Academic literature on the topic 'Postpolymerization'

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Journal articles on the topic "Postpolymerization"

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Jain, Sarthak, Kevin Neumann, Yichuan Zhang, Jin Geng, and Mark Bradley. "Tetrazine-Mediated Postpolymerization Modification." Macromolecules 49, no. 15 (July 25, 2016): 5438–43. http://dx.doi.org/10.1021/acs.macromol.6b00867.

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Romulus, Joy, John T. Henssler, and Marcus Weck. "Postpolymerization Modification of Block Copolymers." Macromolecules 47, no. 16 (August 18, 2014): 5437–49. http://dx.doi.org/10.1021/ma5009918.

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Ren, Juntao, Baojian Ni, Heng Liu, Yanming Hu, Xuequan Zhang, and Toshio Masuda. "Postpolymerization modification based on dynamic imine chemistry for the synthesis of functional polyacetylenes." Polymer Chemistry 10, no. 10 (2019): 1238–44. http://dx.doi.org/10.1039/c8py01793j.

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Walsh, Dylan J., Eric Su, and Damien Guironnet. "Catalytic synthesis of functionalized (polar and non-polar) polyolefin block copolymers." Chemical Science 9, no. 20 (2018): 4703–7. http://dx.doi.org/10.1039/c8sc00450a.

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Mao, Tengfei, Xianzhe He, Guoqiang Liu, Yen Wei, Yanzi Gou, Xingui Zhou, and Lei Tao. "Fluorescent polymers via post-polymerization modification of Biginelli-type polymers for cellular protection against UV damage." Polymer Chemistry 12, no. 6 (2021): 852–57. http://dx.doi.org/10.1039/d0py00503g.

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Reese, Cassandra M., Brittany J. Thompson, Phillip K. Logan, Christopher M. Stafford, Michael Blanton, and Derek L. Patton. "Sequential and one-pot post-polymerization modification reactions of thiolactone-containing polymer brushes." Polymer Chemistry 10, no. 36 (2019): 4935–43. http://dx.doi.org/10.1039/c9py01123d.

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Polymer brushes carrying pendent thiolactone functional groups were explored for the design of multifunctional homopolymer brush architectures using sequential and one-pot postpolymerization strategies.
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Dai, Yunkai, Zhitao Hu, Xiaoying Wang, Xingliang Liu, Yuanchao Li, Yi Shi, and Yongming Chen. "Synthesis of fully degradable cationic polymers with various topological structures via postpolymerization modification by using thio-bromo “click” reaction." Polymer Chemistry 12, no. 17 (2021): 2592–97. http://dx.doi.org/10.1039/d1py00106j.

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Poly(ε-caprolactone) (PCL) based and fully degradable cationic polymers with various topological structures and tunable charge densities were prepared via postpolymerization modification using thio-bromo “click” chemistry.
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Ilundain, Pedro, Rafael Salazar, Daniel Alvarez, Louis Da Cunha, María J. Barandiaran, and José M. Asua. "Modeling and Optimization of Postpolymerization Processes." Industrial & Engineering Chemistry Research 43, no. 5 (March 2004): 1244–50. http://dx.doi.org/10.1021/ie030440+.

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Jain, Sarthak, Kevin Neumann, Yichuan Zhang, Elsa Valero, Jin Geng, and Mark Bradley. "Correction to Tetrazine-Mediated Postpolymerization Modification." Macromolecules 49, no. 19 (September 28, 2016): 7608. http://dx.doi.org/10.1021/acs.macromol.6b02018.

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Wilson, Tiffany M. S., Douglas A. Chinn, David B. Robinson, and F. P. Doty. "Postpolymerization alignment of bulk conjugated polymers." Applied Physics Letters 93, no. 14 (October 6, 2008): 143304. http://dx.doi.org/10.1063/1.2978247.

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Dissertations / Theses on the topic "Postpolymerization"

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Lecamp, Laurence. "Photopolymérisation radicalaire de films de diméthacrylate : étude cinétique et transposition à un système épais." Rouen, 1997. http://www.theses.fr/1997ROUES061.

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Ce travail porte sur la photopolymérisation radicalaire de films de polyéther diméthacrylate de bisphénol A. La rapidité et l'exothermie de cette réaction engendrent des défauts qui altèrent fortement les qualités optiques des verres ophtalmiques obtenus par cette méthode. Une étude cinétique sur des films puis une transposition à des systèmes épais ont été réalisées dans le but de pouvoir contrôler l'homogénéité des verres ainsi formés. Un photocalorimètre différentiel à balayage a été utilisé pour suivre la réaction de photopolymérisation radicalaire et caractériser l'influence de quatre paramètres (température, intensité du rayonnement UV, concentration et nature du photoamorceur). Une relation linéaire entre le taux de conversion et la Tg des matériaux photoréticulés a notamment été établie. L'étude de la réaction de postpolymérisation en isotherme a par ailleurs montré combien l'évolution du réseau dans le temps peut être importante. Deux modèles cinétiques ont été appliqués. Le premier conduisant à une expression de la vitesse au cours de la réaction est totalement phénoménologique. Le deuxième modèle prend en compte les réactions existant entre les différentes espèces chimiques présentes au cours de la photopolymérisation et conduit à la détermination de l'évolution des principales constantes de vitesse. Enfin, une simulation numérique des transferts thermiques a été réalisée afin de modéliser les profils de conversion et de température dans un matériau épais.
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Vrbata, David. "Syntéza a polymerizace substituovaných derivátů kaprolaktonu." Master's thesis, 2011. http://www.nusl.cz/ntk/nusl-312751.

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Copper (I) mediated Huisgen 1,3 dipolar cycloaddition of 4-(piperidine-1-yl)-N-(prop-1-yne- 3-yl)-1,8-naphtalimide (PN) to poly(αN3εCL-co-εCL) of three different molar ratio of αN3εCL was performed. Reaction was succesfull for poly(αN3εCL-co-εCL) with molar fraction of αN3εCL f = 0,22. No degradation of substituted PCL was observed during the synthetic path, therefore the PN molecule is suitable for click coupling to well defined polyester. New aliphatic polyester based on polycaprolactone was synthesized and characterized by means of 1 HNMR spectra and Gel permeation chromatography calibrated with polystyrene standards. The spectra of other two copolymers coupled with PN were not measured due to their low solubility in common organic solvents. Keywords: living polymerization, α-chloro-ε-caprolactone, click reaction
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Books on the topic "Postpolymerization"

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Functional Polymers by PostPolymerization Modification. Wiley-VCH Verlag GmbH, 2012.

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Book chapters on the topic "Postpolymerization"

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Bouranis, D. L. "Designing Synthetic Soil Conditioners Via Postpolymerization Reactions." In Handbook of Soil Conditioners, 333–62. CRC Press, 2020. http://dx.doi.org/10.1201/9781003064688-16.

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