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Volumn 31, Issue 21, 1998, Pages 7570-7571

Synthesis of π-conjugated poly(dithiafulvene) by cycloaddition polymerization of aldothioketene with its alkynethiol tautomer

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; CHARGE TRANSFER; DERIVATIVES; DRYING; INFRARED SPECTROSCOPY; MOLECULAR WEIGHT; MOLECULAR WEIGHT DISTRIBUTION; MONOMERS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; ORGANIC POLYMERS; STRUCTURE (COMPOSITION); SYNTHESIS (CHEMICAL);

EID: 0032180333     PISSN: 00249297     EISSN: None     Source Type: Journal    
DOI: 10.1021/ma980969w     Document Type: Article
Times cited : (36)

References (23)
  • 9
    • 0000529367 scopus 로고
    • For recent reviews, see: (a) Bryce, M. R. Chem. Soc. Rev. 1991, 20, 335. (b) Hansen, T. K.; Becher, J. Adv. Mater. 1993, 5, 288. (c) Roncali, J. J. Mater. Chem. 1997, 7, 2307.
    • (1991) Chem. Soc. Rev. , vol.20 , pp. 335
    • Bryce, M.R.1
  • 10
    • 0343743800 scopus 로고
    • For recent reviews, see: (a) Bryce, M. R. Chem. Soc. Rev. 1991, 20, 335. (b) Hansen, T. K.; Becher, J. Adv. Mater. 1993, 5, 288. (c) Roncali, J. J. Mater. Chem. 1997, 7, 2307.
    • (1993) Adv. Mater. , vol.5 , pp. 288
    • Hansen, T.K.1    Becher, J.2
  • 11
    • 0000660319 scopus 로고    scopus 로고
    • For recent reviews, see: (a) Bryce, M. R. Chem. Soc. Rev. 1991, 20, 335. (b) Hansen, T. K.; Becher, J. Adv. Mater. 1993, 5, 288. (c) Roncali, J. J. Mater. Chem. 1997, 7, 2307.
    • (1997) J. Mater. Chem. , vol.7 , pp. 2307
    • Roncali, J.1
  • 18
    • 85034484547 scopus 로고    scopus 로고
    • note
    • The elemental analysis agreed. Found: C, 63.09; H, 4.45; N, 1.50; S, 30.96. Calcd: C, 63.07; H, 4.10; N, 1.44; S, 31.39.
  • 19
    • 85034485456 scopus 로고    scopus 로고
    • note
    • Gel permeation chromatography was carried out on Shodex K-803 plus K-804 columns by using DMSO as an eluent at 50 °C after calibration with standard poly(8-oxa-6-azabicyclo-[3.2.1]octan-7-one) samples.
  • 20
    • 85034480125 scopus 로고    scopus 로고
    • note
    • 2SO) δ 6.73 (s, 1H), 7.19 (m, 1H), 7.30-7.55 (m, 10H).
  • 21
    • 85034485528 scopus 로고    scopus 로고
    • note
    • 3) δ 1.30 (m, 2H), 1.65 (m, 4H), 3.57 (t, 2H), 4.28 (t, 2H), 4.35 (s, 2H), 7.33 (m, 5H).
  • 22
    • 0032556195 scopus 로고    scopus 로고
    • and references therein
    • For syntheses of diyne monomers, see: Matsumi, N.; Naka, K.; Chujo, Y. J. Am. Chem. Soc. 1998, 120, 5112 and references therein.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 5112
    • Matsumi, N.1    Naka, K.2    Chujo, Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.