Search results for "Isomerization"

showing 10 items of 281 documents

Isomerization and increase in the antioxidant properties of lycopene from Momordica cochinchinensis (gac) by moderate heat treatment with UV-Vis spec…

2014

International audience; Momordica cochinchinensis (gac) is a plant rich in lycopene. This pigment tends to solubilize in oil and get damaged during extraction. The impact of heating on cis-isomerization of oil-free lycopene in hexane was studied at 50 and 80°C during 240min with UV-Vis spectrometry, DAD-HPLC and TEAC test. The initial all-trans-form isomerized to the 13-cis isomer more rapidly at 80°C. After this treatment, 16% of the lycopene compounds were in the 9-cis-form. This isomer triggered an increase in the antioxidant properties which was detectable from concentrations above 9% and resulted in a change from 2.4 to 3.7μmol Trolox equivalent. It is thus possible to increase the bio…

IsomerizationAntioxidantHot TemperatureMomordica cochinchinensismedicine.medical_treatmentExtractionMomordica cochinchinensis (gac)Heat treatmentAntioxidantsAnalytical Chemistrychemistry.chemical_compoundPigmentLycopeneIsomerismmedicineOrganic chemistry[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyMomordicaChromatographybiologyPlant ExtractsExtraction (chemistry)General MedicineMarkerbiology.organism_classificationCarotenoidsLycopeneHexanechemistrySpectrophotometryvisual_artNatural carotenoidsvisual_art.visual_art_mediumTroloxAntioxidantIsomerizationFood ScienceFood chemistry
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Tuneable Emission of Polyhedral Oligomeric Silsesquioxane Based Nanostructures that Self-Assemble in the Presence of Europium(III) Ions: Reversible t…

2020

[EN] Hybrid nanostructures with switchable and reversible "blue-red-green" emission were efficiently synthesized. These nanostructures comprise polyhedral oligomeric silsesquioxanes (POSS) that behave as a nanocage that can be functionalized with terpyridine-based organic ligands, which can be easily complexed with europium (III) ions. The complexes were characterized by UV-Vis and fluorescence spectroscopy and their stoichiometry was also confirmed by H-1 NMR spectroscopy. In the presence of the Eu(III) ions, the octafunctionalized nanocages self-assemble to form 3D architectures that display an intense red-emission, especially in the solid state. The presence of an alkenyl group bridging …

IsomerizationNanostructureMaterials scienceLuminescenceSilsesquioxanesSelf assemblechemistry.chemical_element010402 general chemistry01 natural sciencesisomerizationIonchemistry.chemical_compoundQUIMICA ORGANICAEuropiumPolymer chemistryluminescenceeuropium010405 organic chemistryself-assemblyGeneral ChemistrySelf-assemblySilsesquioxane0104 chemical sciencessilsesquioxaneschemistrySelf-assemblyLuminescenceEuropiumIsomerization
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A DFT mechanistic study of the synthesis of trans-Z,Z-[PtIICl(NH3){HN = C(NH2)Me}2]Cl from addition of NH3 to trans-[PtIICl2(N CMe)2]

2020

Abstract The reaction mechanism between trans-[PtIICl2(N CMe)2] and ammonia to give trans-Z,Z-[PtIICl(NH3){HN = C(NH2)Me}2]Cl has been studied at DFT level. Results showed that, in dichloromethane solution at 263.15 K, the chloride substitution by the ammonia on platinum is a process kinetically more favoured than the ammonia nucleophilic addition to the nitrile of about three orders of magnitude, and hence the nucleophilic addition reaction occurs after. Finally, both nucleophilic addition steps are geometrically driven to give products in the E configuration even if the final products were experimentally observed in the Z configuration. For trans-Z,Z-[PtIICl(NH3)(N CMe)2, the isomerizatio…

KineticPlatinum complexeReaction mechanismNucleophilic additionPlatinum complexesNitrilechemistry.chemical_elementDFTMedicinal chemistryInorganic ChemistryAmidineNucleophilic substitutionchemistry.chemical_compoundDeprotonationchemistryNitrilesMaterials ChemistryNucleophilic substitutionPhysical and Theoretical ChemistryNucleophilic additionPlatinumNitrileIsomerizationDFT; Kinetic; Nitriles; Nucleophilic addition; Nucleophilic substitution; Platinum complexesInorganica Chimica Acta
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Thermal degradation of long-chain polyunsatured fatty acids during deodorization of fish oil

2006

International audience; Long-chain polyunsaturated fatty acids (LC-PUFA) of the n-3 series, particularly eicosapentaenoic (EPA) and docosahexaenoic (DHA) acid, have specific activities especially in the functionality of the central nervous system. Due to the occurrence of numerous methylene-interrupted ethylenic double bonds, these fatty acids are very sensitive to air (oxygen) and temperature. Non-volatile degradation products, which include polymers, cyclic fatty acid monomers (CFAM) and geometrical isomers of EPA and DHA, were evaluated in fish oil samples obtained by deodorization under vacuum of semi-refined fish oil at 180, 220 and 250 °C. Polymers are the major degradation products g…

LONG-CHAIN POLYUNSATURED FATTY ACIDDEODORIZATIONlipids (amino acids peptides and proteins)[SDV.BBM.BC]Life Sciences [q-bio]/Biochemistry Molecular Biology/Biochemistry [q-bio.BM][SDV.BBM.BC] Life Sciences [q-bio]/Biochemistry Molecular Biology/Biochemistry [q-bio.BM]GEOMETRICAL ISOMERIZATIONTHERMAL DEGRADATION
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Coordination networks incorporating halogen-bond donor sites and azobenzene groups

2016

Two Zn coordination networks, {[Zn(1)(Py)2]2(2-propanol)}n (3) and {[Zn(1)2(Bipy)2](DMF)2}n (4), incorporating halogen-bond (XB) donor sites and azobenzene groups have been synthesized and fully characterized. Obtaining 3 and 4 confirms that it is possible to use a ligand wherein its coordination bond acceptor sites and XB donor sites are on the same molecular scaffold (i.e., an aromatic ring) without interfering with each other. We demonstrate that XBs play a fundamental role in the architectures and properties of the obtained coordination networks. In 3, XBs promote the formation of 2D supramolecular layers, which, by overlapping each other, allow the incorporation of 2-propanol as a gues…

MOF Supramolecular Chemistry Halogen Bonding AzobenzeneStereochemistry116 Chemical sciencesSupramolecular chemistry02 engineering and technology010402 general chemistryRing (chemistry)01 natural sciencesIUPAC RECOMMENDATIONS 2013chemistry.chemical_compoundMETAL-ORGANIC FRAMEWORKSdell'Università e della RicercaCHEMISTRYTO-CRYSTAL ISOMERIZATIONMinistero dell'IstruzioneMoleculeGeneral Materials Scienceta215SUPRAMOLECULAR SYNTHESISHalogen bondMETAL-ORGANIC FRAMEWORKS; IUPAC RECOMMENDATIONS 2013; TO-CRYSTAL ISOMERIZATION; SUPRAMOLECULAR SYNTHESIS; VISIBLE-LIGHT; POLYMERS; FLUOROAZOBENZENES; COCRYSTALS; COMPLEXES; CHEMISTRYLigandChemistryFLUOROAZOBENZENESMinistero dell'Istruzione dell'Università e della RicercaGeneral ChemistryCOCRYSTALS021001 nanoscience & nanotechnologyCondensed Matter PhysicsAcceptor0104 chemical sciencesCrystallographyAzobenzeneMIURMetal-organic frameworkCOMPLEXESSettore CHIM/07 - Fondamenti Chimici Delle TecnologieVISIBLE-LIGHTPOLYMERS0210 nano-technology
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Stimuli-responsive hybrid materials: breathing in magnetic layered double hydroxides induced by a thermoresponsive molecule

2014

[EN] A hybrid magnetic multilayer material of micrometric size, with highly crystalline hexagonal crystals consisting of CoAl-LDH ferromagnetic layers intercalated with thermoresponsive 4-(4-anilinophenylazo)benzenesulfonate (AO5) molecules diluted (ratio 9 : 1) with a flexible sodium dodecylsulphate (SDS) surfactant has been obtained. The resulting material exhibits thermochromism attributable to the isomerization between the azo (prevalent at room temperature) and the hydrazone (favoured at higher temperatures) tautomers, leading to a thermomechanical response. In fact, these crystals exhibited thermally induced motion triggering remarkable changes in the crystal morphology and volume. In…

Magnetic couplingsMagnetismLayered double hydroxidesFerromagnetic layersINTERCALATION COMPOUNDengineering.materialThermotropismNI-ALQuantitative Biology::Subcellular ProcessesCondensed Matter::Materials ScienceMETAL-ORGANIC FRAMEWORKSchemistry.chemical_compoundCrystallinityQUIMICA ORGANICANuclear magnetic resonanceCrystal morphologiesPHOTOISOMERIZATIONQUIMICA ANALITICANANOPARTICLESPhysics::Chemical PhysicsAZOBENZENEPhysics::Atmospheric and Oceanic PhysicsThermochromismPRUSSIAN BLUEChemistryMagnetismLayered double hydroxidesFísicaQuímicaGeneral ChemistryMoleculesequipment and suppliesChemistryMagnetic multilayersCrystallographyAzobenzeneFerromagnetismHYDROTALCITEengineeringTHERMAL-EXPANSIONHybrid materialhuman activitiesCOORDINATION POLYMERSChemical Science
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cis- and trans-1,2-diphenylaziridines: induction of xenobiotic-metabolizing enzymes in rat liver and mutagenicity in Salmonella typhimurium.

1986

trans-Stilbene imine (trans-1,2-diphenylaziridine) is the nitrogen analog of trans-stilbene oxide, a potent inducer of several microsomal and cytosolic xenobiotic-metabolizing enzymes. Although the acute toxicity of cis- and trans-stilbene imines prevents their application at the usual dose for trans-stilbene oxide (400 mg/kg/day), it is apparent that the imines nevertheless potently induce several xenobiotic-metabolizing enzymes in rat liver. The IP administration of trans-stilbene imine resulted in statistically significant increases in the activities of aminopyrine N-demethylase, microsomal epoxide hydrolase, glutathione transferase (toward 1-chloro-2,4-dinitrobenzene, 1,2-dichloro-4-nit…

MaleSalmonella typhimuriumStereochemistryHealth Toxicology and MutagenesisImineAziridines10050 Institute of Pharmacology and Toxicology610 Medicine & healthMutagenToxicologymedicine.disease_causeAmes testchemistry.chemical_compound2307 Health Toxicology and MutagenesismedicineAnimalsToxicology and MutagenesisEnzyme inducerchemistry.chemical_classificationbiologyAzirinesMutagenicity Tests3005 ToxicologyRats Inbred StrainsStereoisomerismGeneral MedicineCis trans isomerizationRatsEnzymechemistryBiochemistryLiverHealthMicrosomal epoxide hydrolaseEnzyme InductionMicrosomebiology.protein570 Life sciences; biologyMutagensArchives of toxicology
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Halogen bonding stabilizes a cis-azobenzene derivative in the solid state : A crystallographic study

2017

Crystals oftrans- andcis-isomers of a fluorinated azobenzene derivative have been prepared and characterized by single-crystal X-ray diffraction. The presence of F atoms on the aromatic core of the azobenzene increases the lifetime of the metastablecis-isomer, allowing single crystals of thecis-azobenzene to be grown. Structural analysis on thecis-azobenzene, complemented with density functional theory calculations, highlights the active role of the halogen-bond contact (N...I synthon) in promoting the stabilization of thecis-isomer. The presence of a long aliphatic chain on the azobenzene unit induces a phase segregation that stabilizes the molecular arrangement for both thetrans- andcis-i…

Materials Chemistry2506 Metals and Alloys116 Chemical sciencesCrystal structure010402 general chemistryPhotochemistry01 natural sciencesazobenzene; halogen bonding; isomerization; Electronic Optical and Magnetic Materials; Atomic and Molecular Physics and Optics; 2506; Materials Chemistry2506 Metals and Alloysisomerizationchemistry.chemical_compoundPhase (matter)Atomic and Molecular PhysicsMaterials ChemistryElectronicOptical and Magnetic MaterialsHalogen bondta114010405 organic chemistryChemistrySynthonMetals and AlloysAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic MaterialsCrystallographyazobenzeneAzobenzenehalogen bondingDensity functional theorySettore CHIM/07 - Fondamenti Chimici Delle Tecnologieand Optics2506IsomerizationDerivative (chemistry)
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Time-Resolved Photochemistry of Stiffened Stilbenes

2019

Broadband transient absorption spectroscopy is used to study the photoisomerization of stiffened stilbenes in solution, specifically E/ Z mixtures of bis(benzocyclobutylidene) (t4, c4) and ( E)-1-(2,2-dimethyltetralinylidene)-2-2-dimethyltetraline (t6). Upon excitation to S

Materials science010304 chemical physicsPhotoisomerization0103 physical sciencesUltrafast laser spectroscopyMaterials ChemistryPhysical and Theoretical Chemistry010402 general chemistryPhotochemistrySpectroscopy01 natural sciences0104 chemical sciencesSurfaces Coatings and FilmsThe Journal of Physical Chemistry B
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Highly Robust but Surface‐Active: An N‐Heterocyclic Carbene‐Stabilized Au 25 Nanocluster

2019

Surface organic ligands play a critical role in stabilizing atomically precise metal nanoclusters in solutions. However, it is still challenging to prepare highly robust ligated metal nanoclusters that are surface-active for liquid-phase catalysis without any pre-treatment. Now, an N-heterocyclic carbene-stabilized Au25 nanocluster with high thermal and air stabilities is presented as a homogenous catalyst for cycloisomerization of alkynyl amines to indoles. The nanocluster, characterized as [Au25 (i Pr2 -bimy)10 Br7 ]2+ (i Pr2 -bimy=1,3-diisopropylbenzimidazolin-2-ylidene) (1), was synthesized by direct reduction of AuSMe2 Cl and i Pr2 -bimyAuBr with NaBH4 in one pot. X-ray crystallization…

Materials science010405 organic chemistryHomogeneous catalysisGeneral MedicineGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesCatalysislaw.inventionNanoclustersMetalchemistry.chemical_compoundCrystallographyCycloisomerizationchemistrylawvisual_artvisual_art.visual_art_mediumThermal stabilityCrystallizationCarbeneAngewandte Chemie International Edition
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