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  • 1995-1999  (46)
  • 1980-1984  (32)
  • 1900-1904  (1)
  • Chemistry  (76)
  • Biochemistry and Biotechnology  (13)
  • Tyr(P)-containing peptides  (3)
  • 1
    Electronic Resource
    Electronic Resource
    A small-angle x-ray scattering study of alginate solution and its Sol-Gel transition by addition of divalent cations (1995)
    New York : Wiley-Blackwell
    Biopolymers 35 (1995), S. 227-238 
    Details
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The small-angle x-ray scattering (SAXS) technique has been applied to investigate solution and gel structures of alginate in the absence and presence of two divalent cations: Ca(II) and Cu(II). We have observed a broad maximum in the scattering curve, a characteristic of polyelectrolyte, for the purified alginate sample. The scattering maximum disappears in excess of added simple salt and shifts toward the higher angle region with increasing alginate concentration. Concentration dependence of the position and intensity of the maximum follows power law relations with exponents close to those predicted by theory. Data analysis shows an increase in correlation length ξ and cross-sectional diameter d0, of polymer chains upon gelation and suggests that a dimeric structure is adopted in the junction zone, consistent with the “egg-box” model previously proposed. In the Ca(II)-alginate system, the molecular parameters ξ and d0 are found to have good correlation with the macroscopic properties of gelation, such as gel point determined by viscosity measurements. However, for the Cu(II)-alginate system there is no clearly transitional behavior observed in ξ and d0, implying that the junction zone may be replaced by a more uniformly distributed site binding of Cu(II) ions to the carboxyl groups of both mannuronate and guluronate residues, in confirmation of previous 13C-nmr results. © 1995 John Wiley & Sons, Inc.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bip.360350211
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  • 2
    Electronic Resource
    Electronic Resource
    Crystal Smectic-B Phase from a Mesomorphic Ferrocene Derivative (1995)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 78 (1995), S. 1215-1218 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal properties of two ferrocene derivatives, substituted by either one or two cholesteryloxycarbonyl units, were investigated. While the monosubstituted ferrocene derivative 1 was found to be non-mesomorphic, the disubstituted ferrocene derivative 2 exhibited a crystal smectic-B phase. This result shows that ferrocene-containing thermotropic liquid crystals, despite the bulkiness of the metallocene core, are not limited to disordered calamitic phases.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19950780514
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  • 3
    Electronic Resource
    Electronic Resource
    Synthese stereoisomerer Pinanthromboxane und Evaluation der Verbindungen als PlättchenaggregationsinhibitorenHerrn Professor Dr. A. Hürlimann zum 60. Geburtstag gewidmet (1983)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 66 (1983), S. 989-1008 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis of Stereisomeric Pinanthromboxane Derivatives and Evaluation of the Compounds as Platelet Aggregation InhibitorsStarting from the two enantiomeric myrtenols ((-)-1 and (+)-1; cf. Scheme 1), the synthesis of twelve stereoisomeric pinanthromboxane derivatives ((+)- and (-)-10, -11, -14, -15, -21 and -22) is described (cf. Schemes 1-4). Biological data from the evaluation as platelet aggregation inhibitors (cf. Table 6 and 7), thromboxane synthetase inhibitors (cf. Table 8) and from the assessment as antagonists of leukotriene E4 induced bronchoconstriction (cf. Table 9) are presented.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19830660331
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  • 4
    Electronic Resource
    Electronic Resource
    New Triterpenes from the Bark of Western White Pine (Pinus monticola DOUGL.)See [1]. (1981)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 64 (1981), S. 1183-1207 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Eleven new triterpenes with the lanostene-type skeleton were isolated from the benzene extract of western white pine bark. Their structures were determined mainly on the basis of physical and spectral data.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19810640424
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  • 5
    Electronic Resource
    Electronic Resource
    Supermolecules Containing a Tetrahedral Core: A New Class of Liquid-Crystalline Siloxanes (1996)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 129 (1996), S. 521-525 
    Details
    ISSN: 0009-2940
    Keywords: Liquid crystals ; Siloxanes ; Phase behaviors ; Defined topology ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It is shown that supermolecules with a tetrahedral symmetry and appropriate side-chains exhibit liquid-crystalline phase behaviour. The use of an optimised hydrosylation reaction allows for the synthesis of materials that have four mesogenic groups attached to a siloxane core, where the conformation and the configuration are unambiguous. The materials show low glass transition temperatures and, depending on the spacer length, complex liquid-crystalline morphologies.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19961290508
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  • 6
    Electronic Resource
    Electronic Resource
    Tetrathiafulvalene. XIX. Synthese und Eigenschaften elektronenleitender Poly-Dithiolenkomplexe mit Ethylentetrathiolat und Tetrathiafulvalentetrathiolat als Brückenliganden (1983)
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 325 (1983), S. 957-975 
    Details
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Tetrathiafulvalenes. XIX. Synthesis and Properties of Electron Conducting Poly-Dithiolene Complexes with Ethylene Tetrathiolat and Tetrathiafulvalene Tetrathiolat as Bridge Ligands[1,3]-Dithiolo[4,5-d]-1,3-dithiol-2,5-dione 7 and 5-(5-oxo[1,3]-dithiolo[4,5-d]1,3-dithiole-2-ylidene)[1,3]-dithiolo[4,5-d]1,3-dithiol-2-one 8 were synthesised from 1,3-dithiole-2-thione-4,5-dithiolat. The ligands react with salts of iron, cobalt, nickel, palladium, platinum and copper to give the polymer complexes 22a-g and 23a-e, respectively. Irradiation of 7 in the presence of iron penta-, dicobalt octa- or nickel tetracarbonyl gives the corresponding dithiolene complexes 21a-c.The amorphous insoluble polymer complexes from types 21, 22, and 23 have been characterised by i.r.-spectroscopy, susceptibility and conductivity measurements.The nickel complexes have the highest electrical conductivity (σRT ∼ 10-1Ω-1cm-1, pellets) with a very low activation energy (0,045 eV, 100-300 K)A high electron delocalization in the direction of the polymer chain and an easy charge transfer from chain to chain is supposed.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/prac.19833250612
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  • 7
    Electronic Resource
    Electronic Resource
    Accelerated photo-oxidation of polyethylene. II. Further evaluation of selected additives (1981)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 2917-2926 
    Details
    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: A number of additives previously observed to promote photo-oxidative degradation of polyethylene films have been evaluated with respect to their relative photoinitiating effectiveness at wavelengths near 300 nm and their effects on thermal-oxidative stability of polyethylene. Depending on the nature of the additive, the photo-oxidation process may display autoretarding or autoaccelerating behavior. Thermomechanical analyses and gel content measurements on UV-exposed films containing substituted anthraquinones suggest that at short exposure times, photo-oxidative degradation is accompanied by photochemical crosslinking.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1981.070260908
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  • 8
    Electronic Resource
    Electronic Resource
    Drawing rate effects on morphological parameters in nylon-6, PET, and PBT filaments (1982)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 27 (1982), S. 2369-2375 
    Details
    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: Influence of drawing velocity on morphological parameters of nylon-6, PET, and PBT filaments has been studied. The drawing was carried out at approximately 20°C above the effective glass transition temperature of these materials. The results are explained in terms of drawing-induced changes in temperature and in rate of crystallization.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1982.070270706
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  • 9
    Electronic Resource
    Electronic Resource
    Polyamides incorporating phosphine oxide groups. III. Polymerisation of bis[4-(2-aminoethyl)aminophenyl]-phenylphosphine oxide with dicarboxylic acids (1997)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 2865-2870 
    Details
    ISSN: 0887-624X
    Keywords: phosphine oxide ; aromatic-aliphatic polyamides ; polycondensation ; thermal properties ; fire retardant materials ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The new polymerisation monomer bis[4-(2-aminoethyl)aminophenyl]-phenylphosphine oxide (p-BAPPO) was prepared in good yield by the nucleophilic substitution reaction between bis(4-fluorophenyl)phenylphosphine oxide and a large excess of 1,2-diaminoethane. Five novel polyamides, incorporating phosphine oxide groups within the polymer backbone were synthesised by the condensation reaction of p-BAPPO with a series of aromatic and aliphatic dicarboxylic acids. The thermal properties of these polymers were investigated by differential scanning calorimetry and thermogravimetric analysis. Glass transition temperatures in the 180-215°C range were recorded. Although we observed their thermooxidative stabilities (5% weight loss 〉 345°C) to be lower by 40-70°C than those previously found for wholly aromatic polyamides with phosphine oxide groups within the parent chain, char yields upon prolonged heating at 650°C were still excellent (26-38%). Also, good solubility in aprotic polar solvents was observed for all polyamides synthesised. The new polyamides clearly represent significant progress in the quest for processible fire retardant materials. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 2865-2870, 1997
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Reaction path and free energy calculations of the transition between alternate conformations of HIV-1 proteaseThe content of this publication does not necessarily reflect the views or policies of the Department of Health and Human Services, nor does mention of trade names, commercial products, or organization imply endorsement by the U.S. Government. (1998)
    New York, NY : Wiley-Blackwell
    Proteins: Structure, Function, and Genetics 32 (1998), S. 7-16 
    Details
    ISSN: 0887-3585
    Keywords: conformational change ; free energy calculations ; HIV protease ; molecular dynamics simulations ; protein structure ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Two different structures of ligand-free HIV protease have been determined by X-ray crystallography. These structures differ in the position of two 12 residue, β-hairpin regions (or “flaps”) which cap the active site. The movements of the flaps must be involved in the binding of substrates since, in either conformation, the flaps block the binding site. One of these structures is similar to structures of the ligand-bound enzyme; however, the importance of both structures to enzyme function is unclear. This transformation takes place on a time scale too long for conventional molecular dynamics simulations, so the process was studied by first identifying a reaction path between the two structures and then calculating the free energy along this path using umbrella sampling. For the ligand-free enzyme, it is found that the two structures are nearly equally stable, with the ligand-bound-type structure being less stable, consistent with X-ray crystallography data. The more stable open structure does not have a lower potential energy, but is stabilized by entropy. The transition occurs through a collapse and reformation of the β-sheet structure of the conformationally flexible, glycine-rich flap ends. Additionally, some problems in studying conformational changes in proteins through the use of a single reaction path are addressed. Proteins 32:7-16, 1998. © 1998 Wiley-Liss, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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