Cyclopolymerization. 22. Radical Polymeri- zation of N-Methyl-N-allyl-2-(methoxycarbon- yl)allylamine: Design of Unconjugated Dienes with High Polymerizability and High Cyclization Tendency Using Functional Groups of Low Polymerizabilities-Reference-Cited by-同舟云学术

Cyclopolymerization. 22. Radical Polymeri- zation of N-Methyl-N-allyl-2-(methoxycarbon- yl)allylamine: Design of Unconjugated Dienes with High Polymerizability and High Cyclization Tendency Using Functional Groups of Low Polymerizabilities

Published:1996-01-01 Issue:1 Volume:29 Page:484-485
ISSN:0024-9297
Container-title:Macromolecules
language:en
Short-container-title:Macromolecules

Author:

Kodaira Toshiyuki¹,Fujisawa Tadahiro¹,Liu Qing-Qing¹,Urushisaki Michio¹

Affiliation:

1. Department of Materials Science and Engineering, Faculty of Engineering, Fukui University, Fukui 910, 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/ma951092t

Reference15 articles.

1. Cyclopolymerization. II. Mechanism of the free-radical polymerization of N-n-propyldimethacrylamide

2. Cyclopolymerization. V. Monomer design for the synthesis of highly cyclized polymer from unsymmetrical unconjugated dienes: Synthesis and polymerization of N-methyl-N-allylmethacrylamide

3. Cyclopolymerization. IV. Monomer design for the synthesis of highly cyclized polymer from symmetrical unconjugated diene. Synthesis and polymerization of sym-dimethacryloyldimethylhydrazine

4. Radical polymerization, co-polymerization, and chain transfer of α-substituted acrylic esters

5. Cyclopolymerization of ether dimers of α-(hydroxymethyl)acrylic acid and its alkyl esters: substituent effect on cyclization efficiency and microstructures

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