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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    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.
    Additional Material: 7 Ill.
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  • 2
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Poly[(4-N-ethylene-N-ethylamino)-α-cyanocinnamate] was prepared by solution esterification of (4-N-ethyl-N-(2-hydroxyethyl) amino)-α-Cyanocinnamic acid and by melt transesterification of ethyl (4-N-ethyl-N-(2-hydroxyethyl) amino)-α-cyanocinnamate. The melt transesterification generally yielded polymer with a number-average molecular weight of about 10,200 by gel permeation chromatography (GPC) versus polystyrene standards. The polymer was found to be amorphous with a glass transition temperature of about 103°C by differential scanning calorimetry (DSC). The solution esterification generally gave a polymer with a number-average molecular weight of about 2200 by GPC versus polystyrene standards. This polymer was found to have a glass transition temperature varying between 60 and 90°C by DSC. The infrared (IR) spectrum of the polymer made from both methods were analyzed in detail. The 1H- and 13C-NMR spectra of the meltsynthesized ethyl cinnamate derivative polymer are consistent with the reported structure.
    Additional Material: 6 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 3099-3108 
    ISSN: 0887-624X
    Keywords: poly(arylene ether)s ; poly(N-arylene benzimidazole)s ; high-temperature polymers ; high-performance polymers ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Poly(arylene ether)s containing N-arylenebenzimidazole groups were prepared by the aromatic nucleophilic displacement reaction of two new bis(hydroxyphenyl-N-arylenebenzimidazole)s with activated aromatic difluorides in sulfolane at 200°C in the presence of anhydrous potassium carbonate. The bis(hydroxyphenyl-N-arylenebenzimidazole)s were prepared from bis(o-aminoanilino) arylenes and phenyl-4-hydroxybenzoate. The polymers were soluble in N-methyl-2-pyrrolidinone and m-cresol and exhibited inherent viscosities from 0.37-0.86 dL/g and glass transition temperatures from 219-289°C. Thermogravimetric analyses showed 5% weight losses from 463-506°C in air and 467-522°C in nitrogen. Unoriented thin films exhibited tensile strengths, moduli, and break elongations at 23°C of 10.2-12.5 ksi, 318-365 ksi, and 4-7%, respectively, and at 177°C of 5.1-6.9 ksi, 256-296 ksi, and 1-5%, respectively. A 50 : 50 random copolymer prepared from 1,3-bis(4-fluorobenzoyl) benzene, 1,1'-(4,4'-biphenylene)-bis[2-(4-hydroxyphenyl)benzimidazole], and 5,5'-bis[2-(4-hydroxyphenyl)benzimidazole] exhibited higher moisture absorption and lower tensile properties than those predicted by a rule of mixtures relationship. The chemical, physical, and mechanical properties of these polymers are discussed. © 1993 John Wiley & Sons, Inc.
    Additional Material: 6 Tab.
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 2899-2906 
    ISSN: 0887-624X
    Keywords: high-glass transition temperature nonlinear optical polymer ; syndioregic ; mainchain chromophore ; accordion polymers ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new main-chain syndioregic (head-to-head) NLO polymer was synthesized. The glass transition temperature of high molecular weight polymer was found to be 208°C, and the polymer has minimal weight loss at temperatures to at least 250°C owing to the incorporation of hydrogen bonding moieties and rigid bridging groups. The polymer was further characterized using nuclear magnetic resonance (NMR) and Fourier transform infrared spectroscopy (FTIR). The study of the nonlinear optical properties of this polymer are in progress. © 1993 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 12 (1989), S. 116-119 
    ISSN: 0935-6304
    Keywords: HPLC ; Estradiol-17 β ; Cortisol ; Subambient temperature ; Thoracic rabbit aorta ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 19 (1996), S. 151-154 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Atomic emission spectroscopy ; Enantiomeric separation ; Cyclodextrins ; Chemical warfare agents ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of the organophosphorus nerve agents sarin, tabun, and cyclohexyl methylphosphonofluoridate (GF) produces a mixture of two stereoisomers except for soman where four stereoisomers are produced. Significant differences exist in the reported toxicity and AChE inhibition rates of the various stereoisomers. This makes the ability to distinguish between the different stereoisomers desirable. Five different derivatized cyclodextrin stationary phases developed for gas chromatography were tested for their ability to resolve the nerve agent stereoisomers using a gas chromatograph interfaced to an atomic emission detector. Of the five columns that we examined, only the 2,6-di-O-pentyl-3-O-trifluoroacetyl or 2,6-di-O-pentyl-3-O-butyryl γ-cyclodextrins were able to successfully resolve all four soman stereoisomers. The elution order for each column was determined using solutions of isolated soman stereoisomers. Enantiomers of sarin, tabun, and GF were resolved with varying degrees of success on the different cyclodextrin stationary phases. Only the butyryl γ-cyclodextrin was able to separate the enantiomers of all four of the nerve agents examined in this study. The capacity (k) and selectivity (α) factors were determined for each of the chemical warfare agents successfully separated. The TNO Prins Maurits Laboratory in the Netherlands has previously developed several different chromatographic methods to resolve the stereoisomers of soman, sarin, and tabun. The advantage of the method described here is that commercially available cyclodextrin gas chromatography columns were used to resolve the stereoisomers, thereby facilitating rapid and routine analysis of organophosphorus nerve agents.
    Additional Material: 3 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 8 (1994), S. 82-88 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Thermospray mass spectrometry was used to analyze fumonisin B1 (FB1) from two corn samples that were known to contain fumonisins, and from a FB1-spiked meat sample. The mass spectrometer was operated in the negative-ion discharge-on, filament-off, mode with the fragmentor set at 200 V. Selected-ion monitoring (SIM) was used for quantitative analysis. The mobile phase was CH3CN (containing 1% CICH2CN, v/v)+0.1M ammonium acetate, pH 3.65 (65:35, v/v). Quantitative analysis was done by integrating the peak areas traced by ion currents of 5 selected ions in SIM, and by the method of standard additions. Responses to the selected ions were linear within the range of 2-200 ng. Fumonisins were easily identified in the corn and muscle tissue matrices without any apparent matrix interferences and were detectable down to 0.1 μ/mL (2 ng injected).
    Additional Material: 8 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 20 (1991), S. 717-723 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The major metabolites and breakdown products of some toxic organophosphonates are their respective alky-methylphosphonic acids. These acids ionize at physiological pH and are not amenable to gas chromatographic analysis in their underivatized forms. Their detection in biological samples has been difficult because of their presence at only trace levels. Existing analytical methods were developed mainly for measuring these phosphonic acids in environmental samples and at higher concentrations. In this study, we devised a gas chromatographic/mass spectrometric method to provide confirmation and quantification of the organophosphonic acids of soman (GD), sarin (GB) and GF in blood and urine. This report describes the various derivatization conditions that we have studied and demonstrates the characteristic mass spectra by different ionization techniques.
    Additional Material: 5 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 3 (1992), S. 373-381 
    ISSN: 1042-7147
    Keywords: Polyimides ; Diels-Alder reaction ; Thermally stable polymers ; Soluble polyimides ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Four new bisdienes were prepared from 2-bromomethyl-1,3-butadiene and N,N-diethyl benzidine; bis[4-(N-ethyl) aminophenyl]-p-diisopropylbenzene, 1,4-diamino-2,3,5,6-tetramethylbenzene and α,α′ bis(4-amino-3,5-dimethyl phenyl)-p-diisopropyl benzene. Polyimides were synthesized by the Diels-Alder reaction of these bisdienes and bis(4-maleimidylphenyl)methane and bis(3-maleimidylphenyl) sulfone. The polymers were soluble in m-cresol, dimethyl sulfoxide and chlorinated hydrocarbon solvents. Moderate thermal stability was observed by thermogravimetric analysis in air and nitrogen.
    Additional Material: 2 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 47 (1993), S. 2257-2267 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Silicone-release coatings are used by the pressure-sensitive adhesive industry for labeling applications. Typical release coatings are prepared by the platinum-catalyzed addition reaction of a silicone hydride fluid with a silicone vinyl polymer. Methodology has been developed to determine the network structure of cured release coatings, which involves degradation of the network with trifluoromethane sulfonic acid in excess hexamethyldisiloxane. Gas chromatography-mass spectrometry (GC-MS) and gas chromatography (GC) were employed to identify and quantify residual functionality and cross-links. Residual hydride functionality was also determined by attenuated total reflectance-Fourier transform infrared spectroscopy (ATRFTIR). The observation of network structure by solid-state 29Si-NMR using cross polarization (CP) and magic angle spinning (MAS) is also discussed. The networks underwent a postcure as evidenced by a decrease in residual hydride functionality and an increase in silane content and/or cross-links. © 1993 John Wiley & Sons, Inc.
    Additional Material: 11 Ill.
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