Search results for "thiourea"

showing 10 items of 96 documents

Thiourea Organocatalysts as Emerging Chiral Pollutants: En Route to Porphyrin-Based (Chir)Optical Sensing

2021

Environmental pollution with chiral organic compounds is an emerging problem requiring innovative sensing methods. Amino-functionalized thioureas, such as 2-(dimethylamino)cyclohexyl-(3,5-bis(trifluoromethyl)phenyl)thiourea (Takemoto’s catalyst), are widely used organocatalysts with virtually unknown environmental safety data. Ecotoxicity studies based on the Vibrio fischeri luminescence inhibition test reveal significant toxicity of Takemoto’s catalyst (EC50 = 7.9 mg/L) and its NH2-substituted analog (EC50 = 7.2–7.4 mg/L). The observed toxic effect was pronounced by the influence of the trifluoromethyl moiety. En route to the porphyrin-based chemosensing of Takemoto-type thioureas, their s…

Circular dichroismSupramolecular chemistrychiralitymonitorointiEnvironmental pollutionchiral amineVibrio fischeriQD415-436010402 general chemistryBiochemistry01 natural sciencesMedicinal chemistrysupramolecular chemistrybakteeritAnalytical Chemistry<i>Vibrio</i> <i>fischeri</i>chemistry.chemical_compoundkatalyytitrikkiyhdisteetsupramolekulaarinen kemiaMoiety[CHIM]Chemical Sciences[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical Chemistrythioureaorgaaniset yhdisteetchiral pollutantsTrifluoromethyl010405 organic chemistrytoxicityhost–guest bindingPorphyrin0104 chemical sciencesTakemoto’s catalystcircular dichroismekotoksikologiachemistryThiourea13. Climate action[SDV.TOX.ECO]Life Sciences [q-bio]/Toxicology/Ecotoxicology[SDE.BE]Environmental Sciences/Biodiversity and EcologyChirality (chemistry)porphyrinorganocatalyst
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Enantioselective sensing of dicarboxylates. Influence of the stoichiometry of the complexes on the sensing mechanism

2009

Two new cyclohexane-based thiourea chiral ligands have been synthesized in their enantiomerically pure forms. Both the ability of these ligands in the complexation of chiral dicarboxylates and their sensing properties have been studied. The influence of the stoichiometry of the formed complexes on the fluorescent properties of the systems has been established. The effect of additional substitution in the cyclohexyl moiety was considered by comparing the properties of the newly prepared ligands with those of similar compounds previously described.

CyclohexaneChemistryStereochemistryorganic chemicalsOrganic ChemistryEnantioselective synthesisFluorescenceCombinatorial chemistryCatalysisInorganic Chemistrychemistry.chemical_compoundThioureaMoietyheterocyclic compoundsPhysical and Theoretical ChemistryStoichiometryTetrahedron: Asymmetry
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Fluorescent Sensing of Maleate versus Fumarate by a Neutral Cyclohexane Based Thiourea Receptor.

2006

A new cyclohexyl based fluorescent anion receptor, is able to recognize maleate versus fumarate both as their TMA salts. Costero Nieto, Ana Maria, Ana.Costero@uv.es ; Colera Llavata, Manuel, Manuel.Colera@uv.es ; Gaviña Costero, Pablo, Pablo.Gavina@uv.es ; Gil Grau, Salvador, Salvador.Gil@uv.es

CyclohexaneUNESCO::QUÍMICAurologic and male genital diseases:QUÍMICA [UNESCO]Medicinal chemistryCatalysischemistry.chemical_compoundhemic and lymphatic diseasesNeutral cyclohexaneMaterials ChemistryFluorescentOrganic chemistryUNESCO::QUÍMICA::Química orgánicaReceptorneoplasmsAnion receptorThiourea receptorFumarateMaleate:QUÍMICA::Química orgánica [UNESCO]Metals and AlloysGeneral ChemistryGeneral MedicineFluorescenceSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsFluorescent ; Neutral cyclohexane ; Thiourea receptor ; Maleate ; FumarateThioureachemistryCeramics and CompositesChemInform
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Differences between cysteine and homocysteine in the induction of deoxyribose degradation and DNA damage.

2001

The effect of two naturally occurring thiols, such as cysteine and homocysteine, has been examined for their ability to induce deoxyribose degradation and DNA damage. Copper(II) ions have been added to incubation mixtures and oxygen consumption measurements have been performed in order to correlate the observed damaging effects with the rate of metal catalyzed thiol oxidation. Ascorbic acid plus copper has been used as a positive control of deoxyribose and DNA oxidation due to reactive oxygen species. Cysteine or homocysteine in the presence of copper ions induce the degradation of deoxyribose and the yield of 8-hydroxy-2'-deoxyguanosine (8-OHdG), although important differences are observed…

DNA damageAscorbic AcidThymus GlandBiochemistrySuperoxide dismutasechemistry.chemical_compoundOxygen ConsumptionPhysiology (medical)DeoxyguanosineAnimalsCysteineHomocysteineElectrophoresis Agar GelbiologyDeoxyriboseSuperoxide DismutaseThiourea8-Hydroxy-2'-deoxyguanosineDeoxyguanosineDNA oxidationAscorbic acidCatalasechemistryDeoxyriboseBiochemistry8-Hydroxy-2'-DeoxyguanosineSpectrophotometrybiology.proteinCattleReactive Oxygen SpeciesOxidation-ReductionCopperCysteineDNA DamageFree radical biologymedicine
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Synthesis, properties and crystal structure of bis(metiamide)bis(isothiocyanato)nickel(II)

1991

Abstract The crystal structure of Ni(metiamide)2(NCS)2 was determined by X-ray diffraction methods. Unlike cimetidine, which is a tridentate ligand, metiamide (C9H16N4S2): N-Methyl-N-[2-{(5-methylimidazol-4-yl)methylthio}ethyl]thiourea (which also possesses three potential donor sites) is bidentate, coordinated to the nickel atom through N(imidazole) and S(thioether) atoms. The S(thiourea) atom does not take part in the coordination; instead, the isothiocyanate ion is coordinated through nitrogen to the metal atom. The nickel atom lies on a centre of symmetry in an elongated octahedral environment: the nitrogen atoms occupy equatorial positions (NiN = 2.04 and 2.06 A) and S(thioether) atom…

DenticityHydrogen bondStereochemistrychemistry.chemical_elementCrystal structureInorganic ChemistryNickelchemistry.chemical_compoundCrystallographychemistryThioureaThioetherMaterials ChemistryImidazoleMoleculePhysical and Theoretical ChemistryPolyhedron
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Addition of thiourea and hydrochloric acid: Accurate nanogram level analysis of mercury in humic-rich natural waters by inductively coupled plasma ma…

2020

Abstract An analytical method was developed for the direct determination of total mercury in natural waters at low ng L−1 level by inductively coupled plasma mass spectrometry (ICP-MS). The presented method overcomes previously observed problems relating to poor spike recoveries by adding 0.12% thiourea in addition to 3% HCl to all samples and standards. The sample preparation is fast and easy to perform by the developed method since it requires only the addition of HCl and thiourea to the water samples. A very low instrument detection limit (0.4 ng L−1) was obtained without time-consuming preconcentration procedures. The accuracy and precision of the developed method were found excellent b…

Detection limitAccuracy and precisionChromatographyChemistry010401 analytical chemistrychemistry.chemical_elementHydrochloric acid02 engineering and technology021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesAnalytical ChemistryMercury (element)chemistry.chemical_compoundThioureaSample preparation0210 nano-technologyMethylmercuryInductively coupled plasma mass spectrometryTalanta
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Phenoloxidase-dependent cytotoxic mechanism in ascidian (Styela plicata) hemocytes active against erythrocytes and K562 tumor cells.

1997

The cytotoxic activity against rabbit erythrocytes (RE) and human K562 tumor cells by Styela plicata hemocytes was significantly related to the phenoloxidase (PO) which converts phenols to quinone and initiates the melanogenic pathway. The effector hemocyte population, separated in a Percoll density gradient band, enriched in a granulocyte type named "morula cells", was examined with RE in a hemocyte cytotoxic assay and plaque forming cell assay. Inhibition experiments with the copper chelating agents 1-phenyl-2-thiourea and tropolone, the substrate analogue sodium benzoate and sodium ascorbate support the notion that hemocyte cytotoxic activity is a PO-dependent mechanism. Treatments of he…

ErythrocytesHemocytesMonophenol MonooxygenaseCytotoxicitySettore BIO/05 - ZoologiaHemocyteHydrogen PeroxideTunicateCell FractionationNitric OxidePhenylthioureaTropoloneErythrocytePhenoloxidaseCentrifugation Density GradientTumor Cells CulturedAnimalsHumansQuinoneRabbitsUrochordataK562Settore BIO/06 - Anatomia Comparata E CitologiaReactive Oxygen SpeciesEuropean journal of cell biology
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The Se … Hal halogen bonding: Co-crystals of selenoureas with fluorinated organohalides

2021

Abstract Synthesis and structural characterization of binary co-crystals 1–4 is reported in the present paper. Selenourea and 1,1-dimethylselenourea were used as selenium-containing halogen bond (XB) acceptors and iodopentafluorobenzene (IPFB), 1,4-diiodotetrafluorobenzene (1,4-DIFB) and 1,4-dibromotetrafluorobenzene (1,4-DBrFB) as XB donors. A comparative analysis of the similar binary co-crystals of selenourea and thiourea with a halogen donor revealed that Se … Hal halogen bonds are up to 13.12% shorter than the sum of vdW radii, while in case of S … Hal halogen bonds this value is 11.4%. Therefore, selenium tends to form stronger bonds with halogens than sulfur does. Comparisons of XB i…

Halogen bondSelenoureachemistry.chemical_element02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesAcceptorSulfur0104 chemical sciencesElectronic Optical and Magnetic MaterialsInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryThioureaHalogenMaterials ChemistryCeramics and CompositesPhysical and Theoretical Chemistry0210 nano-technologySeleniumJournal of Solid State Chemistry
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Dithiametacyclophane mit Dreifachbindungen

1994

Dithiametacyclophanes with Triple Bonds Schemes 1 and 2 show the syntheses of dithia[8]metacyclo-phanes 4a-d and tetrathia[m.n]metacyclophanes 9, 10 by cyclization reactions applying the cesium effect. All these cyclophanes contain C—C triple bonds which influence the molecular dynamics; especially the halogen substituents in 4b-d obstruct the topomerization.

Inorganic ChemistryMolecular dynamicschemistry.chemical_compoundThioureaChemistryHalogenTriple bondm-XylenePhotochemistryMedicinal chemistryCyclophaneChemische Berichte
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Organocatalytic Enantioselective Synthesis of α-Hydroxyketones through a Friedel−Crafts Reaction of Naphthols and Activated Phenols with Aryl- and Al…

2016

[EN] An efficient organocatalytic asymmetric synthesis of alpha-hydroxyketones has been developed. Quinine-derived thiourea catalyzed the enantioselective Friedel Crafts alkylation of naphthols and activated phenols with aryl- and alkylglyoxal hydrates, providing the corresponding chiral alpha-hydroxyketones with high yields (up to 97%) and excellent enantioselectivities (up to 99% ee).

Intramolecular Cannizzaro reactionOne-pot synthesisAlkylation010402 general chemistry01 natural sciencesBiochemistryCatalysisReaccions químiqueschemistry.chemical_compound(R)-Alpha-Hydroxy ketonesCatàlisiCinchona alkaloidsHighly efficientStereoselective-SynthesisOrganic chemistryPhenolsPhysical and Theoretical ChemistryFriedel–Crafts reactionDynamic kinetic resolutionElectron-Rich phenols010405 organic chemistryArylOrganic ChemistryEnantioselective synthesisOne-Pot synthesis0104 chemical scienceschemistryThioureaCarbonyl-CompoundsFISICA APLICADAAsymmetric benzoin condensationQuímica orgànica
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