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  • Physics  (2,540)
  • Cell & Developmental Biology  (1,658)
  • Weizen
  • 1975-1979  (4,029)
  • 1925-1929
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Year
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Gamete Research 2 (1979), S. 153-162 
    ISSN: 0148-7280
    Keywords: spermatozoa ; cell surface ; epididymis ; surface labeling ; gel electrophoresis ; proteins ; membrane ; spermatozoa ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Differences in the exposure of spermatozoa surface components during epididymal passage have been examined using lactoperoxidase-catalyzed 125I-iodination or labeling with 125I-diazodiiodosulfanilic acid. Labeled surface proteins obtained from caput and cauda epididymides were solubilized in detergent, separated by sodium dodecylsulfate polyacrylamide slab gel electrophoresis, and identified by radiography. Densitometer scans of autoradiograms revealed increased amounts or exposures of surface proteins of ∼35,000, ∼39,000, ∼50,000, and ∼78,000 molecular weight on the cauda epididymal spermatozoa.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Gamete Research 2 (1979), S. 177-185 
    ISSN: 0148-7280
    Keywords: multiple enzyme forms ; acid nitrophenyl phosphatase ; sea urchin ; development ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Acid nitrophenyl phosphatases from sea urchin eggs and embryos were investigated by gel filtration. Four different forms were found in Hemicentrotus pulcherrimus, and three forms in Anthocidaris crassispina and Pseudocentrotus depressus.The first and second forms (designated AcP-1 and AcP-2) had the highest activity in the range of pH 5.6-6.0. The third (designated AcP-3) had an apparent optimum pH between pH 4.3 and 4.8, and the fourth (designated AcP-4) showed the maximum activity at pH 3.0. AcP-1 was much more thermolabile than AcP-2 and AcP-3 at 56°C. NaF inhibited AcP-2, AcP-3, and AcP-4 but not AcP-1. AcP-1, AcP-2, and AcP-3 were observed in the three species, whereas AcP-4 was not detected in A. crassispina and P. depressus. AcP-1, AcP-2, and AcP-3 were separted by gel filtration.AcP-1 and AcP-2 of A. crassispina and H. pulcherrimus were studied in developing embryos. The behavior of these forms in gel filtration changed during development, from unfertilized eggs to the pluteus stage.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Gamete Research 2 (1979), S. 187-192 
    ISSN: 0148-7280
    Keywords: zona isolation ; collagenase ; receptor for sperm ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Zonae pellucidae were collected from bovine ovaries by chopping, dispersing the chopped tissue with collagenase, sieving through nylon mesh screens, and pipetting. The zonae were free of corona cell processes when examined under the scanning electron microscope. Solutions of zonae obtained with collagenase exhibited the same antigenic and sperm receptor properties as those obtained without enzyme treatment.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Gamete Research 2 (1979), S. 207-211 
    ISSN: 0148-7280
    Keywords: sperm ; capacitation ; acrosome ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Suspensions of nearly 100% viable golden hamster sperm were prepared by passing washed cauda epididymal sperm through a column of 0.25-0.3 mm glass beads. Incubations of these viable sperm under in vitro capacitation conditions in volumes of 0.1 or 1 ml (2-2.5 × 106/ml) resulted in 85-92% viable sperm after four hours and 45 minutes of incubation. More than 70% of these sperm were judged to have been capacitated after four hours and 45 minutes of incubation on the basis of their having undergone acrosome reactions and the presence of high numbers of sperm exhibiting the activated motility characteristic of capacitated hamster sperm.Thus, for the first time, procedures are available that will yield large numbers of viable capacitated sperm for biochemical analysis and that will also allow other studies of hamster sperm capacitation with minimum interference from molecules released from dead sperm.
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  • 5
    ISSN: 0148-7280
    Keywords: speramtozoon-copepoda (My tilicola intestinalis) ; external morphology ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The external structure of the male gamete of Mytilicola intestinalis is studied under a scanning electron microscope and compared with transmission electron micrographs of thin sections corresponding to the different parts of same. The cell in question is long and filiform, showing, along a significant part of its length, two ridges or expansions helicoidally arranged and diametrically opposed. Four different parts or segments can be identified in this spermatozoon: segment A, characterized by its screw-like aspect; segment B, the longest, provided with well-developed helicoidal expansions; segment C, showing an uneven surface and lacking expansions; and segment D, with a smooth surface and decreasing diameter. The significance of this original structure in a spermatozoon, considered immobile until now, is discussed, stating different hypotheses with regard to the possible mobility of the cell just before fertilization takes place.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Gamete Research 2 (1979), S. 283-293 
    ISSN: 0148-7280
    Keywords: in vitro fertilization ; mouse ; second polar body formation ; second meiotic division ; spindle ; polarizing microscopy ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The second meiotic division and polar body formation in mouse eggs fertilized in vitro were observed by phase-contrast and polarizing microscopy, and recorded by time-lapse cinematography. Eggs were collected from oviducts of mice that had been superovulated by injections of PMS and HCG. Some eggs, inseminated with spermatozoa that had been collected from caudae epididymides of mature male mice and cultured for two to three hours before insemination, were observed continuously on a glass slide under a phase microscope. Other eggs were inseminated in Petri dishes in a 5% CO2 incubator and examined every 20 minutes for 180 minutes. Compatible results in both sets of eggs showed that formation of the second polar body began 25-40 minutes after fusion of spermatozoon with the vitellus; it was completed 40-60 minutes later; anaphase II lasted approximately five minutes before the appearance of the furrow abstricting the second polar body. It is suggested that the furrowing associated with second polar body formation is guided by the same kind of forces that divide a cell mitotically.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Gamete Research 2 (1979) 
    ISSN: 0148-7280
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Gamete Research 2 (1979), S. 193-199 
    ISSN: 0148-7280
    Keywords: double spermatozoa ; human prolactin-secreting adenoma ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: In a man with a pituitary prolactin-secreting adenoma almost only double spermatozoa were produced. These cells were almost completely enveloped in a unique membrane, a common bilocular acrosome capped two paired nuclei, and all the other organelles were double. After 120 days of treatment with 2-brom-α-ergocryptine the prolactin level was corrected, and only normal, single spermatozoa were produced. The authors suggest that a high prolactin level inhibits cell division.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Gamete Research 2 (1979), S. 201-206 
    ISSN: 0148-7280
    Keywords: zona pellucida ; antibody ; ovary ; calf ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Treatment of bovine ovary sections with rabbit antibovine zona serum followed by fluorescein-conjugated goat antirabbit IgG produced a specific fluorescent staining only of the zonae pellucidae. Fluorescence was greater near the inner and outer surface of the zona, suggesting that either the same antigen occurs in higher concentration in these regions or that there is more than one antigen, the most immunogenic being located peripherally. In some atretic follicles fluorescent material appeared to diffuse into the degenerating oocyte and into the intercellular spaces of the cumulus oophorus.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Gamete Research 2 (1979), S. 213-222 
    ISSN: 0148-7280
    Keywords: urethan effect ; cleavage induction ; parthenogenesis ; sea urchin ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The effect of urethan on artificial induction of cleavage in eggs of the sea urchin, Hemicentrotus pulcherrimus, was studied. When the eggs were exposed for 20 minutes to seawater containing urethan (final concentration, 0.08 M) after butyric acid-activation and then treated with hypertonic seawater, the cleavage rate was enchanced by about 1.5 times as compared with the nontreated eggs. In the eggs exposed to urethan-seawater for over 70 minutes many clear spots appeared throughout the cytoplasm. Simultaneously, the pigment granules, which had been embedded within the cortex, migrated to the inner cytoplasm and encircled a monastral centrosphere and clear spots. The clear spots were composed of microtubules much like cytasters, and in the central region of them centrioles were not yet found. The eggs in which the pigment granules disappeared from the cortex may be more susceptible to cleavage induction by succeeding hypertonic treatment.
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  • 11
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Gamete Research 2 (1979) 
    ISSN: 0148-7280
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
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  • 12
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Gamete Research 2 (1979), S. 35-42 
    ISSN: 0148-7280
    Keywords: activated motility ; temperature dependence of motility ; sperm transport ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The motility of rabbit spermatozoa recovered from the vagina, endocervix, uterus, and four regions of the oviduct was assessed visually by phase-contrast microscopy at intervals from one minute to 16 hours after a single mating. The percentage of motile cells in each sample was dependent on the temperature of recovery, ie, 23° vs 37°C, but was not influenced by the temperature of observation. Spermatozoa in the lower isthmus of the oviduct were the most temperature sensitive population to recovery at 23°C. When all manipulations and observations were performed at 37°C, the percentage of spermatozoa with progressive motility varied according to the region sampled and interval after mating. Populations from the vagina, uterus and upper regions of the oviduct usually had a high proportion of progressively motile cells with vigorous flagellar activity. Fewer spermatozoa showed progressive movement on recovery from the endocervix and lower 2 cm of the tubal isthmus and their flagellar activity was generally depressed. The decrease in flagellar beat frequency noted in the latter regions may be a major factor limiting sperm ascent in the female tract. A unique pattern of “activated” motility was seen exclusively in populations taken from the oviducts at 6 to 16 hours after mating. This motility pattern, consisting of alternating episodes of linear progressive and vigorous nonprogressive movement, may be analogous to the activated motility described for capacitated rodent spermatozoa.
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  • 13
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Gamete Research 2 (1979), S. 75-87 
    ISSN: 0148-7280
    Keywords: acrosin ; activation ; inhibitor ; proacrosin ; spermatozoa ; zymogen ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The sperm-specific proteinase acrosin (EC 3.4.21.10) is found in spermatozoa as a zymogen. We have looked for different forms of this zymogen in testicular, epididymal, and ejaculated spermatozoa from ram and have compared total sperm extracts made immediately after cell disruption with extracts made later from isolated sperm heads. We have concluded that the autoactivatable zymogen form, known generally as proacrosin, is the only form of acrosin within intact mature ram spermatozoa; no other zymogen form was detected, although lower levels of proacrosin were found in some samples of testicular spermatozoa. From studies of the activation process, it appears that ram proacrosin is truly autoactivatable; no evidence could be found for the involvement of any auxiliary enzyme. Estimations of the molecular weight of proacrosin using gel chromatography (60,000) and SDS-polyacrylamide gel electrophoresis (51,300) indicated that the zymogen is monomeric. Comparison with the molecular weight of ram acrosin (44,000 or 40,000, using the two respective methods) indicated that a single acrosin molecule is derived from each zymogen molecule. The sperm acrosin inhibitor (molecular weight 11,000 or 8,000) was present in testicular spermatozoa as well as in ejaculated spermatozoa; there was no evidence that it was produced as a result of zymogen activation.
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  • 14
    ISSN: 0148-7280
    Keywords: spermatozoon-ostracoda (Heterocypris incongruens) ; external morphology ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: In various papers on the original spermatozoon of the Ostracoda, its helicoidal disposition has been indicated as the principle characteristic of this gamete, at cell structure level as well as in its external morphology. Through a combined study with scanning electron microscope (SEM) and transmission electron microscope (TEM), we have been able to establish the corresponding relationship between the cell architecture and the spermatozoon's external morphology. In the case of Heterocypris incongruens, the helicoidal relief of the gamete's external surface along the greatest part of its length, is the result of the twisting and undulating of a structure derived from the nucleus' external membrane, endoplasmic reticulum, and Golgi apparatus, called “feather-like organelle.” In keeping with the shape of this surface relief, the spermatozoon can be divided into three regions: An anterior one with a corkscrew form, a middle one showing a relief in the form of a screw with four threads, and a posterior or tail one without helicoidal relief. Finally, we discuss the different criteria existing on the possible orientation of this spermatozoon when it moves, as well as the functional advantages that the possession of a filiform, helicoidal, and mobile gamete represents.
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  • 15
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Gamete Research 2 (1979), S. 121-124 
    ISSN: 0148-7280
    Keywords: oocyte maturation ; LH ; ovum culture ; germinal vesicle breakdown ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Immature rats, aged 27 days, were stimulated to develop preovulatory follicles by subcutaneous injection of 15 IU of pregnant mare serum gonadotrophin (PMSG). Two days later their oocytes were collected. They were cultured under conditions that permitted continuous observation. Times of the initial stages of maturation were carefully noted, in the absence and the presence of 10 μg/ml of bovine luteinizing hormone (LH). LH did not accelerate germinal vesicle disappearance. It was concluded that the immature PMSG-treated rat was not an appropriate model for the study of LH action; it was speculated that persistence of PMSG mimicked LH in all the oocytes from such donors.
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  • 16
    ISSN: 0148-7280
    Keywords: lysin ; protease inhibitor ; sea urchin ; vitelline coat ; fertilization ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: To search the spermatozoa of sea urchins for their lysins, the eggs were inseminated in the presence of various protease inhibitors. Among them, two chymotrypsin-specific inhibitors, chymostatin and N-tosyl-L-phenylalanyl-chloro-methane, as well as p-nitrophenyl p′-guanidinobenzoate, inhibit fertilization of the sea urchins, Hemicentrotus pulcherrimus and Strongylocentrotus intermedius.A chymotrypsin-like protease is presumed to be a lysin of the sea urchins, since the inhibition of fertilization by chymostatin is remarkably diminished if the eggs are pretreated with trypsin or chymotrypsin to break the vitelline coat before insemination, and since N-tosyl-L-phenylalanyl-chloromethane, and p-nitrophenyl p′-guanidinobenzoate, as well as chymostatin, inhibit the fertilization.In all the sea urchins so far studied, elevation of fertilization envelopes is inhibited by leupeptin, antipain, soybean trypsin inhibitor, and p-nitrophenyl p′-guanidinobenzoate, all of which are potent trypsin inhibitors.Synthetic inhibitors have cytotoxic side effects on the eggs, but the microbial and plant inhibitors have no such effects.
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  • 17
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Gamete Research 2 (1979), S. 223-233 
    ISSN: 0148-7280
    Keywords: seminal plasma DNase ; nicked sperm DNA ; sperm decondensation ; DNA template ; DNA phosphorylation ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Ejaculated rabbit spermatozoa washed with buffer prior to decondensation by Triton X-100 and dithiothreitol were good templates for DNA synthesis by Escherichia coli DNA polymerase. This result agrees with the observations of Zirkin and Chang [1977], and implies that the sperm DNA is nicked. Template activity, however, was reduced if spermatozoa were extensively washed before decondensation, and if DNase inhibitors EDTA or Na2SO4 were present during decondensation. Template activity was also low if decondensation was induced with DNase inhibitors thioglycollic acid, Na2SO3 or sodium dodecylsulphate and dithiothreitol instead of with Triton X-100 and dithiothreitol. Calf thymus DNA was completely degraded when incubated with rabbit seminal plasma or buffer-washed spermatozoa, but much less degradation was observed if EDTA, Na2SO4, thioglycollic acid, Na2SO3 or sodium dodecylsulphate were also present, or if spermatozoa were extensively washed with buffer. Centrifugation of spermatozoa through 2.05 M sucrose completely removed contaminating DNase, and such spermatozoa were inactive as DNA templates after decondensation. The DNA template activity of swollen rabbit sperm nuclei thus parallels the activity of a contaminating seminal plasma DNase. This suggest that the nicks in sperm DNA enabling it to act as a template for DNA synthesis were generated by the DNase during decondensation and thus are not a natural structural feature of the DNA. The presence of breaks in the DNA of decondensed buffer-washed spermatozoa (DNase contaminated) was confirmed by their incorporation of phosphate from [γ-32 P] ATP in the presence of the enzyme polynucleotide kinase. These spermatozoa were found to contain as few as two breaks/mole of DNA, but sucrose-washed spermatozoa (DNase free) were free of breaks. The possible use of this enzymic procedure for the assessment of sperm genome damage and the evaluation of the quality of a sperm population are discussed.
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  • 18
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Gamete Research 2 (1979) 
    ISSN: 0148-7280
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
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  • 19
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Gamete Research 2 (1979), S. 265-282 
    ISSN: 0148-7280
    Keywords: sperm chromatin ; nuclease digestion ; sperm decondensation ; chromatin structure ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The structure of rabbit, fowl, and Xenopus laevis sperm chromatin was explored by study of the reaction of their decondensed nuclei with DNase 1 and micrococcal nuclease. Those of rabbit and fowl were readily digested by DNase 1, and the polyacrylamide gel electrophoresis profiles of DNAs extracted from the digests were similar, each being polydisperse with a single discrete band of DNA smaller than 72 base pairs. There were differences, however, between the sperm chromatins in the course of their digestion by micrococcal nuclease. A limit digest at about 45% acid solubility was obtained with Xenopus sperm chromatin, while 90% of fowl sperm DNA was rendered acidsoluble by the enzyme. The gel profiles of the limit digests were polydisperse, but only those of rabbit and fowl sperm chromatins possessed a discrete band of DNA smaller than 72 base pairs. Bleomycin did not react with DNA of rabbit, fowl, or Xenopus spermatozoa. Since bleomycin reacts with somatic cell chromatin, and the course of DNase 1 or micrococcal nuclease digestion of sperm chromatin was different from that found for somatic cell chromatin, it would appear that sperm chromatin does not have the repeating nucleosometype structure of somatic cell chromatin. The nuclease digestion studies further suggest that the organization of rabbit and fowl sperm chromatins is similar, and is different from that of Xenopus sperm chromatin. The dependence of the structure of sperm chromatin on the composition of its basic proteins, and a possible structure for a protamine-type sperm chromatin, are discussed.
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  • 20
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Gamete Research 2 (1979), S. 295-304 
    ISSN: 0148-7280
    Keywords: in vitro fertilization ; mouse ; sperm penetration ; zona pellucida ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Sperm penetration through the zona pellucida and fusion of the sperm head with the vitellus were observed continuously and filmed under phase optics in cumulus-free living mouse eggs inseminated in vitro with capacitated epididymal sperm. Most spermatozoa penetrated the zona pellucida, traversed the perivitelline space, and fused with the vitellus at an angle nearly perpendicular to the surface. The mean duration required for sperm to penetrate the zona pellucida was 20 minutes with a range of 15-26 minutes. Sperm traversed the perivitelline space in less than one second. The initial contact of sperm with the vitellus generally took place at the tip of the sperm head. When the tip of the sperm head contacted the vitellus there was an immediate reduction in the rate of flagellation, followed by the gradual sinking of the sperm head into the vitellus.
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  • 21
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    New York, NY : Wiley-Blackwell
    Gamete Research 2 (1979), S. 357-366 
    ISSN: 0148-7280
    Keywords: ova ; spermatozoa ; cryopreservation ; fertilization ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Mature unfertilized ova from superovulated hamsters were freed from all investments and frozen at -50°C. They were cooled at about 1°C/min to 0°C then at 0.8° to 0.6°C/min to -50°C. At 0°C, dimethyl sulfoxide was added to a final concentration of 1.25 M. The ova were stored at -50°C for up to four months. Thawing was performed at 2-4°C/min and followed by several washes with insemination medium. Approximately 90% of the ova were normal in appearance after thawing. The frozen and thawed ova with normal appearance could be penetrated by hamster or human spermatozoa at a rate comparable to unfrozen controls. The ability of hamster ova to tolerate storage at a relatively convenient temperature (-50°C) for long periods (tested for up to four months) makes possible their shipment at low cost to institutions lacking this resource. There they can be used for basic biological studies of sperm-egg interaction or in the clinical assessment of human sperm quality.
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  • 22
    Electronic Resource
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    New York, NY : Wiley-Blackwell
    Gamete Research 2 (1979), S. 1-13 
    ISSN: 0148-7280
    Keywords: capacitation ; acrosomal enzymes ; rabbit sperm ; acrosomal membranes ; fertilization ; lysosomal enzymes ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Significant release of the acrosomal enzymes arylsulfatase, β-N-acetylhexosaminidase and hyaluronidase was observed following the treatment of ejaculated rabbit spermatozoa for 12 hours in 20% rabbit serum for inducing in vitro capacitation, and these sperm were capable of in vivo fertilization; however, the treatment of sperm for 15 minutes in high ionic strength (380 mOsm/kg) or low ionic strength medium (305 mOsm/kg) for in vitro capacitation did not result in any significant release of the above enzymes nor were the sperm capable of in vivo fertilization. Serum-treated spermatozoa remained significantly motile following the 12 hour treatment, 51% underwent the acrosome reaction and were capable of fertilizing 66% of the ova in vivo. Identical serum treatment of lysosomes from rabbit liver resulted in a comparable release of the lysosomal enzymes. Serum treatment for in vitro capacitation resulted in vesiculation of the anterior margin of half the spermatozoa, but left their inner acrosomal membranes and equatorial segments intact. A biochemical relationship between the release of acrosomal enzymes and capacitation is suggested.
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  • 23
    ISSN: 0148-7280
    Keywords: fertilization ; acrosome reaction ; sea urchins ; cross-fertilization ; species specificity ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Sperm of Hemicentrotus pulcherrimus undergo the acrosome reaction in the jelly coat or on the surface of the vitelline layer of Pseudocentrotus depressus eggs and can fertilize the latter, whereas those of P depressus do not undergo the acrosome reaction even after they strike the vitelline layer of H pulcherrimus eggs and cannot cross-fertilize.In the latter combination, however, if cross-insemination is performed in the presence of homologous egg water, cross-fertilization becomes less difficult than in normal seawater, and percentage cross-fertilization rises as does percentage acrosome reaction. It is suggested that the cross-fertilizability of this combination depends highly on the inductivity of the acrosome reaction. The reason why such a causal relation is observed is discussed.
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  • 24
    Electronic Resource
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    New York, NY : Wiley-Blackwell
    Gamete Research 2 (1979), S. 25-34 
    ISSN: 0148-7280
    Keywords: spermatozoa ; spermiogenesis ; male germ cells ; centriole ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: In the course of the reorganization and degeneration of the proximal centriole in the mature acentriolate spermatozoon of the Mongolian gerbil, both the proximal and distal centrioles appear in the early cap phase of spermatid development. During the acrosome phase, both distal and proximal centrioles become highly active in the formation of a segmented column. The proximal centriole becomes actively involved in the formation of the capitulum, while the distal centriole forms the axonemal complex and dense fibers. During the maturation phase of spermatid development, the “pinwheel” arrangement of the proximal centriole becomes an “S”-shaped structure, turned 90° on its vertical axis. The few “doublet” microtubules that can be detected later in that stage completely disappear during spermiation. The distal centriolar area develops a single central pair of microtubules and membranous elements. Another prominent feature in the neck region of the gerbil spermatozoa is the presence of two dense rudimentary columns in association with the mitochondria. Although their density is similar to that of the other columns, these two columns have no connection with the dense fibers; in fact, they are closely associated with the mitochondria.
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  • 25
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    Gamete Research 2 (1979), S. 53-64 
    ISSN: 0148-7280
    Keywords: spermatozoa ; plasma membrane ; glycoproteins ; free acidic groups ; farm mammals ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Ejaculated spermatozoa of boars, bulls, rabbits, and rams were embedded in glycolmethacrylate and thin sections stained with phosphotungstic acid at low pH in order to observe the distribution of glycoproteins of the plasma membrane. Colloidal iron hydroxide was also used to detect the free acidic groups present on the sperm surface. Species-specific patterns of localizations of glycoproteins and linked negative charges were observed. The distribution was sometimes homogeneous as in bull, but generally heterogeneous in the other species. The significance of the results on sperm surface components and the practical interest to know their normal distribution are discussed.
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  • 26
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    Gamete Research 2 (1979), S. 43-51 
    ISSN: 0148-7280
    Keywords: spermatozoa ; acrosome ; glycoproteins ; farm mammals ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Ejaculated spermatozoa of boars, bulls, rabbits, and rams were fixed with glutaraldehyde and embedded in glycolmethacrylate. Thin sections were treated with phosphotungstic acid at low pH in order to localize cellular glycoproteins stained by the PAS technique at the light microscope level. At the ultrastructural level the glycoproteins were segregated in the anterior segment of mature spermatozoa. The distribution of these glycoproteins in the anterior segment was not homogeneous; it appeared species-specific in detail, but as a rule, the maximum concentration was observed in a superficial layer, especially in the marginal thickening. The localization of other acrosomal components (eg, crystalline and basic proteins) is also reviewed. The origin and significance of the segregation of proteins and glycoproteins in the acrosome are discussed in relation to the fact that the acrosomal enzymes analyzed so far are glycoproteins.
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  • 27
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    Gamete Research 2 (1979), S. 65-73 
    ISSN: 0148-7280
    Keywords: embryo transfer ; embryo culture ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Embryo transfer experiments were carried out to study the developmental capacity of cultured rabbit embryos when transferred to recipients of variable postovulatory maturity. Rabbit embryos were flushed from the oviduct at 26 hours postcoitum (pc) and cultured in a modified Ham's F-10 medium supplemented with bovine serum albumin (BSA) for a period of 70 hours. At 96 hours pc the cultured embryos, which ranged from the early morula to the expanding blastocyst stage, were transferred to pseudopregnant recipients mated to vasectomized males 36 to 96 hours prior to the transfer procedure. Greatest embryo survival occurred when transfers were made to either the oviducts or uterine horns of recipients at 48 hours pc. Intermediate results for both implantation rates and number of young born were obtained with recipients at 36, 60, 72, and 84 hours pc. Transferred embryos consistently failed to survive the uterine environment of recipients 96 hours pc at transfer although this group was synchronous with embryonic chronological age. Oviductal transfers were generally more successful than uterine transfers. Markedly higher rates of embryo survival resulted from embryos that were collected 60 and 72 hours pc and transferred directly to synchronous recipients without an interim period of culture. Dissimilarity of development for in vivo grown rabbit embryos and those cultured in synthetic medium is demonstrated.
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  • 28
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    Gamete Research 2 (1979), S. 99-104 
    ISSN: 0148-7280
    Keywords: sperm penetration ; premature cortical reaction ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The method of in vitro fertilization was applied to test a previous suggestion that the lowered fertilizability of the tubal oocytes of female KE strain mice and the high resistance of their zona pellucida to proteolytic enzymes, are due to the premature cortical reaction taking place near the time of ovulation. Therefore higher fertilizability of ovarian oocytes is expected.The effectiveness of F1 hybrid sperm penetration into ovarian and tubal KE oocytes confirmed these assumptions. The ovarian KE oocytes recovered 9-10 hours after administration of human chorionic gonadotropin (HCG) showed significantly higher penetrability (70-83%) than did the tubal oocytes recovered 12 hours after HCG (about 50%) and 14-16 hours after HCG (20%).Similar results were obtained with C57 oocytes. Sperm penetration into ovarian oocytes (10 hours after HCG) was much more effective (67%) than into tubal oocytes (18%); this finding correlated with more rapid zona dissolution by chymotrypsin. On the basis of these results one might speculate that premature cortical reaction takes place also in the C57 strain.
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  • 29
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    Gamete Research 2 (1979), S. 105-105 
    ISSN: 0148-7280
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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  • 30
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    Gamete Research 2 (1979) 
    ISSN: 0148-7280
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
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  • 31
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    Gamete Research 2 (1979), S. 137-145 
    ISSN: 0148-7280
    Keywords: progesterone-induced maturation ; methylxanthines ; chloera toxin ; phosphorylation ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: During the course of maturation of Xenopus laevis oocyte a burst of phosphorylation occurs around germinal vesicle breakdown. At the same time a relative drop in a unique phosphoprotein (protein I; mot wt ∼40,000) is observed. Enucleation of [32P] labeled oocytes has shown the cytoplasmic localization of protein I. Methylxanthines and cholera toxin, which inhibit progesterone-induced maturation, block the burst of phosphorylation and do not change the amount or the distribution of [32P] phosphoproteins.
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  • 32
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    Gamete Research 2 (1979), S. 125-135 
    ISSN: 0148-7280
    Keywords: oogenesis ; oocyte growth ; Xenopus laevis ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: When female Xenopus laevis are injected with [3H]-vitellogenin or [14C] N-acetyl glucosamine, most of the labeled material becomes associated three days later with oocytes having a diameter of 0.9-1.1 mm; smaller and larger oocytes are less labeled. With time, the pattern of labeling shifts to larger oocytes, indicating that those oocytes initially labeled continue to grow. We have measured such shifts as a function of time to provide estimates for oocyte growth rates from the end of stage III (diameter = 0.6 mm) to stage VI (diameter = 1.2 mm). The total time required for oocytes to progress through this size increase is 16-24 weeks in unstimulated females and 9-12 weeks in human chorionic gonadotropin (hCG)-stimulated females. The fastest rate of growth occurs from mid-stage IV (approximately 0.8 mm diameter) until midstage V (1.2 mm diameter), which corresponds to the period of most pronounced vitellogenin uptake. The relative proportion of oocytes within this size range is also reduced, as predicted under steady-stage conditions. Evidence is also presented which indicates that the steady-state level of full-grown oocytes is maintained by a combination of replenishment and atresia. These results provide the first description of the kinetics of oocyte growth in X laevis females maintained under normal laboratory conditions and should be useful for any considerations of macromolecular events occurring during oogenesis.
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  • 33
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 1-7 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of thermal polymerization of methyl methacrylate initiated by the redox system Mn(III)-glycerol was studied in aqueous sulfuric acid in the temperature range of 30-40°C, and the rates of polymerization, Rp, and Mn3+ disappearance, etc., were measured. The effect of certain water-miscible organic solvents and certain cationic and anionic surfactants on the rates of polymerization has been investigated. A mechanism involving the formation of a complex between Mn3+ and glycerol whose decomposition yields the initiating free radical with the polymerization being terminated by the metal ion has been suggested.
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  • 34
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 9-18 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Eleven N-substituted carbazoles (CZ) with terminal vinyl groups were synthesized by five sequences of reaction: N-(p-vinylbenzyl)- and N-β-(vinyloxyethyl)CZ by N-alkylations of potassium CZ with corresponding chlorides; N-(β-acryloyloxyethyl)CZ by the esterification of N-(β-hydroxyethyl)CZ with acryloyl chloride; N-acrylamido-or methacryl-amido-methyl CZ from N-hydroxymethyl CZ and acryl- or methacrylamide; N-(3-acryloyl- or methacryloyl-oxy-2-hydroxypropyl)CZ and N-[3-(p- or m-vinylanilino)-2-hydroxypropyl] CZ from N-(2,3-epoxypropyl)CZ and acrylic or methacrylic acid and p- or m-vinylaniline, respectively; and 2-[β-(N-carbazyl)propionyloxy]ethyl acrylate or methacrylate by the Michael addition of CZ to 2-hydroxyethyl acrylate or methacrylate, followed by esterifications. The vinyl polymers with pendant carbazyl groups more or less distant from the polymer backbones, prepared by conventional radical or cationic polymerization procedures, indicated charge-transfer spectra with 2,4,7-trinitrofluorenone (TNF) in tetrahydrofuran (THF) solutions that are spread over most of the visible range.
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  • 35
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 69-80 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polymerization of tetrahydrofuran (THF) in CH3NO2 solvent was initiated with 1,3-dioxolan-2-ylium cations with AsF6- and SbF6- anions, as well as with esters of FSO3H and CF3SO3H acids. Polymerization shows in this solvent a living feature: values of kp (determined directly from the semilogarithmic kinetic plots) were the same for all of the listed above initiators; thus kp is the same for AsF6-, CF3SO3-, FSO3-, and SbF6- anions. The identity of the kp values for complex and noncomplex (ester-forming) anions comes from the fact that in CH3NO2 solvent equilibrium between macroesters and macroion pairs is shifted almost completely (Ke = 33.0 at 25°C and |THF|0 = 7.0M) to the macroions side. Dissociation constants of the polytetrahydrofuranium ion pairs (CF3SO3- and SbF6- anions) were measured (e.g., KD = 2 × 10-3 M at 25°C and |THF|0 = 7.0M; i.e., at D = 22.8, ΔHD = -3.8 ± 6 kcal mole; ΔSD = -25 ± 2 eu). On the basis of the known values of KD, and therefore dissociation degrees α, rate constants of propagation on the free and paired THF cations (kp+ and k+±) were determined for a large range of degrees of dissociation (α from 0.15 to 0.52). The rate constants kp+ and kp± were found to be the same within an experimental error of measurements (± 15% of the value of kp). Apparently, the polytetrahydrofuranium cations are highly solvated or even separated from their anions by molecules of THF itself. At these conditions the reactivities of the solvated “free” and solvated (or separated) paired cations became undistinguishable.
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  • 36
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Poly(N-aryl maleimide)s of characteristic structures have been synthesized and some of their physical properties studied. These include N-(2-fluoro phenyl), N-(3-fluoro phenyl), N-(4-fluoro phenyl), N-(2,4-difluoro phenyl), N-(2,5-difluoro phenyl), N-(2,3,5,6-tetrafluoro phenyl), and N-(pentafluoro phenyl). The polymerization of N-(fluoro phenyl) maleimides by free-radical initiation in bulk or in solution and by anionic catalyst have been studied to compare the characteristics of polymerization by γ-ray irradiation with that by free-radical initiation. The polymers were characterized by elemental analysis, intrinsic viscosity, spectroscopy (IR and NMR), programmed thermogravimetric analysis, and x-ray diffraction. Spectra of polymers prepared by radiation and anionic polymerization were nearly identical with those of polymers prepared by free-radical polymerization initiated by AIBN in bulk or in solution and by the self-initiated thermal polymerization. A variety of reaction conditions were tried, but all attempts to change the molecular structure of the polymers were unsuccessful. Rates of thermal degradation for poly[N-(fluoro phenyl) maleimide]s have been analyzed by using a multiple-heating-rate procedure. Overall activation energy, order of reaction, and frequency factor have been evaluated. On the basis of the comparison between the overall activation energy of the thermal degradation of poly[N-(fluoro phenyl) maleimide]s and NMR spectra of their corresponding monomers, it can be concluded that the 1H shifts due to ethylenic protons are so characteristic in sign and magnitude as to be useful in thermal stability elucidation. Some qualitative explanations were given on the stability of these polymers as affected by the type and size of the substituent. The x-ray diffractograms of all samples show two rather broad peaks indicative of noncrystalline structures. The location of the peaks does not depend upon preparation conditions and temperature. Poly(N-maleimide)s of fluoroanilines have not been hitherto described.
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  • 37
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 97-109 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The triethylamine-initiated polymerization of glycine-NCA [N-carboxylic acid anhydrides (oxazolidine-2,5-diones)], L-alanine-NCA, and sarcosine-NCA, as well as the pyridine-initiated polymerization of sarcosine-NCA, were carried out in the presence of potential cocatalysts. The 11 electrophilic reagents tested in this work can be divided into two classes: N-acyllactams and similar compounds, which are less reactive than the monomers and have no influence on the polymerization; and isocyanates and N-acyl-NCAs or -NTAs [N-thiocarboxylic acid anhydrides (thiazolldine-2,5-diones)], which are more electrophilic than the monomers and behave as cocatalysts in the case of glycine-NCA and alanine-NCA, since their base-initiated polymerization proceeds via the attack of NCA anions on the electrophilic N-acyl NCA chain and (“activated monomer mechanism”). In the case of sarcosine-NCA, however, the propagation involves a nucleophilic chain end (“carbamate mechanism”) and the strong electrophilic reagents behave as inhibitors.
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  • 38
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The size, distribution, and number of PTFE particles formed by radiation-induced emulsifier-free polymerization were measured by electron microscope and automatic particle analyzer (centrifugation method). From the electron micrographs we found that the particles are formed within 5 min. The change in the number of polymer particles (np) with reaction time (t) depends on the relative concentration of growing polymer chains to stabilizing species produced by the radiolysis of water and monomer; that is, it was governed by TFE pressure/dose rate ratio and classified into three cases: case I, dnp/dt = 0 (e.g., at 3 × 104 rad/hr and 20 kg/cm2); case II, dnp/dt 〈 0 (e.g., at dose rate below 1.9 × 104 rad/hr and 20 kg/cm2); case III, dnp/dt 〉 0 (e.g., at 3 × 104 rad/hr and 2 kg/cm2). The polymer molecular weight above 106 is almost independent of the particle size. The polymerization loci are mainly on the surface of polymer particles dispersed in the aqueous phase in cases I and II except in the initial stage. In case III new particles are formed successively during polymerization. Therefore the polymerization loci are mainly in the aqueous phase. Especially in case I, we concluded that after the generation of particles the propagation proceeds mainly on the surface of polymer particles like the core shell model proposed by Granico and Williams.
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  • 39
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 139-145 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reaction of poly(vinyl chloride) (PVC) with superoxide anion was carried out in tetrahydrofuran (THF) at 40°C in a nitrogen atmosphere. Remarkable changes in infrared (IR) spectra of the samples treated with superoxide anion were observed in the following regions: ca. 3300, 1680, 1620, and 765 cm-1, which suggested the formation of hydroxyl groups, α,β-unsaturated ketone groups, and ethylenic structures. Ultraviolet-visible spectra also showed the formation of polyene structures. The content of chlorine in the polymer decreased and that of oxygen increased with reaction time. The reaction mechanism was discussed on the basis of these results.
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 147-154 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In order to assess the effect of the methylol group at the 4-position of 1,3-dioxolane on polymerization, the photopolymerization of 2-vinyl-4-hydroxymethyl-1,3-dioxolane (VHDO) was carried out in benzene at 40°C. The reaction scheme of VHDO was considered to be the same as that of 2-vinyl-1,3-dioxolane (VDO). The rate of polymerization and the molecular weight of polymer were small because of the degradative chain transfer by allylidene group. Moreover, the rate of polymerization of VHDO was greater than that of VDO, whereas the molecular weight of polymer of VHDO was less than that of VDO.
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  • 41
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 155-162 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: To determine the content of trans-gauche-trans (TGT) conformation in poly(ethylene glycol) (PEG) 1H-NMR spectra were measured with tris(1,1,1,2,2,3,3-heptafluoro-7,7-dimethyl-1,4,6-octanedinato)europium(III) [Eu(fod)3] as a shift reagent. As a result the peaks assigned to the ethylene protons in the polymeric segments separated from those assigned to four ethylene protons as the “near-end” groups, and the singlet peak in the former at the lowest field was assigned to the TGT conformation of the COCCOC sequence. It was confirmed that the conformation of the polymeric segments in PEG complexed with Eu(fod)3 remained unchanged with benzene-d6 content as the solvent. The concentration of TGT conformation increased with the number-average molecular weight (Mn): it increased rapidly until about 70% at Mn = 1500.
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  • 42
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 129-138 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Simultaneous formation of hydrofluoric acid (HF) in the radiation-induced polymerization of tetrafluoroethylene (TFE) was investigated. HF concentration in PTFE latex was determined mainly by conductometric titration with 0.01 and 0.001N NaOH. The amount of HF formed is almost independent of agitation speed and the amount of n-hexadecane added and is maximal at ca. 70°C corresponding to the rate of polymerization.The rate of HF formation increases with the initial pressure of TFE monomer and dose rate and decreases with polymerization or TFE consumption. This fact suggests that HF is formed mainly by TFE reactions and not by the degradation of PTFE.The mechanism of HF formation in this reaction system in the absence of oxygen is shown in the following two schemes: scheme I is the reaction of TFE with primary radicals (OH·, H·, eaq-) from the radiolysis of water; scheme II is the reaction of water with the species from the radiolysis of TFE. On the assumption that HF is formed only according to scheme I, the G value of HF formation G(HF)calc can be calculated as 11.25. All observed G values G(HF)obs are larger than G(HF)calc. When the polymerization is carried out at 20 kg/cm2 under various dose rates, G(HF)obs increases with the dose rate. When the polymerization is carried out at 3.0 × 104 rad/hr under various pressures, G(HF)obs decreases with the decrease in pressure from 20 to 2 kg/cm2 and is fairly close to G(HG)calc at 2 kg/cm2. This indicates that HF formation is due mainly to scheme II at high pressure (in the presence of enough TFE) and to scheme I as the pressure is lowered.
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  • 43
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 163-172 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polybenzimidazoles (PBI) with p-phenylene and/or cis-vinylene groups in the backbone were prepared from terephthalic acid (T), maleic acid (M), and 3,3′ diamino-benzidine tetrahydrochloride dihydrate (DAB) in poly(phosphoric acid) (PPA). Five polymer samples were prepared by varying the M:T molar ratios in the following order: 1:0, 1:1, 2:1, 1:2, and 1:4. The polymers were characterized by intrinsic viscosity, density, electronic fluorescence, and IR spectra. The effect of composition on the solubility of the polymers in various organic solvents was also investigated. The relative thermal stability of the polymers was evaluated by dynamic thermogravimetry in air and polybenzimidazoles (PBI) with cis-vinylene groups were found to be less stable.
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  • 44
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 193-202 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Potentiometric titrations in water of high-molecular-weight partly hydrolyzed polyacrylamides were analyzed by the Lifson - Katchalsky rodlike model. A fair concordance was found between theory and experimental curves with pK0 of acid functions of about 4.75 when 0 〈 τ 〈 0.49. Two methods were derived to calculate the parameter n of the extended Henderson-Hasselbach equation by using a series expansion of pKa vs. α, not yet reported in the literature. A new equation for n was established and comparison between two sets of values of n, obtained by using the theoretical ΔpK curves and series expansion is discussed.
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  • 45
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 271-275 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 46
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 255-266 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Alternating polyampholytes (MA-VA) containing two acidic groups and one basic group were prepared by the copolymerization of maleic anhydride (M1) and N-vinylsuccinimide (M2) at 60°C with AIBN as the initiator, followed by acid hydrolysis with 1N hydrochloric acid at 140°C for 24 hr. The monomer reactivity ratios r1 and r2 are 0.025 and 0.06, respectively. The structure of polymers was discussed on the basis of the data of their elementary, infrared (IR), and thermal analyses and the binding ability of heavy metal ion. Polyampholytes were soluble in strong acidic and basic media but were precipitated in the pH range 3-4. An isoelectric point at pH 3 was determined by potentiometric titration and the turbidimetric method. By thermal treatment above 205°C the polyampholyte turned quantitatively into a cyclized lactam. This suggests that the polyampholyte MA-VA has an intramolecular hydrogen bond between the amino and γ-carboxyl groups. The binding of Cu2+ and Hg2+ by the polyelectrolyte was evaluated by equilibrium dialysis.
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  • 47
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 277-279 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
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  • 48
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 287-291 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 281-286 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
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  • 50
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 293-297 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 51
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 313-318 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new, easily processed, organic semiconductor was prepared from poly(vinyl alcohol) (PVA). The Cu2+ chelate of PVA exhibited excellent surface resistivity around 103 Ω cm-2 when modified with iodine. Favorable conditions for preparing the chelate effective for the conduction were investigated. The resistivity was significantly affected by the amounts of cupric salts and iodine, satisfactory results being given by more than 15 wt% of cupric salts and about 4 wt% of iodine. Effects of molecular weight of PVA and the chelate structure were also studied.
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  • 52
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 301-312 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Behavior of the free radical copolymerization of N-β-methacryloyloxyethyl derivatives of adenine with that of thymine was studied in chloroform solution, taking account of the specific base-base interaction of these monomers. Hydrogen bonding interaction between such monomers was observed by NMR spectroscopy. The acceleration of copolymerization was found to be greater either at lower monomer concentration or at lower polymerization temperature. When N-β-methacryloyloxyethylcarbazole was used as a comonomer, the rate of copolymerization showed a similar trend as in the case of usual free radical copolymerizations. From r1 and r2 values obtained, the copolymerization was found to be alternating, particularly in the case of copolymerization between monomers having complementary nucleic acid bases. The results suggest that the hydrogen bonding interaction between adenine and thymine plays a role in the propagation step.
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  • 53
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 331-349 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1-Methyl-3-methylenecyclobutene (MMCB) and 1,2-dimethylenecyclobutane (DMCB) copolymerized readily with isobutene with aluminum chloride as initiator in methyl chloride solution at temperatures from -95 to -78°C. No polymers were obtained with methylenecyclobutene (MCB) under similar conditions. The copolymerization of MMCB with isobutene took place through a 1,5-addition reaction while that of DMCB through both 1,2- and 1,4-addition reactions. Large amounts of gel were present in the copolymers obtained from DMCB if the reaction was carried to high conversion. The commonly observed effects of dienes (i.e., rate retardation and molecular weight depression) on cationic copolymerization reactions were observed but to a much higher degree with these small ring dienes. The thermal crosslinking behavior of the resulting copolymers was investigated. In conjunction with the copolymerization studies, homopolymers of MMCB, DMCB, and 3,3-dimethyl-1-isopropylidene-2-methylenecyclobutane (IMCB) were prepared and their chemical structures examined.
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  • 54
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 377-384 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2,2,4-Trimethyl-3-on-1-pentyl methacrylate (TMPM) was first synthesized from the condensation reaction of 2,2,4-trimethyl-1-pentanol-3-on with methacrylic acid. Second, the polymerization of TMPM and the copolymerization of TMPM with styrene (St) were carried out in benzene at 60°C, using 2,2′-azobisisobutyronitrile (AIBN) as an initiator. As the result of kinetic investigation, the rate of polymerization (Rp) could be expressed by: Rp = k[AIBN]0.5 [TMPM]1.0. Kinetic constants of polymerization of TMPM were obtained as follows: kp/kt1/2 = 0.27 dm3/2 mole-1/2 sec-1/2, 2fkd = 1.23 × 10-5 sec-1, f = 0.73, Cm = 2.6 × 10-5, Cs = 1.1 × 10-5. From the results the reactivity of TMPM was found to be larger than that of methyl methacrylate. The overall activation energy was calculated to be 110 kJ mole-1. The following monomer reactivity ratios and Q, e values were obtained: TMPM(M1) - St(M2): r1 = 1.50, r2 = 0.14, Q1 = 2.63, E1 = 0.45.
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  • 55
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 393-404 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of dose rate on the rate of polymerization and molecular weight distribution of radiation-induced polymerization of styrene adsorbed on silica gel was studied in a wide dose rate range of 4.4 × 104 to 3 × 108 rad/hr by γ rays of 60Co and electron beams with a Cockcroft-Walton-type accelerator. Dose rate dependence on the initial rate of polymerization was about 1 below 3 × 107 rad/hr, and it decreased gradually at high dose rates. Throughout the dose rate range, graft polymerizations and homopolymerizations by cationic and radical mechanisms proceeded simultaneously. Dose rate dependence of the cationic polymerization was 1 below 3 × 107 rad/hr, while dose rate dependence of the radical polymerization was 0.65 below 3 × 107 rad/hr. At high dose rates, molecular weight and fraction of graft polymer decreased, and fraction of cationic polymerization increased. A very high-molecular-weight graft polymer was formed above 4.4 × 105 rad/hr at the initial stage of the polymerization. The dose rate dependence of this polymerization was larger than 1 and decreased with increase in dose rate. The polymerization seems to be related to an excitation of monomer or growing chain.
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  • 56
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 435-439 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The color stability of high nitrile polymers is increased by dienophilic stabilizers; however, the stabilization reaction is greatly affected by the presence of residual metal ions. This effect is correlated with electronegativity considerations of the metal ion. Metal ions affect the stability of the polymer whether they are used to coagulate the latex or postadded to the dry resin. Coagulation with group IIA metal ions results in polymer capable of stabilization by dienophiles. The mechanisms of stabilization and degradation in the presence of residual metals are discussed.
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  • 57
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 455-464 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the intermediates in unterminated polymerization reactions were studied. It was found that in a first-order initiation (A) all intermediates accumulate monotonically. In a second-order initiation (B) the first intermediates pass through a maximum, whereas the later ones strictly accumulate. An initiator-started polymerization can follow course A or course B, depending on the initial ratio of the concentrations of the initiator and monomer.
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  • 58
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    Topics: Chemistry and Pharmacology
    Notes: Photooxidative degradation of cellulose resulted in decreases of degree of polymerization (DP) and α-cellulose content, concurrently producing chromophoric groups; namely, carbonyl, carboxyl, and hydroperoxide groups within the polymer. Electron spin resonance (ESR) studies revealed that cellulosic carbon free radicals readily reacted with oxygen molecules at 143-160 K to produce peroxy radicals, whereas cellulosic oxygen free radicals were inert toward oxygen molecules throughout the photooxygenation reactions. At 77 K it is feasible that only photoexcited oxygen molecules reacted with cellulosic carbon free radicals to produce peroxide radicals. These radicals were themselves stabilized at 273 K by abstraction of hydrogen atoms from cellulose to produce polymer hydroperoxides. Simultaneously, new radical sites, which exhibited three-line ESR spectra, were generated in cellulose.
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  • 59
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 613-616 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
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  • 60
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 603-612 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The aqueous polymerization of methyl methacrylate with sodium bisulfite as initiator was catalyzed by PbO—SiO2, PbO (70 mole %)—SiO2 (30 mole %) with a particle size 〈 200 mesh had the highest catalytic effect. The average molecular weight obtained in the presence of amorphous PbO—SiO2 glass was higher than that obtained in the presence of crystalline PbO - SiO2 glass powder. In this system mild shaking increased the rate of polymerization. Silicon dioxide catalyzed the rate of polymerization to a higher extent than PbO, which had a slightly higher catalytic effect than lead silicate powder. The average molecular weight formed in the presence of PbO was higher than that formed in the presence of lead silicate, which in turn was higher than that formed in the presence of silicon dioxide. Increasing the initiator concentration decreased the average molecular weight. Mild shaking decreased the average molecular weight obtained when polymerization was carried out in air but increased it in a nitrogen atmosphere. Methanol decreased the conversion percentage of monomer to polymer and the average molecular weight due to its transfer reaction.
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  • 61
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 619-626 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal reaction of equimolar quantities of isophthalonitrile and o-carborane has been shown to produce an adduct oligomer of isophthalonitrile. The structure was determined to involve condensation of three to five isophthalonitrile molecules to form a triazine-type system. This type of bonding gave rise to a trimer and pentamer. Further, the reaction was a homogeneous liquid phase reaction in which o-carborane is involved in a catalytic manner in the oligomerization. The overall reaction has first-order kinetics with an activation energy of 32.2 kcal/mole.
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  • 62
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 627-638 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Sample charging phenomena arising in the ESCA experiment have been investigated for gold and polymer films of known thickness ranging from 5 Å to 20 μ deposited on gold either insulated from or in electrical contact with the spectrometer. Charging induced by a monochromatic x-ray source is typically an order of magnitude greater than that induced by a nonmonochromatized source and exhibits a marked time dependence. A novel source of secondary electrons which employs a low-power, low-pressure mercury lamp external to the spectrometer source chamber as an alternative to an electron flood gun is described, and the charging and biasing characteristics of polymer films as a function of film thickness are discussed and demonstrated to provide an extra informational dimension for the study of polymeric materials.
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  • 63
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    Topics: Chemistry and Pharmacology
    Notes: SAXS measurements on dilute solutions of polyisobutene in n-hexane (Mν = 25,600-3.55 × 106, c 〈 53 g/liter) were carried out by combining conventional slit collimation with the new cone collimation technique. With a fractionated sample (Mν = 25,600; U 〈 0.2) the radius of gyration (R = 48 Å), the cross-sectional radius of gyration (Rq = 3.9 Å), the molecular weight per unit length (M/L = 22.8 Å-1), and the Porod persistence length (a* = 8.1 Å) are found. The persistence length appears to be dependent on the molecular weight. The partial specific volume ν of polyisobutene in n-hexane also depends on the molecular weight according to ν = 1.025 + 105/Mν (cm3/g).
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  • 64
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 649-658 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The electric properties of polymer composites with highly conductive 7,7,8,8-tetracyanoquinodimethan (TCNQ) salts such as quinolinium-TCNQ complex salt (), acridinium-TCNQ complex salt (), and N-methylacridinium-TCNQ complex salt () were studied. Polyacrylonitrile (PAN), poly(N-vinylcarbazole) (PVK), and poly(4-vinylpyridine), (P4VP), etc., were chosen as matrix polymers. The resistivity (ρ) of the was 0.37 Ω cm at the content of 20 wt % in the film. When the content of was increased up to 40 wt%, a phase separation of the needle crystals was observed and the ρ value increased. When was dispersed into PAN or PVK, the separation was also observed and the samples showed low conductivity. The uniform films were obtained in the and systems, but the values of ρ were high because of the degradation of the TCNQ salts. Uniform films with the naked eye were obtained in the and systems, and the values of Ω were 0.37, 1.05, and 3.40 Ω cm, respectively. was stable even when dispersed into P4VP. The properties of the composites were influenced by the combination of the TCNQ salts and the polymers. The uniformity and the stability of the composites were necessary to obtain the high conductive composites.
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 659-672 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of ionization (α) and added salts (NaCl, CaCl2, MgCl2) on the dimensions of commercially available high-molecular-weight polyacrylamides (Mw ≃ 4 × 106), hydrolyzed at various extents (0.04 〈 τ 〈 0.49) and which have been characterized, was investigated by viscosity and light-scattering measurements performed at 25°C. The data point with evidence to the strong dependence of the chain dimensions on the charge density (ατ) and the effect of the nature and concentration of added salts. From a practical point of view it is shown that there is no advantage to using too highly hydrolyzed samples (τ 〉 0.45) in media containing large amounts of salts that lead to precipitation of polymers, especially in the presence of divalent ions.
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  • 66
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 683-692 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The crosslinking mechanism and kinetics of low-molecular-weight polybutadiene, its mixtures with maleic anhydride, and the products of its grafting with maleic anhydride and styrene, using dicumyl peroxide (DCP) as an initiator, were studied. It was shown that for all systems crosslinking is a radical polymerization of the double bonds. Modification of polybutadiene changes only the kinetic parameters of the crosslinking reaction and causes mainly a decrease of the termination step velocity. From DSC data the crosslinking reaction order, activation energy, and reaction heats were calculated.
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 673-681 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate of n-butyl vinyl ether polymerization by chromyl chloride is first order in [catalyst] and second order in [monomer]. Added H2O (after a certain concentration) and HCl increase the rate, thiophene retards the rate, while pyridine inhibits the rate. DP is independent of [chromyl chloride] and increases with increasing [monomer] up to 1M, thereafter becoming independent of it. Both rate and DP increase over the range 10-32°C and decrease at higher temperatures.
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 703-713 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polyimides with different proportions of m-phenylene and p-phenylene (or p,p′-biphenylene) were prepared by polymerizing different molar ratios of m-phenylene diamine and p-phenylene diamine (or p,p′-diaminobiphenyl) with pyromellitic dianhydride in dimethylformamide at 0°C. Chemical cyclodehydration of polyamic acids resulted in the corresponding polyimides. Polymers were characterized by infrared (IR), viscosity, and density measurements. Viscosity and density of polymers decreased with an increase on m-phenylene groups in the backbone. The thermal and thermooxidative stabilities were investigated by dynamic thermogravimetry. Stability decreased when m-phenylene groups were introduced in the backbone.
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  • 69
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 693-701 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thermoelastic (stress-temperature) measurements in elongation have been carried out on polyurethane elastomers obtained from poly(ethylene adipate), poly(ethylene maleate), poly(ethylene glycol), and 4,4′-diphenylmethane diisocyanate. The elastomers were crosslinked by an excess of diisocynate and some of them were additionally crosslinked by dicumyl peroxide. Values of the temperature coefficient d ln r02/dT of the unperturbed dimensions of the network chains and the fraction fe/f of the stress, which is due to energetic effects, were calculated from measurements of unswollen samples and samples swollen in benzene to a constant volume fraction ν2 of about 0.6. The coefficient d ln r02/dT and the ratio fe/f for unswollen samples were positive but dependent on the extension ratio α and crosslinking density. The fe/f ratio displayed a tendency to decrease with increasing α and this decrease was smaller for elastomers of higher crosslinking density. Additional crosslinking due to dicumyl peroxide reduced the dependence of fe/f on α. Swollen samples had lower positive values of fe/f; which were somewhat independent of α and crosslinking density. Departures from the molecular theories of rubberlike elasticity are explained by intermolecular effects, which, in general, are influenced by crosslinking.
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 715-729 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We have studied the rose bengal-sensitized photooxygenation of cis- and trans-polyisoprene model compounds that contain one unit in methanolic solution, characterized the resulting monohydroperoxides, and determined their yield. We have also demonstrated the possibility of a second addition of singlet oxygen on the same unit and have undertaken a kinetic study to determine the rate constants of all the reactions of 4-methyl-4-octene.
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  • 71
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    Topics: Chemistry and Pharmacology
    Notes: In the presence of Et2SO4, (S)-1-(N-phenyl-carbamoyl)-2-methylaziridine gave an oligomer with a structure of [CH2—CHCH3—N(CONHPh)]n. The oligomer has optically active isotactic configuration and narrow molecular weight distribution (DP ca. 8). The net polymerization behavior of the monomer and chemical property, such as absorptivity of Et2SO4, of the oligomer are analogous to the case of 1-(N-phenyl-carbamoyl)-aziridine. The ring opening occurs with retention of the configuration at the asymmetric carbon atom and the oligomer can be crystallized at around 90°C.
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 747-757 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In due consideration of the specific base-base interaction that exists between nucleic acid molecules, the free radical polymerization of N-β-methacryloyloxyethyl derivatives of adenine, thymine, and theophylline initiated by azobisisobutyronitrile (AIBN) was studied in the presence of N-β-methacryloyloxyethyl-type polymers which have complementary nucleic acid bases as template polymers. The rate of polymerization of N-β-methacryloyloxyethyladenine was accelerated when poly(N-β-methacryloyloxyethyluracil) or -thymine was present in the polymerization system. The effect of the stereoregularity of the template polymers, as well as polymerization temperature and the sort of solvents used on the rate of polymerization, was studied and discussed in some detail. The results suggest that the interaction between complementary bases plays a role in template polymerization behavior.
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 759-768 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The radiation-induced copolymerization of tetrafluoroethylene (A) and styrene (B) was studied in bulk and in perfluorotoluene at 22°C at autogenous pressure and 260 and 510 MPa. The reactivity ratio for addition to A-ended radicals, rA, is effectively zero at the two lower pressures and is in the range 0.002-0.008 at 510 MPa. The other reactivity ratio, rB, is 6 at autogenous pressure and also at 260 and 510 MPa if the A content of the charge is less than 50%. If the A content is greater than 95%, rB appears to be 100 at pressures of 260 and 510 MPa. The apparent variation in rB cannot be explained by invoking a penultimate unit effect for B-ended radicals. Polymerization rates scatter somewhat, but all rates are quite small when the A content of the charge is in the range 95-99.8%. Polymers containing as much as 66% A appear to be inherently benzene soluble but frequently contain some gel because of radiation-induced crosslinking after their formation. No very high polymers were formed that contained more than a few percent A, even at high pressure. Features that complicated the study were immiscibility of the liquid monomers, extreme variation of the monomer - copolymer compatibility with charge composition, and freezing of B at high pressure.
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 769-775 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The aminolysis of benzoic mesitoic anhydride was studied in a model system to select the reaction site by steric effect and was found to occur exclusively at the carbonyl group of the benzoic acid. Solution polycondensation of new linear bisanhydrides, terephthalic bis(mesitoic anhydride) and adipic bis(mesitoic anhydride), with aromatic diamines in polar aprotic solvents that contained lithium chloride at room temperature, afforded polyamides with high molecular weight. The interfacial polycondensation in a dichloromethane-water system also successfully yielded polyamides from aliphatic diamines.
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 777-782 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photocrosslinking has been observed in a number of polymers derived by chemical modification of poly(vinylbenzyl chloride). Included are polymers bearing pendant benzophenone, stilbazolium, fluorenone, carbazole, and sulfonylazido moieties. The synthesis and properties of these polymers are described.
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  • 76
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 783-787 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Catalytic actions of various additives were studied in the polycondensation of di(4-nitrophenyl) isophthalate with bis(4-aminophenyl) ether in N-methyl-2-pyrrolidone, and 1-hydroxybenzotriazole (HOBt) was found to be a highly effective catalyst that yielded high-molecular-weight polyamide. In addition to the polycondensation of the 4-nitrophenyl ester, the polymerization of negatively substituted phenyl esters like di(2,4,5-trichlorophenyl) isophthalate was also accelerated by HOBt. For the HOBt-catalyzed aminolysis of esters a bifunctional concerted mechanism that involves an eight-membered transition state was proposed.
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 797-806 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: On the basis of the simultaneously measured free radical generation and HCl evolution a mechanism accounting for the effect of the oxygen on the degradation of poly(vinyl chloride) (PVC) is proposed. The mechanism is based on the reaction of oxygen with radicals generated in PVC to form unstable peroxy radicals. In addition, it is proposed that oxygen reacts directly with conjugated polyenes to form peroxy linkage.
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  • 78
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 789-796 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: To enhance its solubility in common solvents poly(γ-methyl-L-glutamate) (PMG) was transesterificated with ethylene chlorohydrin, ethylene cyanohydrin, and β,β,β-trichloroethanol, respectively. The aminolyses of the resulting polymers proceeded easily in pendant ester groups to give the corresponding amides in reasonable yields without main chain fission. By these procedures the incorporation of functional groups such as azide, amino acid, and thiol into PMG is successfully performed.
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  • 79
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 807-813 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The equilibrium constants of the coordination reaction of chlorodimethylformamide·cobaloxime with 4-vinylpyridine-styrene copolymers (PPS) were determined. The constants for PPS, which contain 20-50% 4-vinylpyridine (4VP) unit, measured about 1.3 × 105 liter/mole larger than those in the pyridine system (6.8 × 104 liter/mole). When the polymer ligand is 4VP homopolymer or contains less than 20% 4VP unit, K values are lower. The rate constants (kf) of the coordination reactions of the cobaloxime with polymer ligands were also measured in dimethylformamide (DMF) and benzene. In DMF kf decreased with an increase in 4VP unit content of the polymer ligand; in benzene it was increased by the 4VP fraction. These results can be explained by the variation in conformation of the polymer chain in each solvent. The effect of the polymer chain on complexation was discussed on the basis of the kinetic data.
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  • 80
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 821-833 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The neighboring effect of sodium carboxylate groups on the saponification of diallyl phthalate prepolymer was investigated in detail in dioxane solutions that contained various amounts of water at 50°C by using different types of model compound; this procedure is also compared with the neighboring effect of hydroxyl groups.
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  • 81
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 815-820 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photopolymerization of cyclohexene oxide in the presence of electron acceptors was studied in a bulk system (in liquid as well as in solid states). The polymerization was proved to proceed by a cationic mechanism in both states by the effect of inhibitors. In a liquid phase the light intensity dependence of the rate of polymerization and the molecular weight distribution showed a contribution of a free ionic polymerization. Any discontinuous phenomenon in the rate as well as in the molecular weight was not discerned between liquid(above -36°C) and plastic crystal (between -36 and -81°C) phases. A quantum yield of monomer consumption as high as 8 × 103 was observed in the plastic crystal phase. Below -81°C in the normal crystal phase the rate as well as the molecular weight was remarkably suppressed.
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  • 82
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 835-841 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Selective formation of biscarbamates from diphenyl carbonate (DPC) and diamines and the preparation of polyurethanes from the carbamates and diols under mild conditions were studied. The reaction of DPC and diamines was significantly affected by catalysts, biscarbamates being exclusively prepared in high yields in the presence of 2-hydroxypyridine. The polycondensation reaction of the biscarbamates with diols was facilitated by catalysts such as metal salts; among the catalysts examined magnesium chloride in pyridine gave the best results. Metal chlorides in pyridine also promoted the reaction of DPC with aromatic amines to give the corresponding ureas, and the direct synthesis of polyureas was achieved by the polycondensation of DPC with diamines in the presence of the chloride.
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  • 83
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
    Notes: Methyl methacrylate (MMA) and styrene (St) copolymerize in the presence of zinc chloride at 3°C under photoirradiation. The contents of methyl methacrylate in the copolymers obtained at a [ZnCl2]/[MMA] molar ratio of 0.4 are systematically larger than 53 mole %, which is the limiting value at a small feed ratio of methyl methacrylate. The resulting copolymers are confirmed as the sole products and not the mixtures by thin layer chromatography. The effect of dilution of the monomer feed mixture with toluene on copolymer composition suggests that it depends chiefly on the feed concentration of styrene and hardly at all on monomer feed ratios. Copolymerizations are also conducted in the presence of stannic chloride at -17°C under photoirradiation and in the presence of ethylaluminium sesquichloride at 0°C with spontaneous initiation. The contents of methyl methacrylate in both copolymers obtained at feed ratios lower than 60 mole % almost correspond to the 1:1 alternating copolymer and increase systematically with higher feed ratios. The systematic deviations of copolymer composition obtained in the presence of metal halides are reasonably interpreted by the participation of the binary molecular complex composed of metal halide and methyl methacrylate in the polymerization of the ternary molecular complex composed of metal halide, methyl methacrylate, and styrene.
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  • 84
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 877-888 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The structure of the 1:2 copolymer of divinyl ether and maleic anhydride was investigated by 13C-NMR spectroscopy. The polymer contains the bicyclic unit composed of one molecule of each monomer and the maleic anhydride unit. The carbon chemical shift for these units was calculated on the basis of the chemical shift of many model compounds. The major peaks of the cyclopolymer prepared in chloroform were consistent with the presence of the symmetrical bicyclic unit with cis junction and the trans monocyclic anhydride unit. The carbonyl carbon spectrum for the copolymer obtained in a mixed solvent of acetone and CS2 suggested the predominant formation of the unsymmetrical bicyclic unit. The polymerization process was discussed on the basis of these results.
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  • 85
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 1103-1116 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The excited state of pyrene observed in fluorescence and pulsed laser techniques is used to show that pyrene is solubilized in the polymer coil of aqueous solution of polymethacrylic acid (PMA) at pH 〈 4-5. This leads to a decreased access of molecules such as I-, Tl+, CH3NO2, and O2 to excited pyrene in the polymer coil. The protection of the excited state by solubilization in the polymer is sufficient to enable 3-bromopyrene phosphorescence to be observed at room temperature in these systems. Increasing the pH of the system uncoils the polymer and leads to increased accessibility of excited pyrene to CH3NO2; eventually, at pH 〉5, the pyrene is ejected into the aqueous phase of the system. In the presence of micellar solutions of surfactants increasing pH transports the pyrene from the polymer to the micellar aggregates. These fluorescence techniques are used to investigate the kinetics of expansion of the polymer coil. The system is suggested as a suitable model for the interaction of pyrene with biopolymers such as DNA.
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  • 86
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 1129-1144 
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    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We have screened various multifunctional Friedel-Crafts alkylation and acylation reagents for their charring ability in impact polystyrene. Only benzyl chloride reagents with Sb2O3-halogen catalysts promoted crosslinking; the result is increased char yields and decreased fuel production and thereby improved fire resistance. Selected systems were evaluated for ignition, extinction, flamespread, and smoke generation; chars were fully characterized.
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  • 87
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 1153-1161 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: To elucidate mechanisms in electroinitiated polymerization reactions a comparison was conducted between ultraviolet (UV) photoinitiation and electroinitiation of N-vinyl phthalimide with zinc chloride as a catalyst. Both methods give low yields of a complex polymer product. A detailed analysis, infrared (IR), gel permeation chromatography (GPC), elemental, and molecular weight, conducted on the polymeric products, indicated that phthalimide ring opening was occurring and that complex mixtures of poly(N-vinyl phthalimide) derivatives were formed. Both initiation methods gave comparable results, which further indicated mechanistic similarity between photo-and electroinitiation in these donor-acceptor charge transfer polymerizations.
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  • 88
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 1175-1186 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The electronic structure of a clean copolymer of ethylene and tetrafluoroethylene is investigated by measuring the ESCA spectra of the core and valence levels. The chemical composition and alternating (〉95%) structure of the copolymer, characterized separately by classical methods, is verified by analyzing the C 1s core-level spectrum. The comparison of the experimental valence band with an original EHCO band-structure calculation, and with similar data for a model of polymer with block structure, shows that the combined methods allow us to distinguish between the two compounds through their valence-band spectra.
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  • 89
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 1235-1238 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 90
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 1199-1213 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: When a cation exchange membrane is immersed in a cationic polyelectrolyte solution to form a thin layer on the membrane surface, the membrane properties are changed: permselectivity between cations with different electric charges (a relative transport number of the calcium ions to sodium ions, PNaCa), current efficiency, and electric resistance of the membrane. Here the more compact the cationic polyelectrolyte layer, the more outstanding the change in permselectivity. To make a more compact layer, an electrodeposition method was adopted and a change in the permselectivity of the resultant cation exchange membrane was investigated. By using the electrodeposition method a strongly basic polyelectrolyte with a larger molecular weight effectively changed the permselectivity of the cation exchange membrane: the PNaCa value dropped to about 0.3 from about 2.5 of the PNaCa of the untreated membrane during electrodialysis of the sodium chloride - calcium chloride system, and an increase in the electric resistance of the membrane (i.e., organic fouling) due to a cationic surface-active agent could be prevented. It is noteworthy that by using the strongly basic polyelectrolyte with a larger molecular weight the electrodeposition method was effective, whereas the immersion method was ineffective. Furthermore, even with the electrodeposition method the cationic polyelectrolyte which had a relatively smaller molecular weight resulted in a more remarkable change in the PNaCa value than did that with a larger molecular weight. In the electrodeposition method the amount of polyelectrolyte cohered onto the membrane surface in creased with an increase in the concentration of the polyelectrolyte, and weakly basic polyelectrolyte, and weakly basic polyelectroyte (polyethyleneimine) was also available independent of its molecular weight.
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  • 91
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 1247-1248 
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    Keywords: Physics ; Polymer and Materials Science
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  • 92
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 1249-1249 
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    Keywords: Physics ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
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  • 93
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 3183-3191 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Among the four 1,1-disubstituted 2-vinylcyclopropanes, diethyl 2-vinylcyclopropane-1,1-dicarboxylate (Ia), 2-vinylcyclopropane-1,1-dicarbonitrile (Ib), ethyl 1-cyano-2-vinylcyclopropanecarboxylate (Ic), and 1,1-diphenyl-2-vinylcyclopropane (Id), Ib and Ic polymerized well with sodium cyanide in N,N-dimethylformamide. Ib was most reactive and a polymer (IIb) from Ib exhibited an inherent viscosity of 1.05 dl/g (concentration of 1.0 g in 100 ml of 95% H2SO4). All experimental results indicated that the polymerization proceeded by ring opening and that the structure of the polymers had pendant vinyl groups. The polymer IIc from Ic was soluble in common solvents like acetone, but IIb was soluble only in 95% H2SO4. Reactions of those compounds with benzenethiolate ion in ethanol yielded addition products that supported the ring-opening polymerization of those monomers. In the postulated mechanism of polymerization cyanide ion attacks the carbon of a cyclopropane ring with electron-releasing vinyl group and the resulting anion is thereby stabilized by two electron-withdrawing substituents. The propagation takes place by the reaction of the anion with another monomer molecule.
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  • 94
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 3217-3239 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Esterification-hydrolysis and condensation-glycolysis are the principal equilibria entailed in a system comprised of benzoic acid, ethanediol, ethanediol monobenzoate, ethanediol dibenzoate, and water. These equilibria are characterized by three interrelated equilibrium constants that pertain to the hydrolysis of both ethanediol monobenzoate and ethanediol dibenzoate and to the condensation of ethanediol monobenzoate. The rate constants related to these reactions and to the corresponding reverse reactions were all found to be functions of the concentration of carboxy groups. Antimony triacetate, a well-known transesterification catalyst, catalyzed the condensation reaction strongly but did not affect the esterification reaction. Based on a mechanism that entailed the considered three principal equilibrium reactions, a set of both the kinetic and thermodynamic parameters was obtained by a nonlinear regression procedure. With these parameters the nonlinear rate equations were integrated numerically, using the fourth-order Runge-Kutta method. Excellent agreement between the values thus calculated and the experimental data were obtained in all cases except when considerable concentrations of both benzoic acid and ethanediol dibenzoate were present in the system. It has been concluded that in these instances the formation of the dibenzoate is paralleled by a pyrolysis reaction that is strongly catalyzed by carboxy groups.
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  • 95
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 3273-3278 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Transfer constants to monomer at 55°C have been measured in 2 and 4-vinylpyridine radical polymerizations. In addition, the transfer constants to ethanol, octan-1-ol, toluene, benzyl alcohol, chloroform, and nitroethane have been measured. These values, which increase in the order above, show no significant variation between the two isomeric monomers.
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  • 96
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 3241-3254 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The process of esterification of terephthalic acid is characterized by a mechanism that involves three equilibrium reactions. Two are esterification-hydrolysis equilibria entailing the reactions of the two terephthalic acid carboxyl groups with alcoholic hydroxyl groups, whereas the third one is a transesterification-acidolysis equilibrium that is concerned with the reaction between two terminal terephthalic acid moieties. The products of these three interrelated equilibria are terephthalic acid, its monoester and diester, the particular alcohol, and water. The alcohol used in the present study was 2-(2-methoxyethoxy)ethanol. Equilibrium constants and rate constants were developed from experimental data obtained at 230°C. The esterification-hydrolysis reactions were found to be catalyzed by carboxyl groups, and the rate of transesterification was found to be a function of the terephthalic acid concentration. With the constants developed, the system of nonlinear differential equations, as derived from the mechanism postulated, was integrated numerically using the Runge-Kutta method. Good agreement between calculated and experimental values was observed.
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  • 97
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 3255-3271 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: N,N′-(pyromellitoyl)diglycine (1) was synthesized by reacting pyromellitic anhydride with glycine in polar solvents such as DMAC, NMP, or DMF at 60°C and then refluxed azeotropically with toluene. Among these solvents, it is easy to form DMF-insoluble salt (1″) in DMF, but this salt can be converted to 1 by treating first with NaHCO3 and then with HCl. Reacting monomer N,N′-(pyromellitoyl)diaminoacetyl chloride (2) can be obtained by treating with thionyl chloride, and N,N′-(pyromellitoyl)dimethyl aminoacetate (3) can be obtained by treating 2 with methanol. As 2 reacts with aromatic diamine in polar solvents, such as DMAC, DMF, or NMP, a series of copolypyromellitimide amides (5a-h) can be obtained. These copolymers can be processed by using DMAC + LiCl (5%) as solvent to produce flexible film of good weather resistivity and heat resistivity. Monomer 2 can also react with aromatic dihydrazides in polar solvents to produce copolypyromellitimide hydrazides (6a-c), and 6a-b can be condensated again to produce copolypyromellitimide oxadiazoles (7a-b) in polyphosphoric acid (PPA). Besides, 3 reacts with aromatic tetraamine by carrying out polycondensation in PPA to produce copolypyromellitimide benzimidazole (8). Structures of copolymers mentioned above were identified by comparing IR spectra with those of model compounds. Heat resistivity was measured by the thermogravimetric method, and their solubilities in various solvents were also investigated.
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  • 98
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 3291-3295 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The radiation-initiated graft polymerization of 4-vinylpyridine to high-density polyethylene has been studied under diffusion-free conditions by the mutual irradiation technique. The reaction rate is 1/2 order in radiation intensity over the range 0.00076-0.011 Mrad/hr. The reaction rate is first order in monomer at 0.00076 Mrad/hr, over the complete range of monomer concentrations; at 0.021 Mrad/hr, up to 60 vol % monomer; and at 0.21 Mrad/hr, up to 50 vol % monomer.
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  • 99
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 3279-3289 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several copolymers of 2-hydroxyethyl methacrylate (HEMA) with methyl acrylate (MA), ethyl acrylate (EA), n-butyl acrylate (BA), and methyl methacrylate (MMA) were prepared at 70°C in nitrogen atmosphere using 0.2% (w/v) benzoyl peroxide as initiator. The copolymer composition was evaluated by estimation of hydroxyl group in the copolymers. Intrinsic viscosity of HEMA-EA, HEMA-BA, and HEMA-MMA copolymers was determined at 35°C in dimethyl formamide. Molecular weight distribution of copolymer samples was evaluated by gel permeation chromatography. Thermal behavior of the copolymers was investigated by dynamic thermogravimetry. Thermal stability decreased on increasing HEMA content in MA, EA, and BA copolymers. However, a reverse trend was observed in HEMA-MMA copolymers.
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  • 100
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    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 1483-1491 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Wholly aromatic polysulfonamides of high molecular weight were prepared by the solution poly-condensation of aromatic disulfonyl chlorides with aromatic diamines in tetramethylene sulfone and substituted pyridines as the acid acceptor. Polysulfonamides with inherent viscosities as high as 1.2 were readily obtained by initiating polycondensation at a temperature of 5-10°C to control the side reactions. The polycondensation was fairly fast and was completed in 10 min at 60°C. All the aromatic polysulfonamides dissolved in a wide range of solvents, including acetone and tetrahydrofuran. These polymers were less thermally stable than the corresponding aromatic polyamides.
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