2001
DOI: 10.1021/ma012491t
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Syndiospecific Living Polymerization of Propene with [t-BuNSiMe2Flu]TiMe2 Using MAO as Cocatalyst. Volume 34, Number 10, May 8, 2001, pp 3142−3145.

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Cited by 10 publications
(13 citation statements)
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“…General Procedure. All reactions and manipulations were conducted under a nitrogen atmosphere using the standard 49 The resulting TMA-free MAO was diluted in toluene to the desired concentration before use. Me 2 C(Cp)(Flu)-ZrCl 2 , 50,51 2-bromo-3-hexylthiophene, 52 and lithium diisopropylamide (LDA) 52 were synthesized using the method described in the literature.…”
Section: ■ Experimental Sectionmentioning
confidence: 99%
“…General Procedure. All reactions and manipulations were conducted under a nitrogen atmosphere using the standard 49 The resulting TMA-free MAO was diluted in toluene to the desired concentration before use. Me 2 C(Cp)(Flu)-ZrCl 2 , 50,51 2-bromo-3-hexylthiophene, 52 and lithium diisopropylamide (LDA) 52 were synthesized using the method described in the literature.…”
Section: ■ Experimental Sectionmentioning
confidence: 99%
“… 11,17 The TMA in MAO can be divided into two kinds: “bound TMA” which is incorporated in the MAO and “free TMA” which can be removed under vacuum to form TMA-depleted MAO (DMAO). 18 Free TMA can be effectively trapped by adding a sterically hindered phenol such as 2,6-di- tert -butyl-4-methylphenol (BHT). 19,20 The catalytic productivity and polymer molecular weight depends on the amount of free TMA in MAO and its synthesis history.…”
Section: Introductionmentioning
confidence: 99%
“…Poly(propylene-ran-norbornene) showed a higher T g value than poly(ethylene-ran-norbornene) with the same norbornene content and molar mass, but the catalysts which copolymerize propylene and norbornene are very limited. 13 We have previously reported that [t-BuNSiMe 2 Flu]TiMe 2 (1) activated by Me 3 -Al-free dried aluminoxane (dMAO) not only conducted living polymerization of propylene and norbornene 14,15 but also copolymerized propylene and norbornene with high activity to produce random copolymers, of which T g values showed a good linear relationship with norbornene content in the copolymers. 16 We have recently found that the introduction of the tert-butyl substituents on the fluorenyl ligand of 1 at the 3,6-position [t-BuNSiMe 2 (3,6-t-Bu 2 Flu)]TiMe 2 (2) improved the activity and syndiospecificity in propylene polymerization to give living polypropylene (PP) with the syndiotactic triad of 0.93 and melting point of 142 °C.…”
mentioning
confidence: 99%