Search results for "Thiol"

showing 10 items of 485 documents

Oktakarboksyftalocyjaniny jako katalizatory utleniania związków siarki

2007

Zbadano aktywność katalityczną oktakarboksyftalocyjaniny kobaltu (CoPcOC), żelaza (FePcOC) i miedzi (CuPcOC) w aerobowym utlenianiu 2-tioetanolu, siarczku sodu i L-cysteiny. Kompleksy kobaltu i żelaza okazały się efektywnymi katalizatorami homofazowymi tych reakcji. Na aktywność katalityczną wpływ mają takie czynniki, jak rodzaj skompleksowanego metalu, pH, asocjacja ftalocyjanin w roztworze.

siarczkioctacarboxyphthalocyaninessulfideskatalityczne utlenianietioleoktakarboksyftalocyjaninythiolscatalytic oxidationEcological Chemistry and Engineering. S = Chemia i Inżynieria Ekologiczna. S
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Total Structure and Electronic Structure Analysis of Doped Thiolated Silver [MAg24(SR)18]2– (M = Pd, Pt) Clusters

2015

With the incorporation of Pd or Pt atoms, thiolated Ag-rich 25-metal-atom nanoclusters were successfully prepared and structurally characterized for the first time. With a composition of [PdAg24(SR)18](2-) or [PtAg24(SR)18](2-), the obtained 25-metal-atom nanoclusters have a metal framework structure similar to that of widely investigated Au25(SR)18. In both clusters, a M@Ag12 (M = Pd, Pt) core is capped by six distorted dimeric -RS-Ag-SR-Ag-SR- units. However, the silver-thiolate overlayer gives rise to a geometric chirality at variance to Au25(SR)18. The effect of doping on the electronic structure was studied through measured optical absorption spectra and ab initio analysis. This work d…

ta114ChemistryStereochemistryDopingAb initioGeneral ChemistryElectronic structureengineering.materialpalladiumBiochemistryCatalysissilver nanoclustersNanoclustersCatalysisOverlayerCrystallographyColloid and Surface ChemistryengineeringNoble metalplatinumChirality (chemistry)ta116thiolsJournal of the American Chemical Society
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A Unified AMBER-Compatible Molecular Mechanics Force Field for Thiolate-Protected Gold Nanoclusters.

2016

We present transferable AMBER-compatible force field parameters for thiolate-protected gold nanoclusters. Five different sized clusters containing both organo-soluble and water-soluble thiolate ligands served as test systems in MD simulations, and parameters were validated against DFT and experimental results. The cluster geometries remain intact during the MD simulations in various solvents, and structural fluctuations and energetics showed agreement with DFT calculations. Experimental diffusion coefficients and crystal structures were also reproduced with sufficient accuracy. The presented parameter set contains the minimum number of cluster-specific parameters enabling the use of these p…

ta114Chemistrythiolate ligands02 engineering and technologyCrystal structure010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesMolecular mechanicsForce field (chemistry)0104 chemical sciencesComputer Science ApplicationsNanoclustersComputational chemistryChemical physicsCluster (physics)Physical and Theoretical Chemistry0210 nano-technologyta116gold nanoclustersJournal of chemical theory and computation
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CCDC 953879: Experimental Crystal Structure Determination

2013

Related Article: Huayan Yang, Yu Wang, Huaqi Huang, Lars Gell, Lauri Lehtovaara, Sami Malola, Hannu Hakkinen, Nanfeng Zheng|2013|Nat.Commun.|4|2422|doi:10.1038/ncomms3422

tetrakis(Tetraphenylphosphonium) tetracosakis(mu3-34-difluorobenzenethiolato)-hexakis(mu2-34-difluorobenzenethiolato)-dodeca-gold-dotriaconta-silver dichloromethane solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 953883: Experimental Crystal Structure Determination

2013

Related Article: Huayan Yang, Yu Wang, Huaqi Huang, Lars Gell, Lauri Lehtovaara, Sami Malola, Hannu Hakkinen, Nanfeng Zheng|2013|Nat.Commun.|4|2422|doi:10.1038/ncomms3422

tetrakis(Tetraphenylphosphonium) tetracosakis(mu~3~-4-(trifluoromethyl)benzenethiolato)-hexakis(mu~2~-4-(trifluoromethyl)benzenethiolato)-dodeca-gold-dotriaconta-silverSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1020496: Experimental Crystal Structure Determination

2014

Related Article: Huayan Yang , Yu Wang , Juanzhu Yan , Xi Chen , Xin Zhang , Hannu Häkkinen , and Nanfeng Zheng|2014|J.Am.Chem.Soc.|136|7197|doi:10.1021/ja501811j

tetrakis(tetraphenylphosphonium) icosakis(mu-4-(trifluoromethyl)benzenethiolato)-trideca-gold-dodeca-copper dichloromethane solvate tetrahydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Protein tyrosine nitration and thiol oxidation by peroxynitrite-strategies to prevent these oxidative modifications.

2013

The reaction product of nitric oxide and superoxide, peroxynitrite, is a potent biological oxidant. The most important oxidative protein modifications described for peroxynitrite are cysteine-thiol oxidation and tyrosine nitration. We have previously demonstrated that intrinsic heme-thiolate (P450)-dependent enzymatic catalysis increases the nitration of tyrosine 430 in prostacyclin synthase and results in loss of activity which contributes to endothelial dysfunction. We here report the sensitive peroxynitrite-dependent nitration of an over-expressed and partially purified human prostacyclin synthase (3.3 μM) with an EC50 value of 5 μM. Microsomal thiols in these preparations effectively co…

thiol oxidationprotein tyrosine nitrationlcsh:Chemistrychemistry.chemical_compoundCytochrome P-450 Enzyme SystemSf9 CellsTyrosinelcsh:QH301-705.5Spectroscopychemistry.chemical_classification0303 health sciencesbiologySuperoxide030302 biochemistry & molecular biologyGeneral MedicineComputer Science ApplicationsIntramolecular OxidoreductasesBiochemistryThiolprostacyclin synthasesuperoxideOxidation-ReductionPeroxynitriteOxidative phosphorylationSpodopteraCatalysisArticleperoxynitriteNitric oxideProstacyclin synthaseInorganic Chemistry03 medical and health sciencesnitric oxideddc:570NitrationPeroxynitrous AcidAnimalsHumansSulfhydryl CompoundsPhysical and Theoretical ChemistryMolecular Biology030304 developmental biologyOrganic Chemistrynitric oxide; superoxide; peroxynitrite; protein tyrosine nitration; thiol oxidation; peroxynitrite scavengers; prostacyclin synthasechemistrylcsh:Biology (General)lcsh:QD1-999biology.proteinTyrosineCattleperoxynitrite scavengersProtein Processing Post-TranslationalInternational journal of molecular sciences
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MODIFICATION OF HYDROPHOBIC SURFACE WITH POLYASPARTAMIDE-BASED POLYCATIONS FOR BIOMEDICAL APPLICATION

2013

A convenient way for the achievement of polymer-based solid materials for specific biomedical applications is grafting the appropriate macromolecules onto the surfaces in order to confer them specific properties. To date many approaches have been used to covalently modify polymeric surfaces, and among them chemoselective coupling reactions, usually referred as “click” reactions, gained much attention thanks to simple procedure with high reaction rate under mild reaction conditions (at normal temperature and pressure) [1]. In particular, radical-initiated thiol-yne “photo-click” chemistry has been demonstrated as an effective way to functionalize efficiently surfaces. This method gives also …

thiol-yne click reactionPHEA; lipoic acid; antibacterial PLA surfaces; thiol-yne click reaction.antibacterial PLA surfacesSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoPHEA lipoic acid antibacterial PLA surfaces thiol-yne click reaction.PHEAlipoic acid
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Deposition of tin sulfide thin films from tin(iv) thiolate precursors

2001

AACVD (aerosol-assisted chemical vapour deposition) using (PhS)(4)Sn as precursor leads to the deposition of Sn3O4 in the absence of H2S and tin sulfides when H2S is used as co-reactant. At 450 degreesC the film deposited consists of mainly SnS2 while at 500 degreesC SnS is the dominant component. The mechanism of decomposition of (PhS)(4)Sn is discussed and the structure of the precursor presented.

tin sulfidestin thiolatesMössbauer spectroscopybusiness.industryChemistryInorganic chemistrychemistry.chemical_elementGeneral ChemistryChemical vapor depositionDecompositionSemiconductorchemical vapour depositionSettore CHIM/03 - Chimica Generale E InorganicaX-ray crystallographyMaterials ChemistryThin filmbusinessElectronic band structureTinDeposition (chemistry)thermal decompositionJournal of Materials Chemistry
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CCDC 996582: Experimental Crystal Structure Determination

2014

Related Article: Matteo Atzori, Flavia Pop, Pascale Auban-Senzier, Carlos J. Gómez-García , Enric Canadell, Flavia Artizzu, Angela Serpe, Paola Deplano, Narcis Avarvari, and Maria Laura Mercuri|2014|Inorg.Chem.|53|7028|doi:10.1021/ic501001r

tris(2-(56-Dihydro[13]dithiolo[45-b][14]dithiin-2-ylidene)-56-dihydro[13]dithiolo[45-b][14]dithiin-1-ium) tris(36-dichloro-45-dioxocyclohexa-26-diene-12-diolato)-iron(iii) dichloromethane solvate monohydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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