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Ring-Opening Polymerization: from Hybrid Block Copolymers to Porous Polymers
来源: 日期2019-10-31 16:59 点击:

报告题目: Ring-Opening Polymerization: from Hybrid Block Copolymers to Porous Polymers

报告时间: 2019年11月4日,星期一,09:00

报告地点:仲英楼B249

报告人: David Pahovnik 教授

报告人简介:

Dr. David Pahovnik received his B.S. in Organic chemistry at the Faculty of Chemistry and Chemical Technology, University of Ljubljana, Slovenia, in 2007, and his Ph.D. in Polymer Chemistry in 2012 at the Department of Polymer Chemistry and Technology, National Institute of Chemistry, Slovenia. Between 2013 and 2014 he was a postdoctoral fellow at prof. Nikos Hadjichristidis group in the Polymer Synthesis Laboratory, King Abdullah University of Science and Technology (KAUST), Saudi Arabia. After his postdoc he returned to National Institute of Chemistry, where he is currently a Research fellow. His main research interests are synthesis and characterization of polymers, with special focus on ring-opening polymerization of NCAs for preparation of synthetic polypeptide-based materials.

报告摘要:

Ring-opening polymerization (ROP) of heterocyclic monomers such as lactones, lactides, epoxides and α-amino acid N-carboxyanhydrides (NCA) is an invaluable tool for the preparation of biocompatible and (bio)degradable polymers as well as hybrid copolymers in a controlled manner. However, polyesters/polyethers prepared by ROP propagate through a hydroxyl group, which is unfortunately a very slow initiating group for ROP of NCA, where chain propagation takes place through the amine group. Therefore, the synthesis of polypeptide-based hybrid block copolymers demands multistep reactions with expensive and time-consuming intermediate steps needed for end-group transformation. To overcome the issue of slow initiation by the hydroxyl group, we developed the procedure that enables separation of initiation from the propagation step, which are instead performed in a successive manner. By using simple alcohol initiators and hydroxyl-terminated macroinitiators we have been able to prepare both the homopolypeptides and polypeptide-based block copolymers, respectively. This approach was further developed to allow for one-pot sequential ROP, where cyclic esters/carbonates are first polymerized, followed by addition of NCA monomer and its polymerization.

Additionally, several examples of porous polymers prepared by employing ROP will be discussed. Since ROP and free-radical polymerizations are orthogonal they can be performed in situ simultaneously to prepare the semi-interpenetrating polymer networks. By selectively removing the degradable polyester component, the porous non-degradable polystyrene monoliths were prepared. Final morphology of the porous network was controlled by tuning the relative polymerization rate of both monomers. On the other hand, fully degradable scaffolds were synthesized by ROP within the oil-in-oil high internal phase emulsions (HIPE). In this way, the macroporous cross-linked poly(ε-caprolactone)-based (PCL) polyHIPE foams were synthesized, which demonstrate cross-linking degree dependant shape memory behaviour. HIPE templating was extended to ROP of NCA to prepare HIPE templated synthetic polypeptide scaffolds, where experimental conditions were carefully tuned to prevent foaming of the scaffold due to CO2 evolution during polymerization.

 
 
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