Reversible addition fragmentation transfer RAFT polymerization

To make further use of the azo-initiator, tethered diblock copolymers were prepared using reversible addition fragmentation transfer (RAFT) polymerization. Baum and co-workers [51] were able to make PS diblock copolymer brushes with either PMMA or poly(dimethylacrylamide) (PDMA) from a surface immobihzed azo-initiator in the presence of 2-phenylprop-2-yl dithiobenzoate as a chain transfer agent (Scheme 3). The properties of the diblock copolymer brushes produced can be seen in Table 1. The addition of a free initiator, 2,2 -azobisisobutyronitrile (AIBN), was required in order to obtain a controlled polymerization and resulted in the formation of free polymer chains in solution. 

There are several techniques for performing CRP, but the most popular and successful ones so far are as follows stable free radical (SFR) or nitroxide-mediated radical polymerization (NMRP) [44, 45, 49], atom transfer radical polymerization (ATRP) [50, 51], and degenerative transfer techniques, including particularly reversible addition-fragmentation transfer (RAFT) polymerization [3]. These are examined in some detail in the following sections. 

It is of obvious interest to explore the use of other polymerization techniques that, being more tolerant to the experimental conditions and monomers, can produce amphiphilie azobenzene BCPs with no need for post reactions. Notably, Su et al. have reeently reported the synthesis of such an amphiphilic diblock copolymer with PAA as the hydrophilic block using reversible addition-fragmentation transfer (RAFT) polymerization (structure d in Fig. 6.2) (Su et al., 2007). Using RAFT, they prepared PAA capped with dithiobenzoate and used it as the macro-RAFT transfer agent to polymerize the hydrophobic azobenzene polymer successfully. It ean be expected that more amphiphilic azobenzene BCPs will be synthesized using the eontrolled radical polymerization techniques (ATRP and RAFT) because of their simplicity, versatility, and efficiency. 

Molecularly imprinted polymers (MIPs) that are capable of sensing specific organophosphorus compounds, such as pinacolyl methylphosphonate (PMP), by luminescence have been synthesized and characterized. The polymers have been synthesized using conventional free radical polymerization and using Reversible Addition Fragmentation Transfer (RAFT) polymerization. The RAFT polymers exhibited many advantages over conventional free radical processes but are more difficult to make porous. 

Heteroarm or miktoarm star copolymers have attracted considerable attention in recent years due to the imique properties of these polymers, for example, they exhibit dramatic difference in morphology and solution properties. In comparison with the linear block and star-block copolymers, the s)mthesis of heteroarm or miktoarm star copolymers has been one of the more challenging projects available. A typical example is that the synthesis of the heteroarm H-shaped terpolymers, [(PLLA)(PS)]-PEO-[(PS)(PLLA)], in which PEO acts as a main chain and PS and PLLA as side arms (Fig. 4.11). The copolymers have been successfully prepared via combination of reversible addition-fragmentation transfer (RAFT) polymerization and ring-opening polymerization (ROP) by Han and Pan [166]. Another interesting example is that Pan et al. [167] successfully... 

Reversible Addition-Fragmentation Transfer (RAFT) Polymerization... 

Indeed, because copper-based ATRP was the first robust CRP process, and reversible addition fragmentation transfer (RAFT) polymerization processes and second-generation mediators for nitroxide-mediated polymerization (NMP) capable of controlled polymerization of acrylates were not developed until later than 1995, many materials initially prepared by copper-based ATRP are materials that were prepared for the first time by any CRP process. ... 

A polyhedron silsesquioxane ladder polymer containing polymerizable components was prepared in a three-step process to address this concern. The process initially entailed preparing the reversible addition-fragmentation transfer (RAFT) ladder iniferter, polysilsesquioxane dithiocarbamate. This intermediate was then polymerized with methyl methacrylate at ambient temperature by irradiating with ultraviolet (UV) light and poly(si Isesquioxane-g-methyl methacrylate) was obtained. 

The fifty chapters submitted for publication in the ACS Symposium series could not fit into one volume and therefore we decided to split them into two volumes. In order to balance the size of each volume we did not divide the chapters into volumes related to mechanisms and materials but rather to those related to atom transfer radical polymerization (ATRP) and to other controlled/living radical polymerization methods reversible-addition fragmentation transfer (RAFT) and other degenerative transfer techniques, as well as stable free radical pol5mierizations (SFRP) including nitroxide mediated polymerization (NMP) and organometallic mediated radical polymerization (OMRP). 

Controlled Radical Polymerization (CRP) is the most recently developed polymerization technology for the preparation of well defined functional materials. Three recently developed CRP processes are based upon forming a dynamic equilibrium between active and dormant species that provides a slower more controlled chain growth than conventional radical polymerization. Nitroxide Mediated Polymerization (NMP), Atom Transfer Radical Polymerization (ATRP) and Reversible Addition Fragmentation Transfer (RAFT) have been developed, and improved, over the past two decades, to provide control over radical polymerization processes. This chapter discusses the patents issued on ATRP initiation procedures, new functional materials prepared by CRP, and discusses recent improvements in all three CRP processes. However the ultimate measure of success for any CRP system is the preparation of conunercially viable products using acceptable economical manufacturing procedures. 

Controlled/ living radical polymerization (CLRP) processes are well-established synthetic routes for the production of well-defined, low-molecular weight-dispersity polymers [99]. The types of CLRP processes (initiator-transfer agent-terminator (INIFERTER), atom transfer radical polymerization (ATRP), nitroxide-mediated radical (NMRP) polymerization, reversible addition-fragmentation transfer (RAFT)) and their characteristics are described in Section 3.8 of Chapter 3 and in Section 14.8 of Chapter 14. 

Luo Y, Gu H (2007) Nanoencapsulation via interfaciaUy confined reversible addition fragmentation transfer (RAFT) miniemulsion polymerization. Polymer 48 3262-3272... 

Several acronyms are used to describe these polymerizations Reversible Addition-Fragmentation Transfer (RAFT), Group transfer polymerization, Ring Opening Metathesis Polymerization (ROMP), Group Transfer polymerization. 

Heterogeneous controlled radical polymerization Reversible addition fragmentation transfer (RAFT) process... 

Currently three systems seem to be the most efficient processes for conducting a CRP nitroxide mediated polymerization (NMP) (eq. 1 in Fig. 5), atom transfer radical polymerization (ATRP) (eq. 2 in Fig. 5) and degenerative transfer systems (eq. 3 in Fig. 5) such as reversible addition-fragmentation transfer (RAFT) or iodine degenerative transfer (IDT) processes (88-90). The key feature of all CRPs is the dynamic equilibration between active radicals and various types of dormant species. 

Three basic concepts concerning stable free-radical polymerization (SFRP) also called nitroxide-mediated radical polymerization (NMP), atom-transfer radical polymerization (ATRP) and reversible addition-fragmentation transfer (RAFT) have been developed during the last decade. 

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