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  • Polymer and Materials Science  (438)
  • Lunar and Planetary Science and Exploration  (47)
  • Biochemistry and Biotechnology  (45)
  • 1
    ISSN: 0025-116X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The η3, η2, η2-dodeca-2(E), 6(E), 10(Z)-trien-1-yl-nickel(II) complexes [Ni(C12H19)]X (X = SbF6, O3SCF3) were treated in toluene with amorphous aluminium trifluoride (which was prepared from AlEt3 and BF3 · OEt2) in a mole ratio 1 : 10 to 20, forming a highly active catalyst for the 1,4-cis polymerization of butadiene. This catalyst is comparable in its activity and selectivity, and in the molar mass distribution of the polybutadiene, with the technical nickel catalyst Ni(O2CR)2/BF3ċOEt2/AlE3 developed by Bridgestone Tire Company thirty years ago. The existence of the C12-allynickel(II) cation [Ni(C12H19)]+ on the AlF3 support could be proved by FAB mass spectroscopic measurements. In agreement with our reaction model for the allyl nickel complex catalyzed butadiene polymerization, it is concluded that the technical nickel catalyst in its effective structure can be described as a polybutadienylnickel(II) complex co-ordinated to a polymeric fluoroaluminate anion via a fluoride bridge.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    ISSN: 0003-3146
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: Metallocen-Katalysatoren eröffnen neue Wege zur Synthese von Olefinoligomeren und -polymeren, deren Molekulargewichte und Schmelzpunkte in weiten Bereichen variieren. Einige wichtige Besonderheiten bei der Herstellung von Oligomeren, von wachsartigen sowie von hochmolekularen Polymeren durch Metallocen-Katalyse werden hier behandelt. Am Beispiel der Oligomerisation von Hexen wird ein einfaches kinetisches Modell entwickelt, das geeignet erscheint, den Reaktionsverlauf und die resultierende Oligomerenverteilung beim Einsatz von Metallocen-Katalysatoren zu beschreiben. Die Herstellung von Propylenpolymeren mit niedrigen und hohen Molekulargewichten durch Metallocen-Katalyse wird hinsichtlich der Reaktionsbedingungen und der Produkteigenschaften mit bekannten Prozessen verglichen. Ferner wurde der Einfluß von verschiedenen Unregelmäßigkeiten der Polymerketten, wie Kettenenden, Regioirregularitäten und Comonomersegmenten auf die Schmelzpunkte untersucht.
    Notizen: Metallocenes offer new synthetic routes to olefin oligomers and polymers covering a wide range of molecular weights and melting points. This paper deals with some important features of the preparation of oligomers, wax-like polymers as well as highmolecular-weight polymers via metallocene catalysis. Taking the oligomerization of hexene as an example, a simple kinetic scheme is established, which is suitable to describe the course of the reaction and the resulting oligomer distribution with metallocenes as catalysts. For low and high-molecular-weight polymers, the metallocene route to polypropylene is compared to existent processes in terms of reaction conditions and product properties. An attempt is made to separate the effect of different chain defects like chain ends, regioirregularities and comonomers on the melting point.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    ISSN: 0006-3525
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Small- and wide-angle x-ray scattering is used for structural characterization of amylose solutions and gets. Recently published coordinates determined by x-ray fiber structure analysis and electron diffraction [A. Imberty and S. Perez: (1988) Biopolymers, Vol. 27. pp. 1205-1212: H. C. Wu and A. Sarko (1978) Carbohydrate Research, Vol. 6.1, pp. 7-40]. X-ray crystallography [W. Hinrichs & W. Saenger (1990) Journal of the American Chemical Society, Vol. 112. pp. 2789-2796], and theoretically calculated atomic coordinates for energy-minimized conformers of amylose molecules in solution and crystals served to simulate small- and wide-angle x-ray scattering curves. The simulation of scattering curves renders possible a quick screening and detection of special features in experimental curves and the decision of whether they are significant or not. The scattered intensities of the models were calculated using the atomic scattering factors and van der Waals radii within the framework of the improved cube method [J. J. Müller (1983) Journal of Applied Crystallography, Vol. 16, pp. 74-82]. All model data and the scattering curves are stored for a fast information retrieval in the database OBIOSCAT controlled by the ORACLE management system.In the context of a mixture of diflerent structures existing in an amylose solution or gel, theparallel-stranded left-handed B-form double helices (Imberty and Perez) do not scatter in a way that is significantly different from that of the parallel-stranded right-handed duplex proposed by Wu and Sarko. The structure of the energy-minimized left-handed parallel-stranded double helix is very similar to that of the canonical B form, but energy-minimized right-handed duplexes with parallel or antiparallel strands have structures that produce new scattering features. Up to now, such features have not been experimentally detected. Extended or collapsed single helices, too, can be discriminated by their scattering features from double helices for scattering vectors larger than 5 nm-1, and the energy-minimized left-handed single helices are nearly identical with the V-forms experimentally found in fibres [G. Rappenecker and P. Zugenmaier (1981) Carbohydrate Research, Vol. 89, pp. 11-19.].Because the investigated amylose gels contain crystallites. The growing of V- and B-form nanocrystallites up to dimensions of 20 nm was simulated with atomic resolution. The scattering curves of independently scattering nunocrystals hold information about crystallite shape, size, surrounding, and the structure, factors of the asymmetric unit in the unit cell, hence, they differ remarkably from the recently published fiber-structure factors and provide this structure information at an early stage of crystallization.Experimental scattering data of wheat amylose recorded during the gelation process can explained by a remarkable amount of V-helices with 6-12 glucopyranosyl residues in solution at 70°C. Extended single helices probably exist also under these conditions. A mixture of independently scattering V- and B-form nanocrystallites is detectable in freshly cooled samples (40°C), and pure B-form nanocrystallites embedded in a matrix of an electron density comparable to that in the crystallites exist together with amorphous material afterjve weeks of aging at 21°C. From the scattering of the amylose sample during the gelation process it follows that Gidley's gelation model [M. J. Gidley (1989) Macromolecules, Vol. 22, pp. 351-358], which assumes crystallization during the phase separation, is prejerred to the model proposed by Miles et al. [M. J. Miles, V. J. Morris, and S. G. Ring (1985) Carbohydrate Research, Vol. 135, pp. 257-269], where crystallization is preceded by phase separation. © 1995 John Wiley & Sons, Inc.
    Zusätzliches Material: 14 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    ISSN: 0003-3146
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: This paper is concerned with the ring opening of the uretdione group in presence of nucleophilic partners and of the technological significance of this reaction. It is shown that at temperatures from 100° to 120°C both polyesters containing hydroxyl groups and low-molecular weight compounds carrying Zerewitinow-active hydrogen atoms react in solution as well as in the molten state with free NCO groups of uretdione diisocyanates by the diisocyanate polyaddition process. Under these conditions no opening of the uretdione ring occurs.These results give rise to the use of uretdione diisocyanates for chain extensions yielding polyuretdione polyurethanes. Reactions with blocking agents (e.g. ε-caprolactam) result in new types of blocked uretdione and blocked polyuretdione polyurethanes. It is shown that the four-membered rings are split completely at temperatures from 140° to 180°C. Compounds containing hydroxyl groups which are available in the reaction mixture react with the latent NCO groups of the uretdiones to form urethanes. By selection and combination of suitable starting compounds crystalline, high-melting polyuretdione polyurethane powders of good milling properties can be obtained. The new syntheses of technical usefulness yield non-polluting polyurethane powder coatings for application by electrostatic spraying.
    Notizen: Die Ringöffnung der Uretdiongruppe in Gegenwart von nukleophilen Reaktionspartner und die technische Bedeutung dieser Reaktionsind Gegenstand der vorliegenden Arbeit. Die Untersuchungen machen deutlich, daß hydroxylgruppenhaltige Polyester und niedermolekulare Zerewitinow-aktive Wasserstofftome tragende Verbindungen sich bei Temperaturen von 100-120°C in Lösung, aber auch in der Schmelze mit den freien NCO-Gruppen der Uretdiondiisocyanate nach dem Diisocyanat-Polyadditionsver-faren umsetzen lassen, ohne daß nennenswerte Uretdionringöffnung eintritt. Auf Grund dieser Erkenntnis können mit den Uretdiondiisocyanaten Kettenverlängerungen zu Poly-uretdionpolyurethanen durchgeführt werden. Durch Umsetzung mit Blockierungsmitteln (z.B.ε-Caprolactam) werden neuartige blockierte Uretdione und blockierte Polyuretdion-polyurethane erhalten. Es wird nachgewiesen, daß die Vierringe im Temperaturbereich von 140-180°C vollständig aufspalten. Gleichzeitig vorliegende hydroxylgruppenhaltige Verbindungen reagieren mit den latenten NCO-Gruppen der Uretdione unter Urethanbildung. Durch geeignete Wahl und Kombinatio der Asgangsverbindungen lassen sich kristalline, hochschmelzende, gut mahlbare Polyuretdionpolyurethanpulver gewinnen. Die neuen technisch verwertbaren Synthesen führen zu umweltfreundlichen, lösungsmittel-freien Verfahen der elektrostatischen Pulverbeschichtung.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    ISSN: 0173-0835
    Schlagwort(e): Two-dimensional polyacrylamide gel electrophoresis ; Protein sequencing ; Amino acid analysis ; Matrix assisted laser desorption ionization-mass spectrometry ; Database ; Chemistry ; Biochemistry and Biotechnology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie , Chemie und Pharmazie
    Notizen: The master gel of the human myocardial two-dimensional electrophoresis (2-DE) gel database contains about 3300 protein spots characterized in terms of isoelectric point (pI) and molecular mass. A high-performance technique was applied, using large gels (23 × 30 cm). Isoelectric focusing with anodic sample preparation and nonequilibrium running conditions (NEPHGE) was combined with sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) in 15% acrylamide gels in the second dimension. The range of pI extends from pH 4.5 to 9.6. Seventy proteins were identified by combinations of amino acid analysis, N-terminal and internal sequencing, immunostaining, matrix assisted laser desorption/ionization-mass spectrometry (MALDI-MS) peptide mass fingerprinting, post-source decay MALDI-MS and ladder sequencing by carboxypeptidase P. The identification of additional proteins, not found in the master gel, was achieved by immunoblotting. Unequivocal identification with high sensitivity and good yield was obtained by combining internal sequencing and MALDI-MS. In-gel digestion, the concentration and purification of peptides in a peptide collecting device, and the improved FRAGMOD program for peptide mass fingerprinting have added to the security and sensitivity of identification. The high-performance human myocardial 2-DE database was built up with proteins detected by the TOPSPOT program. Spots within six sections of the whole pattern are clickable. Protein description includes detailed information about identification, characterization, and links to the related SWISS-PROT, other 2-DE databases and Medline entries. The database is constructed in accordance with four of the rules for a federated database.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Rapid Communications 13 (1992), S. 289-298 
    ISSN: 0173-2803
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 7
    ISSN: 0173-0835
    Schlagwort(e): Matrix assisted laser desorption ; ionization-mass spectrometry ; Peptide mass fingerprinting ; Two-dimensional polyacrylamide gel electrophoresis ; Enzymatic in-gel digestion ; Myocardial proteins ; Heat shock protein 27 ; Phosphorylated proteins ; Chemistry ; Biochemistry and Biotechnology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie , Chemie und Pharmazie
    Notizen: Immunostaining of heat shock protein 27 (Hsp27) protein species on two-dimensional electrophoresis (2-DE) gels with enhanced sensitivity yields 59 spots reacting with anti-Hsp27 antibodies. Recombinant Hsp27 exists in 2-DE as two major protein species which comigrate in the human myocardial pattern with Hsp27 spots C754 and D899 as defined in the heart high-performance 2-DE database (http://www.mdc-berlin.de/∼emu/heart/). Preparative electrophoresis of human myocardial proteins and analysis of the enriched mass range 20-30 kDa by 2-DE revealed eight protein spots (C438, C582, C658, C697, C754, C595, C750) from the human myocardial database and a new spot not previously detected on silver-stained gels. These spots were identified as Hsp27 protein species by enzymatic in-gel-digestion and analysis by matrix assisted laser desorption-ionization (MALDI) peptide mass fingerprinting and, in part, MALDI-post source decay sequencing of single fragments. Possible post-translational modifications were investigated: immunostaining tests with anti-phospho-serine/-threonine/-tyrosine antibodies, although positive for other myocardial proteins, were negative for presumed Hsp27 protein species; likewise, periodate-glycostaining assays and biotinylation screening did not detect modifications in the investigated Hsp27 protein species.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 8
    ISSN: 0173-0835
    Schlagwort(e): Chemistry ; Biochemistry and Biotechnology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie , Chemie und Pharmazie
    Notizen: Targeting to specific sites of the body via colloidal carriers is sought in order to reduce drug side effects. The adsorption of plasma proteins on intravenously injected particles is regarded as the key factor in explaining their organ distribution: total bound protein, or, more likely, the presence of specific proteins and their conformation, are expected to influence macrophage uptake. Polystyrene beads, 60 nm in diameter, were used as model carriers; their surface was differentially modified by adsorption of increasingly hydrophilic block copolymers, poloxamers 184, 188 and 407. After incubation in plasma, the patterns of protein adsorption onto coated beads were analyzed by high-resolution two-dimensional polyacrylamide gel electrophoresis (2-D PAGE). The behavior of some representative proteins was monitored, including albumin, fibrinogen, IgG, factor B and the apolipoproteins, A-I, A-IV, C-III, E and J. The more hydrophobic the particles, the larger the total amount of bound protein. However, this correlation was not valid for all of the analyzed protein species, which proves that it is insufficient to look only at physico-chemical data to predict organ distribution. On the contrary, it is essential to use 2-D PAGE to establish the correlation between adsorbed proteins and carrier behavior in vivo.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 156 (1988), S. 123-137 
    ISSN: 0003-3146
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: Samples of polyoxymethylene (unstabilized and stabilized with the antiozonants N-isopropyl-N′-phenyl-p-phenylenediamin (IPPD) and bis-(1,2,3,6-tetrahydrobenzaldehyd)pentaerithritylacetal (Vulkazon AFS)) were ozonized under mechanical load in a special climate chamber. Surface damages were determined by IR-spectroscopy and scanning electron microscopy. During the ozonolysis a damaged layer is formed, the thickness of which increases with increasing time of ozonization. During this damaging reaction acetal groups are attacked and oligomers are formed.
    Notizen: Proben von unstabilisiertem und mit den Antiozonantien N-Isopropyl-N′-phenyl-p-phenylendiamin (IPPD) und Bis-(1,2,3,6-tetrahydrobenzaldehyd)-pentaerithrityl-acetal (Vulkazon AFS) stabilisiertem Polyoxymethylen wurden unter mechanischer Belastung in einer Klimakammer ozonisiert. Die Schädigungen auf der Oberfläche wurden IR-spektroskopisch und rasterelektronenmikroskopisch untersucht. Während der Ozonisierung von POM bildet sich eine geschädigte Schicht, deren Dicke mit zunehmender Ozonisierungszeit wächst. Hierbei wird das Polymere an den Acetalbindungen angegriffen, wodurch Ketten gespalten werden und Oligomere entstehen.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 10
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 179 (1990), S. 5-19 
    ISSN: 0003-3146
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: A new spectroscopic method for determining the permeability of ammonia in transparent polymer layers is presented. It is based on the quantitative proof of the ammonia passing the test layer into a sensor layer, containing 4-nitrophenol as an NH3-sensitive probe, which is placed under the test film. The permeability (P) of the test layer is calculated from the slope of extinction with time in the sensor layer. The lag time (t1) gives the diffusion coefficient (D). The suitability of this method is confirmed by comparison with literature values. Diffusion coefficients obtained from t1 correspond well to those obtained by the sorption method.The temperature dependence of P and D in more than five different polymers (CDA, PVB, PVAc, PVC and different polyvinyl alcohols) demonstrates that peculiarities in the temperature dependence of the permeability result from the behaviour of the NH3-solubility (P/D) which is strongly dependent on the polymer structure.
    Notizen: Es wird eine neuartige spektroskopische Methode zur Messung der Ammoniak-Permeabilität in transparenten Polymerfilmen vorgestellt. Sie beruht auf dem quantitativen Nachweis des den Testfilm durchdringenden Ammoniaks in einer darunter befindlichen Sensorschicht mit Hilfe der NH3-empfindlichen Sonde 4-Nitrophenol. Aus dem Anstieg der Extinktion mit der Zeit (ΔE/Δt) in der Sensorschicht wird die Permeabilität (P) und aus der Verzögerungszeit (lag time (t1)) der Diffusionskoeffizient (D) berechnet. Die Eignung der Methode wird durch Vergleich mit Literaturwerten belegt. Die aus t1 zugänglichen Diffusionskoeffizienten stimmen sehr gut mit denen überein, die mit der Sorptionsmethode gefunden werden.Die Temperaturabhängigkeiten von P und D in mehr als fünf verschiedenen Polymeren (CDA, PVB, PVAc, PVC und in verschiedenen Polyvinylalkoholen) zeigen, daß Besonderheiten im Temperaturgang der Permeabilität aus dem vom Aufbau des Polymeren stark abhängigen Verhalten der NH3-Löslichkeit (P/D) resultieren.
    Zusätzliches Material: 2 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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