Organic Catalyst-Mediated Ring-Opening Polymerization for the Highly Efficient Synthesis of Polyester-Based Star Polymers

2012 ◽  
Vol 1 (6) ◽  
pp. 681-686 ◽  
Author(s):  
Jing M. Ren ◽  
Qiang Fu ◽  
Anton Blencowe ◽  
Greg G. Qiao
2020 ◽  
Vol 11 (20) ◽  
pp. 3475-3480
Author(s):  
Yu-Jia Zheng ◽  
Guan-Wen Yang ◽  
Bo Li ◽  
Guang-Peng Wu

A highly stereoregular polyphosphoester with a rigid cyclohexylene structure in the main chain was constructed via ring-opening polymerization (ROP) in the presence of an organic catalyst system.


RSC Advances ◽  
2015 ◽  
Vol 5 (43) ◽  
pp. 34466-34474 ◽  
Author(s):  
Li Ma ◽  
Yichao Lin ◽  
Haiying Tan ◽  
Jun Zheng ◽  
Feng Liu ◽  
...  

Two series of 3–12 multiarm star polymers and 4-miktoarm star copolymer of butadiene and styrene, in which the Mn of arm was higher than 20 kg mol−1, were synthesized with high efficiency (from 85.0% to 96.1%) via click chemistry.


2018 ◽  
Vol 5 (16) ◽  
pp. 2458-2462 ◽  
Author(s):  
Giacomo Berton ◽  
Giuseppe Borsato ◽  
Roberta Zangrando ◽  
Andrea Gambaro ◽  
Fabrizio Fabris ◽  
...  

C3-Symmetric tris-benzyl-O-substituted hexahydroxytriphenylene (HHTP) was prepared through selective ring opening with DIBAL-H in 48% yield (38% from HHTP in a two-step synthesis).


Author(s):  
Kai Cheng ◽  
Shiyao Lu ◽  
Kai Wang ◽  
Guangsheng Luo

Ring-opening polymerization (ROP) of lactones catalyzed by 1,5,7-triazabicyclo[4,4,0]decane-5-ene (TBD) is a highly efficient method for synthesizing aliphatic polyester materials. In order to create a green and sustainable synthetic route of...


2021 ◽  
Author(s):  
Xuejin Yang ◽  
Laura M. Murphy ◽  
Farihah M. Haque ◽  
Scott M. Grayson ◽  
Andrew J. Boydston

We have developed a highly efficient synthesis of linear polydicyclopentadiene (pDCPD) via photoredox mediated metal-free ring-opening metathesis polymerization (MF-ROMP) and investigated the Tg–Mn dependence of linear pDCPD.


2012 ◽  
Vol 476-478 ◽  
pp. 1897-1900 ◽  
Author(s):  
Shu Xiao ◽  
Lin Dai ◽  
Jing He

Dissolution and homogeneous graft copolymerization of cellulose were performed in an ionic liquid 1-allyl-3-methylimidazolium chloride (AmimCl) with L-lactide. The best synthetic condition of the cellulose-graft-poly (L-) (cellulose-g-PLLA) was that cellulose 0.6g, L-lactide 5.34g and 4-dimethylaminopyri lactide dine (DMAP) as an organic catalyst 0.69g reacted for 12 hours at 80°C. The synthesized AmimCl and cellulose graft copolymers were characterized by FT-IR, 1H-NMR, GPC, TG and WAXD. The results indicated that AmimCl dissolved cellulose directly by destroying intermolecular and intramolecular hydrogen bonds in cellulose and the grafting rate of the polymer reached 4.44, which was higher than that reported in AmimCl with Sn(oct)2 as a catalyst.


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