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showing 10 items of 2156 documents

Calorimetric investigation of the complex formation between surfactants and α-, β- and γ-cyclodextrins

1992

Abstract A calorimetric technique has been used to study complex formation between α-, β- and γ-cyclodextrins (αCD, βCD and γCD) and some surfactants (sodium dodecylsulphate (SDS), hexadecyl trimethylammonium bromide (CTAB) and p-(1,1,3,3-tetramethylbutyl) phenoxypoly(oxyethyleneglycol) (Triton X-100)). The experimental data indicate that some complexes (SDS-αCD, SDS-βCD and CTAB-αCD) are very stable and allow direct determination of their stoichiometry and molar enthalpy of complex formation. Those for other complexes closely fit a model based on an equilibrium reaction between surfactant, cyclodextrin and a single complex. According to the model, data analysis allows determination of the …

chemistry.chemical_classificationCyclodextrinStereochemistryChemistryEnthalpyCondensed Matter PhysicsStandard enthalpy of formationchemistry.chemical_compoundPulmonary surfactantStability constants of complexesBromidePhysical chemistryPhysical and Theoretical ChemistryChemical equilibriumInstrumentationStoichiometryThermochimica Acta
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Screening of ligands for the Ullmann synthesis of electron-rich diaryl ethers

2012

In the search for new ligands for the Ullmann diaryl ether synthesis, permitting the coupling of electron-rich aryl bromides at relatively low temperatures, 56 structurally diverse multidentate ligands were screened in a model system that uses copper iodide in acetonitrile with potassium phosphate as the base. The ligands differed largely in their performance, but no privileged structural class could be identified.

chemistry.chemical_classificationC–O bond formationDenticityBase (chemistry)catalysisArylOrganic Chemistrynucleophilic aromatic substitutiondiaryl ethersUllmann-type couplingCombinatorial chemistryFull Research PaperCatalysislcsh:QD241-441Chemistrychemistry.chemical_compoundchemistrylcsh:Organic chemistryNucleophilic aromatic substitutionPotassium phosphateOrganic chemistrylcsh:QAcetonitrilelcsh:ScienceCopper iodideBeilstein Journal of Organic Chemistry
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Description of a Simple, Specific, and Sensitive Test for the Detection of Detergent-Solubilized C3b Receptor

1981

Abstract The C3b receptor was isolated from detergent-solubilized human erythrocyte membranes by a previously described technique (1). The receptor glycoprotein was shown to enhance EAC14oxy23b rosette formation with Raji lymphoblastoid cells. This provided a specific and sensitive test to detect the solubilized C3b receptor either in crude or highly purified form. The property of the C3b receptor tested by this assay appears to be analogous to properties of β1H.

chemistry.chemical_classificationErythrocytesRosette FormationChemistryLymphoblastImmunologychemical and pharmacologic phenomenaHematologyBurkitt LymphomaMolecular biologyCell LineReceptors ComplementMembraneBiochemistryRosette formationSolubilizationHumansImmunology and AllergyReceptorGlycoproteinGlycoproteinsImmunobiology
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Understanding the domino reactions of alkyne-tethered N-tosylhydrazones yielding fused polycyclic pyrazoles. An MEDT study

2019

Abstract The domino reactions of alkyne-tethered N-mesylhydrazones yielding fused polycyclic pyrazoles have been studied within the Molecular Electron Density Theory (MEDT). Analysis of the Gibbs free energies indicates that the more favourable reactive path is the one in which the elimination of mesylate anion takes place before the intramolecular [3 + 2] cycloaddition (IM32CA) reaction, which corresponds with the rate-determining step of these domino processes. ELF topological analysis of the bond formation along the IM32CA reaction indicates that in spite of the high activation energy associated to this intramolecular reaction, it shows a pmr-type mechanism characterised by the presence …

chemistry.chemical_classificationIntramolecular reaction010405 organic chemistryChemistryOrganic ChemistryAlkyneBond formation010402 general chemistry01 natural sciencesBiochemistryCycloadditionDomino0104 chemical sciencesIonGibbs free energysymbols.namesakeComputational chemistryIntramolecular forceDrug DiscoverysymbolsTetrahedron
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Some monomers, oligomers and polymers with conjugated triple bonds

1991

In the first part new monoaminodiacetylenes with different numbers of CH2-groups, the formation of Perowskit-type Mn complexes and their polymerizability are described. Symmetrical diaminodiacetylenes and some derivatives therefrom have also been prepared. The second part deals with different types of polymers with diacetylene units in the backbone. Under irradiation color formation and crosslinking take place. Well-defined low molecular weight model compounds of polydiacetylenes is the subject of the third part. Finally rod-like but soluble polymers with alternating p-phenylene and acetylene units are described.

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsDiacetyleneOrganic ChemistryPolymerConjugated systemCondensed Matter PhysicsTriple bondchemistry.chemical_compoundMonomerchemistryAcetylenePolymer chemistryMaterials ChemistryColor formationPolydiacetylenesMakromolekulare Chemie. Macromolecular Symposia
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Confinement-induced screening of hydrodynamic interactions and spinodal decomposition: Multiscale simulations of colloid-polymer mixtures

2012

Phase separation kinetics of a colloid-polymer mixture confined between two planar repulsive walls is studied by a multiscale simulation approach. Colloids and polymers are described by particles interacting with continuous potentials suitable for molecular-dynamics simulation, while hydrodynamic interactions mediated by solvent particles are accounted for by the multiparticle collision dynamics method. Varying the distance D between the walls and the character of the boundary conditions, the interplay of structure formation parallel and perpendicular to the walls is studied, and the effect of hydrodynamics on the growth of domain size ld(t) with time t is elucidated. Only for slip boundary…

chemistry.chemical_classificationMaterials scienceStructure formationSpinodal decompositionKineticsGeneral Physics and AstronomySlip (materials science)PolymerCondensed Matter::Soft Condensed MatterColloidClassical mechanicschemistryChemical physicsPhase (matter)Boundary value problemEPL (Europhysics Letters)
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Carbon nitride as photocatalyst in organic selective transformations

2020

Abstract Graphitic carbon nitride (g-C3N4) is a metal-free conjugated polymer which has become a new research hotspot in photocatalysis. It can be used for solar energy exploitation like in solar energy organic synthesis, one of the most new and appealing green applications of heterogeneous photocatalysis. This chapter resumes the state-of-the-art and progresses in the application of heterogeneous visible light photocatalysis in organic selective transformations by using C3N4 as photocatalyst.

chemistry.chemical_classificationMaterials sciencebusiness.industryGraphitic carbon nitrideNanotechnologyPolymerConjugated systemSolar energychemistry.chemical_compoundchemistryC-C formation Carbon nitride Coupling reactions Organic synthesis Organic transformations Partial oxidationPhotocatalysisOrganic synthesisSettore CHIM/07 - Fondamenti Chimici Delle TecnologiebusinessCarbon nitrideVisible spectrum
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Understanding the origin of the asynchronicity in bond-formation in polar cycloaddition reactions. A DFT study of the 1,3-dipolar cycloaddition react…

2012

The origin of the asynchronicity in bond-formation in polar cycloadditions has been studied by an ELF analysis of the electron reorganisation along the 1,3-dipolar cycloaddition of Padwa's carbonyl ylide 4 with the 1,2-benzoquinone 8. This reaction presents an unexpected asynchronous bond-formation, which is initialised through the nucleophilic attack of Padwa's carbonyl ylide on the carbonyl oxygen atom of the strongly electrophilically activated 1,2-benzoquinone. The present study allows for the establishment that along an asynchronous bond-formation, the more favourable two-center interaction begins at the most electrophilic center, which is the center with the highest spin density achie…

chemistry.chemical_classificationNucleophileChemistryYlideGeneral Chemical EngineeringElectrophile13-Dipolar cycloadditionPolarGeneral ChemistrySpin densityBond formationPhotochemistryCycloadditionRSC Adv.
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Spermidine and morphogenesis in single cell cultures of Sideritis angustifolia lag.

1990

Abstract Single cells from hypocotyl-derived callus of Sideritis angustifolia were evaluated for morphogenesis when cultured in either solidifier or liquid Murashige and Skoog medium supplemented with various concentrations of spermidine, naphthaeneacetic acid (NAA), benzyladenine (BA) and dicyclohexylamine (DCHA). Spermidine (Spd) did not replace the hormonal requirements for cell division and callus formation, but affected growth induced by NAA or BA. This polyamine increased the plating efficiency of cells cultured in the presence of NAA (0.05, 0.54 and 5.40 μM) or BA (0.40, 4.40 and 8.80 μM). In contrast, Spd reduced growth induced by 10.80 μM NAA, optimal auxin concentration for callus…

chemistry.chemical_classificationPlating efficiencyCallus formationfungiPlant ScienceGeneral MedicineBiologySpermidinechemistry.chemical_compoundMurashige and Skoog mediumchemistryBiochemistryAuxinCallusmental disordersCytokininGeneticsPolyamineAgronomy and Crop SciencePlant Science
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Hydrogen bonds in unpolar matrix — Comparison of complexation in polymeric and low molecular-weight systems

1991

By ene-reaction of 4-phenyl-1,2,4-triazoline-3,5-dione with double bonds, polar 4-phenyl-1,2,4-triazolidine-3,5-dione (phenyl urazole) groups are introduced into unpolar matrices. Hydrogen-bond complexes are formed between two amide-like units. The temperature dependence of complex formation in dilute hydrocarbon medium is obtained from remperature-dependent IR spectra in the region of the C=O stretching vibration. Results obtained for a low molecular-weight model system are compared with modified polybutadienes, where the groups are attached statistically along the polymer backbone. The enthalpy and the entropy of complex formation (ΔH f =−28.6 kJ/mol; ΔS f =−52 J/mol K−1) obtained for the…

chemistry.chemical_classificationPolymers and PlasticsDouble bondChemistryStereochemistryHydrogen bondEnthalpyInfrared spectroscopyPolymerStandard enthalpy of formationCrystallographyColloid and Surface ChemistryHydrocarbonMaterials ChemistryPhysical and Theoretical ChemistryEquilibrium constantColloid and Polymer Science
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