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  • 1995-1999  (4)
  • 1997  (4)
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  • 1995-1999  (4)
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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    International journal of theoretical physics 36 (1997), S. 3079-3084 
    ISSN: 1572-9575
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The generators and irreducible representation coherent state of the multimodeSU(2) group are constructed by using the inverse operators of the multimode bosonic harmonic oscillator, and the inhomogeneous inverse differential realization of the multimodeSU(2) group are derived.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    International journal of theoretical physics 36 (1997), S. 1965-1971 
    ISSN: 1572-9575
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The charge and current quantum zero-point fluctuations in a squeezed vacuum state of a nondissipative mesoscopic capacitance coupling circuit with source are given. The quantum noise of this circuit at absolute zero temperature is derived. It is found that there is a squeezing effect in this coupling circuit.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 3403-3408 
    ISSN: 0887-624X
    Keywords: star-shaped ; poly(THF) ; ion-coupling ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The prepoly(tetrahydrofuran) [poly(THF)] capped with hydroxyl and tetrahydrothiophenium groups was prepared using tetrahydrothiophene to terminate the living cationic polymerization of THF initiated by BF3·OEt2 and epichlorohydrin (ECH) at low conversion. Well-defined star-shaped poly(THF) polyols were synthesized by an ion-coupling reaction of the prepoly(THF) with tri- or tetrafunctional benzenecarboxylates, respectively, and this process proceeded by precipitation when the solution of the prepolymer in THF was added to an aqueous solution containing an excess of the corresponding coupling reagent. GPC studies showed that all of the carboxylate groups of every coupling reagent molecule took part in the ion-coupling reaction simultanously. This was confirmed by IR spectra. Almost all of the prepolymers were coupled to form star polymers after repeating the precipitation four times. 1H-NMR illustrated that both the star-shaped polymers and the prepolymers contained primary and secondary hydroxyl end groups. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 3403-3408, 1997
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 198 (1997), S. 2613-2622 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The cationic polymerization of 1,3-dioxepane (DOP) initiated with trifluoromethanesulfonic acid (I) in the presence of ethylene glycol (EG) was investigated. At sufficiently low concentration of the initiator ([I] 〉 0.01 mol/L vs. [EG] 〈 0.20 mol/L), the molecular weights of the obtained polyacetal oligodiols are controlled by the mole ratio of consumed DOP to initial EG. Gel-permeation chromatography studies revealed that the concentration of cyclic oligomers in the products are negligible. The mechanism of the polymerization was investigated by means of kinetic studies. The results showed that the polymerization proceeds according to the active chain end mechanism (ACF) in combination with the activated monomer mechanism (AM); thus the cyclic oligomer in the obtained polymer is reduced, and intermolecular chain transfer to EG in ACE is dominant. It was also demonstrated that as [DOP]2[I]/[EG] decreases the contribution of ACE to the polymerization decreases and that of AM increases. In addition, 1H and 13C NMR data illustrated that each macromolecule of polyDOP oligodiols contained one EG unit on average and that no EG end groups exist.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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