메뉴 건너뛰기




Volumn 122, Issue 38, 2000, Pages 9109-9119

Molecular design and polymer structure control based on polymer crystal engineering. Topochemical polymerization of 1,3-diene mono- and dicarboxylic acid derivatives bearing a naphthylmethylammonium group as the countercation

Author keywords

[No Author keywords available]

Indexed keywords

CARBOXYLIC ACID DERIVATIVE; CATION; DICARBOXYLIC ACID DERIVATIVE; METHYLAMMONIUM; MUCONIC ACID; NAPHTHYL GROUP; POLYMER; SORBIC ACID;

EID: 0034721418     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja001093n     Document Type: Article
Times cited : (84)

References (69)
  • 2
    • 0000241161 scopus 로고    scopus 로고
    • Controlled Radical Polymerization
    • American Chemical Society: Washington, DC
    • (b) Matyjaszewski, K., Ed. Controlled Radical Polymerization; ACS Symp. Ser. No. 685; American Chemical Society: Washington, DC, 1998.
    • (1998) ACS Symp. Ser. No. 685 , vol.685
    • Matyjaszewski, K.1
  • 5
    • 0000264611 scopus 로고    scopus 로고
    • Reinhoudt, N. D., Ed.; Pergamon: Oxford
    • (b) Miyata, M. Comprehensive Supramolecular Chemistry; Reinhoudt, N. D., Ed.; Pergamon: Oxford, 1996; Vol. 10, pp 557-582.
    • (1996) Comprehensive Supramolecular Chemistry , vol.10 , pp. 557-582
    • Miyata, M.1
  • 6
    • 0001615160 scopus 로고    scopus 로고
    • Schlüter. A.-Dieter, Ed.; Wiley-VCH: Weinheim
    • (c) Stupp, S. I.; Osenar, P. Synthesis of Polymers; Schlüter. A.-Dieter, Ed.; Wiley-VCH: Weinheim, 1999; pp 513-547.
    • (1999) Synthesis of Polymers , pp. 513-547
    • Stupp, S.I.1    Osenar, P.2
  • 16
    • 0039931522 scopus 로고    scopus 로고
    • Controlled/Living Radical Polymerization
    • Matyjaszewski, K., Ed.; American Chemical Society: Washington, DC, Chapter 7
    • (c) Matsumoto, A.; Odani, T. Controlled/Living Radical Polymerization; ACS Symp. Ser. No. 768; Matyjaszewski, K., Ed.; American Chemical Society: Washington, DC, 2000; Chapter 7; pp 93-106.
    • (2000) ACS Symp. Ser. No. 768 , vol.768 , pp. 93-106
    • Matsumoto, A.1    Odani, T.2
  • 27
    • 0034682334 scopus 로고    scopus 로고
    • (b) Ward, M. D. Nature 2000, 405, 293-294.
    • (2000) Nature , vol.405 , pp. 293-294
    • Ward, M.D.1
  • 29
    • 0033312815 scopus 로고    scopus 로고
    • Preliminary results for the polymerization of 6: Matsumoto, A.; Odani, T. Polym. J. 1999, 31, 717-719.
    • (1999) Polym. J. , vol.31 , pp. 717-719
    • Matsumoto, A.1    Odani, T.2
  • 31
    • 0003756176 scopus 로고    scopus 로고
    • Crystal Engineering: The Design and Application of Functional Solids
    • Kluwer Academic: Dordrecht, The Netherlands
    • (b) Seddon, K. R.; Zaworotko, M. J., Eds. Crystal Engineering: The Design and Application of Functional Solids; NATO ASI Series C, Vol. 539; Kluwer Academic: Dordrecht, The Netherlands, 1999.
    • (1999) NATO ASI Series C , vol.539
    • Seddon, K.R.1    Zaworotko, M.J.2
  • 32
    • 0003449950 scopus 로고    scopus 로고
    • Crystal Engineering: From Molecules and Crystals to Materials
    • Kluwer Academic: Dordrecht, The Netherlands
    • (c) Braga, D.; Grepioni, F.; Orpen, A. G., Eds. Crystal Engineering: From Molecules and Crystals to Materials; NATO ASI Ser. C, Vol. 538; Kluwer Academic: Dordrecht, The Netherlands, 1999.
    • (1999) NATO ASI Ser. C , vol.538
    • Braga, D.1    Grepioni, F.2    Orpen, A.G.3
  • 49
    • 0000954898 scopus 로고
    • Bassett, D. C., Ed.; Applied Science Publishers: London
    • (e) Bloor, D. Developments in Crystalline Polymers II; Bassett, D. C., Ed.; Applied Science Publishers: London, 1982; pp 151-193.
    • (1982) Developments in Crystalline Polymers II , pp. 151-193
    • Bloor, D.1
  • 50
    • 0343603161 scopus 로고    scopus 로고
    • The (E.Z)-isomer seemed to photoisomerize to 5 at a much lower rate, compared with the isomerization of 4 to 5, although the 4 crystals were contaminated by a small amount of the (E,Z)-isomer
    • The (E.Z)-isomer seemed to photoisomerize to 5 at a much lower rate, compared with the isomerization of 4 to 5, although the 4 crystals were contaminated by a small amount of the (E,Z)-isomer.
  • 58
    • 0342733222 scopus 로고    scopus 로고
    • For the general rule of the topochemical polymerization of diacetylenes, see ref 4c
    • For the general rule of the topochemical polymerization of diacetylenes, see ref 4c.
  • 60
    • 84935624129 scopus 로고
    • Blackwell Scientific Publications: Oxford
    • In some polymer science textbooks, the terms meso and racemic are used. However, the IUPAC committee on nomenclature recommends the use of "racemo" but not "racemic". See, IUPAC Macromolecular Division, Commission on Macromolecular Nomenclature. Compendium of Macromolecular Nomenclature, Blackwell Scientific Publications: Oxford, 1991. See also; Pure Appl. Chem. 1981, 53, 733-752.
    • (1991) Compendium of Macromolecular Nomenclature
  • 61
    • 84935624129 scopus 로고
    • In some polymer science textbooks, the terms meso and racemic are used. However, the IUPAC committee on nomenclature recommends the use of "racemo" but not "racemic". See, IUPAC Macromolecular Division, Commission on Macromolecular Nomenclature. Compendium of Macromolecular Nomenclature, Blackwell Scientific Publications: Oxford, 1991. See also; Pure Appl. Chem. 1981, 53, 733-752.
    • (1981) Pure Appl. Chem. , vol.53 , pp. 733-752
  • 65
    • 0021756405 scopus 로고
    • (d) Mason, S. F. Nature 1984, 311, 19-23.
    • (1984) Nature , vol.311 , pp. 19-23
    • Mason, S.F.1
  • 69
    • 0342733221 scopus 로고
    • Freeman, J. P., Ed.; Wiley: New York
    • (b) Bankston, D. Organic Syntheses; Freeman, J. P., Ed.; Wiley: New York, 1993; Vol. VIII, pp 490-492.
    • (1993) Organic Syntheses , vol.8 , pp. 490-492
    • Bankston, D.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.