Search results for "ALK"

showing 10 items of 4314 documents

Anionic Polymerization of Alkyl (Meth)acrylates Using Metal-Free Initiators:  Effect of Ion Pairing on Initiation Equilibria

1999

Metal-free anionic polymerizations of alkyl (meth)acrylates using tetrabutylammonium salts of diethylphenylmalonate, fluorene, and 9-ethylfluorene as initiators were performed in THF at 30 °C. A poor control of molecular weights, inconsistent initiator efficiencies, and broad or bimodal molecular weight distributions were obtained. The effect of counterion nature was studied from the polymerization of methyl methacrylate using the 1,1-diphenylhexyl anion with tetrabutylammonium, tetramethyldiethylguanidinium, and lithium as counterions under otherwise identical conditions. Metal-free initiators resulted in incomplete initiation which is attributed to the fact that the initiation is an equil…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistrySolution polymerizationPolymerInorganic Chemistrychemistry.chemical_compoundAnionic addition polymerizationchemistryPolymerizationPolymer chemistryMaterials ChemistryHofmann eliminationCounterionMethyl methacrylateAlkylMacromolecules
researchProduct

Synthesis and properties of aromatic ionenes

1993

Cationic polyelectrolytes with aromatic segments can be synthesized by a repetitive alkylation reaction. The structure of the products, their synthesis and their solubility are described. All ionenes are not, or only in small amounts, water soluble. The best solubility can be achieved by mixtures of polar protic and aprotic solvents. Variations of the counterion produces sufficient solubility in THF. All ionenes show a typical polyelectrolyte effect. The thermal stability of aromatic ionenes and the glass transition temperature is dominated by the nature of the counterion. The molecular weight of oligomers can be described by using a combination of a conductive titration method and an ion s…

chemistry.chemical_classificationPolymers and PlasticsOrganic Chemistryfood and beveragesAlkylationPolyelectrolyteIon selective electrodechemistryPolymer chemistryMaterials ChemistryTitrationThermal stabilityCounterionSolubilityGlass transitionPolymer International
researchProduct

Structural variations in amphiphiles: Discoidal multivalent cations

1986

Fourteen cationic multipolar amphiphiles have been synthesized with pyridinium or trimethylammonium head groups. The hydrophobic cores are planar ring systems (benzene or triphenylene) to which two, three, four, or six decylene or undecylene alkyl chains are attached by ester linkages. The hydrophilic head groups are bound to the outer ends of the alkyl chains.

chemistry.chemical_classificationPolymers and PlasticsStereochemistryChemistryCationic polymerizationTriphenyleneRing (chemistry)Micellechemistry.chemical_compoundColloid and Surface ChemistryLiquid crystalPolymer chemistryAmphiphileMaterials Chemistrylipids (amino acids peptides and proteins)PyridiniumPhysical and Theoretical ChemistryAlkylColloid & Polymer Science
researchProduct

Electron-transfer reduction of selected alcohols with alkalide K−, K+(15-crown-5)2 via organometallic intermediates

2004

Abstract The course of the reaction of alkalide K − , K + (15-crown-5) 2 1 with selected alcohols depends on the kind of alcohol and the mode of substrate delivery. In the case of methanol, potassium methoxide formed initially undergoes destruction at the excess of 1 . It results in potassium oxide and methylpotassium. The latter opens the crown ether ring giving potassium tetraethylene glycoxide vinyl ether and methane. A similar course of the process is observed for propanol. Potassium glycidoxide is the main product formed in the reaction of 1 with glycidol. Its oxirane ring is opened at the excess of 1 . Organopotassium alkoxides, i.e., potassium potassiomethoxide and dipotassium potass…

chemistry.chemical_classificationPotassium methoxideAlkalidePotassiumOrganic Chemistrychemistry.chemical_elementVinyl etherBiochemistryPotassium oxideInorganic Chemistrychemistry.chemical_compoundchemistry15-Crown-5Polymer chemistryMaterials ChemistrymedicineOrganic chemistryMethanolPhysical and Theoretical ChemistryCrown ethermedicine.drugJournal of Organometallic Chemistry
researchProduct

Crown ethers derived from bicyclocalix[4]arenes as chromoionophores

2001

The synthesis of calix[4]arenes in which opposite phenolic units are connected by a poly(oxyethylene) bridge at the narrow rim and a 2,6-dimethylene-4-nitrophenol bridge at the wide rim is reported. For two derivatives with tetra- (4) and penta(oxyethylene) (5) bridges UV-Vis spectrophotometric studies were carried out in buffered solution in the presence of alkali metal ions. Their complexation was associated with changes in their UV-Vis spectra, especially with an increase of the absorption band at 450 nm. For 4 and 5 this was most intense in the presence of potassium and caesium ions, respectively, indicating that the calixarene with the shorter crown ether bridge is selective towards po…

chemistry.chemical_classificationPotassiumchemistry.chemical_elementGeneral ChemistryAlkali metalCatalysisIonchemistry.chemical_compoundchemistryAbsorption bandCaesiumPolymer chemistryCalixareneMaterials ChemistryOrganic chemistryPhenolCrown etherNew Journal of Chemistry
researchProduct

Complexation Selectivities of Pillar[5]arenes with Primary Ammonium Salts

2013

The complexation of alkyl-substituted pillar[5]arenes with primary ammonium salts is investigated. 1,4-Bis(methoxy)pillar[5]arene (MeP5) can form strong complexes with the primary ammonium salts in CDCl3. However, 1,4-bis(ethoxy)pillar[5]arene (EtP5) shows weak interaction with these guests, and 1,4-bis(butoxy)pillar[5]arene (BuP5) can not form such a complex at all. These results indicate that the modified alkyl chains of pillar[5]arene play an important role in the complexation selectivity.

chemistry.chemical_classificationPrimary (chemistry)Binding propertiesPillarGeneral ChemistryMedicinal chemistrychemistry.chemical_compoundchemistryAlkoxy groupOrganic chemistryAmmoniumSelectivityHost–guest chemistryAlkylChinese Journal of Chemistry
researchProduct

Zur C-17-Oxidation von Clavinalkaloiden mit primärer alkoholischer Hydroxylgruppe

1975

Die Oppenauer-Oxidation von 1 mit Cyclohexanon fuhrt zu dem Aldolkondensationsprodukt 4 und der Carbonsaure 3. Analog konnte Lysergsaure (8) in geringer Menge aus 6 gewonnen und im Reaktionsgemisch von 7 nachgewiesen werden. Damit wurden erstmals Clavinalkaloide mit primarer alkoholischer Hydroxylgruppe chemisch zu den entsprechenden Carbonsauren oxidiert. C-17-Oxidation of Clavine Alkaloids with a Primary Alcoholic Hydroxyl Group. 1 is converted by Oppenauer oxidation with cyclohexanone to the aldol condensation product 4 and to the carboxylic acid 3. Lysergic acid (8) was obtained in a small yield by the analogous reaction of 6 and was found in the reaction mixture of 7. Thus clavine alka…

chemistry.chemical_classificationPrimary (chemistry)StereochemistryCarboxylic acidClavine AlkaloidsPharmaceutical ScienceCyclohexanoneOppenauer oxidationLysergic acidchemistry.chemical_compoundchemistryYield (chemistry)Drug DiscoveryAldol condensationArchiv der Pharmazie
researchProduct

Generation and transformation of the [3.3.1]propellane skeleton by thermal rearrangements

1994

Abstract In a sequence of unexpected thermal rearrangements the strained monocyclic alkyne 4 is transformed into the tricyclic system 5 which yields in a flash vacuum pyrolysis again a monocyclic compound 10 .

chemistry.chemical_classificationPropellanechemistry.chemical_compoundFlash vacuum pyrolysischemistryComputational chemistryOrganic ChemistryDrug DiscoveryThermalAlkynePhotochemistryBiochemistryTransformation (music)Tetrahedron Letters
researchProduct

1-Alkyl- and azeto[1,2-a][1,5]benzodiazepine derivatives in the reaction of o-phenylenediamine with 3-(dimethylamino)propiophenones

2000

The reaction of o-phenylenediamine (4) with one, two or three equivalents of p-substituted 3-dimethylaminopropiophenone hydrochlorides 5a−e was studied. 4-Aryl-2,3-dihydro-1H-1,5-benzodiazepine derivatives 6a−e were obtained in good yields, along with the 1:2-adducts 7c−e and the unexpected 1:3-adducts rac-8c−e. The type of adduct formed is determined by the molar ratio of the reactants 4 and 5 and by the nature of the substituent in the para position of the propiophenone 5.

chemistry.chemical_classificationPropiophenonesBenzodiazepineChemistrymedicine.drug_classOrganic ChemistrySubstituentMedicinal chemistryAdductPara positionchemistry.chemical_compoundPropiophenoneo-PhenylenediaminemedicinePhysical and Theoretical ChemistryAlkyl
researchProduct

Structure of Polymers

2014

The structure and thermodynamics of polymers are discussed both with an adapted version of Flory’s regular solution theory and the concept of scaling and random walks. The salient properties of polymers like segregation and elasticity are discussed in terms of these concept. The Flory-Stockmayer theory of gelation is introduced and related to the percolation concept.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceRegular solutionPolymer architecturePolymerRandom walkCondensed Matter::Soft Condensed MatterSupramolecular polymerschemistryPercolationStatistical physicsElasticity (economics)Scaling
researchProduct