Search results for "stereochemistry"

showing 10 items of 4831 documents

Enhancement of Hydrolysis through the Formation of Mixed Heterometal Species: Al3+/CH3Sn3+ Mixtures

2013

ABSTRACT: The hydrolysis of mixed-metal cations (Al3+/CH3Sn3+) was studied in aqueous solutions of NaNO3, at I = 1.00 ± 0.05 mol·dm−3 and T = 298.15 K, by potentiometric technique. Several hydrolytic mixed species are formed in this mixed system, namely, Alp(CH3Sn)q(OH)r with (p, q, r) = (1, 1, 4), (1, 1, 5), (1, 1, 6), (2, 1, 4), (1, 2, 5), (1, 4, 11), (1, 3, 8), and (7, 6, 32). The stability of these species, expressed by the equilibrium: pAl3+ + qCH3Sn3+ + rOH− = Alp(CH3Sn)q(OH)r 3(p+q)−r, βpqr OH, can be modeled by the empirical relationship: log βpqr OH = −3.34 + 2.67p + 9.23(q + r). By using the equilibrium constant Xpqr relative to the formation reaction: pAl(p+q)(OH)r + q(CH3Sn)(p+q…

equilibrium analysiequilibrium analysis; mixed hydrolysis of metal ions; aluminium(III); monomethyltin(IV)monomethyltin(IV)Aqueous solutionChemistryStereochemistryGeneral Chemical EngineeringPotentiometric titrationEmpirical relationships Formation reaction Mixed species Mixed systems Potentiometric techniqueGeneral ChemistryPotentiometric techniqueMedicinal chemistryTurn (biochemistry)HydrolysisMixed systemsMixed speciesMixed systemsMixed speciesEmpirical relationshipsSettore CHIM/01 - Chimica AnaliticaSolubilityaluminium(III)mixed hydrolysis of metal ionFormation reactionEquilibrium constantJournal of Chemical & Engineering Data
researchProduct

Highly Syndiotactic or Isotactic Polyhydroxyalkanoates by Ligand-Controlled Yttrium-Catalyzed Stereoselective Ring-Opening Polymerization of Function…

2017

International audience; Reported herein is the first stereoselective controlled ROP of a specific family of racemic functional β-lactones, namely 4-alkoxymethylene-β-propiolactones (BPL(OR) s). This process is catalyzed by an yttrium complex stabilized by a nonchiral tetradentate amino alkoxy bisphenolate ligand _ONOO(R'2) ₍2-) , which features both a good activity and a high degree of control over the molar masses of the resulting functional poly(3-hydroxyalkanoate)s. A simple modification of the R' substituents in ortho and para position on the ligand platform allows for a complete reversal from virtually pure syndioselectivity (Ps up to 0.91 with R'=cumyl) to very high isoselectivity (Pi…

esteritStereochemistryring-opening polymerizationchemistry.chemical_element010402 general chemistry01 natural sciencesRing-opening polymerizationCatalysisCatalysispolymerointiTacticity[CHIM]Chemical SciencesYttriumpolymeeritta116β-lactonespolymersMolar mass010405 organic chemistryLigand[CHIM.ORGA]Chemical Sciences/Organic chemistrystereoselective catalysisGeneral MedicineGeneral ChemistryYttrium0104 chemical scienceschemistrykatalyysiAlkoxy groupStereoselectivitybeta-lactonesAngewandte Chemie International Edition
researchProduct

Synthesis and Antiproliferative Activity of 2,5-bis(3′-Indolyl)pyrroles, Analogues of the Marine Alkaloid Nortopsentin

2013

2,5-bis(3′-Indolyl)pyrroles, analogues of the marine alkaloid nortopsentin, were conveniently prepared through a three step procedure in good overall yields. Derivatives 1a and 1b exhibited concentration-dependent antitumor activity towards a panel of 42 human tumor cell lines with mean IC50 values of 1.54 μM and 0.67 μM, respectively. Investigating human tumor xenografts in an ex-vivo clonogenic assay revealed selective antitumor activity, whereas sensitive tumor models were scattered among various tumor histotypes.

ex-vivo xenograftsIndolesStereochemistryPharmaceutical ScienceMice NudeAntineoplastic AgentsArticleInhibitory Concentration 50MiceCell Line TumorNeoplasmsDrug Discoverybis-indolyl-pyrroles; nortopsentin analogues; marine alkaloids; antitumor; <i>ex-vivo </i>xenograftsIc50 valuesAnimalsHumansnortopsentin analoguePyrrolesClonogenic assayPharmacology Toxicology and Pharmaceutics (miscellaneous)lcsh:QH301-705.5Tumor Stem Cell AssayMice nudeantitumorAntitumor activityDose-Response Relationship DrugChemistryAlkaloidbis-indolyl-pyrroles; nortopsentin analogues; marine alkaloids; antitumor; ex-vivo xenograftsImidazolesTumor Stem Cell AssaySettore CHIM/08 - Chimica FarmaceuticaXenograft Model Antitumor Assaysbis-indolyl-pyrrolemarine alkaloidHuman tumornortopsentin analogueslcsh:Biology (General)Cell culturebis-indolyl-pyrrolesmarine alkaloidsMarine Drugs
researchProduct

One-pot synthesis of fluorinated 2-amino-pyrimidine-N-oxides. Competing pathways in the four-atom side-chain rearrangements of 1,2,4-oxadiazoles

2006

Abstract Trifluoromethylated 2-amino-pyrimidine N-oxides have been synthesized by reaction of the 3-amino-5-methyl-1,2,4-oxadiazole with trifluoromethyl-β-diketones in the presence of perchloric acid, followed by hydrolysis. In this ring-to-ring transformation an initial formation of (unisolated) 1,2,4-oxadiazole-pyrimidinium salts, and subsequent ring-opening at the oxadiazole moiety occurs. Isolation of 2-(hydroxyamino)-pyrimidine from the reaction mixture evidenced the presence of a competing pathway where the N(4) nitrogen of the oxadiazole is involved in the formation of a regioisomeric pyrimidinium salt. The effect of the trifluoromethyl group on the product distribution is discussed.…

fluoropyrimidine derivativecrystal structurepyrimidine N-oxidePyrimidinesynthesisStereochemistryOne-pot synthesisOxadiazoleX ray analysis3 diketoneBiochemistryMedicinal chemistryperchloric acidnitrogenchemistry.chemical_compoundside-chain rearrangementDrug DiscoveryStructural isomerSide chainMoietyPerchloric acidring openingfluorinated heterocycle3 diketone fluoropyrimidine derivative ketone derivative nitrogen oxide perchloric acid; article crystal structure hydrolysis priority journal reaction analysis ring opening synthesis X ray analysisTrifluoromethylChemistryOrganic Chemistryarticle124-oxadiazoleketone derivativereaction analysishydrolysispriority journaloxide
researchProduct

Physical chemical properties and kinetics of redox processes in water/soybean oil microemulsions

2008

Microemulsoes de agua em oleo (ME w/o) constituidas de agua, oleo de soja, SDS (dodecil sulfato de sodio) e diversos alcoois de cadeia curta foram caracterizadas sob o ponto de vista fisico-quimico e de propriedades eletroanaliticas. Foram testados diferentes co-surfactantes e razoes surfactante:cosurfactante, sendo a ME com a composicao mais favoravel utilizada para estudar a cinetica de processos redox. Para tanto, realizaram-se medidas de voltametria ciclica utilizando como eletrodo de trabalho um ultramicroeletrodo de disco de Pt e, como eletrodo de referencia e auxiliar, foram usados Ag/AgCl e Pt, respectivamente, e ferroceno como uma sonda. Verificou-se que a estabilidade termodinâmic…

food.ingredientAqueous solutionChemistryStereochemistryKineticsGeneral ChemistryReference electrodeRedoxSoybean oilchemistry.chemical_compoundfoodMicroemulsionSodium dodecyl sulfateCyclic voltammetryNuclear chemistryJournal of the Brazilian Chemical Society
researchProduct

New 2-Methoxy Acetylenic Acids and Pyrazole Alkaloids from the Marine Sponge Cinachyrella sp.

2017

Three new 2-methoxy acetylenic acids (1–3) and a known derivative (4), in addition to three new natural pyrazole alkaloids (5–7) were isolated from an Indonesian marine sponge of the genus Cinachyrella. Compounds 5 and 6 have previously been reported as synthetic compounds. The structures of the new compounds were established on the basis of one- and two-dimensional NMR spectroscopy as well as by mass spectrometric data. The absolute configuration of the new acetylenic acid derivatives (1–3) was established by ECD spectroscopy. All isolated compounds were evaluated for their cytotoxicity against L5178Y mouse lymphoma cells. Compounds 1–4 exhibited strong activity with an IC50 value of 0.3 µ…

food.ingredientLymphomaStereochemistrynatural productsCinachyrella sp.Pharmaceutical ScienceAntineoplastic AgentsPyrazole010402 general chemistry01 natural sciencesArticlepyrazole alkaloidMicechemistry.chemical_compoundAlkaloidsfoodTermészettudományokCell Line TumorDrug DiscoveryAnimalsOrganic chemistryKémiai tudományokCytotoxicitynatural products; marine sponge; Cinachyrella sp.; 2-methoxy acetylenic acid; pyrazole alkaloidPharmacology Toxicology and Pharmaceutics (miscellaneous)lcsh:QH301-705.5biology010405 organic chemistryChemistryAcetylenic acidAbsolute configurationNuclear magnetic resonance spectroscopybiology.organism_classificationMass spectrometricBiosynthetic PathwaysPorifera0104 chemical sciencesSpongelcsh:Biology (General)IndonesiaAlkynesddc:540Fatty Acids UnsaturatedPyrazolesDrug Screening Assays AntitumorCinachyrella2-methoxy acetylenic acidmarine spongeMarine Drugs
researchProduct

Efficient stabilisation of a dihydrogenphosphate tetramer and a dihydrogenpyrophosphate dimer by a cyclic pseudopeptide containing 1,4-disubstituted …

2017

A cyclic pseudooctapeptide 2 is described containing 1,4-disubstituted 1,2,3-triazole moieties. This compound features eight converging hydrogen bond donors along the ring, namely four amide NH and four triazole CH groups, which enable 2 to engage in interactions with anions. While fully deprotonated sulfate anions exhibit only moderate affinity for 2, protonated anions such as dihydrogenpyrophosphate and dihydrogenphosphate anions are strongly bound. Complexation of the phosphate-derived anions involves sandwiching of a dihydrogenpyrophosphate dimer or a dihydrogenphosphate tetramer between two pseudopeptide rings. X-ray crystallography provided structural information, while 1H NMR spectro…

fosfaatit010405 organic chemistryStereochemistryChemistryHydrogen bondDimerTriazoleIsothermal titration calorimetryProtonationGeneral Chemistry010402 general chemistry01 natural sciencesphosphate oligomers0104 chemical sciencesoligomeeriCrystallographychemistry.chemical_compoundDeprotonationpseudopeptidesTetramerAmidestabilisationta116orgaaniset yhdisteetChemical Science
researchProduct

Structure and optical properties of a monolayer single crystal of a cyanine dye

1992

Abstract Molecularly thin single crystals of a cyanine dye prepared by adsorption at a charged surfactant monolayer are studied by polarized optical spectroscopy and electron diffraction. Both techniques independently show a herringbone arrangement of the dye with the long axes of translationally inequivalent molecules forming an angle of 80°. The dye arranges in a primitive rectangular unit cell (a=21.2 A, b=6.14 A) adjacent to an epitaxially related hexagonal cell of the aliphatic tails of the surfactant.

genetic structuresChemistryStereochemistryGeneral Physics and AstronomyEpitaxychemistry.chemical_compoundCrystallographyElectron diffractionPulmonary surfactantMonolayerMoleculePhysical and Theoretical ChemistryCyanineSpectroscopySingle crystalChemical Physics Letters
researchProduct

Communication between iron(II) building blocks in cooperative spin transition phenomena

2003

[EN] In the present article we discuss the cooperative nature of the spin crossover phenomenon in iron(II) complexes, providing a perspective of the state of the art in this area. The first aspect we discuss is the role of the intermolecular interactions, more precisely the ¿-interactions, in mononuclear complexes. We show that by playing with the nature of the ligands, aliphatic, aromatic, or extended aromatic, it is possible to create stronger cohesive forces and receive a more cooperative response from the compound. In the next step the singular family of bipyrimidine-bridged iron(II) dinuclear compounds is presented as the simplest example of polynuclear spin crossover complexes exhibit…

genetic structuresStereochemistryChemistryIntermolecular forceSupramolecular chemistrySpin transitionSpin transitionIron(II) complexesInorganic ChemistryChemical physicsSpin crossoverFISICA APLICADAIntramolecular forceMaterials ChemistryMolecular magnetismPhysical and Theoretical ChemistrySupramolecular chemistryTopology (chemistry)Curse of dimensionalityCoordination Chemistry Reviews
researchProduct

Optical and electrical properties of oriented thin films of oligomer containing betaine-type moiety in side chain

2005

Non-linear optical and electrical properties of polymer films obtained by dipole orientation of active units are reported. Novel polar oligomer with N-(indan-1,3-dion-2-yl)pyridinium betaine (IPB) as a side group is studied. Orientation of polar groups in oligomer thin films causes an increase of the photo-induced change of surface potential on irradiation in the region of photo-induced electron transfer (PIET) where the IPB group exhibits a reversible change of the value and sign of the dipole moment. At longer wavelengths, the value of the surface potential of the oligomer may be determined by transport of photogenerated charge carriers.

genetic structuresStereochemistryInstitut für Physik und AstronomieCondensed Matter PhysicsOligomerElectronic Optical and Magnetic MaterialsDipoleCrystallographychemistry.chemical_compoundElectron transferBetainechemistrySide chainMoietyPyridiniumsense organsPendant group
researchProduct