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Functional Polymers by Post-Polymerization Modification (eBook)

Concepts, Guidelines and Applications
eBook Download: EPUB
2013
Wiley-VCH (Verlag)
978-3-527-65544-1 (ISBN)

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n modern polymer science a variety of polymerization methods for the direct synthesis of polymers bearing functional groups are known. However, there is still a large number of functional groups that may either completely prevent polymerization or lead to side reactions. Post-polymerization modification, also known as polymer-analogous modification, is an alternative approach to overcome these limitations. It is based on the polymerization of monomers with functional groups that are inert towards the polymerization conditions but allow a quantitative conversion in a subsequent reaction step yielding a broad range of other functional groups. Thus, diverse libraries of functional polymers with identical average degrees of polymerization but variable side chain functionality may easily be generated.

Filling the gap for a book dealing with synthetic strategies and recent developments, this volume provides a comprehensive and up-to-date overview of the field of post-polymerization modification.

As such, the international team of expert authors covers a wide range of topics, including new synthetic techniques utilizing different reactive groups for post-polymerization modifications with examples ranging from modification of biomimetic and biological polymers to modification of surfaces.

With its guidelines this is an indispensable and interdisciplinary reference for scientists working in both academic and industrial polymer research.

Patrick Theato is Associate Professor for polymer chemistry at the University of Hamburg. He studied chemistry at Mainz (Germany) and Amherst (USA), and received his Ph.D. in 2001 from the University of Mainz with Prof. R. Zentel. After postdoctoral research with Prof. D.Y. Yoon (Seoul National University, Korea) and Prof. C.W. Frank (Stanford University, USA), he joined the University of Mainz as a young faculty member and completed his Habilitation in 2007. From 2009 to 2012 he held a joint appointment with the School of Chemical and Biological Engineering at Seoul National University within the World Class University program. In 2011 he accepted a prize senior lectureship at the University of Sheffield, UK. Shortly after he moved to University of Hamburg, Germany. He serves as an Editorial Advisory Board Member of "Macromolecules". His current research interests include the defined synthesis of reactive polymers, block copolymers, design of multi stimuli-responsive polymers, versatile functionalization of interfaces, hybrid polymers, polymers for electronics and templating of polymers. Harm-Anton Klok is Full Professor at the Institutes of Materials and Chemical Sciences and Engineering at the Ecole Polytechnique Fédérale de Lausanne (EPFL) (Switzerland). He received his Ph.D. in 1997 from the University of Ulm (Germany) after working with Prof. M. Möller. After postdoctoral research with Prof. D. N. Reinhoudt (University of Twente) and Prof. S. I. Stupp (University of Illinois at Urbana-Champaign, USA), he joined the Max Planck Institute for Polymer Research in Mainz (Germany) in early 1999 as a project leader in the group of Prof. K. Müllen. In November 2002, he was appointed to the faculty of EPFL. Harm-Anton Klok is recipient of the 2007Arthur K. Doolittle Award of the American Chemical Society (ACS) and is Associate Editor of the ACS journal "Biomacromolecules".

HISTORY OF POST-POLYMERIZATION MODIFICATION
Introduction
Post-polymerization Modification via Thiol-ene Addition
Post-polymerization Modification of Epoxides, Anhydrides, Oxazolines, and Isocyanates
Post-polymerization Modification of Active Esters
Post-polymerization Modification via Thiol-Disulfide Exchange
Post-polymerization Modification via Diels-Alder Reactions
Post-polymerization Modification via Michael-Type Addition
Post-polymerization Modification via Azide Alkyne Cycloaddition Reactions
Post-polymerization Modification of Ketones and Aldehydes
Post-polymerization Modifications via Other Highly Efficient Reactions
Concluding Remarks

POST-POLYMERIZATION MODIFICATIONS VIA ACTIVE ESTERS
Introduction
Active Esters in the Side Group
Star Polymers
Active Esters at the End Groups
Controlled Positioning of Active Ester Moieties
Summary

THIOL-ENE BASED FUNCTIONALIZATION OF POLYMERS
Introduction
General Considerations and Mechanisms
Functionalization of Polymers
Summary

THIOL-YNE CHEMISTRY IN POLYMER AND MATERIALS SCIENCE
Introduction
The Thiol-yne Reaction in Small-Molecule Chemistry
The Thiol-yne Reaction in Polymer and Material Synthesis

DESIGN AND SYNTHESIS OF MALEIMIDE GROUP CONTAINING POLYMERIC MATERIALS VIA THE DIELS-ALDER/RETRO DIELS-ALDER STRATEGY
Introduction
Maleimide Functional Group Containing Polymeric Materials
The Diels-Alder/Retro Diels-Alder Cycloaddition-Cycloreversion Reactions
Application of Diels-Alder/Retro Diels-Alder Reaction to Synthesize Maleimide-Containing Polymers
Conclusions

THE SYNTHESIS OF END-FUNCTIONAL RING-OPENING METATHESIS POLYMERS
Introduction
End-Functionalization Methods in General
Functionalization during Initiation
Functionalization after Propagation
Functionalization during Propagation
Conclusions and Outlook

FUNCTIONAL POLYMERS WITH CONTROLLED MICROSTRUCTURE BASED ON STYRENE AND N-SUBSTITUTED MALEIMIDES
Introduction
Background on Radical Copolymerization of Styrene and Maleimides
Precise Incorporation of Maleimide Units on Polystyrene Backbone
Tuning a Simple Technique for the Preparation of Sequence-Controlled Polymers to the Elaboration of Functionalized Well-Defined Macromolecules
Summary and Outlook

TEMPERATURE-TRIGGERED FUNCTIONALIZATION OF POLYMERS
Introduction
Temperature-Triggered Alteration of Polymer Property
Conclusions

NEW FUNCTIONAL POLYMERS USING HOST?GUEST CHEMISTRY
Introduction
Polymers with Responsive Three-Dimensional Structures
Polymer Probes for Specific Chemical Sensing
Responsive Soft Materials
Functional Polyrotaxanes

GLYCOPOLYMERS VIA POST-POLYMERIZATION MODIFICATION TECHNIQUES
Introduction
Synthesis and Controlled Polymerization of Glycomonomers
Post-polymerization Modification of Polymer Scaffolds to Synthesize Glycopolymers
Azide - Alkyne Click Reactions
Utilizing Thiol-Based Click Reactions
Thiol-ene Click Reactions
Thiol-yne Click Reactions
Thiol-Halogen Substitution Reactions
Alkyne/Alkene Glycosides: 'Backward' Click Reactions
Post-polymerization Glycosylation of Nonvinyl Backbone Polymers
Conclusions and Outlook

DESIGN OF POLYVALENT POLYMER THERAPEUTICS
Introduction
Polyvalent Polymer Therapeutics
Conclusions

POSTTRANSLATIONAL MODIFICATION OF PROTEINS INCORPORATING NONNATURAL AMINO ACIDS
Posttranslational Modification of Existing Amino Acids within Protein Chain
Exploiting Biosynthetic Machinery: Cotranslational Approach
Intein-Inspired Ligation Approach
Combined Approach
Protein and Polymer Conjugates
Modulating the Physicochemical Properties of Protein Polymers via NAA Incorporation
Future in Combined Technologies to Fabricate Tailored Protein-Polymer Conjugates as New Materials
Conclusion and Future Perspectives

FUNCTIONALIZATION OF POROUS POLYMERS FROM HIGH-INTERNAL-PHASE EMULSIONS AND THEIR APPLICATIONS
Introduction
Functionalization of polyHIPEs
Applications
Conclusions

POST-POLYMERIZATION MODIFICATION OF POLYMER BRUSHES
Introduction
Synthesis and Strategies for Functional Polymer Brushes
Applicatio

Erscheint lt. Verlag 12.2.2013
Sprache englisch
Themenwelt Naturwissenschaften Chemie Organische Chemie
Wirtschaft
Schlagworte alternative approach • bearing • Chemie • Chemistry • completely • Direct • Functional • groups • Industrial Chemistry • known • Large • Limitations • Materials Science • Materialwissenschaften • Methods • Methods - Synthesis & Techniques • Modern • modification • Number • Organische Chemie / Methoden, Synthesen, Verfahren • Organische Synthese • Polymer • polymeranalogous • Polymere • Polymerization • Polymers • Polymer Science & Technology • Polymersynthese • polymer synthesis • Polymerwissenschaft u. -technologie • Reactions • Science • synthesis • Technische u. Industrielle Chemie • variety
ISBN-10 3-527-65544-1 / 3527655441
ISBN-13 978-3-527-65544-1 / 9783527655441
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