Academic literature on the topic 'Group transfer polymerization'

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Journal articles on the topic "Group transfer polymerization"

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Webster, Owen W., and D. Y. Sogah. "Group transfer polymerization." Kobunshi 36, no. 11 (1987): 808–11. http://dx.doi.org/10.1295/kobunshi.36.808.

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BLEDZKI, ANDRZEJ K. "Group - transfer polymerization." Polimery 30, no. 08 (1985): 293–95. http://dx.doi.org/10.14314/polimery.1985.293.

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Chen, Yougen, and Toyoji Kakuchi. "Organocatalyzed Group Transfer Polymerization." Chemical Record 16, no. 4 (2016): 2161–83. http://dx.doi.org/10.1002/tcr.201600034.

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Hertler, Walter R. "Chain transfer in group-transfer polymerization." Macromolecules 20, no. 12 (1987): 2976–82. http://dx.doi.org/10.1021/ma00178a004.

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Sogah, Dotsevi Y., Walter R. Hertler, Owen W. Webster, and Gordon M. Cohen. "Group transfer polymerization - polymerization of acrylic monomers." Macromolecules 20, no. 7 (1987): 1473–88. http://dx.doi.org/10.1021/ma00173a006.

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Brittain, William J., and Ira B. Dicker. "Termination in group-transfer polymerization." Macromolecules 22, no. 3 (1989): 1054–57. http://dx.doi.org/10.1021/ma00193a010.

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Brittain, William J. "A Review of Group-Transfer Polymerization." Rubber Chemistry and Technology 65, no. 3 (1992): 580–600. http://dx.doi.org/10.5254/1.3538630.

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Abstract Group-transfer polymerization is a very useful synthetic method for the preparation of acrylic ester polymers. This living polymerization process works well at room temperature and can be used to prepare a wide variety of complex polymer structures. Mechanistic work suggests that GTP is a form of anionic polymerization where propagation occurs via a small concentration of enolate anions which are in equilibrium with dormant silyl ketene acetal chain ends. GTP will find the most use in specialty applications including dispersants, toners, photoresists, and rheology control agents.
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Ute, Koichi, Toshiyuki Tarao, and Koichi Hatada. "Group Transfer Polymerization of Methyl Crotonate." Polymer Journal 29, no. 11 (1997): 957–58. http://dx.doi.org/10.1295/polymj.29.957.

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Bywater, Stanley. "Group transfer polymerization - A critical overview." Makromolekulare Chemie. Macromolecular Symposia 67, no. 1 (1993): 339–50. http://dx.doi.org/10.1002/masy.19930670127.

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Quirk, Roderic P., Jie Ren, and Gregory Bidinger. "Mechanistic aspects of group transfer polymerization." Makromolekulare Chemie. Macromolecular Symposia 67, no. 1 (1993): 351–63. http://dx.doi.org/10.1002/masy.19930670128.

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Dissertations / Theses on the topic "Group transfer polymerization"

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Hellstern, Ann Marie. "Synthesis, characterization and kinetic investigations of heterophase materials prepared using group transfer polymerization." Diss., Virginia Polytechnic Institute and State University, 1989. http://hdl.handle.net/10919/54788.

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The impact of multiphase polymeric materials has been enhanced by the preparation of well defined block and graft copolymers. Hence, there has been a growing emphasis on new synthetic methods for the preparation of blocks and grafts. Group Transfer Polymerization (GTP) is a relatively new synthetic method which provides a means to obtain poly(alkyl acrylate)s and poly(alkyl methacrylate)s via a "living" mechanism over a broad temperature range. The degree of control over molecular weight and molecular weight distribution rivals that afforded through living anionic techniques for the preparatio
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Raynaud, Jean. "Carbènes N-hétérocycliques comme activateurs "multi-tâches" des réactions de polymérisations par transfert de groupe des (meth)acryliques et par ouverture de cycle des oxiranes." Thesis, Bordeaux 1, 2010. http://www.theses.fr/2010BOR13995/document.

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L’utilisation de carbènes N-hétérocycliques (NHCs), en tant qu’activateurs organiques « multitâches », a permis la polymérisation de deux classes de monomères : les monomères vinyliques de type (méth)acrylique et les monomères cycliques de type époxyde. En particulier, la polymérisation par transfert de groupe (GTP) catalysée par les NHCs a été utilisée pour polymériser les monomères acryliques et méthacryliques, dans des solvants polaires comme apolaires, en présence d’un amorceur de type acétal de cétène silylé. Sur cette base des copolymères à blocs « tout-acrylique » ont été synthétisés. D
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Salzinger, Stephan [Verfasser], Bernhard [Akademischer Betreuer] Rieger, Wolfgang [Akademischer Betreuer] Eisenreich, and Kai-Olaf [Akademischer Betreuer] Hinrichsen. "Expansion of Rare Earth Metal-Mediated Group Transfer Polymerization to New Monomers / Stephan Salzinger. Gutachter: Wolfgang Eisenreich ; Kai-Olaf Hinrichsen ; Bernhard Rieger. Betreuer: Bernhard Rieger." München : Universitätsbibliothek der TU München, 2013. http://d-nb.info/1044395842/34.

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Soller, Benedikt Simon [Verfasser], Bernhard [Akademischer Betreuer] [Gutachter] Rieger, Wolfgang [Gutachter] Eisenreich, and Tom [Gutachter] Nilges. "Rare Earth Metal-Mediated Group Transfer Polymerization of Vinylphosphonates: Initiation, Propagation, and Stereoregularity / Benedikt Simon Soller. Betreuer: Bernhard Rieger. Gutachter: Wolfgang Eisenreich ; Tom Nilges ; Bernhard Rieger." München : Universitätsbibliothek der TU München, 2016. http://d-nb.info/1113182466/34.

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Schaffer, Andreas Friedrich Josef [Verfasser], Bernhard [Akademischer Betreuer] Rieger, Ralf [Gutachter] Huss, Wolfgang [Gutachter] Eisenreich, and Bernhard [Gutachter] Rieger. "From C-H bond activation to function: Diversification of smart materials generated via rare earth metal-mediated group transfer polymerization / Andreas Friedrich Josef Schaffer ; Gutachter: Ralf Huss, Wolfgang Eisenreich, Bernhard Rieger ; Betreuer: Bernhard Rieger." München : Universitätsbibliothek der TU München, 2021. http://d-nb.info/123634328X/34.

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Labalme, Etienne. "Synthesis and characterizations of new fluorinated membranes bearing pendant phosphonic acid groups for PEMFC application." Thesis, Montpellier, Ecole nationale supérieure de chimie, 2013. http://www.theses.fr/2013ENCM0013.

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Ce travail de thèse s'inscrit dans la continuité des travaux de recherche réalisés sur le développent de nouvelles membranes échangeuses de protons pour piles à combustibles de type PEMFC, porteuses de groupements protogènes acides phosphoniques. L'objectif de ces travaux est d'apporter des solutions permettant l'amélioration des propriétés physico-chimiques d'un copolymère phosphoné, le poly(CTFE-alt-VEPA) obtenu à partir de la polymérisation radicalaire de vinyl éthers et de CTFE. La première stratégie employée est une stratégie Blend. Elle consiste à ajouter un polymère fluoré commercial, l
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Öktem, Gözde. "Oligo(3-hexylthiophene) Wires for needs of Single-Molecule Nanoelectronics." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2017. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-227736.

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A material to function as a molecular electronic device should have a strong coupling with electrodes through appropriate and well-defined anchoring groups and have to support an effective traveling of charges via a conjugated molecular backbone. Oligo(3-hexylthiophene)s are π-conjugated molecules having large applicability in several areas of organic electronics owing interesting semiconducting properties and they also hold great promises in the field of single-molecule electronics. Polymerization methods, in principle, allow construction of long conjugated systems in a single synthetic step,
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NIU, ZHAO-WEN, and 牛昭文. "Potassium bifluoride-catalyzed group transfer polymerization." Thesis, 1987. http://ndltd.ncl.edu.tw/handle/83329561026738834330.

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Mputumana, Nomfusi Augusta. "Siloxyl and Hydroxyl functionalized polymers by atom transfer radical polymerization." Thesis, 2010. http://hdl.handle.net/10500/3927.

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The syntheses of siloxyl and hydroxyl chain end functionalized polystyrene and poly(methyl methacrylate) by Atom Transfer Radical Polymerization (ATRP) were effected by the following methods: (a) α-Siloxyl functionalized polymers were prepared in quantitative yields via a one-pot ATRP synthesis method for the polymerization of styrene or methyl methacrylate using a new siloxyl functionalized initiator adduct, formed in situ by the reaction of (1-bromoethyl)benzene with 1-(4-t-butyldimethylsiloxyphenyl)-1- phenylethylene in the presence of CuBr/bpy or CuBr/PMDETA as catalysts in dipheny
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Γκοτζαμάνης, Γεώργιος. "Ανάπτυξη νέων "ευφυών" κατά συστάδες συμπολυμερών τύπου ομοπολυμερές-στατιστικό συμπολυμερές". Thesis, 2007. http://nemertes.lis.upatras.gr/jspui/handle/10889/613.

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Στην παρούσα Διδακτορική Διατριβή σχεδιάστηκαν και συντέθηκαν με πολυμερισμό μέσω μεταφοράς ομάδας (group transfer polymerization, GTP) τέσσερα νέα πρότυπα “ευφυή” υδατοδιαλυτά συμπολυμερή, τα οποία αυτοοργανώνονται σε υδατικά διαλύματα σε δομές μικκυλίων ή ελαστικού φυσικού δικτύου, αποκρινόμενα άμεσα σε μεταβολές του pH, της θερμοκρασίας και της ιοντικής ισχύος του διαλύματος. Η καινοτομία των πολυμερών που συντέθηκαν οφείλεται στο γεγονός ότι σε ένα συσταδικό συμπολυμερές ενσωματώθηκε μία στατιστική συστάδα, η οποία παρουσιάζει ιδιότητες που είναι συνδυασμός των ιδιοτήτων των μονομερών που
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Books on the topic "Group transfer polymerization"

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Banerjee, Krishna G. The stereochemistry of group transfer polymerization of methyl, diphenylmethyl, and triphenylmethyl methacrylates. 1988.

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Chan-Seng, Delphine. "Living"/controlled radical group polymerization: From emulsion atom transfer radical polymerization to the synthesis of new nitroxides for stable free radical polymerization. 2007.

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Book chapters on the topic "Group transfer polymerization"

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Hertler, W. R. "Group Transfer Polymerization." In Silicon in Polymer Synthesis. Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-79175-8_2.

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Webster, O. W., and B. C. Anderson. "Group Transfer Polymerization." In New Methods for Polymer Synthesis. Springer US, 1992. http://dx.doi.org/10.1007/978-1-4899-2356-1_1.

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Chen, Yougen, Keita Fuchise, Toshifumi Satoh, and Toyoji Kakuchi. "Group Transfer Polymerization of Acrylic Monomers." In Anionic Polymerization. Springer Japan, 2015. http://dx.doi.org/10.1007/978-4-431-54186-8_10.

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Müller, Axel H. E. "Kinetics of Group Transfer Polymerization." In Recent Advances in Mechanistic and Synthetic Aspects of Polymerization. Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-3989-9_2.

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Spinelli, Harry J. "Methacrylate Star Polymers via Group Transfer Polymerization." In Progress in Pacific Polymer Science. Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-642-84115-6_29.

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Heuts, Johan P. A., David A. Morrison, and Thomas P. Davis. "End-Group Control in Catalytic Chain Transfer Polymerization." In ACS Symposium Series. American Chemical Society, 2000. http://dx.doi.org/10.1021/bk-2000-0768.ch022.

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Sitz, Hans-Dieter, and Friedhelm Bandermann. "Group Transfer Polymerization of Methyl Methacrylate with Basic Catalysts." In Recent Advances in Mechanistic and Synthetic Aspects of Polymerization. Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-3989-9_3.

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Asami, R., Y. Kondo, and M. Takaki. "Synthesis of Poly(Methyl Methacrylate) Macromonomer by Group Transfer Polymerization, and Polymerization of the Macromonomer." In Recent Advances in Anionic Polymerization. Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-3175-6_25.

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Webster, Owen W. "Group Transfer Polymerization and Its Relationship to Other Living Systems." In Macromolecular Engineering. Springer US, 1995. http://dx.doi.org/10.1007/978-1-4615-1905-8_1.

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Webster, O. W., and D. Y. Sogah. "Recent Advances in the Controlled Synthesis of Acrylic Polymers by Group Transfer Polymerization." In Recent Advances in Mechanistic and Synthetic Aspects of Polymerization. Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-3989-9_1.

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