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  • 1
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 23 (1990), S. 5170-5172 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1573-4994
    Keywords: Anisotropy ; heavy atom ; phosphorescence ; water-soluble polymer
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract A hydrophobically modified water-soluble polymer, based upon acrylic acid and styryl derivatives, was synthesized. A proportion (ca. 75 mol%) of the styryl residues in the copolymer contain a bromine substituent as a “heavy-atom” functionality. It has been shown that room-temperature phosphorescence (RTP) can be induced in an acenaphthylene (ACE) label, covalently bound to the polymer chain, through intramacromolecular interactions in dilute solutions of the copolymer. This is the first instance in which RTP has been generated in either label or solubilized guest, in such a fashion. The conformational behavior of the functionalized copolymer, BrSTY/STY/AA, has been studied using RTP, fluorescence lifetime, and time-resolved anisotropy measurements and compared to that of both its unbrominated, styrene-modified analogue, STY/AA, and poly(acrylic acid) PAA itself. The conformation transition which accompanies conversion of each polyacid into the corresponding fully neutralized polysalt is much more dramatic in either hydrophobically modified species than in poly(acrylic acid). Intramacromolecular aggregation leading to the creation of hydrophobic domains within the coils of the macromolecules is enhanced at a low pH and severely impedes segmental motion in the two styrene-modified polyacids. The effect is greater in the bromine-containing polymer, which suggests that more densely packed domains are formed in this species than in STY/AA. In addition to altering the magnitude of the effect that neutralization has upon the molecular dynamics of the polyacid in aqueous media, hydrophobic modification raises the pH range over which the change in conformational behavior of the macromolecule is apparent.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1573-3505
    Keywords: hemodialysis ; behavioral controls ; compliance ; noncompliance
    Source: Springer Online Journal Archives 1860-2000
    Topics: Psychology
    Notes: Abstract The present study was conducted to examine the hypothesis that compliant chronically ill patients, typically described as “adjusted,” reinforce more positive social environments using behavioral controls than noncompliant patients, typically described as “maladjusted.” Specifically, it is hypothesized that diet-compliant chronic hemodialysis patients emit significnatly more active involvement-in-treatment behaviors and more social behaviors than diet-noncompliant chronic hemodialysis patients. Subjects, who ranged in age from 30 to 77 years, were outpatients at a kidney center. Behavioral observations were conducted to assess the occurrence or frequency of (1) four involvement-in-treatment behaviors that are routinely taught to all patients and (2) two social behaviors, which were patient verbalizations and smiles. The results showed that compliant patients emitted significantly more involvement-in-treatment behaviors and smiles than noncompliant patients. Results support the proposed control framework that compliant, in contrast to non-compliant, chronically ill patients have recourse through positive behavioral controls when adjusting to the stresses of illness. It was proposed that through these controls, compliant patients reinforce positive environments rather than simply respond to life circumstances as given.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 963-978 
    ISSN: 0887-6266
    Keywords: carbazole ; excimer ; fluorescence ; migration ; photophysics ; trapping ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Steady-state and time-resolved fluorescence techniques have been used to study the photophysical behaviors of poly(N-vinyl carbazole), PNVCz and a series of N-vinyl carbazole-methyl acrylate (NVCz-co-MA) copolymers in dilute solution as a function of both NVCz composition and temperature. A kinetic scheme, intended to describe intramolecular excimer formation across the entire NVCz composition range, is proposed. In low aromatic content copolymers, two monomer species (unquenched and quenched monomer) and two excimer species (the sandwich-like excimer and a higher energy excimer) exist. The contribution from monomer emission to the overall fluorescence decreases with increasing NVCz content through increased excimer formation: this is likely to be consequent upon (1) an increase in the number of excimer forming sites, and (2) increasing efficiency of energy transfer from the excited monomers to the excimer forming sites. In the homopolymer, PNVCz, the only emission that can be observed on a nanosecond timescale is excimeric. This fluorescence appears to originate from three excimer species (the sandwich-like excimer, and two higher energy forms). For the homopolymer, the current observations are consistent with the model proposed by Vandendriessche and De Schryver [Polym. Photochem. 7, 153 (1986)]. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 963-978, 1997
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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