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  • 1985-1989  (4,985)
  • 1988  (4,985)
  • Polymer and Materials Science  (3,199)
  • Life and Medical Sciences  (1,786)
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Years
  • 1985-1989  (4,985)
Year
  • 101
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 3151-3158 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The solid-state 1,3,5-trithiane polymerization initiated by UV-irradiation was studied at various irradiation times and various polymerization temperatures. The conversion of monomer to polymer reaches limiting values (at longest) in about 30 min of reaction. The apparent activation energy of this process is somewhat higher than in the chemically initiated polymerization. Generated by UV, active centers, which initiate the polymerization, are stable. On the basis of X-ray diffraction studies it was found that the prepared polythiomethylene has a hexagonal structure and high degree of crystallinity. In the polymer investigated, a new additional crystal phase is formed, which is not stable.
    Additional Material: 8 Ill.
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  • 102
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Monofunctional compounds (benzoic acid, heptyl alcohol, and 2-butoxy-ethanol) were used to investigate the kinetics of the esterification and the alcoholysis reactions. Carboxylic acids (benzoic acid) are the only catalysts present in the reaction medium. The factors which influence the kinetics of the esterification reaction were studied: the nature of the carboxylic acid (substituents on the benzene ring), the nature of the alcohol, the composition of the reaction medium (alcohol alone or with another solvent, ester, or water). The results point out for an acyl type (AAC2) mechanism. The alcoholysis reaction needs the presence of carboxylic acid as a catalyst to occur significantly. A similar mechanism is proposed for both reactions: nucleophilic attack by the oxygen atom of the alcohol at the ion pair formed by protonation of the acid (esterification reaction) or by protonation of the ester (alcoholysis).
    Additional Material: 6 Ill.
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  • 103
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactions of model molecules were considered to study the kinetics and the mechanism of the esterification and the alcoholysis reactions catalyzed by various metal compounds (Li, Na, K, Zn, Co, Mn, Ti). Ti was found to be the most active catalyst for both reactions and to be acting via a different mechanism (concerted). The possible structure of the active titanium intermediate was investigated by means of 1H- and 13C-NMR spectroscopy, FT-IR spectroscopy, and electroconductivity.
    Additional Material: 10 Ill.
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  • 104
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 2225-2234 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new series of 16 aramids and 16 polyarylates having perfluoro-substituents on the benzene ring was prepared by a low temperature solution or an interfacial polycondensation. The effects of fluorine substituents on the structure and properties of polymers were examined. Fluorinated aramids exhibited higher crystallinity, while fluorinated polyarylates show lower crystallinity. The melting point (Tm) of aramids decreased with fluorine substitution, whereas Tm of polyarylates from fluorinated aromatic diols was higher than that of those from unfluorinated ones. The temperature of 10% weight loss and the residue at 900°C decreased with fluorine substitution except for the aramids from fluorinated diamines. Solubility and contact angle also increased with fluorine substitution. Some polyarylates were found to exhibit an optical anisotropy.
    Additional Material: 4 Ill.
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  • 105
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Lithiated isopropylidene-telechelic polyisobutylenes (i.e., PIBs capped with end groups) are most interesting novel intermediates for further transformations, e.g., functionalization, polymerization. This report concerns model lithiation experiments of 2,4,4-trimethyl-1-pentene (TM1P) that guided us toward the subsequent quantitative lithiation of isopropylidene-telechelic PIBs. Thus, lithiation of TM1P with, n-, s-, and t-butyllithium, in the presence of various complexing agents (i.e., TMEDA, t-BuOK, 1,2-DPE, CH3OCH2CH2OCH3, THF, and 12-crown-4) followed by silylation with Me3SiCl (for the purpose of quantitation) gave three products: 2(trimethylsilylmethyl)-4,4-dimethyl-1-pentene (TM1P-Si), 2(trimethylsilylmethyl)-4,4-dimethyl-2-pentene (TM2P-Si2). The relative product composition strongly depends on the BuLi/complexing agent ratio and temperature. Among the different butyllithiums and complexing agents the best overall results were obtained with the s-BuLi/TMEDA combination. Complete lithiation of TM1P with minimum dilithiation was obtained using the molar ratio [s-BuLi]: [TMEDA]: [TM1P] = 2 : 2 : 1. The apparent activation energy of lithiation by s-BuLi/TMEDA was found to be 6.7 ± 0.8 kcal/mol. Guided by TM1P model experiments, quantitative monolithiation of isopropylidene-capped polyisobutylene (including ca. 4% chain and isomerization) was achieved using the molar ratio [s-BuLi] : [TMEDA] : [C—C] = 5 : 4 : 1.
    Additional Material: 10 Ill.
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  • 106
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    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 3323-3336 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The following reactions of pyrylium salts with amines are described: (1)bis(pyrylium salts) with amines; (2) diamines with pyrylium salts; and (3) bis(pyrylium salts) with diamines. Both (1) and (2) give bis(pyridinium salts) in high yields, and (3) gives the corresponding polymers which are isolated and characterized. This procedure was applied to cationic bis(pyrylium salts) to give cationic dimers and polymers, and further to zwitterionic bis(pyrylium salts) to yield the corresponding zwitterionic dimers and polymers.
    Additional Material: 2 Tab.
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  • 107
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    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 3391-3395 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 108
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    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 3403-3407 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 5 Ill.
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  • 109
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Time studies of evaporation from liquid-saturated poly[(Sty)98-co-(DVB)2] particles enmeshed in poly(tetrafluoroethylene) microfibers show that it is possible to distinguish kinetically between volatile sorbed molecules not absorbed to the polymer chain and those that are adsorbed to it. Elimination of the nonadsorbed molecules occurs first, and it follows zero-order kinetics. The subsequent elimination of the residual volatiles, namely the adsorbed molecules, follows first-order kinetics, with a rate constant that remains constant only until the enmeshed microparticles undergo transition from the gel to the glass state. Thereafter, is observed a sequence of up to six independent rate constants in a series of intervals, the durations of which increase exponentially. This is interpreted to mean that after evaporation to the glass transition composition, the total weight of residual adsorbed molecules is given by a linear combination of exponential decay functions for up to six populations of adsorption sites, the rate constants for which reflect the force of association between the sites and the retained molecules.
    Additional Material: 7 Ill.
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  • 110
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    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 3409-3413 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 5 Ill.
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  • 111
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    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 2295-2303 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 9 Ill.
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  • 112
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    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. xi 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 113
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    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 2355-2357 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Perfume alcohols such as 2-phenyl ethanol and eugenol were supported to sulfochlorinated poly(styrene-co-divinyl benzene) beads in the presence of base such as triethyl amine, pyridine, and sodium bicarbonate and their hydrolysis at different temperature was studied.
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  • 114
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    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 2307-2343 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of emulsion copolymerizing systems during intervals II and III (i.e., after completion of latex particle formation) has been studied through the pseudo-homopolymerization approach. The Smith-Ewart equations for copolymers are reduced to the corresponding equations for homopolymers by introducing suitable pseudo-homopolymerization parameters. Analogies and differences between our results and those of previously reported treatment are critically discussed. On the grounds of the probabilistic approach developed in Part I of this series, a detailed description of the copolymer chain structure is derived for systems containing no more than one growing radical per particle. In particular explicit algebraic relationships are reported for both the two-dimensional molecular weight distribution and the unidimensional marginal distribution functions of molecular weight and chemical composition. A complete description of the chain microstructure is also reported. Equations are derived specifying the time evolution of the monomer sequence distribution and polymer end groups.
    Additional Material: 5 Ill.
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  • 115
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    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 2369-2380 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bis(neomenthyl cyclopentadienyl)zirconium dichloride/methyl aluminoxane (η5-(NMCp)2ZrCl2/MAO) catalyst has been investigated for ethylene polymerization. About 51% of the Zr forms active sites more or less instantaneously according to quenching with tritiated methanol. There is an initial drop of rate of polymerization, Rp, of about 30% which remains constant thereafter. The catalytic activity increases monotonically with temperature; it is proportional to [MAO]1.75 at a constant [Zr] = 1.5 μM and proportional to [Zr]-1.2 at a constant [MAO] = 64.5 mM. At very large [MAO]/[Zr], the catalyst has extremely high activity; κp = 5 × 103 (Ms)-1 at 50°C. There is also facile chain transfer to aluminum, κtrA = 0.14 s-1 at 50°C. Both κp and κtrA are about 30 times greater than the corresponding rate constants for MgCl2 supported TiCl3 catalysts. The TiCl3/MgCl2 and (NMCp)2/MAO catalysts have nearly the same activation energy for propagation (ca. 7 kcal/mol-1). The higher activity of the latter is due to its larger preexponential factor in κp. The dependence of catalytic activity on the [MAO]/[Zr] ratio may be explained by rapid association-dissociation equilibria of MAO involving acid-base and/or electron deficient bridge complexation.
    Additional Material: 6 Ill.
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  • 116
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    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 2435-2447 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of fumaronitrile with triethylamine in bulk at 295-353 K gives in high yields dark-colored polymers. The polymerization occurs at one of the two nitrile groups and not at the (C—C) double bond. The kinetics of the reaction were investigated and the polymers characterized analytically.
    Additional Material: 5 Ill.
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  • 117
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 26 (1988), S. 449-449 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 118
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 26 (1988), S. 465-468 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 119
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 26 (1988), S. 491-492 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 120
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 26 (1988), S. 511-516 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
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  • 121
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    Journal of Polymer Science: Polymer Letters Edition 26 (1988), S. 54-55 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 122
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 26 (1988), S. 539-539 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 123
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    Journal of Polymer Science: Polymer Letters Edition 26 (1988), S. 421-427 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
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  • 124
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    Journal of Polymer Science: Polymer Letters Edition 26 (1988), S. 416-416 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 125
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 26 (1988), S. 135-138 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
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  • 126
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    Journal of Polymer Science: Polymer Letters Edition 26 (1988), S. 153-157 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 4 Ill.
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  • 127
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    Journal of Polymer Science: Polymer Letters Edition 26 (1988), S. 166-167 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 128
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    Journal of Polymer Science: Polymer Letters Edition 26 (1988), S. 247-247 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 129
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    Journal of Polymer Science: Polymer Letters Edition 26 (1988), S. 275-275 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 130
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    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 26 (1988), S. 277-279 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 131
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    Journal of Polymer Science: Polymer Letters Edition 26 (1988), S. 305-311 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 132
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    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 9 (1988), S. 1-8 
    ISSN: 0886-1544
    Keywords: substrate attached materials (SAM) ; chemotaxis ; leukocytes ; adherence ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: We describe a technique to visualize substrate-attached materials (SAM) of polymorphonuclear leukocytes (PMN) using the fluorescent lipid analog 1, 1′-dioctadecyl-3,3,3′,3′,-tetramethylindocarbocyanine-perchlorate (DiC18Icc). DiC18Icc was incorporated into the membranes of living cells or SAMs. Since cell preparation does not require fixation, SAMs can be rapidly visualized by fluorescence microscopy. SAMs are generated by subjecting attached cells to a shearing force by rinsing with phosphate-buffered saline (PBS). The SAM-labeling protocol identified a membrane compartment as shown by detergent extraction. The SAMs of PMN leukocytes observed with this technique display complex patterns of interconnecting filaments, foci with radiating filaments, and smooth membranous areas with interconnecting filaments. The sensitivity and nondestructive nature of the DiC18Icc-labeling procedure have allowed us to observe filopodia of motile cells. The results are consistent with the hypothesis that locomotion involves a series of attachment and detachment steps. After 60 minutes of locomotion, these trailing filopodia have been measured at lengths up to 100 μm. The amount of membrane associated with these filopodia accounts for roughly 10% of the total membrane are of resting cells. These data set limits for models of membrane flow during chemotaxis.
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  • 133
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    Cell Motility and the Cytoskeleton 9 (1988), S. 60-72 
    ISSN: 0886-1544
    Keywords: villin ; actin ; rat brush border ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The biochemical properties of villin purified from the brush borders of chicken and rat small intestines were compared, with emphasis on their physical properties and their Ca++-dependent interaction with actin. Like chicken villin, rat villin exists as two isoforms present in equimolar concentrations; the rat isoforms are slightly more acidic than those of chicken villin (6.08 and 6.11 versus 6.26 and 6.34). Rabbit antisera raised against either villin crossreacted with the other one. Like the avian protein, rat villin bundled F-actin at calcium concentrations below 0.1 μM. Above ∼1 μM calcium, it accelerated the rate of actin assembly and restricted filament lengths of F-actin formed either during coassembly with villin or by addition of villin to preformed filaments. The threshold calcium concentration required for effective severing of preformed filaments was approximately tenfold higher than that required for restricting lengths during coassembly. The extent of filament shortening was proportional to the amount of villin present. At a fixed villin concentration, filament length decreased with increasing [Ca++] over a broad range from 10-7-10-4 M. In general, the mean filament lengths and the dispersion about the mean value were lower in samples where filaments were coassembled with villin than when villin was added to preformed filaments.
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  • 134
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    Cell Motility and the Cytoskeleton 9 (1988), S. 48-59 
    ISSN: 0886-1544
    Keywords: axon ; growth cone ; retraction ; taxol ; slow transport ; axonal transport ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Axons in tissue culture retract and shorten if their tips are detached from the substrate. The shortening reaction of the axon involves contractile forces that also arise during normal axonal motility, elongation, and retraction. We studied shortening in axonal segments isolated from their parent axons by transecting the axon between the growth cone and the most distal point of adhesion to the substrate. Within 15-20 minutes after transection, an isolated axonal segment shortened and pulled its tail end toward the growth cone. During the shortening process, long sinusoidal bends arose along the axon. The identical shortening reaction occurs without transection, when the axon tip is detached from the substrate. Pharmacological studies with inhibitors of glycolysis indicate that the shortening mechanisms utilize metabolic energy, presumably ATP. The rate of sinusoidal shortening is similar to both the rate of polymer translocation in the axon by slow axonal transport and the rate of normal axonal elongation. Taxol inhibits the shortening reaction with a similar dose dependence to its inhibition of axonal growth. Together, all these observations suggest that the same basic intracellular motility mechanisms are involved in normal axonal growth, in slow axonal transport, and in the shortening reaction: the intracellular dynamic system that utilizes ATP to generate longitudinal movements of polymers within the axon may be the same mechanism underlying both the retraction and the elongation of the axon.
    Additional Material: 9 Ill.
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  • 135
    ISSN: 0886-1544
    Keywords: actinogelin ; α-actinin ; reconstituted actin-gel ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: We studied the properties of actinogelin, a Ca2+-regulated actin cross-linking protein isolated from Ehrlich tumor cells or rat liver. Chicken gizzard α-actinin was used as a Ca2+-insensitive control. Actinogelin, which has very high gelation activity under low Ca2+ conditions, was found using electron microscopic or fluorescence studies to induce formation of a characteristic structure in which actin filaments and bundles radiate to (or converge from) all directions from spot-like core structures. A similar structure was induced with actinogelin, even in the presence of 0 7 saturation of tropomyosin. No such structure was detected with actinogelin under high Ca2+ conditions, and only a few were found with gizzard α-actinin. Because reconstituted structures are similar to those observed intracellularly, actinogelin may be important in the formation of similar microfilament organization in the cells. It seems also important that these structures are reconstituted with only two purified protein components, i.e., actinogelin and actin.Immunocompetition studies showed that actinogelin and gizzard α-actinin partially shared antigenicity, and their molecular shape and peptide maps were similar. Their amino acid compositions [Kuo et al., 1982], subunit and domain structures, and binding sites on actin [Mimura and Asano, 1987] are also very similar. Therefore, it is concluded that actinogelin belongs to α-actinin superfamily proteins. Furthermore, the presence of functionally different subfamilies concerned with Ca2+ sensitivy, gelation-efficiency, and others is discussed. Actinogelin, which induces networks of actin filaments, may be classified as high gelation type.
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  • 136
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    Cell Motility and the Cytoskeleton 10 (1988), S. 349-362 
    ISSN: 0886-1544
    Keywords: immunofluorescence ; cytoplasmic actins ; muscle actins ; epitope ; isoactins ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Two IgG1, κ monoclonal antibodies (Mab) against actin have been obtained from a fusion in which chicken gizzard actin was used as the immunogen. One Mab, designated B4, shows a preferential reactivity toward enteric smooth muscle actin but also cross-reacts with skeletal, cardiac, and aorta actins on the basis of immunoblots, ELISA assays, and indirect immunofluorescence. However, this antibody does not react with either cytoplasmic actin in any of these assay systems. A second Mab, designated C4, reacts with all six known vertebrate isoactins as well as Dictyostelium discoideum and Physarum polycephalum actins. Thus B4 Mab appears to react with an epitope that is at least partially shared among the muscle actins but not found in cytoplasmic actins, while C4 Mab binds to an antigenic determinant that has been highly conserved among the actins. The binding sites of both Mabs on skeletal actin overlap that of pancreatic DNase I. Both antibodies bind a SV8 proteolytic product comprising the amino-terminal two-thirds of the actin molecule, and their epitopes appear to overlap since C4 can compete for the binding of B4 to skeletal actin. Neither antibody is able to prevent actin polymerization.
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    Cell Motility and the Cytoskeleton 9 (1988) 
    ISSN: 0886-1544
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
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  • 138
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    Cell Motility and the Cytoskeleton 9 (1988), S. 9-16 
    ISSN: 0886-1544
    Keywords: adaptation ; cAMP ; cell motility ; chemotaxis ; Dictyostelium discoideum ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: When developing amebae of Dictyostelium discoideum are treated with constant concentrations of cAMP above 10-8 M, the average rate of motility is depressed, with maximum inhibition at roughly 10-6 M. It is demonstrated that shifting the concentration of cAMP from 0 M to concentrations ranging from 10-8 to 10-6 M in a perfusion chamber results in the immediate inhibition of motility. After shifting from 0 M to 10-8 or 10-7 M, the rate of cell motility remains low, then rebounds to a higher level, exhibiting a standard adaptation response. No adaptation is exhibited after a shift from 0 M to 10-6 M, a concentration resulting in maximum inhibition. It is demonstrated that the level of inhibition and the extent of the adaptation period are dependent upon the concentration of cAMP after the shift, and that submaximal inhibition is additive. The characteristics of adaptation in this motility response are very similar to the characteristics of adaptation for the relay system and phosphorylation of the putative cAMP receptor.
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  • 139
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    Cell Motility and the Cytoskeleton 9 (1988), S. 17-29 
    ISSN: 0886-1544
    Keywords: sequestered actin bundles ; polygonal arrays ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Using mainly fluorescence microscopy after rhodamine-phalloidin staining, the F-actin distribution in the mouse lens epithelium was studied with regard to the effects of age, genetic strain, and mechanical injury.These studies have revealed that aside from its association with the plasma membrane the structural organization of F-actin in the mouse lens epithelium in situ is characterized by two major configurations: (1) a filamentous arrangement in such patterns as stress fibers, polygonal arrays (PAs), and meshworks, and (2) a highly concentrated structure called a sequestered actin bundle (SAB).The aging study indicated that the SAB is a consistent character in C57BL/6 mice from the age of 5 wk on, but not in CF1 mice. The size and shape of the SAB change gradually with age as inferred from two-dimensional measurements. The genetic study on the SAB character using hybrids and congenic strains showed that it is inherited as a Mendelian dominant, probably multigenic mode. Finally, the injury study revealed a structural modification in cells around the wound, including flattening of cells at the edge and extension of processes into the wound space. In the rest of the epithelium, injury amplified membrane infolding and fluorescence of polygonal arrays but diminished the size and fluorescence intensity of SABs. These changes are thought to be correlated with wound repair involving cell division and migration.These studies illustrate the variability in F-actin expression in situ in lens epithelial cells that can be induced by intrinsic and extrinsic factors.
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  • 140
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    Cell Motility and the Cytoskeleton 10 (1988), S. 217-228 
    ISSN: 0886-1544
    Keywords: immunogold ; microtubules ; optical sectioning ; video microscopy ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The distribution of F-actin cables in dividing endosperm cells of a higher plant, Haemanthus, was visualized with the immunogold-silver-enhanced method and compared with the arrangement of immunogold-stained microtubules in the same cells. The three-dimensional distribution of F-actin cables and microtubules during mitosis and cell plate formation was analyzed using ultrathin optical sectioning of whole mounts in polarized light video microscopy. F-actin cables form a loose irregular network in the interphase cytoplasm. Much of this network remains outside of the spindle during mitosis. A few F-actin cables were detected within the spindle. Their pronounced rearrangement during mitosis appears to be related to the presence and growth of microtubule arrays. During prometaphase, actin cables located on the spindle surface and those present within the spindle tend to arrange parallel to the long axis of the spindle. Cables outside the spindle do not reorient, except those at the polar region, where they appear to be compressed by the elongating spindle. Beginning with mid-anaphase, shorter actin cables oriented in various directions accumulate at the equator. Some of them are incorporated into the phragmoplast and cell plate and are gradually fragmented as the cell plate is formed and ages. Actin cables adjacent to microtubule arrays often show a regular punctate staining pattern. Such a pattern is seldom observed in the peripheral cytoplasm, which contains few microtubules. The rearrangement of F-actin cables mimicks the behavior of spindle inclusions, such as starch grains, mitochondria, etc., implying that F-actin is redistributed passively by microtubule growth or microtubule-related transport. Thus F-actin or actomyosin-based motility does not appear to be directly involved in mitosis and cytokinesis in higher plants.
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  • 141
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    Cell Motility and the Cytoskeleton 9 (1988), S. 73-84 
    ISSN: 0886-1544
    Keywords: cilia ; metachronal waves ; electron microscopy ; calcium ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Structural and behavioral features of intact and permeabilized Paramecium tetraurelia have been defined as a basis for study of Ca2+ control of ciliary reversal. Motion analysis of living paramecia shows that all the cells in a population swim forward with gently curving spirals at speeds averaging 369 ± 19 μm/second. Ciliary reversal occurs in 10% of the cell population per second. Living paramecia, quick-fixed for scanning electron microscopy (SEM), show metachronal waves and an effective stroke obliquely toward the posterior end of the cell. Upon treatment with Triton X-100, swimming ceases and both scanning and transmission electron microscopy reveal cilia that uniformly project perpendicularly from the cell surface. Thin sections of these cells indicate that the ciliary, cell, and outer alveolar membranes are greatly disrupted or entirely missing and that the cytoplasm is also disrupted. These permeabilized paramecia can be reactivated and are capable of motility and regulation of motility. Motion analysis of cells reactivated with Mg2+ and ATP in low Ca2+ buffer (pCa7) shows that 71% swim forward in straight or curved paths at speeds averaging 221 ± 20 μm/second. When these cells are quick-fixed for SEM the metachronal wave patterns of living, forward swimming cells reappear. Motion analysis of permeabilized cells reactivated in high Ca2+ buffers (pCa 5.5) shows that 94% swim backward in tight spirals at a velocity averaging 156 ± 7 μm/second. SEM reveals a metachronal wave pattern with an effective stroke toward the anterior region. Although the permeabilized cells do not reverse spontaneously, the pCa response is preserved and the Ca2+ switch remains intact. The ciliary axonemes are largely exposed to the external environment. Therefore, the behavioral responses of these permeabilized cells depend on interaction of Ca2+ with molecules that remain bound to the axonemes throughout the extraction and reactivation procedures.
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  • 142
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    Cell Motility and the Cytoskeleton 9 (1988), S. 101-110 
    ISSN: 0886-1544
    Keywords: prokaryotic motility ; periplasmic flagella ; hydrodynamics ; model ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Spirochetes are a group of bacteria with a unique ultrastructure and a fascinating swimming behavior. This article reviews the hydrodynamics of spirochete motility, and examines the motility of the spirochete Leptospira in detail. Models of Leptospira motility are discussed, and future experiments are proposed.The outermost structure of Leptospira is a membrane sheath, and within this sheath are a helically shaped cell cylinder and two periplasmic flagella. One periplasmic flagellum is attached subterminally at either end of the cell cylinder and extends partway down the length of the cell. In swimming cells, each end of the cell may assume either a spiral or a hook shape. Translational cells have the anterior end spiral shaped, and the posterior end hook shaped. In the model of Berg et al., the periplasmic flagella are believed to rotate between the sheath and the cell cylinder. Rotation of the anterior periplasmic flagellum causes the generation of a gyrating spiral-shaped wave. This wave is believed sufficient to propel the cells forward in a low-viscosity medium. The cell cylinder concomitantly rolls around the periplasmic flagella in the opposite direction - which allows the cell to literally screw through a gel-like viscous medium without slippage. This model is presented, and it is contrasted to previous models of Leptospira motility.
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  • 143
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    Cell Motility and the Cytoskeleton 9 (1988), S. 117-128 
    ISSN: 0886-1544
    Keywords: centrosome ; aster-forming activity ; tubulin polymerization ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Mitotic apparatuses (MAs) isolated from sea urchin metaphase eggs were chilled on ice to depolymerize microtubules, homogenized, and incubated with tubulin. This caused formation of many small asters with microtubules focusing on granules which were probably fragments of the centrosome. The aster-forming protein components of the granules in the homogenized MAs were solubilized in 0.5 M KCl containing 50% glycerol. After dialysis against low-ionic-strength buffer solution, proteins congregated to form granular assembly capable of initiating aster formation. Phosphocellulose column chromatography enabled the separation of the aster-forming protein fraction which contained a 51,000 molecular weight protein (51-kd protein) as a major component. The protein fraction possessing the aster-forming activity was also prepared from methaphase whole egg homogenate, and the elution profile of the 51-kd protein on phosphocellulose column also coincided with that of the aster-forming activity. The granular assembly reconstituted from the phosphocellulose fraction formed asters whose microtubules show the same growth rate and length distribution as those of asters reconstructed from the granules in the homogenized MAs. Anti-51-kd protein antibody that was raised in rabbit and affinity-purified stained the center of asters which were reconstructed either from the granules in the homogenized MAs or from the granular assembly reconstituted from the phosphocellulose fraction. These results suggest that the 51-kd protein is a component in the aster-forming activity of the centrosomal component in vitro.
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    Cell Motility and the Cytoskeleton 9 (1988), S. 312-324 
    ISSN: 0886-1544
    Keywords: flagella ; sea urchin spermatozoa ; waveform analysis ; Ciona spermatozoa ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Data obtained by manual digitization of photographs of flagellar bending waves have been analyzed by determining size parameters for the bends by least-squares fitting of a model waveform. These parameters were then used to normalize the data so that the average shape of the bends could be determined. Best fits were obtained with a model waveform derived from the constant curvature waveforms used previously but with provision for a linear change in curvature across the central region of the bend-the gradient curvature model (GCM). The central regions of the GCM bending waves are separated by transition regions with length determined by a parameter called the truncation factor (FT). Fitting the GCM to sine-generated bending waves give optimal fit when FT = 0.34. Fitting the GCM to four different samples of flagellar bending waves gave best fits with values of FT ranging from 0.17 for ATP-reactivated Lytechinus spermatozoa beating at approximately 10 Hz to 0.32 for live spermatozoa of Arbacia. The difference between the Arbacia waveforms and a sine-generated waveform is therefore very small, but a sine-generated waveform lacks the degree of freedom represented by FT that is required to fit other waveforms optimally.The residual differences between the waveform data and optimal GCM waveforms were averaged and found to be small. In most cases, the curvature in the central region of the optimal GCM decreased in magnitude towards the tip of the flagellum; however, this slope was highly variable and sometimes positive. Significant variations in both this slope and FT were found in individual bends as they propagated along a flagellum.
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  • 145
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    Cell Motility and the Cytoskeleton 9 (1988), S. 325-336 
    ISSN: 0886-1544
    Keywords: anaphase ; aster ; mitosis ; motility ; spindle ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: An earlier, laser microbeam study produced evidence that, in Fusarium solani, extranuclear polar forces function at anaphase B of mitosis to pull apart the incipient daughter nuclei, whereas the central spindle functions primarily to limit the rate at which they separate. To elucidate further the various dynamics of mitotic anaphase, 8-14 mitoses in hyphae of F. solani were analyzed at 0.5-2.0-sec intervals using high-resolution, digitally processed, videotaped sequences. The spindle growth rate, although fluctuating frequently, averaged 0.6 μm/min during metaphase, increased to 3.6 μm/min during anaphase A and was maximal at 6.1 μm/min during anaphase B. Commonly, chromosomes migrated poleward during anaphase A at fluctuating rates, the average rate being an unprecedented 7.5 μm/min. During anaphase the mitotic apparatus migrated to and fro in the hyphae at rates of 3-15 μm/min, an apparent effect of opposing, fluctuating and typically unequal cytoplasmic forces applied to the two spindle poles. Thus, the molecular mechanisms underlying the various anaphase movements in F. solani do not operate entirely smoothly and uniformly. Accelerated growth of the central spindle is temporally associated with anaphase A and the development of asters. Thus, chromosome disjunction may allow the polar forces to increase the rate of spindle elongation. Microtubule dynamics and motor molecules appear to be adequate to account for the observed rates of mitotic movements.
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  • 146
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    Cell Motility and the Cytoskeleton 9 (1988), S. 361-374 
    ISSN: 0886-1544
    Keywords: microtubular cytoskeleton ; Dinoflagellates ; immunofluorescence ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The cytoskeletal microtubule system has been studied in six species of unarmoured Dinoflagellates using immunofluorescence and electron microscopy. Several structures have been detected and described: (1) a subpellicular layer of microtubules, constituting the microtubular cytoskeleton, running singly or in bundles from the anterior part of the cell to the posterior; (2) a feeding apparatus, containing a ribbon of microtubules, which corresponds to a small peduncle in some species and is simply represented by a cytostome in some other species; and (3) the longitudinal flagellum that runs in a long intracytoplasmic pocket before becoming free at the extremity of the sulcus. A thorough study of the organization of the microtubular structures in a wide spectrum of Dinoflagellates is a prerequisite for understanding the evolutionary history of the group.
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  • 147
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    Cell Motility and the Cytoskeleton 10 (1988), S. 380-390 
    ISSN: 0886-1544
    Keywords: stress fiber ; cytoskeleton ; microvilli ; tubulin ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: We present the first study of the changes in the assembly and organization of actin filaments and microtubules that occur in epithelial cells subjected to the hydrostatic pressures of the deep sea. Interphase BSC-1 epithelial cells were pressurized at physiological temperature and fixed while under pressure. Changes in cell morphology and cytoskeletal organization were followed over a range of pressures from 1 to 610 atm. At atmospheric pressure, cells were flat and well attached. Exposure of cells to pressures of 290 atm or greater caused cell rounding and retraction from the substrate. This response became more pronounced with increased pressure, but the degree of response varied within the cell population in the pressure range of 290-400 atm, Microtubule assembly was not noticeably affected by pressures up to 290 atm, but by 320 atm, few microtubules remained. Most actin stress fibers completely disappeared by 290 atm. High pressure did not simply induce the overall depolymerization of actin filaments for, concurrent with cell rounding, the number of visible microvilli present on the cell surface increased dramatically. These effects of high pressure were reversible. Cells re-established their typical morphology, microtubule arrays appeared normal, and stress fibers reformed after approximately 1 hour at atmospheric pressure. High pressure may disrupt the normal assembly of microtubules and actin filaments by affecting the cellular regulatory mechanisms that control cytological changes during the transition from interphase into mitosis.
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  • 148
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    Cell Motility and the Cytoskeleton 10 (1988), S. 410-419 
    ISSN: 0886-1544
    Keywords: calcium ; Ca2+ ; shape change ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: When flagellates of Physarum polycephalum were treated with Triton X-100 and more than 10-5 M Ca2+, the microfilamentous cytoskeleton disintegrated, as seen by staining with rhodamine-phalloidin, and myxamoebal fragmin became associated with the Triton-insoluble cytoskeleton as demonstrated by immunofluorescence microscopy and immunoblotting. The association of myxamoebal fragmin with the cytoskeleton was reversed by the subsequent addition of excess EGTA. When flagellates were permeabilized in the absence of Ca2+, myxamoebal fragmin did not associate with the cytoskeleton and diffused out of the cells. Subsequent treatment of these cells with Ca2+ was ineffective in inducing either the association of myxamoebal fragmin with the cytoskeleton or the disintegration of the microfilamentous cytoskeleton. However, treatment of these permeabilized flagellates with 10 μg/ml purified myxamoebal fragmin and 1 mM Ca2+ caused the disintegration of the microfilaments. Therefore, we conclude that myxamoebal fragmin participates in the Ca2+-induced disintegration of the microfilamentous cytoskeleton in these permeabilized cells. Rapid cooling of flagellates caused the reversible association of myxamoebal fragmin with the Triton-insoluble cytoskeleton in vivo. Thus myxamoebal fragmin may also participate in the reorganization of the microfilamentous cytoskeleton induced in vivo by the cold treatment.
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    Cell Motility and the Cytoskeleton 10 (1988), S. 438-449 
    ISSN: 0886-1544
    Keywords: tyrosinated microtubules ; organelle distribution/transport ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: We have recently shown that acetylated α-tubulin containing microtubules (acety1-MTs; labeled by antibody 6-11B-1) constitute a cold-stable subset of the microtubule network of nonneuronal cells in rat primary forebrain cultures [Cambray-Deakin and Burgoyne: Cell Motil. 8(3):284-291, 1987b]. In contrast, tyrosinated α-tubulin containing MTs (tyr-MTs; labeled by antibody YL1/2) are cold-labile. Here we have examined the distribution of acety1-MTs and tyr-MTs in cultures of newborn rat forebrain astrocytes and simultaneously investigated the distribution of mitochondria and glial filaments. In double-label immunofluorescence experiments a marked colocalisation of acetyl-MTs and glial filament bundles was observed. Tyr-MTs did not show a similar colocalisation with glial filament bundles. Furthermore, the distribution of mitochondria closely followed that of the acetyl-MT and glial filament bundles. When cells were exposed to short-term (30-min) treatments with MT-disrupting agents such as colchicine and nocodazole, the tyr-MT network was removed but the distributions of acetyl-MTs, glial filaments, and mitochondria were unchanged. Increased exposure to colchicine (9-16 hr) caused a progressive disruption of the acetyl-MTs and the collapse of glial filaments and mitochondria to the perinuclear region. These results suggest that acetyl-MTs and glial filaments but not tyr-MTs may be involved in the intracellular transport of organelles and/or in the control of their cytoplasmic distribution.
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    Cell Motility and the Cytoskeleton 10 (1988), S. 482-495 
    ISSN: 0886-1544
    Keywords: organelle motility ; kinesin ; cytoplasmic dynein ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Directed movements of organelles have been observed in a variety of cultured cells. To study the regulation and molecular basis of intracellular organelle motility, we have prepared extracts from cultured chick embryo fibroblasts (CEF cells) which support the movement of membranous organelles along microtubules. The velocity, frequency and characteristics of organelle movements in vitro were similar to those within intact cells. Organelles and extract-coated anionic beads moved predominantly (80%) toward the minus ends of microtubules that had been regrown from centrosomes, corresponding to retrograde translocation. Similar microtubule-dependent organelle movements were observed in extracts prepared from other cultured cells (African green monkey kidney and 3T3 cells).Organelle motility was ATP and microtubule dependent. The frequency of organelle movement was inhibited by acidic (pH〈7) or alkaline (pH〉8) solutions, high ionic strength ([KCl] = 0.1 M), and the chelation of free magnesium ions. Treatment of the extracts with adenylyl imidodiphosphate (AMP-PNP, 7 mM), sodium orthovanadate (vanadate; Na3VO4, 20 μM), or N-ethylmaleimide (NEM, 2 mM) blocked all organelle motility. The decoration of microtubules with organelles was observed in the presence of AMP-PNP or vanadate. Motility was not affected by cytochalasin D (2 μM) or cAMP (1 mM). Kinesin (Mr= 116,000), an anterograde microtubule-based motor, was partially purified from the CEF extract by microtubule affinity purification in the presence of AMP-PNP, and was able to drive the movement of microtubule on glass coverslips. A similar preparation made in the presence of vanadate contained a different subset of proteins and did not support motility. These results demonstrate that intracellular organelle motility can be reproduced in vitro and provide the basis for investigating the roles of individual molecular components involved in the organelle motor complex.
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    Cell Motility and the Cytoskeleton 10 (1988), S. 518-527 
    ISSN: 0886-1544
    Keywords: 9 + 2 flagellar beating ; aprotinin ; axonemes ; protease inhibitor ; sperm motility ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The effects of protease substrates and inhibitor, which have been previously shown to inhibit mammalian sperm motility (de Lamirande, E., and Gagnon, C. [1986] J. Cell Biol. 102:1378-1383), were investigated using reactivated sea urchin and carp spermatozoa as models of “9 + 2” flagella. Aprotinin in the 2 to 20 μM range interfered with sperm motility by reducing both the beat frequency and the percentage of motile spermatozoa. These inhibitory effects of aprotinin were reversible either by dilution or by the addition of high concentrations of MgATP to the incubation medium. Protease substrates with a lys-ester bond, such as N-α-benzyloxycarbonyl-lys thiobenzyl ester (BLT), also affected motility, but in the 0.1 to 0.5 mM range. As with aprotinin, both the flagellar beat frequency and the percentage of motile spermatozoa were partially and completely decreased, respectively. Analysis of the beat frequencies as a function of MgATP concentration in the presence and absence of 6 μM aprotinin indicated that this protease inhibitor affects sperm motility by decreasing the maximal flagellar beat frequency rather than by altering the axoneme's apparent Km for MgATP. Furthermore, aprotinin concentrations that blocked flagellar reactivation completely inhibited the sliding of microtubules from trypsinized axonemes. Basic proteins or polypeptides of pI close to that of aprotinin (10.3) were also potent inhibitors of the reactivation of motility. However, the characteristics of their inhibition of flagellar beat frequencies and reversibility of their effects suggested that they might be acting on sites different from those sensitive to aprotinin. The inhibitory effects of protease inhibitor and substrates, as well as results of experiments showing the absolute requirement of an intact ester bond for the inhibitory action of protease substrates, suggest that the involvement of a protease in the reactivation of 9 + 2 flagellar beating might be considered as a possible mechanism to explain aprotinin and BLT actions.
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  • 152
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    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 89-98 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: α-Trifluoromethylstyrene (TFMST) does not undergo radical homopolymerization with azobis(isobutyronitrile) (AIBN) in bulk at 60°:C. Low-temperature initiation was not effective either. Radical copolymerization of TFMST (M2) with styrene (ST, M1) has yielded monomer reactivity ratios as follows: r1 =: 0.60 and r2 =: 0.00. It has been found that the cyclohexyl radical generated by reaction of cyclohexylmercuric chloride with sodium borohydride adds to the β-carbon of TFMST 7.5 times faster than that of ST. Combination of the copolymerization analysis and the “mercury method” has allowed us to estimate Alfrey-Price Q and e parameters for TFMST to be 0.43 and 0.90, respectively. Thus, due to the strongly electron-withdrawing effect of the trifluoromethyl group, this styrene is highly electron deficient. In spite of the favorable electronic effect, however, the ceiling temperature appears very low, presumably due to the steric hindrance.
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 117-129 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymerization of three optically active β-1,1-dichloroalkyl β-propiolactones has been investigated in toluene, at 55°C, using aluminum triisopropoxide (Al(OiPr)3) as initiator in a range of monomer/initiator molar ratios smaller than 150. β-1,1-dichloroethyl β-propiolactone polymerizes according to a living mechanism. However, the ability to polymerize decreases with an increase in the length of the alkyl substituent. For instance, β-1,1-dichloro-n-propyl β-propiolactone is obtained only in low yields, whereas β-1,1-dichloro-n-butyl β-propiolactone does not polymerize at all. Actually, each of the lactones investigated reacts with Al(OiPr)3 in an initiation step that obeys a coordination-insertion mechanism. However, the size of the chloroalkyl substituent has a critical effect on the propagation: when the alkyl group contains more than two methylene units, the insertion of a second monomer becomes exceedingly slow.
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 223-233 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Although isocyanate group (NCO) introduced onto carbon black surface was inactivated rapidly upon storage, it could be stabilized by masking the NCO group with active hydrogen compounds such as acetylacetone, diethyl malonate, and sodium hydrogensulfite. Upon heating these carbon blacks having masked NCO group at 150°C, the NCO group was regenerated on carbon black by the decomposition of the masked NCO group. On the other hand, acyl azide (CON3) group introduced onto carbon black was stable at below 20°C, but readily decomposed to NCO group by heating. By means of the reaction of NCO group on carbon black with functional polymers having hydroxyl, amino, and carboxyl group, these polymers were effectively grafted onto carbon black surface. When carbon black having CON3 group was used as reactive carbon black, the grafting ratio of diol-type polyethylene glycol (Mn = 8.2 × 103), polyethyleneimine (Mn = 2.0 × 104), polyvinyl alcohol (Mn = 2.2 × 104), and bifunctional carboxyl-terminated polystyrene (Mn = 1.1 × 105) was determined to be 29.7, 81.7, 32.2, and 50.4%, respectively. The number of grafted polymer chain decreases with an increase in molecular weight of the polymers, because the shielding effect of NCO group by grafted polymer chain is enhanced with an increase in molecular weight of the polymer.
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 701-712 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 29Si-NMR spectra are reported for poly(methylphenylsilylene), 1, poly(1,1,2-trimethyl-2-phenyldisilene) 2, two samples of poly(dimethylsilylene-co-phenylmethylsilylene), 3a and 3b, and poly(phenylmethylsilylene-co-n-hexylmethylsilylene), 4. The spectra of 3a, 3b, and 4 indicate that these polymers contain blocklike regions with considerable segregation of RMeSi and PhMeSi groups. The spectrum of 2 shows no evidence for stereospecific polymerization. The preparation of 2 from 1,1,2-trimethyl-2-phenyldichlorosilane is also described.
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  • 156
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 677-700 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Esters of ω-alkenoic acids have been homopolymerized with transition metal initiating systems. The key to the successful polymerization was the complexation of the monomer prior to its addition to the initiating system. Titanium trichloride, aluminum activated, was found to be best as the transition metal part of the initiator systems, with diethyl-, or better, diisobutylaluminum chloride as the reducing agents and n-hexane or toluene as the solvents. Best results for polymerizations were obtained with 2,6-dimethylphenyl esters of the functional α-olefin monomers; however, other phenyl esters also polymerized well. Attempts to polymerize methyl 10-undecenoate gave the corresponding polymer in only low yields. Polymers of the 2,6-dimethylphenyl esters, obtained in high molecular weight, were characterized. Polymers were also obtained from 2,6-dimethylphenyl 7-octenoate, but not from ω-alkenoates with less than three methylene units between the ester group and the terminal olefin group.Poly(2,6-dimethylphenyl 10-undecenoate) was hydrolyzed in an aqueous sodium hydroxide/1,4-dioxane solution to poly(sodium 10-undecenoate) that in turn was neutralized with acetic acid to poly(10-undecenoic acid).
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  • 157
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 713-720 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The silicon-29 nuclear magnetic resonance spectra of a number of dialky- and alkylmethylpoly-silanes are reported. Polysilanes composed of asymmetrically substituted silylenes (i.e., alkylmethylsilylenes) exhibited very broad resonance lines attributed to diastereomeric chemical shifts of stereogenic silylenes alpha and beta to the observed nucles Symmetrically substituted polysilanes showed a single narrow peak. The 29Si chemical shifts for these polysilanes decrease with increasing steric bulk of the substituents, varying inversely with the electronic excitation energy.
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  • 158
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 765-781 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Uracil esters and acids containing both a chiral center and a halogen atom at the 5-position (fluoro, chloro and bromo) were preapred. The esters of these species were then grafted onto polyethylenimine via an amide bond. The precise nature of this bond was examined using 1H, 13C, 19F, and 13C-1H coupled spectroscopies. The results show that the polymers obtained under our experimental conditions possess both covalent and ionic bonds at the grafting position.
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  • 159
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 529-540 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the photopolymerization of styrene in bulk and in dilute systems in the presence of benzoin isobutyl ether as photoinitiator have been examined. The values of the intensity exponent, calculated at different temperatures or at different styrene concentrations, and the monomer exponent, calculated at various intensities, showed significant departure from those predicted by the ideal kinetic scheme, particularly at high intensity, at low temperature, or at low styrene concentrations. Low molecular weight polymer was the dominant product when high light intensity or low polymerization temperature was used. As the temperature was raised, however, or as the intensity was reduced, a high molecular weight polymer became progressively more important. Kinetic and molecular weight data suggest that at low temperature, high intensity, and/or at low monomer concentration, the benzoyl radical is the dominant initiating species; and the benzyl ether radical was consumed mainly in the termination step. At low intensity, high temperature and/or high monomer concentration, however, it appears that both benzoyl and benzyl ether radicals initiated polymerization.
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  • 160
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 819-826 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetic expressions for a dead-end polymerization initiated by the photolysis of a sensitizer are derived. The phenomenon of dead ending amplifies the inherent differences between the kinetics of photoinitiated and thermally initiated polymerizations. The analysis clearly shows that photoinitiation has distinct advantages over thermal initiation for improving yields in a polymerization which exhibits dead ending.
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  • 161
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 827-834 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The copolyether-polyester system resulting from the anionic graft polymerization of pivalolactone onto poly(2,6-dimethylphenylene oxide) has been formulated with differing graft densities and graft segment lengths. Wide angle x-ray scattering studies on these materials indicated an increased crystalline order with increased PVL segments/graft for similarly annealed specimens and a decrease in such order with increasing carboxylation.
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  • 162
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 1769-1778 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Celluloses from a variety of common sources were analyzed for availabilities of O(2)H, O(3)H, and O(6)H in order to estimate the extent of hydrogen bonding on accessible fibrillar surfaces. Celluloses from flax, ramie, sisal, and wood (both cellulose I and II from wood) together with liquid NH3-swollen cotton and NaOH-swollen cotton (cellulose II) had relative availabilities similar to those of native cotton. Celluloses from Valonia centricosa and in rayon samples stood apart from each other and from the “cotton family.” The difference between Valonia and cotton celluloses appears to result, in addition to the accepted smaller, less perfect crystallites in cotton, from an O(2)H hydrogen bond which is likely the intramolecular bond between O(2)H and O(6′)H that is present in Valonia and absent in cotton. Rayon samples also showed evidence of similar bonds involving O(2)H on accessible surfaces. Since the regenerated rayons had relative availabilities different from those of mercerized cotton and wood cellulose samples, it is proposed that chain packing arrangements are not the same in these two types of cellulose II.
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  • 163
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 1819-1834 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of new bisbenzocyclobutene-terminated aromatic imide monomers has been synthesized from the condensation reaction of 4-aminobenzocyclobutene and the perspective dianhydride in refluxing acetic acid/toluene. The differential scanning calorimetric studies of the foregoing monomers indicated that polymerization exotherms began at 229-250°C and reached their maxima at 258-263°C. The cured samples (250-254°C; N2; 8 h) were surprisingly stable toward thermo-oxidative degradation; only 7-10% weight loss was observed after 200 h (in air) at 314°C (600°F). At higher temperatures (650 and 700°F), the most rigid structure was the most thermo-oxidatively stable. An approach to enhance both the final glass-transition temperature (Tg cure) and the thermo-oxidative stability of the bisbenzocyclobutene system was to dilute the cure-site density since the cure-site structure is the weakest part of the polymeric structure. Therefore, a series of bisbenzocyclobutene-terminated aromatic imide oligomers were prepared, using various aromatic amines as the chain-extending agents. Meta-phenylenediamine was apparently the most effective in the advancement of both the Tg (cure) and thermo-oxidative stability.
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 1835-1865 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A simple, probabilistic approach describing the number distribution of the molecular weight (MWD) of polymers formed by emulsion polymerization is presented. The radical populations of the reacting system are formally split into infinite, quickly convergent series of particularly tagged radical populations. These populations are characterized by the nature and the number of the state transitions of the associated latex particles. For each kind of single radical or radical pairs a distribution function is then defined. These functions can be specified on the basis of αi and Qi, the growth probabilities, within a latex particle in state i, of a single radical and a radical pair respectively. The overall MWDs are then given by summation over all the distributions of the radical populations and over all the allowed states. Only one set of ordinary differential equations (the Smith-Ewart equations) are involved in the mathematical formulation, single distribution functions being obtained by solving simple exponential-type integrals. In this paper, analytic solutions are presented for the zero-one, zero-one-two and general systems. Analogies and differences between our approach and previously reported treatments are critically discussed.
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  • 165
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 1867-1883 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rates of epoxidation of polybutadiene homopolymers and styrene-butadiene triblock copolymers with monoperoxyphthalic acid were measured at four temperatures in homogeneous solution. Dioxane and mixed solvents with chloroform were used as reaction media. Activation energy values were also calculated for polymers different in microstructure and styrene content. Viscometry in a modified viscometer was performed and combined with kinetic measurement to monitor the conformational change during epoxidation. Cis-content in polybutadiene and styrene content in SBS exhibit only slight effect on epoxidation in dioxane. The addition of chloroform promotes the reaction rate remarkably and enlarges the difference between polymers. Explanations were given including the solvent effect on reduced viscosity, which was used to correlate the conformational change of polymer chains. NMR and GPC analysis confirmed the absence of ring opening and degradation during epoxidation up to 54% epoxy group content.
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  • 166
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 1885-1902 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several new phosphorylated or nonphosphorylated maleimide or nadimide systems containing s-triazine rings were synthesized. Their synthesis was accomplished by simple methods utilizing readily available and relatively inexpensive starting materials. All polymer precursors were characterized by infrared (IR) and proton nuclear magnetic resonance (1H-NMR) spectroscopy. They were thermally polymerized to heat-resistant laminating resins. Thermal characterization of monomers and their cured resins was achieved using differential thermal analysis (DTA), dynamic thermogravimetric analysis (TGA) and isothermal gravimetric analysis (IGA). The cured resins were stable up to 304-330°C both in nitrogen and air atmospheres and formed anaerobic char yield 49-59% at 800°C. The phosphorylated polymers showed a lower temperature of initial weight loss but afforded higher anaerobic char yield than did the corresponding nonphosphorylated polymers. The thermal properties of the polymers were correlated with their chemical structure.
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  • 167
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 913-933 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The dissociation of 2,2′-disubstituted thioindigo whites into captodative radicals and the recombination of these radicals have been examined in solution and in polymeric matrix. For the methyl- and ethyl-substituted TIW the quantum yield of dissociation in solution is equal to 4 × 10-4 and 5 × 10-4, respectively. Using the iodine scavenging method the quantum yield of formation of free radicals was almost 3 to 4 × 10-4, i.e. 20-25% radicals recombine in cage. For the isopropyl and aryl TIWs partial dissociation occurs already at room temperature. Their dissociation enthalpies have been evaluated in solution on the basis of the ESR signal surfaces at different temperatures. For the aromatic substituted Δ Hdiss amounts to 88-95 kJ mol-1, while for i-PrTIW ΔHdiss is 150 kJ mol-1. The behavior of these compounds was studied in three different matrices: polymethyl methacrylate (PMMA), polypropyl methacrylate (PPMA), and polystyrene (PST). In the cases of the aryl substituted derivatives, cage dimensions of the TIW-radical pairs were measured at low temperature, and their apparent dissociation enthalpies above their glass transition temperatures were evaluated using ESR spectrometry; they are equal to 118 ± 3 kJ mol-1 in PPMA and around 155 kJ in PMMA and PST. The decay kinetics of the radicals after photolysis of the TIWs below Tg were interpreted on the basis of Waite's equations for diffused controlled reactions. The great influence of steric effects in the cases of the 2-orthochlorophenyl and the 2,4-dichlorophenyl TIWs is stressed as well as the importance of the merostabilization of the captodative radicals on these kinetic characteristics. The nature of the polymeric matrix is also underlined; below Tg the diffusion rate constant is only one-third in PST compared to PMMA. The radicals generated from Ph TIW and its para-nitro and p-methoxy derivatives show a strong inhibiting effect toward the polymerization of methyl methacrylate, while the alkyl TIWs behave as free radical initiators.
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  • 168
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 935-951 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The interpolymeric electron donor-acceptor (EDA) complex of donor poly[(N-ethylcarbazol-3-yl)methyl methacrylate] (PHMCM-2) with acceptor poly-(2-[(3,5-dinitrobenzoyl)oxy]ethyl methacrylate) (PDNBM-2) presents a single glass transition temperature and a decomplexation endotherm on differential scanning calorimetric (DSC) thermograms. This system is considered a “polymer blend model” which exhibits a lower critical solution temperature (LCST). Phase separation of this blend is kinetically controlled and positive deviations of the glass transition temperatures from weight average values suggest that it behaves as a thermally reversible crosslinked network. Calorimetric methods to determine the heats of mixing of small molecule complexes in solution were adapted for this solid state blend to estimate the equilibrium constant (Keq) and other thermodynamic parameters. Applying a computer iterative procedure and assuming 1 : 1 stoichiometry, a least-squares fit was found for several different donor molecular weights with three different high molecular weight acceptors. At moderate molecular weights, Keq rises to represent saturation fractions near unity as found in biological systems. Keq decreases for higher molecular weights, possibly due to trapped chain entanglements. These results are supported by a composition-independent, “horizontal line” phase diagram, thus resembling the completely complexed/denaturation process in DNA.
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 973-983 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In the present study, dynamic differential scanning calorimetry has been used to investigate the effect of an alkali lignin in amounts up to 20% by weight, on the crosslinking kinetics of an epoxy prepolymer cured with an aliphatic polyamine. Lignin presence does not significantly affect the overall reaction order, but the activation energy increases and the slowing of the overall curing process with lignin content could be explained by the interaction between lignin and the polyamine hardener. The possibility of having a “false compensation” in the case of the use of single DSC scans is also discussed.
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 993-1001 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymeric membrane crosslinked by a viologen structure was prepared by the reduction of the homopolymer with a pendant cyanopyridinium structure, poly(1-vinylbenzyl-4-cyanopyridinium perchlorate), chemically or electrochemically. The homopolymer in the state of membrane was reduced chemically by aqueous sodium dithionite (Na2S2O4) to obtain the polymer containing viologen group (64 mol%) despite a heteogeneous reaction. When the membrane was reduced electrochemically, the resulting viologen moiety in the membrane showed reversible one- and two-electron redox behavior.
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 1021-1033 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The activity of 10 water soluble photoinitiators derived from thioxanthone, benzophenone, and benzil were studied comparatively. The mechanisms of initiation were determined by time resolved laser spectroscopy and steady state polymerization. The characteristic features of each series of compounds are pointed out. The possible contribution of biphotonic processes to the initiation step is considered.
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 1979-1983 
    ISSN: 0887-624X
    Keywords: 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 26 (1988), S. 2537-2551 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polystyrene was crosslinked in either 1,2-dichloroethane or carbon tetrachloride in the presence of aluminum chloride. Apparently, the reactions involve Friedel-Crafts substitution of phenyl ring with CH2CH2Cl or CCl3 groups, which than participate in crosslinking, giving CH2CH2 or CCl2, CCl, and C bridges. In the first stage a charge-transfer complex is formed between AlCl3, polystyrene and the solvent. After heating this complex above 35-40°C a rapid formation of HCl occurs and a crosslinked polymer is formed. This final product is insoluble, infusible, and inflammable. It decomposes at 400°C without melting.
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 2589-2596 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis and characterization of pseudo or semi- and full-interpenetrating polymer networks (IPNs) of poly(2,6-dimethyl-1,4-phenylene oxide) and polydimethylsiloxane were performed. We observed that in full IPNs, the elasticity of the IPN samples increased very drastically, as the composition of polydimethylsiloxane increased (i.e. 0-60%) while the tensile strength (TS) and the glass transition temperature (Tg) decreases. The pseudo IPNs appeared to consist of two phases while the full IPNs of lower siloxane content were miscible.
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 2603-2612 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Copolymerization of 1-(trimethylsilyl)-1-propyne (MeC ≡ CSiMe3) with several aromatic and aliphatic disubstituted acetylenes (MeC ≡ CPh, n-BuC ≡ CPh, 2-octyne, and 4-octyne) were examined by using Ta and Nb catalysts. The TaCl5-Ph3Bi catalyst was effective in copolymerization with the aromatic acetylenes, whereas the NbCl5-Ph3Bi catalyst was preferable in copolymerization with the aliphatic acetylenes. The copolymerization products were not mixtures of homopolymers but copolymers. The relative reactivity of monomer tended to decrease with increasing steric effect of monomer: 2-octyne 〉 MeC ≡ CSiMe3 〉 4-octyne 〉 MeC ≡ CPh 〉 n-BuC ≡ CPh. The copolymers of MeC ≡ CSiMe3 with MeC ≡ CPh [copoly(TMSP/PP)s] had high molecular weight (Mw 〉 1 × 106), and provided thermally stable tough films. With increasing MeC ≡ CPh content of copoly(TMSP/PP), the oxygen permeability coefficient (PO2) decreased, while the separation factor (PO2/PN2) increased.
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 2597-2602 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A film forming polyester was obtained from the title compound and 1,4-butanediol. In addition oxidation of the title compound gave rise to 7,8-dicarbomethoxy-7,8-diphenylquinodimethane as a mixture of Z and E isomers. The 1H-NMR and the electronic characterization of this polymer are discussed. The quinodimethane will undergo 1,6-nucleophilic addition to form an aromatic compound.
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 2651-2667 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The substitution of polychlorotrifluoroethylene (PCTFE) with sulfur, selenium, and phosphorus nucleophiles is reported. The primary reaction, which extends throughout the bulk of the polymer, is the incorporation of the nucleophile with concommitant loss of chloride. The substituted PCTFE's are studied by 1H-, 13C-, 19F-, and 31P-NMR, as well as IR, and elemental analysis.
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 1639-1647 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermoxidative behavior of atactic and isotactic polypropylene under dynamical thermoxidative conditions has been studied. It has been established that, with the increase of the heating rate, the development of the oxidative processes are diminished and consequently a modification in the reaction mechanism takes place. One can notice at the same time that the oxidative processes are more intense in the case of the atactic polymer. The 5-15°C/min heating rates determine significant differences between the thermal behavior of the samples, permitting the elaboration of the standard curves useful in fast determination of the atactic content of the industrial products by routine analysis.
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    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 2039-2046 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of various phase transfer agents on the interfacial polycondensation of bisphenol A with isophthaloyl chloride was investigated. It was found that the transfer rate of bisphenolate and, thus, the reaction rate of polycondensation were increased with an increasing lipophilicity of the phase transfer agent, i.e. TBAC 〉 TEBAC 〉 TEAC, whereas the equilibrium of bisphenolate between the organic phase and the aqueous phase was hardly affected. Moreover, experimental evidence indicated that a phase transfer agent of high lipophilicity reduced the hydrolysis of the acid chloride, an important aspect in interfacial polycondensation.
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  • 180
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 2077-2083 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The direct polycondensation of isophthalic acid (IPA) and aromatic diamines with a new phosphorus compound, phenylphosphonic dichloride (PPDC), was studied. PPDC could actually react with nearly a two molar amount of carboxyl groups, but more than 75 mol % PPDC with respect to the carboxyl groups of IPA were satisfactorily used in the polycondensation. The initial reaction of IPA with PPDC in pyridine at room temperature and then at 120°C was needed to complete the activation, and the subsequent aminolysis at 120°C for 3 h was most effective. The polyamides of high inherent viscosity were obtained even from weakly basic aromatic diamines, and their values were more than those obtained by the conventional method. In their thermal properties determined by the DTA, they showed Tgs and Tms higher than those reported before.
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  • 181
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of methacrylates and acrylates containing 4-methoxy-4′-hydroxy-α-methylstilbene and 4-hydroxy-4′-methoxy-α-methylstilbene constitutional isomers attached to the polymerizable group through flexible spacers containing 11, 8, 6, 3, and respectively 2 methylenic units is described. The radical copolymerization of a 1/2 or 2/1 mole ratio of the two constitutional isomeric monomers led to thermotropic side-chain liquid crystalline polymers in all cases. The synthesis of copolysiloxanes based on the same constitutional isomeric mesogens as side groups, and flexible spacers containing 11, 8, 6, 5, and respectively 3 methylenic units is also described. All polymers were characterized by differential scanning calorimetry and optical polarization microscopy. The polymers containing 11 methylenic units in the spacer exhibit Sc mesomorphism, while the other polymers are nematic. Copolymethacrylates do not undergo side-chain crystallization. Only the copolyacrylate containing 11 methylenic units in the spacer exhibits side-chain crystallization. All the copolysiloxanes display side-chain crystallization. The number of melting transitions seen for these polymers decreases with increasing spacer length. Copolysiloxanes containing dissimilar spacer length were also prepared. Only the copolymer synthesized with highly dissimilar spacer lengths, i.e., containing 3 and 11 methylenic units, does not undergo side-chain crystallization. These results have demonstrated that while the type of mesophase is dictated only by the spacer length, the degree of decoupling of the motion of the side-groups from the motion of the main chain is strongly dependent on the nature of the polymer backbone. For the same mesogenic unit and spacer length, the thermal stability of the mesophase is also dictated by the nature of the polymer backbone. The use of constitutional isomers of mesogenic units as side groups in liquid crystalline polymers provides at least qualitative information on the degree of decoupling of the side groups from the polymer main chain.
    Additional Material: 13 Ill.
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  • 182
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 2085-2097 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The radical polymerizations of diallylsilanes such as diallyldimethylsilane (1) and diallylmethylphenylsilane (2) have been conducted. Both poly(diallyldimethylsilane) (3) and poly(diallylmethylphenylsilane) (4) are soluble in benzene, methyl ethyl keton (MEK), and chloroform, slightly soluble in acetone, and insoluble in methanol and ethanol. No insoluble fraction of either polymer was obtained. Very little evidence of vinyl protons in the 1H-NMR spectra can indicate that both polymerizations predominantly proceed with intramolecular cyclization. In order to study the ring size of cyclic structure in the repeating unit of the polymers, a model compound, allyl(2-chloropropyl)dimethylsilane (5), was synthesized and cyclized with Bu3SnH in the presence of azobisisobutyronitrile (AIBN) in benzene, under similar condition of those for the cyclopolymerizations. The product was analyzed with GC-MS which showed that the five-membered ring compound, 1,1,3,4-tetramethylsilacyclopentane, was not formed. From the result of the cyclization of the model compound, it can be suggested that the polymerizations undergo with only h-t intramolecular cyclization to form a six-membered ring in the repeated unit. The 13C-NMR spectra of 3 and 4 were measured to study the ring size and the configuration of the cyclic structures. The two peaks at -1.6 and -3.4 ppm of the spectrum of 3 show that there are two kinds of methyl carbons in the repeating unit. From consideration of the model reaction and the number of the peaks of the NMR spectrum, it can be considered that the polymer main chain is assembled with the six-membered ring in cis-form, and the two signals are assigned to equatorial and axial methyl carbons, respectively. The two peaks at -1.5 and -5.1 ppm of the 13C-NMR spectrum of 4 can be assigned similarly. The radical cyclopolymerizations of triallylsilanes such as methyltriallylsilane (6) and phenyltriallylsilane (7) were conducted. The 1H-NMR spectra of poly(methyltriallylsilane) (8) and poly(phenyltriallylsilane) (9) show broad peak around 5 ppm for vinyl protons and around 2 ppm for alkyl protons. Comparisons of the relative intensities of the peaks indicate that both polymerizations undergo with single ring closure to form a polymer with monocyclic structure moiety, cyclosilahexane, and an allyl group in a repeating unit of 8 and 9.
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  • 183
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 1199-1205 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The results of XPS measurements and molecular orbital calculations performed on the fluorine containing polyimide, PMDA-BDAF, are presented. The calculated carbon 1s (C1s) core energy level positions are compared with the level positions inferred from the XPS measurements. Within Koopman's approximation, the observed shape of the main XPS peak is consistent with the calculated distribution of C1s levels under this peak. Comparison of the magnitude of the carbonyl XPS peak intensity with the main peak intensity indicates a carbonyl C1s signal deficiency compared with that expected for “ideal bulk stoichiometry” i.e., for a polymer with no crosslinks or chain terminations. Comparison of data obtained from a grazing emission (surface sensitive) geometry with that obtained from a normal emission geometry, which probes more deeply into the bulk, indicates a signal enhancement of the C1s levels associated with carbon atoms of the CF3 groups as one nears the polymer surface. Such enhancement might be due to either actual differences in chemical composition, or to preferential structural ordering near the polymer surface.
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  • 184
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 1231-1237 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The photopolymerizations of 4-vinylbenzophenone (VBP) in various solvents were investigated to make clear the photoininiation characteristics. It was found that direct photoirradiation produces polymers, oligomers (trimers), and dimers. The dimers were identified as trans- and cis-1,2-bis(4-benzoylphenyl)cyclobutanes. The fraction of trans-form in the cyclobutane dimers produced was about 80%, and was little affected by the reaction conditions. The quantum yields ([VBP] = 0.1M in benzene) was estimated to be 3 × 10-2 for the dimerization and 2 × 10-4 for the initiation of polymerization. The photoreactions via π,π* triplet state of the monomer was suggested from the results.
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  • 185
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 1249-1251 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
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  • 186
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 1207-1229 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The emulsifier-free emulsion polymerizations of styrene in the presence of about 1 wt% (related to styrene) of the water soluble comonomer, sodium methallyl sulfonate (NaMS), which has short hydrophobic group and strong hydrophilic ionic group, and of the initiator, potassium persulfate, are carried out. Under constant ionic strength, the number density of polymer particles (Np) is found to depend on 0.5-power of the initiator concentration and shows a minimum in the comonomer concentration plot. Under constant concentration of monomer, comonomer and initiator, Np is found to depend on -1.1-power of the ionic strength. In the earlier period, the presence of styrene oligomer having MW about 1000 and water soluble poly(NaMS) or copolymer with high NaMS content suggests a micellar nucleation mechanism, by which the styrene oligomer behaves as emulsifier and the poly(NaMS) can either stabilize or destabilize the existing particles, depending on its concentration in the aqueous phase. The particle size is rather uniform having an uniformity very close to 1 (ca. 1.001) throughout the entire process. It is much larger than that of the conventional emulsion polymerization or emulsifier-free emulsion polymerization with the other comonomers by about 3 to 4 times in diameter or 27 to 64 times in volume, leading to that the average radical number in the particle could be much greater than 0.5. The (conversion)2/3 versus time plot is found to be linear from 6 to 50% conversion. During this period, for the conversion from 10 to 40% the polymerization rate increases twice but the particle volume increases four-fold. In addition, MWD shows bimodal (excluding the styrene oligomer peak in the earlier period) during the growth period. But the lower MW peak shifts to higher MW and become larger, while the higher MW peak decreases, and finally the MWD becomes single mode after 58.6% conversion. These results suggest a “gradient polymerization” or “transition stage to core-shell structure” in the earlier stage of particle growth and a “shell part polymerization” in the later stage.
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  • 187
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 1253-1257 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
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  • 188
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 1239-1248 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Novel copolymers containing both donor and acceptor chromophores have been synthesized by free radical polymerization of 2-N-carbazolylethyl acrylate and 2′-acrylylethyl-4,5,7-trinitrofluorenone-2-carboxylate. The charge transfer complexation occurs in copolymers in a similar way to poly(2-N-carbazolylethyl acrylate) molecularly doped with 2,4,7-trinitrofluorenone (TNF) and a model compound, ethyl 4,5,7-trinitrofluorene-2-carboxylate (Et-TNF). Copolymer and doped systems exhibit obvious CT bands in a 440-600 nm region, where the former shows higher absorption than the latter. Glass-transition temperatures show positive deviations from the weight-average values of copolymers, indicating the partial interchain interaction of copolymers in solid state. Quantum efficiency of hole photogeneration of the copolymer with the 0.05 to 1.0 molar ratio of TNF to carbazole chromophores is higher than those of the corresponding molecularly TNF- and Et-TNF-doped poly(2-N-carbazolylethyl acrylate), especially at lower electric fields.
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  • 189
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 1809-1817 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The highly conjugated aromatic polymers, poly(2,5-dimethoxyphenylene vinylene) and poly(2,5-dimethylphenylene vinylene), were obtained from their water soluble, sulfonium salt precursor polymers. Films of these polymers were reacted with either AsF5 or I2 vapor. Poly(2,5-dimethoxyphenylene vinylene) showed increases in electrical conductivity of up to 14 to 15 orders of magnitude for these two dopants, while an 8 to 9 order of magnitude increase was observed for poly(2,5-dimethylphenylene vinylene) with the same dopants. The synthesis of the precursor polymers, the properties and elimination reactions of films of the precursors, the doping reactions, and the conductivities of the resulting phenylene vinylene films are discussed.
    Additional Material: 4 Ill.
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  • 190
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 1791-1807 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Soluble copolymers of diethyl 2-(methacryloyloxy) ethyl phosphate (DMP) with methyl methacrylate (MMA), methyl acrylate (MA), ethyl acrylate (EA) and butyl acrylate (BA) were synthesized by radical copolymerization in benzene solution using azobis(isobutyronitrile) (AIBN) as initiator. The monomer reactivity ratios of these systems at 60°C were determined by the conventional schemes using the methods of Fineman-Ross, Joshi-Joshi, and Kelen-Tüdos. DMP underwent a completely random and azeotropic copolymerization with MMA whereas in its reaction with the other acrylates DMP entered preferentially into the polymer chain. The reactivities of DMP-terminated polymer radicals towards the acrylate monomers were found to be in the order: MMA 〉 EA 〉 MA 〉 BA. An increase in solvent polarity decreased the relative reactivity of DMP for the DMP-MMA pair. An examination of the molecular weights of the copolymers revealed the occurrence of chain transfer caused by DMP. The copolymer glass transition temperatures were determined and the variations of Tg with copolymer compositions were discussed according to the theory of Johnston, taking into account the effect of the sequence distributions of the comonomers on Tg. The Tgs of the alternating copolymers of DMP with the four alkyl acrylates were calculated.
    Additional Material: 12 Ill.
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  • 191
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 2561-2572 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thermal degradation of polychloroprene under nitrogen, especially at the initial stages, has been studied by using 1H-NMR, 13C-NMR and FT-IR spectroscopy. A model polymer of low molecular weight (Mn = 6300) was prepared to avoid gelation during degradation. None of isomerized 1,2 unit has been found in the original polymer. Allylic rearrangement of 1,2 unit was the first-stage reaction, which was finished within 30 min at 150°C. The extent of HCl loss was proportional to the decrease of isomerized 1,2 unit. It has been suggested that the next-stage reaction is dehydrochlorination of the isomerized 1,2 unit. The presence of terminal vinyl group and the increased amount of olefinic proton were not found in the degraded polymer. The back-biting mechanism involving a six-membered cyclization process is proposed for the dehydrochlorination. The thermal racemization has been also found to take place in the 3,4 unit.
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  • 192
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 2573-2579 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Tri-n-butyltin hydride (Bu3SnH) was employed for the synthesis of organotin polymers via radical process. The polymers having both organotin and carbonate groups were obtained by the reaction of Bu3SnH with monomers such as diallylcarbonate and diethylene glycol bis(allyl carbonate) via hydrostannation. The copolymerization of diethylene glycol bis(allyl carbonate) and the mono-hydrostannated derivative was also conducted to obtain the corresponding polymers.
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  • 193
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 3103-3117 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several compatible mixtures of 2,2-bis[4-(N-4-benzocyclobutenyl) phthalimid-4-phenyl]hexafluoropropane (BCB) and 1,1′-(methylene di-4,1-phenylene)bismaleimide (BMI) were prepared according to the molar ratios (BCB : BMI): 1 : 1; 1 : 1.5; 1 : 3; 1.5 : 1. Complete compatibility of the mixtures was evidenced by a single initial Tg. All mixtures showed relatively low initial Tg's (61-70°C) and characteristic polymerization exotherms of benzocyclobutene-based systems (onset: 221-225°C; maximum: 257-259°C), providing an excellent processing window (ca. 155°C). The cured sample of the mixtures, pure BCB and BMI (250°C; N2; 8 h) were subjected to comparative isothermal gravimetric analysis (ITGA). After 200 h at 650°F (343°C) in circulating air, the cured BMI sample retained only 3% of its original weight, whereas the mixtures of BCB and BMI exhibited thermo-oxidative stabilities similar to BCB (13-15% weight loss). A model compound was synthesized from the intimate mixture of N-phenylmaleimide and N-benzocyclobutenyl phthalimide in 63% yield. The ITGA results and isolation of the model Diels-Alder adduct render strong support to the conviction that Diels-Alder polymerization is indeed the predominant curing process in the BCB/BMI system.
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  • 194
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 3127-3130 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Tab.
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  • 195
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 3141-3149 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Successful chromatograms were obtained for trifluoroacetylated nylon 12 (N-TFA-N) in gel permeation chromatography (GPC) with dichloromethane as eluent. It was confirmed that the method of universal calibration was applicable for N-TFA-N and polystyrene. The average molecular weights of nylon 12 were obtained from the chromatogram of N-TFA-N by use of the calibration curve for polystyrene. The stability of N-TFA-N in solution was examined from various angles. Satisfactory results are obtained, if the sample solution is measured within 48 h after preparation.
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  • 196
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 3159-3166 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Graft copolymerization of acrylonitrile (AN) onto sisal fibers (chemically modified) was studied using the Mn(III)/EDTA redox system in aqueous solution. The effects of time, monomer (AN), metal ion [Mn(III)] substrate [ethylene diamine tetraacetic acid (EDTA)], temperature, and acid concentration on graft yield have been studied. The effects of thiourea on the graft yield has also been studied. A suitable mechanism is proposed.
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  • 197
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 1343-1359 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of addition reactions between methyl α-eleostearate which forms the main chain of tung oil and cresols when catalyzed by an acid, p-toluene sulfonic acid, have been studied. The addition reactions, carried out with any one of the o-, m-, and p-cresols were shown to be first order with regard to both methyl α-eleostearate and cresol concentrations. The reactions were additions of two cresol molecules to one methyl α-eleostearate molecule, and it was presumed that they proceed in the two steps given below in which the first step in rate-determining. 1$$ E + C \to E{\rm - }C $$ 2$$ E{\rm - }C + C \to C{\rm - }E{\rm - }C $$ (E: methyl/α-eleostearate, C: cresols)The apparent reaction rate constants (L/mol min) were found to be 0.046 for o-cresol, 0.038 for m-cresol, and 0.033 for p-cresol. The apparent activation energies (kcal/mol) were found to be 0.95, 3.66, and 4.05, in the cases of o-, m-, and p-cresols, respectively.
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  • 198
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 3269-3274 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Copolycondensations of 3,5-dimethoxy-4-hydroxybenzoic (syringic acid, SGA), 4-hydroxybenzoic(PHB), and 4-aminobenzoic (PAB) acids with diphenyl chlorophosphate(DPCP)/LiCl/pyridine were studied. Random copolycondensations of a wide range of monomer compositions afforded copolymers exhibiting birefringence at room temperature. However, when the sequence of PHB and PAB was fixed by using a newly prepared monomer, 4-(4′-aminobenzoyloxy) benzoic acid (PABBA), the ordered copolymers thus prepared showed birefringence above 200°C, but not at room temperature. Variations in solubility and thermal behavior were also observed in randomly and sequentially prepared copolymers. The monomer sequences in copolymers in random copolycondensations could be changed by controlling the reaction of monomers with DPCP.
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  • 199
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polyamides containing thymine photodimer units in the main chain were synthesized, and their photolysis by ultraviolet irradiation below 260 nm were studied in film state. Photodimers of thymine derivatives were obtained by photochemical reaction of the carboxylic acid derivatives of thymine in aqueous solution irradiated above 270 nm. An attempt was made to resolve the isomers of the photodimers, and the two kinds of cis isomers [cis-syn(head to head), and cis-anti(head to tail)] were isolated successfully. The polyamides were prepared by condensation of the photodimers with diamine using an activated ester method. The photodissociation of the thymine photodimer in the polymer main chain caused the breakage of the polymer chains, leading to the production of oligomers and dimer compounds containing thymine bases at the ends of the molecule. The dissociation rate of the polymer did not depend on the kind of the thymine photodimer which was in the main chain of the polymer.
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  • 200
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    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 3337-3360 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Preparation of novel model polymers of polynucleotides with copoly(vinylamine-vinylalcohol) [P(Vam-Val)] backbone and a pair of adeninyl and thyminyl pendant groups is described. At first, direct, low temperature esterification was used to attach (-) and (±)-2-(thymin-1-yl)propionic acid [(-)TPA and (±)TPA], to the N-Cbz protected hydroxy polymer P(Vamz-Val) which was prepared by selective N-protection of N-benzyloxycarbonyloxy-5-norbornene-2,3-dicarboximide (CbzONB) with P(Vam-Val), at the hydroxy group via an ester bond. Two novel precursors P(Vamz-Ve(-)T) and P(Vamz-Ve(±)T) were obtained. Then the Cbz protecting group of P(Vamz-Ve(-)T) and P(Vamz-Ve(±)T) were removed by hydrobromic acid to give the hydrobromide salt of P(Vam-Ve(-)T) and P(Vam-Ve(±)T), respectively. Finally, the attachment of (±)-2-(adenine-9-yl)propionic acid [(±)APA] to linear P(Vam-Ve(-)T) and P(Vam-Ve(±)T) by selective N-acylation with N-hydroxy-5-norbornene-2,3-dicarboximide (HONB). This procedure gave the corresponding P(Vam-Val) having a pair of adeninyl and thyminyl pendant groups, such as P(Va(±)Ad-Ve(-)T) and P(Va(±)Ad-Ve(±)T). In contrast to the corresponding polymer models, the related segment model compounds were also prepared from threo-2-amino-4-pentanol without N-blocking-deblocking operations. The segment model compounds including four stereoisomers of highly optical purities, were separated and purified by reverse phase HPLC technique.
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