Functionalized syndiotactic polystyrene polymers prepared by the combination of metallocene catalyst and borane comonomer

J. Y. Dong, E. Manias, T. C. Chung

Research output: Contribution to journalArticle

76 Citations (Scopus)

Abstract

This paper discusses an effective route in the functionalization of s-PS polymer that involves the direct copolymerization of styrene with a borane-containing styrenic monomer, i.e., 4-[B-(n-butylene)-9-BBN]styrene (B-styrene). The reactivity ratios of the two comonomers are quite close, with r1 = 0.9 for styrene and r2 = 1.2 for B-styrene in the Cp*Ti(OMe)3/MAO catalyst system. A broad composition range of syndiotactic poly(styrene-co-B-styrene) copolymers has been prepared with narrow molecular weight and composition distributions. The random copolymer structure was further evidenced by DSC and 13C NMR analyses. With increasing B-styrene concentration, the copolymers show a systematic decrease in glass transition temperature, melting point, crystallization temperature, and crystailinity. At above 8.4 mol % B-styrene content, the crystallinity of the copolymer completely disappears. In turn, the borane groups in the copolymer are very versatile and can be quantitatively converted to other functional groups, such as hydroxy and anhydride groups, or transformed to free radical initiators for in situ free radical graft polymerization to prepare s-PS-g-PMMA graft copolymers.

Original languageEnglish (US)
Pages (from-to)3439-3447
Number of pages9
JournalMacromolecules
Volume35
Issue number9
DOIs
StatePublished - Apr 23 2002

Fingerprint

Boranes
Styrene
Polystyrenes
Polymers
Catalysts
Copolymers
Free Radicals
Free radicals
Anhydrides
Graft copolymers
Monoamine Oxidase
Polymethyl Methacrylate
Crystallization
Chemical analysis
Grafts
Copolymerization
Functional groups
Melting point
metallocene
Monomers

All Science Journal Classification (ASJC) codes

  • Organic Chemistry
  • Polymers and Plastics
  • Inorganic Chemistry
  • Materials Chemistry

Cite this

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abstract = "This paper discusses an effective route in the functionalization of s-PS polymer that involves the direct copolymerization of styrene with a borane-containing styrenic monomer, i.e., 4-[B-(n-butylene)-9-BBN]styrene (B-styrene). The reactivity ratios of the two comonomers are quite close, with r1 = 0.9 for styrene and r2 = 1.2 for B-styrene in the Cp*Ti(OMe)3/MAO catalyst system. A broad composition range of syndiotactic poly(styrene-co-B-styrene) copolymers has been prepared with narrow molecular weight and composition distributions. The random copolymer structure was further evidenced by DSC and 13C NMR analyses. With increasing B-styrene concentration, the copolymers show a systematic decrease in glass transition temperature, melting point, crystallization temperature, and crystailinity. At above 8.4 mol {\%} B-styrene content, the crystallinity of the copolymer completely disappears. In turn, the borane groups in the copolymer are very versatile and can be quantitatively converted to other functional groups, such as hydroxy and anhydride groups, or transformed to free radical initiators for in situ free radical graft polymerization to prepare s-PS-g-PMMA graft copolymers.",
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Functionalized syndiotactic polystyrene polymers prepared by the combination of metallocene catalyst and borane comonomer. / Dong, J. Y.; Manias, E.; Chung, T. C.

In: Macromolecules, Vol. 35, No. 9, 23.04.2002, p. 3439-3447.

Research output: Contribution to journalArticle

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