Search results for "Inorganic Chemical"

showing 10 items of 491 documents

TAP reactor study of the deep oxidation of propane using cobalt oxide and gold-containing cobalt oxide catalysts

2009

Abstract A transient reactor study of the oxidation of propane to CO 2 on gold-free and gold-doped CoO x catalysts has been carried out. It has been demonstrated that the presence of gold markedly promotes the catalytic reactivity of cobalt oxide in the total oxidation of propane. Both catalysts oxidised propane directly to CO 2 via a Mars–Van Krevelen mechanism, and this was confirmed using isotopically labelled oxygen experiments. The increased activity of the gold catalyst is related to the faster reoxidation of the cobalt oxide when gold is present in the catalyst, since the reaction step in which the catalyst is reduced, due to propane oxidation, is similar for both catalysts. The fast…

inorganic chemicalsChemistryorganic chemicalsProcess Chemistry and TechnologyCatalyst supportInorganic chemistrychemistry.chemical_elementHeterogeneous catalysisOxygenCatalysisCatalysischemistry.chemical_compoundCatalytic oxidationTransition metalPropaneheterocyclic compoundsCobalt oxideApplied Catalysis A: General
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Halogen bonding and host-guest chemistry between

2019

Single crystal X-ray structures of halogen-bonded assemblies formed between host N-hexylammonium resorcinarene bromide (1) or N-cyclohexylammonium resorcinarene chloride (2), and 1,4-diiodooctafluorobutane and accompanying small solvent guests (methanol, acetonitrile and water) are presented. The guests’ inclusion affects the geometry of the cavity of the receptors 1 and 2, while the divalent halogen bond donor 1,4-diiodooctafluorobutane determines the overall nature of the halogen bond assembly. The crystal lattice of 1 contains two structurally different dimeric assemblies A and B, formally resulting in the mixture of a capsular dimer and a dimeric pseudo-capsule. 1H and 19F NMR analyses …

inorganic chemicalsChemistryresorcinarene saltshalogen bondingcapsuleOrganic Chemistryhost–guest chemistryFull Research Paperdimeric assembliesX-ray crystallographyBeilstein journal of organic chemistry
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Incorporation of dynamic boronate links and Ag nanoparticles into PVA hydrogels for pH-Regulated and prolonged release of methotrexate

2021

Abstract In this study, pH-responsive hydrogels based on PVA-boronate crosslinks were prepared via a simple route and used for controlled and targeted delivery of anticancer drug methotrexate. A double network (DN) hydrogel composed of didiol-boronate/PVA complex as the first network and PVA crystallites generated by a freeze-thaw process as the second one was developed. The swelling of PVA-boronate DN hydrogels demonstrated high sensitivity to multiple stimuli including the pH, temperature, and ionic strength of the media thanks to the dynamic boronate links in the first network. Moreover, unlike previously reported hydrogels based on the boronate linkages, the new DN hydrogels preserved t…

inorganic chemicalsChemistrytechnology industry and agricultureCancer therapyPharmaceutical ScienceAg nanoparticlesmacromolecular substances02 engineering and technology021001 nanoscience & nanotechnologycomplex mixtures030226 pharmacology & pharmacyAnticancer drug03 medical and health sciences0302 clinical medicineChemical engineeringProlonged releaseIonic strengthSelf-healing hydrogelsmedicineMethotrexateSwellingmedicine.symptom0210 nano-technologymedicine.drugJournal of Drug Delivery Science and Technology
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Crystal structure of a CsF-uranyl-salen complex. An unusual cesium-chlorine coordination.

2006

Complexation of CsF with the ditopic uranyl-salen receptor results in a solid-state structure, in which the coordination sphere of cesium is filled by ligation to one of the chlorine atoms of the solvent chloroform. This X-ray structure is the first example of chloroform ligation to an alkali-metal ion.

inorganic chemicalsChloroformCoordination sphereInorganic chemistrychemistry.chemical_elementCrystal structureUranylIonInorganic ChemistrySolventchemistry.chemical_compoundchemistryCaesiumPolymer chemistryChlorinePhysical and Theoretical ChemistryInorganic chemistry
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Redox modulation of Rubisco conformation and activity through its cysteine residues

2008

Treatment of purified Rubisco with agents that specifically oxidize cysteine-thiol groups causes catalytic inactivation and increased proteolytic sensitivity of the enzyme. It has been suggested that these redox properties may sustain a mechanism of regulating Rubisco activity and turnover during senescence or stress. Current research efforts are addressing the structural basis of the redox modulation of Rubisco and the identification of critical cysteines. Redox shifts result in Rubisco conformational changes as revealed by the alteration of its proteolytic fragmentation pattern upon oxidation. In particular, the augmented susceptibility of Rubisco to proteases is due to increased exposure…

inorganic chemicalsChloroplastsbiologyPhysiologyCatabolismCysteamineRibulose-Bisphosphate CarboxylasefungiRuBisCOMutagenesisfood and beveragesChlamydomonas reinhardtiiPlant ScienceOxidative phosphorylationPlantsbiology.organism_classificationRedoxChloroplastBiochemistryPlant Cellsbiology.proteinAmino Acid SequenceOxidation-ReductionCysteineJournal of Experimental Botany
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Chiral cyclohexane based fluorescent chemosensors for enantiomeric discrimination of aspartate

2008

Some new chiral cyclohexyl based fluorescent anion receptors have been synthesized and their absolute configuration has been determined by using circular dichroism (CD). Complexation experiments have been carried out with several dicarboxylates, and stoichiometries and complexation constants for the corresponding complexes have been determined. The chiral discrimination ability of these ligands for chiral dicarboxylates has been studied and the best results have been obtained with TMA aspartate.

inorganic chemicalsCircular dichroismCyclohexaneChemistryStereochemistryorganic chemicalsOrganic ChemistryAbsolute configurationBiochemistryFluorescenceIonCrystallographychemistry.chemical_compoundDrug Discoveryhealth occupationspolycyclic compoundsheterocyclic compoundsEnantiomerStoichiometryTetrahedron
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Characterization of gas flow through low-permeability claystone: laboratory experiments and two-phase flow analyses

2014

For the characterization of gas migration through a low-permeability clay host rock for deep underground repositories, a comprehensive understanding of the relevant phenomena of gas and fluid flow through low-permeability clay is required. The National Cooperative for the Disposal of Radioactive Waste (Nagra) in Switzerland has developed a comprehensive programme to characterize gas flow in low-permeability Opalinus Clay through laboratory tests and detailed numerical analyses for developing appropriate constitutive models. Laboratory tests were performed on cores by two different laboratories, the Laboratory for Soil Mechanics at EPFL and the Department of Geotechnical Engineering and Geos…

inorganic chemicalsClay soilsGeologyOcean EngineeringSòls argilososOverburden pressurecomplex mixturesGas flowPermeability (earth sciences)Void ratioBedFluid dynamicsCompressibilityGeotechnical engineeringTwo-phase flow:Enginyeria civil::Geotècnia::Mecànica de sòls [Àrees temàtiques de la UPC]Soil mechanicsGeologyWater Science and Technology
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Analysis of the Cellular Roles of MOCS3 Identifies a MOCS3-Independent Localization of NFS1 at the Tips of the Centrosome

2019

The deficiency of the molybdenum cofactor (Moco) is an autosomal recessive disease, which leads to the loss of activity of all molybdoenzymes in humans with sulfite oxidase being the essential protein. Moco deficiency generally results in death in early childhood. Moco is a sulfur-containing cofactor synthesized in the cytosol with the sulfur being provided by a sulfur relay system composed of the L-cysteine desulfurase NFS1, MOCS3, and MOCS2A. Human MOCS3 is a dual-function protein that was shown to play an important role in Moco biosynthesis and in the mcm(5)s(2) U thio modifications of nucleosides in cytosolic tRNAs for Lys, Gln, and Glu. In this study, we constructed a homozygous MOCS3 …

inorganic chemicalsCoenzymesBiochemistry03 medical and health scienceschemistry.chemical_compoundRNA Transferddc:570Sulfite oxidaseMetalloproteinsHumansnatural sciencesInstitut für Biochemie und BiologieAconitate HydrataseCentrosome0303 health sciencesPteridinesSulfite Oxidase030302 biochemistry & molecular biologyNucleotidyltransferasesIsocitrate DehydrogenaseCell biologyCarbon-Sulfur LyasesHEK293 CellschemistryCentrosomeSulfurtransferasesbacteriaCRISPR-Cas SystemsMolybdenum cofactorMolybdenum CofactorsHeLa CellsBiochemistry
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Phosphorylation of the Goodpasture antigen by type A protein kinases.

1995

Collagen IV is the major component of basement membranes. The human alpha 3 chain of collagen IV contains an antigenic domain called the Goodpasture antigen that is the target for the circulating immunopathogenic antibodies present in patients with Goodpasture syndrome. Characteristically, the gene region encoding the Goodpasture antigen generates multiple alternative products that retain the antigen amino-terminal region with a five-residue motif (KRGDS). The serine therein appears to be the major in vitro cAMP-dependent protein kinase phosphorylation site in the isolated antigen and can be phosphorylated in vitro by two protein kinases of approximately 50 and 41 kDa associated with human …

inorganic chemicalsCollagen Type IVAnti-Glomerular Basement Membrane DiseaseMolecular Sequence DataBiochemistryAutoantigensSerineAntigenmedicineSerineGoodpasture syndromeHumansAmino Acid SequencePhosphorylationProtein kinase AMolecular BiologyBasement membranebiologyBase SequenceKinaseCell Biologymedicine.diseaseMolecular biologyCyclic AMP-Dependent Protein Kinasesenzymes and coenzymes (carbohydrates)medicine.anatomical_structureOligodeoxyribonucleotidesbiology.proteinPhosphorylationCollagenAntibodyThe Journal of biological chemistry
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A new general fragmentation reaction in mass spectrometry: The hydrogen-carbon, carbon-carbon double rearrangement of 2 heteroalkyl substituted diphe…

1995

Diphenylmethyl cations formed by benzylic cleavage of the molecular ions of ortho heteroalkyl substituted 1,1-diphenylalkanes undergo the double rearrangement process (H to C followed by C to C) previously reported for ortho-methoxy derivatives. Hence the formation of substituted benzyl (or tropylium) ions allowing this double rearrangement process constitutes an interesting type of fragmentation reaction characteristic for 1,1-diphenylalkanes bearing ortho substituents (OMe, OEt, OiPr, SMe, NHMe, NMe2) which are able to transfer a hydride to the charged benzyl carbon of diphenylmethyl cations formed by benzylic cleavage of the molecular ion.

inorganic chemicalsCollision-induced dissociationHydrogenChemistryHydrideorganic chemicalsPolyatomic ionReinforced carbon–carbonAnalytical chemistrychemistry.chemical_elementMass spectrometryMedicinal chemistryIonFragmentation (mass spectrometry)heterocyclic compoundsSpectroscopyEuropean Journal of Mass Spectrometry
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