ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Elsevier  (515)
  • Wiley-Blackwell  (62)
  • 1975-1979  (319)
  • 1970-1974  (258)
Collection
Years
Year
  • 1
    Publication Date: 1979-02-01
    Print ISSN: 0021-9673
    Electronic ISSN: 1873-3778
    Topics: Chemistry and Pharmacology
    Published by Elsevier
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Publication Date: 1970-10-01
    Print ISSN: 0006-2952
    Electronic ISSN: 1873-2968
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Published by Elsevier
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 18 (1979), S. 3077-3087 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We present evidence for structures of two ordered forms of polyxanthylic acid based on ir spectroscopy, pH titrations, and thermal transitions. Over the pH range ∼6-9.5, the structure is a four-stranded helix with alkali metal ions specifically complexed in the central channel. These internal counterions stabilize the structure by complexing with carbonyl oxygens and by partial screening of electrostatic repulsion caused by ionization of the xanthine residues in this pH range. Below pH 5, the structure is quite different and much more stable. Our data are consistent with a six-stranded helix in which both carbonyl oxygens and both NH protons are hydrogen bonded.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 9 (1975), S. 1-8 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In this paper a calculation of the static quadrupole polarizabilities and the shielding factors of the atoms and ions of the 2p open shell systems is presented. A fully coupled Hartree-Fock method using the Roothaan formalism is adopted. Calculations have been done for the ground as well as for some valence excited states. An antishielding effect is observed for all the atoms and ions under study.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 11 (1977), S. 441-450 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of LCAO-MO-SCF calculations, using various basis sets of Gaussian-type functions, has been made in order to study the effects of p, d, and f polarization functions for a 10-electron isoelectronic series of oxygen hydrides and for an 18-electron isoelectronic series of sulfur hydrides. Conclusions from these results suggest that meaningful proton affinities cannot be calculated without the inclusion of a d function on the heavy atom and a p function on the hydrogen atoms.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 9 (1975), S. 495-504 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In this paper we include the rearrangement correction (discussed in the preceding paper) in a coupled Hartree-Fock (CHF) calculation of atomic hyperpolarizabilities and other related properties. We have studied the effect of these corrections on properties like electric dipole hyperpolarizabilities, uniform electric field quadrupole polarizabilities and shielding factors in two-electron ions and have noticed significant changes in the computed values over the CHF results.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 12 (1977), S. 1-9 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In this paper static dipole polarizabilities and shielding factors of 3p open-shell atomic systems from A1 to C1 are presented using coupled Hartree-Fock theory in the Roothaan scheme. The calculation was made for the ground as well as for some valence excited states of the ions. A variational approach was adopted to obtain the polarizability values and the results are compared with the existing data wherever possible. The shielding factor values are in good agreement with the theoretical N/Z ratio.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 11 (1977), S. 17-20 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A derivation of most general existence conditions for surface states of a semi-infinite Kronig-Penney crystal is reported. They reduce to Steslicka's conditions under a subsidiary restriction and also indicate that the surface-state energies may lie in the allowed bulk bands. Numerical computations supporting the qualitative conclusions are provided.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 9 (1975), S. 75-81 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The time-dependent variational principle is used to calculate the frequency-dependent dipole polarizabilities of 2p open-shell atomic systems. A general theory is built up to include frequency-dependent perturbations using the Roothaan-Hartree-Fock (HFR) formalism. The excitation energies corresponding to the low-lying excited states of the system are obtained from the poles of the dynamic polarizability values. A fairly accurate knowledge of transition oscillator strengths is also obtained from a knowledge of the polarizability values near the poles. The excitation energies and oscillator strengths are compared with available data.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 177 (1976), S. 75-88 
    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: Die Kinetik der Polymerisation von Methylmethacrylat (MMA), initiiert durch Butan-thiol/Dimethylsulfoxid in Benzol, wurde gravimetrisch untersucht. Das Thiol stellt die reduzierende Komponente des Katalysatorsystems dar und gleichzeitig das Übertragungs-reagenz. Die Reaktionsordnung in bezug auf Butanthiol ist 0,48. In den niederen Konzen-trationsbereichen zwischen 4,69.10-4 und 9,38.10-2mo11-1 verhalt sich DMSO wie die oxidierende Komponente des Initiatorsystems und die Polymerisationsgeschwindigkeit ist der Quadratwurzel der DMSO-Konzentration proportional. Oberhalb dieser Konzen-tration bis 1,40 moll- verhält sich DMSO sowohl als Oxidans als auch als Hemmsub-stanz, indem es ein Addukt mit dem wachsenden Radikal bildet, dessen Wachstumge-schwindigkeit vermindert ist. Die Reaktionsordnung in bezug auf das Monomere ist 1,04, wenn die DMSO-Konzentration im unteren Bereich liegt, und sie steigt an auf 1,25, wenn die DMSO-Konzentration großer als 9,38.10-2 mol 1-1 ist. Die Struktur des Thiols hat einen deutlichen Einfluß auf die Polymerisationsgeschwindigkeit, die außerdem von der Polarität und Viskosität des Löosungsmittels abhangig ist; sie ist am größten in Benzol und am kleinsten in Äthylacetat. Die «efficiency» der Initiierung liegt zwischen 60 und 80% und die Aktivierungsenergie betragt 72,45 kJ mol-1. Ein kinetischer Ausdruck zur Beschreibung der Ergebnisse wurde abgeleitet.
    Notes: The kinetics of butanethiol/dimethylsulfoxide (DMSO) initiated polymerization of methyl methacrylate in benzene medium was studied gravimetrically. The thiol acts as the reducing component of the initiator system and also as a transfer agent. The order with respect to [Butanethiol] is 0,48. In the lower concentration region between 4,69.10-4 and 9,38.10-2mol 1-1, DMSO behaves simply as the oxidant of the initiator system, and the rate of polymerization has the usual square root dependence on [DMSO]. But above the concentration of 9,38.10-2mol 1-1 and up to 1,40mol 1-1, DMSO acts both as an oxidizing agent and as a retarder, forming an adduct with the growing radicals, which propagates the reaction with a retarded rate. The order with respect to monomer concentration is 1,04, when DMSO is used in the lower concentration range and it increases to 1,25 when [DMSO] is higher than 9,38.10-2mol 1-1. Thiols of different structures affect the rate significantly. The rate of polymerization is also dependent on the polarity and viscosity of the solvent being a maximum in benzene and a minimum in ethyl acetate. The efficiency of initiation of the initiator system is 60-80% and the overall activation energy is 72,45 kJ mol-1. An appropriate kinetic expression was derived to explain the results.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...