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  • Chemistry  (50)
  • Electronic structure and strongly correlated systems
  • Molecular Sequence Data
  • 1990-1994  (41)
  • 1970-1974  (11)
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 2809-2813 
    ISSN: 0887-624X
    Keywords: Malachite Green vinyl polymer ; ionic conductivity ; photoinduced switching ; single-ionic ; carrier generation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Copolymers of bis[4-(N,N-dimethylamino)phenyl]-4-vinylphenylmethanenitrile (vinyl Malachite Green leuconitrile) with methyl methacrylate or ω-methoxyoligo(oxyethylene) methacrylate have been synthesized, aiming at designing one-component-type organic polymers for photoswitchable ion-conducting films. The triphenylmethanenitrile copolymers with ω-methoxyoligo(oxyethylene) methacrylate were found to undergo ionic-conductivity switching by turning on and off UV light at ambient temperature, owing to their low glass transition temperature. © 1993 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 181-185 
    ISSN: 0887-624X
    Keywords: poly(bisthiazole-imide) ; heterocyclic polyimide ; solubility ; high-temperature polymers ; thermal properties ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 5 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 1243-1254 
    ISSN: 0887-624X
    Keywords: tetraphenylporphyrin-containing polymer ; homopolymer ; water-soluble polymer ; radical polymerization ; manganese(III) complex ; ligand substitution reaction ; anionic ligand ; thiocyanate ; electrostatic effect ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A vinyl monomer containing the pendant tetraphenylporphyrin (TPP) group, 4-vinyltetraphenylporphyrin (VTPP), was synthesized. A homopolymer (PVTPP) which is insoluble in water, and three water-soluble polymers were obtained by radical polymerization. The water-soluble polymers are two anionic polymers (PVPTSPP and PVTPP-StSO3) and a cationic polymer (PVTPP-VPyM). PVPTSPP has sulfonic acid groups in a TPP group and very high charge density. PVTPP-StSO3 was obtained by copolymerization of VTPP and sodium 4-styrenesulfonate. PVTPP-VPyM was obtained by quarternarization of a copolymer of VTPP and 4-vinylpyridine. Polymeric manganese(III) complexes (PMn-VTPP, PMnVPTSPP, PMnVTPP-StSO3, and PMnVTPP-VPyM) were prepared from the polymers and manganese acetate. The acetate ligand in PMnVTPP can be easily substituted by another ligand such as Cl-, AcO-, OH-, and SCN-. The substitution reaction occurs in the interface between water and chloroform. The sulfonated homopolymer, PMnVPTSPP, cannot incorporate with anionic ligands because of the strong electrostatic repulsion. In the anionic copolymer, PMnVTPP-StSO3, the ligand substitution reaction with SCN ligand needs activation energy of 53 kJ/mol. In the cationic polymer complex, PMnVTPP-VPyM, the OH ligand can be easily substituted with the SCN ligand and the equilibrium constant of the reaction was estimated at 1.38 × 10-3. © 1994 John Wiley & Sons, Inc.
    Additional Material: 14 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 29 (1991), S. 777-779 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 5
    ISSN: 1042-7163
    Keywords: Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 4,6-Disubstituted thianthrene-5-oxides reacted with n-butyllithium to afford sterically crowded 1,9-disubstituted dibenzothiophenes (3) in moderate yields. The structures of the phenylthio derivative 3a and its monooxide 6a were determined by X-ray crystallographic analysis, which revealed that the distances between the two outer sulfur atoms are 3.012 Å (3a) and 3.016 Å (6a). 1,9-Disubstituted dibenzothiophenes 3 and their monooxides 6 afforded the corresponding dithia dications on dissolution in conc. sulfuric acid. The lower oxidation potentials of compounds 3 compared with other dibenzothiophene derivatives reveal evidence for strong transannular interaction between the two outer sulfur atoms.
    Additional Material: 2 Ill.
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  • 6
    ISSN: 1018-5054
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The conformation of the ethoxy tail flanking the cyanobiphenyl core has been studied in the liquid-crystalline phase as well as in the isotropic solution. In solution, the vicinal coupling constant 3JCH for the moiety CphO—CH (Cph: phenyl carbon) provided the information regarding the rotation around the O—C bond. Phenetole was mostly used as a model compound. The conventional rotational isomeric state (RIS) analysis yielded the energy difference between the gauche and trans state to be of the order of 1,6 to 1,4 kcal/mol in CDCl3, C6D6 and dimethyl-d6 sulfoxide. In this treatment, the rotational state around the neighboring bond (Cph—O) was taken to occur at 0 or π. The deuterated compound, 4-ethoxy-4′-biphenylyl-d7 cyanide, was prepared and studied in the liquid-crystalline state by 2H NMR. The orientational order parameters of the mesogenic core were determined by the analysis of dipolar and quadrupolar splitting data due to aromatic deuterons. The quadrupolar splitting data were also obtained for the deuterated ethoxy tail. The conformation of the tail was elucidated according to the RIS simulation scheme previously proposed. The fraction of the trans conformation ft was estimated to be 0,79 around the nematic-isotropic transition temperature (TNI = 91,9°C). It was suggested that the conformation of the ethoxy tail remains nearly unaffected by the phase transition in the immediate vicinity of TNI. The fraction ft increases moderately toward an asymptotic value as temperature decreases.
    Additional Material: 8 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 4 (1993), S. 205-208 
    ISSN: 1042-7147
    Keywords: Polymer electrolytes ; lonic conductivity ; Organogels ; Photopolymerization ; Polyaniline ; Rechargeable battery ; 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: Gel-type solid polymer electrolytes (SPE) which consisted of LiBF4 as the electrolyte, a mixture of propylene carbonate and 1,2-dimethoxyethane as the solvents, and a mixture of ethoxypolyoxyethyleneacrylate and trimethylolpropanetriacrylate as the monomers, were prepared by photopolymerization. The composition range for the gelation and the SPE formation was defined. Relationships between the composition of the SPE, and the ionic conductivity and modulus were clarified. The ionic conductivity of the SPE film, the composition of which was 13 wt% monomer, 20 wt% LiBF4 and 67 wt% solvent, was 2.7 × 10-3 S/cm, and the modulus was 103 dyn/cm2 at 25°C. When a polyaniline(PANI)/SPE interface was formed on polyaniline films by photopolymerization at the optimal composition, the redox behavior of PANI was almost equivalent to that in nonaqueous electrolyte solutions. The discharge capacity of a Li/SPE/PANI film rechargeable battery was 116 mAh/g-PANI (based on the weight of PANI), almost the same as that of a Li/nonaqueous electrolyte solution/PANI cell.
    Additional Material: 7 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 20 (1991), S. 493-497 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A sensitive and rapid method to analyse fuel components in blood from rats exposed to kerosene or light oil vapour was developed by making use of capillary gas chromatography/mass spectrometry. The aliphatic hydrocarbons with carbon numbers 8-10 and aromatics such as toluene, xylene, 3- and 4-ethyltoluene and trimethylbenzenes were clearly detected in blood from rats exposed to kerosene or light oil vapour, using the head-space method combined with the salting-out technique. The concentration ratio of pseudocumene to toluene in blood exposed to light oil was higher than that in the case of exposure to kerosene. The lower limits of detection were 50 pg and 1 ng in toluene and pseudocumene, respectively. Our suggestion is that this method is useful in forensic investigations to detect fuel components in blood and for the purposes of differentiating kerosene and light oil in blood tissues.
    Additional Material: 2 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 15 (1971), S. 2065-2072 
    ISSN: 0021-8995
    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
    Notes: For the rapid identification of additives such as antioxidant, ultraviolet absorber, and slipping agent, polypropylene containing such additives was heated in a tube connected directly to the inlet system of a mass spectrometer. The vapor of the additives evaporating out of the polypropylene was led to the reservoir and then submitted to mass spectrometry to give spectra for identification.
    Additional Material: 3 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 1749-1759 
    ISSN: 0021-8995
    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
    Notes: Nuclear magnetic resonance absorption spectra of linter cellulose containing various amounts of water were studied to clarify the relation between the amount of absorbed water in cellulose fiber and the molecular motion in such a cellulose-water system. An amorphous cellulose sample was used for the sake of comparison. The changes in line width and second moment of the spectra were measured at various temperatures. From the variation with temperature of the first-derivative curves and the second moments, it has been inferred that the proton movement of absorbed water changes markedly over the approximate range 180°-200°K and that the absorbed water lowers the glass transition temperature of cellulose to room temperature.
    Additional Material: 13 Ill.
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