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  • 1990-1994  (10,932)
  • 1990  (10,932)
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  • 2015-2019
  • 1990-1994  (10,932)
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  • 1
    ISSN: 0886-1544
    Keywords: polycentric chromosome ; light microscopy ; electron microscopy ; high-pressure freezing ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Mitosis in the hemipteran Agallia constricta (leafhopper) cell line AC-20 was examined by light microscopy of living and fixed cells. During early prometaphase the numerous small (0.30-3.0-μm) chromosomes appear as discrete units that lack a primary constriction. However, by late prometaphase the chromosomes are tightly packed at the spindle equator and are no longer clearly resolvable as individuals. When viewed from the side the metaphase chromatin appears as a 2-3-μm wide band that spans the width of the spindle; when viewed from the pole it appears as a fenestrated disk. The metaphase chromatin splits at anaphase into two sister chromatin plates, each of which exhibits holokinetic poleward movement, i.e., all parts of each plate move as a single unit with the same velocity. In many early-to-mid anaphase cells the separating sister plates are connected by chromatin-containing bridges that break as anaphase progresses. Ultrastructural analyses of serial thick and thin sections from cells fixed by conventional, OsO4/KFeCN, or high pressure rapid freezing methods, reveal that by metaphase all of the chromosomes are interconnected to form a large, irregularly shaped fenestrated disk of chromatin. Similar analyses reveal that adjacent chromatids remain interconnected throughout anaphase. Each disk of metaphase and anaphase chromatin contains numerous kinetochores recessed within its polefacing surface. Kinetochores consist of a fine, faintly staining fibrillar material arranged along the chromatin surface as thin (0.1-0.3 μm dia.) rods varying considerably (0.15-2.3 μm) in length. From these observations we conclude that the polycentric metaphase chromatin of A. constricta, and its holokinetic behavior during anaphase, arises from the aggregation or cohesion of smaller prometaphase chromosomes, each of which contains a single, diffuse kinetochore.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 15 (1990), S. 271-272 
    ISSN: 0886-1544
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
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  • 3
    Electronic Resource
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    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 15 (1990) 
    ISSN: 0886-1544
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
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  • 4
    Electronic Resource
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    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 15 (1990), S. 199-203 
    ISSN: 0886-1544
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
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  • 5
    ISSN: 0886-1544
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Cytoskeleton alterations of NIH/3T3 fibroblast monolayers transfected with Haras-activated oncogene were studied by immunofluorescence, immunoelectron microscopy, and immunoelectrophoretic analysis of actin isoforms. Transformation foci were found to consist of cells with a round shape and rare stress fibers that spread sparsely, forming rare focal contacts and fibronexuses. The loss of stress fibers in transformed cells was confirmed by staining with rhodamine-phalloidin and with a fluorescinated anti-non-muscle cell actin antibody. The transformed cells were anchored to the substrate prominently by filaments that contained fibronectin, as showed by immunoelectron microscopy. A down-regulation of α-actin isoform was observed by immunofluorescence and immunoblotting analysis using a specific monoclonal antibody. The diffuse distribution of α-actin, lacking a specific association with stress fibers, challenges the hypothesis of a connection between α-actin down-regulation and stress fiber loss.
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  • 6
    Electronic Resource
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    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 17 (1990), S. 250-263 
    ISSN: 0886-1544
    Keywords: myosin ; microinjection ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: We present microinjection data in support of an indirect approach by which cytoplasmic protein interactions important in the processes of bone resorption can be elucidated. Three polyclonal antibodies (M1, M3, M5) raised against myosin II from perfused rat liver differently affected the actin-activated Mg ATPase of myosin II. These antibodies microinjected into isolated rat osteoclasts affected osteoclast morphology and activity in bone resorption. M1, which completely inhibited myosin ATPase activity at a antibody:myosin ratio of 10:1, initially promoted the extension/retraction motility of lamellipodia but eventually reduced the spread area of osteoclasts along the substrate after 20 hr. M3, which inhibited ATPase activity by 70%, had similar effects; however, M5, which weakly inhibited ATPase activity, neither promoted extension/retraction nor reduced spread area of osteoclasts. Immunofluorescence showed that these antibodies removed myosin II from the majority of actin filaments in injected osteoclasts. Because antibodies that did not bind to a myosin II column had little effect on the extension/retraction of lamellipodia or the osteoclast spread area, these data suggest that myosin II participates in the stabilization of osteoclast lamellipodia along the substrate. M1 injection strongly inhibited injected osteoclasts from excavating resorption lacunae in bone slices, compared to control antibody. M3 and M5 were less effective but also inhibited bone resorption. These data show that myosin II is functionally important in bone resorption and that the osteoclast-differentiated activity of bone resorption is a more sensitive assay for myosin activity than lamellipodia motility or cell morphology.
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  • 7
    Electronic Resource
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    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 17 (1990), S. 309-316 
    ISSN: 0886-1544
    Keywords: digitization ; flagellum ; image analysis ; microcomputer ; simplex ; spermatozoa ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Methods are described for computerized analysis of digitized images obtained by scanning photomicrographs of swimming sperm flagella. After storing a series of image frames in computer memory, the entire series is analyzed automatically. For each sperm image, the sperm head is located to obtain a starting point for analysis of the flagellum. This location is obtained by minimizing image intensity along a model of the sperm head outline. The flagellum is modelled by a series of straight segments of equal length: 0.5 or 1 μm. The angles between these segments are adjusted to give minimum image intensity along the line of the model as well as minimizing smoothing functions. Extensions to analyze a series of images in each frame, and to measure the positions of beads attached to the flagellar microtubules, are also described.
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  • 8
    Electronic Resource
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    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 16 (1990), S. 58-67 
    ISSN: 0886-1544
    Keywords: subunit composition ; Western blotting ; monoclonal antibody ; affinity-purified polyclonal antibody ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Sea urchin sperm outer arm dynein is a multi-subunit protein composed of heavy chains, intermediate chains, and light chains. We prepared monoclonal and affinity-purified polyclonal antibodies to heavy and intermediate chain subunits and examined whether the embryonic ciliary axonemes ofthe same species contain the polypeptides sharing epitopes with them. Ciliary axonemes contained a high molecular weight polypeptide with the exact same mobility as flagellar β-heavy chain. This polypeptide also shared epitopes with it. In contrast, no polypeptide had the exact same molecular weight as flagellar α-heavy chain and shared epitopes with it. Western blots showed that ciliary axonemes also contain three polypeptides sharing epitopes with the respective flagellar intermediate chain. The present results revealed that the α-heavy chains of flagellar and ciliary outer arm dyneins are different.
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  • 9
    Electronic Resource
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    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 15 (1990), S. 1-6 
    ISSN: 0886-1544
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
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  • 10
    Electronic Resource
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    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 15 (1990), S. 121-134 
    ISSN: 0886-1544
    Keywords: clathrin ; cell-substrate adhesion ; freeze fracture ; quick-freeze ; deep-etch ; rotary- replication ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: We have used antibodies to clathrin light chains in immunocytochemical studies of acetylcholine receptor (AChR) clusters of cultured rat myotubes. Immunofluorescence and ultrastructural experiments show that clathrin is present in coated pits and in large plaques of coated membrane. Coated membrane plaques are spatially and structurally distinct from AChR-rich membrane domains and the bundles of microfilaments that are also present in AChR clusters. Clusters contain a relatively constant amount of clathrin light chain protein, which is not dependent on the amount of AChR. Clathrin plaques remain after AChR domains are disrupted by azide, or after microfilament bundles are destabilized by cytochalasin D. Extraction of myotubes with saponin removes clathrin without disrupting AChR domains. Thus, clathrin plaques, microfilament bundles, and AChR-rich domains are independently stabilized.
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  • 11
    Electronic Resource
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    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 16 (1990), S. 33-46 
    ISSN: 0886-1544
    Keywords: dynein structure ; cilia ; development ; microtubule-based motility ; antibodies to dynein ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The determination of the structure and the expression of dynein during embryonic development are central to the understanding of dynein function. As an important first step toward these objectives, cDNAs encoding portions of sea urchin ciliary dynein were identified by antibody screening of a sea urchin cDNA expression library. Bacause of the complete lack of protein sequence data, it was first necessary to prove the identity of the dynein cDNAs. Of the five cDNA inserts initially cloned, one, designated P72A1, was characterized extensively. Four independent criteria demonstrated that P72A1 encoded a portion of a dynein heavy chain. (1) The β-galactosidase-P72A1 fusion protein affinity-purified dynein-specific antibodies from crude antiserum. (2) Two other antisera to dynein, raised independently of the antiserum used to screen the cDNA library, reacted with the fusion protein. (3) A new antiserum raised against the fusion protein reacted with authentic dynein heavy chain on Western blots and stained embryonic cilia by indirect immunofluorescence microscopy. (4) Two new antisera, elicited against opposite ends of the P72A1 open reading frame, each reacted with authentic dynein heavy chain protein. Western blot analyses of dissociated dynein heavy chains revealed that P72A1 encoded a portion of the β heavy chain. Epitope mapping experiments confirmed the identity of P72A1 as part of the βheavy chain and also demonstrated that P72A1 encoded epitopes of the carboxyl-terminal fragment B domain of the dynein β heavy chain. Northern blot analyses of poly(A)+ RNA revealed that P72A1 hybridized with a large RNA species ca. 12.5 kb in length. The dynein mRNA concentration increased during embryonic development. Dot blot analyses of RNA isolated at various times after embryo deciliation demonstrated that the dynein β heavy chain mRNA accumulated rapidly in response to deciliation. The accumulation was similar to but not identical with the induction of tubulin mRNA in response to the same stimulus.
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  • 12
    Electronic Resource
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    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 16 (1990), S. 68-79 
    ISSN: 0886-1544
    Keywords: monoclonal antibody ; centrosome ; kinetochore ; midbody ; cell cycle ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Salt-extracted proteins of taxol-stabilized microtubules from Chinese hamster ovary cells arrested at mitosis were used to immunize mice for hybridoma production. From a group of related monoclonal antibodies (MAbs), one, C9, recognized an epitope on antigens localized by immunofluorescence microscopy to interphase centrosomes and nuclei. The availability of the nuclear antigen was cell cycle-dependent; however, permeabilization of cells before fixation revealed that the antigen was present throughout the cell cycle. The nuclear antigen was exposed during prophase and was released from the nucleus upon nuclear envelope breakdown filling the cytoplasm of the mitotic cell. Antigenic material re-accumulated at daughter nuclei and was concealed during Gl phase. Detergent extraction of the cytoplasmic antigen from mitotic cells enabled localization of antigens to centrosomes, kinetochores, and the furrowing region/midbody. Immunoblot analysis of cells of a variety of species of origin identified an approximate 250 kD polypeptide as corresponding to the nuclear antigen, whereas polypeptides of 107/117 kD as well as approximately 250 kD accounted for the mitotic cytoplasmic antigens. No polypeptides could be associated with antigens at centrosomes, kinetochores, or midbodies. This MAb joins the antibody preparations previously reported that describe nuclear antigens, or epitopes on antigens, enhanced at mitosis.
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  • 13
    Electronic Resource
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    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 16 (1990), S. 190-203 
    ISSN: 0886-1544
    Keywords: mitosis ; calcium ; diacylglycerol ; protein kinase C ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: We have treated living, intact stamen hair cells from the spiderwort plant, Tra-descantia virginiana, with 0.5 μg/ml or 60 μg/ml 1,2-dioctanoylglycerol, a potent and permeant activator of protein kinase C, and have observed the rates of progression of mitosis from prophase through anaphase. We have found that in addition to the concentration used, the time of initial treatment with 1,2-di-octanoylglycerol defines the response by the cells. The cells rapidly undergo nuclear envelope breakdown when this diglyceride is added in very late prophase, 0 to ∼8 min prior to the time of normal nuclear envelope breakdown. Anaphase onset occurs 28 min after nuclear envelope breakdown, rather than after the 33 min interval observed in untreated cells. Rapid progression through metaphase is also observed if cells are treated with 0.5 μg/ml 1,2-dioctanoylglycerol during prometaphase, up to 15 min after nuclear envelope breakdown. The addition of 0.5 μg/ml 1,2-dioctan oylglycerol in late metaphase, ∼26 min after nuclear envelope breakdown, results in sister chromatid separation slightly ahead of its normal time, 33 min after nuclear envelope breakdown, and in precocious cell plate vesicle aggregation, 3-5 min earlier than that observed in untreated cells. Treatment of cells with 60 μg/ml of 1,2-dioctanoylglycerol at any point during the interval from 0 to ∼5 min prior to nuclear envelope breakdown results in precocious entry into anaphase. If cells are treated with either 0.5 μg/ml or 60 μg/ml 1,2-dioctanoylglycerol earlier than 20 min before nuclear envelope breakdown, they do not enter mitosis, but instead revert to interphase without dividing. When 1,2-dioctanoylglycerol is added atother times during mitosis, the rate of subsequent mitotic progression is dramatically slowed; the cells require 〉55 min to progress from nuclear envelope breakdown to anaphase onset, though once in anaphase, the cells progress onward to cytokinesis at normal rates. Treatments of cells with 1,3-dioctanoylglycerol at any point during prophase, prometaphase, or metaphase are without effect on the rate of subsequent mitotic progression. The shifts in response by cells treated at specific times with 1,2-dioctanoylglycerol during mid- and late metaphase may be indicative of the existence of one or more regulatory switch points (i.e., checkpoints) just prior to anaphase onset.
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  • 14
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    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 16 (1990), S. 167-181 
    ISSN: 0886-1544
    Keywords: metachronal wavelength ; metachronal wave direction ; asymmetry of beating ; ciliary beating ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: A mathematical model is proposed to explain the dependence of the direction and the length of the metachronal wave on parameters that characterize the ciliary beat, the dimensions of the cilia, and the geometry of their arrangement on the ciliated surface. The metach/onal wave is decomposed into two mutually perpendicular components, which are chosen in such a way that the direction of one of them is in the direction of the effective stroke. The magnitudes of the two components are determined by using the concept of the time of delay between adjacent cilia. The properties of the metachronal wave are then calculated as a function of the ciliary parameters.The results obtained with the present model predict that the direction of the wave propagation is strongly dependent on the type of metachronism in the direction of the effective stroke and the polarization in time and in space of the ciliary beat. The metachronal wavelength is found to depend on four parameters: the ciliary length, the angle of the arc projected on the cell surface by the ciliary tip during the recovery stroke, the degree of asymmetry of ciliary beat, and the portion of the cycle occupied by the pause. The metachronal wavelength is also found to be only weakly dependent on the ciliary frequency.At this stage there exists relatively little experimental information with which t o characterize fully the metachronal properties of ciliary systems. Even when only partial information exists, the model allows prediction, to within a certain range, of the direction of the wave propagation. It also suggests a possible mechanism for the influence of changes in environmental conditions on wave direction and wavelength. In severalcases in which full information does exist, good agreement between the experimental findings and the predictions of the model is found. According to this model it will be worthwhile to invest more effort in measuring the time and space polarization of ciliary beating and the times of delay between cilia.
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  • 15
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    Cell Motility and the Cytoskeleton 16 (1990), S. 204-213 
    ISSN: 0886-1544
    Keywords: kinesin ; molecular structure ; immunoaffinity purification ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Previous studies with monoclonal antibodies indicate that sea urchin kinesin contains two heavy chains arranged in parallel such that their N-terminal ends fold into globular mechanochemical heads attached to a thin stalk ending in a bipartitetail [Scholey et al. 1989]. In the present, complementary study, we have used the monoclonal antikinesin. SUK4, to probe the quaternary structure of sea urchin (Strongylocentrotus purpuratus) kinesin. Kinesin prepared from sea urchin cyto-sol sedimented at 9.6 S on sucrose density gradients and consisted of 130-kd heavy chains plus an 84-kd/78 kd doublet (1 mol heavy chain: 1 mol doublet determined by gel densitomctry). Low levels of 110-kd and 90-kd polypeptides were sometimes present as well. The 84-kd/78 kd polypeptides are thought to be light chains because they were precipitated from the kinesin preparation at a stoichiometry of one mol doublet per 1 mol heavy chain using SUK4-Sepharose immunoaffinity resins. The 110-kd and 90-kd peptides, by contrast, were removed using this immunoadsorption method. SUK4-Sepharose immunoaffinity chromatography was also used to purify the 130-kd heavy chain and 84-kd/78-kd doublet (1 mol heavy chain: 1 mol doublet) directly from sea urchin egg cytosolic extracts, and from a MAP (microtubule-associated protein) fraction eluted by ATP from microtubules prepared in the presence of AMPPNP but not from microtubules prepared in ATP. The finding that sea urchin kinesin contains equi-molar quantities of heavy und light chains, together with the aforementioned data on kinesin morphology, suggests that native sea urchin kinesin is a tetramer assembled from two light chains and two heavy chains.
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  • 16
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    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 16 (1990) 
    ISSN: 0886-1544
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
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  • 17
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    Cell Motility and the Cytoskeleton 17 (1990) 
    ISSN: 0886-1544
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
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  • 18
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    Cell Motility and the Cytoskeleton 16 (1990), S. 251-265 
    ISSN: 0886-1544
    Keywords: Ciliary motility ; inclination ; polarity of beating ; active sliding velocity ; sliding translocation rate ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Depolarization-induced cycles of a frontal cirrus of Stylonychia were investigated by applying methods of axial-view analysis of the cilia, high-speed microcinématography, and step voltage-clamp. Rising depolarization (from 3 mV to 7ge; 30mV) increased the rate of beating from zero to maximally 58 Hz. During cyclic activity, the axis of the beat cone of a proximal segment of the cirrus was inclined by 60° (0° = perpendicular to cell surface), and was always oriented 90° counterclockwise to the power stroke. With the stimulus amplitude rising, the orientations of the power stroke and inclination were increasingly shifted in more counterclockwise directions by up to 80° After correction for inclination ( = normalization), and following planification of the track of the segment, we determined the following properties of the cycle during depolarization: The course of the cycle tended to be rounded, i.e., the ratio of major over minor amplitudes (= spatial polarity) approximated a value of 1.6 which is only two thirds of maximal spatial polarity observed during hyperpolarization. The angular velocity generally increased with rising steps of depolarization; up to +5 mV (and comparable to hyperpolarization-induced responses), the velocity maximum occurred during the return stroke. With depolarizations ≥7 mV the angular velocity maximum shifted to the power stroke so that the temporal polarity (rates of power stroke over rates of return stroke) increased from 0.4 to 1.6. Calculations of the angular velocity as referred to the proximal ciliary segment level suggest active sliding rates (between 5 and 30 nm/ms) of identified pairs of doublet microtubules. Ciliary frequency is a function of the rate of reorientation of the cyclic track; this parameter, which corresponds to the rate of translocation of active sliding between pairs of doublets, grew with the amplitude of depolarization. Translocation rates were high during transitions between the beat phases (power stroke, return stroke), and were reduced during these phases. Orientational polarograms of the mean rates of both active sliding and sliding translocation show properties of discreteness as well as continuity. The depolarization-induced changes in inclination, and the inferred patterns of sliding rate and sliding translocation rate, are compared with previous results from hyperpolarization-dependent activation of the same motor organelle.
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  • 19
    ISSN: 0886-1544
    Keywords: Cell motility ; chemotaxis ; mathematical model ; alveolar macrophages ; C5a ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Phenomenological parameters from a mathematical model of cell motility [1] are used to quantitatively characterize chemosensory migration responses of rat alveolar macrophages migrating to C5a in the linear under-agarose assay, simultaneously at the levels of both single cells and cell populations. This model provides theoretical relationships between single-cell and cell-population motility parameters. Our experiments offer a critical test of these theoretical linking relationships, by comparison of results obtained at the cell population level to results obtained at the single-cell level.Random motility of a cell population is characterized by the random motility coefficient, μ (analogous to a particle diffusion coefficient), whereas single-cell random motility is described by cell speed, s, and persistence time, P (related to the period of time that a cell moves in one direction before changing direction). Population chemotaxis is quantified by the chemotactic sensitivity, χo, which provides a measure of the minimum attractant gradient necessary to elicit a specified chemotactic response. Single-cell chemotaxis is characterized by the chemotactic index, CI, which ranges from 0 for purely random motility to 1 for perfectly directed motility. Measurements of cell number versus migration distance were analyzed in conjunction with the phenomenological model to determine the population parameters while paths of individual cells in the same experiment were analyzed in order to determine the single-cell parameters.The parameter μ shows a biphasic dependence on C5a concentration with a maximum of 1.9 × 10-8 cm2/sec at 10-11 M C5a and relative minima of 0.86 × 10-8 cm2/sec at 10-7 M C5a and 1.1 × 10-8 cm2/sec in the absence of C5a; s and P remain fairly constant with C5a concentration, with s ranging from 2.1 to 2.5 μm/min and P varying from 22 to 32 min. χo is equal to 1.0 × 10-6 cm/receptor for all C5a concentrations tested, corresponding to 60% correct orientation for a difference of 500 bound C5a receptors across a 20 μm cell length. The maximum CI measured was 0.2.Values for the population parameters μ and χo were calculated from single-cell parameter values using the aforementioned theoretical linking relationships. The values of μ and χo calculated from single-cell parameters agreed with values of μ and χo determined independently from population migrations, over the full range of C5a concentrations, confirming the validity of the linking equations. Experimental confirmation of such relationships between single-cell and cell-population parameters has not previously been reported.
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  • 20
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    Cell Motility and the Cytoskeleton 17 (1990), S. 34-45 
    ISSN: 0886-1544
    Keywords: detyrosinated α-tubulin ; Drosophila embryo ; confocal microscopy ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The distribution of microtubules (MTs) enriched in detyrosinated α-tubulin (Glu-tubulin) was studied in Drosophila embryos by immunofluorescence micro-scopy by using a monoclonal antibody (ID5) which was raised against a 14-residue synthetic peptide spanning the carboxyterminal sequence of Glu-tubulin (Wehland and Weber: J. Cell Sci. 88:185-203, 1987). While all MT arrays contained tyrosinated α-tubulin (Tyr-tubulin), MTs rich in Glu-tubulin were not found during early stages of development even by using an image intensification camera. Elevated levels of microtubular Glu-tubulin were first detected after CNS condensation in neurone processes. In addition, sperm tails, which remained remarkably stable inside the embryo until late stages of development, were decorated by ID5. This was in marked contrast to the distribution of microtubule arrays containing acetylated α-tubulin, which could already be detected during the cellular blastoderm stage. Additional experiments with taxol suggested that the absence of MTs rich in Glu-tubulin during early stages of development was not due to the rapid turnover rate of MTs, which would be too fast for α-tubulin to be detyrosinated. The possible significance of the differential detyrosination and acetylation of microtubules during development is discussed.
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  • 21
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    Cell Motility and the Cytoskeleton 17 (1990) 
    ISSN: 0886-1544
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
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  • 22
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    Cell Motility and the Cytoskeleton 17 (1990), S. 71-74 
    ISSN: 0886-1544
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
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  • 23
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    Cell Motility and the Cytoskeleton 17 (1990), S. 87-94 
    ISSN: 0886-1544
    Keywords: benzimidazole ; anti-microtubule agents ; carbendazim ; nocodazole ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: We are using molecular genetic techniques to identify sites of interaction β-tubulin with benzimidizole anti-microtubule agents. We have developed a marker-rescue technique for cloning mutant alleles of the benA, β-tubulin gene of Aspergillus nidulans and have used the technique to clone two mutant benA alleles, benA16 and benA19. These are the only A. nidulans alleles known to confer resistance to the benzimidazole antimicrotubule agent thiabendazole and supersensitivity to other benzimidazole antimicrotubule agents including benomyl and its active breakdown product, carbendazim. benA16 has been shown, moreover, to reduce thiabendazole binding to β-tubulin. We have sequenced the two mutant alleles and have found that they carry different nucleotide changes that cause the same single amino acid substitution, valine for alanine at amino acid 165. Since thiabendazole and carbendazim differ at only one side chain, the R2 group, we conclude that the region around amino acid 165 is involved in the binding of the R2 group of benzimidazole antimicrotubule agents to β-tubulin.
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  • 24
    ISSN: 0886-1544
    Keywords: Wheat germ agglutinin ; Limax flavus agglutinin ; axonal cytoskeleton ; actin ; cytochalasin D ; axoplasmic transport ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Goldfish retinal ganglion cell (RGC) axons regenerating in vitro exhibit a novel mode of axoplasmic transport that entails a rapid bidirectional bulk redistribution of axoplasm, “packaged” as protruding varicosities and non-protruding phase-dense inclusions (Koenig et al.: J. Neurosci. 5:715-729, 1985; Edmonds and Koenig Brain Res. 406:288-293, 1987). We have used phase-contrast video microscopy to study transmembrane effects of surface-binding lectins on bulk transport and transport of single visible organelles in RGC axons. Our findings show that certain lectins which crosslink sialoglycoconjugates, such as wheat germ agglutinin (WGA) and the more specific sialic acid-binding lectin Limax flavus agglutinin (LFA), induce a rapid inhibition of transport activity. The LFA-induced inhibition of transport can be reversed by appropriate simple sugar haptens, and can also be antagonized by pretreatment with cytochalasin D. One of the consequences of LFA binding is an increase in RITC-conjugated phalloidin fluorescence staining of preterminal axons. The latter observation in conjunction with the antagonistic action of cytochalasin D suggests that one possible explanation for the transmembrane arrest of transport induced by crosslinking of surface sialoglycoconjugates may involve a polymerization and/or reorganization of the actin filament network which hinders translocation of mobile axoplasmic components.
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  • 25
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    Cell Motility and the Cytoskeleton 17 (1990) 
    ISSN: 0886-1544
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
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  • 26
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    Journal of Chemometrics 4 (1990), S. 47-50 
    ISSN: 0886-9383
    Keywords: Classification ; Pattern recognition ; Preprocessing ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Over the past 15 years the linear learning machine has been applied to a large number of chemical problems. The learning machine approach is conceptually simple and does not require knowledge about the statistical distribution of the data. However, there are problems associated with this approach. One problem which has not been investigated is the influence of mislabeled samples on the positioning of the hyperplane in feature space. If a few samples in a data set are incorrectly tagged prior to training (i.e. the samples are labeled as members of class 2 even though they are actually members of class 1), it is still possible using the linear learning machine to achieve a classification success rate of 100% for the training set. However, unfavorable results will be obtained for the prediction set. The magnitude of this effect and its potential implications regarding the proper use of the linear learning machine are discussed.
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  • 27
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    Journal of Chemometrics 4 (1990), S. 51-59 
    ISSN: 0886-9383
    Keywords: Deconvolution ; Jansson's method ; Peak restoration ; Iterative deconvolution ; Peak resolution ; Non-linear deconvolution ; Super-resolution ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In previous papers Jansson's method was found to be successful at deconvolving severely overlapped gas chromatographic peaks. In the most recent paper the method was evaluated with respect to quantitative accuracy, peak area and retention time repeatability. The problems associated with deconvolving noisy data and some alternatives which can improve the ability of Jansson's method to deconvolve noisy data are discussed. These alternatives include presmoothing the data with a nine-point, third-order polynomial filter and data reblurring. This paper will test these methods on peaks with various degrees of resolution and signal-to-noise ratios.
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  • 28
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    Journal of Chemometrics 4 (1990), S. 61-77 
    ISSN: 0886-9383
    Keywords: Infrared ; Spectroscopy ; Spectrometry ; Retrieval ; Confirmation ; Chemometrics ; Adequate peaks ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In the series of analytical techniques for identification of chemical substances, infrared spectrometry presents by far the highest information content. However, the information is most complicated too. It concerns a multitude of band positions, band intensities and band shapes, which, moreover, can be disturbed by matrix and other effects. The high redundancy, however, allows conclusions to be made by a qualitative, subjective procedure.IR is often used to prove the equality between a sample and a reference material, e.g. in quality control of a production process. In forensic control, the question to be answered is mostly not to prove equality, but whether or not the presence of a compound in a sample, e.g. a drug, can be proved. Moreover, testing has to be performed according to objective rules.To fulfil these requirements, a new retrieval algorithm, the ‘Adequate Peaks Search’, is presented. It concerns representing the reference spectra by sets of adequate peak positions and the sample spectrum by a set of all peak positions, whereafter the cross-sections of the sample set and the reference sets are determined. The concept ‘adequate peak’ is defined and criteria have been formulated to evaluate the results into a positive (presence of the analyte is proved) or negative (presence is not proved) conclusion.The detection limit when the Adequate Peaks Search (APS) method was applied was four to seven times lower than that attained by a number of experts.
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  • 29
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    Journal of Chemometrics 4 (1990), S. 79-90 
    ISSN: 0886-9383
    Keywords: PLS ; Three-way matrices ; Calibration ; Residual bilinearization ; Background correction ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: When using hyphenated methods in analytical chemistry, the data obtained for each sample are given as a matrix. When a regression equation is set up between an unknown sample (a matrix) and a calibration set (a stack of matrices), the residual is a matrix R.The regression equation is usually solved by minimizing the sum of squares of R. If the sample contains some constituent not calibrated for, this approach is not valid. In this paper an algorithm is presented which partitions R into one matrix of low rank corresponding to the unknown constituents, and one random noise matrix to which the least squares restrictions are applied. Properties and possible applications of the algorithm are also discussed.In Part 2 of this work an example from HPLC with diode array detection is presented and the results are compared with generalized rank annihilation factor analysis (GRAFA).
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    Journal of Chemometrics 4 (1990), S. 91-96 
    ISSN: 0886-9383
    Keywords: Sample size ; Monte Carlo ; Multivariate, normal ; Q-Q plots ; Classification ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Because many pattern recognition techniques are predicated on the assumption of mutivariate normal data, Monte Carlo simulation studies were performed to determine the number of samples that are necessary to describe a multivariate normal population adequately. From these studies we have learned that hundreds of samples are required. These results suggest that parametric procedures should only be used to analyze very large data sets.
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    Journal of Chemometrics 4 (1990), S. 97-100 
    ISSN: 0886-9383
    Keywords: Matrix decomposition ; NIPALS ; Principal component ; SIMCA ; PLS ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Non-linear Iterative Partial Least Squares (NIPALS) algorithm is used in principal component analysis to decompose a data matrix into score vectors and eigenvectors (loading vectors) plus a residual matrix. NIPALS starts with some guessed starting vector. The principal components obtained by NIPALS depends on the starting vector; the first principal component could not always be computed. Wold has suggested a starting vector for NIPALS, but we have found that even if this starting vector is used, the first principal component cannot be obtained in all cases. The reason why such a situation occurs is explained by the power method. A simple modification of the original NIPALS procedure to avoid getting smaller eigenvalues is presented.
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    Journal of Chemometrics 4 (1990), S. 101-101 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Topics: Chemistry and Pharmacology
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    Journal of Chemometrics 4 (1990), S. 102-102 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Topics: Chemistry and Pharmacology
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    Journal of Chemometrics 4 (1990) 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of Chemometrics 4 (1990), S. 102-102 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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    Journal of Chemometrics 4 (1990), S. i 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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  • 37
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    Journal of Chemometrics 4 (1990), S. 103-121 
    ISSN: 0886-9383
    Keywords: Kalman filter ; Recursive digital filter ; Square-root filter ; Information filter ; Parameter estimation ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The use of recursive filtering techniques for parameter estimation in a variety of areas is reviewed. In particular, the Kalman filter algorithm is described, along with several variations, including square-root, UDUT and information filters. The solution to parameter estimation problems is discussed for both linear and non-linear models. Applications described include calibration, curve resolution in spectroscopy, chromatography, electrochemistry, kinetic analysis and process monitoring.
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    Journal of Chemometrics 4 (1990), S. i 
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    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
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  • 39
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    Journal of Chemometrics 4 (1990), S. 337-354 
    ISSN: 0886-9383
    Keywords: Chemometrics ; Chemometrics Society ; History of chemometrics ; Pioneers of modern chemometrics ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This is a first foray into the historical start and early years of chemometrics from about 1972 onwards. We have gathered interviews with three originators (Kowalski, Wold and Massart) as well as with a selected group of six other well-known chemometricians who gradually became active in the 1970s (Christie, Clementi, Hopke, Martens, Brown and Deming). The interviews include amongst a host of subjective recollections a succinct record of the key historical literature as highlighted by the interviewees' own rankings of ‘earliest’ and ‘best’.A discussion of the most general commonalities in these interviews together with other historical material is presented in the second part of the paper.
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    Journal of Chemometrics 4 (1990), S. 355-360 
    ISSN: 0886-9383
    Keywords: Pattern recognition ; U.K. chemometrics usage ; Quantitative structure-activity relationships ; Artificial intelligence ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A survey of members of the U.K. QSAR Discussion Group has been made to determine the extent of use and development of chemometric and artificial intelligence (AI) methods in the analysis of multivariate quantitative structure-activity relationship (QSAR) data in the U.K. Chemometric methods were found to be well established in both industrial and educational establishments and there was significant method development occurring. AI methods were not employed to any great extent and the general level of interest in these techniques was low compared to chemometric methods. A requirement for more education in multivariate statistical methods and regression methods was indicated. A need for a user-friendly, comprehensive, commercially available multivariate statistical package containing multivariate stability testing and regression diagnostic methods was identified.
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    Journal of Chemometrics 4 (1990), S. 361-377 
    ISSN: 0886-9383
    Keywords: Abstract factor analysis ; Exploratory data analysis ; Principal components ; Simulated equilibria ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract factor analyses were performed on databases consisting of simulated samples from aqueous equilbria. The program COMPLEX was used to generate equilibrium species in a system of three reactant metals and five reactant bases. Reactant concentrations and pH were drawn from random-normal distributions so that sample data vectors comprised a multivariate log-normal distribution of equilibrium concentrations. In addition, sample groups were created containing different distributions for pH and reactant concentrations.Equilibrium species were shown to contain variance contributed by change in pH among samples as well as change in reactant concentrations. Factor modelling revealed the qualitative relationships among the species and how the relationships change with pH. Factors also revealed those reactants containing variance in the data matrix. In some cases, reactant variance obscured relationships between pH and the equilibrium species.Since factor modelling of a simulated data matrix revealed the expected chemical equilibrium interactions, a potentially powerful tool exists for investigating the effects of outliers and error.
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  • 42
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    Journal of Chemometrics 4 (1990), S. 389-412 
    ISSN: 0886-9383
    Keywords: Chemometrics ; Chemometrics Society ; History of chemometrics ; Pioneers of modern chemometrics ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This is a first foray into the historical start and early years of chemometrics from about 1972 onwards. We have gathered interviews with three originators (Kowalski, Wold and Massart) as well as with a selected group of six other well-known chemometricians who gradually became active in the 1970s (Christie, Clementi, Hopke, Martens, Brown and Deming). The interviews include amongst a host of subjective recollections a succinct record of the key historical literature as highlighted by the interviewees' own rankings of ‘earliest’ and ‘best’.A discussion of the most general commonalities in these interviews together with other historical material is presented in the second part of the paper.
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  • 43
    ISSN: 0886-9383
    Keywords: Discriminant analysis ; Size-exclusion chromatography ; Wheat proteins ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Continuous digitalized signals such as spectra, electrophoregrams or chromatograms generally have a large number of data points and contain redundant information. It is therefore troublesome performing discriminant analysis without any preliminary selection of variables. A procedure for the application of canonical discriminant analysis (CDA) on this kind of data is studied. CDA can be presented as a succession of two principal component analyses (PCAs). The first is performed directly on the raw data and gives PC scores. The second is applied on the gravity centres of each qualitative group assessed on the normalized PC scores. A stepwise procedure for selection of the relevant PC scores is presented. The method has been tested on an illustrative collection of 165 size-exclusion high-performance (SE-HPLC) chromatograms of proteins of wheat belonging to 55 genotypes and grown in three locations. The discrimination of the growing locations was performed using seven to nine PC scores and gave more than 86% accurate classifications of the samples both in the training sets and the verification sets. The genotypes were also rather well identified, with more than 85% of the samples correctly classified. The studied method gives a way of assessing relevant mathematical distances between digitalized signals according to qualitative knowledge of the samples.
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  • 44
    ISSN: 0886-9383
    Keywords: Principal components ; Multiple and stepwise regression ; Non-parametric density and regression estimation ; Bootstrap inference ; Canonical correlation ; PLS regression ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A statistical study of the dependence between various critical fusion temperatures of a certain kind of coal and its chemical components is carried out. As well as using classical dependence techniques (multiple, stepwise and PLS regression, principal components, canonical correlation, etc.) together with the corresponding inference on the parameters of interest, non-parametric regression and bootstrap inference are also performed.
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 75-87 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Wholly aromatic liquid crystalline main chain polyesters derived from terephthalic acid, phenyl- or (1-phenylethyl)hydroquinone modified with either 3,4′- or 4,4′-dicarboxydiphenylether and p-hydroxybenzoic acid, have been prepared by acidolysis and thermally investigated. All prepared polyesters exhibit excellent thermal stability up to about 400°C, however, the (1-phenylethyl)hydroquinone polyesters generally showed lower stability. Melting points could be decreased to around 200°C without any decrease in the thermal stability or the nematic range.
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    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Soapless emulsion copolymerization of styrene (S) and n-butyl acrylate (BuA) has been investigated using two types of initiator and different comonomer feed mixtures. When using K2S2O8 as initiator, the particle size and size distribution of the final latexes (500 nm and 1.003, respectively) is not significantly affected by the comonomer feed composition, whereas the molecular weight and surface characteristics were found to sharply change at high butyl acrylate content. Based on the most probable particle nucleation mechanism and type of chain termination in the monomer swollen particles, a tentative explanation of these results has been proposed. Replacing persulfate by a carboxylic initiator (4-4′-azobiscyanopentanoic acid) results in the formation of stable particles as α observed with the persulfate, provided the aqueous phase pH is fixed in between 6 and 7. Results on the initiator residue location as a function of the conversion point out that the particle flocculation mechanism is strongly significant in the preparation of such latexes.
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 193-204 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction rates and products of remote oxygen plasma treatment, corona discharge, and ozone treatment of high and low density polyethylenes have been examined using x-ray photoelectron spectroscopy. The oxygen uptake by remote plasma treatment was faster than that of other surface treatments using excited oxygen species. A steady state concentration of 18 ± 1% oxygen can be attained within 1 s of exposure in the remote plasma.
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 231-243 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Due to the particular rheological properties of thermotropic liquid crystalline polymers (TLCP), their application for imaging technology has been investigated. The first class of polymers investigated in this study are the thermotropic liquid crystalline polycarbonates prepared from the solution polycondensation of p,p-dihydroxybiphenyl with bischloroformate as the aliphatic flexible spacer. From the variety of bischloroformates employed, smectic TLCP's were generally obtained with the possible presence of a nematic mesostate. The introduction of comonomers such as substituted hydroquinones or bisphenols were found to lower both the melting transitions and mesophasic range of the TLCP. From rheological characterization, the amount of nonmesogenic moieties present in the copolycarbonates were found to correlate with the increase in the melt viscosity of TLCP.
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 285-298 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Homopolyesters based on bicyclo[2.2.2]oct-2-ene as a mesogenic group were prepared and characterized. The use of bicyclo[2.2.2]oct-2-ene in these homopolyesters lowered the symmetry of the resulting systems enough to lead to the observation of melting behavior.
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 323-331 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of new polyimides containing fluorinated alkoxy side chains are prepared from novel fluorinated alkoxy diamines. The dieletric constant at 1 kHz in the fluorinated polyimides decreases from 3.3 to 2.6 as fluorine content increases. The refractive index also changes from 1.58 to 1.48, dependent on the fluorine content. In addition, the fluorinated polyimides exhibit lower water absorption than the reference polyimides prepared from m-phenylenediamine.
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 411-424 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The emulsion polymerization of vinyl acetate using potassium persulfate and cyclohexanone sodium bisulfite as redox pair initiation system was studied. The rate of polymerization, maximum conversion, and the number of polymer particles produced were found to change with redox initiator, monomer and emulsifier concentrations, and temperature variation. The rate of polymerization was found to be dependent on the initiator, the monomer, and the emulsifier concentrations to the 0.88, 0.22, and 0.20 powers, respectively. The K2S2O8-NaHSO3 redox system was found to decrease maximum conversion and doesn't form a stable emulsion. The apparent arrhenius activation energy (Ea) estimated for the polymerization system was 65.6 kJ/mol. The viscosity average molecular weights for some obtained poly(vinyl acetate) were determined.
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 479-503 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The preparation of a variety of silicon-containing epoxy monomers and oligomers is described and their reactivity in photoinitiated cationic polymerization examined. Monomers and oligomers having terminal cycloaliphatic epoxy groups were found to be especially reactive in cationic polymerization. These materials are attractive candidates for use in coatings, adhesives, and elastomers.
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 551-558 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Six new gem-dicyanocyclobutanes containing carbomethoxy and hydroxyl/acetoxy functions were synthesized by cycloaddition of the appropriate vinyl ethers or alkoxystyrenes to methyl β,β-dicyanoacrylate. They proved to be too thermally labile to allow polycondensation to potentially piezoelectric linear polyesters.
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 573-583 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2-(Chloromethyl)oxetane was prepared in 8% overall yield from 2-propen-1-ol by protection of the alcohol with dihydropyran, epoxidation, ring expansion with dimethylsulfoxonium methylide, acid deprotection, and chlorination with triphenylphosphine in CCl4. 3-(Chloromethyl)oxetane was prepared in 22% overall yield by hydroboration-oxidation of 3-chloro-2-chloromethyl-1-propene followed by base-catalyzed cyclization. Each of the oxetanes was converted to the corresponding elastomeric homopolymer by treatment with a triethylaluminum-acetylacetone-water mixture. Poly[2-(chloromethyl)oxetane] was found to be similar to polyepichlorophydrin in reactivity toward benzoate ion, whereas poly[3-(chloromethyl)oxetane] is more reactive by a factor of 2.
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  • 55
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 679-691 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Twelve structurally different bis- and tetramaleimides were synthesized by Friedel-Crafts reaction between 4-maleimido-benzoylchloride or 3,5-bismaleimido-benzoylchloride and various aromatic reagents. They were characterized by infrared (IR) and proton nuclear magnetic resonance (1H-NMR) spectroscopy. Crosslinked resins were obtained by curing the monomers at 250°C/6 h. Thermal characterization of monomers and cured resins was accomplished by differential thermal analysis (DTA), dynamic thermogravimetric analysis (TGA), and isothermal gravimetric analysis (IGA). Tetramaleimides were polymerized at lower temperatures than did the respective bismaleimides. The cured resins were stable up to 317-385°C in N2 atmosphere and formed an anaerobic char yield of 52-66% at 800°C.
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  • 56
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 717-730 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Small and large unilamellar liposomes composed of 1,2-bis(2,4-octadecadienoyl)-sn-glycero-3-phosphorylcholine (DODPC) are prepared by sonication and extrusion, respectively. They are polymerized with water-insoluble radical initiator, azobis(isobutyronitrile) (AIBN) which can selectively polymerize diene groups in 1-acyl chains of the lipids. Polymerized liposomes are freeze-dried to obtain the polymerized liposome powder. There are two methods to redisperse lyophilized liposomes into water. The extrusion is an effective method to disperse them because the energy at extrusion is necessary only for redispersion, whereas the excess energy at sonication gives damage on liposome structure. There is no difference in stability between polymerized liposomes before and after redispersion with extrusion. DODPC polymers, obtained from free radical-initiated polymerization with AIBN, are linear and have polymerizable diene groups in 2-acyl chains. The liposome powder is therefore soluble in organic solvents. Reconstruction of polymerized liposomes is performed with lipid polymers having low or high molecular weight. The lipid polymers having high molecular weight provide stable large unilamellar liposomes by ethanol injection, but unstable small unilamellar liposomes are formed by sonication. The liposomes reconstructed from lipid polymers having low molecular weight are unstable regardless of their size. After reconstruction of liposomes selectively polymerized by AIBN, diene groups in 2-acyl chains are polymerized by water-soluble radical initiator or UV-irradiation to yield highly crosslinked structure. Their stability is improved remarkably by this postpolymerization.
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  • 57
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 803-809 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New reaction products have been generated on polyethylene and polystyrene surfaces using a novel two-step process. The first stage involves exposure to a downstream nitrogen plasma, and the second to either ozone or a corona discharge. It is observed that each of the two-step reactions yields very different reaction products, with an apparent increase in the formation of C—O functional groups in the former case and the formation of surface — NO2 groups in the latter case.
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  • 58
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 825-835 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Poly(L-glutamate) esters (3a-3d) with long alkyl side chains containing a mesogenic aromatic segment at the terminal position were synthesized. The superstructure of these polypeptides in solution and film were found to hold a α-helical conformation which was confirmed by CD, IR, and dichroic IR spectroscopy. The thermotropic liquid crystalline behavior was investigated by DSC, x-ray diffraction, and polarizing microscopy with hot stage. Polymers 3a and 3b, having transesterification over 60%, were assumed at least to have two liquid crystalline states. Polymer 3c-H-95 exhibited one crystalline state and two liquid crystalline states; however, 3d-H-97 did not show distinct liquid crystalline states.
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  • 59
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 923-929 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Plasma polymers derived from iodobenzene and four copolymers with benzene of varying monomer ratios have been synthesized. Samples were analyzed for qualitative and quantitative information using x-ray photoelectron spectroscopy. The optimum conditions whereby a higher iodine content is obtained in the plasma polymer have been achieved. The results indicate that the use of a copolymerization approach is better. These plasma polymers were subsequently exposed to an oxygen plasma and it was found that oxidation and etching of the surfaces of the plasma polymers does occur. The extent of iodine loss via oxygen plasma etching appears dependent on the character of the plasma polymer.
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  • 60
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 935-943 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 61
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 967-972 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A novel monomer, 2-acryloyl thioxanthone (TXA), was prepared by reaction of 2-hydroxy thioxanthone with acryloyl chloride. Copolymerization of TXA with methyl methacrylate (MMA) in DMF at 80°C was studied in order to evaluate relative reactivities of these monomers. Values of 1.36 and 0.5 were found for the respective reactivity ratios of MMA and TXA, respectively. The resonance stabilization and polar properties were determined and discussed in terms of spectroscopic data.
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  • 62
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 837-855 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The results observed in 44 time-studies that monitored evaporation from liquid-saturated poly(Sty-co-DVB) particles enmeshed in poly(tetrafluoroethylene) microfibers under conditions that precluded decrease in area of the microporous composite film sample verified that after the enmeshed particles undergo transition from the gel-state to the glass-state, the number of residual adsorbed molecules per phenyl group of polymer is given by a linear combination of n 〈 7 exponential decay functions, the first order rate constants of which are related to one another by the equation: log ki = log k0 - mi, where m is characteristic of the polymer, and k0 is characteristic of the sorbed liquid such that k1 is about 105 times faster than k6. The results also show that k1 of the set of nki for desorption from poly(Sty-co-DVB) in the glass-state is equal to kgel, the first-order rate constant for desorption of the test-liquid from that polymer in the gel-state. These results are interpreted to mean that i, the identification number of the ith population, reflects the number of phenyl groups in the “host” polymer with which the “guest” volatile molecule is associated simultaneously as discussed in the text.
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  • 63
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 987-1009 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A mathematical model for the unseeded emulsion copolymerization of styrene and methyl methacrylate has been developed. This model, which includes a new rate coefficient for radical desorption, was used to analyze the effect of the styrene/methyl methacrylate molar ratio in the initial charge on the number of particles, overall conversion and copolymer composition. It was found that the number of particles increased with the methyl methacrylate content and that a drift of the copolymer composition resulted during the polymerization of styrene/methyl methacrylate molar ratios other than 50/50. Good agreement between experimental results and model predictions was achieved.
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 955-965 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An extremely efficient process has been developed for the synthesis of linear silylene-acetylene and disilylene-acetylene polymers. Trichloroethylene is quantitatively converted by n-butyllithium to dilithioacetylene. Quenching with dialkyl-or diaryldichlorosilanes affords high yields of the polymers, \documentclass{article}\pagestyle{empty}\begin{document}$ \rlap{--} [{\rm SiR}_{\rm 2} \hbox{---} {\rm C} \equiv {\rm C\rlap{--} ]}_n ,{\rm and }\rlap{--} [{\rm SiMe}_{\rm 2} {\rm SiMe}_{\rm 2} - {\rm C} \equiv {\rm C\rlap{--} ]}_n $\end{document} if ClMe2SiSiMe2Cl is employed. Molecular weights are much higher with this route than when acetylene is used as the dilithio- or dimagnesium acetylide precursor. Some of these polymers can be pulled into continuous fibers, and all can be cast into coherent films and thermally converted into silicon carbide.
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  • 65
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 1011-1031 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A model is presented for the simulation of the structuration of polymer particles under conditions in which the new polymer chains are compatible with the polymer previously formed. The model involves the calculation of the monomer concentration gradients within the particles due to discrepancies in thermodynamic interactions between the monomer and the different polymers present in each part of the polymer particle. In addition, the distribution of free radicals in the latex particle is taken into account. This distribution results from the anchoring of the hydrophilic end-group of the growing polymer chain on the surface of the particle. The model was applied to the simulation of the polymerization of vinyl acetate on a butyl acrylate-vinyl acetate copolymer seed. It was found that the development of the particle morphology was mainly due to the profile of concentration of radicals in the particle. On the other hand, the effect of the monomer-polymer thermodynamic interactions on the particle morphology was found to be negligible. However, it has to be pointed out that this is because, for the system studied, the interaction parameters of vinyl acetate with polyvinyl acetate and polybutyl acrylate are nearly identical.
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  • 66
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 1073-1078 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We have observed that homopolymers of certain (meth)acrylate esters, prepared by the Schotten-Baumann method of (meth)acryloyl chloride and desired alcohol, in the presence of triethylamine or pyridine, formed gels. The mechanism of gelation was investigated and found to be due to a diene impurity, (meth)acrylic anhydride, which cannot be easily separated from many (meth)acrylate esters. For preparation of pure (meth)acrylate esters, the SN2 displacement reaction of (meth)acrylate anion with the desired chloro compound is recommended. The yields of the two reactions are comparable, and even t-butoxycarbonylmethyl methacrylate is produced in 73% yield by the recommended method.
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  • 67
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 1137-1148 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Carboxylic acid or primary amine-terminated poly(isobutyl vinyl ethers) were synthesized by living cationic polymerizations with functionalized initiators (CH3CHIO—CH2CH2 — X; X: that are the adducts of the corresponding vinyl ethers (CH2 = CH — OCH2CH2—X) with hydrogen iodide. In the presence of iodine, these initiators induced living cationic polymerization of isobutyl vinyl ether to give polymers with the α-end group of X originating from the initiators. The polymer molecular weights were regulated by the monomer to initiator feed ratio and the molecular weight distributions were very narrow (Mw/Mn ≤ 1.15). Subsequent deprotection of the terminal group X led to polymers with a terminal carboxylic acid or primary amine. 1H- and 13C-NMR analyses showed that the end functionalities of these polymers were all close to unity.
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  • 68
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    Keywords: Chemistry ; Polymer and Materials Science
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    Topics: Chemistry and Pharmacology
    Notes: Amphiphilic block polymers of vinyl ethers (VEs).\documentclass{article}\pagestyle{empty}\begin{document}$\rlap{--} [{\rm CH}_{\rm 2} {\rm CH}\left( {{\rm OCH}_{\rm 2} {\rm CH}_{\rm 2} {\rm NH}_{\rm 2} } \right)\rlap{--} ]_m \rlap{--} [{\rm CH}_{\rm 2} {\rm CH}\left( {{\rm OR}} \right)\rlap{--} ]_n \left( {{\rm R: }n{\rm - C}_{{\rm 16}} {\rm H}_{{\rm 33}} ,{\rm }n{\rm - C}_{\rm 4} {\rm H}_{\rm 9} ;m \simeq 40,{\rm n} = 1 - 10} \right)$\end{document} were prepared, each of which consists of a hydrophilic segment with pendant primary amino groups and a hydrophobic poly(alkyl VE) segment. Their precursors were obtained by the HI/I2-initiated sequential living cationic polymerization of an alkyl VE and a VE with a phthalimide pendant (CH2 = CHOCH2CH2Im; Im; phthalimide group), where the segment molecular weights and compositions (m/n ratio) could be controlled by regulating the feed ratio of two monomers and the concentration of hydrogen iodide. Hydrazinolysis of the imide functions gave the target polymers which were readily soluble in water under neutral conditions at room temperature. These amphiphilic block polymers lowered the surface tension of their aqueous solutions (0.1 wt%, 25°C) to a minimum ≃ 30 dyn/cm when the hydrophobic pendant R was n-C4H9 (n = 4-9). The polymers with n-C4H9 pendants in the hydrophobic segment exhibited a higher surface activity than those with n-C16 H33 pendants. The surface activity of the polymers also depended on the pH of the polymer solutions; the surface activity increased in more basic solutions where the ionization of the amino group (—NH2)2—NH3⊕) is suppressed.
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 1179-1183 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of bis(ethyl-3-oxo-butanolato-O1,O3)-bis(2-propanolato)titanium(Tyzor DCR and 2-isocyanatoethyl methacrylate (IEM) in refluxing hexane produced a mixture of trimer and polymers of 2-isocyanatoethyl methacrylate which varied considerably from 23 to 92% polymer as the molar ratio of bis(ethyl-3-oxo-butanolato-O1,O3)-bis(2-propanolato)titanium(Tyzor DCR) to 2-isocyanatoethyl methacrylate (IEM) varied from 1:4 to 1:32. The IEM 1-nylon polymer which was soluble in cresol and phenol was characterized by FTIR, 1H-NMR, and 13C-NMR. This analysis also showed that the methacrylate carbon-carbon double bond survived our reaction conditions intact. Based on atomic absorption determination of titanium, the molecular weight of the polymer ranged between 3000 and 4000 g/mol. Thermal gravimetric analysis (TGA) showed the polymer to be stable in air to approximately 250°C.
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 1221-1236 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymerization of phenylacetylene initiated by MoCl5 and WCl6 based initiators was monitored directly in the NMR sample tube and demonstrated the presence of backbiting and intramolecular cyclization reactions. It was shown that the ratio of cis to trans structural units obtained by isomerization prior to double bond formation dictates the degree of backbiting and intramolecular cyclization reactions. This cis-trans ratio determines the length of cis-transoidal sequences present in the polymer backbone which are available for both backbiting and intrachain cyclization reactions. The cyclic trimers obtained in the metathesis polymerization of phenylacetylene are formed only through the cis-cisoidal-induced backbiting and/or intramolecular reactions. The o-trimethylsilylphenylacetylene follows a living mechanism of polymerization. This is due to the fact that the size of the ortho substituent suppresses the cis-transoidal to cis-cisoidal isomerization reactions and therefore eliminates the backbiting reactions. The steric hindrance provided by the size of the ortho substituent also eliminates interchain and intrachain reactions.
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 1289-1296 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: No abstract.
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 1303-1327 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Zerovalent palladium catalysts, dispersed within functional, porous, crosslinked styrene-divinylbenzene copolymers were prepared by impregnation of lipophylic [(C8H17)2NH+][PdCl4 = ] complexes followed by reduction with hydrazine or formaldehyde. A qualitative survey of the catalytic reactivity in hydrogenation of various alkenes differing in substitution degrees (styrene, +-methylstyrene, etc.), and competitive reduction of exo/endo bonds (4-vinylcyclohexene) was performed. The functional groups in the polymer, 2,4-dinitrophenyl, aminomethyl, methoxybenzyl, dialkylaminomethyl, and pseudocrown were shown to have a major effect on catalyst activity. In the two series of polymeric supports, the polymeric adsorbents (Amberlites XAD-2, XAD-4, and XAD-7) and functionalized Amberlite XE-305, the general trend indicated preference of Pd0 catalysts dispersed on hydrophobic π-acceptor type supports over hydrophobic supports, over polar basic or hydrophilic supports. This is generally true for both non-polar (e.g., styrene) and polar (e.g., allylacrylate) olefins. The most active catalysts, carrying 2,4-dinitro phenyl groups, also showed higher selectivity in reduction of the exo over endo double bond in 4-vinylcyclohexene, in comparison to commercial Pd/C catalyst. Electron microscopy (SEM) showed very little change in the inner porous polymer structure and almost homogeneous metal distribution profiles. TEM provided particle sizes. The activity of the catalyst was 8-fold higher with the smallest crushed particles (0.05-0.12 μm) than with the large (600 μm) noncrushed beads. The catalyst showed exceptional stability on storage (98% activity after 1 year) and marginal loss of activity after 21,000 catalytic cycles per Pd atom.
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 1377-1386 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In the sulfonation of polynorbornene in dilute solution, the nature of the sulfonation agent mainly influences the reaction rate, according to its strength and also affects some side reactions (chain scission and crosslinking). The sulfonation can be carried out in suspension after swelling the highly porous powder in dichloroethane up to a 55% sulfonation ratio with preservation of the initial particular nature of the polymer; the latter may be then either partly or totally water soluble, depending on the initial size of the particles. Partial sulfonation, leading to ionomers, may be carried out in bulk at moderate temperature, in a mixing chamber, after gelification of the polymers, plasticized with CCl4.
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 1841-1846 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: For a potential use of spiroorthoesters which polymerize with essentially zero shrinkage during polymerization, the preparation of spiroorthoester (I) bearing the perfluoroalkyl group was carried out. Spiroorthoester I was prepared by the reaction of ε-caprolactone with 2-(F-octyl)ethyl glycidyl ether (II), obtained from 2-(F-octyl)ethanol and epichlorohydrin, in the presence of catalytic amount of BF3OEt2. Spiroorthoester I underwent the cationic ring-opening polymerization by virtue of BF3OEt2 to obtain poly(ether-ester) with 2.7% expansion on polymerization. The presence of the perfluoroalkyl group had no significant effect on the polymerization of the spiroorthoester.
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 1519-1526 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Poly(2-hydro-2-oxo-1,3,2-dioxaphosphorinane) was quantitatively chlorinated, and the resulting polymer was reacted with excess of imidazole, giving the highly reactive polyesteramide. This polymer, treated with N1-hydroxyethyluracil, gave polyphosphates with N1-oxoethyleneuracil in the side chains. The final polymers (M̄n ≈ 104) as well as the intermediate products were characterized by 1H-, 13C- and 31P-NMR spectroscopy.
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 1569-1578 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1,2-Bis(p-aminophenyl)tetramethyldisilane was synthesized from 1,2-dichlorotetramethyldisilane and 4-[N,N-bis(trimethylsilyl)amino]phenyllithium. The diamine was reacted with various aromatic diacid chlorides giving disilane-containing aromatic polyamides (aramids), whose inherent viscosities were between 0.27 and 0.70 dL/g, depending on the diacid chlorides used. The aramids had glass transition temperatures between 194 and 255°C. No weight loss was observed below 350°C. Some of the polymers were found to be semicrystalline based on their x-ray diffractograms. The aramid films showed a strong ultraviolet (UV) absorption at 287 nm, which decreased during irradiation with UV light, suggesting that cleavage of the silicon-silicon bond in the aramid backbone occurs. A decrease in the inherent viscosity and molecular weight of the soluble aramid derived from phenylindanedicarbonyl chloride was also observed by irradiation with UV light.
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 1623-1636 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of modified polyacrylonitriles have been obtained with several primary amines, such as ethanolamine, ethylenediamine, ethylamine, n-butylamine, and n-octylamine, without any catalysts in DMSO. This paper presents the syntheses of these new modified polymers and discusses the resultant structures and reaction mechanism by IR, NMR, and UV spectra. Composition was obtained by elemental analysis. Moreover, some physical properties of polymer were also investigated. It was found that all these primary amines could initiate coloration of polyacrylonitrile, which involves linking up of adjacent nitrile groups, and also reactions of the amines with the nitrile groups. However, the product of polyacrylonitrile with ethanolamine and with ethylenediamine were soluble in water when the mole ratio of amine group to nitrile group was 2. This interesting fact promoted a more detailed study of the modification of polyacrylonitrile with these amines. Crosslinking of the products of PAN with ethanolamine (or with ethylenediamine) was achieved by heat treatment. A mechanism for the formation of crosslinking was proposed.
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 1909-1921 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Monodisperse crosslinked polystyrene beads of varied size and crosslink density are prepared by emulsion copolymerization of styrene and divinylbenzene in the absence of emulsifier. Tumbling and internally stirred reactors were used for synthesis, with minimal agglomeration at at least 0.22 wt % potassium persulfate and up to 10% by weight of styrene in aqueous emulsion in the absence of oxygen. Particle sizes decreased from 800 to 200 nm on raising the polymerization temperature from 60 to 95°C. The glass transition temperature of the beads increased from 104.4 to 133°C by the inclusion of up to 10% by weight of divinylbenzene. The thermal stability of the beads was higher for peroxide than for persulfate initiation. The crosslink density estimated from the degree of swelling was about one third that expected from stoichiometry. The polystyrene beads are used as filler particles in polymer composites.
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 1989-1994 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 80
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 2237-2247 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of polyamides and polyureas containing cyclic (1b, 1c, and 1d) or acyclic (2b, 2c, and 2d) bipyridinediyl diamino units in the polymer backbone were prepared. By introducing aliphatic or aromatic comonomers, it was possible to influence the degree of rigidity of the resulting polymers. In the synthesis of the polymers 2c and 2d two new azamacrocycles 5 and 6, respectively, were also produced and they were isolated and characterized. 1H-NMR and IR spectral data support the structure of the synthesized compounds. Thermal analysis data indicate that the polyureas posses lower PDT (polymer degradation temperature) values with respect to the corresponding polyamides.
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  • 81
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 2275-2292 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In order to graft a vinyl acetate-methyl acrylate mixture onto cellulose, an exploration of the way of addition of the reactants has been made. The influence of several factors on the grafting parameters was studied, i.e., the order of addition of the ceric ion initiator and the monomer mixture, the removal of the ceric ion solution after a cellulose-ceric ion contact time, and the delayed addition along the polymerization period of the more reactive monomer (methyl acrylate) towards the cellulosic radicals. Some grafting parameters were determined: grafting yield, grafting efficiency, cellulose conversion, molecular weight, ceric ion consumption, grafting frequency, number of grafted chains, and synthetic copolymer composition. After a short period (ca. 15 min) for the ceric adsorption on cellulose, a fast formation of cellulosic radicals arises in the initial stages of the polymerization. These initial cellulosic radicals should be trapped by a sufficiently reactive monomer if high grafting yield and high number of grafted chains are to be reached. A portion of the synthetic polymer chains anchored to cellulose that are formed in the first stages of the polymerization, which are generated from cellulosic hemiacetal groups, should constitute block copolymer.
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  • 82
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 1995-1997 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 83
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 2085-2095 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Monosized droplets of 2-hydroxyethyl methacrylate (HEMA) and glycerol monomethacrylate (GMA) were made by passing the monomers under pressure through a nozzle coupled to an energized piezoelectric crystal. The droplets were allowed to fall into liquid nitrogen where they vitrified. The radiation post-polymerization of the monomer spheres was investigated. Uniform monosized poly-HEMA particles in the 100-300 μm diameter range were prepared with a coefficient of variation of 1.57% for particles of 155 μm in diameter. Monosized poly-GMA was also prepared. The post-polymerization conversion of pre-irradiated GMA vitrified monomer droplets as a function of thawing rate and radiation dosage was investigated.
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  • 84
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 2169-2178 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Four diimide-diacids 3a-d were synthesized from pyromellitic dianhydride and amino acids of the formula HOOC — (CH2)m — NH2, with m = 1, 3, 5, 10. These diacids were condensed directly with various aromatic diamines using triphenyl phosphite in N-methyl-2-pyrrolidone (NMP)-pyridine solution in the presence of calcium chloride. The resulting poly(amide-imide)s have an aliphatic-aromatic structure and the relation between the general properties and the amount of the aliphatic part in the repeat unit was studied. IR spectroscopy, elemental analysis, and inherent viscosity measurements were used for the characterization. Studies of solubility, DSC traces, thermal stability, and crystallinity were also made.
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  • 85
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Radical copolymerizations of α-trimethylsilyloxystyrene (TMSST), a silyl enol ether of acetophenone, with electron-accepting monomers such as maleic anhydride (MA) and fumaronitrile (FN) were investigated. TMSST underwent alternating copolymerizations with both MA and FN irrespective of the feed composition, whereas it failed to copolymerize with diethyl fumarate (DEF). The alternating copolymers of TMSST with MA and FN were desilylated with concentrated hydrochloric acid as a catalyst to form polymers containing γ-lactone rings. The formation of the lactone rings was also observed in the desilylation of an alternating copolymer of TMSST with acrylonitrile (AN) under the similar conditions.
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  • 86
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 2475-2483 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dicyanoimidazole (I) was attached to a polystyrene backbone in order to prepare polymers containing electron-accepting pendant groups to complement the existing body of electron-donating polymers. The preparation of poly[4,5-dicyano-1-(vinylbenzyl)imidazole] (III), poly[4,5-dicyano-1-(vinylbenzyl)imidazole-co-9-(vinylbenzyl) carbazole] and attempted polymerization of 4,5-dicyano-1-vinylimidazole are described. Cyclic voltammetry and charge transfer studies are used to characterize the electron-accepting strength of the cyanoimidazole model compounds. These studies show that while cyanoimidazoles are moderate electron acceptors, they do not form charge transfer complexes with the donor molecules investigated.
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  • 87
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of novel photosensitive polybenzoxazole precursors were prepared from polycondensation of 2,2-bis(3,3′-amino-4,4′-hydroxyphenyl)hexafluoropropane with photosensitive dicarboxylic acid chlorides such as p-phenylenediacryloyl chloride and benzophenone-4,4′-dicarboxylic chloride. The precursors are soluble in common organic solvents owing to the presence of perfluoromethyl groups in the chain structure, and insolubilized in the solvents on irradiation with the light. Polybenzoxazole patterns with high resolution as well as high aspect ratio were reproduced by baking the precursor patterns at 300°C. The pattern shrinkage on the conversion to polybenzoxazole was slight. The polybenzoxazole films offered good heat-resistance up to 400°C in addition to good electrical properties.
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  • 88
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 2597-2607 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: N-phenyl-α-methylene-β-lactam (PML), a cyclic analog of N,N-disubstituted methacrylamides which do not undergo radical homopolymerization, was synthesized and polymerized with α,α′-azobis (isobutyronitrile) (AIBN) in solution. Poly (PML) (PPML) is readily soluble in tetrahydrofuran, chloroform, pyridine, and polar aprotic solvents but insoluble in toluene, ethyl acetate, and methanol. PPML obtained by radical initiation is highly syndiotactic (rr = 92%), exhibits a glass transition at 180°C, and loses no weight upto 330°C in nitrogen. The kinetics of PML homo-polymerization with AIBN was investigated in N-methyl-2-pyrrolidone. The rate of polymerization (Rp) can be expressed by Rp = k[AIBN]0.55[PML]1.2 and the overall activation energy has been calculated to be 87.3 kJ/mol. Monomer reactivity ratios in copolymerization of PML (M2) with styrene (M1) are r1 = 0.67 and r2 = 0.41, from which Q and e values of PML are calculated as 0.60 and 0.33, respectively.
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  • 89
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 2651-2663 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new method is described for the preparation of sterically stabilized nanoparticles of defined size and polydispersity which are stabilized in aqueous solution by the presence of covalently linked monomethoxy-poly (oxyethylene) (MeOPOE) chains. The nanoparticles (100-270 nm mean diameter) were prepared by a process of desolvation of a graft copolymer prepared from poly(2-aminoethylmethacrylate) (PAEMA) and MeOPOE. Reproducible desolvation was achieved by the addition of sodium phosphate buffer to the copolymer in aqueous solution to give particles which were crosslinked in situ with the addition of glutaraldehyde. The size (mean diameter) and polydispersity (Q) of the particles were determined by Photon Correlation Spectroscopy (PCS). The temperature at which the desolvation reaction was performed was found to influence the particle size; at low temperatures (5-12°C), small particles were produced (99-121 nm, Q = 0.090-0.121), whereas at much higher temperatures (40-55°C), particles as large as 224-275 nm (Q = 0.138-0.127) were generated. Other parameters such as the graft copolymer concentration, the amount of glutaraldehyde added, the pH of the sodium phosphate buffer added, and the reaction time were found to be of relative insignificance in influencing the particle size. In addition to those involved in drug delivery, our method of nanoparticle preparation may be of interest to those engaged in the preparation of particulate materials and colloidal dispersions for other specific applications (e.g. stabilized photographic emulsions).
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  • 90
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 2729-2739 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of solution polymerization of methyl methacrylate using trioctylmethylammonium persulfate (aliquat persulfate) at 60°C has been studied in t-butyl alcohol, N,N-dimethyl formamide, acetonitrile, dioxane, acetone, and methyl ethyl ketone. The rate of polymerization depends markedly on the solvent used. The initiator exponent is close to 0.5 in the first three solvents but larger than this value in the other three solvents. The overall activation energy of the polymerization has been determined in all the solvents. The rate constants and activation parameters for the primary decomposition of the initiator have been determined in the first three solvents where ideal polymerization conditions prevail. The activation parameters for the decomposition of AQ2S2O8 in the organic solvents depend on the type of solvent. They are very different from those of the free S2O2-8 ion in water. These differences have been explained taking into consideration the various ionic forms in which the initiator exists in the studied solvents using a previously postulated model of the activated state.
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  • 91
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 2765-2775 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The radical polymerization behavior of alkoxyallene containing the epoxy group, allenyl glycidyl ether (I), was investigated to obtain the more reactive polymer. The desired polymer was successfully synthesized only by the copolymerization of I with acrylonitrile (AN) at 80°C in DMF, although the homopolymer of I was converted to the crosslinked polymer during its purification. The same number of epoxy and two kinds of methylene groups were simultaneously introduced onto the polymer through propagating allyl radical. The obtained copolymer, therefore, was readily converted to the gelled polymer with methods such as heating and treating with Lewis acids or amines. Further, the copolymer containing two kinds of methylene groups was prepared similarly from methoxyallene (II) and AN, and was also converted to the crosslinked polymer with the cationic catalyst. These copolymers of I or II with AN will be expected to be new types of reactive polymers.
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  • 92
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 2877-2879 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 93
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 2917-2922 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Initiation with a combined initiator n-butyllithium/lithium tert-butoxide in the ratio 1:6 brings the anionic polymerization of 2-ethylhexylacrylate (EtHA) in toluene and n-heptane at temperatures between -78 and -20°C up to a quantitative conversion. In the initial stages of the process the molecular weight distribution (MWD) of the products is polymodal as a result of the stablizing function of the alkoxide; MWD of the final product after a complete consumption of the monomer is medium, being visibly dependent on the reaction temperature and without any distinct content of low-molecular weight components, which suggests a sufficient activity of all growth centers, and thus an essential restriction of side termination reactions.
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  • 94
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 2845-2856 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2-Trimethylsilyloxy-1,3-butadiene (TMSBD), the silyl enol ether of methyl vinyl ketone, was homopolymerized with a radical initiator to afford polymers with a molecular weight of ca. 104. Radical copolymerizations of TMSBD with styrene (ST) and acrylonitrile (AN) in bulk or dioxane at 60°C gave the following monomer reactivity ratios: r1 = 0.64 and r2 = 1.20 for the ST (M1)-TMSBD (M2) system and r1 = 0.036 and r2 = 0.065 for the AN (M1)-TMSBD (M2) system. The Q and e values of TMSBD determined from the reactivity ratios for the former copolymerization system were 2.34 and -1.31, respectively. The resulting polymer and copolymers were readily desilylated with hydrochloric acid or tetrabutylammonium fluoride as catalyst to yield analogous polymers having carbonyl groups in the polymer chains.
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  • 95
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 2857-2866 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: For emulsion polymerization in the zero order region (Interval II) a relation between the average number of free radicals per particle, n̄(t), and the particle number average volume of a particle, v̄n(t), is derived as dv̄n(t)/dt = Kn̄(t), where K is volume growth rate of a particle containing one free radical and is constant. This relation is also extended to copolymerization systems with an appropriate modification of the definition of K. By use of the data of particle size distribution (PSD), n̄ can be calculated without knowing the total number of particles. In conjunction with this relation, the recently developed light-scattering technique for measuring the PSD in addition to the conventional transmission electron microscope technique can provide a quick route for determination of n̄. Styrene and methyl methacrylate emulsion homopolymerizations are taken as calculation examples.
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  • 96
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 3123-3135 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymerization of methyl methacrylate with cupric laurate in combination with N,N-dimethyl formamide as initiator was studied in carbon tetrachloride medium at 60°C. The rate of polymerization was found to be proportional to the 3/2th power of the monomer concentrations and to the square root of both cupric laurate and DMF concentrations. Spectroscopic investigations indicated a ternary complex formation involving cupric ion, methyl methacrylate, and DMF. A reaction scheme is suggested on the basis of these results and various kinetic constants have been evaluated.
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  • 97
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 3155-3163 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Copolymers of 2-ethylacrylic acid (EAA) and methacrylic acid (MAA) were prepared in bulk and in N,N-dimethylformamide (DMF). Although precipitation of the copolymers was observed in bulk, the reaction mixtures remained apparently homogeneous in DMF. Best-fit terminal-model reactivity ratios were determined by a nonlinear least squares technique to be rMAA = 1.14 and rEAA = 0.23 in bulk, and rMAA = 1.91 and rEAA = 0.09 in 50% DMF solution. Examination of 13C-NMR spectra provided convincing evidence for the formation of statistical copolymers. Copolymerizations richer in MAA provided copolymers of higher molecular weights.
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 3179-3184 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 99
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 3241-3250 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: High purity 2,7-fluorenedicarboxylic acid chloride was synthesized in a multistep reaction scheme from 2,7-dibromofluorene. Subsequent polycondensation in polyphosphoric acid of 2,5-diamino-1,4-benzenedithiol dihydrochloride with terephthaloyl chloride and 2,7-fluorenedicarboxylic acid chloride led to rigid-rod benzobisthiazole polymers with reactive fluorene moieties. The proportion of fluorene in the resultant polymers was controlled through reaction stoichiometry. Soluble polymers with intrinsic viscosities as high as 33.7 dL/g (methanesulfonic acid, 30°C) were obtained if the polymerization temperature was not allowed to exceed 165°C. Insoluble, presumably crosslinked polymers were obtained at higher temperature (190-200°C). Thermal characterization of the polymers by differential thermal analysis and thermal gravimetric analysis/mass spectroscopy did not disclose any thermal transition to 450°C. Onset of weight loss in air did not occur until over 550°C.
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    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 3261-3269 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New photosensitive polymides containing photosensitive disilane unit were synthesised from 1,2-bis(4-aminophenyl)tetramethyldisilane and various aromatic tetracarboxylic dianhydrides by the usual two-step procedure that includes ring-opening polyaddition to yield the precursor polyamic acids, followed by cyclodehydration giving the respective polyimides. The polymaic acids had inherent viscosities between 0.63 and 0.85 dL/g depending on the tetracarboxylic dianhydride used. Excepting the polyimide obtained from pyromellitic dianhydride, all other polyimides were soluble in N-methyl-2-pyrrolidone, m-cresol, and pyridine. While the polyimide containing diphenyl sulfone unit was amorphous, the other polyimides were semi-crystalline polymers based on their x-ray diffractograms. The polyimides had glass transition temperatures between 235 and 304°C. They were thermally stable up to 380°C in both air and nitrogen atmospheres. All the polyamic acids showed a drastic decrease in the inherent viscosity upon UV light irradiation, implying the inherent photosensitivity of the polymers containing the disilane moiety.
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