 2 (saloph) 2 O. This behaviour shows that the planar saloph 2− ligand, as the analogous salen 2− , is easily distorted, and is not as rigid as generally considered. Iron(III) porphyrin Fe(TPPS) 3− with catechol gives the complex [Fe(TPPS)(Hcat)] 4− . Deprotonation of the unidentate Hcat − ligand cannot be studied because the smaller stability of the complex, and the dimerization of the metalloporphyrin dominates in basic medium. T…

Steric effectsCatecholDenticitybiologyStereochemistryLigandActive siteMedicinal chemistryPorphyrinInorganic Chemistrychemistry.chemical_compoundDeprotonationchemistryMaterials Chemistrybiology.proteinChelationPhysical and Theoretical ChemistryInorganica Chimica Acta
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Studies on DNA interaction of organotin(IV) complexes of meso-tetra(4-sulfonatophenyl)porphine that show cellular activity.

2016

PubMedID: 27393277 The interaction of the diorgano- and triorganotin(IV) derivatives of meso-tetra-(4-sulfonatophenyl)porphine (Me2Sn)2TPPS, (Bu2Sn)2TPPS, (Me3Sn)4TPPS and (Bu3Sn)4TPPS to natural DNA was analysed (together with free meso-tetra-(4-sulfonatophenyl)porphine (TPPS4 -) for comparison purposes). Particular attention was paid to (Bu3Sn)4TPPS, a species that shows significant cellular action. Preliminary tests were done on the solution properties of the organotin(IV) compounds (pKA and possible self-aggregation). Spectrophotometric and spectrofluorometric experiments showed that all the investigated organotin(IV) derivatives strongly interact with DNA, the binding energy depending …

Steric effectsCellular activityOrganometallic compounds External binding Negative porphyrins Aggregation ViscosityNegative porphyrinsPorphyrinsStereochemistryBinding energyDna interactionOrganometallic compounds010402 general chemistry01 natural sciencesMedicinal chemistryBiochemistryInorganic Chemistrychemistry.chemical_compoundAggregationmetal complexequilibrium constantDNA conformation changescomplex formationOrganotin CompoundsHumansDNA bindingEquilibrium constantGroup 2 organometallic chemistrybiology010405 organic chemistryViscosityDNAbiology.organism_classificationExternal binding0104 chemical sciencesAggregation External binding Negative porphyrins Organometallic compounds Viscosity Biochemistry Inorganic Chemistry metal complex equilibrium constant DNA conformation changes DNA binding complex formationchemistrySettore CHIM/03 - Chimica Generale E InorganicaA549 CellsTetraNucleic Acid ConformationDNAJournal of inorganic biochemistry
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An unprecedented, bridged dihydrogen complex of a cofacial metallodiporphyrin and its relevance to the bimolecular reductive elimination of hydrogen

1990

Recently, the authors characterized the first metalloporphyrin dihydrogen complex, Os(OEP)(H{sub 2}), and proposed that a similar ruthenium porphyrin dihydrogen complex, Ru(OEP)(H{sub 2}), is involved as an intermediate in the catalytic H/D isotopic exchange between water and hydrogen. They now report that treatment of a metal-metal-bonded cofacial ruthenium porphyrin dimer with a sterically bulky ligand in the presence of hydrogen gas has yielded the first known complex containing a dihydrogen ligand bound between two metals. Such a bridged dihydrogen complex is proposed as an intermediate in the bimolecular elimination of dihydrogen from two metalloporphyrin hydrides.

Steric effectsLigandDimerchemistry.chemical_elementGeneral ChemistryReaction intermediateBiochemistryPorphyrinMedicinal chemistryCatalysisReductive eliminationRutheniumchemistry.chemical_compoundColloid and Surface ChemistrychemistryDihydrogen complexJournal of the American Chemical Society
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The 5/2,3/2 Spin Admixture in the Chloroiron(III) Derivative of the Sterically Crowded 2,3,7,8,12,13,17,18-Octaethyl-5,10,15,20-tetraphenylporphyrin

1999

Despite similar ring deformations in solution and in the solid state, the chloroiron(III) derivative of 2,3,7,8,12,13,17,18-octaethyl-5,10,15,20-tetraphenylporphyrin ([FeCl(oetpp)], shown schematically) prepared in this study exhibits only a very weak quantum-mechanical admixture of spin S=3/2 (only 4-10 %) with spin S=5/2. In contrast, for the variety of [FeCl(oetpp)] studied earlier by other researchers a 40 % contribution of the S=3/2 state was found.

Steric effectsSolid-stateGeneral ChemistryRing (chemistry)Catalysislaw.inventionchemistry.chemical_compoundCrystallographyNuclear magnetic resonancechemistrylawTetraphenylporphyrinMössbauer spectroscopySpin (physics)Electron paramagnetic resonanceDerivative (chemistry)Angewandte Chemie International Edition
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Shape-persistent poly-porphyrins assembled by a central truxene: synthesis, structure, and singlet energy transfer behaviors

2013

Four dyad systems composed of a central truxene and either one or three β-substituted zinc(II) porphyrins (ZnP: TruZnP (7) and TruTriZnP (9)) or free-bases (H2P: TruP (6) and TruTriP (8)) have been prepared. The presence of β-methyl groups minimizes π-conjugation through the quasi right angle made by the porphyrin and the truxene planes, and renders these dyads relatively rigid. The position of the absorption and emission 0–0 peaks confirms the role of the truxene and porphyrin as the energy donor and acceptor, respectively. Selective excitation of the truxene results in an efficient singlet energy transfer (S1 ET) from the truxene to the porphyrin unit. The rates for S1 ET (k ET ) are ext…

Steric effectschemistry.chemical_compoundchemistryEnergy transferTemperature independentchemistry.chemical_elementGeneral ChemistrySinglet stateZincPhotochemistryFluorescencePorphyrinAcceptorJournal of Porphyrins and Phthalocyanines
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Dual-Mode Chiral Self-Assembly of Cone-Shaped Subphthalocyanine Aromatics

2020

This document is the Accepted Manuscript version of a Published Work that appeared in final form in Journal of the American Chemical Society, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/jacs.0c07291

SubphthalocyanineChemistryThermodynamic equilibriumDimerStackingSupramolecular chemistryPorphyrinoidsSelf-assemblyQuímicaGeneral Chemistry010402 general chemistry01 natural sciencesBiochemistryCatalysis0104 chemical scienceschemistry.chemical_compoundColloid and Surface ChemistryEnantiopure drugPolymerizationChemical physicsLiquid crystalSupramolecular PolymersSelf-assembly
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Porphyroblast crystallization kinetics: the role of the nutrient production rate

2011

The mechanisms that govern porphyroblast crystallization are investigated by comparing quantitative textural data with predictions from different crystallization models. Such numerical models use kinetic formulations of the main crystallization mechanism to predict textural characteristics, such as grain size distributions. In turn, data on porphyroblast textures for natural samples are used to infer which mechanism dominated during their formation. Whereas previous models assume that the rate-limiting step for a porphyroblast producing reaction is either transport or growth, the model advanced in this study considers the production of nutrients for porphyroblasts as a potentially rate-limi…

SupersaturationNucleationMineralogyThermodynamicsGeologyTexture (geology)Grain sizelaw.inventionGeochemistry and PetrologylawPhase (matter)MetastabilityPorphyroblastCrystallizationGeologyJournal of Metamorphic Geology
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Synthesis and Spectral and Structural Characterization of a New Series of Bis-Strapped Chiral Porphyrins Derived from L-Proline

2001

International audience; New chiral porphyrins were obtained in reasonable yields in three steps, starting from the áâáâ atropisomer of mesotetrakis(o-aminophenyl)porphyrin (TAPP). These potential catalysts for the enantioselective epoxidation of alkenes were obtained by the reaction of different linkers on the same Lprolinoyl-picket porphyrin. Their 1H NMR spectral characteristics, as well as the crystal structure of one of them, clearly indicate that the orientation of the proline cycle depends on the linker used to tether the two pickets on each side of the porphyrin. The same linker is employed for both sides of the porphyrin; hence the resulting D2-symmetric superstructure.

SuperstructureAtropisomerPorphyrinsStereochemistryOrganic ChemistryEnantioselective synthesisStructure-activity relationshipsCrystal structure[ CHIM ] Chemical SciencesPorphyrinCatalysischemistry.chemical_compoundCrystallographychemistryProton NMRAmino acids[CHIM]Chemical SciencesPhysical and Theoretical ChemistrySynthesis designLinkerChiral auxiliaries
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