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Volumn 30, Issue 19, 1997, Pages 5612-5615

Novel synthesis of poly(thioarylene)s via reaction between arenethiols and bromo compounds with a free radical initiator

Author keywords

[No Author keywords available]

Indexed keywords

COPOLYMERIZATION; FOURIER TRANSFORM INFRARED SPECTROSCOPY; GEL PERMEATION CHROMATOGRAPHY; INITIATORS (CHEMICAL); MOLECULAR WEIGHT; ORGANIC POLYMERS; STRUCTURE (COMPOSITION); SYNTHESIS (CHEMICAL); THERMOANALYSIS;

EID: 0031235622     PISSN: 00249297     EISSN: None     Source Type: Journal    
DOI: 10.1021/ma970395f     Document Type: Article
Times cited : (13)

References (35)
  • 3
    • 5244332507 scopus 로고    scopus 로고
    • U.S. Patent 4,028,341, 1977
    • Hay, A. S. U.S. Patent 4,028,341, 1977.
    • Hay, A.S.1
  • 4
    • 5244296272 scopus 로고    scopus 로고
    • U.S. Patent 3294760, 1966
    • Hay, A. S. U.S. Patent 3294760, 1966.
    • Hay, A.S.1
  • 26
    • 85086526661 scopus 로고    scopus 로고
    • note
    • w higher than 20 000.
  • 27
    • 0031117586 scopus 로고    scopus 로고
    • Cyclic(arylene disulfide) oligomers form PPS poly(arylene disulfide)s by a ring-opening polymerization reaction, see: Ding, Y.; Hay, A. S. Polymer 1997, 38, 2239. An equilibrium exists between diphenyl disulfide and diphenyl sulfide at around 300 °C (see: Harpp, D. N.; Kader, H. A.; Smith, R. A. Sulfur Lett. 1982, 1, 59 and references therein). The use of a cyclic(arylene disulfide) as an initiator introduces a small excess of sulfur in the resulting polymer, which would probably be present as disulfide linkages or terminal SH groups.
    • (1997) Polymer , vol.38 , pp. 2239
    • Ding, Y.1    Hay, A.S.2
  • 28
    • 0031117586 scopus 로고    scopus 로고
    • and references therein
    • Cyclic(arylene disulfide) oligomers form PPS poly(arylene disulfide)s by a ring-opening polymerization reaction, see: Ding, Y.; Hay, A. S. Polymer 1997, 38, 2239. An equilibrium exists between diphenyl disulfide and diphenyl sulfide at around 300 °C (see: Harpp, D. N.; Kader, H. A.; Smith, R. A. Sulfur Lett. 1982, 1, 59 and references therein). The use of a cyclic(arylene disulfide) as an initiator introduces a small excess of sulfur in the resulting polymer, which would probably be present as disulfide linkages or terminal SH groups.
    • (1982) Sulfur Lett. , vol.1 , pp. 59
    • Harpp, D.N.1    Kader, H.A.2    Smith, R.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.