author_facet Simon, Peter F. W.
Radke, Wolfgang
Müller, Axel H. E.
Simon, Peter F. W.
Radke, Wolfgang
Müller, Axel H. E.
author Simon, Peter F. W.
Radke, Wolfgang
Müller, Axel H. E.
spellingShingle Simon, Peter F. W.
Radke, Wolfgang
Müller, Axel H. E.
Macromolecular Rapid Communications
Hyperbranched methacrylates by self‐condensing group transfer polymerization
Materials Chemistry
Polymers and Plastics
Organic Chemistry
author_sort simon, peter f. w.
spelling Simon, Peter F. W. Radke, Wolfgang Müller, Axel H. E. 1022-1336 1521-3927 Wiley Materials Chemistry Polymers and Plastics Organic Chemistry http://dx.doi.org/10.1002/marc.1997.030180915 <jats:title>Abstract</jats:title><jats:p>The synthesis of hyperbranched methacrylates was achieved by self‐condensing group transfer polymerization of 2‐(2‐methyl‐1‐triethylsiloxy‐1‐propenyloxy)ethyl methacrylate (<jats:bold>1</jats:bold>). “Back‐biting” is shown to be the predominant side reaction. In spite of this, the compact nature of the hyperbranched molecules was demonstrated through SEC‐viscosity measurements and comparison with a linear analogue. The degree of branching can be controlled by copolymerization with conventional monomers, e.g. MMA, and the living polymers can be used as macroinitiators for star‐shaped polymers.</jats:p> Hyperbranched methacrylates by self‐condensing group transfer polymerization Macromolecular Rapid Communications
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title Hyperbranched methacrylates by self‐condensing group transfer polymerization
title_unstemmed Hyperbranched methacrylates by self‐condensing group transfer polymerization
title_full Hyperbranched methacrylates by self‐condensing group transfer polymerization
title_fullStr Hyperbranched methacrylates by self‐condensing group transfer polymerization
title_full_unstemmed Hyperbranched methacrylates by self‐condensing group transfer polymerization
title_short Hyperbranched methacrylates by self‐condensing group transfer polymerization
title_sort hyperbranched methacrylates by self‐condensing group transfer polymerization
topic Materials Chemistry
Polymers and Plastics
Organic Chemistry
url http://dx.doi.org/10.1002/marc.1997.030180915
publishDate 1997
physical 865-873
description <jats:title>Abstract</jats:title><jats:p>The synthesis of hyperbranched methacrylates was achieved by self‐condensing group transfer polymerization of 2‐(2‐methyl‐1‐triethylsiloxy‐1‐propenyloxy)ethyl methacrylate (<jats:bold>1</jats:bold>). “Back‐biting” is shown to be the predominant side reaction. In spite of this, the compact nature of the hyperbranched molecules was demonstrated through SEC‐viscosity measurements and comparison with a linear analogue. The degree of branching can be controlled by copolymerization with conventional monomers, e.g. MMA, and the living polymers can be used as macroinitiators for star‐shaped polymers.</jats:p>
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author Simon, Peter F. W., Radke, Wolfgang, Müller, Axel H. E.
author_facet Simon, Peter F. W., Radke, Wolfgang, Müller, Axel H. E., Simon, Peter F. W., Radke, Wolfgang, Müller, Axel H. E.
author_sort simon, peter f. w.
container_issue 9
container_start_page 865
container_title Macromolecular Rapid Communications
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description <jats:title>Abstract</jats:title><jats:p>The synthesis of hyperbranched methacrylates was achieved by self‐condensing group transfer polymerization of 2‐(2‐methyl‐1‐triethylsiloxy‐1‐propenyloxy)ethyl methacrylate (<jats:bold>1</jats:bold>). “Back‐biting” is shown to be the predominant side reaction. In spite of this, the compact nature of the hyperbranched molecules was demonstrated through SEC‐viscosity measurements and comparison with a linear analogue. The degree of branching can be controlled by copolymerization with conventional monomers, e.g. MMA, and the living polymers can be used as macroinitiators for star‐shaped polymers.</jats:p>
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spelling Simon, Peter F. W. Radke, Wolfgang Müller, Axel H. E. 1022-1336 1521-3927 Wiley Materials Chemistry Polymers and Plastics Organic Chemistry http://dx.doi.org/10.1002/marc.1997.030180915 <jats:title>Abstract</jats:title><jats:p>The synthesis of hyperbranched methacrylates was achieved by self‐condensing group transfer polymerization of 2‐(2‐methyl‐1‐triethylsiloxy‐1‐propenyloxy)ethyl methacrylate (<jats:bold>1</jats:bold>). “Back‐biting” is shown to be the predominant side reaction. In spite of this, the compact nature of the hyperbranched molecules was demonstrated through SEC‐viscosity measurements and comparison with a linear analogue. The degree of branching can be controlled by copolymerization with conventional monomers, e.g. MMA, and the living polymers can be used as macroinitiators for star‐shaped polymers.</jats:p> Hyperbranched methacrylates by self‐condensing group transfer polymerization Macromolecular Rapid Communications
spellingShingle Simon, Peter F. W., Radke, Wolfgang, Müller, Axel H. E., Macromolecular Rapid Communications, Hyperbranched methacrylates by self‐condensing group transfer polymerization, Materials Chemistry, Polymers and Plastics, Organic Chemistry
title Hyperbranched methacrylates by self‐condensing group transfer polymerization
title_full Hyperbranched methacrylates by self‐condensing group transfer polymerization
title_fullStr Hyperbranched methacrylates by self‐condensing group transfer polymerization
title_full_unstemmed Hyperbranched methacrylates by self‐condensing group transfer polymerization
title_short Hyperbranched methacrylates by self‐condensing group transfer polymerization
title_sort hyperbranched methacrylates by self‐condensing group transfer polymerization
title_unstemmed Hyperbranched methacrylates by self‐condensing group transfer polymerization
topic Materials Chemistry, Polymers and Plastics, Organic Chemistry
url http://dx.doi.org/10.1002/marc.1997.030180915