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Journal articles on the topic 'Oligostyrenes'

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Author: Grafiati

Published: 4 June 2021

Last updated: 20 February 2023

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1

Konishi, Toshiki, Takenao Yoshizaki, and Hiromi Yamakawa. "Determination of Stereochemical Compositions of Oligostyrenes by 13C NMR." Polymer Journal 20, no. 2 (February 1988): 175–78. http://dx.doi.org/10.1295/polymj.20.175.

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2

David, Ghislain, Bernard Boutevin, Jean-Jacques Robin, Cedric Loubat, and Nathalie Zydowicz. "Synthesis of carboxy-terminated telechelic oligostyrenes by Dead End Polymerization." Polymer International 51, no. 9 (2002): 800–807. http://dx.doi.org/10.1002/pi.957.

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3

Ahmetli, Gulnare, Nejdet Sen, Erol Pehlivan, and Sancaktar Durak. "Adhesive and anticorrosive polymeric coatings obtained from modified industrial waste oligostyrenes." Progress in Organic Coatings 55, no. 3 (March 2006): 262–67. http://dx.doi.org/10.1016/j.porgcoat.2005.11.011.

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4

Pasch, Harald, Wolf Hiller, and Ronald Haner. "Investigation of the tacticity of oligostyrenes by on-line h.p.l.c./1H n.m.r." Polymer 39, no. 8-9 (January 1998): 1515–23. http://dx.doi.org/10.1016/s0032-3861(97)00446-1.

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5

Shalliker, Ross Andrew. "Two-dimensional HPLC analysis of oligostyrenes: Comprehensive and online heart-cutting techniques." Journal of Separation Science 32, no. 17 (September 2009): 2903–11. http://dx.doi.org/10.1002/jssc.200900175.

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6

Gray, Michael J., Gary R. Dennis, Patrick J. Slonecker, and R. Andrew Shalliker. "Utilising retention correlation for the separation of oligostyrenes by coupled-column liquid chromatography." Journal of Chromatography A 1073, no. 1-2 (May 2005): 3–9. http://dx.doi.org/10.1016/j.chroma.2004.10.071.

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7

Braun, Dietrich, Inka Henze, and Harald Pasch. "Functionality type analysis of carboxy-terminated oligostyrenes by gradient high performance liquid chromatography." Macromolecular Chemistry and Physics 198, no. 11 (November 1997): 3365–76. http://dx.doi.org/10.1002/macp.1997.021981103.

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8

Rodrigues, Anne-Sophie, Evgueni Kirillov, Bruno Vuillemin, Abbas Razavi, and Jean-François Carpentier. "Binary ansa-lanthanidocenes/dialkylmagnesium systems versus single-component catalyst: Controlled synthesis of end-capped syndiotactic oligostyrenes." Journal of Molecular Catalysis A: Chemical 273, no. 1-2 (August 2007): 87–91. http://dx.doi.org/10.1016/j.molcata.2007.03.072.

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9

Meppelder, Geert-Jan M., Klaus Beckerle, Ramanujachary Manivannan, Bing Lian, Gerhard Raabe, Thomas P. Spaniol, and Jun Okuda. "Enantiomerically Pure Titanium Complexes Containing an [OSSO]-Type Bis(phenolate) Ligand: Synthesis, Structure, and Formation of Optically Active Oligostyrenes." Chemistry - An Asian Journal 3, no. 8-9 (September 1, 2008): 1312–23. http://dx.doi.org/10.1002/asia.200800064.

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10

Shimada, Kayori, Marina A. Lusenkova, Keisuke Sato, Takeshi Saito, Shigetomo Matsuyama, Hisae Nakahara, and Shinichi Kinugasa. "Evaluation of mass discrimination effects in the quantitative analysis of polydisperse polymers by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry using uniform oligostyrenes." Rapid Communications in Mass Spectrometry 15, no. 4 (2001): 277–82. http://dx.doi.org/10.1002/rcm.224.

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11

Busko, N. A., V. K. Grishchenko, A. V. Barantsova, N. V. Gudzenko, Ya V. Kochetova, and S. N. Ostapyk. "SILICON-CONTAINING OLIGOMERIC AZOINITIATORS IN THE SYNTHESIS OF BLOCK COPOLYMERS." Polymer journal 43, no. 2 (June 9, 2021): 123–32. http://dx.doi.org/10.15407/polymerj.43.02.123.

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The aim of the work was to develop methods for the synthesis and study of the properties of silicon-containing oligomeric azo- and polyazoinitiators based on bis-γ-hydroxypropylpolysiloxane (HPS) and bis-γ-aminopropylpolysiloxane (APS). Silicon-containing oligomeric azoinitiators using HPS were synthesized on the basis of cyclohexanone azo-bis-isobutyrohydrazone (AGN-CH) and bis-γ-hydroxypropylpolysiloxane bifunctional macrodiisocyanate (MDIHPS). MDIHPS was obtained by the interaction of GPS with 2,4 toluene diisocyanate (2,4-TDI). Oligomeric azoinitiators have been obtained, which have the structure RXR and (RX)nR, where R is a propylpolysiloxane block, X is a azo initiator block. For the synthesis of an oligomeric azo initiator based on bis-γ-aminopropyl polysiloxane (APS), a method was first developed for the synthesis of a monomeric azo initiator with terminal oxadiazolinylcarbamanate isocyanate groups (AGN-NCO) by the interaction of AGN-CH and 2,4-TDI at a molar ratio of 1: 2. On the basis of the obtained AGN-NCO and APS at a molar ratio of AGN-NCO: APS = 1: 1, an oligomeric azo initiator (OAI APS-P) was synthesized, which has the structure (RX)nR, where R is a propylpolysiloxane block, X is an azo initiator block. The structures of monomeric and oligomeric azo initiators have been studied by UV and IR spectroscopy, and the kinetic regularities of their synthesis have been calculated. On the basis of oligomeric azo initiators and styrene, block copolymers of the (AB)nA type were obtained by the method of thermal and photoinitiated radical polymerization, where A is a propylpolysiloxane block, B is an oligosyrene block with a constant value of the organosilicon block and a different size of the oligostyrene block. The structure of block copolymers was investigated by IR spectroscopy. It was shown that during photopolymerization, oligostyrene blocks of shorter length are formed than during thermopolymerization, and possible oxidation processes. The study of relaxation transitions by DSC in oligostyrene and propylpolysiloxane blocks of the BCP showed that the common heat capacity curves are the presence of two jumps in the heat capacity at the glass transition temperatures of the polysiloxane and oligostyrene microphase. A slight shift in the glass transition temperature of polysiloxane microphases in BCP towards higher temperatures compared to the homopolymer may be associated with the effect of oligostyrene microphase. With a decrease in the length of the oligosyrene block, a low-temperature shift in the glass transition temperature of oligostyrene blocks relative to the homopolymer and a depression of ∆Cp,2 are observed, which is associated with the suppression of mobility in oligodienic microphases by less mobile propylpolysiloxane blocks.

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12

Wang, Hanfu, and Yanchun Han. "Vesicles Formed by Oligostyrene-block-Oligoaniline-block-Oligostyrene Triblock Oligomer." Macromolecular Rapid Communications 30, no. 7 (April 1, 2009): 521–27. http://dx.doi.org/10.1002/marc.200800705.

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13

Rimmer, Stephen, and John R. Ebdon. "Synthesis of telechelic oligostyrenes by the ozonoloysis of poly(styrene-stat-butadiene): Protection of styrene units against ozone attack by the use of Di-N-alkyl amides as sacrificial ozone scavengers." Journal of Polymer Science Part A: Polymer Chemistry 34, no. 17 (December 1996): 3573–83. http://dx.doi.org/10.1002/(sici)1099-0518(199612)34:17<3573::aid-pola12>3.0.co;2-b.

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14

Matsumiya, Y., H. Watanabe, T. Inoue, K. Osaki, and M. L. Yao. "Rheo-Dielectric Behavior of Oligostyrene and Polyisoprene." Macromolecules 31, no. 22 (November 1998): 7973–75. http://dx.doi.org/10.1021/ma980465y.

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15

Chang, Bong Ho, Hee Cheon Cho, Young Chan Bae, Attila R. Imre, and W. Alexander Van Hook. "Modified Double Lattice Model for Oligoethylene/Oligostyrene Blends." Monatshefte f�r Chemie / Chemical Monthly 135, no. 5 (May 1, 2004): 493–99. http://dx.doi.org/10.1007/s00706-003-0148-4.

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16

Kimura, Takao, Kazunobu Tanji, and Masahiro Minabe. "Grafting of Hydrophobic Oligostyrene onto Hydrophilic 6,6-Type Polyamide." Polymer Journal 24, no. 11 (1992): 1311–15. http://dx.doi.org/10.1295/polymj.24.1311.

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17

Zhdanov, A. A., B. G. Zavin, and O. G. Blokhina. "Graft anionic copolymerization of octamethyl cyclotetrasiloxane with oligostyrene carbocyclosiloxane." Polymer Science U.S.S.R. 28, no. 10 (January 1986): 2428–34. http://dx.doi.org/10.1016/0032-3950(86)90064-x.

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18

Inoue, Tadashi, Takayuki Onogi, and Kunihiro Osaki. "Dynamic birefringence of oligostyrene: A symptom of ?polymeric? mode." Journal of Polymer Science Part B: Polymer Physics 38, no. 7 (April 1, 2000): 954–64. http://dx.doi.org/10.1002/(sici)1099-0488(20000401)38:7<954::aid-polb6>3.0.co;2-f.

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19

Kiepen, F., and W. Borchard. "Pressure-pulse-induced critical scattering of oligostyrene in n-pentane." Macromolecules 21, no. 6 (November 1988): 1784–90. http://dx.doi.org/10.1021/ma00184a041.

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20

Nose, Takuhei. "Interfacial Tension of Oligostyrene/Oligo(dimethylsiloxane) near the Critical Point." Macromolecules 28, no. 10 (May 1995): 3702–6. http://dx.doi.org/10.1021/ma00114a025.

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21

Islam, Molla Rafiquel, and Pudupadi R. Sundararajan. "Nano-scale self-assembly impeded by CH⋯π interaction in block selective solvents in the case of oligostyrene–perylenediimide–oligostyrene (coil–rod–coil) molecule." European Polymer Journal 49, no. 8 (August 2013): 2042–51. http://dx.doi.org/10.1016/j.eurpolymj.2013.04.037.

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22

Cifre, J. G. Hernández, and J. García de la Torre. "Radiation Scattering by Dilute Polymer Solutions in Shear Flow: An Example of Mesoscale Modeling and Brownian Dynamics Simulation." Applied Rheology 13, no. 4 (August 1, 2003): 200–208. http://dx.doi.org/10.1515/arh-2003-0014.

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Abstract The intention of the paper is to illustrate the ability of the Brownian dynamics simulation technique applied to mesoscale polymer models in order to reproduce light scattering experiments of dilute polymer solution under flow. After suitable parameterization of a real polymeric system, polystyrene solved in a oligostyrene/toluene mixture at 299 K (good solvent conditions), a bead-spring model of the polymer chain is built and used to generate molecular trajectories on a computer. Such trajectories will capture the deformational and orientational processes experienced by the real polymer chain under flow. Then, from the set of molecular conformations generated, several polymer properties as well as typical scattering patterns can be reproduced quite accurately. FENE springs were used and excluded volume and non-preaveraging hydrodynamic interaction were taken into account in order to build a chain model as realistic as needed.

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23

Ahmedova, G., H. Kara, Y. Cengeloglu, E. Özcan, Y. Burdurlu, M. Ersöz, and A. Koçak. "The Synthesis of Styrene-Oligoester Copolymer and Investigation of Their Physico-mechanical Properties." Eurasian Chemico-Technological Journal 2, no. 2 (April 16, 2016): 157. http://dx.doi.org/10.18321/ectj373.

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<p>The copolymerization reaction of commercial propylene oxide with glycidylmethacrilate in the presence of BF<sub>3</sub>·O(C<sub>2</sub>H<sub>5</sub>)<sub>2</sub> catalyst have been investigated. The composition and structure of copolymerization products and anchored functional groups have been determined using IR and gel chromatographic methods. The physico-mechanical properties and utility of polyfunctional unsaturated oligoester were investigated. The obtained thermoset product via the reaction of the oligoester with both styrene and oligostyrene obtained from the bottom of column as a waste material during the rectification operation of styrene in the presence of radicalic initiator has a good adhesion capability, hardness and high heat and water resistance. Thus the waste material was converted to the high valuable polymeric material.</p>

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24

Hensel-Bielowka, Stella, Patryk Wlodarczyk, Michal Mierzwa, Marian Paluch, and Kia L. Ngai. "Dynamics of α-Tetralone at Elevated Pressure and in Mixture with Oligostyrene." Journal of Physical Chemistry B 116, no. 1 (December 21, 2011): 22–29. http://dx.doi.org/10.1021/jp207071y.

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25

Sui, Yan, Xiangkai Fu, Xuebing Ma, Jingrong Chen, and Renquan Zeng. "Study of preparation and reaction mechanisms of new types of phosphonous acid-teminated oligostyrene." Reactive and Functional Polymers 64, no. 1 (July 2005): 55–62. http://dx.doi.org/10.1016/j.reactfunctpolym.2005.04.003.

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26

Ling, Gerald H., Yangyang Wang, and R. A. Weiss. "Linear Viscoelastic and Uniaxial Extensional Rheology of Alkali Metal Neutralized Sulfonated Oligostyrene Ionomer Melts." Macromolecules 45, no. 1 (December 19, 2011): 481–90. http://dx.doi.org/10.1021/ma201854w.

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27

Adames, W., A. Michalczyk, and W. Borchard. "Differential vapour pressure osmometry—II. Determination of the thermodynamic properties of oligostyrene/cyclohexane solutions." European Polymer Journal 25, no. 9 (January 1989): 951–55. http://dx.doi.org/10.1016/0014-3057(89)90116-x.

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28

Imre, Attila R., and W. Alexander Van Hook. "The effect of branching of alkanes on the liquid–liquid equilibrium of oligostyrene/alkane systems." Fluid Phase Equilibria 187-188 (September 2001): 363–72. http://dx.doi.org/10.1016/s0378-3812(01)00548-9.

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29

Wendorff, Joachim, Armido Studer, Caren Röben, Michael Stasiak, Birgit Janza, and Andreas Greiner. "Immobilization of Oligostyrene-Prolinol Conjugates into Polystyrene via Electrospinning and Applications of these Fibers in Catalysis." Synthesis 2008, no. 14 (June 18, 2008): 2163–68. http://dx.doi.org/10.1055/s-2008-1067146.

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30

Ganß, Martin, Ulrike Staudinger, Bhabani K. Satapathy, Andreas Leuteritz, and Roland Weidisch. "Mechanism of strengthening and toughening of a nanostructured styrene-butadiene based block copolymer by oligostyrene-modified montmorillonites." Polymer 213 (January 2021): 123328. http://dx.doi.org/10.1016/j.polymer.2020.123328.

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31

Gray, Michael J., Gary R. Dennis, Patrick J. Slonecker, and R. Andrew Shalliker. "Separation of oligostyrene isomers in a complex mixture using two-dimensional heart-cutting reversed-phased liquid chromatography." Journal of Chromatography A 1028, no. 2 (March 2004): 247–57. http://dx.doi.org/10.1016/j.chroma.2003.10.123.

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32

Dahan, Elianne, and Pudupadi R. Sundararajan. "Solvent-dependent nanostructures of gels of a Gemini surfactant based on perylene diimide spacer and oligostyrene tails." European Polymer Journal 61 (December 2014): 113–23. http://dx.doi.org/10.1016/j.eurpolymj.2014.09.023.

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33

Imre, Attila R., W. Alexander Van Hook, Bong Ho Chang, and Young Chan Bae. "The Effect of Alkane Chain Length on the Liquid?Liquid Critical Temperatures of Oligostyrene/Linear-Alkane Mixtures." Monatshefte f�r Chemie / Chemical Monthly 134, no. 12 (December 1, 2003): 1529–39. http://dx.doi.org/10.1007/s00706-003-0077-2.

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34

Imre, Attila R., c. Galina Melnichenko, W. Alexander Van Hook, and Bernhard A. Wolf. "On the effect of pressure on the phase transition of polymer blends and polymer solutions: Oligostyrene–n-alkane systems." Physical Chemistry Chemical Physics 3, no. 6 (2001): 1063–66. http://dx.doi.org/10.1039/b008406i.

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35

Abetz, Volker, Gunther Müller, Reimund Stadler, and Shulamith Schlick. "The glass transition of mixtures of polystyrene with alkyl-terminated oligostyrene — experimental evidence for microphase separation in a polymer blend." Macromolecular Chemistry and Physics 196, no. 11 (November 1995): 3845–57. http://dx.doi.org/10.1002/macp.1995.021961134.

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36

David, Ghislain, Jean-Jacques Robin, and Bernard Boutevin. "Synthesis of carboxy-telechelic oligostyrene by dead-end polymerization: Evaluation of primary radical termination by kinetic study and kinetic simulation model." Journal of Polymer Science Part A: Polymer Chemistry 39, no. 16 (2001): 2740–50. http://dx.doi.org/10.1002/pola.1252.

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37

Abetz, Volker, Gunther Müller, Reimund Stadler, and Shulamith Schlick. "Correction to “The glass transition of mixtures of polystyrene with alkyl-terminated oligostyrene – experimental evidence for microphase separation in a polymer blend”1." Macromolecular Chemistry and Physics 198, no. 7 (July 1997): 2333–35. http://dx.doi.org/10.1002/macp.1997.021980724.

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38

Harmandaris, Vagelis A., Kurt Kremer, and George Floudas. "Dynamic Heterogeneity in Fully Miscible Blends of Polystyrene with Oligostyrene." Physical Review Letters 110, no. 16 (April 18, 2013). http://dx.doi.org/10.1103/physrevlett.110.165701.

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