Search results for "Pyridine"

showing 10 items of 2516 documents

Thermodynamic control over energy dissipation modes in dual-network hydrogels based on metal-ligand coordination.

2020

Modern polymeric hydrogels use reversible bonds to mimic biological functionalities. However, true biological materials benefit from several supramolecular elements and deliver multiple functions at the same time. To approach similar creation and control of multiple different functional elements in a synthetic soft material, we develop a model dual-network hydrogel in which multiple energy dissipating modes are formed by metal–ligand coordination and regulated by their association thermodynamics. This idea is realized by using linear and tetra-arm poly(ethylene glycol) (PEG) precursors with complementary reactive end groups. The former also carries terpyridine ligands on both ends, which fo…

Materials scienceLigandMetal ions in aqueous solutionSupramolecular chemistry02 engineering and technologyGeneral ChemistryDissipation010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesIonMetalchemistry.chemical_compoundchemistryChemical physicsvisual_artSelf-healing hydrogelsvisual_art.visual_art_mediumTerpyridine0210 nano-technologySoft matter
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Ruthenium-Containing Block Copolymer Assemblies: Red-Light-Responsive Metallopolymers with Tunable Nanostructures for Enhanced Cellular Uptake and An…

2015

The use of self-assembled nanostructures consisting of red-light-responsive Ru(II)-containing block copolymers (BCPs) for anticancer phototherapy is demonstrated. Three Ru-containing BCPs with different molecular weights are synthesized. Each BCP contains a hydrophilic poly(ethylene glycol) block and an Ru-containing block. In the Ru-containing block, more than half of the side chains are coordinated with [Ru(2,2':6',2''-terpyridine)(2,2'-biquinoline)](2+) , resulting in more than 40 wt% Ru complex in the BCPs. The Ru complex acts as both a red-light-cleavable moiety and a photoactivated prodrug. Depending on their molecular weights, the BCPs assemble into micelles, vesicles, and large comp…

Materials scienceLightStereochemistryCell SurvivalPolymersBiomedical EngineeringPharmaceutical Sciencechemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesMicelleRutheniumPolyethylene GlycolsBiomaterialschemistry.chemical_compoundNeoplasmsSide chainCopolymerMoietyHumansProdrugsMicellesPhototherapy021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical sciencesRutheniumNanostructuresMolecular WeightchemistrySelf-assemblyTerpyridine0210 nano-technologyEthylene glycolHydrophobic and Hydrophilic InteractionsHeLa CellsAdvanced healthcare materials
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Exploring the effect of the cyclometallating ligand in 2-(pyridine-2-yl)benzo[d]thiazole-containing iridium(III) complexes for stable light-emitting …

2018

The preparation and characterization of a series of iridium(III) ionic transition-metal complexes for application in light-emitting electrochemical cells (LECs) are reported. The complexes are of the type [Ir(C^N)2(N^N)][PF6] in which C^N is one of the cyclometallating ligands 2-(3-(tert-butyl)phenyl)pyridine (tppy), 2-phenylbenzo[d]thiazole (pbtz), 1-phenyl-1H-pyrazole (ppz) and 1-phenylisoquninoline (piq), and N^N is 2-(pyridine-2-yl)benzo[d]thiazole (btzpy). The variation in the C^N ligands allows the HOMO energy level to be tuned, leading to HOMO–LUMO gaps in the range 2.76–3.01 eV and values of Eox1/2 of 0.81–1.11 V. In solution, the complexes are orange to deep-red emitters (λmax in t…

Materials sciencePhotoluminescenceLigandIonic bondingchemistry.chemical_element02 engineering and technologyGeneral ChemistryElectroluminescence010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceschemistry.chemical_compoundCrystallographychemistryPyridineMaterials ChemistryDensity functional theoryIridium0210 nano-technologyThiazole
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X-ray powder diffraction and LIESST-effect of the spin transition material [Fe(bpp)2](NCS)2·2H2O

2006

Abstract We have studied the X-ray powder diffraction of the spin transition material [Fe(bpp)2](NCS)2 · 2H2O (bpp: 2,6-bis(pyrazol-3-yl)pyridine) at room temperature. Two crystallographic phases have been observed depending on the sample history of this material. The results obtained corroborate the earlier observations from magnetic and calorimetric studies. Relatively prolonged exposure of the sample to X-rays caused a structural change. LIESST and Reverse-LIESST effects, characterised by 57Fe Mossbauer spectroscopy, have been observed in this material.

Materials scienceSAMPLE historySpin transitionX-rayGeneral Physics and AstronomyLIESSTchemistry.chemical_compoundCrystallographychemistryStructural changeMössbauer spectroscopyPyridinePhysical and Theoretical ChemistryPowder diffractionChemical Physics Letters
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Chemically Selective Imaging of Individual Bonds through Scanning Electron Energy-Loss Spectroscopy: Disulfide Bridges Linking Gold Nanoclusters

2020

As proof-of-principle of chemically selective, spatially resolved imaging of individual bonds, we carry out electron energy-loss spectroscopy in a scanning transmission electron microscopy instrument on atomically precise, thiolate-coated gold nanoclusters linked with 5,5'-bis(mercaptomethyl)-2,2'-bipyridine dithiol ligands. The images allow the identification of bridging disulfide bonds (R-S-S-R) between clusters, and X-ray photoelectron spectra support the finding.

Materials scienceScanning electron microscopeDisulfide bondDithiolElectronNanoclusterschemistry.chemical_compoundCrystallographyBipyridinechemistryScanning transmission electron microscopyGeneral Materials SciencePhysical and Theoretical ChemistrySpectroscopyThe Journal of Physical Chemistry Letters
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Anomalous Spin Transition Observed in Bis(2,6-bis(pyrazol-3-yl)pyridine)iron(II) Thiocyanate Dihydrate

2003

Bis(2,6-bis(pyrazol-3-yl)pyridine)iron(II) thiocyanate dihydrate undergoes a two-step singlet (1A1) ⇄ quintet (5T2) transition in which both steps are associated with thermal hysteresis. Thermal cycling of the sample results in its conversion to a second phase which displays a single-step transition with a very narrow hysteresis loop. This second phase slowly reverts to the initial phase on standing at 300 K. The interconversions are completely reversible. The spin state changes have been monitored by measurement of magnetism and Mossbauer spectra and by differential scanning calorimetry (DSC) studies.

Materials scienceSpin statesThiocyanateInorganic chemistrySpin transitionCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundCrystallographyDifferential scanning calorimetrychemistryPhase (matter)Mössbauer spectroscopyPyridineElectrochemistrySinglet stateAdvanced Functional Materials
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Luminescent copper(i) complexes with bisphosphane and halogen-substituted 2,2′-bipyridine ligands

2018

Heteroleptic [Cu(P^P)(N^N)][PF6] complexes, where N^N is a halo-substituted 2,2'-bipyridine (bpy) and P^P is either bis(2-(diphenylphosphino)phenyl)ether (POP) or 4,5-bis(diphenylphosphino)-9,9- dimethylxanthene (xantphos) have been synthesized and investigated. To stabilize the tetrahedral geometry of the copper(I) complexes, the steric demands of the bpy ligands have been increased by introducing 6- or 6,6'-halo-substituents in 6,6'-dichloro-2,2'-bipyridine (6,6'-Cl2bpy), 6-bromo-2,2'- bipyridine (6-Brbpy) and 6,6'-dibromo-2,2'-bipyridine (6,6'-Br2bpy). The solid-state structures of [Cu(POP)(6,6'-Cl2bpy)][PF6], [Cu(xantphos)(6,6'-Cl2bpy)][PF6].CH2Cl2, [Cu(POP)(6-Brbpy)][PF6] and [Cu(xantp…

Materials scienceXantphosF100F200Tetrahedral molecular geometrychemistry.chemical_element02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCopper22'-Bipyridine0104 chemical sciencesInorganic ChemistryCrystallographyBipyridinechemistry.chemical_compoundchemistryDensity functional theoryTriplet state0210 nano-technologySingle crystalDalton Transactions
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Distinct effects of atypical 1,4-dihydropyridines on 1-methyl-4-phenylpyridinium-induced toxicity.

2006

Our previous data obtained from in vivo experiments demonstrated high neuroprotective effects of three novel atypical neuronal non-calcium antagonistic 1,4-dihydropyridine (DHP) derivatives cerebrocrast, glutapyrone and tauropyrone. The present studies were carried out in vitro to clarify, at least in part, their mechanism of action in primary culture of cerebellar granule cells by use of 1-methyl-4-phenylpyridinium (MPP+) as a neurotoxic agent which causes dramatic oxidative stress. Cerebrocrast (highly lipophilic, with a classical two-ring structure) dose-dependently (0.01-10.0 microM, EC50 = 13 nM) reduced MPP+-induced cell death. At the same time, the calcium antagonist nimodipine (refe…

Membrane potentialNeurons1-Methyl-4-phenylpyridiniumDihydropyridinesCell DeathMolecular Structure1-Methyl-4-phenylpyridiniumClinical BiochemistryCell BiologyGeneral MedicineMitochondrionPharmacologyBiologymedicine.disease_causeBiochemistryNeuroprotectionMechanism of actionmedicinemedicine.symptomMode of actionReactive Oxygen SpeciesOxidative stressIntracellularCells CulturedCell biochemistry and function
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Novel 1H-pyrrolo[2,3-b]pyridine derivative nortopsentin analogues: synthesis and antitumor activity in peritoneal mesothelioma experimental models.

2013

In this study, we describe the synthesis of new nortopsentin analogues, 1H-pyrrolo[2,3-b]pyridine derivatives and their biological effects in experimental models of diffuse malignant peritoneal mesothelioma (DMPM), a rare and rapidly fatal disease, poorly responsive to conventional therapies. The three most active compounds, 1f (3-[2-(5-fluoro-1-methyl-1H-indol-3-yl)-1,3-thiazol-4-yl]-1H-pyrrolo[2,3-b]pyridine), 3f (3-[2-(1H-indol-3-yl)-1,3-thiazol-4-yl]-1-methyl-1H-pyrrolo[2,3-b]pyridine), and 1l (3-[2-(5-fluoro-1-methyl-1H-indol-3-yl)-1,3-thiazol-4-yl]-1-methyl-1H-pyrrolo[2,3-b] pyridine), which were shown to act as cyclin-dependent kinase 1 inhibitors, consistently reduced DMPM cell prol…

MesotheliomaMagnetic Resonance SpectroscopyCell growthKinasePyridinesAntineoplastic AgentsPharmacologyCell Linechemistry.chemical_compoundchemistryPaclitaxelApoptosisCell cultureDrug DiscoveryPyridineSurvivinMolecular MedicineCytotoxic T cellHumansSpectrophotometry UltravioletPeritoneal NeoplasmsJournal of medicinal chemistry
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Metallogel formation in aqueous DMSO by perfluoroalkyl decorated terpyridine ligands.

2016

Terpyridine based ligands 1 and 2, decorated with a C8F17 perfluorinated tag, are able to form stable thermoreversible gels in the presence of several d-block metal chloride salts. The gel systems obtained have been characterized by NMR, X-ray diffraction, electron microscopies and Tgel experiments in order to gain insights into the observed different behaviour of the two similar ligands, also in terms of the effect of additional common anionic species. peerReviewed

Metal chlorideAqueous solutiongelation capabilitiesligands02 engineering and technologyligandit010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundchemistrymetallogel formationPolymer chemistryOrganic chemistryTerpyridine0210 nano-technologyDMSOta116Dalton transactions (Cambridge, England : 2003)
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