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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 36 (1995), S. 599-605 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A continuum hydration model based upon the atomic charges provided with the CFF91 force field [A. B. Schmidt and R. M. Fine (1994) Molecular Simulation, 13. 347-365] has been extended to the octanol-water transfer. The electrostatic component of the transfer free energy is calculated using the finite-difference solution to the Poisson-Boltzmann equation while the nonpolar contributions are assumed to be proportional to the solute-excluded volume in water. All atomic charges and radii besides the aromatic carbon radius are equal in both solvents. The octanol dielectric constant and the probe radius are the main fitting parameters defining the octanol phase. The model has been tested for 38 organic molecules related to the amino acid residues and generally provides a high accuracy. In particular, the mean unsigned error for N-acetyl amino acid amides is 0.5 kcal/mol. © 1995 John Wiley & Sons, Inc.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 174 (1990), S. 69-80 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: It is shown, that hydroxyterminated polydienes of good microstructure and functionality and a narrow molecular weight distribution can be prepared using di-hydroxyethyl-azo-bis-isobutyramide as an initiator. The activation energy of the initiator decay has been determined by volumetric measurement of the nitrogen evolved in this reaction.
    Notes: Es wird gezeigt, daß hydroxyterminierte Polydiene mit guter Mikrostruktur und Funktionalität sowie enger Molekulargewichtsverteilung unter Verwendung von Azobis-isobuttersäure-di-hydroxyethylamid hergestellt werden können. Die Aktivierungsenergie des Initiatorzerfalls wurde durch volumetrische Messung des bei dieser Reaktion freiwerdenden Strickstoffs bestimmt.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 2 (1951), S. 93-95 
    ISSN: 0947-5117
    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
    Notes: Allgemeine Eignung von Graphit als Apparatewerkstoff  -  Entwicklung von Graphitwärmeaustauschern durch die I. G. Farbenindustrie, Bitterfeld  -  Imprägniermittel und -verfahren zur Verringerung der Porosität des Graphits  -  Verbindung von Bauelementen aus Graphit.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 64 (1992), S. 871-872 
    ISSN: 0009-286X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 40 (1959), S. 277-278 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: By addition of 1-isocyanat-tetraacetylglucose to the hydroxylgroups of unsubstituted amylose we introduced branches are introduced in linear polysaccharides. The degree of branching attained was calculated from acetyl and nitrogen values. The highest degree of branching was about 0.8. The desacetylated branched polysaccharides were soluble in water.
    Notes: Mit Hilfe der Additionsreaktion von 1-Isocyanato-tetraacetylglucose an die Hydroxylgruppen von Polysacchariden wurden in unsubstituierte Amylose Glucoseverzweigungen eingeführt. Der Verzweigungsgrad konnte aus Stickstoff- und Acetylbestimmungen ermittelt werden. Es wurden Verzweigungsgrade von über Z = 0,8 erreicht. Die von den Acetylgruppen befreiten Substanzen waren z. T. gut wasserlöslich.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 622 (1996), S. 1038-1046 
    ISSN: 0044-2313
    Keywords: Binuclear antimony(V) complexes ; structure ; dynamics ; NMR spectra ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: d, h-μ-Benzylalkoxophosphonato-e-μ-alkoxo-f-μ-oxo-bis[trichloroantimony(V)] CompoundsThe binuclear antimony(V) complexes Cl3Sb(O)[R3(R1O)PO2](OR2)SbCl3 1 - 6 with R1 = R2 = CH3, C2H5 and R3 = C6H5CH2, (CH3)3C6H2CH2 in solution slowly exchanges the R2 groups between the oxygen atoms of the Sb2O2 ring. The SbOPOSb ringsystem makes rapid pseudorotation. The isomeres are detected by nmr spectroscopy. 1 (R1 = R2 = CH3) crystallizes in the orthorhombic space group Pnma with a = 1247.0, b = 1324.1, c = 1207.9 pm and Z = 4. 2 (R1 = CH3, R2 = C2H5) and 5 (R1 = R2 = CH3, R3 = (CH3)3 · C6H2CH2) crystallizes triclinic in the space group P-1 with a = 984.1, b = 1026.7, c = 1079.9 pm, α = 87.93, β = 75.70, γ = 87.62° and Z = 2 and a = 1164.6, b = 1296.9, c = 1712.9 pm, α = 109.9, β = 96.3, γ = 100.2° and Z = 4 resp., with two crystallographically independent molecules in the asymmetric unit.
    Notes: Die zweikernigen Antimon(V)-Komplexe Cl3Sb(O)[R3(R1O)PO2](OR2)SbCl3 1 bis 6 mit R1 = R2 = CH3, C2H5 und R3 = C6H5CH2, (CH3)3C6H2CH2 tauschen bei RT in Lösung langsam die R2-Gruppen aus. Daneben erfolgt rasches Umklappen des SbOPOSb-quasi-Fünfringes. Die Isomerenbildung wird NMR-spektroskopisch nachgewiesen. 1 (R1 = R2 = CH3) kristallisiert orthorhombisch in der Raumgruppe Pnma mit a = 1247,0, b = 1324,1, c = 1207,9 pm und Z = 4. 2 (R1 = CH3, R2 = C2H5) und 5 (R1 = R2 = CH3, R3 = (CH3)3C6H2CH2) kristallisieren triklin in der Raumgruppe P-1 mit a = 984,1, b = 1026,7, c = 1079,9 pm, α = 87,93, β = 75,70, γ = 87,62° und Z = 2 bzw. a = 1164,6, b = 1296,9, c = 1712,9 pm, α = 109,9, β = 96,3, γ = 100,2° und Z = 4 mit zwei kristallographisch unabhängigen Molekülen in der asymmetrischen Einheit.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 621 (1995), S. 640-644 
    ISSN: 0044-2313
    Keywords: Binuclear antimony(V) complexes ; ligand exchange ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: d,h-m̈-Alkoxoalkylphosphonato-e-m̈-alkoxo-f-m̈-oxo-bis[trichloroantimony(V)] CompoundsThe binuclear antimony(V) complexes Cl3Sb(O)[R3(R1O)PO2](OR2)SbCl3 1 to 7 with R1, R2 and R3 = Me or Et in solution slowly exchanges the R2 groups between the equatorial oxygen atoms of the Sb2O2 ring. The SbO(3)PO(3)Sb ringsystem makes rapid pseudorotation. The resulting isomeres are detected by nmr spectroscopy.
    Notes: Die zweikernigen Antimon(V)-Komplexe Cl3Sb(O)[R3(R1O)PO2](OR2)SbCl3 mit R1, R2 und R3 = Me bzw. Et (1 bis 7) tauschen bei 20°C in Lösung langsam die R2-Gruppen der e-m̈-O-Atome (O(1)-Atome) aus. Daneben erfolgt rasche Pseudorotation des SbO(3)PO(3)Sb-quasi-Fünfringes. Die Isomerenbildung wird NMR-spektroskopisch nachgewiesen.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0323-7648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Liquid crystalline side chain polymers containing photoreactive azobenzene chromophores in the dark-adapted trans form and phenylbenzoate groups as co-mesogens have been prepared and investigated as monomolecular layers at the water/air interface and as multilayer assemblies deposited onto solid supports by the Langmuir-Blodgett-Kuhn (LBK) technique. Pressure area isotherms at variable temperatures together with reflection absorption spectra and Brewster angle microscopic pictures have been taken and analyzed (i) to derive information about the structural order and the packing properties of the mesogenic side groups within the monolayers of different homo- and co-polymeric systems and ii) to optimize the conditions for the transfer of the monolayers.The resulting multilayer assemblies were primarily characterized by X-ray reflectometry studies, which yield the film thickness, the electron density modulations indicative of any internal (double) layer periodicity, and two roughness parameters characterizing the substrate/film and the film/air interfaces, respectively. These investigations were complemented by surface plasmon, UV-vis and IR spectroscopic measurements which provided further information as to the optical/structural properties of the samples.It was found that those systems containing only azobenzene side groups (or a high percentage of them) are composed of metastable double layer subunits which can be easily assembled to thicker films even capable of carrying waveguide modes. The azobenzene chromophores forming various types of aggregates have an average tilt angle of 36° relative to the film normal presumably with a broad angular distribution.If the azobenzene mesogens are diluted by phenylbenzoate co-mesogens in the radio 1:2, only the first few dipping cycles show a good monolayer transfer so that only thin multilayer assemblies can be built up. Moreover, all these preparations though deposited in the Y-type mode show no indication of a doublelayer structure in the transferred film, but instead exhibit the so-called mesogen peak with a smectic periodicity corresponding to only a single monolayer. A structural model with interdigitating side groups is proposed to account for these experimental results.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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