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Volumn 32, Issue 1, 1999, Pages 48-54

Synthesis of functionalized polymers by means of anionic living polymerization. 1. Synthesis of functionalized polymers with α-methylstyryl groups by anionic reactions with use of 1-{4-[3-(4-isopropenylphenyl)propyl]phenyl}-1-phenylethylene

Author keywords

[No Author keywords available]

Indexed keywords

ANIONIC POLYMERIZATION; BLOCK COPOLYMERS; FLUORINE CONTAINING POLYMERS; METALLORGANIC POLYMERS; MOLECULAR STRUCTURE; MONOMERS; POLYISOPRENES; POLYMETHYL METHACRYLATES; POLYSTYRENES; REACTION KINETICS; SYNTHESIS (CHEMICAL);

EID: 0032730558     PISSN: 00249297     EISSN: None     Source Type: Journal    
DOI: 10.1021/ma9811730     Document Type: Article
Times cited : (33)

References (16)
  • 13
    • 0030572119 scopus 로고    scopus 로고
    • 4 mediated coupling reaction between 1,3-dibromopropane and the 4-isopropenylphenylmagnesium chloride in THF, similar to the method previously reported. See: Hirao, A.; Hayashi, M.; Nakahama, S. Macromolecules 1996, 29, 3353.
    • (1996) Macromolecules , vol.29 , pp. 3353
    • Hirao, A.1    Hayashi, M.2    Nakahama, S.3
  • 16
    • 85034553652 scopus 로고    scopus 로고
    • note
    • We examined separately the reaction of s-BuLi with 1-{4-[3-(4-vinylphenyl)propyl]phenyl}-1-phenylethylene, a DPE derivative substituted with a styryl group, in THF at -78°C for 30 min. Unlike the reaction of s-BuLi with 1, insoluble polymeric material and a small amount of soluble polymer with a very broad molecular distribution were obtained in the reaction. This clearly indicates that undesirable side reactions such as polymerization and/or addition reactions of both the styryl and 1,1-diphenylethenyl groups occur simultaneously. Accordingly, the anionic functionalization reaction using the DPE substituted with a styryl group was unsuccessful under the conditions employed here.


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