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Hyperbranched polymers : synthesis, properties, and applications / edited by Deyue Yan, Chao Gao, Holger Frey.

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Format:
Book
Contributor:
Yan, Deyue.
Gao, Chao.
Frey, Holger.
Series:
Wiley series on polymer engineering and technology.
Wiley series on polymer engineering and technology
Language:
English
Subjects (All):
Dendrimers.
Polymers.
Physical Description:
1 online resource (482 p.)
Edition:
1st ed.
Place of Publication:
Hoboken, N.J. : Wiley, 2011.
Language Note:
English
Summary:
A much-needed overview of the state of the art of hyperbranched polymers The last two decades have seen a surge of interest in hyperbranched polymers due to their ease of synthesis on a large scale and their promising applications in diverse fields, from medicine to nanotechnology. Written by leading scientists in academia and industry, this book provides for the first time a comprehensive overview of the topic, bringing together in one complete volume a wealth of information previously available only in articles scattered across the literature. Drawing on their work at the
Contents:
CONTENTS; Preface; Contributors; 1. Promising Dendritic Materials: An Introduction to HyperbranchedPolymers; 1.1 Importance of Branching; 1.2 Polymer Architecture; 1.3 Dendritic Polymers; 1.4 Hyperbranched Polymers; 1.4.1 Concept and History; 1.4.2 Structure and Properties; 1.4.3 Synthesis Philosophy; 1.4.4 Applications; 1.5 Conclusions; 1.6 References; 2. Polycondensation of AB x Monomers; 2.1 Introduction; 2.2 Statistical Consideration; 2.2.1 Polymerization Behavior; 2.2.2 Degree of Branching; 2.3 Polymerization of AB x -Type Monomers; 2.3.1 C-C Coupling Reactions
2.3.1.1 Metal-Catalyzed Cross Couplings2.3.1.2 Diels-Alder Reactions; 2.3.1.3 Nucleophilic Substitution by Activated Methylenes; 2.3.1.4 Electrophilic Acylations; 2.3.2 C-O Coupling Reactions; 2.3.2.1 Nucleophilic Substitution Reactions by Phenoxides orAlkoxides; 2.3.2.2 Esterification of Carboxylic Acid Derivatives; 2.3.2.3 Ring-Opening Reaction of Epoxides; 2.3.3 C-N Coupling Reactions; 2.3.3.1 Condensation of Amines and Carboxylic AcidDerivatives; 2.3.3.2 Nucleophilic Addition of Amines; 2.3.3.3 Other C-N Coupling Reactions; 2.3.4 Si-C or Si-O Coupling Reactions
2.3.4.1 Hydrosilylation Reactions2.3.4.2 Condensation Reactions; 2.3.4.3 Other Si-Containing Reactions; 2.3.5 Other Coupling Reactions; 2.3.5.1 C-O or C-N Coupling Reactions of Isocyanates; 2.3.5.2 C-S Coupling Reactions; 2.4 References; 3. Synthesis of Hyperbranched Polymers via Polymerization ofFunctionally Symmetric Monomer Pairs; 3.1 Introduction; 3.2 Theoretical Treatment of A 2 + B 3 Polymerization; 3.3 Polymerization of Symmetrical Monomer Pairs; 3.3.1 Polycondensation of A 2 and B 3 Monomers; 3.3.1.1 Polyamides; 3.3.1.2 Polyimides; 3.3.1.3 Polyethers; 3.3.1.4 Polyesters
3.3.1.5 Polycarbonates3.3.1.6 Polyurethanes; 3.3.2 Proton-Transfer Polymerization of A2 and B3 Monomers; 3.3.3 The Michael Addition Polymerization of A2 and B3 Monomers; 3.4 Conclusions; 3.5 References; 4. Synthesis of Hyperbranched Polymers via Polymerization ofAsymmetric Monomer Pairs; 4.1 Introduction; 4.2 General Description of Polymerization of Asymmetric MonomerPairs; 4.3 Hyperbranched Polymers Prepared by Polymerization of AsymmetricMonomer Pairs; 4.3.1 Poly(Sulfoneamine); 4.3.2 Poly(Ester Amine); 4.3.3 Poly(Amidoamine); 4.3.4 Multihydroxyl Hyperbranched Poly(Amine Ester)s
4.3.5 Poly(Ester Amide)s4.3.6 Polyesters; 4.3.7 Poly(Urea-Urethane)s; 4.3.8 Other Polymers; 4.3.9 Highly Branched Copolymers; 4.4 Conclusions; 4.5 References; 5. Self-Condensing Vinyl Polymerization; 5.1 Introduction; 5.2 Self-Condensing Vinyl Polymerization; 5.2.1 General Principles; 5.2.2 Various Mechanisms of SCVP; 5.2.3 Kinetics and MWD; 5.2.4 Degree of Branching; 5.2.5 Comparison with Experimental Data; 5.3 Self-Condensing Vinyl Copolymerization (SCVCP); 5.3.1 Experimental Data; 5.3.2 Kinetics and MWD; 5.3.3 Degree of Branching; 5.3.4 Comparison with Experimental Data
5.4 Self-Condensing Processes in Presence of Initiators
Notes:
Description based upon print version of record.
Includes bibliographical references and index.
ISBN:
9786613025548
9780470934760
047093476X
9781283025546
128302554X
9780470928998
0470928999
9780470929001
0470929006
OCLC:
710974947

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