Copolymerization of lactones and bioaromatics via concurrent ring-opening polymerization/polycondensation

2017 ◽  
Vol 19 (8) ◽  
pp. 1877-1888 ◽  
Author(s):  
Ha Thi Hoang Nguyen ◽  
Gabriel N. Short ◽  
Pengxu Qi ◽  
Stephen A. Miller

Concurrent ring-opening polymerization/polycondensation of lactones and bioaromatic hydroxy-acids yields random copolymers with improved and controlled thermal properties.

2021 ◽  
Vol 03 (01) ◽  
pp. 041-050
Author(s):  
Xiaoqian Wang ◽  
Ai Lin Chin ◽  
Rong Tong

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.


2010 ◽  
Vol 76 ◽  
pp. 30-35 ◽  
Author(s):  
Naomi Cohen-Arazi ◽  
Ilanit Hagag ◽  
Michal Kolitz ◽  
Abraham J. Domb ◽  
Jeoshua Katzhendler

Optically active α-hydroxy acids derived from amino acids have been synthesized and polymerized into new biodegradable polyesters. The variety of functional side chains enables the design of positively charged, negatively charged, hydrophobic and hydrophilic chiral building blocks or any combination of these constituents. Hydroxy acids of 15 natural amino acids were prepared with retention of configuration using a straightforward and reliable method of diazotization of α-amino acids. Polyesters were synthesized from these hydroxy acids by a number of methods: direct condensation in bulk, microwave assisted synthesis and ring opening polymerization. The molecular weight of the prepared polymers ranges between 2000 to 5000Da for the direct condensation and the microwave methods, whereas the ring opening polymerization results in high molecular weight polymers (20000 to 30000Da). The polymers were analyzed for their optical activity (Circular Dichroism Spectroscopy), thermal properties (DSC), solubility, molecular weight and polydispersity (GPC), and aqueous degradation. These polymers were tested for their compatibility to neuronal cells growth and differentiation.


RSC Advances ◽  
2015 ◽  
Vol 5 (80) ◽  
pp. 65635-65645 ◽  
Author(s):  
Mohamed Gamal Mohamed ◽  
Ruey-Chorng Lin ◽  
Jia-Huei Tu ◽  
Fang-Hsien Lu ◽  
Jin-Long Hong ◽  
...  

A salicylaldehyde azine-functionalized benzoxazine monomer formed zinc ion complexes not only improved the thermal properties but also facilitated ring-opening polymerization.


2018 ◽  
Vol 20 (21) ◽  
pp. 4995-5006 ◽  
Author(s):  
Masayoshi Honda ◽  
Hideki Abe

Various biomass-derived poly(aliphatic carbonate)s were synthesized by bulk ring-opening polymerization over a heterogeneous H3PW12O40/CeO2 catalyst, and thermal properties were investigated.


2012 ◽  
Vol 1 (4) ◽  
pp. 441-444 ◽  
Author(s):  
Yanbing Lu ◽  
Lichen Yin ◽  
Yanfeng Zhang ◽  
Zhonghai Zhang ◽  
Yunxiang Xu ◽  
...  

2016 ◽  
Vol 2016 ◽  
pp. 1-9 ◽  
Author(s):  
Yixiu Liu ◽  
Xizhuang Bai ◽  
A. Liang

Random copolymers of poly(d,l-lactide-co-glycolide-co-ε-caprolactone) (PLGC) were synthesized by the ring-opening polymerization of d,l-lactide (DLLA), glycolide (GA), andε-caprolactone (CL). The effects of CL on the copolymers were evaluated to prepare suitable copolymers with controlled properties. Our results showed that the CL content significantly influenced the thermal and mechanical properties of the copolymers and that the CL content in compositions could be altered to control properties of random copolymers. The in vitro hydrolytic degradation of the resulting implants showed that the degradation rate of PLGC was lower than that of PLGA, which could markedly reduce acidic degradation products. Finally, we demonstrated that higher CL contents in compositions slowed degradation rates.


Polymers ◽  
2021 ◽  
Vol 13 (24) ◽  
pp. 4365
Author(s):  
Grażyna Adamus ◽  
Adrian Domiński ◽  
Marek Kowalczuk ◽  
Piotr Kurcok ◽  
Iza Radecka

The feasibility of synthesis of functionalized poly(3-hydroxybutanoic acid) analogue and its copolymers via ring-opening polymerization of β-butyrolactone mediated by activated anionic initiators is presented. Using these new synthetic approaches, polyesters with a defined chemical structure of the end groups, as well as block, graft, and random copolymers, have been obtained and characterized by modern instrumental techniques, with special emphasis on ESI-MS. The relationship between the structure and properties of the prepared polymeric materials is also discussed.


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