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  • Wiley-Blackwell  (94)
  • 1995-1999  (48)
  • 1990-1994  (46)
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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 3249-3254 
    ISSN: 0887-624X
    Keywords: unsymmetric Schiff base monomer ; linear polymeric Schiff base complexes ; polymeric catalyst ; unfunctionalized olefins ; epoxidation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A polymerizable unsymmetric tetradentate Schiff base with one vinyl group 3 was synthesized and copolymerized with styrene in toluene. Mn(III) ion was quantitatively incorporated into the copolymers by the functional moieties. The resulting linear polymer-bound manganese complexes (4a′ and 4b′) were used as catalyst under homogeneous condition for selective epoxidation of unfunctionalized olefins (i.e. styrene, α-methylstyrene and cyclohexene) at room temperature in the presence of iodosylbenzene (PhIO) as the terminal oxidant. The efficacy of epoxidation using the polymeric catalysts was comparable to that of the monomolecular analog. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 3249-3254, 1997
    Additional Material: 3 Tab.
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  • 2
    ISSN: 0887-624X
    Keywords: N-(2-(vinyloxy)ethyl)-1,8-naphthalimide ; fluorescence structural self-quenching effect ; C60 ; electron donor ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A vinyloxy monomer bearing electron-accepting chromophore, N-(2-(vinyloxy)ethyl)-1,8-naphthalimide (VOENI), was synthesized by reaction of potassium 1,8-naphthalimide with 2-chloroethyl vinyl ether. VOENI can be homopolymerized by cationic initiation and copolymerized with maleic anhydride (MAn) under radical initiation. The fluorescence behaviors of VOENI and its polymers were investigated. It has been found that the fluorescence intensity of the VOENI monomer is much lower than that of its polymers at the same chromophore concentration. This means that a “structural self-quenching effect” (SSQE) has been also observed in the vinyloxy monomer consisting of an electron-accepting chromophore, which has opposite electronic structure in comparison with acrylates bearing electron-donating chromophores as we have reported previously. The SSQE is attributed to the charge-transfer interaction between the electron-accepting chromophore and the electron-donating double bond in the same molecule. The fluorescence quenching of 1,8-naphthalic anhydride and P(VOENI-co-MAn) by ethyl vinyl ether (EVE), dihydrofuran, triethylamine (TEA), etc. evidences that the electron-rich vinyloxy group does act as an important role in the SSQE of VOENI. C60 can also quench the fluorescence of the polymers, and an upward deviation from the linearity of the Stern-Volmer plot was observed showing that C60 acted as a powerful electron donor to quench the fluorescence of the copolymer. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 1111-1116, 1998
    Additional Material: 6 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Molecular Reproduction and Development 35 (1993), S. 251-256 
    ISSN: 1040-452X
    Keywords: B-50/GAP-43 ; Development ; Hippocampus ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Protein phosphorylation has been suggested to be correlated with brain development and with the molecular mechanism of behavioral effects of neuropeptides. The present study reports in vitro endogenous phosphorylation of P46, a membrane-associated protein that is changed during development of the rat hippocampus. This study indicated that the degree of endogenous phosphorylation may be correlated with the establishment of synaptic connections. Interestingly, P46 was proved to be identical to a well-known growth-associated protein B-50/GAP-43 in its identical apparent molecular weight, isoelectric point, phosphorylation dependence, and the cross immunoreaction of monoclonal anti-B-50/GAP-43 antibody and P46. Moreover, neonatal administration of neuropeptide ZNC(G)PR could facilitate the developmental progress of P46 endogenous phosphorylation. It is suggested that the changes in P46 phosphorylation could be involved in the cellular mechanism of ZNC(C)PR behavioral effects on learning. © 1993 Wiley-Liss, Inc.
    Additional Material: 6 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 7 (1996), S. 257-264 
    ISSN: 1042-7147
    Keywords: interpenetrating polymer networks ; semi-IPN ; phase diagrams ; poly(ethylene oxide) ; poly(methyl methacrylate) ; phase separation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Interpenetrating polymer networks (IPNs) of poly(ethylene oxide) (PEO) and poly(methyl methacrylate) (PMMA) were prepared by simultaneous network formation. The PEO network was produced by acid-catlayzed self-condensation of α,ω-bis(triethoxysilane)-terminated PEO in the presence of small amounts of water. The PMMA network was formed by free radical polymerization of MAA in the presence of divinylbenzene as crosslinker. The reaction conditions were adjusted to obtain similar crosslinking kinetics for both reactions. An attempt was made to construct a phase diagram of the IPNs by measuring the composition of the IPNs at the moment of the appearance of the phase separation, as indicated by the onset of turbidity. This composition could be determined because the siloxane crosslinks of the PEO network could be hydrolyzed in aqueous NaOH with the formation of linear, soluble PEO chains. The phase diagram was compared with phase diagrams of blends of linear polymers and of semi-IPNs (crosslinked PMMA and linear PEO), obtained under similar conditions, i.e. polymerization of MMA in the presence of varying amounts of PEO. It was observed that the form of the phase diagrams of the linear polymers is similar to that of the IPNs, but is quite different from that of the semi-IPNs. Thus, homogeneous transparent materials containing up to 60% of PEO could be prepared in the blends and the IPNs, but in the semi-IPNs, phase separation occurred with PEO contents as low as 10%.
    Additional Material: 7 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 62 (1996), S. 1185-1192 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A polymerizable photosensitizer, 2-(N-acridonyl)ethyl methacrylate (AEMA), containing both aromatic ketone and aromatic tertiary amine moieties in the same molecule, was prepared by reaction of N-hydroxyethyl acridone (HEA) and methacryloyl chloride in the presence of triethylamine (TEA). HEA was obtained by reaction of acridone with ethylene carbonate. The photochemical behavior including photoinitiation and fluorescence properties of AEMA and its polymer P(AEMA) were studied. It was found that the photoinitiation efficiency of monomeric AEMA is lower than that of its polymer for the photopo-lymerization of acrylonitrile (AN) in DMF. By the kinetic study and the analysis of recorded electron spin resonance spectra of the photoinitiation systems of AEMA or AEMA-di-methylaminoethyl methacrylate (DMAEMA) trapped by 2-methyl-2-nitritopropane (MNP), the mechanism is deduced to be similar to that of the benzophenone-TEA system. The recorded fluorescence spectra show that AEMA and P(AEMA) possess a strong fluorescence emission peak at 410 and 439 nm, respectively. The concentration self-quenching effect was observed with maximum intensities at a concentration of 8.6 × 10-5 mol/L in DMF for both AEMA and P(AEMA). Even though AEMA has a tertiary amino group and an electron-deficient acrylic double bond in the same molecule, it did not display structural self-quenching effect as we reported previously. This may be due to the two benzene rings in acridone that lessen the electron-donating ability of the N atom. The fluorescence quenching of AEMA and P(AEMA) by electron-donating and electron-accepting compounds was also investigated. © 1996 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 55 (1995), S. 1733-1738 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: (3,4-Difuryl-2,5-dimethyl)phenyl-polyvinyl silicon oils (DDP-C-gum) were synthesized by Diels-Alder reaction of polyvinyl silicon oil (C-gum) with 3,4-difuryl-2,5-dimethylcyclopentadienone (DDCP) in diphenyl ether at reflux temperature under atmospheric pressure. Their structures were characterized by 1H-NMR, UV, and IR spectra. Properties such as viscosity, refractive index, color, and thermal stability of some DDP-C-gums were obtained. © 1995 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
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  • 7
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: In a model polyurethane/poly(methyl methacrylate) (PU/PMMA) system, the partitioning of unreacted methyl methacrylate monomer (MMA) is studied in the late stages of its polymerization, simulated by incorporating controlled amounts of MMA in otherwise fully cured simultaneous interpenetrating networks (SIN) samples. Glass transitions temperatures (Tg) were determined using dynamic mechanical spectroscopy and differential scanning calorimetry as a function of MMA content of the SINs. The lowering of Tg in each phase due to the plasticization effect of MMA is used to calculate a plasticization coefficient for each phase, finally allowing calculation of the partition coefficient of MMA between the two phases. It is found that the MMA monomer distributes itself almost uniformly across the two phases of the current SIN system, leading to speculation as to the locus of late SIN polymerization. © 1995 John Wiley & Sons, Inc.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 51 (1994), S. 2139-2144 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A polymerizable photoredox system consisting of 4-methacryl oxbenzophenone (MABP) and N,N-dimethlaminoethyl methacrylate (DMAEMA) used for the photopolymerization of acrylonitrile (AN) was studied. It was found that the polymerization rate is proportional to the 0.93th power for the AN concentration, the 0.28th power for the MABP concentration, and the 0.25th power for the DMAEMA concentration. The overall activation energy of the polymerization obtained is 30.43 kJ/mol. The recorded ESR spectrum indicates that the excited-state MABP abstraets hydrogen mainly from the methyl group of the dimethylamino moiety. The comparison of the initiation ability of polymeric MABP or polymeric DMAEMA with their monomeric forms has also been done and the results indicate that in good solvents P (MABP) has a much higher initiation ability than that of monomeric MABP, but monomeric DMAEMA and P (DMAEMA) display almost the same initiation ability. In poor solvent, the initiation ability of P (MABP) is not so obviously higher than that in good solvents. The result of UV analysis of P (AN) initiated by the MABP-DMAEMA system indicates that both MABP and DMAEMA not only initiate the photopolymerization of AN, but also enter into P (AN) polymer chains. © 1994 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 58 (1995), S. 331-346 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Any simultaneous interpenetrating network (SIN) synthesis contains three key events. These are gelation of polymer I, gelation of polymer II, and phase separation of polymer I from polymer II. Metastable phase diagrams of SINs are developed, in which the time occurrence of these three events is represented. A polyurethane/poly(methyl methacrylate) (PU/PMMA) system was chosen as a model. Polymerization kinetics were followed in situ for both PU and PMMA using Fourier Transform Infrared Spectroscopy (FTIR) with the aid of a heated demountable cell. Glass transitions of fully cured samples were determined by dynamic mechanical spectroscopy (DMS) and differential scanning calorimetry (DSC). Phase separation was determined by the onset of turbidity, and gelation of the first gelling polymer was determined by the sudden resistance of the system to flow. As a result, a metastable phase diagram was constructed for the four-component SIN system (the two monomers and their respective polymers) as a tetrahedron in three dimensions with the two monomers and two polymers at the four apexes. Phase separation and gelations of the two polymers are indicated by various surfaces. These surfaces intersect at lines and curves, representing unique conditions of an SIN synthesis, e.g., simultaneous gelation of both polymers, or simultaneous phase separation and gelation of polymer I, etc. These conditions are critical in terms of the development of the SIN morphology, dividing the reaction space into specific regions. Finally, it is shown how the tetrahedron diagram helps visualize the course of the three key events during SIN synthesis, and provides direction for controlling them. © 1995 John Wiley & Sons, Inc.
    Additional Material: 14 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 43 (1991), S. 1323-1326 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: We have investigated the effects of 1,3-bis (methylphenylethynylvinyl) disiloxane (BMPVDS) as crosslinker on heat-curable silicone rubber and measured sol fractions and crosslink density of vulcanizates by benzene-extract and toluene-swelling methods, respectively. The experimental results show that, adding suitable amounts of BMPVDS, the vulcanizates exhibited rather fine mechanical properties. The tear strength of some vulcanizates could reach as high as 60.31 kN/m, the tensile strength 13.46 MPa, and the modulus at 100% extension 2.45 MPa, and the permanent deformation is rather low. BMPVDS is also a good curing retarder of hydrosilation curing silicone rubber. When adding 0.08 part of BMPVDS or more, the stocks can store at 20 ± 1°C more than 50 days without curing.
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