Search results for "Nitrophenol"

showing 10 items of 111 documents

CCDC 899064: Experimental Crystal Structure Determination

2012

Related Article: A.Valkonen, E.Kolehmainen, A.Grzegorska, B.Osmialowski, R.Gawinecki, K.Rissanen|2012|Acta Crystallogr.,Sect.C:Cryst.Struct.Commun.|68|o279|doi:10.1107/S0108270112025589

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters(E)-2-(([4-(diethylamino)phenyl]imino)methyl)-4-nitrophenolExperimental 3D Coordinates
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CCDC 1519434: Experimental Crystal Structure Determination

2017

Related Article: Arto Valkonen, Giuseppe M. Lombardo, Kari Rissanen, Francesco Punzo, Massimo Cametti|2017|Dalton Trans.|46|5240|doi:10.1039/C6DT04773D

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters(acetonitrile)-(22'-[12-phenylenebis(iminomethyl)]bis(4-nitrophenolato))-dioxo-uranium(vi)Experimental 3D Coordinates
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CCDC 1919134: Experimental Crystal Structure Determination

2020

Related Article: Julie Echaubard, Asmae Bousfiha, Mathieu Berthelot, Julien Roger, Paul Fleurat-Lessard, Hélène Cattey, Sophie Fournier, Charles H. Devillers, Dominique Lucas|2020|Eur.J.Inorg.Chem.|2020|551 |doi:10.1002/ejic.201900849

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersaqua-[515-bis(4-methylphenyl)-10-phenyl-20-(quinolin-8-yl)porphyrinato]-zinc 4-nitrophenolExperimental 3D Coordinates
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CCDC 855780: Experimental Crystal Structure Determination

2012

Related Article: K.Salorinne, E.Nauha, M.Nissinen|2012|Chem.Asian J.|7|809|doi:10.1002/asia.201100969

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersbis(mu~3~-281420-Tetraethyl-6121824-tetramethoxy-410:1622-bis(369-trithiaundecane-111-dioxy)calix(4)arene)-bis(246-trinitrophenolato)-bis(acetonitrile)-tetra-silver bis(246-trinitrophenolate) acetonitrile solvateExperimental 3D Coordinates
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CCDC 1555144: Experimental Crystal Structure Determination

2018

Related Article: Yann Bernhard, Philippe Richard, Richard A. Decréau|2018|Tetrahedron|74|1047|doi:10.1016/j.tet.2018.01.029

Space GroupCrystallographyCrystal SystemCrystal Structure[56781415161723242526-dodecafluoro-21120282930-hexaazaheptacyclo[19.6.1.1310.11219.049.01318.02227]triaconta-1(28)2468101214161820222426-tetradecaenato](4-nitrophenolato)boronCell ParametersExperimental 3D Coordinates
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CCDC 762043: Experimental Crystal Structure Determination

2011

Related Article: M.Clemente-Leon, E.Coronado, M.Lopez-Jorda|2010|Dalton Trans.|39|4903|doi:10.1039/c001067g

Space GroupCrystallographycatena-(bis((22'-(25811-Tetra-azadodeca-111-diene-112-diyl-N^2^N^5^N^8^N^11^)-bis(4-nitrophenolato-O))-iron) hexakis(mu~2~-oxalato)-di-chromium-di-manganese nitromethane solvate monohydrate)Crystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Reaction Rate Modeling in Cryoconcentrated Solutions: Alkaline Phosphatase Catalyzed DNPP Hydrolysis

2000

The hydrolysis of disodium p-nitrophenyl phosphate catalyzed by alkaline phosphatase was chosen as a model to study the kinetics of changes in frozen food products. The initial reaction rate was determined in concentrated sucrose solutions down to -24 degrees C, and the enzymatic characteristics K(M) and V(max) were calculated. The experimental data were compared to the kinetics predicted by assuming that the reaction was viscosity dependent. Indeed, an analysis of the enzymatic reaction demonstrated that both the diffusion of the substrate and the flexibility of the enzyme segments were controlled by the high viscosity of the media. When the temperature was too low for the viscosity to be …

StereochemistryChemistryHydrolysisDiffusionInorganic chemistryKineticsTemperatureSubstrate (chemistry)Concentration effectGeneral ChemistryAlkaline PhosphataseCatalysisCatalysisNitrophenolsSolutionsReaction rateViscosityOrganophosphorus CompoundsGeneral Agricultural and Biological SciencesGlass transitionJournal of Agricultural and Food Chemistry
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Synthesis and biological evaluation of 4-nitro-substituted 1, 3-diaryltriazenes as a novel class of potent antitumor agents

2011

Abstract We describe the synthesis and biological activity of a new class of 1,3-diaryltriazenes, namely 4-nitro-substituted 1,3-diaryltriazenes. Structure–activity relationship analysis reveals that 1,3-diaryltriazenes can be modified from inactive to highly cytotoxic compounds by the introduction of two nitro groups at the para positions of benzene rings and two additional electron-withdrawing groups (bromo, chloro, trifluoromethyl or fluoro substituents) at their ortho position. In order to increase the solubility of the modified compounds, we introduced various acyl groups to their triazene nitrogen. The results of LC-MS/MS analysis showed that N -acyltriazenes can be considered as prod…

StereochemistryNitro compoundAntineoplastic AgentsApoptosis1 ; 3-diaryltriazenes ; synthesis ; cytotoxicity ; ROS induction ; apoptosisChemical synthesisNitrophenolschemistry.chemical_compoundStructure-Activity RelationshipCell Line TumorDrug DiscoveryCytotoxic T cellHumansProdrugsTriazeneCell ProliferationPharmacologychemistry.chemical_classificationChemistryOrganic ChemistryBiological activityGeneral MedicineDNA NeoplasmProdrugEndoplasmic Reticulum StressIn vitroDrug Resistance NeoplasmNitroCisplatinTriazenesReactive Oxygen Species
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Synthesis, mechanical and thermal rheological properties of new gellan gum derivatives

2017

New derivatives of gellan gum (GG) were prepared by covalent attachment of octadecylamine (C18- NH2) to polysaccharide backbone via amide linkage by using bis(4-nitrophenyl) carbonate (4-NPBC) as a coupling agent. The effect of the alkyl chain grafted onto hydrophilic backbone of high molecular weight GG was investigated in terms of physicochemical properties and ability of new derivatives to form hydrogels. A series of hydrogels was obtained in solutions with different kind and concentration of ions and their stability and mechanical properties were evaluated. The obtained derivatives resulted soluble at temperature lower than starting GG and physicochemical properties of obtained hydrogel…

Thermal scanning rheologyCarbonateCarbonatesPhysical hydrogelsMechanical properties02 engineering and technology010402 general chemistryPolysaccharide01 natural sciencesBiochemistryGellan gumNitrophenolschemistry.chemical_compoundRheologyPhysical hydrogelStructural BiologyAmidePolymer chemistryThermalAminesMolecular BiologyAlkylAminechemistry.chemical_classificationScience & TechnologyNitrophenolTissue EngineeringChemistryPolysaccharides BacterialTemperatureOctadecylamineHydrogelsGeneral Medicine021001 nanoscience & nanotechnologyGellan gum0104 chemical sciences3. Good healthHydrogelCovalent bondSelf-healing hydrogels0210 nano-technologyRheologyMechanical propertie
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Degradation of 4-nitrophenol (4-NP) using Fe–TiO2 as a heterogeneous photo-Fenton catalyst

2010

Photocatalytic degradation of 4-nitrophenol was investigated using Fe-doped (1, 3, 5 and 8 wt.% Fe) TiO(2) catalysts under UV light irradiation in aqueous dispersions in the presence of H(2)O(2). Photocatalysts with the lowest Fe content (1%) showed a considerably better behavior with respect to the unloaded TiO(2) and the catalysts with higher Fe contents. Photocatalytic degradation was studied under different conditions such as amounts of 1% Fe-TiO(2) catalyst, H(2)O(2) dose and initial pH of 4-NP solution. The results indicated that about 67.53% total organic carbon of a solution containing 20 mg L(-1) 4-NP was removed at pH 6.17 by using 4.9 mM of H(2)O(2) and 0.4 g L(-1) of the catalys…

TitaniumPhotolysisEnvironmental EngineeringUltraviolet RaysIronHealth Toxicology and MutagenesisInorganic chemistry4-NitrophenolHydrogen PeroxidePollutionCatalysisHeterogeneous photocatalysis 4-Nitrophenol Fe–TiO2 photocatalystsCatalysisTitanium oxideNitrophenolschemistry.chemical_compoundchemistryTitanium dioxidePhotocatalysisEnvironmental ChemistryDegradation (geology)Hydrogen peroxideWaste Management and DisposalChemical decompositionJournal of Hazardous Materials
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