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  • Chemistry  (10,148)
  • Inorganic Chemistry  (732)
  • 1990-1994  (10,148)
  • 1970-1974
  • 1992  (10,148)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Chemometrics 6 (1992) 
    ISSN: 0886-9383
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 2
    ISSN: 0886-9383
    Keywords: Derivatization reaction ; Factorial design ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A number of nucleophiles have been successfully identified and quantified using the Kröhnke reaction with 2,3-diphenyl derivatives of quinolizinium salts. Optimization of the reaction conditions by means of a mathematical model involving analysis of the response surface has led to a better understanding of the factors exerting an influence on the above reaction.The parameters chosen were temperature, reaction time, base concentration, water concentration and nucleophile concentration. The reaction was developed in polar aprotic solvents (acetone, acetonitrile). To facilitate the nucleophilic attack, the presence of an organic base (triethylamine) was necessary, although concentrations in excess of 0·15M did not alter the development of the reaction. Since pharmaceutical solutions are often aqueous, the influence of water on the reaction was studied. Low water volumes have no significant influence on the opening of the quinolizinium ring by the nucleophilic reagent. However, when the water proportion exceeded that of the organic solvent, the fluorescence intensity was lower than expected. Development of the fluorescent reaction product was first detected 5 min after the reaction started. The fluorescence intensity reached its optimum value after 138 min.
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  • 3
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    New York, NY : Wiley-Blackwell
    Journal of Chemometrics 6 (1992), S. i 
    ISSN: 0886-9383
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 4
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    New York, NY : Wiley-Blackwell
    Journal of Chemometrics 6 (1992), S. 65-83 
    ISSN: 0886-9383
    Keywords: Trilinear decomposition ; Receptor modeling ; Source identification ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In many cases, monitoring data for ambient airborne particles can be organized in the form of a three-way data table with one way for chemical species, one for sampling periods and one for sites. A direct trilinear decomposition followed by a matrix reconstruction (DTDMR) is developed to analyze such a data table as a whole. The three-way data set is composed into three two-way matrices by a direct trilinear decomposition (DTD). The column vectors of each of the matrices are called ‘source profiles’, ‘emission patterns’ and ‘site coefficients’ respectively. Particulate sources are identified by examining both their source profiles and emission patterns. After the sources have been identified, emission patterns and site coefficients are used to produce a three-way matrix that gives estimates of mass contributions of sources to the samples collected at every site in every period. By simulation study, not only has the method been verified, but a good indicator has been found that shows the number of factors (i.e. sources) in the system. Unlike other receptor models, DTDMR does not require source profile data and does not involve trial-and-error procedures. Since DTDMR identifies sources based on variations in two dimensions, it has a higher potential to distinguish two sources that have similar chemical compositions. The DTDMR model has provided excellent results with simulated data and has been applied in a real world three-way data set.
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  • 5
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    New York, NY : Wiley-Blackwell
    Journal of Chemometrics 6 (1992), S. 163-175 
    ISSN: 0886-9383
    Keywords: Multiple-correspondence analysis ; Starch granule description ; Image analysis ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Raw starch is composed botanically of characteristic granules of various sizes and shapes, so that each kind of starch may be characterized by the population of its granules. In the present study ten commercial starch species were studied: wheat, rice, manioc, potato, arrowroot, amylomaize, normal maize, waxy maize and two different banana species. Six variables measuring the size and shape of granules were obtained by image analysis. The objective was to find a method to describe and compare the granule populations of the ten species. For such a study, multiple-correspondence analysis (MCA) was applied. MCA makes it possible to draw similarity maps of categories and objects. For each starch species the frequency distributions (histograms) of the six variables were assessed and each granule was characterized by its species and the classes of histograms to which it belonged. MCA was applied to the granule table and a description of the histogram classes and the granules was obtained. From the variables description a general typology of the granules was deduced. The similarity maps showed considerable scatter of the granules for all species except rice. A particular species could therefore not be identified by a single granule, but the granule distribution seemed to be characteristic. MCA was an appropriate method to analyse these data because it points out non-linear relationships between quantitative and qualitative variables.
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  • 6
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    New York, NY : Wiley-Blackwell
    Journal of Chemometrics 6 (1992), S. 177-188 
    ISSN: 0886-9383
    Keywords: PLS ; Prediction error ; Background constituents ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A modification of a technique proposed by Lorber and Kowalski for the estimation of prediction errors is presented. The method is applied to five data sets. The results show that for some data sets the estimated prediction errors are close to the actual prediction errors for samples within the calibration range, while samples outside the calibration range must be background corrected before quantification of the prediction error.
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  • 7
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    New York, NY : Wiley-Blackwell
    Journal of Chemometrics 6 (1992), S. 199-216 
    ISSN: 0886-9383
    Keywords: MARS ; Splines ; Multivariate calibration ; Non-linear ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This tutorial paper presents a simplified view of one of the more recently published multivariate calibration methods particularly suited to dealing with non-linear data sets. The method is referred to as MARS and stands for multivariate adaptive regression splines. Simple examples are provided to explain the workings of the method.
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  • 8
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    New York, NY : Wiley-Blackwell
    Journal of Chemometrics 6 (1992), S. 247-255 
    ISSN: 0886-9383
    Keywords: Analysis of variance ; Assumptions ; Graphics ; Models ; Validation of model ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The computer has made it possible to scrutinize data rapidly by means of graphics. This should be done prior to the application of any model to the data, since the model must be validated before using it as a means of analyzing the data. The procedure is illustrated in terms of two examples of real experimental data.
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  • 9
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    New York, NY : Wiley-Blackwell
    Journal of Chemometrics 6 (1992), S. 284-285 
    ISSN: 0886-9383
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 10
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    New York, NY : Wiley-Blackwell
    Journal of Chemometrics 6 (1992), S. 307-334 
    ISSN: 0886-9383
    Keywords: Non-linear PLS ; Quadratic regression ; Non-linear models ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We treat here an extension of linear PLS regression to include regression on quadratic PLS components. The quadratic regression can be viewed as a natural extention of linear PLS regression to quadratic PLS according to the H-principle of mathematical modelling. The numerical implementation is treated in detail. It is shown that this approach can be used for models with large numbers of variables. Some modelling strategies are discussed depending on the purpose of the modelling. Applications of this approach are treated.
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  • 11
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    New York, NY : Wiley-Blackwell
    Journal of Chemometrics 6 (1992), S. 357-357 
    ISSN: 0886-9383
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 12
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    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 13-19 
    ISSN: 0887-624X
    Keywords: cationic ; copolymerization ; radiation-initiation ; reaction pathways ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A method of analysis of copolymerization systems involving multiple reaction pathways is presented. The method involves fractionation and separate analysis of the individual product populations comprising each sample. Modification of the Kelen-Tüdos linearization techniques into the form necessary to deal with high conversion copolymerizations involving multiple reaction pathways is presented. The method is applied to the ionizing radiation initiated copolymerization of styrene derivatives in dichloromethane, in which case simultaneous copolymerization via cationic and free radical mechanisms is found to occur. Reactivity ratios corresponding to each mechanism are calculated and discussed.
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  • 13
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 63-69 
    ISSN: 0887-624X
    Keywords: rare earth coordination catalyst ; 1-octene ; polymerization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The study of rare earth coordination catalysts for polymerization of 1-octene has been successfully carried out for the first time. Some features and kinetic behavior of polymerization of 1-octene by Nd(naph)3-AIEt3 catalyst system in tetrachloro-methane are described. The overall polymerization activation energy Ea measured was 74.5 kJ/mol and the rate equation could be expressed as Rp = kp [Nd] [M] (kp = 3.21 × 10-3 L/mol s, at 50°C). The catalytic activity of various rare earth elements in Ln (naph)3 and ligands in NdL3 for the polymerization was compared. A 1-octene oligomer with double bonds was obtained. It is either a white or pale yellow waxy semi-solid. Its number-average molecular weight is about 103 and the molecular weight distribution is less than 2.
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  • 14
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 83-89 
    ISSN: 0887-624X
    Keywords: polyarylate ; polycondensation ; mechanism ; catalysts ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Alternate syntheses of polyarylate from dimethyl iso/terephthalate (DMI/DMT) and bisphenol-A (BPA) or bisphenol-A diacetate (BPAOAc) were investigated using a variety of catalysts. The model exchange of DMT with 4-t-butylphenol with loss of methanol proceeded moderately rapidly at rather low temperature (170°C) to produce to mono- and di-t-butylphenyl terephthalates. Dibutyltin oxide is the preferred catalyst. Alkali metal phenoxides are almost as effective but were less soluble. The model reaction of DMT with 4-tert-butylphenyl acetate involving loss of methyl acetate gave comparable results using dibutyltin oxide as catalyst. Based on these model results, polycondensations of DMI/DMT with BPAOAc under optimal conditions, gave polyarylate having an inherent viscosity 0.34 dL g-1 in quantitative yield and light brown color. Polycondensation with BPA was unsatisfactory in terms of yield, molecular weight, and color.
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  • 15
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    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 119-124 
    ISSN: 0887-624X
    Keywords: synthesis ; corrosion ; polymer ; sulfide thiol ; dibromide ; condensation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Binary condensation copolymers of 1,2-ethane dithiol and 1,3-propane dibromide, 1,4-butane dibromide, and 1,6-hexane dibromide were prepared. Yields ranged from 55 to 89% with molecular weights of 1-2 × 104 Daltons. The polymers were synthesized via an SN2 process with and without the presence of water. The polymers were characterized by DSC, viscosity, FT-IR, and 1H-and 13C-NMR spectra.
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  • 16
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    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 145-148 
    ISSN: 0887-624X
    Keywords: multi-armed vinyl monomer ; methacrylate with pendant cyclotriphosphazene ; radical polymerization ; radical copolymerization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 17
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    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 169-169 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 18
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    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 137-144 
    ISSN: 0887-624X
    Keywords: fillers ; emulsifier free emulsion polymerization ; monodisperse beads ; polymethacrylates ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Monodisperse polymethacrylate beads of varied size and crosslink density are prepared by emulsion copolymerization of methacrylate and divinyl monomers in the absence of emulsifiers. The sizes of polybutyl and polyethyl methacrylate beads decreased with increasing polymerization temperature, while polymethyl methacrylate beads were largely unchanged in size. The molar mass of polymer in polymethyl metnacrylate beads markedly exceeded that in polystyrene beads. The rate of polymerization increased, and bead size decreased, with increasing initiator concentration or decreasing monomer concentration. The polymethacrylate beads are used as filler particles in polymer composites.
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  • 19
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 501-504 
    ISSN: 0887-624X
    Keywords: ring-opening polymerization ; polypropyleneimine ; N-benzyl phthalimides ; thermo-initiated polymerization ; thermal catalyst ; latent catalyst ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 20
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    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 509-511 
    ISSN: 0887-624X
    Keywords: chloromethyl styrene ; bis(vinylbenzyl)-ether ; phase transfer catalysis ; 13C CP/MAS NMR ; crosslinking ; styrylmethyl ether ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 21
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1-11 
    ISSN: 0887-624X
    Keywords: ring-opening polymerization ; epoxide polymerization ; cationic polymerization ; transition metal initiators ; rhodium initiators ; rhodium colloid initiators ; hydrosilylation reactions ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organometallic rhodium complexes are described which are highly efficient initiators for the ring-opening polymerization of expoxides and other heterocyclic compounds. A cocatalyst, consisting of a compound or polymer containing silicon-hydrogen bonds must also be present. These same catalyst-cocatalyst mixtures are also highly active for hydrosilylation reactions. Other complexes bearing phosphine ligands have been discovered, which while active for hydrosilylation, are not catalysts for epoxide polymerizations. Polymer supported rhodium catalysts are also described which permit the synthesis of epoxy-functional silanes in high yields without competing ring-opening polymerization.
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  • 22
    ISSN: 0887-624X
    Keywords: telechelic oligomers ; halogenated telomers ; monodispersed α,ω-diols ; redox telomerization of allyl acetate ; α,ω-di(trichloromethyled) end grouped telomers ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The redox bistelomerization of allyl acetate with telogens which exhibit α, ω-di(trichloromethyled) end groups catalyzed by copper, iron salts, or a ruthenium complex led to monoadducts and telechelic oligomers. These diacetates were quantitatively changed into diols. Such compounds have been characterized by both 1H- and 13C-NMR. A reactivity series has been determined and shows that both end groups must be activated to obtain the expected telechelic products in satisfactory yields.
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  • 23
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 835-843 
    ISSN: 0887-624X
    Keywords: interpenetrating polymer networks ; poly(urethane carbonate) ; polyvinyl pyridine ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Simultaneous interpenetrating polymer networks (IPN's), pseudo IPN's, and liner blends of aliphatic poly(carbonate-urethane) (PCU) and polyvinyl pyridine (PVP) have been prepared and characterized by DSC, DMA, and TEM. The full IPN's of PCU and PVP had a single phase morphology only above 50 wt % PCU, as determined by both DSC and DMA and confirmed by transmission electron microscopy (TEM). However, in both pseudo IPN's of PCU and PVP and in their linear blends there exist multiple glass transitions and melting points seen by DSC and DMA indicating phase incompatibility. The full IPN's exhibited superior ultimate mechanical properties and solvent resistance as compared to the pseudo IPN's, liner blends, and the pure crosslinked PCU and PVP networks.
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  • 24
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 873-877 
    ISSN: 0887-624X
    Keywords: poly(phenylacetylene) ; trifluoromethyl group ; gas permeation ; oxygen permselectivity ; membrane ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Poly(phenylacetylene)s containing trifluoromethyl groups on their benzene rings were synthesized, and gas permeation behaviors of their films were examined. Permeability coefficients for O2 and N2, diffusion selectivity (Do2/DN2) and solubility selectivity (SO2/SN2) were estimated. The gas permeability of polymer films were found to be enhanced remarkably with introduction of trifluoromethyl groups into the polymers: poly[2,4,5-tris(trifluoromethyl)phenylacetylene], Po2 = 7.8 × 10-8 [cm3 (STP) cm cm-2 s-1 cm Hg-1], Po2/PN2 = 2.1. The relationship between the polymer structures and their gas permeability was discussed.
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  • 25
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 929-932 
    ISSN: 0887-624X
    Keywords: protein adsorption ; phospholipid polymer ; membrane ; biocompatibility ; biosensor ; permeability ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 26
    ISSN: 0887-624X
    Keywords: oxidative coupling polymerization ; poly(2,6-dimethyl-1,4-phenylene)oxide ; 2,6-dimethylphenol ; PPO-dimer ; PPO-trimer ; specificity ; reactivity ; flory principle of equal reactivity ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In the oxidative coupling polymerization, catalyzed by copper-amine complexes, the oxidation rates of 2,6-dimethylphenol (DMP) and its C—O-coupled dimer [4-(2′,6′-dimethylphenoxy)-2,6-dimethylphenol] and trimer [4-(-4′-(2″,6″-dimethylphenoxy)-2′,6′-dimethylphenoxy))-2,6-dimethylphenol] have been determined. The DMP concentration dependence shows a Michaelis-Menten-type behavior. On the other hand, the dimer and trimer showed a first-order rate-dependence in the respective phenol concentrations. This indicates that the slow reaction step, following an equilibrium complex formation between DMP and copper complex, is relatively fast for both the dimer and the trimer. Therefore, coordination of dimer or trimer to the copper complex appears to be rate-determining. Furthermore, the dimer and trimer gave overall reaction rates approximately eight times higher than found for DMP. Following the Flory principle of equal reactivity for functional groups of oligomers in polycondensations, all PPO oligomers can be assumed to have equally high oxidation rates as the dimer and trimer. The yield of undesired DPQ side product is strongly reduced when starting with the dimer (0.18%), or trimer (0.17%), compared to 3.3% for DMP. This is not unexpected, since DPQ can only be formed from two monomeric DMP residues. In fact, using a 1/10 molar mixture of dimer/DMP already results in a DPQ yield of only 1.7%. Furthermore, when starting from DMP, it has been observed that DPQ was predominantly formed during the first 30% conversion. Starting from dimer (or trimer) DPQ was formed at an almost constant very low rate during the whole course of the reaction. From these experiments it can be concluded that the most important polymerization reaction involves oxidation of copper-coordinated DMP anion to its corresponding cations, followed by coupling with a copper coordinated PPO chain.
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  • 27
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 941-944 
    ISSN: 0887-624X
    Keywords: polymerization ; methyl methacrylate ; manganic laurate-substituted thiols ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 28
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 955-955 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 29
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 211-220 
    ISSN: 0887-624X
    Keywords: block copolymer ; dextran ; polyamide ; aminolysis ; terminal group ; macromolecular activator ; chemical modification ; protection ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A novel AB-type block copolymer composed of dextran and polyamide sequences was prepared through the following two approaches. One is a coupling reaction of a terminal functional group introduced in the dextran chain with that in the polyamide chain, such as the reaction of an amine group with an acyllactam group or that of a lactone group with an amine group at the corresponding chain ends. The other is an anionic polymerization of a bicyclic lactam activated with a trimethylsilylated dextran derivative having an acyllactam end group. The latter procedure was found to be more effective for the preparation of the block copolymer having a high molecular weight polyamide sequence.
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  • 30
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 245-256 
    ISSN: 0887-624X
    Keywords: microspheres, aggregation ; divinylbenzene, copolymerization ; seeded emulsion polymerization ; particle morphology ; gel, phase separation ; monodisperse macrospheres ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Monodisperse porous styrene-divinylbenzene copolymer particles were prepared via seeded emulsion polymerization using a mixture of linear polymer (polystyrene seed) and non-solvent as inert diluent. Experimental evidence was presented to describe the mechanism of formation of porous polymer particles during the copolymerization and solvent extraction stages, in which porosity was a consequence of phase separation in the presence of diluents. Pore structure formation was investigated by changes in copolymerization kinetics, gel content, crosslinking density, particle morphology, surface area, pore volume, and pore size distribution. The process of copolymerization was presented, based on the concepts of production, agglomeration, and fixation of the interior gel microspheres of polymer particles. A portion of linear polymer used as diluent was found to participate in the network structure while the porous matrix was built-up. The influence of the removal of the linear polymer from the matrix pores during the solvent extraction process on the porous structure was also discussed.
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  • 31
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 299-304 
    ISSN: 0887-624X
    Keywords: polyformal ; polycarbonate ; copoly(carbonate formal) ; phase-transfer catalyst ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A linear, high molecular weight polyformal is readily synthesized by direct transformation of commercially available polycarbonate. The reaction is best carried out in dibromomethane with 8.0 equiv. of potassium hydroxide pellets in the presence of a phase-transfer catalyst at 90-95°C. A random copoly(carbonate formal) can also be obtained simply by reducing the amount of potassium hydroxide used in the reaction. The molecular weight of the resulting polymer is governed by the starting polycarbonate.
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  • 32
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 329-331 
    ISSN: 0887-624X
    Keywords: azlactone (oxazolone) styrene monomer ; functional styrene monomer ; polymeric reagents ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 355-362 
    ISSN: 0887-624X
    Keywords: amphiphilic polymers ; graft copolymers ; poly(ethylene glycol) ; GPC ; inverted micelles ; partition chromatography ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Amphiphilic comb polymers were prepared through grafting poly(ethylene glycol) methyl ether (MPEG 2000) onto acrylic and methacrylic copolymers. The graft copolymers were purified from unreacted MPEG by partition chromatography on methanol pretreated fibrous cellulose using ethyl acetate and methanol as eluents. The separation was found to depend on the water contents of the cellulose and the eluents. It is proposed that one parameter of importance for the chromatographic separation is the formation of hydrated inverted micelles. The amphiphilic comb polymers were shown by gel chromatography on Sepharose to form high molecular weight aggregates in water. On addition of sodium lauryl sulphate or inorganic salts to the eluent at low ionic strengths these aggregates dissociated and were fractionated by the gel. It was also shown that on GPC in THF solution on Styragel columns the polymers exhibited apparent molecular weights equal or smaller than those of the corresponding backbones. This effect may be a consequence of the graft copolymers having relatively small hydrodynamic volumes, and this idea is supported by the fact that their intrinsic viscosities generally were lower than those of the backbones. However, adsorption on the Styragel columns also may be of importance.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 371-377 
    ISSN: 0887-624X
    Keywords: inorganic polymer ; silicic acid ; polytitanosiloxane ; SiO2-TiO2 ; oxide fibers ; tensile strength ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: From polytitanosiloxanes (PTS), SiO2-TiO2 oxide fibers with fairly good tensile strength were prepared, and their mechanical and thermal properties were investigated. The precursor fibers PTS-0.5 and PTS-1.0 were obtained by dry spinning of a highly viscous PTS solution which were formed as the reaction mixture of silicic acid (SA) with bis(2,4-pentanedionato)titanium diisopropoxide (PTP) in the molar ratios (SA/PTP) of 0.5 and 1.0. The precursor fibers PTS-0.5 were too brittle to measure their tensile strength, whereas PTS-1.0 and the heat-treated fibers were found to have tensile strength of 130 (precursor), 540 (500°C), and 450 (900°C) MPa, respectively. Heat-treatment of the fibers PTS-1.0 at above 1000°C forms anatase and rutile of titanium dioxide. The crystallization is resulted from the unreacted PTP which is not incorporated into the polymer network.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 409-418 
    ISSN: 0887-624X
    Keywords: plasma polymerization ; microwave and pulsed power ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Pulsed microwave power was used to polymerize a variety of monomers containing different functional groups. We examined the effects of pulse frequency and duty cycle on the deposition rates and the composition of the polymers. For monomers that do not contain oxygen we find that there is an increase in deposition rate with increasing pulse frequency and that the pulsed deposition rate is always less than the continuous power deposition rate. For monomers that contain oxygen, or for co-depositions of hydrocarbon monomers with O2 or CO, we find that there is a decrease in deposition rate with increasing frequency, however the deposition rate using pulsed power is greater than the rate using continuous power. This result is shown to be related to the amount of etching that takes place during the deposition process. Infrared studies reveal that pulsed power can alter the composition of plasma polymers of some oxygen-containing monomers. The presence or absence of vinyl unsaturation, nitrile groups, or a cyclic structure have no effect on the polymerization process.
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    ISSN: 0887-624X
    Keywords: Scholl reaction ; cation-radical polymerization ; 1,5-bis(phenoxy)pentanes ; polymerization mechanism ; polymerizability of monomers ; proton transfer reactions ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis and the oxidative polymerization of 1,5-bis(phenoxy)pentane, 1,5-bis(phenoxy)pentane substituted with various electron-donating groups, and 1,5-bis(phenylthio)pentane is described. The polymers derived from methyl substituted 1,5-bis(phenoxy)pentane monomers contain diphenyl methane, 1,2-diphenylethane, and benzyl chloride structural units. The mechanism for the generation of these structural units is presented. It consists of the proton transfer reactions from the cation-radical propagating species and subsequent reactions of the resulting benzyl radicals. The polymerizability of monomers with 1,5-pentanedioxy group is lower than that of the monomers with diphenyl sulfone group. This dissimilarity was attributed to the difference between both the reactivity and the concentration of the cation-radical propagating species resulted from these two classes of monomers.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1219-1221 
    ISSN: 0887-624X
    Keywords: acid additives ; cationic salts ; grafting ; homopolymer ; photosensitized ; polypropylene ; styrene ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1247-1259 
    ISSN: 0887-624X
    Keywords: polyarylethersulfone ; polyethersulfone ; HTA ; oscillations ; chemiluminescence ; XPS ; oxidation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chemiluminescence in conjunction with x-ray photoelectron spectroscopic surface analysis has been used to elucidate the thermooxidation of polyarylethersulfone HTA film between 85 and 110°C. Oscillations have been observed in chemiluminescence at different wavelengths and in the concentration of newly identified sulfine intermediates. A reaction mechanism is proposed to account for the chemiluminescence and product behaviors. This mechanism features parallel intramolecular and intermolecular pathways branching from a common sulfinyl sulfonate intermediate; each branch produces different emittering species. Oscillating behavior appears to be general for polyarylsulfone films.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1287-1298 
    ISSN: 0887-624X
    Keywords: microsphere ; concentration effects ; growth mechanism ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effects of the monomer concentration were investigated on the preparation of diethylene glycol dimethacrylate (2G) microspheres by radiation-induced polymerization. The monomer concentration strongly affected the conversion and the shape of the microspheres. The particles were obtained in the range from 2 to 24 vol % of 2G monomer. The effective concentration for the preparation of monodisperse microspheres is around 10 vol %. Higher monomer concentrations up to 24 vol % gave rough surface particles. Considering the effects on the number of microspheres in the solution, the authors introduced the inhibiting region, where one microsphere disturbs the existence of another microsphere, and tried to explain the mechanism of the microsphere growth. The competition between the propagation and the crosslinking reactions is balanced to give the microspheres.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1327-1333 
    ISSN: 0887-624X
    Keywords: aromatic polyamides ; polyisophthalamides ; phenylthio pendent groups ; 5-phenylthioisophthalic acid ; phosphorylation polycondensation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of polyisophthalamides containing pendent phenylthio groups was prepared from seven aromatic diamines and 5-phenylthioisophthalic acid by the phosphorylation polycondensation method. The properties of these polymers were compared with those of the analogous unmodified ones. The modified polymers exhibited better solubility in organic solvents than their unmodified counterparts. They also showed glass transition temperatures that were lower by approximately 30°C. However, the presence of the side groups did not bring about any substantial lowering of the thermal stability as measured by TGA. Other properties investigated were mechanical strength and water sorption.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1347-1354 
    ISSN: 0887-624X
    Keywords: radical polymerization ; monomer-isomerization polymerization ; fumarate ; maleate ; copolymerization ; thermal degradation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Radical polymerization of isopropyl tert-butyl fumarate (iPtBF) and monomer-isomerization radical polymerization of isopropyl tert-butyl maleate (iPtBM) were investigated with 2,2′-azobisisobutyronitrile as initiator in the presence and absence of morpholine (Mor) as isomerization catalyst. It was found that iPtBF gave high molecular weight polymers in high yield as previously observed for diisopropyl fumarate (DiPF) and di-tert-butyl fumarate (DtBF). It was confirmed that iPtBF produced by in situ monomer isomerization of iPtBM homopolymerized to give a polymer. Radical copolymerization of iPtBM with styrene in the presence and absence of Mor was also performed and monomer reactivity ratios obtained were compared. From the kinetic study of the isomerization of iPtBM, it was revealed that the isomerization rate showed first-order dependence on the concentration of iPtBM and Mor, and that the apparent activation energy was 29.4 kJ/mol. On pyrolysis of the poly(iPtBF) at 180°C, isobutene and isopropanol were eliminated rapidly to yield polymer containing carboxyl groups and anhydrides. The pyrolytic behavior was different from that of a copolymer of DiPF with DtBF.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1355-1361 
    ISSN: 0887-624X
    Keywords: polyether ; cesium ; phenoxide ; liquid crystalline ; dibromodecane ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of a poly(azine-ether) via Williamson etherification using the cesium salt of 4-hydroxyacetophenone azine and 1,10-dibromodecane was carried out in N-methyl-2-pyrrolidone. The heterogeneous reaction proceeded readily at temperatures from ambient to 150°C. Polymers of varying molecular weight with essentially alkyl bromide end groups were produced either by changing the polymerization temperature or by using an excess of the organic substrate. The thermal stability of the polymers was molecular weight dependent and those with the highest DPn exhibited monotropic nematic mesomorphism.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1535-1540 
    ISSN: 0887-624X
    Keywords: polymer support ; dichlorotriazine ; cooperative effect ; pseudo crown ether ; phase transfer catalyst ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Poly(2,4-dichloro-6-vinyl-1,3,5-triazine-co-styrene)s were prepared by the reaction of poly(2,4-diamino-6-vinyl-1,3,5-triazine-co-styrene)s with hydrochloric acid, and followed by treatment with thionyl chloride and N,N-dimethylformamide. The chlorine atoms in the resulted polymers were replaced readily by several nucleophiles such as amide, alkoxide, and mercaptide to afford the corresponding polymers in moderate yields. Among these, polymers containing oligo (oxyethylene) groups at both 2 and 4 positions of 1,3,5-triazine ring worked effectively as phase transfer catalysts for the reaction of n-octyl bromide with alkali metal thiocyanates in toluene-water systems. However, polystyrenes containing only one oligo (oxyethylene) group in monomer unit scarcely exhibited the activity under these conditions although the degree of loading of the functional group was almost the same. The activity depended on the number of oxyethylene units, and the selectivity to alkali metal ions was also observed. © 1992 John Wiley & Sons, Inc.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1567-1573 
    ISSN: 0887-624X
    Keywords: nickel ; coupling polymerization ; aromatic dichloride ; polyamide ; poly[(2,5-dimethyl-1,4-piperazinediyl) (4,4′-biphenyldicarbonyl)] ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Four aryl dichlorides containing secondary amide structural units as monomers were synthesized from substituted piperazines and chlorobenzoyl chlorides. Polyamides were prepared by the nickel-catalyzed coupling polymerization of these monomers. Polymerizations were carried out in N-methyl-2-pyrrolidinone (NMP) in the presence of nickel chloride, zinc, triphenylphosphine, and bipyridine, and resulted in polyamides with inherent viscosities up to 0.38 dL/g under mild conditions. The structure of polymer was determined by IR and 13C-NMR spectroscopies. The polyamide, poly[4,4′-biphenyldicarbonyl (2,5-dimethylpiperazine)] 6d, was readily soluble in dipolar aprotic solvents and chloroform. Thermogravimetry of polyamides, poly[(4,4′-biphenyldicarbonyl piperazine)]s 6, showed 10% weight loss at around 425 and 450°C in air and under nitrogen, respectively. © 1992 John Wiley & Sons, Inc.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1511-1518 
    ISSN: 0887-624X
    Keywords: polymerization anionic ; acrylates ; complex initiators ; 2-ethylhexylacrylate ; tert-alkoxides ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The anionic polymerization of 2-ethylhexyl acrylate (EtHA) initiated with the complex butyllithium/lithium-tert-butoxide (BuLi/t-BuOLi) was investigated at -60°C in a medium of various solvating power, i.e., in mixtures of toluene and tetrahydrofuran and in neat tetrahydrofuran. With increasing amount of THF in the mixture the attainable limiting conversion of polymerization decreases; the monomer can be polymerized quantitatively only in a toluene/THF mixture (9/1). Molecular weights of the polymers thus obtained, their distribution, and initiator efficiency are not appreciably affected by the polymerization medium. The molecular weight distribution of the products is medium-broad (Mw/Mn = 2-2.4), with a hint of bimodality. The 1H-13C-NMR, and IR spectra suggest that during the polymerization there is neither any perceptible reesterification of the polymer with the alkoxide nor transmetalation of the monomer with the initiator. In a suitable medium, autotermination of propagation proceeds to a limited extent only, predominantly via intramolecular cyclization of propagating chains; in a medium with a higher content of polar THF, it prevails and terminates propagation before the polymerization of the monomer has been completed. © 1992 John Wiley & Sons, Inc.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1525-1533 
    ISSN: 0887-624X
    Keywords: polycarbonate ; photo-Fries ; photolysis ; fluorescence ; diphenylcarbonate ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of polymer matrices on a photoinduced rearrangement process has been shown to be dependent upon whether the photoreactive group is attached to a polymer backbone, or free. If diphenylcarbonate is simply embedded in a polymer matrix, the rearrangement process is independent of whether the host film is above or below its glass transition. However, if the diphenylcarbonate group is incorporated as part of a polycarbonate backbone, the Fries rearrangement process is significantly reduced for photolyses conducted at temperatures well below the glass transition of polycarbonate. The utility of fluorescence spectroscopy in identification of the initial salicylate type photo-Fries type rearrangement product of polycarbonate is also demonstrated. The broad, structureless fluorescence spectrum with peak maximum at 470 nm produced by photolysis of polycarbonate films for short time periods is assigned to emission from phenyl salicylate type photoproducts. © 1992 John Wiley & Sons, Inc.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1609-1614 
    ISSN: 0887-624X
    Keywords: conducting polypyrrole ; chemical synthesis ; cyclic voltammetry ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The conducting polypyrrole chemically synthesized in water, using the variable concentrations of FeCl3 and CuCl2 as oxidizing agents, was chemically and electrochemically characterized and compared with electrochemically generated polypyrrole. According to the results of elemental analysis and counter ion determinations, it can be concluded that a mixture of dimer and trimer was obtained using CuCl2, i.e., a dimer composition using FeCl3 as an oxidant. Cyclic voltammetric studies of polypyrrole obtained by using FeCl3 as an oxidant showed no evidence of polypyrrole decomposition after repetitive cycling. The voltammograms showed also that after the oxidation reaction a high capacitive current remained, confirming the assumption that the capacitive current is intrinsically associated with polypyrrole, irrespective of the way of its preparation. Cyclic voltammogram of the polypyrrole synthesized by oxidation with CuCl2 showed different shape, probably influenced by the presence of copper ions incorporated in polymers. © 1992 John Wiley & Sons, Inc.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1655-1665 
    ISSN: 0887-624X
    Keywords: microstructure ; N-vinylcarbazole ; methyl acrylate ; NMR ; sequence distribution ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The microstructure of a series of high conversion copolymers of methyl acrylate (MA) and N-vinylcarbazole (NVC) was characterized by NMR. 1H- and 13C-NMR spectra were assigned by comparison to the homopolymers and by using heteronuclear shift correlation spectroscopy. MA-centered triad distributions were obtained from the carbonyl carbon. Distributions of NVC sequences were determined from aromatic carbons 1 and 8a, and aromatic proton 1 These experimentally determined sequence distributions were compared to those calculated from reactivity ratios approximated from the copolymer compositions. Agreement was very good for low NVC content copolymers. Three signals were particularly useful in providing rapid assessment of the distribution of NVC units within low NVC content copolymers: proton 1 and carbon 1 of NVC and the carbonyl carbon of MA. © 1992 John Wiley & Sons, Inc.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1675-1679 
    ISSN: 0887-624X
    Keywords: fluoropolymers ; low dielectric constant ; thermally stable ; aromatic polyethers ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of fluorinated aromatic polyethers was synthesized via aromatic nucleophilic substitution of highly fluorinated aromatics (1,2,4,5-tetrafluorobenzene, hexafluorobenzene, and decafluorobiphenyl) with bisphenol AF or bisphenol A. Polymerization with 1,2,4,5-tetrafluorobenzene was not observed, and polymerization of hexafluorobenzene with bisphenol proceeded only if the potassium carbonate-bisphenol ratio was carefully controlled. The polymer condensed from decafluorobiphenyl and bisphenol AF was prepared in 77% yield with an inherent viscosity of 1.01 dL/g. The polymer prepared from the condensation of decafluorobiphenyl with bisphenol A was obtained in 48% yield with an inherent viscosity of 0.28 dL/g. These polymers were very soluble in common organic solvents, formed clear, colorless films, and were thermally stable (〉 450°C by TGA). The fully fluorinated polymer exhibited low water uptake (0.3%) and dielectric constant (2.17). © 1992 John Wiley & Sons, Inc.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1477-1487 
    ISSN: 0887-624X
    Keywords: bisimido-bisphthalonitriles ; thermally stable monomers ; 4-aminophthalonitrile ; aromatic tetracarboxylic dianhydride ; NMR study ; synthesis ; structural assignments ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Various melt-polymerizable bisimido-bisphthalonitrile polymer precursors were synthesized by the reaction of 4-aminophthalonitrile (4-APN) with bis(3,4-dicarboxyphenyl) dimethylsilane dianhydride (SIDA), 4,4′-hexafluoroisopropylidene diphthalic anhydride (6FDA), bis(3,4-dicarboxyphenyl)ether dianhydride (ODPA), and 3,3′, 4,4′-tetracarboxylichenzophen+ne dianhydride (BTDA) in an aprotic solvent. The synthesized monomers showed crystalline melting at 269 and 271°C. Elemental analysis, differential thermal analysis (DTA), infrared (IR), nuclear magnetic resonance (1H-NMR) and mass spectral studies were carried out to characterize the synthesized monomers. Thermogravimetric analysis (TGA) of the synthesized monomers showed their thermal stability at 410-400°C. A detailed study and NMR investigation of the first step of condensation reaction was carried out and indicated the formation of a transient charge transfer complex. Thermal cyclization of the formed intermediate, however, gave the required monomers. A preliminary study demonstrated that melt-polymerization of the synthesized monomers gave thermallystable, tough polymers.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1503-1506 
    ISSN: 0887-624X
    Keywords: polymer catalyst ; phase transfer catalyst ; triphenylphosphine oxide ; Chemistry ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1508-1508 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1507-1508 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1519-1523 
    ISSN: 0887-624X
    Keywords: polymerization anionic ; acrylates ; lithium-tert-butoxide ; 2-ethylhexylacrylate ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymerization of 2-ethylhexyl acrylate (EtHA) initiated with lithium-tert-butoxide (t-BuOLi) in tetrahydrofuran (THF) and in the temperature range between -60 and 20°C was investigated. The reaction rate is distinctly temperature-dependent and at -60°C is already very low, similarly to the polymerization of methacrylates. Molecular weights of the polymers thus formed, particularly at higher temperatures, are inversely proportional to conversion of the monomer due to the slow initiation reaction. This is documented by the low consumption of alkoxide even at long reaction times, which also depends on the reaction temperature. At higher temperatures the polymerization stops spontaneously, due to the greater extent of autotermination reactions. The weak initiating efficiency of the alkoxide decreases still more with decreasing concentration of the monomer during the polymerization, as confirmed by the concentration dependence of the reaction rate in toluene at -20°C. The results suggest a negligible initiating effect of alkoxides in complex bases, particularly at lower polymerization temperatures. © 1992 John Wiley & Sons, Inc.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1559-1565 
    ISSN: 0887-624X
    Keywords: radical copolymerization ; dialkyl fumarate ; substituent effect ; monomer reactivity ratio ; steric effect ; polar effect ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Radical copolymerization of dialkyl fumarates (DRF) with various vinyl monomers was carried out in benzene at 60°C. The monomer reactivity ratios, r1 and r2, were determined from the comonomer-copolymer composition curves. The relative reactivity of DRFs with various ester substituents toward a polystyryl radical was revealed to depend on both steric and polar effects of the ester groups. It has also been clarified that α-substituents of the polymer radical have a significant role in addition of DRF, from the comparison of the monomer reactivity ratios determined in copolymerizations with monosubstituted and 1,1-disubstituted ethylenes. The absolute cross-propagation rate constants were also evaluated and discussed. © 1992 John Wiley & Sons, Inc.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 125-132 
    ISSN: 0887-624X
    Keywords: maleamic acids ; maleimides ; Diels-Alder polymerization ; polyimides ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactions of monomaleamic acid derived from an aromatic diamine with furfural afforded a novel class of furfurylidene-substituted maleamic acids 2a-2d. The latter were cyclodehydrated to yield maleimides 3a-3d which are AB-monomers for a Diels-Alder polymerization. In addition, N-furfurylmaleamic acid (4) was synthesized by reacting furfurylamine with maleic anhydride at ambient temperature. Cyclodehydration of 4 afforded N-furfurylmaleimide (5). The polymer precursors were characterized by IR and 1H-NMR spectroscopy. Their curing behavior was investigated by DTA and correlated with chemical structures. Diels-Alder polymerization of monomers occurred at the temperature range of 113-210°C. Thermal stability of monomers was evaluated by TGA and isothermal gravimetric analysis (IGA). It was shown that thermal stability of the polymer derived from maleamic acid 4 was dramatically improved upon curing at high temperatures due to the formation by dehydration of a stable aromatic structure.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 149-152 
    ISSN: 0887-624X
    Keywords: radical polymerization ; monomer ; diethyl-2-acetamido-2-vinylbenzyl malonate ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1767-1770 
    ISSN: 0887-624X
    Keywords: decafluorobiphenyl ; polyarylether ; polyether ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 185-195 
    ISSN: 0887-624X
    Keywords: radiation ; polybutadiene ; crosslinking ; solid-state NMR ; 13C-NMR ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Solid-state 13C NMR spectroscopy has been used to determine the decrease in C=C bonds, formation of crosslinks and cis to trans isomerization during the γ irradiation of (a) 〉 99% cis, 1,4-polybutadiene, (b) 54% trans, 41% cis, 1,4-polybutadiene, and (c) 86% 1,2-polybutadiene. G(-cis C=C) and G(-trans C=C), were similar and decreased with dose from ≈ 40 for 0-1 MGy to 5 for 5-10 MGy. G(-double bonds) and G(crosslink) were comparable, indicating that crosslinking occurred through the double bonds. G(crosslink) was much higher than values derived from physical properties, confirming that NMR measures the total of inter- and intramolecular crosslinking (cyclization). The 1,2 polybutadiene was much more sensitive to crosslinking, and a value of G(-C=C) = 240 was obtained at low doses. Crosslinking evidently proceeds by a kinetic chain reaction in all three types of polybutadiene.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1667-1673 
    ISSN: 0887-624X
    Keywords: electrochemical polymerization ; polythiophene ; 2,5-bis(trimethylsilyl)thiophene ; bis(2-thienyl)silanes ; oxidative elimination ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Electrochemical polymerization of 2,5-bis(trimethylsilyl) thiophene produced highly conducting films which showed infrared spectra, visible-near infrared absorption spectra, and cyclic voltammograms identical to films prepared from thiophene. Elemental analysis indicated that almost all silicon atoms were eliminated during the electrochemical polymerization. However, scanning electron microscopy showed a morphological difference between the films from 2,5-bis(trimethylsilyl)thiophene and from thiophene. The electrochemical polymerization of bis(2-thienyl)dimethylsilane, 1,2-bis(2-thienyl)tetramethyldisilane, and bis(2-thienyl)diphenylsilane also produced polythiophene films having unique morphologies quite different from the conventional ones. These findings indicate that these electrochemical procedures must be useful for preparation of new conjugated polymers. © 1992 John Wiley & Sons, Inc.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1705-1716 
    ISSN: 0887-624X
    Keywords: amphiphilic gels ; copoly(styrene-acrylamide)s ; copoly(styrene-trichlorophenyl acrylate) ; peptide synthesis ; polymer reactivity ; polymeric reagents ; polymer supports ; polymer swelling ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new class of “amphiphilic” copoly(styrene-acrylamide)s of potential interest for peptide synthesis is described. As examples of the new polymers, those carrying nitrophenol or piperazine functionality were used for model reactions in peptide synthesis, and were found to be substantially more efficient than similar reagents derived from polystyrene, polydimethylacrylamide or silica gel. Due to their amphiphilic structure, the new resins have general substrate compatibility and are permeated by all of the commonly used solvents, including toluene and ethyl acetate on the one hand, through dimethylformamide, to dimethylsulfoxide and water on the other. The improved performance of the new polymers is attributed to their alternating amphiphilic structure and favorable polymer-solvent-substrate interactions. © 1992 John Wiley & Sons, Inc.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1725-1729 
    ISSN: 0887-624X
    Keywords: gel ; display device ; electrochromism ; electrochromic device ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polymer gel films [poly(1-vinyl-2-pyrrolidinone-co-N,N′-methylenebisacrylamide) (PVPD)] which contain simple organic electrochromics [p-diacetylbenzene (p-DAB), dimethyl- or diethyl terephthalate (p-DMP or p-DEP)] are prepared and their optical responses to applied voltage are investigated. p-DAP/PVPD film is colored in green by the application of 1.2 V vs. Pt wire (quasireference electrode) across the film, and p-DMP/PVPD and p-DEP/PVPD films are colored in red by the application of -2.5 and -1.5 V vs. Pt, respectively. Their coloring responses are about a few seconds and the bleaching process also occurs rapidly. The films have no optical memory effect. © 1992 John Wiley & Sons, Inc.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1741-1746 
    ISSN: 0887-624X
    Keywords: electrically conducting polymers ; 3,3′-dimethoxy-2,2′-bithiophene ; 3-methoxythiophene ; synthesis ; polymerization ; electrochemistry ; Chemistry ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
    Notes: A new electroactive polymer, namely poly(3,3′-dimethoxy-2,2′-bithiophene) has been prepared by voltammetric polymerization of 3,3′-dimethoxy-2,2′-bithiophene. Due to a different coupling pattern (equivalent to “head-to-head,” and “tail-to-tail” coupled alkoxythiophene rings), poly(3,3′-dimethoxy-2,2′-bithiophene) exhibits different voltammetric properties than the corresponding “head-to-tail” coupled polymer, i.e., poly(3-methoxythiophene). Poly(3,3′-dimethoxy-2,2′-bithiophene) gives very sharp oxidation and reduction peaks indicating an abrupt insulator to conductor transition. This hypothesis was corroborated by the studies of relative resistance as a function of electrode potential. Sharper and better-defined redox peaks may indicate better stereoregularity of poly(3,3′-dimethoxy-2,2′-bithiophene) as compared to poly(3-methoxythiophene) since in this compound the 5,5′-coupling positions are geometrically equivalent and no coupling defects are expected. © 1992 John Wiley & Sons, Inc.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1761-1765 
    ISSN: 0887-624X
    Keywords: polythiophenes ; soluble ; steric hindrance ; UV spectroscopy ; nuclear magnetic resonance ; high resolution in solid state ; Chemistry ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1775-1776 
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    Keywords: agar-agar hydrogel ; thermal property ; carbohydrates ; irradiation ; Chemistry ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1778-1778 
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    Keywords: Chemistry ; Polymer and Materials Science
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 1778-1778 
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    Keywords: Chemistry ; Polymer and Materials Science
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2045-2048 
    ISSN: 0887-624X
    Keywords: siloxanes ; epoxy resins ; synthesis ; curing ; Chemistry ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2055-2057 
    ISSN: 0887-624X
    Keywords: end group effect ; end-to-end linking ; radiation crosslinking ; poly(ethylene glycol) ; Chemistry ; Polymer and Materials Science
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2071-2073 
    ISSN: 0887-624X
    Keywords: polycationic polymer ; poly(allylbiguanido-co-allylamine) ; potentiometric titration ; thermogravimetric analysis ; Chemistry ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2075-2075 
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    Keywords: Chemistry ; Polymer and Materials Science
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2099-2108 
    ISSN: 0887-624X
    Keywords: amphiphilic polyelectrolyte ; compartmentalization ; photoinduced electron transfer ; molecular composite ; polymer-bound chromophore ; Chemistry ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
    Notes: A molecular composite of an amphiphilic polyanion and cationic surfactants was prepared by treating a terpolymer [consisting of sodium 2-acrylamido-2-methylpropanesulfonate, N-(1-adamantyl)methacrylamide, and a small mole fraction of N-(1-pyrenylmethyl)methacrylamide] with didodocyldimethylammonium bromide in aqueous solution. The molecular composite was soluble in organic solvents with a wide range of polarities. Fluorescence spectra indicated that the pyrenyl (Py) residues in the molecular composite experienced polar microenvironments even though the composite was dissolved in nonpolar solvents. Exciplex formation of the Py residue with 4,4′-dicyanobenzene was strongly suppressed due to the polar microenvironments and steric “protection” of the chromophore. Photoinduced electron transfer (ET) from the Py residue to pyromellitic dianhydride (PMDA) in acetonitrile showed characteristics of long-range ET between fixed donor and acceptor sites and yielded long-lived transient Py cation radicals and PMDA anion radicals which persisted for tens of milliseconds. These findings imply that the micellelike structure of the parent amphiphilic polyelectrolyte formed in aqueous solution is retained, to some degree, in the molecular composite dissolved in organic solvents. © 1992 John Wiley & Sons, Inc.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2131-2141 
    ISSN: 0887-624X
    Keywords: polypropylene, catalyst dynamics for ; Ziegler-Natta ; heterogeneous catalysis of; catalysis ; polyolefins, fragmentation of ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Recently considerable detail has become available on the initial morphology and the morphological changes that occur for silica based Cr catalysts for ethylene polymerization. These catalysts are produced as a dry powder and may be employed either in gas phase or in slurry processes. MgCl2-supported Ziegler-Natta polymerization catalysts are often prepared and employed as slurries. They usually are never dried and thus few studies have employed the spectra of physical techniques common to the characterization of pore structure. In the current study, we have carefully removed the solvent for both ball-milled and precipitated MgCl2-supported catalysts. These catalysts are characterized by physical sorption, mercury porosimetry, and electron microscopy both as prepared and during the initial stages of polymerization (to ∼ 100 g of polymer/g of catalyst). We find that the initial catalyst may be represented by a complex agglomerate of small crystallites as contrasted with the branched pore network found in Cr/silica catalysts. As a result, it is concluded that the initial fragmentation of the MgCl2 based systems is more uniform as contrasted with the progressive fragmentation of the silica-based system. This fragmentation mechanism facilitates the retention of greater polymer/catalyst surface during the initial stages of the polymerization. © 1992 John Wiley & Sons, Inc.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2187-2193 
    ISSN: 0887-624X
    Keywords: chitin ; chitosan ; fibers ; crosslinking ; epichlorohydrin ; film ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A need exists for the development of totally biodegradable packaging materials. Chitosan is an under-utilized polymer which possesses many of the desired characteristics for this application. This article describes the crosslinking of chitosan fibers. Epichlorohydrin (ECH) was selected as a convenient base catalyzed crosslinking agent. The strength of chitosan fibers, especially wet tenacity, is improved by crosslinking. © 1992 John Wiley & Sons, Inc.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 577-581 
    ISSN: 0887-624X
    Keywords: organoborazine homopolymers ; organoborazine copolymers ; radical polymerization ; thermal behavior ; monomer reactivity ratios ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymerization and copolymerization with styrene of a series of unsymmetrically B-p-vinylphenyl-N-methyl and N-phenyl borazines [R3(R2)2B3N3(R1)3; R1 = methyl, phenyl, R2 = methyl phenyl, R3 = p-vinylphenyl] has been studied. The polymerization of these monomers yielded both tractable and crosslinked materials. The polymers obtained were characterized by 1H- and 13C-NMR spectroscopy, elemental analysis, gel permeation chromatography, and thermogravimeteric analysis. The reactivity ratios for the copolymerization reaction were calculated by the Mortimer-Tidwell method.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 589-595 
    ISSN: 0887-624X
    Keywords: laser copolymerization ; charge transfer complexes ; N-vinylpyrrolidone ; maleic anhydride ; maleimide ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This article describes the laser-initiated copolymerization of N-vinylpyrrolidone with maleic anhydride and maleimide via charge transfer complexes. The dependence of copolymer yield on the molar ratios of the monomers in the feed and on the irradiation time is described. Based on the ultraviolet and infrared spectroscopy, and chemical analysis results, a tentative mechanism of polymerization is suggested. The rates of polymerization of several monomer systems are compared. The N-vinylpyrrolidone and maleimide system shows the highest rate of polymerization.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 613-623 
    ISSN: 0887-624X
    Keywords: thermolysis of crosslinked polysiloxanes ; redistribution reactions ; Si—C/Si—O and Si—H/Si—O bonds exchange ; thermogravimetric analysis/mass spectroscopy ; solid-state 29Si-NMR ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermolysis under argon of various polysiloxane resins containing D, T, DH, or TH units was investigated using thermogravimetric analysis combined with mass spectroscopy (TG/MS analysis) and solid-state 29Si-NMR. Redistribution reactions involving the exchange of Si—C/Si—O bonds or Si—H/Si—O bonds were evidenced in addition to the exchange of Si—O/Si—O bonds reported to date. These reactions significantly modify the initial siloxane units and lead to an escape of volatile silanes or siloxanes. The exchange of Si—H/Si—O bonds takes place at lower temperatures (300°C) than the exchange of Si—C/Si—O bonds (500°C).
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 625-634 
    ISSN: 0887-624X
    Keywords: catalysis ; mechanism ; kinetics ; aminolysis ; tautomer ; molten state ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The aminolysis of poly(styrene-co-methyl acrylate) (SMA) by octadecylamine was studied in solution and in the melt at temperatures around 200°C. This reaction is rather slow, so several types of catalysts were tested to accelerate it. The most efficient is 2-pyridone, a compound in tautomeric equilibrium with 2-hydroxypyridine. A mechanism of the catalytic reaction is proposed whereby the tautomeric nature of the catalyst plays a key role in a very important step of the reaction, namely the proton transfer. This mechanism is confirmed by the kinetic data determined in a 1,2,4-trichlorobenzene solution and in the melt. In addition, it was found that the kinetic data obtained in both media are very close, indicating no significant difference of local polarity in the two reaction media. Data also show only a minor effect due to difference in viscosity. Finally, the question of the homogeneity of the molten medium is discussed.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 679-683 
    ISSN: 0887-624X
    Keywords: coordination polymerization ; vinylcyclohexane ; Ziegler-Natta catalyst ; isomerization ; monomer-isomerization copolymerization ; 2-butene ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polymerization of vinylcyclohexane (VCHA) with TiCl3-aluminum alkyl catalysts was investigated. The polymerization rate of VCHA was low due to the branch at the position adjacent to the reacting double bond. The effects of aluminum alkyl on the polymerization and monomer-isomerization were observed; the polymer yield decreased in the following order: (CH3)3Al 〉 (i-C4H9)3Al 〉 (C2H5)3Al. Isomerization of VCHA was observed with the TiCl3-(i-C4H9)3Al and the TiCl3-(C2H5)3Al catalysts during the polymerization, while with the TiCl3-(CH3)3Al catalyst such isomerization was not observed. Monomer-isomerization copolymerization of VCHA and trans-2-butene took place to give copolymers consisting of VCHA and 1-butene units.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 689-690 
    ISSN: 0887-624X
    Keywords: radical polymerization ; ring-opening polymerization ; 4-methylene-1,3-dioxolanes ; Chemistry ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 723-729 
    ISSN: 0887-624X
    Keywords: bismaleimides ; structure effect ; crosslinking reaction ; heat resistance ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Novel bismaleimides (BMIs) were prepared from functional monomaleimides and diglycidyl ether of bisphenol A (DGEBA) and some of them were shown to have good processibility and improved water resistance while retaining characteristic thermal stability of polyimide. Functional monomaleimides were synthesized via the condensation reaction of maleic anhydride with either aminobenzoic acid or aminophenol. Crosslinking reaction of thus obtained BMIs was carried out with or without catalyst at the temperature range of 100-250°C. The type of the functional group species and their position in monomaleimides significantly affected the crosslinking behavior of the resulting BMIs and the thermal property of their crosslinked products. BMIs with meta linkage, obtained from meta monomaleimides, exhibited much faster thermal crosslinking behavior than corresponding para BMIs. When the molecular weight of BMI was larger, the crosslinking density became smaller and Tg was lower as expected, while the viscosity started to increase at a higher temperature. Glass transition temperatures of the crosslinked resins were in the range of 160-250°C and these resins showed excellent thermal stability up to 370°C.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 787-796 
    ISSN: 0887-624X
    Keywords: template polymerization ; crosslinked PMAA ; calorimetry ; morphology ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of crosslinked poly(methacrylic acid) (c-PMAA) on the polymerization of N-vinylimidazole in aqueous solution was studied using UV, calorimetry, SEM, and TEM. It was established that synthetic lightly crosslinked PMAA samples behaved intermediate between rigid crosslinked PMAA particles functioning as microreactors, and linear conventional PMAA, where template and conventional polymerization in the surrounding solution are integrated. A modified calorimetric technique was used to measure monomer conversion, and to correct for the rapid adsorption process. Rate enhancements up to a factor of 4 were obtained for the c-PMAA's, which were lower than those obtained for linear conventional PMAA, and which slightly decreased with increasing crosslink density of the samples. Template complexes possessed a platelet-like morphology similar to template complexes obtained for linear PMAA.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2085-2097 
    ISSN: 0887-624X
    Keywords: imide-aryl ether ketone block copolymers ; multiphase morphologies ; mechanical and thermal properties ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Imide-aryl ether ketone block copolymers were prepared and their morphology and thermal and mechanical properties investigated. Two aryl ether ketone blocks were incorporated; the first was an amorphous block derived from bisphenol-A and the second block was a semi-crystalline poly(aryl ether ether ketone) prepared from a soluble and amorphous ketimine precursor. Bis(amino) aryl ether ketone and aryl ether ketimine oligomers were prepared via a nucleophilic aromaic substitution reaction with molecular weights ranging from 6,000 to 12,000 g/mol. The oligomers were co-reacted with 4,4′-oxydianiline (ODA) and pyromellitic dianhydride (PMDA) diethyl ester diacyl chloride in N-methyl-2-pyrrolidone (NMP) in the presence of N-methylmorpholine. The copolymer compositions, determined by H-NMR, of the resulting amic ester based copolymers ranged from 8 to 50 wt % aryl ether ketone or ketimine content. Prior to imide formation, the ketimine moiety of the aryl ether ketimine block was hydrolyzed (p-toluene sulfonic acid) to the ketone form producing the aryl ether ether ketone block. Compositions of this block were maintained low to retain solubility. Solutions of the copolymers were cast and cured to effect imidization, producing clear films with high moduli (ca. 2200 MPa) and elongations (33-100%). The copolymers displayed good thermal stability with decomposition temperatures in excess of 450°C. Multiphase morphologies were observed irrespective of the co-block type, block length or composition. © 1992 John Wiley & Sons, Inc.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2203-2210 
    ISSN: 0887-624X
    Keywords: allyl ether ; star polymers ; rheology ; curing kinetics ; molecular architecture ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of allyl ether-maleate functional star-shaped esters with from one to four arms has been synthesized. The structures that have been made are an analogous series with increasing molecular weight and functionality where the increase in molecular weight has been made nonlinear, i.e., star-shaped. The resins are monodisperse in the sense that each arm has a well-defined structure and that, within a certain sample, only one type of molecule exists. The viscosity and rheological behavior of the resins have been studied. The curing kinetics of the star-shaped (branched) resins and the properties of the films formed have also been studied. These properties have been related to differences in functionality and to differences in the molecular architecture of the resins. © 1992 John Wiley & Sons, Inc.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2247-2250 
    ISSN: 0887-624X
    Keywords: polymer catalyst ; formose reaction ; thiazolium salt ; hydrocarbons ; dihydroxy acetone ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thiazolium salt polymers synthesized by quaternization of 4-(4′-vinylphenyl)thiazole (VPT) polymers with methyl iodide had a highly catalytic activity for “the formose reaction.” Their catalytic activities were comparable to that of a low molecular weight analog, 3-methyl-4-phenylthiazolium iodide (MPTI). In the reaction catalyzed by the polymer catalyst, a main product, dihydroxyacetone (DHA), was detected by gas-liquid chromatography. The polymer catalysts were easily recovered from the reaction mixture and reused with a sustained catalytic activity. © 1992 John Wiley & Sons, Inc.
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  • 86
    ISSN: 0887-624X
    Keywords: para-xylylenes ; 1,4-benzoquinodimethanes ; conducting polymers ; poly(arylene vinylene)s ; poly(phenylene vinylene)s ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: para-Xylylenes are generated by treatment of various 1,4-bis(dialkylsulfoniomethyl)arene dihalides with base in water, methanol, and aqueous acetonitrile, as shown by UV-Vis spectroscopy. This procedure allows the monitoring of the transient xylylene monomers that yield polyelectrolyte precursor polymers for poly(arylene vinylene)s, formed by variations of the chemistry developed originally by Wessling and co-workers. Alkoxy, alkyl, and halogen ring substituents on the sulfonium salt precursors do not greatly affect the ability to generate and observe the growth and decay of steady-state concentrations of the para-xylylene intermediates. Use of strong resonance-acceptor substituents - such as cyano or nitro - on the ring reduces production of a strong para-xylylene absorption, possibly due to reluctance of the ylides initially formed from the bis-sulfonium salts to eliminate to the xylylenes. By variation of UV-Vis conditions, it was found that use of 20% aqueous acetonitrile rather than water allowed formation of low to modest molecular weight polyelectrolytes in cyano-substituted cases (Mw = 8000-37,000). Use of UV-Vis test experiments should be useful for screening of bis sulfonium salt precursors that may be expected to give high molecular weight polyelectrolytes - in cases where para-xylylene formation is easy - as well as for finding reaction conditions that will optimize polymer formation. © 1992 John Wiley & Sons, Inc.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2277-2280 
    ISSN: 0887-624X
    Keywords: polyethylene ; photooxidation kinetics ; light intensity ; oxygen uptake ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 88
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2559-2567 
    ISSN: 0887-624X
    Keywords: Diels-Alder polymerization ; polyimides ; bismaleimide ; bismaleamic acid ; bisfurfurylpyromellitimide ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Certain AB or AA and BB Diels-Alder polymer precursors bearing maleimide and furan segments were synthesized, characterized, and polymerized. Particularly, the monomaleamic acid derived from 4,4'-diaminodiphenylmethane, reacted with the monofurfurylpyromellitamic acid to yield a triamic acid which was cyclodehydrated to the corresponding triimide. A polyimide was obtained upon heat-curing of triimide or the intermediate triamic acid. In addition, equimolar amounts of N,N'-bismaleimido-4,4'-diphenylmethane (BMDM) and bisfurfurylpyromellitimide or their intermediate diamic acids were cured to afford a polyimide. The polymer precursors were characterized by IR and 1H-NMR spectroscopy and their curing behavior was investigated by DTA. It was shown that the Diels-Alder polymerization of monomers took place at lower temperature than that required for crosslinking of BMDM. The thermal stabilities of polymers were ascertained by TGA and isothermal gravimetric analysis (IGA). The synthesized Diels-Alder polymers were remarkably more heat-resistant than the crosslinked polymer obtained from BMDM or its intermediate bismaleamic acid. They were stable up to about 360°C in N2 or air and afforded anaerobic char yield of 58% at 800°C. © 1992 John Wiley & Sons, Inc.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2587-2594 
    ISSN: 0887-624X
    Keywords: kinetics of quaternization ; poly(4-vinyl pyridine) ; steric hindrance ; liquidcrystalline copolymers ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics and characteristics of the quaternization of poly(4-vinylpyridine) with very large alkylating agents are studied with the main aim to demonstrate the occurrence of a limitation of the reaction due to steric effect. Kinetics are carried out in sulfolane at different temperatures with two ω-(4'-methoxy-4-biphenylyloxy)alkyl bromides. An important limitation of the reaction is demonstrated: 30% of the pyridine groups are inaccessible at 333 K, 23% at 355.5 K, and 4% at 363 K. Post-quaternization experiments with butyl bromide of already partially quaternized P4VP also demonstrate this limitation. The occurrence of global steric hindrance and hydrophobic effects affecting the conformation of the chain in solution is proposed to explain the limited accessibility of the pyridine groups. The results question the classical neighboring group model generally used to describe the slowing down of the quaternization reaction with increasing quaternization ratio. The thermal stability of the quaternized polymers and the colors of the reaction medium are also discussed. © 1992 John Wiley & Sons, Inc.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2619-2629 
    ISSN: 0887-624X
    Keywords: emulsion polymerization, vinyl acetate ; emulsion polymerization, polymerizable surfactant ; emulsion polymerization, kinetics ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A polymerizable surfactant, sodium dodecyl allyl sulfosuccinate (TREM LF-40; Henkel) and its nonpolymerizable counterpart were used in comparative studies of the emulsion polymerization of vinyl acetate. The conversion-time behavior differed for the two surfactants; the TREM LF-40 showed a decrease in the polymerization rate with increasing concentration while its hydrogenated derivative showed the opposite behavior, the rate increasing with increasing surfactant. Particle size analysis revealed a decreasing particle size with increasing surfactant concentration for both series of reactions. An explanation for the seemingly ambiguous results obtained for the polymerizable surfactant was sought by examining the reactivity of its vinyl group in copolymerization with vinyl acetate and its allylic group in a chain transfer reaction. The results suggest that both the copolymerization and chain transfer reactions can lead to the observed reduction in polymerization rate with increasing TREM LF-40 concentration. © 1992 John Wiley & Sons, Inc.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2663-2663 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 92
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2677-2681 
    ISSN: 0887-624X
    Keywords: polystyrene ; photooxidation ; oxygen ; nitrous oxide ; ultraviolet ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Strips of polystyrene held in a flowing O2 or N2O atmosphere have been exposed to 240-600 nm radiation. The extent of photooxidation has been followed by x-ray photoelectron spectroscopy (XPS). Although N2O is a more reactive gas than O2, it produces a less oxidized polymer surface. This surprising observation can be correlated to the photochemistry occurring at the gas/polystyrene interface. © 1992 John Wiley & Sons, Inc.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2693-2698 
    ISSN: 0887-624X
    Keywords: thermal oxidation ; polymer blends, poly(ethylene oxide) ; poly(methyl methacrylate) ; miscibility ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thermal oxidation of poly(ethylene oxide) (PEO) and its blends with poly(methyl methacrylate) (PMMA) were studied using oxygen uptake measurements. The rates of oxidation and maximum oxygen uptake contents were reduced as the content of PMMA was increased in the blends. The results were indicative of a stabilizing effect by PMMA on the oxidation of PEO. The oxidation reaction at 140°C was stopped at various stages and PMMA was separated from PEO and its molecular weights were measured by gel permeation chromatography (GPC). The decrease in the number-average molecular weight of PMMA was larger as the content of PEO increased in the blends. The visual appearance of the films suggested that phase separation did not occur after thermal oxidation. The activation energy for the rates of oxidation in the blends was slightly increased compared to pure PEO. © 1992 John Wiley & Sons, Inc.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2781-2790 
    ISSN: 0887-624X
    Keywords: poly((E,E)-[6.2]paracyclophane-1,5-diene ; thermal analysis ; thermal degradation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thermal degradation of poly((E,E)-[6.2]paracyclophane-1,5-diene) is studied in inert and oxidative environments by using thermogravimetric analysis, pyrolysis GC/MS, pyrolysis GC/FT-IR, and variable temperature-diffuse reflectance infrared spectroscopy (VT-DRIFTS). Thermal degradation in helium begins by depolymerization yielding a volatile product capable of abstracting hydrogens from the polymer residue. Multiple hydrogen abstractions result in a variety of volatile species containing benzyl-benzyl bonds. In the presence of oxygen, polymer decomposition is dictated by reactions of peroxy and hydroperoxy radicals. At low temperatures, oxygenated species are the primary products. At higher temperatures, increased unsaturation is detected in the polymer residue. In both inert and oxidative environments, the strain associated with alignment of paracyclophane aromatic rings is lost during the initial stages of thermal degradation. © 1992 John Wiley & Sons, Inc.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2349-2355 
    ISSN: 0887-624X
    Keywords: carbonation ; functionalization ; polystyrene ; polyisoprene ; polybutadiene ; poly(styryl)lithium ; poly(butadienyl)lithium ; anionic polymerization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The carbonation of the adduct of poly(styryl)lithium with 1,1-diphenylethylene with gaseous carbon dioxide in benzene proceeds in high yield (〉99%) compared to the inefficient functionalizations for poly(styryl)lithium (66%), poly(isoprenyl)lithium (59%), and polybutadienyl)lithium (27%). The quantitative carboxylation of poly(isoprenyl)lithium and poly(butadienyl)lithium requires the presence of larger amounts of Lewis bases such as THF ([THF]/[Li] = 300) or TMEDA ([TMEDA]/[Li] = 46) compared to poly(styryl)lithium in which a ratio of [TMEDA]/[Li] = 12 is effective. © 1992 John Wiley & Sons, Inc.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2365-2369 
    ISSN: 0887-624X
    Keywords: photolysis ; transient species ; sulfonium salt ; benzyl cation ; time-resolved measurements ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Benzyl cation was detected by transient absorption spectroscopy with a spectroscopic multichannel analyzer on pulse excitation (fourth harmonic of Nd:YAG laser, 266 nm; 10 ns fwhm) of benzyl(4-hydroxyphenyl) methylsulfonium hexafluoroantimonate(BSS) in 1,2-dichloroethane (EDC). The benzyl cation was long-lived (lifetime, 59 ms) at room temperature and quenched by a vinyl ether compound. The formation of the benzyl cation as active species on photolysis of BSS is in contrast to the formation of Brønsted acids in other sulfonium salts so far reported. © 1992 John Wiley & Sons, Inc.
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  • 97
    ISSN: 0887-624X
    Keywords: living cationic polymerization ; alkoxyethyl vinyl ether ; pendant oxyethylene unit ; water-soluble polymer ; phase separation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Living cationic polymerization of alkoxyethyl vinyl ether [CH2=CHOCH2CH2OR; R: CH3 (MOVE), C2H5 (EOVE)] and related vinyl ethers with oxyethylene units in the pendant was achieved by 1-(isobutoxy)ethyl acetate (1)/Et1.5AlCl1.5 initiating system in the presence of an added base (ethyl acetate or THF) in toluene at 0°C. The polymers had a very narrow molecular weight distribution (M̄w/M̄n = 1.1-1.2) and the M̄n proportionally increased with the progress of the polymerization reaction. On the other hand, the polymerization by 1/EtAlCl2 initiating system in the presence of ethyl acetate, which produces living polymer of isobutyl vinyl ether, yielded the nonliving polymer. When an aqueous solution of the polymers thus obtained was heated, the phase separation phenomenon was clearly observed in each polymer at a definite critical temperature (Tps). For example, Tps was 70°C for poly(MOVE), and 20°C for poly(EOVE) (1 wt % aqueous solution, M̄n ∼ 2 × 104). The phase separation for each case was quite sensitive (ΔTps = 0.3-0.5°C) and reversible on heating and cooling. The Tps or ΔTps was clearly dependent not only on the structure of polymer side chains (oxyethylene chain length and ω-alkyl group), but also on the molecular weight (M̄n = 5 × 103-7 × 104) and its distribution. © 1992 John Wiley & Sons, Inc.
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  • 98
    ISSN: 0887-624X
    Keywords: Ziegler-Natta catalysts ; ansa-metallocene catalyst ; thermoplastic elastomeric poly(propylene) ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Racemic-anti-[ethylidene(1-η5-tetramethylcyclopentadienyl) (1-η5-indenyl)dimethyltitanium (6) has been synthesized and its molecular structure determined by x-ray diffraction methods. The two Ti=Me(1) and Ti=Me(2) units have bond distances differing by 0.08 Å and their proton NMR resonances are separated by over 1 ppm. Using this compound and methylaluminoxane (MAO) as the activator, at 25°C the 6/MAO catalyst produced polypropylene having crystalline domain with physical crosslinks. The polymers obtained at lower polymerization temperatures are rheologically liquids. The behaviors of this catalyst system resembles closely the previously reported rac-[anti-ethylidene(1-η5-tetramethylcyclopentadienyl) (1-η5-indenyl)dichlorotitanium (4)/MAO system. The structure of 6 determined here furnishes tangible support for the proposed two-state (isomeric)-switching propagation mechanism. Addition of MAO to 6 causes broadening of the Me(1) resonance in the 1H-NMR spectra, and 6 is decomposed by Ph3C+B(C6F5)-4. © 1992 John Wiley & Sons, Inc.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2645-2652 
    ISSN: 0887-624X
    Keywords: Soluble oligoamide ; internal acetylene ; crosslinking ; melt-processing ; high-temperature polymer ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Aromatic oligoamides of DP = 5 and 11 that have all meta-phenylene linkages were prepared by controlling the ratio of isophthaloyl chloride and diamines [m-phenylenediamine and bis(3-aminophenyl)acetylene], and then end-capped with aniline or 2-aminobiphenylene. Aromatic oligoamides having para-phenylene linkages were also prepared similarly using terephthaloyl chloride as a monomer. The oligoamides that have all m-phenylene linkages were soluble in organic solvents such as N-methyl-2-pyrrolidone and N,N-dimethylacetamide, though the oligoamides having p-phenylene linkages were much less soluble. The oligoamides having acetylene units in the backbone showed exotherm due to crosslinking. The onset of the exotherm appeared at 310-340°C for the oligoamides having all m-phenylene linkages, and 330-370°C for the oligoamides having p-phenylene linkages. They were melt-processed at 350 or 380°C for 1 h, giving tough and insoluble films from oligoamides having all m-phenylene linkages and brittle films from oligoamides having p-phenylene linkages. The films showed excellent thermal properties. For example, viscoelastic analyses showed little decrease of mechanical property up to 370°C, and Tg was not observed below the temperature. Thermogravimetric analyses also showed that thermal stability of the melt-processed films were excellent. © 1992 John Wiley & Sons, Inc.
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    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2657-2662 
    ISSN: 0887-624X
    Keywords: poly(propargylamine) ; poly(1,1-diethylpropargylamine) ; polyacetylene derivatives ; transition metal catalysts ; organoaluminum cocatalysts ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Some polyacetylene derivatives containing an amine functional group were prepared by the polymerization of propargylamine (PA) and 1,1-diethylpropargylamine (DEPA) with various transition metal catalysts. In the polymerization of PA, Mo-based catalysts were more effective than that of W-based catalysts, and organoaluminum compounds, especially EtAlCl2, were found to be very effective cocatalysts. In the polymerization of DEPA, Mo-and W-based catalyst systems showed a similar catalytic activity. The polymerization easily proceeded in polar solvents such as nitrobenzene and DMF as well as nonpolar aromatic solvents such as chlorobenzene, toluene, etc. The resulting poly(PA) and poly(DEPA) were insoluble in organic solvents regardless of polymerization catalysts but the polymers were found to be stable to air oxidation. Thermogravimetric analyses and thermal transitions of poly(PA) and poly(DEPA) were also studied. © 1992 John Wiley & Sons, Inc.
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