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Polymerization mechanisms ring opening

For example, see Slomkowski, S. and Duda, A. Anionic ring-opening polymerization, In Ring-Opening Polymerization, Mechanisms, Catalysis, Structure, and Utility, Brunelle, D. J. (Ed.), Hanser-Verlag, New York, pp. 87-128, 1993. [Pg.139]

Abraham GA, Gallardo A, Lozano AE, San RJ (2000) E-caprolactone/ZnCL complex formation characterization and ring-opening polymerization mechanism. J Polym Sci A Polym Chem 38 1355-1365... [Pg.211]

Slomkowski, S. and A. Duda, Anionic Ring-Opening Polymerization, Chap. 3 in Ring-Opening Polymerization. Mechanism, Catalysis, Structure, Utility, D. J. Brunelle, eds., Hanser, Munich, 1993. [Pg.615]

S. Penczek, P. Kubisa, and K, Matyjaszewski, Cationic ring-opening polymerization—mechanisms, Adv. Polym. Sci. 37 1 (1980). [Pg.542]

BruneUe DJ, editor. Ring-Opening Polymerization Mechanisms, Catalysis, Structure, Utility. New York Hanser 1993. [Pg.159]

ZnC12 complex formation Characterization and ring-opening polymerization mechanism. 2000,... [Pg.794]

Brunelle DJ (ed) (1996) Ring opening polymerization mechanisms, catalysis, structure, utility. Hanser, Munich... [Pg.257]

RUBBERS PRODUCED BY CONDENSATION AND RING-OPENING POLYMERIZATION MECHANISMS... [Pg.379]

A recent computer study of the cationic polymerization of cyclic acetals led to the conclusion that the ring-opening polymerization mechanism is influenced by substitution in the C2 position. In the latter case, the relative stability of the intermediate oxonium and carbenium ions is favored in the direction of carbenium ions. Evidently, assuming independent validity of computer modeling, the critical energy differences between the proposed reaction paths is small. Therefore, the polymerization of each cyclic acetal must be considered individually [48]. [Pg.202]

XU J, zou Y F and pan c y (2002), Study on cationic ring-opening polymerization mechanism of 3-ethyl-3-hydroxymethyl oxetane , J Macromol Sci-Pure Appl Chem, A39(5) 431-445... [Pg.581]

Scheme 6.2 Anionic, cationic chain-end and cationic activated-monomer ring-opening polymerization mechanisms for ethylene oxide. Scheme 6.2 Anionic, cationic chain-end and cationic activated-monomer ring-opening polymerization mechanisms for ethylene oxide.
Scheme 9.15 Cationic ring-opening polymerization mechanism of 3-lactone from alkylating initiator. Scheme 9.15 Cationic ring-opening polymerization mechanism of 3-lactone from alkylating initiator.
Abraham, G. A., Gallardo, A., Lozano, A. E., Roman, J. S., s-C rolactone/ZnC Complex Formation Characterization and Ring-Opening Polymerization Mechanism, Journal of Polymer Science, Part A Polymer Chemistry, 2000, 38, 1355-1365. [Pg.2653]


See other pages where Polymerization mechanisms ring opening is mentioned: [Pg.616]    [Pg.68]    [Pg.6015]    [Pg.6014]    [Pg.94]    [Pg.616]    [Pg.28]    [Pg.72]    [Pg.395]    [Pg.377]    [Pg.948]    [Pg.37]    [Pg.112]   


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Acid-initiated ring-opening polymerization mechanism

General Mechanisms in Ring-Opening Polymerization

Radical Ring-Opening Polymerization Mechanism

Reaction mechanisms, polymers ring-opening polymerization

Ring mechanism

Ring-Opening Polymerizations by a Free-Radical Mechanism

Ring-opening metathesis polymerization mechanism

Ring-opening polymerization base-initiated mechanism

Ring-opening polymerization cationic mechanism

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