Anionic polymerization of primary acrylates as promoted by lithium 2-(2-methoxyethoxy) ethoxide

Some primary acrylates, such as methyl, ethyl, n-butyl, and n-nonyl acrylate (MA, EA, nBuA and nNonA, respectively) have been anionically polymerized by using diphenylmethyl lithium (DPMLi) as an initiator, in the presence of a chelating μ-σ dual ligand, i.e., a polydentate lithium alkoxide, at low temperature. It has been found that lithium 2-(2-methoxyethoxy) ethoxide (LiOEEM) is a very efficient ligand in preventing the anionic polymerization of these monomers from being disturbed by significant secondary transfer and termination reactions. Even for the difficult cases of ethyl and methylacrylate, that approach provides high polymerization yields and low polydispersity, allowing the molecular weight to be predetermined. LiOEEM/initiator molar ratio, solvent polarity, temperature and monomer concentration have proved to be key parameters in the control of the polymerization process. The efficiency of that control is however dependent on the monomer structure and improves with the length of the n-alkyl substituent, i.e., MA < EA < nBuA < nNonA. © 1997 John Wiley & Sons, Inc.     

New initiator system for the anionic polymerization of (meth)acrylates in toluene. IV. Random copolymerization of (meth)acrylates in toluene initiated by s-BuLi ligated by lithium silanolates

Copolymerization of binary mixtures of alkyl (meth)acrylates has been initiated in toluene by a mixed complex of lithium silanolate  (s-BuMe₂SiOLi) and s-BuLi (molar ratio > 21) formed in situ by reaction of s-BuLi with hexamethylcyclotrisiloxane (D₃). Fully acrylate and methacrylate copolymers, i.e., poly(methyl acrylate-co-n-butyl acrylate), poly(methyl methacrylate-co-ethyl methacrylate), poly(methyl methacrylate-co-n-butyl methacrylate), poly(methyl methacrylate-co-n-butyl methacrylate), poly(isobornyl methacrylate-co-n-butyl methacrylate), poly(isobornyl methacrylate-co-n-butyl methacrylate) of a rather narrow molecular weight distribution have been synthesized. However, copolymerization of alkyl acrylate and methyl methacrylate pairs has completely failed, leading to the selective formation of homopoly(acrylate). As result of the isotactic stereoregulation of the alkyl methacrylate polymerization by the s-BuLi/s-BuMe₂SiOLi initiator, highly isotactic random and block copolymers of (alkyl) methacrylates have been prepared and their thermal behavior analyzed. The structure of isotactic poly(ethyl methacrylate-co-methyl methacrylate) copolymers has been analyzed in more detail by Nuclear Magnetic Resonance (NMR). © 1999 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 37: 2525–2535, 1999     

Side-chain crystallinity. III. Influence of side-chain crystallinity on the glass transition temperatures of selected copolymers incorporating n-octadecyl acrylate or vinyl stearate

The influence of side-chain crystallinity on the glass transition temperatures of selected copolymers was investigated. The copolymers were selected, in part, from those whose crystallinity was treated in the preceding paper. These included the lower amorphous acrylate esters, such as methyl, ethyl, n-butyl, and 2-ethylhexyl acrylates, together with methyl methacrylate and acrylonitrile, each copolymerized with n-octadecyl acrylate over the range of composition. The decline in the glass transition temperature was linear with increasing weight fraction of n-octadecyl acrylate for all systems in the composition range where the copolymers were essentially amorphous. The extrapolated T_g for the amorphous state of poly(n-octadecyl acrylate), and for amorphous poly(oleyl acrylate), was close to ?111°C. This coincided with a value previously obtained by an extrapolation of data on homologs. Beyond a critical fraction of octadecyl acrylate (0.3 to 0.5), developing side-chain crystallinity in n-octadecyl acrylate raised the glass temperature steadily for all systems, up to a value of 17-C, obtained for the crystalline homopolymer. Crystallinity did not develop in stiff copolymers until T_g was about 30°C below the melting point of the most perfect crystals. In compositionally heterogeneous copolymers incorporating vinyl stearate, blocks of crystalline units appeared to be dispersed in a glassy matrix of amorphous co-units. An empirical equation was derived which fitted the experimental data for random copolymers, over all composition ranges, with fair accuracy.     

In situ generation of nitroxide from alkoxyamines for controlled acrylate polymerization

A general strategy for the controlled nitroxide-mediated polymerization of acrylates from alkoxyamines without addition of excess free nitroxide is outlined. 2,2-Dimethyl-3-(1-phenylethoxy)-4-phenyl-3-azapentane ( 1 ), prepared in one pot by the addition of 1-phenylethyl radicals to 2-methyl-2-nitrosopropane, is heated prior to the addition of monomer to afford a mixture of alkoxyamine 1 , free nitroxide, and 2,3-diphenylbutane. With a 30 min preheating period at temperatures up to 125 °C, the kinetics of the subsequent polymerization of n-butyl acrylate at 125 °C appear largely unaffected, though the ultimate molecular weight of the polymers is dependent upon the preheating temperature. The poly(n-butyl acrylate) samples, that result from this process, have much narrower molecular weight distributions than those which result in the absence of the preheating process. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 5128–5136, 2006     

A new microwave dielectric method for studying photoinitiated chain radical polymerization processes

Measurements of both real and imaginary parts of the dielectric constant at a fixed microwave frequency have been performed on n-butyl acrylate/poly(n-butyl acrylate) mixtures. The dielectric constant of the mixtures has been compared with that of neat n-butyl acrylate during UV photoinitiated polymerization. The values of the imaginary part of the dielectric constant thus obtained have allowed determination of the instantaneous monomer concentration and verified the kinetic equation for the photoinitiated polymerization process. The limits of validity of the method as well as its capability of providing detailed kinetic information are also discussed.     

Atom transfer radical polymerization of n‐butyl acrylate catalyzed by CuBr/N‐(n‐hexyl)‐2‐pyridylmethanimine

The homogeneous atom transfer radical polymerization (ATRP) of n‐butyl acrylate with CuBr/N‐(n‐hexyl)‐2‐pyridylmethanimine as a catalyst and ethyl 2‐bromoisobutyrate as an initiator was investigated. The kinetic plots of ln([M]₀/[M]) versus the reaction time for the ATRP systems in different solvents such as toluene, anisole, N,N‐dimethylformamide, and 1‐butanol were linear throughout the reactions, and the experimental molecular weights increased linearly with increasing monomer conversion and were very close to the theoretical values. These, together with the relatively narrow molecular weight distributions (polydispersity index ～ 1.40 in most cases with monomer conversion > 50%), indicated that the polymerization was living and controlled. Toluene appeared to be the best solvent for the studied ATRP system in terms of the polymerization rate and molecular weight distribution among the solvents used. The polymerization showed zero order with respect to both the initiator and the catalyst, probably because of the presence of a self‐regulation process at the beginning of the reaction. The reaction temperature had a positive effect on the polymerization rate, and the optimum reaction temperature was found to be 100 °C. An apparent enthalpy of activation of 81.2 kJ/mol was determined for the ATRP of n‐butyl acrylate, corresponding to an enthalpy of equilibrium of 63.6 kJ/mol. An apparent enthalpy of activation of 52.8 kJ/mol was also obtained for the ATRP of methyl methacrylate under similar reaction conditions. Moreover, the CuBr/N‐(n‐hexyl)‐2‐pyridylmethanimine‐based system was proven to be applicable to living block copolymerization and living random copolymerization of n‐butyl acrylate with methyl methacrylate. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 3549–3561, 2002     

Synthesis of tertiary-butyl acrylate polymers and preparation of diblock copolymers using atom transfer radical polymerization

The synthesis of tert-butyl acrylate by atom transfer radical polymerization (ATRP) is reported. This polymer was prepared using FeCl₂ · 4H₂O(PPh₃)₂ catalyst system in conjunction with methyl 2-bromopropionate as initiator, in bulk and in solution using acetone as a solvent. The addition of solvent was necessary in order to decrease the polymerization rate and to afford low polydispersity polymers. The number-average molecular weights of the resulting polymers increased in direct proportion to the monomer conversion, and the polydispersities (M_w/M_n) were as low as 1.2. In addition, the preparation of an AB diblock copolymer of poly (n-butyl methacrylate)-block-poly (tert-butyl acrylate) by ATRP is reported. The resulting polymers and copolymers were characterized by means of size exclusion chromatography and ¹H-NMR Spectroscopy.     

New Segmented Copolymers by Combination of Atom Transfer Radical Polymerization and Ring Opening Polymerization

Atom transfer radical polymerization (ATRP) and ring opening polymerization (ROP) were combined to synthesize various polymers with various structures and composition. Poly(ε-caprolactone)-b-poly(n-octadecyl methacrylate), PCL-PODMA, was prepared using both sequential and simultaneous polymerization methods. Kinetic studies on the simultaneous process were performed to adjust the rate of both polymerizations. The influence of tin(II) 2-ethylhexanoate on ATRP was investigated, which led to development of new initiation methods for ATRP, i.e., activators (re)generated by electron transfer (AGET and ARGET). Additionally, block copolymers with two crystalizable blocks, poly(ε-caprolactone)-b-poly(n-butyl acrylate)-b-poly(n-octadecyl methacrylate), PCL-PBA-PODMA, block copolymers for potential surfactant applications poly(ε-caprolactone)-b-poly(n-octadecyl methacrylate-co-dimethylaminoethyl methacrylate), PCL-P(ODMA-co-DMAEMA), and a macromolecular brush, poly(hydroxyethyl methacrylate)-graft-poly(ε-caprolactone), PHEMA-graft-PCL, were prepared using combination of ATRP and ROP.     

Electron spin resonance study on polymerization of alkyl acrylates with n-butyl titanate(IV)–triethylaluminum catalyst

n-Butyl titanate(IV)–triethylaluminum catalyst at Al/Ti molar ratios greater than 6 polymerizes methyl and n-butyl acrylates at ?78°C. The polymerization system which includes methyl acrylate at ?78°C, gives two ESR signals with g factors of 1.958 and 1.961 that overlap each other. The absorption intensity of the latter signal is approximately proportional to the polymer chain concentration calculated from polymer yield and the molecular weight. The polymerization system at Al/Ti ratios smaller than 3 has no catalytic activity on the polymerization and shows only the ESR signal with the g factor of 1.958. On the basis of these facts the ESR signal with the g factor of 1.961 is attributed to the active growing end of poly(methyl acrylate) with this catalyst. The character of this active growing end is discussed.     

Preparation of PEG-modified urethane acrylate emulsion and its emulsion polymerization

In order to improve stability and reduce droplet size, the PEG-modified urethane acrylates were synthesized by the reaction of polyethylene glycol (PEG) with residual isocyanate groups of urethane acrylate to incorporate hydrophilic groups into the molecular ends. The droplet sizes of the PEG-modified urethane acrylate emulsions were much smaller than those of unmodified urethane acrylate emulsions at the same surfactant composition, and the droplet sizes of these emulsions were significantly effected not by surfactant compositions and types, but by the reaction molar ratio of PEG, because the urethane acrylate containing polyoxyethylene groups as terminal groups aided the interfacial activity of surfactant molecules and acted as a polymeric surfactant. The actions of PEG-modified urethane acrylate were confirmed by the investigation of adsorption of urethane acrylate in a water/benzene interface.For polymerization of emulsions, the stability of emulsion in the process of emulsion polymerization was changed by the type of surfactant or initiator. In the case of emulsion polymerization with a water soluble initiator (K₂S₂O₈), the emulsions prepared using TWEEN 60 were broken in the process of polymerization. However, polymerization of these emulsions could be carried out using an oil soluble initiator (AIBN). The conversion of emulsion polymerization changed with the type of urethane acrylates, that is, the reaction molar ratio of PEG to 2-HEMA.     

Ligated anionic block copolymerization of methyl methacrylate with n-butyl acrylate and n-nonyl acrylate as promoted by lithium 2-(2-methoxyethoxy) ethoxide/diphenylmethyllithium

Poly(methyl methacrylate-b-n-butyl acrylate) (PMMA-b-Pn-BuA) and poly(methyl methacrylate-b-n-nonyl acrylate) (PMMA-b-Pn-NonA) diblock copolymers have been successfully synthesized by the sequential anionic polymerization of methyl methacrylate (MMA) and the n-alkyl acrylate (n-BuA or n-NonA), in a 90/10 toluene/tetrahydrofuran (THF) mixture at −78°C. When diphenylmethyllithium (DPMLi) ligated with lithium 2-(2-methoxyethoxy) ethoxide (LiOEEM) is used as the initiator, the polymerization of each block appears to be living. Molecular weight and composition of block copolymers can be predicted from the monomer over initator molar ratio and the molecular weight distribution is narrow. Size exclusion chromatography (SEC) supports that no homo-PMMA contaminates the final copolymer. Although the reverse polymerization sequence Pn-NonA-b-PMMA always results in some contamination by homo-Pn-NonA, it has no really significant effect on the final product characteristics. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 1543–1548, 1997     

Effect of the chemical natures of a monomer and a leaving group in symmetric trithiocarbonate as a reversible addition-fragmentation chain-transfer agent on the position of the trithiocarbonate group in macromolecules

The mechanism controlling the formation of polymer chains during the polymerization of vinyl monomers-namely, styrene, 4-vinylpyridine, n-butyl acrylates, and tert-butyl acrylate—mediated by symmetric trithiocarbonates (R-S-C(=S)-S-R) with different leaving groups R is studied. It is shown that the position of the trithiocarbonate fragment in a macromolecule depends on the nature of both the monomer and substituent R in trithiocarbonate. Variations in the structure of the leaving group in the initial reversible addition-fragmentation chain-transfer agent and the synthesis conditions makes it possible to direct polymerization to form a structure (symmetric, end, or asymmetric) relative to the trithiocarbonate group.     

Atom transfer radical polymerization of acrylates in an ionic liquid: Synthesis of block copolymers

Atom transfer radical polymerization (ATRP) of acrylates in ionic liquid, 1‐butyl‐3‐methylimidazolium hexaflurophospate, with the CuBr/CuBr₂/amine catalytic system was investigated. Sequential polymerization was performed by synthesizing AB block copolymers. Polymerization of butyl acrylate (monomer that is only partly soluble in an ionic liquid forming a two‐phase system) proceeded to practically quantitative conversion. If the second monomer (methyl acrylate) is added at this stage, polymerization proceeds, and block copolymer formed is essentially free of homopolymer according to size exclusion chromatographic analysis. The number‐average molecular weight of the copolymer is slightly higher than calculated, but the molecular weight distribution is low (M_w/M_n = 1.12). If, however, methyl acrylate (monomer that is soluble in an ionic liquid) is polymerized at the first stage, then butyl acrylate in the second‐stage situation is different. Block copolymer free of homopolymer of the first block (with M_w/M_n = 1.13) may be obtained only if the conversion of methyl acrylate at the stage when second monomer is added is not higher than 70%. Matrix‐assisted laser desorption/ionization time‐of‐flight analysis confirmed that irreversible deactivation of growing macromolecules is significant for methyl acrylate polymerization at a monomer conversion above 70%, whereas it is still not significant for butyl acrylate even at practically quantitative conversion. These results show that ATRP of butyl acrylate in ionic liquid followed by addition of a second acrylate monomer allows the clean synthesis of block copolymers by one‐pot sequential polymerization even if the first stage is carried out to complete conversion of butyl acrylate. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 2799–2809, 2002     

Monodisperse micron-sized crosslinked polystyrene particles. IV. Effect of network structure on polymerization procedure

Monodisperse micron-sized polystyrene particles crosslinked using urethane acrylate were produced by dispersion polymerization in ethanol solution and the effect of the crosslinked network structure on the polymerization procedure was studied. The influences of the concentrations of the initiator and urethane acrylate on the particle diameter (D _n), the particle number density (N _p), and the polymerization rate (R _p) were found to obey the approximate relationships D _n ∝ [initiator]^0.43 [urethane acrylate]^0.05, N _p ∝ [initiator]^−1.30 [urethane acrylate]^0.19, and R _p ∝ [initiator]^{0.24 ± 0.02}. The power-law dependence of D _n and N _p on the initiator concentration showed a similar trend to that of linear polystyrene reported in the literature. Especially, it was found that urethane acrylate does not have a serious effect on D _n and N _p of the particles produced. The dependence of R _p on the initiator concentration was observed to be higher than that of linear polystyrene, suggesting that there is still competition between heterogeneous polymerization and solution polymerization because of the crosslinked network structure of the primary particle. Received: 1 April 1999 Accepted in revised form: 29 June 1999     

Free radical and nitroxide mediated polymerization of hydroxy–functional acrylates prepared via lipase–catalyzed transacylation reactions

3‐Hydroxypropyl acrylate, 4‐hydroxybutyl acrylate, 2‐methyl‐3‐hydroxypropyl acrylate, 2‐hydroxypropyl acrylate, neopentyl glycol acrylate, glyceryl acrylate, and dihydroxyhexyl acrylate were prepared via transacylation reaction of methyl acrylate with diols and triols catalyzed by Candida antarctica lipase B. After removal of the enzyme by filtration and the methyl acrylate by distillation, the monomers were polymerized via free radical polymerization (FRP) with azobisisobutyronitrile as initiator and nitroxide mediated polymerization (NMP) employing Blocbuilder? alkoxyamine initiator and SG‐1 free nitroxide resulting in hydroxy functional poly(acrylates). The NMP kinetics are discussed in detail. In addition, the polymers obtained by FRP and NMP are compared and the results are related to the amount of bisacrylates that are present in the initial monomer mixtures resulting from the transacylation reactions. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 2610–2621, 2010     

Free-Radical Modification of Polypropylene. I. Grafting of Poly(Ethyl Acrylate) on Atactic Polypropylene

The synthesis of atactic poly(propylene-g-ethyl acrylates) of [Mbar]_n ～ 3000–5000 has been accomplished with 80–90% incorporation of the backbone in the graft copolymer. The principle involves free radical initiation of ethyl acrylate polymerization with benzoyl peroxide via chain transfer. At low conversions (up to ～15%), massive homopolymerization took place and the initial rates of both homo- and graft copolymerizations were indistinguishable even with 1% initiator based on monomer. Grafting occurred at higher conversions and the [Mbar]_n of the grafted product increased with increasing initiator concentration for almost similar conversion data. The isothermal stability of the graft copolymer was far superior to that of atactic polypropylene. The initial decomposition temperature of the graft copolymers increased with increasing initiator amount used for grafting. It is proposed that the number of branches of poly (ethyl acrylate) increased, following the abstraction of an increasing number of tertiary hydrogen atoms from the backbone.     

Synthesis,characterization, and rheological properties of hybrid titanium star‐shaped poly(n‐butyl acrylate)

The synthesis of hybrid star‐shaped polymers was carried out by atom transfer radical polymerization of n‐butyl acrylate from a well‐defined multifunctional titanium‐oxo‐cluster initiator. Conditions were identified to prevent possible side reactions among monomer, polymer, and the titanium‐oxo‐cluster ligands. Polymerizations provided linear first‐order kinetics and the evolution of the experimental molecular weight is also linear with the conversion. ¹H DOSY NMR and cleavage of the polymeric branches from the multifunctional initiator by hydrolysis were used to (i) prove the star‐shaped structure of the polymer, and (ii) demonstrate that the shoulder observed on size exclusion chromatograms is not due to a noncontrolled polymerization but to ungrafting of polymeric branches during analysis. Rheological properties of the hybrid star‐shaped poly(n‐butyl acrylate) were studied in the linear regime and show that the Ti‐oxo‐cluster not only increases significantly the viscosity of the polymer relative to its ungrafted arm but has a rheological signature which is qualitatively different from that of stars with organic cores suggesting that the Ti cluster reduces significantly the molecular mobility of the star. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011     

Hydroxy Functional Acrylates: Enzymatic Synthesis and Free Radical Polymerization

Hydroxy functional acrylates were prepared via transacylation of methyl acrylate with 1,2,6-hexanetriol catalyzed by Candida antarctica lipase B. Under the applied reaction conditions, 70% of the substrate was converted into hydroxy functional acrylates. In a subsequent step, after filtration of the enzyme, the monomer mixture containing methyl acrylate and the new monomers was polymerized via free radical polymerization resulting in a functional copolymer with M_n = 14500 g/mol.     

Radical block polymerization of vinyl chloride. II. Synthesis and characterization of vinyl chloride block copolymers

Peroxidized polypropylene has been used as a heterofunctional initiator for a two-step emulsion polymerization of a vinyl monomer (M₁) and vinyl chloride with the production of vinyl chloride block copolymers. Styrene, methyl-, and n-butyl methacrylate and methyl-, ethyl-, n-butyl-, and 2-ethyl-hexyl acrylate have been used as M₁ and polymerized at 30–40°C. In the second step vinyl chloride was polymerized at 50°C. The range of chemical composition of the block copolymers depends on the rate of the first-step polymerization of M₁ and the duration of the second step; e.g., with 2-ethyl-hexyl acrylate block copolymers could be obtained with a vinyl chloride content of 25–90%. The block copolymers have been submitted to precipitation fractionation and GPC analysis. Noteworthy is the absence of any significant amount of homopolymers, as well as poly(M₁)n as PVC. The absence of homo-PVC was interpreted by an intra- and intermolecular tertiary hydrogen atom transfer from polypropylene residue to growing PVC sequences. The presence of saturated end groups on the PVC chains is responsible for the improved thermal stability of these block polymers, as well as their low rate of dehydrochlorination (180°C). Molecular aggregation in solution has been shown by molecular weight determination in benzene and tetrahydrofuran.     

Preparation of ASA (acrylonitrile-styrene-acrylate) structural latexes via seeded emulsion polymerization

Acrylonitrile-styrene-acrylate (ASA) structural latexes were synthesized in a two-stage seeded emulsion polymerization. In the first-stage, partially cross-linked poly (n-butyl acrylate) (PnBA) and poly (n-butyl acrylate-stat-2-ethyl hexyl acrylate) P (nBA-stat-2EHA) (75/25 by wt) rubber cores were synthesized, and then in the second-stage, a hard poly (styrene-stat-acrylonitrile) (SAN) (70/30 by wt) shell was grafted on to the rubber seeds. The effects of surfactant type and second-stage monomer addition mode have been investigated on the final morphology of two-stage emulsion particles. The results indicated that an application of anionic surfactant, that is, sodium dodecyl sulfonate (SDS), along with sodium persulfate (KPS) initiator for both stages, and with first-stage tert-butyl hydroperoxide (t-BHP) and second-stage KPS initiators led to a hemisphere particle morphology. On the other hand, raspberry and core-shell structures were observed for the structural latexes, which were prepared using a non-ionic surfactant, that is, nonylphenol ethoxylated polyethylene glycol (Igepal CO-850), accompanying KPS initiator for both stages. It is clear, however, that the relative surface hydrophilicity of the core phase, altered by the surfactant type considerably affected the type of morphology formed. For obtained structural latexes, the gradual addition of the second-stage monomers to the core latexes resulted in a fairly real core-shell structure with a higher shell thickness. On the contrary, a raspberry structure in which the rubber phase was enlarged by the second-stage polymer microdomains was observed for the second-stage monomer addition batch. In fact, the shell semi-batch polymerization conditions lower the shell plasticizing effect, and increase the kinetic barrier to prevent from further second-stage monomer diffusion and microdomain formation within the rubbery phase.