Complex polymer architectures via RAFT polymerization: From fundamental process to extending the scope using click chemistry and nature's building blocks

2012 ◽  
Vol 37 (1) ◽  
pp. 38-105 ◽  
Author(s):  
Andrew Gregory ◽  
Martina H. Stenzel
2016 ◽  
Vol 7 (35) ◽  
pp. 5536-5543 ◽  
Author(s):  
Johannes C. Brendel ◽  
Guillaume Gody ◽  
Sébastien Perrier

Controlled radical polymerization methods and click chemistry form a versatile toolbox for creating complex polymer architectures.


Author(s):  
Kurt Binder ◽  
Hans-Jürgen Butt ◽  
George Floudas ◽  
Holger Frey ◽  
Hsiao-Ping Hsu ◽  
...  

2021 ◽  
Vol 3 (3) ◽  
pp. 1602-1609
Author(s):  
Flavia Lupi ◽  
Daniele Martella ◽  
Sara Nocentini ◽  
Diego Antonioli ◽  
Michele Laus ◽  
...  

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.


2016 ◽  
Vol 7 (40) ◽  
pp. 6220-6230 ◽  
Author(s):  
Haiwang Lai ◽  
Mingxia Lu ◽  
Hongxu Lu ◽  
Martina H. Stenzel ◽  
Pu Xiao

Prodrug (gemcitabine)-based polymer coated nanodiamonds as stimuli-responsive drug delivery platforms for the treatment of pancreatic cancer.


2007 ◽  
Vol 40 (3) ◽  
pp. 474-481 ◽  
Author(s):  
Sudershan R. Gondi ◽  
Andrew P. Vogt ◽  
Brent S. Sumerlin

RSC Advances ◽  
2016 ◽  
Vol 6 (18) ◽  
pp. 14496-14504 ◽  
Author(s):  
Sofyane Andjouh ◽  
Christine Bressy ◽  
Yves Blache

A series of bromotyramine-based 4-acryloyl-1,2,3-triazole monomers and polymers using click chemistry and RAFT polymerization.


2006 ◽  
Vol 59 (10) ◽  
pp. 719 ◽  
Author(s):  
Christopher Barner-Kowollik ◽  
Thomas P. Davis ◽  
Martina H. Stenzel

Various pathways to generate star polymers using reversible addition–fragmentation transfer (RAFT) are discussed. Similar to other polymerization techniques, star polymers can be generated using arm-first and core-first approaches. Unique to the RAFT process is the subdivision of the core-first approach into the R-group and Z-group approaches, depending on the attachment of the RAFT agent to the multifunctional core. The mechanism of the R- and Z-group approaches are discussed in detail and it is shown that both techniques have to overcome difficulties arising from termination reactions. Termination reactions were found to broaden the molecular weight. However, these side reactions can be limited by careful design of the synthesis. Considerations include RAFT and radical concentration, number of arms, type of RAFT agent and monomer. Despite obvious challenges, the RAFT process is highly versatile, allowing the synthesis of novel polymer architectures such as poly(vinyl acetate) and poly(vinyl pyrrolidone) star polymers.


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