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  • Articles: DFG German National Licenses  (19)
  • Polymer and Materials Science  (13)
  • Column liquid chromatography  (2)
  • Crystal structures  (2)
  • Drosophila melanogaster  (2)
Source
  • Articles: DFG German National Licenses  (19)
Material
  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Inorganica Chimica Acta 224 (1994), S. 163-169 
    ISSN: 0020-1693
    Keywords: Crystal structures ; Polychalcogenide complexes ; Tellurium complexes
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Inorganica Chimica Acta 221 (1994), S. 51-54 
    ISSN: 0020-1693
    Keywords: Crystal structures ; Dithiolato complexes ; Hafnium complexes ; Porphyrin complexes
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Insect Physiology 38 (1992), S. 167-173+175-176 
    ISSN: 0022-1910
    Keywords: Drosophila melanogaster ; Prothoracicotropic hormone ; ecdysone synthesis ; heat-shock protein
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1617-4623
    Keywords: Yolk protein ; Ovarian enhancer 1 ; Enhancer-binding factors ; Drosophila melanogaster
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract It has been reported that three different DNA regions — the fat body enhancer and ovarian enhancers 1 and 2 — direct the tissue-specific expression ofyp1 andyp2 inDrosophila melanogaster. In the present study, we identified ovarian enhancer 1-specific binding proteins. Electrophoretic mobility shift assay revealed that these proteins are present in the adult ovary, but not in adult testis or fat body. Southwestern blot analysis showed that about 130 kDa and 40 kDa proteins, designated OEF1 and OEF2, respectively, from ovarian nuclear or crude extracts bind specifically to the ovarian enhancer 1. The two proteins were partially purified by streptavidin/agarose-DNA affinity chromatography, and their binding activity was confirmed by electrophoretic mobility shift assay. These ovarian enhancer factors may play an important role in the regulation of transcription ofyp1 andyp2 in the ovary.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 1755-1765 
    ISSN: 0887-624X
    Keywords: 1-(trifluoromethyl)-2,3,5,6-benzenetetracarboxylic dianhydride ; amide acid ; poly(amic acid) ; isomeric unit ; nuclear magnetic resonance spectroscopy ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Two different poly(amic acid)s were synthesized by the polycondensations of 1-(trifluoromethyl)-2,3,5,6-benzenetetracarboxylic dianhydride (CF3DAN) with p-phenylene diamine and benzidine. In addition, an amide acid model compound was prepared from CF3DAN and aniline. Isomeric units in the poly(amic acid)s as well as the amide acid were investigated by 1H and 13C-nuclear magnetic resonance (NMR) spectroscopies. Spectroscopic results indicate that the major isomeric component was a CF3-meta-isomeric unit centered on the aromatic carbon substituted with the trifluoromethyl group. In particular, the amide acid compound was determined to be composed of 80 mol % CF3-meta-isomer and 20 mol % H-meta-isomer. Therefore, for the poly(amic acid)s, the minor isomeric component is speculated to be a H-meta-isomeric unit rather than a para-isomeric unit. The result might result mainly from the strong electron-withdrawable and bulky trifluoromethyl substituent in the CF3DAN monomer. The strong electron withdrawability might significantly enhance the reactivities of the adjacent carbons in the monomer to the nucleophilic attack of the amino nitrogen in the aniline and diamines, and consequently overcome the role of the bulkyness, ultimately leading to the amide acid and poly(amic acid)s rich with the CF3-meta-isomeric unit. In addition, a portion of the imide form was detected in the dried AN-CF3DAM-AN amide acid. Thus, the formation of imide linkage might be involved in a small portion for the dried poly(amic acid)s. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 1755-1765, 1998
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Column-switching ; Parathion, and metabolites in serum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A new high-performance liquid chromatographic method with column-switching has been developed for the simultaneous determination of parathion and its metabolites such asp-nitrophenol and paraoxon in serum. Serum samples were injected onto a precolumn packed with LiChroprep RP-8 after simple dilution with 20% phosphoric acid. Polar plasma components were washed with 0.02 M phosphate buffer (pH 3.0). After valve switching, the concentrated compounds were eluted in back-flush mode and separated on a Ultracarb ODS 30 column with a gradient of acetonitrile −0.01 M phosphate buffer (pH 3.0) as mobile phase. The method showed excellent precision, accuracy and speed with detection limit of 0.1 μg mL−1. Total analysis time per sample was 〈40 min and coefficients of variation for intra-and inter-assay were 〈4.5%.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Microbore columns ; Column-switching ; Myristicin ; Serum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A microbore high-performance liquid chromatographic method with column-switching was developed for the analysis of myristicin from rat serum without prepurification. Deproteinization, fractionation, concentration and separation of analyte were carried out by appropriate switching of columns and using solvent mixtures. The method showed excellent precision, accuracy and speed with a detection limit of 10 ng mL−1 from 25 μL of serum. The total analysis time per sample was 25 min and the coefficients of variation for intra- and inter-assay were less than 1.8%.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Materialwissenschaft und Werkstofftechnik 26 (1995), S. 263-268 
    ISSN: 0933-5137
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: Qn the viscosity of glass melts and porous sintered glassesSuspensions of solid phase particles in molten glasses modify their flow behavior and therefore their viscosity. This work deals with the dependence of the effective viscosity (ηeff) of isotropic suspensions on the concentration of the solid phase particles. Independently of the shape of the inclusions the values of the effective viscosities lie between upper [ηeff = ηL (1 - CD)-14 ]and lower bounds [ηeff = ηL (1 - CD)-3], where ηL is the viscosity of the molten glass and CD is the volume fraction of solid inclusions. The lower bound is also valid for the effective viscosity of suspensions containing spherical inclusions.Pores present in a glass matrix affect its flow behavior and consequently its creep and sintering behavior. The effective viscosity of porous glasses (ηP) as a function of the volume fraction of pores, or porosity (P), also varies between and upper [ηP = ηM (1 - P)1.04] and a lower bound [ηP = ηM (1 - P)14], where ηM is the viscosity of the nonporous glass matrix. For spherical porosity the equation is: \documentclass{article}\pagestyle{empty}\begin{document}$${\rm \eta_P = \eta_M(1 - P)^{1.5}}$$\end{document}Measured values for the viscosity of different suspensions as reported in the literature as well as own experimental data on two glass-solid systems are compared with the theoretical values predicted by these equations. In a similar way literature data for the viscosity of porous sintered glasses are compared with the respective equations. In all cases a fair agreement between experiment and theory was found in some cases the agreement was excellent. Therefore the presented equations constitute a reliable approach for the prediction of the viscosity of suspensions and porous sintered glasses and since they do not contain fitting parameters, they are of substantial practical relevance (for a comprehensive english treatment of the matter compare Glastechnische Berichte, Proc. Otto-Schott-Colloquium 1994).
    Notes: Suspensionnen von Festphasenteilchen in Glasschmelzen verändern deren Fließverhalten und damit deren Viskosität. Die vorliegende Arbeit behandelt die Abhängigkeit der effektiven Viskosität (ηeff) isotroper Suspensionnen von der Konzentration der Festphansenteilchen. Unabhängig von deren Form liegen die effektiven Viskositäten zwischen oberen und unteren Grenzwerten, deren Konzentrationsabhängigkeit durch Näherungslösungen gegeben ist: obere Grenzwertgleichung: ηeff = ηL (1 - CD)-14untere Grenzwertgleichung: ηeff = ηL (1 - CD)-3(ηL = Viskosität der Schmelze; CD = Volumenanteil der Festphasenteilchen). Für die effektive Viskosität von Suspensionen mit sphärischen Festphasenteilchen gilt die untere Grenzwertgleichung.Poren in Sintergläsern verändern ebenfalls deren Fließ- und damit Sinter-, Umform- und Kriechverhalten. Die effektive Viskosität poröser Gläser (ηP) als Konzentrationsfunktion ist gegeben durch die Näherungslösungen: obere Grenzwertgleichung: ηP = ηM (1 - P)1.04untere Grenzwertgleichung: ηP = ηM (1 - P)14(ηM = Viskosität des porenfreien Glases; P = Porosität).IM Falle sphärischer Porosität gilt die Viskositätsgleichung \documentclass{article}\pagestyle{empty}\begin{document}$${\rm \eta_P = \eta_M(1 - P)^{1,5}}$$\end{document}Gemessene Werte der Viskosität diverser Suspensionen sowie von Na2O-SiO2-Schmelzen mit dispergierten festen SiO2-Teilchen und Na2O-GeO2-Schmelzen mit dispergierten GeO2-Teilchen werden ebenso mit berechneten Werten verglichen wie die experimentellen Werte der Viskosität von porösen Sintergläsern mit den entsprechenden theoretischen. In allen Fällen wurde hinreichende, vielfach beste Übereinstimmung festgestellt. Die Gleichungen liefern praxisrelevante, verläßliche Aussagen sowohl für Suspensionen wie für poröse Sintergläser.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Advanced Materials 8 (1996), S. 928-932 
    ISSN: 0935-9648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 1 (1990), S. 263-273 
    ISSN: 1042-7147
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Small-angle neutron scattering studies have been used to clarify several aspects of the internal structure of latexes and subsequent film formation modes. This paper reviews work both around the world and at Lehigh University on those subjects. Two points have been made clear: (1) The appearance of core-shell phenomena in latexes depends on the size of the polymer chain to that of the latex particle; the phenomenon is most marked when the radius of gyration of the chain is about one fifth as big as the latex radius. (2) Strength build-up during film formation depends on the extent of interdiffusion of the chains. For moderate molecular weights, interdiffusion distances of one radius of gyration yield maximum strength. For both moderate (250,000 g/mol) and high (2,000,000 g/mol) molecular weights, full strength was achieved in two hour's annealing time at 144°C.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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