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  • Geosciences (General)  (29)
  • Polymer and Materials Science  (23)
  • Organic Chemistry  (20)
  • Animals  (8)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 2 (1991), S. 237-243 
    ISSN: 1042-7147
    Keywords: Thin films ; Heat conductivity ; Thermal instruments and techniques ; 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: The temperature diffusivity β and heat conductivity κ of thin polymer films were measured at room temperature. Temperature waves were excited at one side of the film and detected at the other side with a pyroelectric foil (PVDF). The dependence of β and κ on chemical and structural parameters have been studied. For the first time, Langmuir-Blodgett-Kuhn multilayer assemblies prepared from “hairy rod” polymers were characterized: μm thin films of stiff polyamides prepared by spincoating exhibit heat conductivities an order of magnitude larger than “classical” polymers.
    Additional Material: 4 Ill.
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  • 2
    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: Stable monomolecular layers of a liquid-crystalline homopolymer bearing azobenzene chromophores in the mesogenic side groups could be prepared at the water-air interface by slow compression at room temperature. From the area per monomer unit of A0≈0.25 nm2 a structural model with tightly packed azobenzene groups oriented nearly parallel to the surface normal was deduced. After transfer to a solid support in a Y-type mode the obtained Langmuir-Blodgett-Kuhn (LBK) multilayer assemblies of varying thicknesses (from a double layer to a thick film of d = 238 nm, capable of guiding optical modes) were prepared and analyzed by X-ray reflection and optical evanescent wave techniques. A monolayer thickness of d0 = 2.52 nm, as well as the anisotropic index of refraction of these layers, could thus be evaluated.Photo-isomerization by UV-irradiation (at λ = (360±30)nm) was examined by UV-VIS absorption spectroscopy. X-ray reflectivity data of samples illuminated for 30 min showed a complete loss of the layered structure of the LBK samples. As a result strongly light-scattering films were obtained. Surface plasmon microscopy was used to demonstrate the usefulness of this photo-induced order-disorder transition for optical information storage.
    Additional Material: 10 Ill.
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  • 3
    ISSN: 1042-7147
    Keywords: LBK films ; alternating layers ; ionenes ; NLO chromophores ; surface plasmon spectroscopy ; X-ray reflection and diffraction ; 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: Langmuir-Blodgett-Kuhn films of ionene polymers and nonlinear optically (NLO) active amphiphiles were investigated using several ultrathin film-sensitive techniques to determine multilayer ordering. Studies involved the formation of “passive-active” AB y-type multilayers of the ionenes and the NLO active amphiphiles. Deposition was possible with the use of an alternate three compartment dipping trough. The multilayer structures and thicknesses were verified by X-ray diffraction and reflection measurements and surface plasmon spectroscopy on a gold-coated glass substrate. Two main factors were determined to be responsible for the formation of stable alternating film architectures, namely electrostatic interaction in the hydrophilic layers and the van der Waals interaction in the hydrophobic layers. The use of ionenes as a class of amphiphilic polymers allowed the preparation of films with excellent optical quality.
    Additional Material: 6 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 330 (1988), S. 1015-1021 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 3,3-Bisalkylthioacrylonitriles (2), substituted by a cyano, carboxylate or amido group at position 2 react with derivatives 5 of α-aminoacids by monosubstitution under the formation of 3-carbonylmethylaminoacrylnitriles (6) or by substitution and cyclisation to 5-alkylthio-3-aminopyrrole-2-carboxylates (7) or the tetrahydro-1,4-diazepin-2,7-dione (8).
    Additional Material: 2 Tab.
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 36 (1997), S. 181-189 
    ISSN: 0021-9304
    Keywords: plasma deposition ; film chemistry control ; triethylene glycol monoallyl ether ; PEO (polyethylene oxide) ; protein adsorption ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The direct plasma-induced deposition of tri(ethylene glycol) monoallyl ether is reported. RF plasma polymerization of this monomer was carried out under both continuous wave (CW) and pulsed plasma operation. The major focus of this work was optimization of the degree of retention of the C-O-C bonds of the starting monomer during the deposition process. This successfully was accomplished using low RF power during the CW runs and low RF duty cycles during the pulsed plasma experiments. Spectroscopic analysis of the plasma films revealed a strong dependence of film composition on the RF power and duty cycles employed. In particular, an unusually high level of film chemistry compositional control was demonstrated for the pulsed plasma studies, with film composition varying in a steady, progressive fashion with sequential changes in the ratios of plasma on to plasma off times. This film chemistry controllability is demonstrated despite the relatively low volatility of the starting monomer. The utility of this plasma deposition approach in introducing polyethylene oxide (PEO) structures on solid substrates was evaluated via protein adsorption studies. Radiolabeled bovine albumin adsorption was studied on plasma-modified poly(ethylene teraphthalate) (PET) substrates. Dramatic reductions in both initial adsorption and retention of this protein were observed on PET samples having maximal PEO content relative to its adsorption on untreated PET surfaces. Good stability and adhesion of the plasma films to the underlying PET substrates were observed, as evidenced from prolonged immersion of plasma-treated surfaces in aqueous solution. Overall, the results obtained from the present work provide additional support for the utility of one-step plasma process to reduce biological fouling of surfaces via deposition of PEO surface units. © 1997 John Wiley & Sons, Inc. J Biomed Mater Res, 36, 181-189, 1997.
    Additional Material: 7 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 327 (1985), S. 455-462 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: N-(3-Aminothioacryloyl)-formamidines 3 react with primary amines to give either 4(1H)-pyrimidinthiones 6 or transaminated N-(3-aminothioacryloyl)-formamidines 5. Alkylation of the latter compounds gives rise to cyclised 6(1H)-pyrimidinimines 7. The 4(1H)-pyrimidinthiones 6 can be S-alkylated to 4-alkylmercaptopyrimidinium salts 8. Subsequent substitution of the alkylmercapto group of the 8 results in the formation of 4-aminopyrimidinium salts 9, which can also be obtained starting from the 3 by a reversed reaction sequence that is first by S-alkylation to 3-alkylmercapto-2-azapentamethinium salts 10 and subsequent reaction with primary amines.
    Additional Material: 3 Tab.
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  • 7
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: N, N′-Bis(aminomethylidene)thioureas 1 react with electron acceptor substituted methyl halides 2 under the formation of 2-formamidinothiazoles 4. The reaction of N-(3-aminothioacryloyl)-formamidines 5 with substituted methyl halides 2 gives either 2-formamidinothiophenes 7 or 2-aminovinylthiazoles 8. The 8 can be hydrolysed to corresponding 2-hydroxyvinylthiazoles 9. 2-Aminovinylthiazoles 11 bearing primary amino groups are obtained by transamination of the N-(3-aminothioacryloyl)-formamidines 5 and subsequent reaction of the resulting 10 with substituted methyl halides 2.
    Additional Material: 2 Tab.
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  • 8
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Investigation on Probe Properties of 7-Hydroxy-coumarines in Micellar Cetyl-triethyl-ammoniumbromide Solution - Means for Characterization of Micellar SystemsAnions of 3-substituted 7-hydroxy-coumarines (1a-c) as fluorescence probes have been studied in this work. Acid-base equilibria in water and micellar solution of cetyl-triethylammoniumbromide (cmc = 0,72 mmol l-1), fluorescence properties and fluorescence quenching by octacyano-molybdate-IV have been investigated. It has been confirmed that probe and quencher are completely micellized. Fluorescence life times and quenching constants per one quencher molecule in the micell of about 108 s-1 have been determined. The kinetics of saponification of the probe 3-acetyl-7-hydroxy-coumarine at pH = 12 in micellar solution has been followed by probe fluorescence.
    Additional Material: 6 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 323 (1981), S. 466-470 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Activation Entropies of Free Radical Addition Reactions via MINDO/3-UHF-CalculationsA MINDO/3-UHF study on the additions of methyl radicals to acetone, formaldehyde, ethylene, and isobutene indicates that the transition state occurs later with non-terminal C-addition as compared to terminal C-addition. Distinctly lower activation entropies are obtained for non-terminal addition.
    Additional Material: 1 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 193 (1992), S. 1235-1247 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A series of liquid-crystalline copolymers 1 with a chiral azobenzene moiety as photoreactive mesogenic unit was prepared. The polymers were fractionated and the mesophase behaviour of the high- and low-molecular weight fractions was examined. The copolymers display smectic A and cholesteric phases. For the cholesteric phases the pitch of the helix was determined, which ranges from 3 to 20 μm. Stable monolayers at the air-water interface were obtained from two monomers and one of the homopolymers. Multilayer assemblies of the azobenzene-containing polymers can be used to study photo-induced order/disorder transitions.
    Additional Material: 3 Ill.
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