메뉴 건너뛰기




Volumn 38, Issue 6, 2005, Pages 2122-2130

Synthesis and characterization of sulfur-containing nongeminal cyclic and polymeric alkylarylphosphazenes

Author keywords

[No Author keywords available]

Indexed keywords

LIGANDS; NUCLEOPHILIC SUBSTITUTION; POLYPHOSPHAZENES; SULFONE FUNCTIONAL GROUPS;

EID: 15944426770     PISSN: 00249297     EISSN: None     Source Type: Journal    
DOI: 10.1021/ma048234g     Document Type: Article
Times cited : (24)

References (38)
  • 1
    • 0038319782 scopus 로고    scopus 로고
    • Klabunde, K. J., Ed.; Wiley-Interscience: New York
    • Schmid, G. In Nanoscale Materials in Chemistry; Klabunde, K. J., Ed.; Wiley-Interscience: New York, 2001, pp 15-59.
    • (2001) In Nanoscale Materials in Chemistry , pp. 15-59
    • Schmid, G.1
  • 12
    • 0000356163 scopus 로고
    • Wisian-Neilson, P., Allcock, H. R., Wynne, K. J., Eds; ACS Symposium Series 572; American Chemical Society: Washington, DC
    • Wisian-Neilson, P. In Inorganic and Organometallic Polymers II. Advanced Materials and Intermediates; Wisian-Neilson, P., Allcock, H. R., Wynne, K. J., Eds; ACS Symposium Series 572; American Chemical Society: Washington, DC, 1994, pp 246-257.
    • (1994) Inorganic and Organometallic Polymers II. Advanced Materials and Intermediates , pp. 246-257
    • Wisian-Neilson, P.1
  • 13
    • 1642519534 scopus 로고    scopus 로고
    • De Jaeger, R., Gleria, M., Eds.; Nova Science: Hauppauge, New York
    • (b) Wisian-Neilson, P. In Phosphazenes: A World-wide Insight; De Jaeger, R., Gleria, M., Eds.; Nova Science: Hauppauge, New York, 2002, pp 109-123.
    • (2002) Phosphazenes: A World-wide Insight , pp. 109-123
    • Wisian-Neilson, P.1
  • 22
    • 0028766005 scopus 로고
    • Wisian-Neilson, P.; Claypool, C. L.; Bahadur, M. Macromolecules 1994, 27, 7494-7495. Although, ca. 95% substitution was observed with MeI as the electrophile, almost every other electrophile we have used shows significantly lower substitution, presumably because of steric effects. Attempts to achieve higher substitution of the RS- groups failed to give better results and produced mixtures that were significantly more difficult to purify. Thus, 0.6 equiv of n-BuLi and disulfide appeared to be optimum conditions and gave substitution typical of other electrophiles, as noted in refs 10 and 19 and references therein.
    • (1994) Macromolecules , vol.27 , pp. 7494-7495
    • Wisian-Neilson, P.1    Claypool, C.L.2    Bahadur, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.