Stereospecific Radical Polymerization of α-(Alkoxymethyl)acrylates Controlled by Lewis Acid Catalysts: Mechanistic Study and Effect of Amino Alcohols as Ligand for Zinc Bromide-Reference-Cited by-同舟云学术

Stereospecific Radical Polymerization of α-(Alkoxymethyl)acrylates Controlled by Lewis Acid Catalysts: Mechanistic Study and Effect of Amino Alcohols as Ligand for Zinc Bromide

Published:2001-06-06 Issue:14 Volume:34 Page:4724-4729
ISSN:0024-9297
Container-title:Macromolecules
language:en
Short-container-title:Macromolecules

Author:

Baraki Hideo¹,Habaue Shigeki¹,Okamoto Yoshio¹

Affiliation:

1. Department of Applied Chemistry, Graduate School of Engineering, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8603, Japan

Publisher

American Chemical Society (ACS)

Subject

Materials Chemistry,Inorganic Chemistry,Polymers and Plastics,Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ma0104128

Reference17 articles.

1. Stereoregular polymerization of α-substituted acrylates

2. Chiral auxiliary control of tacticity in free radical polymerization

3. Polymerization and Telomerization of Chiral Acrylamides

4. Stereospecific radical polymerization of 1-phenyldibenzosuberyl methacrylate affording a highly isotactic polymer

5. Pronounced Effects of Temperature and Monomer Concentration on Isotactic Specificity of Triphenylmethyl Methacrylate Polymerization through Free Radical Mechanism. Thermodynamic versus Kinetic Control of Propagation Stereochemistry

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