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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Analytica Chimica Acta 274 (1993), S. 53-58 
    ISSN: 0003-2670
    Keywords: Amperometry ; Carbon paste ; Enzymatic methods ; Enzyme electrodes ; Lactate ; Methylene green mediator
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Analytica Chimica Acta 265 (1992), S. 15-20 
    ISSN: 0003-2670
    Keywords: Amperometry ; Enzymatic methods ; Enzyme electrode ; Pyruvate
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 1481-1490 
    ISSN: 0887-624X
    Keywords: ibuprofen ; ketoprofen ; naproxen ; copolymer reactivity ; thermal stability ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Three nonsteroidal antiinflammatory drugs, 2-(4-isobutylphenyl)-propionic acid (ibuprofen), 2-(3-benzoylphenyl)-propionic acid (ketoprofen), and 2-(6-methoxy-2-naphthyl)-propionic acid (naproxen), were covalently linked with 2-hydroxyethyl methacrylate (HEMA). The drug-linked HEMA (M1) (ibuprofen-linked HEMA abbreviated as HI; ketoprofen-linked HEMA as HK, and naproxen-linked HEMA as HN), were respectively copolymerized with methacrylic acid (M2), MA, to obtain macromolecular prodrugs. The compositions of the copolymers were determined by means of a 1H-NMR spectroscopy and monomer reactivity ratios were estimated using the Kelen-Tüdös linear differential equation. The reactivity ratios are: r1 = 0.101 ± 0.012, r2 = 1.071 ± 0.065 for HI-MA; r1 = 0.344 ± 0.066, r2 = 0.966 ± 0.032 for HN-MA, and r1 = 0.650 ± 0.182, r2 = 1.032 ± 0.106 for HK-MA, respectively. The monomer reactivity toward to MA radical estimated from 1/r2 values is almost same for all three monomers (1/r2 ∼ 1). The glass transition temperatures of three drug-linked homopolymers go hand in hand with the steric hindrance of three drugs, i.e., ketoprofen 〉 naproxen ≫ ibuprofen calculated the minimum energy by computer molecular modeling. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 1481-1490, 1998
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 6 (1993), S. 601-608 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Exhaustive methylation of 1-phenylurazole (1), using ethereal diazomethane as the methylating agent, results in the formation of three products: 1-phenyl-3,5-dimethoxy-1,2,4-triazole (2), 1-phenyl-3-methoxy-4-methyl-Δ2-1,2,4-triazolinev5-one (3) and 1-phenyl-2,4-dimethylurazole (4). Based on the amounts of 2-4 isolated, the overall yields in these reactions are typically 〉90%. When 1 and diazomethane were allowed to react in a fashion that resulted in the formation of monomethylated analogues of 1, 1-phenyl-3-methoxy-Δ2-1,2,4-triazoline-5-one (5) and 1-phenylv2-methylurazole (6) were formed. In separate experiments, the monomethylated species 5 and 6 were allowed to react with diazomethane in efforts to develop a sequence of reactions that reasonably accounts for the formation of 2-4. Whereas N- and O-methylated products were obtained when 5 was treated with ethereal diazomethane, the reaction of 6 and diazomethane produced only the N-alkylated product 1-phenyl-2,4-dimethylurazole (in quantitative yield). The outcomes of these experiments are consistent with a sequence of reactions in which the treatment of 1 with diazomethane results, initially, in the formation of the monomethylated species 5 and 6. In the presence of sufficient diazomethane, 5 and 6 then undergo further mothylation, forming the dimethylated species 2-4.
    Type of Medium: Electronic Resource
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  • 5
    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: Using VO2+ as a spin probe, a new method to obtain microenvironmental information on supports was developed which can be used in the choice of supports for coordination catalysts. Utilizing the above method, NaY was chosen as second support component. A complex support catalyst VOCl3/MgCl2/NaY/Al2Et3Cl3 was prepared and used in ethylene-propylene copolymerization. Higher polymerization activity was obtained with this catalytic system. Alternating the ratio of two kinds of supports, the composition and sequence structure of copolymers could be controlled, which showed that NaY participated in the active species, affected the insertion of monomer, and changed the composition and sequence structure of copolymers. © 1994 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 54 (1994), S. 1439-1447 
    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: Owing to the low Tg of polystyrene, the mechanical properties of polystyrene-block-poly-butadiene-block-polystyrene (SBS) thermoplastic elastomers drop steeply above 60°C. To overcome this behavior, many research groups have considered the replacement of styrene (S) by α-methylstyrene (MS). We also attempted the synthesis of copolymers with a central polybutadiene (poly B) block and rigid blocks consisting of polystyrene (poly S) and poly(α-methylstyrene) (poly MS) blocks. Starting from a dilithium initiator, difunctional poly B's with low 1,2 content (10%) were prepared and toluene was added. After addition of a small amount of styrene, MS was added in the presence of a 15% (in vol) of THF at T ≤ -40°C. The copolymers did not have the expected structure and poor mechanical properties resulted, which were, however, still measurable at 120°C. These results probably resulted from secondary reactions involving the MS carbanions. To identify these reactions and to control the polymer structure, the synthesis of multiblock copolymers was carried out with a monofunctional polybutadienyllithium to which were added successively S and MS (in a mixture of hexane and benzene as solvent). MS was added at low temperature in the presence of small amounts of THF or at room temperature after addition of TMEDA. These attempts were unsuccessful, the copolymer being always multimodal as a result of unwanted coupling reactions involving terminal double bonds. The synthesis of elastomers using a coupling reaction of poly MS-poly S-poly B was also considered but the yield in poly B was low since termination reactions involving the polar additive occurred. © 1994 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Biomedical Chromatography 7 (1993), S. 75-77 
    ISSN: 0269-3879
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Small hydrophilic peptides differing in only one glycine amino acid group have been successfully separated by free-solution capillary electrophoresis (FSCE) using phosphate buffer at acid pH. The effects of column temperature and operating current on the migration times of these small peptides have been investigated. The results from FSCE have been compared with those from reversed phase high performance liquid chromatography.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 28 (1990), S. 317-321 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 5 (1992), S. 1-6 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: With the aid of a thermochemical cycle consisting of acidity and new redox data in dimethyl sulfoxide (DMSO) solution, homolytic N—H bond dissociation energies (ΔBDE values) relative to acetamide (1) (where the N—H BDE for 1 is defined as 0 kcal mol-1) were determined for diacetamide (0), biuret (+ 1), 3,3-dimethylglutarimide (-3), diacetylhydrazine (-16), 4,4-dimethylpyrazolidine-3,5-dione (- 25), 4-dimethylurazole (-29), hydrazoic acid (-15), succinimide (-15) and 1,2-dimethylurazole (-13) (all values in kcal mol-1). These ΔBDE data provide (a) additional evidence for the minimal N—H bond weakening effects of adjacent carbonyl groups, (b) evidence for relatively large N—H bond weakening effects of adjacent  - NHC(O)R moieties in both cyclic and acyclic hydrazides and (c) evidence suggesting that urazolyl radicals are more stable than pyrazolidinedionyl radicals, relative to their hydrogenated precursors. Inserting the appropriate acidity and redox data for hydrazoic acid into a thermochemical cycle that includes a constant that permits comparison of DMSO solution BDEs with gas-phase BDEs yields estimates of 93 kcal mol-1 for the homolytic strengths of the N—H bonds present in succinimide and H—N3. The DMSO N—H BDE determined in this way for H - N3 is in remarkable agreement with a determination of its gas-phase value, whereas the DMSO N—H BDE for succinimide places it intermediate between three published estimates of its gas-phase value.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electroanalysis 7 (1995), S. 92-94 
    ISSN: 1040-0397
    Keywords: Glucose oxidase ; Glucose ; Carbon paste ; Methylene-green mediator ; Enzyme electrode ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An amperometric glucose bioelectrode based on the incorporation of methylene green (MG) within a glucose oxidase (GOD)-containing carbon paste is described. The electrode generates an anodic current in the range of 0.0-0.6 V (vs. SCE). The optimum pH is 8.5. The apparent Michaelis constant for the Cali bration plot is 49.3 mM (at 0.5% MG and 5.0% GOD loadings). The electrode sensitivity is 18.1 μA/mM cm2. The electrode is insensitive to paracetamol and ethanol. At 0.068 V the response to ascorbic acid (40 μM) accounts for 2.4% of that of the normal physiological glucose level in blood. The performance was optimized by systematically altering the electrode composition and electrode potential. The electrode was used to measure glucose in a serum sample and gave an acceptable correlation with the reference method Eksan-G results. Good stability was observed for storage in the dry state in the refrigerator.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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