Localization of Critical Molar Ratio Intervals for Highly Branched Step-Growth Michael Addition Networks
Author:
Affiliation:
1. Lehrstuhl für Chemische Technologie der Materialsynthese, Universität Würzburg, Röntgenring 11, 97070 Würzburg, Germany
2. Fraunhofer-Institut für Silicatforschung, Neunerplatz 2, 97082 Würzburg, Germany
Publisher
American Chemical Society (ACS)
Subject
Materials Chemistry,Inorganic Chemistry,Polymers and Plastics,Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ma200810e
Reference19 articles.
1. Michael addition reactions in macromolecular design for emerging technologies
2. Water-borne,in situcrosslinked biomaterials from phase-segregated precursors
3. Nucleophile-Initiated Thiol-Michael Reactions: Effect of Organocatalyst, Thiol, and Ene
4. Thiol-enes: Chemistry of the past with promise for the future
5. Molecular Size Distribution in Three Dimensional Polymers. I. Gelation1
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1. Synthesis and characterization of hyperbranched poly(ester-amine) by Michael addition polymerization;Designed Monomers and Polymers;2017-01-01
2. Thiol–ene “click” reactions and recent applications in polymer and materials synthesis: a first update;Polym. Chem.;2014
3. Microencapsulation of Alkaline Salt Hydrate Melts for Phase Change Applications by Surface Thiol-Michael Addition Polymerization;Macromolecular Materials and Engineering;2012-04-26
4. A Method of Controlling Dispersity by Monomer Feeding Protocol and Forced Gelation in Nongelling Step-Growth Branched Polymerization Systems;Macromolecules;2011-09-22
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