Kinetic modeling of controlled living microemulsion polymerizations that use reversible addition–fragmentation chain transfer

Reversible addition–fragmentation chain transfer (RAFT) polymerization is a useful technique for the formation of polymers with controlled architectures and molecular weights. However, when used in the polymerization of microemulsions, RAFT agents are only able to control the polymer molecular weight only at high RAFT concentrations. Here, a kinetic model describing RAFT microemulsion polymerizations is derived that predicts the reaction rates, molecular weight polydispersities, and particle size. The model predicts that at low RAFT concentrations, the RAFT agent will be consumed early in the reaction and that this will result in uncontrolled polymerization in particles nucleated late in the reaction. The higher molecular weight polydispersity that is observed in RAFT microemulsion polymerizations is the result of this uncontrolled polymerization. The model also predicts a shift in the conversion at which the maximum reaction rate occurs and a decrease in the particle size with increasing RAFT concentration. Both of these trends are also consistent with those observed experimentally. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 6055–6070, 2006     

Kinetic model of reversible addition fragmentation chain transfer polymerization of styrene in seeded emulsion

A detailed model describing the kinetics of living polymerization mediated by reversible addition‐fragmentation chain transfer (RAFT) in seeded emulsion polymerization is developed. The model consists of a set of population balance equations of the different radical species in the aqueous phase and in the particle phase (accounting for radical segregation) as well as for the dormant species in the particle phase. The entire population of radicals was divided into several distinguished species, based on their length and their chain end group. The model results are helpful in understanding inhibition and retardation phenomena that are typical for RAFT emulsion polymerizations. While inhibition is due to the radical loss in form of the RAFT leaving group, retardation is mostly caused by a small amount of short dormant chains in the particle phase, leading to a slight increase of radical loss via RAFT exchange with radicals entering a particle. The model results are compared to a series of experiments, using cumyl dithiobenzoate as a RAFT agent in polymerizations of styrene. The agreement between experimental and model results is good and, notably, the only parameters considered adjustable were the RAFT exchange rate coefficients. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 6114–6135, 2006     

Isoprene polymerization via reversible addition fragmentation chain transfer polymerization

Until recently, the primary living radical polymerization method available for preparing polyisoprene was nitroxide‐mediated radical polymerization, with reversible addition‐fragmentation chain transfer polymerization being applied only in a few cases within the last couple of years. We report here the preparation of polyisoprene by RAFT in the presence of the trithiocarbonate transfer agent S‐1‐dodecyl‐S′‐(r,r′‐dimethyl‐r′′‐acetic acid)trithiocarbonate and t‐butyl peroxide as the radical initiator. The kinetics of this polymerization at an optimized temperature of 125 °C and radical initiator concentration of 0.2 equiv relative to transfer agent have been studied in triplicate and demonstrate the living nature of the polymerization. These conditions resulted in polymers with narrow polydispersity indices, on the order of 1.2, with monomer conversions up to 30%. Retention of chain‐end functionality was demonstrated by polymerizing styrene as a second block from a polyisoprene macrotransfer agent, resulting in a block copolymer presenting a unimodal gel permeation chromatogram, and narrow molecular weight distribution. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 4100–4108, 2007     

Macromolecular design via reversible addition–fragmentation chain transfer (RAFT)/xanthates (MADIX) polymerization

Among the living radical polymerization techniques, reversible addition–fragmentation chain transfer (RAFT) and macromolecular design via the interchange of xanthates (MADIX) polymerizations appear to be the most versatile processes in terms of the reaction conditions, the variety of monomers for which polymerization can be controlled, tolerance to functionalities, and the range of polymeric architectures that can be produced. This review highlights the progress made in RAFT/MADIX polymerization since the first report in 1998. It addresses, in turn, the mechanism and kinetics of the process, examines the various components of the system, including the synthesis paths of the thiocarbonyl‐thio compounds used as chain‐transfer agents, and the conditions of polymerization, and gives an account of the wide range of monomers that have been successfully polymerized to date, as well as the various polymeric architectures that have been produced. In the last section, this review describes the future challenges that the process will face and shows its opening to a wider scientific community as a synthetic tool for the production of functional macromolecules and materials. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43:5347–5393, 2005     

Dibenzyl trithiocarbonate mediated reversible addition–fragmentation chain transfer polymerization of acrylonitrile

Reversible addition–fragmentation chain transfer polymerization has been successfully applied to polymerize acrylonitrile with dibenzyl trithiocarbonate as the chain‐transfer agent. The key to success is ascribed to the improvement of the interchange frequency between dormant and active species through the reduction of the activation energy for the fragmentation of the intermediate. The influence of several experimental parameters, such as the molar ratio of the chain‐transfer agent to the initiator [azobis(isobutyronitrile)], the molar ratio of the monomer to the chain‐transfer agent, and the monomer concentration, on the polymerization kinetics and the molecular weight as well as the polydispersity has been investigated in detail. Matrix‐assisted laser desorption/ionization time‐of‐flight mass spectrometry and ¹H NMR analyses have confirmed the chain‐end functionality of the resultant polymer. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 490–498, 2006     

Synthesis of arborescent (Dendritic) polystyrenes via controlled inimer‐type reversible addition‐fragmentation chain transfer polymerization

The reversible addition‐fragmentation chain transfer (RAFT) copolymerization of styrene and 4‐vinylbenzyl dithiobenzoate, a RAFT‐based inimer (initiator‐monomer), is described. Controlled polymerization was achieved in bulk conditions using thermal initiation at 110 °C to give arborescent polystyrene (arbPSt). The number‐average molecular weights of the polymers increased linearly with conversion and were much higher than theoretically calculated for a linear polymerization, reaching M_n = 364,000 g/mol with M_w/M_n = 2.65. Branching analysis by NMR showed an average of 3.5 branches per chain. SEC data, which were similar to those measured in arborescent polyisobutylene, supported the architectural analysis. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 7621–7627, 2008     

Influence of the chemical structure of dithiocarbamates with different N‐groups on the reversible addition–fragmentation chain transfer polymerization of styrene

Polymerizations of styrene with azobisisobutyronitrile initiation or thermal initiation have been performed in the presence of dithiocarbamates with different N‐groups, that is, benzyl 4,5‐diphenyl‐1H‐imidazole‐1‐carbodithioate ( 2a ), benzyl 1H‐1,2,4‐triazole‐1‐carbodithioate ( 2b ), benzyl indole‐1‐carbodithioate ( 2c ), benzyl 2‐phenyl‐indole‐1‐carbodithioate ( 2d ), benzyl phenothiazine‐10‐carbodithioate ( 2e ), benzyl 9H‐carbazole‐9‐carbodithioate ( 2f ), and benzyl dibenzo[b,f]azepine‐5‐carbodithioate ( 2g ). The results show that the structure of the N‐group of dithiocarbamates has significant effects on the activity of dithiocarbamates for the polymerization of styrene. 2a , 2b , 2c , 2d , and 2f are effective reversible addition–fragmentation chain transfer (RAFT) agents for the RAFT polymerization of styrene, and the polymerizations have good living characteristics. However, in the cases of 2e and 2g , the obtained polymers have uncontrolled molecular weights and broad molecular weight distributions. The polymerization rate is markedly influenced by the conjugation structure of the N‐group of the dithiocarbamate, and the polymerization rate of 2b is greater than that of 2a . For 2b , the rate of polymerization seems independent of the RAFT agent concentration. However, a significant retardation in the rate of polymerization can be observed in the case of 2c . 2d is more effective than 2c , and the substitution group of phenyl on this dithiocarbamate has obvious effects on the effectiveness of the controlled polymerization of styrene. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 4849–4856, 2005     

A cyclic selenium‐based reversible addition‐fragmentation chain transfer agent mediated polymerization of vinyl acetate

A cyclic selenium‐based reversible addition‐fragmentation chain transfer (RAFT) agent, 5,5‐dimethyl‐3‐phenyl‐2‐selenoxo‐1,3‐selenazolidin‐4‐one (RAFT‐Se), was synthesized and utilized in the RAFT polymerizations of vinyl acetate (VAc). Its analog, 5,5‐dimethyl‐3‐phenyl‐2‐thioxothiazolidin‐4‐one (RAFT‐S), was also used in RAFT polymerizations for comparison under identical conditions. The RAFT polymerizations of VAc with RAFT‐Se were moderately controlled evidenced by the increase of molecular weights with conversion, despite the slightly high M_w/M_n (less than 1.90), whereas the molecular weights were poorly controlled in the presence of RAFT‐S (2.00 < M_w/M_n < 2.30). Thanks to its unusual cyclic structure of RAFT‐Se, one or more RAFT‐Se species was incorporated into the resultant poly(VAc) as revealed by the results of cleavage of polymer and atomic absorption spectroscopy. Considering the biorelated functions of both poly(VAc) and Se element, this work undoubtedly provided a successful methodology of how to incorporate high content of Se into a molecular weight controlled poly(VAc). © 2013 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013     

Reversible addition–fragmentation chain transfer polymerization of methyl methacrylate in emulsion

Theoretical simulations showed that for controlled/living radical polymerization in an emulsion system, some of the earliest born particles could be superswollen to a size close to 1 μm. We hypothesized that the superswelling of these particles would lead to colloidal instability. Under the guidance of the simulation results, reversible addition–fragmentation chain transfer (RAFT) emulsion polymerization of methyl methacrylate (MMA) was carried out. Experimental results showed that increasing the initiation rate, surfactant level, and targeted molecular weight could improve the colloidal stability of the RAFT polymerization of MMA in an emulsion. The experimental results were in full accord with the theoretical predictions. The poor control of the molecular weight and polydispersity index was found to have a close relationship with the colloidal instability. For the first time, we demonstrated that RAFT polymerization could successfully be implemented with little coagulum, good control of the molecular weight, and a low polydispersity index with the same process used for traditional emulsion polymerization but with higher surfactant levels and initiation rates. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44:2837–2847, 2006     

Controlled radical polymerization of styrene and methyl acrylate in the presence of reversible addition–fragmentation chain transfer agents,phenylethyl phenyl dithioacetate and phenyldithioacetic acid

The use of phenyldithioacetic acid (PDA) in homopolymerizations of styrene or methyl acrylate produced only a small fraction of chains with dithioester end groups. The polymerizations using 1‐phenylentyl phenyldithioacetate (PEPDTA) and PDA in the same reaction showed that PDA had little or no influence on the rate or molecular weight distribution even when a 1:1 ratio is used. The mechanistic pathway for the polymerizations in the presence of PDA seemed to be different for each monomer. Styrene favors addition of styrene to PDA via a Markovnikov type addition to form a reactive RAFT agent. The polymer was shown by double detection SEC to contain dithioester end groups over the whole distribution. This polymer was then used in a chain extension experiment and the M_n was close to theory. A unique feature of this work was that PDA could be used to form a RAFT agent in situ by heating a mixture of styrene and PDA for 24 h at 70 °C and then polymerizing in the presence of AIBN to give a linear increase in M_n and low values of PDI (<1.14). In the case of the polymerization of MA with PDA, the mechanism was proposed to be via degradative chain transfer. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 5232–5245, 2005     

Preparation of nanocomposites by reversible addition‐fragmentation chain transfer polymerization from the surface of quantum dots in miniemulsion

Herein, we report the synthesis of quantum dots (QDs)/polymer nanocomposites by reversible addition‐fragmentation chain transfer (RAFT) polymerization in miniemulsions using a grafting from approach. First, the surfaces of CdS and CdSe QDs were functionalized using a chain transfer agent, a trisalkylphosphine oxide incorporating 4‐cyano‐4‐(thiobenzoylsulfanyl)pentanoic acid moieties. Using a free radical initiator (AIBN) to activate the RAFT process, a polystyrene (PS) block was grafted from the surface of the QDs. Quantum confinement effects were identified for the nanocomposite obtained, so attesting to the integrity of the QDs after the polymerization. Free PS chains were also present in the final nanocomposite, indicating that the RAFT polymerization from the surface of the QDs was accompanied by conventional free radical polymerization. After isolating the nanocomposite particles, a second poly(n‐butyl acrylate) block was tentatively grown from the initial PS block. The first results indicated a successful polymerization of the second polymer and show the potential of the current strategy to prepare block copolymers from the surface of the RAFT‐modified QDs. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 5367–5377, 2009     

Dendrimers as scaffolds for multifunctional reversible addition–fragmentation chain transfer agents: Syntheses and polymerization

The synthesis and characterization of novel first‐ and second‐generation true dendritic reversible addition–fragmentation chain transfer (RAFT) agents carrying 6 or 12 pendant 3‐benzylsulfanylthiocarbonylsulfanylpropionic acid RAFT end groups with Z‐group architecture based on 1,1,1‐hydroxyphenyl ethane and trimethylolpropane cores are described in detail. The multifunctional dendritic RAFT agents have been used to prepare star polymers of poly(butyl acrylate) (PBA) and polystyrene (PS) of narrow polydispersities (1.4 < polydispersity index < 1.1 for PBA and 1.5 < polydispersity index < 1.3 for PS) via bulk free‐radical polymerization at 60 °C. The novel dendrimer‐based multifunctional RAFT agents effect an efficient living polymerization process, as evidenced by the linear evolution of the number‐average molecular weight (M_n) with the monomer–polymer conversion, yielding star polymers with molecular weights of up to M_n = 160,000 g mol^?1 for PBA (based on a linear PBA calibration) and up to M_n = 70,000 g mol^?1 for PS (based on a linear PS calibration). A structural change in the chemical nature of the dendritic core (i.e., 1,1,1‐hydroxyphenyl ethane vs trimethylolpropane) has no influence on the observed molecular weight distributions. The star‐shaped structure of the generated polymers has been confirmed through the cleavage of the pendant arms off the core of the star‐shaped polymeric materials. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 5877–5890, 2004     

Reversible addition‐fragmentation chain transfer polymerization of vinyl acetate under high pressure

In this work, high molecular weight polyvinyl acetate (PVAc) (M_n,GPC = 123,000 g/mol, M_w/M_n = 1.28) was synthesized by reversible addition‐fragmentation chain transfer polymerization (RAFT) under high pressure (5 kbar), using benzoyl peroxide and N,N‐dimethylaniline as initiator mediated by (S)‐2‐(ethyl propionate)‐(O‐ethyl xanthate) (X1) at 35 °C. Polymerization kinetic study with RAFT agent showed pseudo‐first order kinetics. Additionally, the polymerization rate of VAc under high pressure increased greatly than that under atmospheric pressure. The “living” feature of the resultant PVAc was confirmed by ¹H NMR spectroscopy and chain extension experiments. Well‐defined PVAc with high molecular weight and narrow molecular weight distribution can be obtained relatively fast by using RAFT polymerization at 5 kbar. © 2015 Wiley Periodicals, Inc. J. Polym. Sci. Part A: Polym. Chem. 2015 , 53, 1430–1436     

Synthesis of statistical and block copolymers containing adamantyl and norbornyl moieties by reversible addition‐fragmentation chain transfer polymerization

The synthesis of statistical and block copolymers, consisting of monomers often used as resist materials in photolithography, using reversible addition‐fragmentation chain transfer (RAFT) polymerization is reported. Methacrylate and acrylate monomers with norbornyl and adamantyl moieties were polymerized using both dithioester and trithiocarbonate RAFT agents. Block copolymers containing such monomers were made with poly(methyl acrylate) and polystyrene macro‐RAFT agents. In addition to have the ability to control molecular weight, polydispersity, and allow block copolymer formation, the polymers made via RAFT polymerization required end‐group removal to avoid complications during the photolithography. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 943–951, 2010     

Synthesis and characterization of block copolymers containing poly(di(ethylene glycol) 2‐ethylhexyl ether acrylate) by reversible addition–fragmentation chain transfer polymerization

Reversible addition–fragmentation chain transfer (RAFT) polymerization has emerged as one of the important living radical polymerization techniques. Herein, we report the polymerization of di(ethylene glycol) 2‐ethylhexyl ether acrylate (DEHEA), a commercially‐available monomer consisting of an amphiphilic side chain, via RAFT by using bis(2‐propionic acid) trithiocarbonate as the chain transfer agent (CTA) and AIBN as the radical initiator, at 70 °C. The kinetics of DEHEA polymerization was also evaluated. Synthesis of well‐defined ABA triblock copolymers consisting of poly(tert‐butyl acrylate) (PtBA) or poly(octadecyl acrylate) (PODA) middle blocks were prepared from a PDEHEA macroCTA. By starting from a PtBA macroCTA, a BAB triblock copolymer with PDEHEA as the middle block was also readily prepared. These amphiphilic block copolymers with PDEHEA segments bearing unique amphiphilic side chains could potentially be used as the precursor components for construction of self‐assembled nanostructures. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 5420–5430, 2007     

Influence of a reversible addition–fragmentation chain transfer agent in the dispersion polymerization of styrene

Dispersion polymerization was applied to the controlled/living free‐radical polymerization of styrene with a reversible addition–fragmentation chain transfer (RAFT) polymerization agent in the presence of poly(N‐vinylpyrrolidone) and 2,2′‐azobisisobutyronitrile in an ethanol medium. The effects of the polymerization temperature and the postaddition of RAFT on the polymerization kinetics, molecular weight, polydispersity index (PDI), particle size, and particle size distribution were investigated. The polymerization was strongly dependent on both the temperature and postaddition of RAFT, and typical living behavior was observed when a low PDI was obtained with a linearly increased molecular weight. The rate of polymerization, molecular weight, and PDI, as well as the final particle size, decreased with an increased amount of the RAFT agent in comparison with those of traditional dispersion polymerization. Thus, the results suggest that the RAFT agent plays an important role in the dispersion polymerization of styrene, not only reducing the PDI from 3.34 to 1.28 but also producing monodisperse polystyrene microspheres. This appears to be the first instance in which a living character has been demonstrated in a RAFT‐mediated dispersion polymerization of styrene while the colloidal stability is maintained in comparison with conventional dispersion polymerization. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 348–360, 2007     

Synthesis and swelling behavior of comb‐type grafted hydrogels by reversible addition–fragmentation chain transfer polymerization

The comb‐type grafted hydrogels poly(N‐isopropylacrylamide)‐g‐poly(N‐isopropylacrylamide) (PNIPAM‐g‐PNIPAM) and poly(acrylic acid)‐g‐poly(N‐isopropylacrylamide) (PAAc‐g‐PNIPAM) were prepared by reversible addition–fragmentation chain transfer polymerization. A macromolecular chain‐transfer agent was prepared first. Then, hydrogels were obtained by a reaction with a comonomer (N‐isopropylacrylamide or acrylic acid) in the presence of N,N‐methylenebisacrylamide as a crosslinker. The equilibrium swelling ratios and the swelling and deswelling kinetics of PNIPAM‐g‐PNIPAM were measured. The effects of the chain length and amount on the swelling behavior were investigated. The deswelling mechanism was illustrated. Meanwhile, the PAAc‐g‐PNIPAM hydrogel was used to confirm the versatility of this novel method. It was prepared in an alcoholic medium, whereas hydrogen‐bonding complexes formed in 1,4‐dioxane, which was chosen as the reaction medium for the PNIPAM‐g‐PNIPAM hydrogel. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 2615–2624, 2005     

Implementing the reversible addition–fragmentation chain transfer process in PREDICI

There is currently a highly controversial debate about the nature of the reversible addition–fragmentation chain transfer (RAFT) mechanism. In this debate, kinetic computer modeling is frequently used as a powerful tool to correlate experimental data with theoretical models to deduce the rate coefficients that govern the process. Frequently, the PREDICI program package has been used as a simulation tool. Recently, the implementation and mathematical basis of the RAFT process, with respect to PREDICI, have been criticized. This communication discusses the mathematical and mechanistic implementation of the RAFT process in the PREDICI program package and elucidates the well‐founded mathematical basis of the approach. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 1441–1448, 2004     

Synthesis and characterization of fluorescence end‐labeled polystyrene via reversible addition‐fragmentation chain transfer (RAFT) polymerization

Fluorescence end‐labeled polystyrene (PS) with heteroaromatic carbazole or indole group were prepared conveniently via reversible addition‐fragmentation chain transfer (RAFT) polymerization using dithiocarbamates, ethyl 2‐(9H‐carbazole‐9‐carbonothioylthio)propanoate (ECCP) and benzyl 2‐phenyl‐1H‐indole‐1‐carbodithioate (BPIC) as RAFT agents. The end functionality of obtained PS with different molecular weights was high. The steady‐state and the time‐resolved fluorescence techniques had been used to study the fluorescence behaviors of obtained end‐labeled PS. The fluorescence of dithiocarbamates resulting PS in solid powder cannot be monitored; however, they exhibited structured absorptions and emissions in solvent DMF and the fluorescence lifetimes of PS had no obvious change with molecular weights increasing. These observations suggested that the polymer chains were possibly stretched adequately in DMF, that is, the fluorescence end group was exposed into solvent molecules and little quenching of excited state occurred upon incorporation into polymer chain. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 6198–6205, 2008     

Controlled radical polymerization of a trialkylsilyl methacrylate by reversible addition–fragmentation chain transfer polymerization

The reversible addition–fragmentation chain transfer (RAFT) polymerization of a hydrolyzable monomer (tert‐butyldimethylsilyl methacrylate) with cumyl dithiobenzoate and 2‐cyanoprop‐2‐yl dithiobenzoate as chain‐transfer agents was studied in toluene solutions at 70 °C. The resulting homopolymers had low polydispersity (polydispersity index < 1.3) up to 96% monomer conversion with molecular weights at high conversions close to the theoretical prediction. The profiles of the number‐average molecular weight versus the conversion revealed controlled polymerization features with chain‐transfer constants expected between 1.0 and 10. A series of poly(tert‐butyldimethylsilyl methacrylate)s were synthesized over the molecular weight range of 1.0 × 10⁴ to 3.0 × 10⁴, as determined by size exclusion chromatography. As strong differences of hydrodynamic volumes in tetrahydrofuran between poly(methyl methacrylate), polystyrene standards, and poly(tert‐butyldimethylsilyl methacrylate) were observed, true molecular weights were obtained from a light scattering detector equipped in a triple‐detector size exclusion chromatograph. The Mark–Houwink–Sakurada parameters for poly(tert‐butyldimethylsilyl methacrylate) were assessed to obtain directly true molecular weight values from size exclusion chromatography with universal calibration. In addition, a RAFT agent efficiency above 94% was confirmed at high conversions by both light scattering detection and ¹H NMR spectroscopy. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 5680–5689, 2005