Search results for "Tact"
showing 10 items of 1313 documents
Über die Autoxydation gesättigter makromolekularer Kohlenwasserstoffe
1973
Die Autoxydation in Losung von isotaktischem Polypropylen bzw. Polyputylen-1 gehorcht einer anderen kinetischen Beziehung als die entsprechende Autoxydation von ataktischem Polypropylen, Polybutylen-1 und Polyathylen. Die Autokatalyse der Autoxydation isotaktischer Produkte wird durch einen bimolekularen Kettenstart der gebildeten Hydroperoxyde hervorgerufen, wahrend bei ataktischen Produkten ein monomolekularer Kettenstart beobachtet wird. Die unterschiedliche Kinetik der Autoxydation kann eindeutig auf Taktizitatsunterschiede zuruckgefuhrt werden. The autoxidation of isotactic polypropylene and poly-butylene-1 in solution shows a kinetic difference from that of atactic fractions of these …
Die oxydation von polyepoxiden mit molekularem sauerstoff
1966
Polypropylenoxid, Polybutylen-1-oxid und Polystyroloxid wurden dargestellt und mit Hilfe von Losungsmitteln in verschiedene taktische Fraktionen getrennt. Diese Fraktionen und Polyathylenoxide mit verschiedenem Molekulargewicht wurden in Substanz autoxydiert und die fluchtigen Reaktionsprodukte gaschromatographisch identifiziert. Die Autoxydation dieser Polymeren in Losung wurde durch Messung der Sauerstoffaufnahme verfolgt. Die Bruttoaktivierungsenergien der taktischen Fraktionen der Polymeren sind groser als die der ataktischen Fraktionen. Die Kinetik der Autoxydation des Polybutylen-1-oxides wurde aufgeklart. Polypropyleneoxide, polybutene-1-oxide, and polystyreneoxide were prepared and …
Cell Adhesive and Antifouling Polyvinyl Chloride Surfaces Via Wet Chemical Modification
2012
Polyvinyl chloride (PVC) is one of the most frequently used polymers for the manufacturing of medical devices. Limitations for its usage are based upon unfavorable surface properties of the polymer including its hydrophobicity and lack of functionalities in order to increase its versatility. To address this issue, wet chemical modification of PVC was performed through surface amination using the bifunctional compound ethylene diamine. The reaction was conducted in order to achieve maximum surface amination while leaving the bulk material unaffected. The initial activation step was characterized by means of various methods including contact angle measurements, colorimetric amine quantificati…
Novel diamine-bis(phenolate) Ti(IV) complexes – tuning the complex structure to control catalytic properties in α-olefin polymerization
2016
Abstract Four monomeric titanium(IV) dichloride complexes of amine-bis(phenolate) ligands having an extra donor arm (2a–2d) and one oxo-bridged complex 3 were successfully synthesized in the reaction of TiCl4 with a sodium salt of the appropriate ligand, and they were characterized by 1H NMR spectroscopy. The ligands had either a dimethylamino side‐arm donor and t-Bu substituents on both (1a) and one (1d) phenolate rings or a diisopropylamino side-arm donor and t-Bu (1b) and t-Bu along with OMe (1c) phenolate substituents. All complexes upon activation with [Ph3CB(C6F5)4] and MAO were used to catalyze polymerization of 1-octene (in liquid monomer) into poly(1-octene). Their activities as we…
Non-steroidal anti-inflammatory agents. Part 23. Synthesis and Pharmacological Activity of Enaminones which inhibit both bovine cyclooxygenase and 5-…
1998
The synthesis and stereochemical characteristics of pyrrolidino-, isoquinolino- and indolo-enaminones 2–11 are reported. The inhibition of cyclooxygenase was determined in a bovine thrombocyte intact cell assay and that of 5-lipoxygenase using intact bovine polymorphonuclear leucocytes. Except compound 2c′ which is a well-balanced dual inhibitor of both enzymes, all other enaminone derivatives are weak inhibitors of both cyclooxygenase and 5-lipoxygenase. Structure-activity relationships of the enaminones in relation to known anti-inflammatory drugs are discussed.
Titanium isodicyclopentadienide hemimetallocenes for ethylene/styrene copolymerization
2004
Abstract The syndiotactic polymerization of styrene with exo-[(η5-isodiCp)TiCl3] 1/methylalumoxane (MAO; isodiCp=isodicyclopentadienyl) was studied as well as the ethylene/styrene copolymerization with exo-[{η5:η1(N)-isodiCp(SiMe2Nt-Bu)}TiCl2] 2/MAO. These two catalytic systems are stable during polymerization. The half-sandwich titanocene 1 exhibits good syndiospecificity and average activity. The bridged half-sandwich amino complex 2 was found to incorporate styrene into polymer chains at 70 °C. Activity results decrease with increasing styrene concentrations.
A Deeper Insight into the Postpolymerization Modification of Polypenta Fluorophenyl Methacrylates to Poly(N -(2-Hydroxypropyl) Methacrylamide)
2014
This work provides a detailed insight into the synthesis of N-(2-hydroxypropyl)methacrylamide (HPMA) polymers employing the activated ester approach. In this approach, polypenta fluorophenyl methacrylate (PFPMA)-activated ester polymers are synthesized by the reversible addition-fragmentation chain transfer (RAFT) polymerization and transferred into HPMA-based systems by the use of 2-hydroxypropylamine. To prove quantitative conversion in the absence of side reactions, special attention is devoted to investigate different reaction conditions by different analytical methods ((1) H, (19) F, inverse-gated (13) C NMR, and zeta potential measurements). Furthermore the influence of common solvent…
Adaptive Wetting-Adaptation in Wetting
2018
Many surfaces reversibly change their structure and interfacial energy upon being in contact with a liquid. Such surfaces adapt to a specific liquid. We propose the first order kinetic model to describe dynamic contact angles of such adaptive surfaces. The model is general and does not refer to a particular adaptation process. The aim of the proposed model is to provide a quantitative description of adaptive wetting and to link changes in contact angles to microscopic adaptation processes. By introducing exponentially relaxing interfacial energies and applying Young's equation locally, we predict a change of advancing and receding contact angles depending on the velocity of the contact line…
Polyreactions in ordered systems: Polymerization of octadecyl methacrylate in monolayers at the gas–water interface
1977
The ultraviolet-initiated polymerization of octadecyl methacrylate (ODMA, octadecyl 2-methyl-2-propenoate) as a monomolecular layer at the gas-water interface was studied. The polymerization was carried out at 27°C at the nitrogen-water interface; air inhibits the polymerization. At 27°C the ODMA monolayer exhibits three different states which were characterized by surface pressure-area diagrams and by surface potential measurements. The ODMA monolayer was polymerized under constant surface pressure in the range between 0 and 10 dyne/cm. The polymerization was followed by recording the contraction of the film. The conversion was determined by comparison of the area per monomer unit during p…
Crystallization Behaviour at High Cooling Rates of Two Polypropylenes
1993
Phase distribution of quenched samples of two isotactic polypropylenes, having different molecular weight distributions, was evaluated by a deconvolution procedure of WAXD spectra. The dependence on cooling rate of the two resins shows the low molecular weights rich polymer is characterized by a faster kinetics with an α-monoclinic to mesomorphic transition taking place at higher cooling rates.