Search results for "tetrahydrofuran"
showing 10 items of 284 documents
Leitfahigkeitsmessungen an Polystyrylnatrium in Dimethoxiäthan (DME) und Tetrahydrofuran (THF)
1971
An Polystyrylnatrium werden in zwei polaren organischen Losungsmitteln Leitfahigkeitsmessungen uber einen groseren Temperaturbereich ausgefuhrt. Aus der Temperaturabhangigkeit der Dissoziationskonstante ergibt sich, das die undissoziierte Verbindung in zwei Formen, dem Kontaktionenpaar (I) und dem solvatgetrennten Ionenpaar (II), vorkommt. Enthalpie- und Entropiedifferenz beim ubergang von I nach II, sowie die entsprechenden thermodynamischen Parameter der Dissoziation von II werden ermittelt. Der effektive Ladungsabstand im solvatgetrennten Ionenpaar betragt etwa 7 A. Conductivity measurements were carried out with polystyryl sodium in two polar solvents within a large temperature range. T…
Zur kinetik der anionischen polymerisation von methyl-methyacrylat in tetrahydrofuran bei −75°C
1973
Die anionische Polymerisation von Methylmethacrylat (MMA) in Tetrahydrofuran (THF) verlauft bei −75°C mit Cumylcasium bzw. oligomerem α-Methylstyrylcasium als Initiatoren ohne erkennbare Nebenreaktionen analog der anionischen Polymerisation von unpolaren Monomeren in atherischen Losungsmitteln. Als Beweis wird hauptsachlich die enge Molekulargewichtsverteilung der unter diesen Bedingungen hergestellten Polymethylmethacrylate angefuhrt. Bei −75°C betragen die Geschwindigkeitskonstanten fur die Monomeranlagerung an das Ionenpaar kw(±) = 80 dm3 mol−1 s−1 und an das freie Anion etwa kw(−) ≈ 6 · 104 dm3 mol−1 s−1. Leitfahigkeitsmessungen ergeben, das die Dissoziationskonstante des Polymethylmeth…
Modelling of the elution behaviour in hybrid micellar eluents with different organic modifiers
1999
Abstract The elution behaviour in reversed-phase liquid chromatography (RPLC), with mobile phases containing micelles, can be described according to a distribution pattern among three phases: bulk water, micellar pseudophase and stationary phase. Several mechanistic equations based on this pattern, previously used to predict the retention in hybrid mobile phases of sodium dodecyl sulphate and propanol, were checked with several organic modifiers and a group of solutes of diverse polarity. The modifiers were the alcohols 1-propanol, 1-butanol and 1-pentanol, and other organic solvents widely used in conventional RPLC such as acetonitrile and tetrahydrofuran. New models were also proposed to …
A combined experimental and theoretical study of the thermal [3+2] cycloaddition of carbonyl ylides with activated alkenes
2018
International audience; 4-Benzoyl-3,5-diaryltetrahydrofuran-2,2-dicarbonitriles were first synthesized from 2,2-dicyano-3-aryloxiranes and chalcones at toluene reflux; the 4,5-cis products proved to be predominantly formed and were isolated. Whereas shortened reaction times were observed by using microwave irradiation or catalytic cuprous chloride, no significant stereoselectivity change was in general noticed. Reacting 2,2-dicyano-3-aryloxiranes with 2-cyclopentenone next afforded 3-aryl-4-oxohexahydro-1H-cyclopenta[c]furan-1,1-dicarbonitriles, and the endo stereoisomers were isolated. That no stereoselectivity change was noticed in the presence of cuprous chloride rather suggests an impac…
Palladium on pumice: new catalysts for the stereoselective semihydrogenation of alkynes to (Z)-alkenes
2001
Abstract High selectivities (93–99%) and excellent stereoselectivities (>99%) in the semihydrogenation of CC triple bonds were achieved using palladium on pumice with a metal loading of 0.5, 1.5 or 3.0% wt as catalyst. The reactions were carried out in ethanol or tetrahydrofuran with only 2.5% of ethylenediamine allowing a self-terminating semihydrogenation independently on the CC triple bond.
ChemInform Abstract: Palladium on Pumice: New Catalysts for the Stereoselective Semihydrogenation of Alkynes to (Z)-Alkenes.
2010
Abstract High selectivities (93–99%) and excellent stereoselectivities (>99%) in the semihydrogenation of CC triple bonds were achieved using palladium on pumice with a metal loading of 0.5, 1.5 or 3.0% wt as catalyst. The reactions were carried out in ethanol or tetrahydrofuran with only 2.5% of ethylenediamine allowing a self-terminating semihydrogenation independently on the CC triple bond.
Ultrasonic and Volumetric Properties of 1-Ethyl-3-methylimidazolium Trifluoromethanesulfonate Ionic Liquid with 2-Propanol or Tetrahydrofuran at Seve…
2011
Densities and speeds of sound of 1-ethyl-3-methylimidazolium trifluoromethanesulfonate mixtures with 2-propanol and tetrahydrofuran (THF), as well as of the pure components, have been measured over the whole range of compositions at T = (278.15 to 328.15) K and P = (101 ± 2) kPa. From these experimental data, the excess molar volume, excess speed of sound, and excess isentropic compressibility have been calculated and fitted to an extended version of the Redlich–Kister equation, which takes into account the dependence on composition and temperature simultaneously. The Prigogine–Flory–Patterson theory has also been used to explain the behavior of these systems.
Reversal of asymmetric induction in stereoselective strecker synthesis on galactosyl amine as the chiral matrix
1988
Abstract The reversal of the direction of asymmetric induction in Lewis acid catalyzed Strecker synthesis using the 2,3,4,6-tetra-O-pivaloyl-β-D-galactopyranosyl amine 1 is described. In isopropanol or tetrahydrofuran 1 had given ( R )-diastereomers of the corresponding α-amino nitriles preferably. However, in chloroform in the presence of heterogeneous zinc chloride the same auxiliary alternatively leads to an excess of the ( S )-diastereomers.
Polymere ester von säuren des Phosphors, 3. Polymerisation des 2-Äthoxy-2-oxo-1,3,2-dioxaphospholans
1975
2-Athoxy-2-oxo-1,3,2-dioxaphospholan (1) wird durch verschiedene Alkoholate sehr schnell und in hoher Ausbeute zu Poly[oxy(athoxyphosphoryl)oxyathylen] (3) polymerisiert. Die Produkte sind hochviskos und farbols. Sie losen sich in Wasser, Alkoholen, Tetrahydrofuran, Dioxan, Methylenchlorid, Chloroform und Dimethylsulfoxid; unloslich sind sie in Ather und in Kohlenwasserstoffen. Polymerisationsgrade bis 83 (M = 12600) wurden gemessen. In wasriger Losung bei Raumtemperatur erfolgte auch nach Tagen kein merklicher hydrolytischer Abbau. Der mutmaslich anionische Polymerisationsmechanismus und mogliche Nebenreaktionen werden kurz diskutiert. 2-Ethoxy-2-oxo-1,3,2-dioxaphospholane (1) is polymeriz…
Studien zum Vorgang der Wasserstoffübertragung, 67. Endioldiester durch acylierende elektroreduktive Dimerisierung von Carbonsäurechloriden mit Lithi…
1983
Aromatische, aliphatische und aromatisch-aliphatische Carbonsaurechloride (und Anhydride) werden mit Lithiumamalgam (Li/Hg) durch acylierende reduktive Dimerisierung in wechselnden Ausbeuten (meist 70%) in cis- und/oder trans-Endioldiester 1–10 ubergefuhrt. Der Einflus des Losungsmittels auf den Reaktionsverlauf wird untersucht. Aus 2,2′-Diphensauredichlorid entsteht das Phenanthrenderivat 7, aus Phthaloyldichlorid Phthalid 8. Li/Hg wandelt Diphenyl-phosphinylchlorid in Tetraphenyldiphosphandioxid (15) um. Auf die Bestimmung der Halbstufenpotentiale von 12 Saurechloriden und vier 1,2-Diketonen grundet sich die Formulierung des Reaktionsmechanismus. 1,2-Diketone sind Zwischenprodukte der acy…