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  • Polymer and Materials Science  (8)
  • diffusion-limited reaction  (1)
  • glass transition temperature  (1)
  • 1
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A novel photoresponsive polymer containing organic chromophores which possess thermal stability as well as substantial and reversible responsiveness upon external photostimulus has been developed. trans-2{4-[2-(Dimethylcarbamoyl)vinyl]phenoxy}ethyl methacrylate (1) was synthesized and copolymerized by free-radical methods with methyl methacrylate giving a copolymer poly[(methyl methacrylate)-co-1] (poly(MMA-co-1)) (2) with cinnamamide moiety chromophores randomly attached as side groups. Photoisomerization and ultraviolet absorbance were used to examine the photostationary states and solubility changes upon photoirradiation. Poly[(methyl methacrylate)-co-1] (90,7 : 9,3 mol%) with 9,3 mol-% cinnamamide content has better solubility in a polar solvent such as acetonitrile (theta temperature ΘPMMA = 30°C) than in a nonpolar solvent such as carbon tetrachloride (ΘPMMA = 27°C). Photoisomerization of the trans-cinnamamide to cis-cinnamamide units significantly shifts the cloud point of poly[(methyl methacrylate)-co-1] (90,7 :9,3 mol-%) in carbon tetrachloride; this cloud point shift is reversible by photoisomerization back to the trans state. However, in a hydrogen-bonding solvent such as tert-butyl alcohol, while photoirradiation of poly[(methyl methacrylate)-co-1] (90,7 :9,3 mol%) yields a significant shift in cloud point, this is not reversible by photoirradiation as hydrogen-bond formation between the tertiary amide and the hydroxylic solvent reduces the isomerization efficiency. Fatigue of the photoreversibility of the copolymer, which is not present in dilute solutions of the cinnamamide chromophore, is noted.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 2667-2681 
    ISSN: 0887-6266
    Keywords: nonradiative energy transfer ; polymer blends ; intermolecular correlations ; miscibility ; phase separation ; modeling ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A theoretical analysis has been developed to predict fluorescence nonradiative energy transfer (NBET) behavior in homogeneous and phase-separated polymer blends. Conditions where intermolecular correlations need to be included are examined by first investigating the effect of including intermolecular correlations in predictions of NRET behavior in donor and trap (acceptor) end-labeled polymer melts. Donor fluorescence decays and energy transfer efficiencies are predicted for several different polymer systems using donor-trap intermolecular correlations in the theoretical analysis. These results are compared quantitatively to the same predictions recalculated without correlations and demonstrate the need to consider the effects of correlations when analyzing NRET measurements used for quantitative study of phase behavior. For the nonradiative energy transfer systems investigated here, correlation effects can often result in substantial differences, up to 60% as compared to the uncorrelated case, in predictions of relative energy transfer efficiency for bulk polymer. In the case of the blends, the effect of including intermolecular correlations is strongly a function of composition. A two-phase model is proposed to establish a quantitative method for relating energy transfer efficiency to phase-separated blend composition, and it is demonstrated that significant errors in interpretation of experimental NRET data may result if correlation effects are not included. © 1994 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    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 B: Polymer Physics 32 (1994), S. 2625-2635 
    ISSN: 0887-6266
    Keywords: fluorene ; fluorescence ; quenching ; in situ monitoring ; free-radical polymerization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A new approach for monitoring in situ the progress of an addition polymerization has been developed based on the fluorescence quenching of fluorene. Fluorene is quenched by the enone functionality on acrylates and methacrylates, but is not quenched after the carbon-carbon double bond in this group is broken by incorporation into the polymer backbone. Ethyl (2-fluorenyl)methacrylate was used as a self-quenching comonomer during the 2,2'-pazo bis(2-methylpropionitrile)-initiated free-radical copolymerization of methyl methacrylate at 60°C. The fluorescence intensity increases by 60% up to the onset of the gel effect (defined as the sudden increase in the temperature profile). The system shows sensitivity well into the glassy state, with fluorescence increasing more than two orders of magnitude from the beginning of the reaction. This sensitivity is compared with that of two free-volume-dependent probes, 1,3-bis(1-pyrene)propane and dimethylaminobenzylidenemalononitrile, and to fluorene. The temperature profile of the test-tube-scale reaction was used as an internal reference for characterizing the sensitivity of the probes with respect to the gel effect region. © 1994 John Wiley & Sons, Inc.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 2795-2802 
    ISSN: 0887-6266
    Keywords: ultrathin polymer films ; fluorescence nonradiative energy transfer ; second harmonic generation ; polymer relaxation ; small-molecule diffusion ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Two optically based, molecular probe techniques are employed to study relaxation and small-molecule translational diffusion in thin and ultrathin (thicknesses 〈 ∼200 nm) polymer films. Second harmonic generation (SHG) is used to study the reorientational dynamics of a nonlinear optical chromophore, Disperse Red 1 (DR1) (previously shown to be an effective probe of α-relaxation dynamics) either covalently attached or freely doped in polymer films. Our studies on films ranging in thickness from 7 nm to 1 μm show little change in Tg with film thickness; however, a substantial broadening of the relaxation distribution is observed as film thickness decreases below approximately 150 nm. Experimental guidelines are given for using fluorescence nonradiative energy transfer (NRET) to study translational diffusion in ultrathin polymer films. Appropriate choice of a fluorescence donor species is important along with ensuring that diffusion is slow enough to be measured appropriately. Initial results on the diffusion of a small-molecule probe, lophine, in poly(isobutyl methacrylate) indicates that there is little change in probe diffusion coefficients in films as thin as 90 nm as compared to bulk films. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2795-2802, 1997
    Additional Material: 6 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 2999-3008 
    ISSN: 0887-6266
    Keywords: chain length effects ; diffusion-limited reaction ; polymer solution ; phosphorescence quenching ; segmental diffusion ; polymer-polymer reactions ; reaction kinetics ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Model interactions have been studied by phosphorescence quenching to obtain a better understanding of the chain length dependence of interpolymeric chain end-chain end reactions such as those involved in the termination step of free radical polymerization. For small molecule-polymer interactions in dilute cyclohexane solution, quenching rate constant (kq) data agree with the Smoluchowski equation prediction that kq scales as polymer molecular weight (MW) to the -½ power, confirming self-diffusion control. For polymer-polymer interactions in dilute solution, the chain length dependence is weaker than that predicted by translational diffusion control, as described by the Smoluchowski equation, but is stronger than that predicted by renormalization group theory. For interactions between 70000 MW benzil-end-labeled polystyrene and varying MWs of anthracene-end-labeled polystyrene at 300 g/L polymer, kq decreases by a factor of 10 in going from MWs of 100 to 1000 g/mol; beyond 1000 g/mol, kq is nearly independent of chain length. Such effects indicate that the importance of oligomeric radical self-diffusion and polymer radical chain-end segmental mobility must be carefully considered in understanding the termination process in free radical polymerization. © 1996 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 2343-2349 
    ISSN: 0887-6266
    Keywords: diffusion ; sorption ; fluorescence monitoring ; polymer coatings ; water ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The fluorescent molecular rotor probes 4-tricyanovinyl-[N-(2-hydroxyethyl)-N-ethyl]-aniline, tricyano-4-(dimethylamino) benzylidene, and tricyanovinyljulolidene have been used as extrinsic fluorescence probes for quantitative monitoring of water uptake in polymeric coatings. The presence of water causes plasticization of the polymer, which results in increased local mobility within the film. The nonradiative decay pathways of the rotor probes are increased as local mobility increases, and the resulting decrease in fluorescence intensity of the probes is directly proportional to the amount of water sorbed. Beyond allowing for the characterization of sorbent content, this fluorescence technique can be used to determine the diffusion coefficient of water in a polymer film. The relative change in fluorescence fits well to a Fickian diffusion model, yielding a diffusion coefficient for water of 3 × 10-8 cm2/s in poly(vinyl acetate), and a value of 6 × 10-9 cm2/s in a room-temperature cured epoxypolyamide, in excellent agreement with diffusion coefficient values determined from gravimetric analysis. Preliminary studies also demonstrate the utility of molecular rotor probes to monitor water uptake in individual layers of multilayered polymer systems. © 1995 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 2987-2997 
    ISSN: 0887-6266
    Keywords: small molecule diffusion ; fluorescence nonradiative energy transfer ; glass transition temperature ; rubbery polymer ; probe shape effects ; probe flexibility effects ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A novel experimental approach involving fluorescence nonradiative energy transfer (NRET) is employed to study the Fickian diffusion of small molecules in rubbery poly(isobutyl methacrylate) (PiBMA) films near the glass transition, using a formalism that directly relates the small molecule translational diffusion coefficient, D, to changes in the normalized nonradiative energy transfer efficiency, EN. Values of D for pyrene, 1,3-bis-(1-pyrene) propane (BPP), 1,3-bis-(1-pyrene) decane (BPD), 9,10-bis-phenyl ethynyl anthracene (BPEA), diphenyl Disperse Red 4 (DPDR4), and decacyclene in PiBMA are measured over temperatures ranging from approximately Tg to Tg + 25°C. Among these chromophores, significant differences in both the magnitude and temperature dependence of D are observed which are attributed to differences in molecule shape and flexibility, as well as molar volume. Other factors being equal, chromophore flexibility was shown both to increase the magnitude of D and to decrease its dependence on temperature, as does an increase in aspect ratio. For BPD, these effects are attributed to the ability of the flexible molecule to diffuse in a piecewise manner, requiring the cooperative mobility of fewer polymer chain segments than a rigid molecule of the same molar volume. For BPEA and DPDR4, this deviation from D being dominated by molar volume effects is attributed the to high aspect ratio of these elongated molecules. © 1996 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Theory and Simulations 6 (1997), S. 931-948 
    ISSN: 1022-1344
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: There has been a great deal of recent interest in monitoring polymer interdiffusion with fluorescence nonradiative energy transfer (NRET), a typical experiment consisting of polymer chains labeled with a donor chromophore interdiffusing with chains labeled with an acceptor chromophore, causing an increase in energy transfer efficiency, E. A factor nearly always ignored in models of this process is the fact that chromophore interactions are screened out because of intermolecular correlation effects, leading to a lower E than would otherwise be expected. The model of Dhinojwala and Torkelson (Macromolecules 27, 4817 (1994)) has been modified to include correlations in order to explore the impact that ignoring correlations has on the diffusion coefficients calculated in such experiments. When correlations are included in the model, E is proportional to (Dpt)1/2/x for t〈x2/(16Dp) (where x is the thickness of the donor-labeled film and Dp is the polymer diffusion coefficient), similar to when correlations are ignored. Within this linear regime errors in Dp associated with ignoring correlations are typically less than 20% for logically defined systems, which may be insignificant given the uncertainty with which diffusion coefficients are normally reported. However, this study clearly demonstrates that precautions should be used in all experiments of this type to stay in this linear regime, as improperly accounting for or ignoring correlation effects at longer diffusion times can lead to the spurious result that apparent diffusion coefficients decrease with annealing time, by factors of 2 to 5 to as much as an order of magnitude or more at sufficiently long time. Systems designed to minimize correlation effects should have a large Förster radius and a sufficiently high ratio of acceptors to donors; with such a situation and the use of NRET data from the linear regime of E vs. t1/2, it is possible under many experimental circumstances to determine diffusion coefficients within small error even when the effects of correlations are ignored.
    Additional Material: 5 Ill.
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