Search results for "ALK"

showing 10 items of 4314 documents

π-Conjugated diimidazolium salts: rigid structure to obtain organized materials.

2015

Phenylene ethynylene based diimidazolium salts differing in the alkyl chain length borne on the imidazolium ion and anion nature were synthesized. Their properties were studied both in solution and in the solid state. Salts obtained were able to aggregate in organic solvent solution. Aggregate formation was studied by performing concentration dependent measurements using UV-vis, fluorescence and Resonance Light Scattering. Furthermore, features of the aggregates were also investigated in the solid state by means of fluorescence and Scanning Electron Microscopy measurements. Finally, Density Functional Theory calculations were performed to obtain insights into the interaction geometry in the…

chemistry.chemical_classificationdiimidazolium salts self-assembly DFT investigationChemistryGeneral Physics and AstronomySalt (chemistry)Settore CHIM/06 - Chimica OrganicaConjugated systemResonance (chemistry)IonSolventPhenylenePhysical chemistryOrganic chemistryDensity functional theoryPhysical and Theoretical ChemistryAlkylSettore CHIM/02 - Chimica FisicaPhysical chemistry chemical physics : PCCP
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A Novel Zeolite-Induced Population of a Planar Viologen Conformation. New Viologen Charge Transfer Complexes and Alkene/Viologen/Zeolite Arrays

2004

A rare example of a novel zeolite-induced conformational change and a mechanism for this process are suggested in order to rationalize an unexpected spontaneous intrazeolite reduction observed during preparation of a new viologen (MQ2+)-doped zeolite (NaY). In addition, the formations of six new alkene/viologen/ zeolite charge transfer (CT) arrays using NaMQY and the previously reported NaMVY are also reported. The binding constants between MQ2+ and MV2+ and 2,3-dimethyl-2-butene (TME) were determined using the Benesi-Hildebrand approach, and the stabilities of these CT complexes are compared to their intrazeolite analogue.

chemistry.chemical_classificationeducation.field_of_studyConformational changeChemistryAlkenePopulationViologenCharge (physics)Settore CHIM/06 - Chimica OrganicaPhotochemistrySurfaces Coatings and FilmsPlanarMaterials ChemistrymedicinePhysical and Theoretical ChemistryeducationZeolitemedicine.drugZeolites Binding constants Electrochromic display devices Oxygenation
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H-NMR and FT-IR study of the state of melatonin confined in membrane models: location and interactions of melatonin in water free lecithin and AOT re…

2004

The state of melatonin confined either in dry lecithin or bis(2-ethylhexyl) sulfosuccinate sodium salt (AOT) reversed micelles has been investigated by H-NMR and FT-IR spectroscopies as a function of the melatonin to surfactant molar ratio (R). The analysis of experimental results leads to hypothesize that, independently of R and the surfactant nature and as a consequence of anisotropic melatonin/surfactant interactions, melatonin is totally solubilized in reversed micelles and mainly located by opportune orientation in the nanodomain constituted by the surfactant head groups. The absence of significant spectral changes related to the protons linked to the first carbon atoms of surfactant a…

chemistry.chemical_classificationendocrine systemfood.ingredientOrganic ChemistryPhotochemistryMicelleLecithinlcsh:QD241-441MelatoninfoodMembranelcsh:Organic chemistrychemistryPulmonary surfactantmedicineProton NMRFourier transform infrared spectroscopyhormones hormone substitutes and hormone antagonistsAlkylmedicine.drugArkivoc
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Serine/Threonine Phosphatase Inhibitors Decrease Adrenergic Arylalkylamine N -Acetyltransferase Induction in the Rat Pineal Gland

2001

Adrenergic regulation of the pineal enzyme serotonin N-acetyltransferase [arylalkylamine N-acetyltransferase (AA-NAT); EC 2.3.1.87] accounts for the circadian rhythm in melatonin formation. In the present study, the role of protein phosphatases in the adrenergic regulation of rat pineal AA-NAT was investigated using specific inhibitors. In cultured pineals, the serine/threonine phosphatase type 1 and type 2A inhibitors okadaic acid and calyculin A significantly decreased adrenergically or cAMP-induced AA-NAT activity, whereas the serine/threonine phosphatase type 2B inhibitor cypermethrin and tyrosine phosphatase inhibitor dephostatin were ineffective. Reverse transcriptase-polymerase chain…

chemistry.chemical_classificationendocrine systemmedicine.medical_specialtyEndocrine and Autonomic SystemsEndocrinology Diabetes and MetabolismfungiPhosphataseAdrenergicProtein tyrosine phosphataseOkadaic acidBiologyMolecular biologySerineCellular and Molecular Neurosciencechemistry.chemical_compoundEndocrinologyEnzymeEndocrinologychemistryInternal medicineArylalkylaminemedicineThreonineJournal of Neuroendocrinology
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Enzymatic Resolution of 3-oxodicyclopentadiene on a Decagram Scale

2018

The chiral building block 3-oxodicyclopentadiene (1) can be readily resolved on a decagram scale by a short sequence consisting of (1) reduction to the corresponding endo-alcohol, (2) enzymatic oxidative resolution with a ketoreductase enzyme to give (+)-1 and the (+)-form of the endo-alcohol, and (3) reoxidation of the (+)-endo-alcohol with another ketoreductase to give (–)-1. With a selectivity factor of 310, the enantiomeric ratios of the resolved (+)-endo-alcohol and (+)-ketone are both >99:1. Both enzymatic oxidations could be performed with a at least 300:1 substrate/catalyst ratio (w/w).

chemistry.chemical_classificationentsyymithapetustetrahydromethanoindenoneResolution (mass spectrometry)alkoholit (yhdisteet)ChemistryStereochemistryoxidationOrganic ChemistrySubstrate (chemistry)resolutionAlcoholCatalysisalcoholsgram-scale synthesischemistry.chemical_compoundEnzymeEnantiomerSelectivity
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Speciation of trialkyltin(IV) cations in natural fluids

2004

The hydrolysis of (CH(3))(3)Sn(+), (C(2)H(5))(3)Sn(+) and (C(3)H(7))(3)Sn(+) has been studied in a Synthetic Seawater (SSW) ionic medium simulating the major composition of natural seawater, at different salinities (5 less than or equal to S less than or equal to 45), and at t = 25 degreesC. Interactions with anionic components of SSW, considered as single sea salt, are determined by means of a complex formation model. By potentiometric measurements (ISE-H(+) and ISE-F(-) electrodes), the model has been extended to also consider interactions of organotins with carbonate and fluoride ions, which are other important components of seawater. Literature and new values of hydrolysis constants in …

chemistry.chemical_classificationfood.ingredientChemistryHydrolysisSea saltmedia_common.quotation_subjectInorganic chemistryIonic bondingArtificial seawaterSalt (chemistry)General ChemistryOceanographytrialkyltin(IV)SpeciationHydrolysisfoodIonic strengthEnvironmental ChemistrySeawaterIonic strength Protonation protonation constantsHydrolysis; trialkyltin(IV); Natural FluidsNatural FluidsWater Science and Technologymedia_commonMarine Chemistry
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Structural Investigation of Water/Lecithin/Cyclohexane Microemulsions by FT-IR Spectroscopy

1995

Abstract FT-IR spectra of water/lecithin/deuterated cyclohexane microemulsions as a function of water/lecithin molar ratio R ( R = [water]/[lecithin]) at various volume fractions ( O ) of the micellar phase have been recorded at 25°C. After elimination of the small spectral contributions due to deuterated cyclohexane and normalization, the shape of the C–H stretching band due to lecithin has been found dependent upon R and O whereas that of the O–H stretching band has been found dependent only upon R . The change in shape of the C–H band was interpreted in terms of a modification of the lecithin alkyl chain packing order. The analysis of the O–H band provides evidence that the hydroxylic gr…

chemistry.chemical_classificationfood.ingredientCyclohexaneHydrogen bondChemistryLecithinSpectral lineSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundColloid and Surface ChemistryfoodDeuteriumPhase (matter)Organic chemistryPhysical chemistryMicroemulsionAlkylJournal of Colloid and Interface Science
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Iodonium complexes of the tertiary amines quinuclidine and 1-ethylpiperidine

2021

Iodonium complexes incorporating tertiary amines have been synthesised to study and explore why such species comprised of alkyl amines are relatively rare. The complexes were characterised in solution (1H and 15N NMR spectroscopy) and the solid state (SCXRD), and analysed computationally. peerReviewed

chemistry.chemical_classificationkemiallinen synteesiamiinit010405 organic chemistryChemistrySolid-state1-ethylpiperidineNuclear magnetic resonance spectroscopykompleksiyhdisteet010402 general chemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesInorganic Chemistryjodichemistry.chemical_compoundAlkylQuinuclidine
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Co(II)-mediated synthesis of 2-carbamimidoylbenzoates and isoindole-1,3-diaminates

2015

Abstract Phthalonitrile, acetoxime and cobalt(II) nitrate hexahydrate are combined in acetone with formation of stable and easy to handle Co(II) complex [Co{C6H4C(NH2)NC(ONCMe2)2}2](NO3)2 (1). Interaction of 1 with excess alcohols ROH (also used as solvents) and 2 equiv of (NH4)2S leads, in one-step, to alkyl 2-carbamimidoylbenzoate nitrates [C6H4COOR{2-C(NH2)2}]NO3 [R=CH3, C2H5, C3H7, CH(CH3)2]. Similarly, N1,N3-dialkyl-1H-isoindole-1,3-diaminate nitrates [C6H4C(NR′)NC(NR′)]NO3 [R=C3H7, C4H9, C(CH3)3, CH2CH2OH, CH2CH2SC2H5) can be directly produced from 1 by its reaction with 4 equiv of amines and 2 equiv of (NH4)2S in alcoholic media.

chemistry.chemical_classificationphthalonitrilesChemistryStereochemistrymetal assisted (mediated) synthesisOrganic Chemistrychemistry.chemical_elementN1oximesBiochemistryMedicinal chemistryPhthalonitrilechemistry.chemical_compoundNitrateDrug DiscoveryAcetone3-diaminatesIsoindoleCobaltta116alkyl 2-carbamimidoylbenzoatesN3-dialkyl-isoindole-1AlkylTetrahedron
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Polyethylene composites filled with n‐alkyl‐functionalized siloxane‐silsesquioxane resins and sol‐gel silicas

2019

High‐density polyethylene (HDPE) composites filled with silicon‐based fillers were prepared by melt blending. The use of non‐functionalized and n‐octyl‐functionalized siloxane‐silsesquioxane resins and the sol‐gel silicas as fillers allowed us to evaluate the influence of functionalization of the fillers on the properties of the composites. The melting and crystallization temperatures of the composites were found to be only slightly affected by the addition of the silicon‐based fillers. In turn, the crystallization degree values were increased, in particular for the materials containing non‐functionalized fillers. The free‐volume properties of the composites did not change significantly in …

chemistry.chemical_classificationpolyethylenethermogravimetric analysisThermogravimetric analysisMaterials sciencePolymers and PlasticsGeneral ChemistryPolyethylenemechanical propertiescompositesSilsesquioxanechemistry.chemical_compoundDifferential scanning calorimetrychemistrySiloxaneMaterials ChemistryCeramics and CompositesComposite materialdifferential scanning calorimetryAlkylSol-gelPolymer Composites
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