Search results for "PORP"

showing 10 items of 567 documents

Dual application of (aqua)(chlorido)(porphyrinato)chromium(III) as hypersensitive amine-triggered ON switch and for dioxygen activation.

2014

Although synthesis and substitution reactions of chlorido chromium(III) porphyrins Cr(III)(TPP)(Cl)(L) (H2TPP = 5,10,15,20-tetraphenyl porphyrin, L = pyridine, H2O, ROH, etc.), have been well-established in coordination chemistry for decades, an unexpected dichotomous reactivity of Cr(III)(TPP)(Cl)(H2O) (1) toward amines is disclosed here. This reactivity leads to the application of 1 as highly sensitive substoichiometric and irreversible ON switch for amine detection by an autocatalytic pathway. The concomitant activation of O2 by the 1/amine system is furthermore exploited in an electrochemically driven epoxidation of norbonene using O2 as initial oxidant.

chemistry.chemical_classificationSubstitution reactionChemistrychemistry.chemical_elementPhotochemistryMedicinal chemistryPorphyrinCoordination complexInorganic ChemistryAutocatalysischemistry.chemical_compoundChromiumPyridineAmine gas treatingReactivity (chemistry)Physical and Theoretical ChemistryInorganic chemistry
researchProduct

Gold(iii) tetraarylporphyrin amino acid derivatives: ligand or metal centred redox chemistry?

2015

EPR spectroscopy and DFT calculations show that the site of reduction of porphyrinato gold(iii) complexes depends on the counterions X, the meso substituents R and the solvent.

chemistry.chemical_classificationValence (chemistry)010405 organic chemistryGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciencesPorphyrin0104 chemical scienceschemistry.chemical_compoundElectron transferChemistrychemistryValence isomerHexafluorophosphateDensity functional theoryElectron configurationCounterionChemical science
researchProduct

Fermentbestimmungen in Erythrocyten von Kranken mit Porphyria cutanea tarda

1969

In Erythrocyten von 12 Kranken mit Porphyria cutanea tarda konnte eine Aktivitatssteigerung der Enzyme G-6-PDH, 6-PGDH sowie der NADH- und der NADPH-abhangigen Glutathionreduktion festgestellt werden, deren Ursache diskutiert wird.

chemistry.chemical_classificationbiologyGlucosephosphate dehydrogenaseGeneral Medicinemedicine.diseaseMolecular medicineMolecular biologyEnzymechemistryDrug Discoverybiology.proteinmedicineMolecular MedicinePorphyria cutanea tardaEnzyme inducerGenetics (clinical)Klinische Wochenschrift
researchProduct

Novel Porphyrin-Cholic Acid Conjugates as Receptors for Biologically Important Anions

2005

A series of novel receptors showing high binding affinity in aqueous media for biologically important anions are reported. These naturally chromophoric porphyrin-based receptors contain cholic acids connected via quaternary alkyl ammonium amido linkages.

chemistry.chemical_classificationchemistry.chemical_compoundAqueous mediumChemistryStereochemistrypolycyclic compoundsCholic acidAmmoniumGeneral ChemistryReceptorPorphyrinAlkylConjugateSupramolecular Chemistry
researchProduct

Spin Switching with Triazolate-Strapped Ferrous Porphyrins

2019

Fe(III) porphyrins bridged with 1,2,3-triazole ligands were synthesized. Upon deprotonation, the triazolate ion coordinates to the Fe(III) ion, forming an overall neutral high-spin Fe(III) porphyrin in which the triazolate serves both as an axial ligand and as the counterion. The second axial coordination site is activated for coordination and binds p-methoxypyridine, forming a six-coordinate low-spin complex. Upon addition of a phenylazopyridine as a photodissociable ligand, the spin state of the complex can be reversibly switched with ultraviolet and visible light. The system provides the basis for the development of switchable catalase- and peroxidase-type catalysts and molecular spin sw…

chemistry.chemical_classificationkemiallinen synteesiSpin states010405 organic chemistryLigandkompleksiyhdisteet010402 general chemistry01 natural sciencesPorphyrin0104 chemical sciencesIonCatalysisInorganic Chemistrychemistry.chemical_compoundCrystallographyDeprotonationchemistrycoordination complexesPhysical and Theoretical ChemistryCounterionta116chemical synthesisVisible spectrumInorganic Chemistry
researchProduct

Ruthenium(II) meso-tetra-(benzo-15-crown-5)-porphyrinates: synthesis and spectroscopic investigation

2007

The synthesis of novel ruthenium(II) meso-tetra-(benzo-15-crown-5)-porphyrinates, meso-[( B 15 C 5)4 Por ] Ru ( CO )( MeOH ) (1) and meso-[( B 15 C 5)4 Por ] Ru ( L )2 (2)-(4) (meso-[( B 15 C 5)4 Por ]2-= 5,10,15,20-tetrakis-(benzo-15-crown-5)-porphyrinato-dianion; L = pyridine (py), pyrazine (pyz), 4,4′-bipyridyl (4,4′-bpy)), where CO and MeOH , or two N -donor ligands are axially coordinated to the central metal, are reported. The metalation of the free ligand performed by the reaction of Ru 3( CO )12 with meso-[( B 15 C 5)4 Por ] H 2 in 1,2,4-trichlorobenzene (TCB, bp = 215°C), gives (1) in a high yield. The synthesis of (2)-(4) involves the decarbonylation of (1) with trimethylamine N …

chemistry.chemical_classificationmetalloporphyrinsPyrazineLigandMetalationInorganic chemistryDecarbonylation[ CHIM.COOR ] Chemical Sciences/Coordination chemistrychemistry.chemical_elementGeneral ChemistryMedicinal chemistryRutheniumchemistry.chemical_compoundchemistry15-Crown-5Pyridine[CHIM.COOR]Chemical Sciences/Coordination chemistryrutheniumCrown etherComputingMilieux_MISCELLANEOUS
researchProduct

Luminescence properties of a cofacial dipalladium porphyrin dimer under argon and in the presence of dioxygen

2001

The preparation and luminescence properties of a dipalladium cofacial porphyrin dimer (DPA) Pd 2 (where DPA is the tetraanion of 1,8-bis(2,8,13,17-tetraethyl-3,7,12,18-tetramethylporphyrin-5-yl)anthracene) are reported and compared together with the photophysical behavior of the known monomeric (OEP)Pd and (TPP)Pd complexes. The effect of dioxygen in the presence and in the absence of the very bulky base, 1-t-butyl-5-phenylimidazole, is also investigated. The title dimer, (DPA) Pd 2, shows fluorescence and phosphorescence in the ps and ms time scale, respectively, with a global intensity lower than that of the porphyrin monomer analogues. The fluorescence sensitivity towards dioxygen quenc…

chemistry.chemical_compoundAnthraceneQuenching (fluorescence)MonomerchemistryDimerGeneral ChemistryLuminescencePhotochemistryPhosphorescenceFluorescencePorphyrinJournal of Porphyrins and Phthalocyanines
researchProduct

Very fast singlet and triplet energy transfers in a tri-chromophoric porphyrin dyad aided by the truxene platform

2015

A trichromophoric dyad composed of an octa-β-alkyl-palladium(II)porphyrin (donor) and two tri-meso-aryl-zinc(II)porphyrins (acceptors) held by a truxene spacer exhibits very fast rates for triplet energy transfers at 77 (kET(T1) = 1.63 × 108 s-1) and 298 K (kET(T1) = 3.44 × 108 s-1), whereas the corresponding singlet energy transfer rates, kET(S1) = 3.9 × 1010 s-1 (77 K) and kET(S1) = 6.0 × 1010 s-1 (298 K), are also considered fast. The interpretation for these results is that the energy transfer processes proceed via a through bond Dexter mechanism (i.e. double electron exchange) supported by comparison with literature data and evidence for a moderate MO coupling between the donor and ac…

chemistry.chemical_compoundChemistryEnergy transferElectron exchangeGeneral ChemistrySinglet stateChromophorePhotochemistryAcceptorPorphyrinJournal of Porphyrins and Phthalocyanines
researchProduct

Evidence for reverse pathways and equilibrium in singlet energy transfers between an artificial special pair and an antenna

2013

A dyad, 1, built on an artificial special pair (bis(meso-nonyl)zinc(II)porphyrin), [Zn2], a spacer (biphenylene), a bridge (1,4-benzene), and an antenna (di-meso-(3,5-di(t-butyl)phenyl)porphyrin free base), FB, is prepared by Suzuki coupling and is analyzed by absorption and steady state, and time-resolved emission spectroscopy at 298 and 77 K. Using bases from the Förster theory, evidence for two pathways for S 1 energy transfer, FB* → [Zn2], and [Zn2]* → FB, along with their respective rates, k ET ( S 1)1 and k ET ( S 1)-1, are extracted from the comparison of the fluorescence decays monitored at the emission maximum. At 77 K, the unquenched (1.79 ([Zn2]) and 10.6 ns (FB)) and quenched c…

chemistry.chemical_compoundChemistryFree baseGeneral ChemistrySinglet stateEmission spectrumSteady state (chemistry)Atomic physicsBiphenyleneAbsorption (electromagnetic radiation)FluorescencePorphyrinJournal of Porphyrins and Phthalocyanines
researchProduct

First highly distorted π-extended Fe(II) porphyrin – a unique model to elucidate factors affecting the electrochemical potentials

2004

The preparation, X-ray crystal structure and electrochemistry of a new poly-substituted air-stable tetrabenzoporphyrin iron(II) bis-pyridine complex (1) is reported.

chemistry.chemical_compoundChemistryInorganic chemistryGeneral ChemistryCrystal structureElectrochemistryPhotochemistryPorphyrinJournal of Porphyrins and Phthalocyanines
researchProduct