2,4.

Osamu Ohara, Chuji Aso, Toyoki Kunitake

研究成果: ジャーナルへの寄稿 › 記事

7 引用 (Scopus)

抄録

Polymerizations of spiro left bracket 2,4 right bracket hepta-4,6-diene were carried out with cationic initiators and Ziegler-type catalysts. This monomer polymerized very rapidly with a variety of cationic initiators, and low monomer and initiator concentrations had to be employed in order to avoid formation of crosslinked polymers. The polymer contained 1,2 and 1,4 addition units, and there was no indication of the opening of the cyclopropyl ring in the monomer unit.

元の言語英語
ページ（範囲）1917-1925
ページ数9
ジャーナルJ Polym Sci Part A-1 Polym Chem
巻11
発行部数8
出版物ステータス出版済み - 1 1 1973
外部発表Yes

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Monomers
Polymers
Polymerization
Catalysts

All Science Journal Classification (ASJC) codes

  • Engineering(all)

これを引用

Ohara, O., Aso, C., & Kunitake, T. (1973). 2,4. J Polym Sci Part A-1 Polym Chem, 11(8), 1917-1925.

2,4. / Ohara, Osamu; Aso, Chuji; Kunitake, Toyoki.

：: J Polym Sci Part A-1 Polym Chem, 巻 11, 番号 8, 01.01.1973, p. 1917-1925.

研究成果: ジャーナルへの寄稿 › 記事

Ohara, O, Aso, C & Kunitake, T 1973, '2,4.', J Polym Sci Part A-1 Polym Chem, 巻. 11, 番号 8, pp. 1917-1925.
Ohara O, Aso C, Kunitake T. 2,4. J Polym Sci Part A-1 Polym Chem. 1973 1 1;11(8):1917-1925.
Ohara, Osamu ; Aso, Chuji ; Kunitake, Toyoki. / 2,4. ：: J Polym Sci Part A-1 Polym Chem. 1973 ; 巻 11, 番号 8. pp. 1917-1925.
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AU - Kunitake, Toyoki

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N2 - Polymerizations of spiro left bracket 2,4 right bracket hepta-4,6-diene were carried out with cationic initiators and Ziegler-type catalysts. This monomer polymerized very rapidly with a variety of cationic initiators, and low monomer and initiator concentrations had to be employed in order to avoid formation of crosslinked polymers. The polymer contained 1,2 and 1,4 addition units, and there was no indication of the opening of the cyclopropyl ring in the monomer unit.

AB - Polymerizations of spiro left bracket 2,4 right bracket hepta-4,6-diene were carried out with cationic initiators and Ziegler-type catalysts. This monomer polymerized very rapidly with a variety of cationic initiators, and low monomer and initiator concentrations had to be employed in order to avoid formation of crosslinked polymers. The polymer contained 1,2 and 1,4 addition units, and there was no indication of the opening of the cyclopropyl ring in the monomer unit.

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ER -

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