Immortal ring-opening polymerization of ε-caprolactone by a neat magnesium catalyst system: an approach to obtain block and amphiphilic star polymers in situ

2014 ◽  
Vol 5 (15) ◽  
pp. 4580-4588 ◽  
Author(s):  
Yang Wang ◽  
Bo Liu ◽  
Xue Wang ◽  
Wei Zhao ◽  
Dongtao Liu ◽  
...  

Building of various functional and topological microstructured PCLs via the immortal catalyst system of MgnBu2/ROH and click reaction.

2012 ◽  
Vol 2012 ◽  
pp. 1-6 ◽  
Author(s):  
Chae Hwan Hong ◽  
Si Hwan Kim ◽  
Ji-Yeon Seo ◽  
Do Suck Han

Polylactide (PLA), which is one of the most important biocompatible polyesters that are derived from annually renewable biomass such as corn and sugar beets, has attracted much attention for automotive parts application. The manufacturing method of PLA is the ring-opening polymerization of the dimeric cyclic ester of lactic acid, lactide. For the stereocomplex PLA, we developed the four unit processes, fermentation, separation, lactide conversion, and polymerization. Fermentation of sugars to D-lactic acid is little studied, and its microbial productivity is not well known. Therefore, we investigated D-lactic acid fermentation with a view to obtaining the strains capable of producing D-lactic acid, and we got a maximum lactic acid production 60 g/L. Lactide is prepared by a two-step process: first, the lactic acid is converted into oligo(lactic acid) by a polycondensation reaction; second, the oligo(lactic acid) is thermally depolymerized to form the cyclic lactide via an unzipping mechanism. Through catalyst screening test for polycondensation and depolymerization reactions, we got a new method which shortens the whole reaction time 50% the level of the conventional method. Poly(L-lactide) was obtained from the ring-opening polymerization of L-lactide. We investigated various catalysts and polymerization conditions. Finally, we got the best catalyst system and the scale-up technology.


2004 ◽  
Vol 856 ◽  
Author(s):  
Alexandru D. Asandei ◽  
Isaac W. Moran ◽  
Gobinda Saha ◽  
Yanhui Chen

ABSTRACTTi(III)Cp2Cl-catalyzed radical ring opening (RRO) of epoxides or single electron transfer (SET) reduction of aldehydes generates Ti alkoxides and carbon centered radicals which add to styrene, initiating a radical polymerization. This polymerization is mediate in a living fashion by the reversible termination of growing chains with the TiCp2Cl metalloradical. In addition, polymers or monomers containing pendant epoxide groups (glycidyl methacrylate) can be used as substrates for radical grafting or branching reactions by self condensing vinyl polymerization. In addition, Ti alkoxides generated in situ by both epoxide RRO and aldehyde SET initiate the living ring opening polymerization of ε-caprolactone. Thus, new initiators and catalysts are introduced for the synthesis of complex polymer architectures.


2011 ◽  
Vol 49 (19) ◽  
pp. 4213-4220 ◽  
Author(s):  
Kubra Dogan Demir ◽  
Mehmet Atilla Tasdelen ◽  
Tamer Uyar ◽  
Asei William Kawaguchi ◽  
Atsushi Sudo ◽  
...  

2008 ◽  
Vol 9 (2) ◽  
pp. 704-710 ◽  
Author(s):  
Mohamad Takwa ◽  
Yan Xiao ◽  
Neil Simpson ◽  
Eva Malmström ◽  
Karl Hult ◽  
...  

2006 ◽  
Vol 39 (13) ◽  
pp. 4374-4379 ◽  
Author(s):  
Donald J. Darensbourg ◽  
Wonsook Choi ◽  
Poulomi Ganguly ◽  
Casseday P. Richers

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.


Sign in / Sign up

Export Citation Format

Share Document