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  • Polymer and Materials Science  (33)
  • Electronic structure and strongly correlated systems  (4)
  • 1
    Electronic Resource
    Electronic Resource
    Tailoring of macromolecule conjugates using reversed micelles as matrix microreactors (1990)
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 191 (1990), S. 2801-2814 
    Details
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Being solubilized in systems of reversed micelles of a surfactant, the macromolecules incorporate into the inner cavities of the micelles, whose size can be changed by varying the degree of hydration, w0 = [H2O]/[surfactant]. The conjugates of proteins (α-chymotrypsin, bovine serum albumin (BSA), monoclonal antibodies to insulin) with linear polyelectrolytes (poly(methacrylic acid), quaternized poly(4-vinylpyridine)) are synthesized in reversed micelles of Aerosol OT (sodium bis(2-ethylhexyl)sulfosuccinate) in the octane with 100% yield. The yield critically depends on the degree of hydration: the reaction does not proceed at low w0, but if w0 exceeds a threshold value (which differs for various macromolecules) the yield increases sharply and reaches 100%. Using the ultracentrifugation it was demonstrated that at low w0 the polyelectrolyte represents a compact globule compressed by the micellar matrix in the inner cavity of a micelle. Under these conditions, there is no space for the protein in a micelle which contains polyelectrolyte, and therefore reaction does not proceed. If w0 exceeds a threshold value the micelles become large enough to entrap the conjugated macromolecules simultaneously. The possibility of regulation of the conjugate composition by variation of w0 (via the size of the micellar matrix) was demonstrated by a conjugate of BSA with quaternized poly(4-vinylpyridine).
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/macp.1990.021911129
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  • 2
    Electronic Resource
    Electronic Resource
    DNA interpolyelectrolyte complexes as a tool for efficient cell transformation (1991)
    New York : Wiley-Blackwell
    Biopolymers 31 (1991), S. 1437-1443 
    Details
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A tool was developed for enhancement of plasmid penetration into an intact cell, based on increasing DNA hydrophobicity via inclusion into a soluble interpolyelectrolyte complex (IPC) with polycations. The characteristics of formation of DNA IPC with synthetic polycations [poly(N-ethyl-4-vinylpyridinium)bromide (PVP) and PVP modified with 3% of N-cetyl-4-vinylpyridinium units (PVP-C)] were studied using ultracentrifugation and polyacrylamide gel electrophoresis methods. The conditions were established under which the mixing of DNA and polycation aqueous solutions results in the selfassembly of soluble IPC species. Incorporation of DNA into IPC results in the enhancement of DNA binding with isolated Bacillus subtilis membranes. A considerable increase in the efficiency of transformation of B. subtilis cells with pBC16 plasmid resulted from incorporation of the plasmid into the IPC with PVP and CVP.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bip.360311210
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  • 3
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    Anharmonic order-parameter oscillations and lattice coupling in strongly driven 1 T-TaS_{2} and TbTe_{3} charge-density-wave compounds: A multiple-pulse femtosecond laser spectroscopy study (2011)
    American Physical Society (APS)
    Details
    Publication Date: 2011-01-11
    Description: Author(s): P. Kusar, T. Mertelj, V. V. Kabanov, J.-H. Chu, I. R. Fisher, H. Berger, L. Forró, and D. Mihailovic The anharmonic response of charge-density wave (CDW) order to strong laser-pulse perturbations in 1 T-TaS_{2} and TbTe_{3} is investigated by means of multiple-pump-pulse time-resolved femtosecond optical spectroscopy. We observe remarkable anharmonic effects hitherto undetected in systems exhibit... [Phys. Rev. B 83, 035104] Published Mon Jan 10, 2011
    Keywords: Electronic structure and strongly correlated systems
    Print ISSN: 1098-0121
    Electronic ISSN: 1095-3795
    Topics: Physics
    Published by American Physical Society (APS)
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  • 4
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    Energy dependence of the electron-boson coupling strength in the electron-doped cuprate superconductor Pr_{1.85} Ce_{0.15} CuO_{4−δ} (2017)
    American Physical Society (APS)
    Details
    Publication Date: 2017-02-04
    Description: Author(s): M. Beck, M. Klammer, I. Rousseau, M. Obergfell, P. Leiderer, M. Helm, V. V. Kabanov, I. Diamant, A. Rabinowicz, Y. Dagan, and J. Demsar In the conventional theory of superconductivity the critical temperature Tc is determined by the electron-phonon coupling constant and the phonon cut-off frequency. The hallmark experiments of McMillan and Rowell demonstrated that bosons (phonons) responsible for pairing can be observed through the frequency dependence of the gap parameter. Determination of the electron-boson coupling strength in high- T c cuprates is, however, not an easy task. One of the promising ways is to measure the energy relaxation rate of photoexcited carriers by using femtosecond real-time techniques. Here, considering the electron relaxation process within the conduction band, it is commonly assumed that the underlying Eliashberg electron-boson coupling function is independent of electron excess energy. Conversely, studies of light-induced suppression of superconductivity in Pr 1 . 85 Ce 0 . 15 CuO 4 reported here imply a strong variation of the electron-boson coupling function on electron energy. Considering the competing scenarios of superconductivity being mediated by either phonons or magnetic excitations, the results suggest that high-energy electrons strongly couple either to phonons or magnetic modes, while the situation is reversed when considering pairing of low-energy electrons. [Phys. Rev. B 95, 085106] Published Fri Feb 03, 2017
    Keywords: Electronic structure and strongly correlated systems
    Print ISSN: 1098-0121
    Electronic ISSN: 1095-3795
    Topics: Physics
    Published by American Physical Society (APS)
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  • 5
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    Collective modes in quasi-one-dimensional charge-density wave systems probed by femtosecond time-resolved optical studies (2014)
    American Physical Society (APS)
    Details
    Publication Date: 2014-01-07
    Description: Author(s): H. Schaefer, V. V. Kabanov, and J. Demsar The interplay between the electronic and structural subsystems has strong implications on the character of collective excitations in cooperative systems. Their detailed understanding can provide important information on the coupling mechanisms and coupling strengths in such systems. With the recent ... [Phys. Rev. B 89, 045106] Published Mon Jan 06, 2014
    Keywords: Electronic structure and strongly correlated systems
    Print ISSN: 1098-0121
    Electronic ISSN: 1095-3795
    Topics: Physics
    Published by American Physical Society (APS)
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  • 6
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    Theory of electronic relaxation in a metal excited by an ultrashort optical pump (2014)
    American Physical Society (APS)
    Details
    Publication Date: 2014-03-05
    Description: Author(s): V. V. Baranov and V. V. Kabanov The theory of the electron relaxation in simple metals excited by an ultrashort optical pump is developed on the basis of the solution of the linearized Boltzmann kinetic equation. The kinetic equation includes both the electron-electron and the electron-phonon collision integrals and assumes that F... [Phys. Rev. B 89, 125102] Published Tue Mar 04, 2014
    Keywords: Electronic structure and strongly correlated systems
    Print ISSN: 1098-0121
    Electronic ISSN: 1095-3795
    Topics: Physics
    Published by American Physical Society (APS)
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  • 7
    Electronic Resource
    Electronic Resource
    Competitive reactions in solutions of DNA and water-soluble interpolyelectrolyte complexes (1995)
    New York : Wiley-Blackwell
    Biopolymers 35 (1995), S. 523-531 
    Details
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of competitive binding of two polyanions - DNA and synthetic fluorescence-tagged poly(methacrylate) (PMA*) - with the polycation-quencher poly(N-ethyl-4-vinyl-pyridinium) (PEVP) was studied by fluorescence quenching technique. It was found that ability of DNA to displace PMA *from the water-soluble nonstoichiometric interpolyelectrolyte complex (NPEC) formed by PMA* and PEVP - NPEC(PMA*-PEVP) - and to form water-soluble NPEC(DNA-PEVP) \documentclass{article}\pagestyle{empty}\begin{document}$$ NPEC(PMA^{*}\hbox{-}PEVP) + DNA \Leftrightarrow NPEC(DNA\hbox{-}PEVP) + PMA^{*}$$\end{document} can be determined by the parameter Ψ = PPMA*/PPEVP where PPMA* and PPEVP are the degrees of polymerization of PMA* and PEVP, respectively. In the case of Ψ 〈 1 the decrease of Ψ leads to the shift of the reaction equilibrium to the right, which can be explained by the gain of entropy due to the increase of the total number of polymeric particles in the solution. Introduction of alkali metal cations into the reaction mixture results in the shift of the reaction equilibrium, and according to their ability to shift the equilibrium to the right the cations can be arranged in the series Na+ 〉 K+ 〉 Li+. The substitution of native DNA by denatured DNA practically does not affect the reaction equilibrium in solutions of NaCl and KCl but considerably shifts it to the right in solutions of LiCl. The data obtained are in accordance with the differences in the selectivity of alkali cations binding with competitive polyanions. © 1995 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bip.360350511
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  • 8
    Electronic Resource
    Electronic Resource
    Some new aspects of polymerization reaction (1979)
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 3 (1979), S. 41-68 
    Details
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: This paper deals with general and also specific aspects of matrix polyreactions on macromolecular templates, namely, mutual assistance of active centres of propagating chains and template units in elementry steps of propagatior. Such assistance has been found in polymerization of 4-vinylpyridine on polyacids and propargyl compounds on poly-4-vinylpyridine. These examples have shown that these kinds of assistance are the crucial points in kinetic template effects.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/macp.1979.020031979103
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  • 9
    Electronic Resource
    Electronic Resource
    Catalytic behaviour of metalcomplexes immobilized in functional polymeric carriers (1981)
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 5 (1981), S. 121-154 
    Details
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The general principles of construction of gel-immobilized catalyst systems (GICS) are reported as well as some peculiarities of the polymerization of ethylene and of the dimerization of ethylene and propylene in the presence of these systems.GICS consist of a transition metal complex and a specially designed polymeric support. Advantages offered by gel-immobilized catalyst systems are discussed with respect to homogeneous and microheterogeneous metal complex catalysts.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/macp.1981.020051981109
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  • 10
    Electronic Resource
    Electronic Resource
    Cooperative interpolyelectrolyte reactions (1985)
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 13 (1985), S. 137-155 
    Details
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Water-soluble nonstoichiometric polyelectrolyte complexes (NPEC) are formed as a result of interaction of opposite charged polyelectrolytes used in nonequivalent ratios. One of the most important properties of NPEC is their ability to participate in intermacromolecular exchange and substitution reactions in aqueous solutions. The kinetics of exchange and substitution reactions has been studied by the method of luminescence quenching. It has been found that such reactions proceed by the contact mechanism and that addition of low molecular electrolytes to the reaction mixtures results in a dramatic increase in the rates of the reactions. The kinetics of the reactions is well described by the equation q = 1-exp(- kt∝) (here q is the degree of conversion and ∝ 〈 1), deduced under the assumption that exchange and substitution occur by the nucleation mechanism and the development of nuclei is inhibited in time. The studied reactions represent a new class of interpolymer reactions and they can be very important, in particular, for understanding the mechanism of functioning of biologically important macromolecules and for the interpretation of the physiological activity of polyelectrolytes.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/macp.1985.020131985111
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