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  • Humans  (16)
  • Polymer and Materials Science  (14)
  • Astrophysics  (12)
  • ASTROPHYSICS
  • 2005-2009  (16)
  • 1995-1999  (17)
  • 1980-1984  (13)
  • 1
    Electronic Resource
    Electronic Resource
    Nearest-neighbor and next-nearest-neighbor effects in the proton NMR spectra of the oligoribonucleotides ApGpX and CpApX (1980)
    New York : Wiley-Blackwell
    Biopolymers 19 (1980), S. 557-573 
    Details
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The variable-temperature proton nmr spectra of the oligoribonucleotides in the series CpApX and the series ApGpX, X = A, G, C, U, together with the parent dimers CpA and ApG have been measured. A complete analysis of all the nonexchangeable base proton resonances and ribose H-1′ proton resonances was made. The presence of trends in the shielding abilities of the various bases at both the nearest-neighbor and next-nearest-neighbor positions were identified. The observed shieldings could be used to predict the chemical shifts of protons in related systems. Based on the empirical results from ribodinucleoside monophosphates, the temperature-dependent behavior of the J1′2′ coupling constants of the triribonucleotides suggested that the compounds in the CpApX series stacked from the 5′-end to the 3′-end, while those in the ApGpX series stacked from the 3′-end to the 5′-end.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bip.1980.360190309
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  • 2
    Electronic Resource
    Electronic Resource
    Conformations of cyclic peptide/calcium complexes in solution (1982)
    New York : Wiley-Blackwell
    Biopolymers 21 (1982), S. 169-179 
    Details
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthetic cyclic octapeptides of general structure cyclo[Glu(γOBzl)-Sar-Gly-(N-R)Gly]2 (R = n-hexyl and cyclohexyl) transport calcium ions selectively across organic phases and phospholipid membranes. We have now used proton nmr spectroscopy (360 MHz) to study the solution conformation(s) of their calcium complexes. When Ca(ClO4)2 was added to solutions of these peptides in CDCl3, nmr spectra of the resulting calcium complexes were characteristic of a single C2-symmetric conformer. From a Karplus-Bystrov analysis of vicinal coupling constants in both the peptide backbone and Glu side chain (treated as an ABCC′MX spin system), in conjuction with model-building studies, a structure was proposed in which the calcium ion is bound in an octahedral-type complex by the four (coplanar) carbonyl groups of the (all-trans) Glu-Sar and Gly-(N-R)Gly peptide bonds. Occurrence of preferred rotamers about Glu side chain Cα-Cβ bonds indicated that restricted rotation in peptide side chains arises upon calcium binding.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bip.360210114
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  • 3
    Electronic Resource
    Electronic Resource
    Carriers for drugs and enzymes based on copolymers of allyl glycidyl ether with acrylamide (1982)
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 183 (1982), S. 781-788 
    Details
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Copolymerization of acrylamide with allyl glycidyl ether yielded water soluble polymers containing an epoxy group; addition of a crosslinking agent, N,N′-methylenebis(acrylamide), to the copolymerization mixtures resulted in the formation of similar though water insoluble polymers. Condensation of a potent beta-adrenergic antagonist Alm—H, which contains a reactive amino group, with a polymer containing an epoxy group yeilded a pharmacologically active polymer. The polymer containing the epoxy group was also converted, by reaction with sodium thiosulfate and subsequent reduction, into a mecapto groups containing polymer which was also water soluble. The latter polymer was converted by condensation with a beta-adrenergic antagonist Alm—COCH2Br, which contains a reactive bromoacetamido group, into a pharmacologically active polymer.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/macp.1982.021830403
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  • 4
    Electronic Resource
    Electronic Resource
    Nearest-neighbor and next-nearest-neighbor effects in the proton NMR spectra of the oligoribonucleotides ApXpG, CpXpG, CpApXpUpG, ApGpXpC, and ApGpXpCpU (1981)
    New York : Wiley-Blackwell
    Biopolymers 20 (1981), S. 1383-1398 
    Details
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The proton nmr spectra of the oligoribonucleotides in the series CpXpG, ApXpG, CpApXpUpG, and ApGpXpC (X = A, G, C, and U), together with the reference compounds CpG, ApG, CpApUpG, and ApGpC, have been measured. A complete analysis of all the nonexchangeable base protons and the ribose H-1′ protons was made. The insertion of a nucleotide X into a oligoribonucleotide led to shift changes at both nearest-neighbor and next-nearest-neighbor positions, which were rationalized in terms of the shielding abilities of the various bases. The derived shielding trends in the ApGpXpC series of compounds were successfully used to predict the chemical shifts of resonances in the related ApGpXpCpU series.
    Additional Material: 13 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bip.1981.360200703
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  • 5
    Electronic Resource
    Electronic Resource
    Protein-nucleic acid interactions and DNA conformation in a complex of human immunodeficiency virus type 1 reverse transcriptase with a double-stranded DNA template-primer (1997)
    New York : Wiley-Blackwell
    Biopolymers 44 (1997), S. 125-138 
    Details
    ISSN: 0006-3525
    Keywords: AIDS ; DNA structure ; polymerase structure ; protein - DNA interaction ; x-ray crystallography ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The conformation of the DNA and the interactions of the nucleic acid with the protein in a complex of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase (RT) and a 19-mer/18-mer double-stranded DNA template-primer (dsDNA) are described. The structure of this HIV-1 RT complex with dsDNA serves as a useful paradigm for studying aspects of nucleotide polymerases such as catalysis, fidelity, drug inhibition, and drug resistance. The bound dsDNA has a bend of approximately 41° at the junction of an A-form region (first five base pairs near the polymerase active site) and a B-form region (the last nine base pairs toward the RNase H active site). The 41° bend occurs smoothly over the four base pairs between the A-form portion and the B-form portion in the vicinity of helices αH and αI of the p66 thumb subdomain. The interactions between the dsDNA and protein primarily involve the sugar - phosphate backbone of the nucleic acid and structural elements of the palm, thumb, and RNase H of p66, and are not sequence specific. Amino acid residues from the polymerase active site region, including amino acid residues of the conserved Tyr-Met-Asp-Asp (YMDD) motif and the “primer grip,” interact with 3′-terminal nucleotides of the primer strand and are involved in positioning the primer terminal nucleotide and its 3′-OH group at the polymerase active site. Amino acid residues of the “template grip” have close contacts with the template strand and aid in positioning the template strand near the polymerase active site. Helix αH of the p66 thumb is partly inserted into the minor groove of the dsDNA and helix αI is directly adjacent to the backbone of the template strand. Amino acid residues of Β1′, αA′, αB′, and the loop containing His539 of the RNase H domain interact with the primer strand of the dsDNA. © 1997 John Wiley & Sons, Inc. Biopoly 44: 125-138, 1997
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Rapid spectroscopic confirmation of the presence of polystyrene in polymer particles of mixed composition (1998)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 999-1004 
    Details
    ISSN: 0887-6266
    Keywords: latex ; polystyrene ; luminescence ; particle ; micron-diameter ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A technique for rapid determination of the presence of polystyrene in individual micron-diameter polymer particles of mixed composition is presented. This technique is based upon observation of visible emission from conjugated regions of the polymer backbone, generated photochemically, while the particle is held in an optical trap. Particle emission characteristics are dependent upon particle size and suspending solvent. Emission spectra are provided for single component polystyrene particles and mixed polymer particles containing poly(methyl methacrylate), poly(N-vinyl pyrrolidone), and polystyrene. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 999-1004, 1998
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Binary and ternary blends of poly(vinyl chloride), hytrel, and a polyurethane (1981)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 3467-3473 
    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: Binary blends of poly(vinyl chloride) and a poly(ether urethane) containing 20 and 40 weight percent, respectively, of poly(vinyl chloride) have been prepared by solution blending from tetrahydrofuran and their degree of mixing investigated using dynamic mechanical analysis. In the polyurethane, transitions were found at -19°C and -119°C. The former was attributed to the glass transition and the latter to a Schatzki type of motion of the polyether sequences. This latter transition occurred at a temperature which is higher than the literature value for the low temperature transition in poly(tetrahydrofuran), which is equivalent to the polyether sequence in the polyurethane. This discrepancy is attributed to the influence of neighboring hard segments present because of incomplete segmental phase separation of the polyurethane. For the blends only one very broad transition was observed, indicating that there was substantial mixing of these two polymers. Three ternary blends were prepared, also by solution blending, containing poly(vinyl chloride), Hytrel, and the polyurethane in the ratios 1:1:1, 1:2:1, and 2:1:1, respectively. In the first two blends there was clear evidence of phase separation. It was only in the 2:1:1 blend that an apparently significantly compatible material resulted.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1981.070261025
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  • 8
    Electronic Resource
    Electronic Resource
    Polymeric systems for acoustic damping. III. Blends of poly(vinyl chloride), segmented poly(ether ester), and poly(methyl acrylate) (1981)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 3487-3491 
    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 solution blend of poly(vinyl chloride) and a segmented poly(ether ester) and blends containing these two polymers plus poly(methyl acrylate) were investigated by dynamic mechanical analysis and electron microscopy. The binary blend, which contained 75% by weight of the poly(ether ester), showed only one loss peak, but also evidence of some phase separation. It is believed that the polyether sequences of the poly(ether ester) are extensively mixed with poly(vinyl chloride). Poly(methyl acrylate) was added to spread the damping range and produce a material of potential use as an acoustic damper. It is evident from both electron microscopy and dynamic mechanical analysis that poly(methyl acrylate) is substantially incompatible in the other polymers.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1981.070261027
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  • 9
    Electronic Resource
    Electronic Resource
    XPS and SEM characterization of hydrated cerium oxide conversion coatings (1995)
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 23 (1995), S. 540-550 
    Details
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Cerium-rich conversion coatings have been deposited onto aluminium 2024-T351 alloy by immersion into a solution containing 10 g L-1 CeCl3 and 1% H2O2 in a process described as ‘cerating’. Prior to deposition the alloy had been prepared either by using a standard chemical pretreatment used for aerospace alloys before conversion coating or by polishing. X-ray photoelectron spectroscopy and scanning electron microscopy have been used to characterize these cerium-containing conversion coatings. It was found that, during deposition, hydrated cerium oxide initially covered the intermetallics present in the alloy surface and then covered the surface generally. Deposition continued over the intermetallics throughout the conversion coating process, resulting in thick, heavily-cracked regions considerably greater than the average thickness of the film (〉0.3 μm). Elsewhere the coating was generally up to 0.2 μm thick, and appeared to comprised of deposited particles around 100 nm in size.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/sia.740230714
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  • 10
    Electronic Resource
    Electronic Resource
    Unusual Peak Shifts in the Core Levels of CeO2 Films Deposited on Si(100) (1996)
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 24 (1996), S. 634-640 
    Details
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: X-ray photoelectron spectroscopy has been used to study 20, 100 and 1000 nm evaporated cerium oxide films on Si(100) single-crystal wafers. Upon exposure to the x-ray source there was loss of oxygen and generation of Ce3+. Furthermore, for the 20 nm coating, there was evidence of a shift to higher binding energies of the C 1s peak and a high binding energy O 1s component relative to the oxygen anion peak at 529.7±0.1 eV with increased exposure time to the x-ray source. No similar shift was observed in the O KLL Auger lines, suggesting that the effect was not due to differential charging of the surface with respect to the bulk of the coating. Hence the relative shift is explained in terms of electronic effects resulting from the formation of anion vacancies in the surface. These include a shift of the Fermi level due to defect states in the bandgap as well as band bending due to the positive charge set up from the anion vacancies.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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