Search results for "Iodide"

showing 10 items of 405 documents

CCDC 774615: Experimental Crystal Structure Determination

2011

Related Article: M.Muller, M.Albrecht, V.Gossen, T.Peters, A.Hoffmann, G.Raabe, A.Valkonen, K.Rissanen|2010|Chem.-Eur.J.|16|12446|doi:10.1002/chem.201001534

bis(Dibenzyl(pentafluorophenylmethyl)ammonium) hemikis(tetraiodide) tri-iodide toluene solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 143351: Experimental Crystal Structure Determination

2001

Related Article: O.Blacque, H.Brunner, M.M.Kubicki, F.Leis, D.Lucas, Y.Mugnier, B.Nuber, J.Wachter|2001|Chem.-Eur.J.|7|1342|doi:10.1002/1521-3765(20010316)7:6<1342::AID-CHEM1342>3.0.CO;2-D

bis(mu~2~-1-Arsa-2-selenaethane)-bis(eta^5^-pentamethyl-cyclopentadienyl)-di-iron iodideSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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The “green” electrochemical synthesis of periodate

2020

Abstract High‐grade periodate is relatively expensive, but is required for many sensitive applications such as the synthesis of active pharmaceutical ingredients. These high costs originate from using lead dioxide anodes in contemporary electrochemical methods and from expensive starting materials. A direct and cost‐efficient electrochemical synthesis of periodate from iodide, which is less costly and relies on a readily available starting material, is reported. The oxidation is conducted at boron‐doped diamond anodes, which are durable, metal‐free, and nontoxic. The avoidance of lead dioxide ultimately lowers the cost of purification and quality assurance. The electrolytic process was opti…

boron-doped diamond540 Chemistry and allied sciencesMaterials scienceflow chemistryoxidationIodideLead dioxideElectrolysis | Hot Paper010402 general chemistryElectrochemistry01 natural sciencesCatalysislaw.inventionchemistry.chemical_compoundlawelectrolysisElectrolytic processIodatechemistry.chemical_classificationElectrolysis010405 organic chemistryCommunicationPeriodateGeneral ChemistryFlow chemistryCombinatorial chemistryCommunications0104 chemical sciencesperiodatechemistry540 Chemie
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Selenium: A Cure for Autoimmune Thyroiditis.

2021

Autoimmune thyroiditis (AT) is a disease whose incidence has increased dramatically over the past few decades. In iodine sufficient areas, this pathological condition affects up to 5% of the general population. The higher incidence of AT observed in areas of the world with low-selenium (Se) soils apperas to be the consequence of a reduced activity of the intracellular Sedependent glutathione peroxidase activity. Se is involved, through selenoproteins, in the regulation of intracellular antioxidant, redox and anti-inflammatory processes. As a component of selenoproteins, Se exerts various structural and enzymatic functions. A low Se/high fat diet can cause selenoprotein changes and promote t…

business.industryEndocrinology Diabetes and MetabolismThyroiditis Autoimmunechemistry.chemical_elementHashimoto Diseasemedicine.diseaseIodide PeroxidaseAutoimmune thyroiditisSeleniumchemistryImmunologyImmunology and AllergyMedicineHumansSettore MED/49 - Scienze Tecniche Dietetiche ApplicatebusinessSelenium autoimmune thyroiditis redox balanceSeleniumEndocrine, metabolicimmune disorders drug targets
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Active caspase-3 detection to evaluate apoptosis induced by Verbena officinalis essential oil and citral in chronic lymphocytic leukaemia cells

2011

Verbena officinalis L., Verbenaceae, commonly known as vervain, is a plant widely used in medicine. Despite of its widespread use in different traditional practices, the mechanisms of pharmacological actions of the plant and its volatile oil are still unclear. We evaluated the pro-apoptotic activity of V. officinalis essential oil and of its main component, citral, on lymphocytes collected from ten patients with chronic lymphocytic leukaemia (CLL), a disease in which a faulty apoptotic mechanism is still retained one of the primary pathogenic events, by adding to treated mononuclear cells, annexin-V, propidium iodide, and CD19. Apoptosis was also evaluated using anti-active-caspase-3 monocl…

caspase-3lcsh:RS1-441Caspase 3PharmacologyCitralCD19law.inventionlcsh:Pharmacy and materia medicachemistry.chemical_compoundlawhemic and lymphatic diseasesPropidium iodideGeneral Pharmacology Toxicology and PharmaceuticscitralEssential oilbiologyflow cytometryVerbena officinalisapoptosisbiology.organism_classificationVerbena officinalisBiochemistrychemistryApoptosisOfficinalisbiology.proteinchronic lymphocytic leukaemiaRevista Brasileira de Farmacognosia
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CCDC 1425262: Experimental Crystal Structure Determination

2016

Related Article: T. Mäkelä, K. Rissanen|2016|Dalton Trans.|45|6481|doi:10.1039/C6DT00414H

catena-((mu2-11'-(2356891112-Octahydro-1471013-benzopentaoxacyclopentadecine-1516-diyl)bis(3-(4-nitrophenyl)urea))-sodium iodide acetone solvate hemihydrate)Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1478713: Experimental Crystal Structure Determination

2016

Related Article: Toni Mäkelä, Anniina Kiesilä, Elina Kalenius and Kari Rissanen|2016|Chem.-Eur.J.|22|14264|doi:10.1002/chem.201602362

catena-[11'1''-(17-(((4-(oxy(oxido)-azanyl)phenyl)carbamoyl)amino)-679101213202123242627-dodecahydrodibenzo[bn][1471013161922]octaoxacyclotetracosine-2316-triyl)tris(3-(4-nitrophenyl)urea)-rubidium iodide chloroform solvate]Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Reaction of LiArMe6 (ArMe6= C6H3-2,6-(C6H2-2,4,6-Me3)2) with indium(I)chloride yields three m-terphenyl stabilized mixed-valent organoindium subhalid…

2016

Abstract Indium(I)chloride reacts with LiAr Me 6 ( Ar Me 6  = C6H3-2,6-(C6H2-2,4,6-Me3)2) in THF to give three new mixed-valent organoindium subhalides. While the 1:1 reaction of InCl with LiAr Me 6 yields the known metal-rich cluster In8( Ar Me 6 )4 (1), the use of freshly prepared LiAr Me 6 led to incorporation of iodide, derived from the synthesis of LiAr Me 6 , into the structures, to afford In4( Ar Me 6 )4I2 (2) along with minor amounts of In3( Ar Me 6 )3I2 (3). When the same reaction was performed in 4:3 stoichiometry, the mixed-halide compound In3( Ar Me 6 )3ClI (4) was obtained. Further increasing the chloride:aryl ligand ratio resulted in the formation of the known mixed-halide spe…

chemistry.chemical_classification010405 organic chemistryArylIodideInfrared spectroscopychemistry.chemical_element010402 general chemistry01 natural sciencesChloride0104 chemical sciencesInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryComputational chemistryTerphenylX-ray crystallographyMaterials ChemistrymedicinePhysical and Theoretical ChemistryStoichiometryIndiummedicine.drugPolyhedron
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Ion pair complexes and anion binding in the solution of a ditopic receptor.

2016

The synthesis and crystal structures with alkali halides of a ditopic benzo-15-crown-5 bis-urea receptor have been presented. In addition, the anion binding properties of and its alkali metal complexes in solution are presented. A comprehensive single-crystal X-ray crystallographic study of , all together 13 crystal structures, including the ion pair complexes with NaCl, NaBr, NaI, KF, KCl, KBr, KI, RbF, RbCl, and RbI, give a detailed view of how behaves in the solid-state with different alkali halides depending on the size of the cation and anion. In the solid-state forms a 1 : 1 complex with a sodium cation and the anion is complexed as a contact (NaCl) or a separate ion pair (NaBr, NaI).…

chemistry.chemical_classification010405 organic chemistryInorganic chemistryIodidechemistry.chemical_elementHalide010402 general chemistryAlkali metal01 natural sciencesChlorideditopic receptors0104 chemical sciencesRubidiumIonanion bindingInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryBromidemedicineion pair complexesAnion bindingta116medicine.drugDalton transactions (Cambridge, England : 2003)
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On Demand One-Pot Mild Preparation of Layered Double Hydroxides and Their Hybrid Forms: Advances through the Epoxide Route.

2019

Epoxide ring opening driven alkalinization process was explored with the aim of preparing layered double hydroxide (LDH) phases on demand, at room temperature. Employing iodide as nucleophilic agent, the precipitation reaction can be driven under much lower halide concentrations. This scenario favors the selective intercalation of concomitant bulky oxo anions as nitrate or perchlorate in the LDH products, allowing for the one-pot synthesis of an LDH able to delaminate in formamide. Even large dicarboxylic acids, - O2 C-(CH2 )n -CO2 - , with n up to 8, can be quantitively intercalated within the growing LDH phase, providing a versatile one-pot route for hybrid LDHs as well. Under the mild co…

chemistry.chemical_classification010405 organic chemistryOrganic ChemistryIntercalation (chemistry)IodideCationic polymerizationLayered double hydroxidesEpoxideGeneral Chemistryengineering.material010402 general chemistry01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundPerchloratechemistryPolymer chemistryengineeringHydroxideSolubilityChemistry (Weinheim an der Bergstrasse, Germany)
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