New ring-opening polymerization via a .pi.-allylpalladium complex. 2. Novel proton-transfer polymerization of vinylcyclopropane derivatives having two electron-withdrawing substituents

1993 ◽  
Vol 26 (18) ◽  
pp. 4748-4750 ◽  
Author(s):  
Masato Suzuki ◽  
Shuji Sawada ◽  
Satoshi Yoshida ◽  
Anke Eberhardt ◽  
Takeo Saegusa
Keyword(s):  
Proton Transfer ◽  
Ring Opening ◽  
Ring Opening Polymerization ◽  
Proton Transfer Polymerization ◽  
Electron Withdrawing Substituents

scholarly journals Hybrid Copolymerization via the Combination of Proton Transfer and Ring-opening Polymerization

2019 ◽  
Vol 38 (3) ◽  
pp. 231-239 ◽  
Author(s):  
Hong-Jun Yang ◽  
Chen-Qiong Chai ◽  
Yong-Kang Zuo ◽  
Jin-Feng Huang ◽  
Yi-Ye Song ◽  
...  
Keyword(s):  
Proton Transfer ◽  
Ring Opening ◽  
Ring Opening Polymerization

A Recommender System for Inverse Design of Polycarbonates and Polyesters

2020 ◽  
Author(s):  
Nathaniel Park ◽  
Dmitry Yu. Zubarev ◽  
James L. Hedrick ◽  
Vivien Kiyek ◽  
Christiaan Corbet ◽  
...  
Keyword(s):  
Ring Opening ◽  
High Performance ◽  
Recommendation System ◽  
Polymeric Materials ◽  
Monomer Conversion ◽  
Design Strategy ◽  
Ring Opening Polymerization ◽  
Inverse Design ◽  
False Negatives ◽  
Accelerate Development

The convergence of artificial intelligence and machine learning with material science holds significant promise to rapidly accelerate development timelines of new high-performance polymeric materials. Within this context, we report an inverse design strategy for polycarbonate and polyester discovery based on a recommendation system that proposes polymerization experiments that are likely to produce materials with targeted properties. Following recommendations of the system driven by the historical ring-opening polymerization results, we carried out experiments targeting specific ranges of monomer conversion and dispersity of the polymers obtained from cyclic lactones and carbonates. The results of the experiments were in close agreement with the recommendation targets with few false negatives or positives obtained for each class.<br>

Bisurea and Bisthiourea H-Bonding Organocatalysts for Ring-Opening Polymerization: Cues for the Catalyst Design

2019 ◽  
Vol 52 (23) ◽  
pp. 9232-9237 ◽  
Author(s):  
Rukshika S. Hewawasam ◽  
U. L. D. Inush Kalana ◽  
Nayanthara U. Dharmaratne ◽  
Thomas J. Wright ◽  
Timothy J. Bannin ◽  
...  
Keyword(s):  
Ring Opening ◽  
Ring Opening Polymerization ◽  
Catalyst Design

Ring-opening polymerization of [2]ferrocenophanes with a hydrocarbon bridge: synthesis of poly(ferrocenylethylenes)

1993 ◽  
Vol 115 (15) ◽  
pp. 7035-7036 ◽  
Author(s):  
James M. Nelson ◽  
Heiko Rengel ◽  
Ian Manners
Keyword(s):  
Ring Opening ◽  
Ring Opening Polymerization

scholarly journals Isoselective Ring-opening Polymerization of Racemic Lactide Catalyzed by N-heterocyclic Olefin/(Thio)urea Organocatalysts

2021 ◽  
Author(s):  
Zhen-Yu Wang ◽  
Guang-Qiang Xu ◽  
Li Zhou ◽  
Cheng-Dong Lv ◽  
Ru-Lin Yang ◽  
...  
Keyword(s):  
Ring Opening ◽  
Ring Opening Polymerization

scholarly journals Controlled Ring-Opening Polymerization of O-Carboxyanhydrides to Synthesize Functionalized Poly(α-Hydroxy Acids)

2021 ◽  
Vol 03 (01) ◽  
pp. 041-050
Author(s):  
Xiaoqian Wang ◽  
Ai Lin Chin ◽  
Rong Tong
Keyword(s):  
Biomedical Engineering ◽  
Ring Opening ◽  
Ring Opening Polymerization ◽  
Metal Catalyst ◽  
Hydroxy Acids ◽  
Controlled Polymerization ◽  
Biodegradable Polyesters ◽  
Recent Advances

Poly(α-hydroxy acids), as a family of biodegradable polyesters, are valuable materials due to their broad applications in packaging, agriculture, and biomedical engineering. Herein we highlight and explore recent advances of catalysts in controlled ring-opening polymerization of O-carboxyanhydrides towards functionalized poly(α-hydroxy acids), especially metal catalyst-mediated controlled polymerization. Limitations of current polymerization strategies of O-carboxyanhydrides are discussed.

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