Preparation of Poly(β-malic acid) by Enzymatic Ring-Opening Polymerization of Benzylβ-Malolactonate

1996 ◽  
Vol 25 (9) ◽  
pp. 795-796 ◽  
Author(s):  
Shuichi Matsumura ◽  
Hideki Beppu ◽  
Kazuhiro Nakamura ◽  
Shuichi Osanai ◽  
Kazunobu Toshima
Keyword(s):  
Malic Acid ◽  
Ring Opening ◽  
Ring Opening Polymerization

Ring-opening polymerization of an O-carboxyanhydride monomer derived from l-malic acid

2011 ◽  
Vol 2 (10) ◽  
pp. 2204 ◽  
Author(s):  
Ryan J. Pounder ◽  
David J. Fox ◽  
Ian A. Barker ◽  
Michael J. Bennison ◽  
Andrew P. Dove
Keyword(s):  
Malic Acid ◽  
Ring Opening ◽  
Ring Opening Polymerization

scholarly journals Preparation of poly(.ALPHA.-D,L-malic acid-co-glycolic acid) by ring-opening polymerization of a novel cyclic diester.

1989 ◽  
Vol 46 (4) ◽  
pp. 281-284 ◽  
Author(s):  
Yoshiharu KIMURA ◽  
Kenji SHIROTANI ◽  
Hideki YAMANE ◽  
Toshio KITAO
Keyword(s):  
Malic Acid ◽  
Ring Opening ◽  
Glycolic Acid ◽  
Ring Opening Polymerization

scholarly journals Polyhydroxybutyrate (PHB)-based triblock copolymers: synthesis of hydrophobic PHB/poly(benzyl β-malolactonate) and amphiphilic PHB/poly(malic acid) analogues by ring-opening polymerization

2016 ◽  
Vol 7 (28) ◽  
pp. 4603-4608 ◽  
Author(s):  
Ghislaine Barouti ◽  
Sophie M. Guillaume
Keyword(s):  
Malic Acid ◽  
Ring Opening ◽  
Triblock Copolymers ◽  
Ring Opening Polymerization

Poly(benzyl β-malolactonate)-b-poly(3-hydroxybutyrate)-b-poly(benzyl β-malolactonate), PMLABe-b-PHB-b-PMLABe, and its analogous poly(β-malic acid), PMLA-b-PHB-b-PMLA, triblock copolymers are synthesized and fully characterized.

New Amphiphilic Poly[(R,S)-β-malic acid-b-ε-caprolactone] Diblock Copolymers by Combining Anionic and Coordination−Insertion Ring-Opening Polymerization

2002 ◽  
Vol 35 (27) ◽  
pp. 9896-9903 ◽  
Author(s):  
Olivier Coulembier ◽  
Philippe Degée ◽  
Sandrine Cammas-Marion ◽  
Philippe Guérin ◽  
Philippe Dubois
Keyword(s):  
Malic Acid ◽  
Ring Opening ◽  
Diblock Copolymers ◽  
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
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