Multimodal Polypropylene Synthesis Using Cyclic Borane Cocatalyst

A strategy for synthesizing bimodal isotactic polypropylene (iPP) using a C2-symmetric zirconocene catalyst is reported. Unlike conventional multimodal polymerization methods requiring multireactor systems or multiple catalysts, our approach exploits multiple counteranions derived from a boron-based cocatalyst 1. Propylene polymerization using zirconocene 2 produced polypropylene with a bimodal molecular weight distribution when combined with cocatalyst 1 without losing stereospecificity. Chain-end analyses of the polymer obtained by using 1 confirmed different chain propagation and termination propensities compared with the polymer from a conventional borane activator, B(C6F5)3, explaining the observed bimodal nature. Notably, this molecular weight distribution could be tuned by the polymerization temperature and solvent, highlighting the potential for the control of these termination reactions.

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Publication Details

Journal
Organometallics
Published
2025-09-22
DOI
https://doi.org/10.1021/acs.organomet.5c00180
Citations
1
Primary Topic
Synthetic Organic Chemistry Methods
Type
article
Field-Weighted Citation Impact
0.94
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article

Multimodal Polypropylene Synthesis Using Cyclic Borane Cocatalyst

Takeshi Shiono, Yuushou Nakayama, Shogo Nishiyama, Ryō Tanaka et al.
1 citations
Organometallics
Synthetic Organic Chemistry Methods
0.94
article

Multimodal Polypropylene Synthesis Using Cyclic Borane Cocatalyst

Takeshi Shiono, Yuushou Nakayama, Shogo Nishiyama, Ryō Tanaka, Daichi Oka
article en
1 citations

Abstract

A strategy for synthesizing bimodal isotactic polypropylene (iPP) using a C2-symmetric zirconocene catalyst is reported. Unlike conventional multimodal polymerization methods requiring multireactor systems or multiple catalysts, our approach exploits multiple counteranions derived from a boron-based cocatalyst 1. Propylene polymerization using zirconocene 2 produced polypropylene with a bimodal molecular weight distribution when combined with cocatalyst 1 without losing stereospecificity. Chain-end analyses of the polymer obtained by using 1 confirmed different chain propagation and termination propensities compared with the polymer from a conventional borane activator, B(C6F5)3, explaining the observed bimodal nature. Notably, this molecular weight distribution could be tuned by the polymerization temperature and solvent, highlighting the potential for the control of these termination reactions.

OrganometallicsVol. 44(19)
Hiroshima University (JP)
Openalex Percentile: Top 21%
Synthetic Organic Chemistry Methods
0.94
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Multimodal Polypropylene Synthesis Using Cyclic Borane Cocatalyst — Takeshi Shiono, Yuushou Nakayama, et al. · Organometallics (2025) | TGRS Research Map | TGRS