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1.
High conversion methyl methacrylate (MMA)-methacrylic acid (MA) copolymers prepared by two different emulsion polymerization processes were characterized in terms of composition and sequence distribution by 1H- and 13C-NMR, taking into account the conversion effect. A rapid and selective counting procedure for calculating the compositional configurational pentads (512 values) in these copolymers is described. From this counting procedure and using the Klesper's assignment of the 18 peaks observed in the 13C-NMR carbonyl resonance spectrum of the copolymers, a relatively good agreement was found between the calculated and experimental fractions of each peak intensity. Moreover, this study allows differences in compositional homogeneity to be characterized as a function of the nature of the emulsion polymerization process.  相似文献   

2.
The preparation of chloroprene–methyl methacrylate copolymers in the presence of Lewis acids (Et1.5AlCl1.5) in hydrocarbon solvent and the effect of Lewis acids concentration on copolymer composition are described. 13C NMR spectra were obtained on these copolymers. In samples of high MMA content, tactic placements of MMA were observed as well as several different kinds of sequences for chloroprene and MMA. In samples of low MMA content, no tactic placements of MMA were found but several different kinds of chloroprene sequences were observed. From the analysis of the 13C NMR spectra of the different copolymers examined, it is apparent that all the various kinds of chloroprene sequences in these copolymers can be determined.  相似文献   

3.
Poly-p-ethylacrylophenone (PPEtAP) and poly-p-chloroacrylophenone (PPClAP) and their copolymers with styrene (PEtAP/S) and (PClAP/S) and with methyl methacrylate (PEtAP/MMA) and (PClAP/MMA) were prepared. Quantum yields of main-chain scissions at 366 nm at room temperature in benzene solution are of the same order as those of the unsubstituted polyacrylophenone and its copolymers. Substitution with chlorine and ethyl group in the para position compared to the unsubstituted polyacrylophenone and its copolymers leads to an increase of the lifetime for the n–π* excited triplet state, as is evident from the measured quenching constants of photolysis. The low-temperature emission spectra of the copolymers are similar to the spectra of the model compounds in a polymer film. For the homopolymer, however, the character of the emission spectrum changes considerably.  相似文献   

4.
This article describes the homopolymerization of isocyanatoethyl methacrylate (IEM) and its copolymerization with methyl methacrylate (MMA) in acetonitrile in the presence of 2,2′‐azobisisobutyronitrile. The constant characteristic of IEM polymerizability (kp2/kte = 128 × 10?3 L mol?1 s?1, where kp is the propagation constant and kte is the termination constant) was determined. The study of IEM reactivity toward MMA gave ratios of 0.88 and 1.20 for IEM and MMA, respectively. The physicochemical properties of the IEM homopolymer and IEM/MMA copolymers were also studied. The glass‐transition temperature of poly(isocyanatoethyl methacrylate) was found to be 47 °C. From the thermogravimetric analysis of the weight‐loss percentage corresponding to the first wave of the thermogram, it was shown that the degradation mechanism of the IEM/MMA copolymers started from the isocyanate group. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 4762–4768, 2006  相似文献   

5.
Triad cotacticities of alternating copolymers of methyl methacrylate with styrene prepared in the presence of zinc chloride, ethylaluminium sesquichloride, and ethylboron dichloride are investigated from the mechanistic point of view by means of 1H- and 13C-NMR. The cotacticities from 1H-NMR spectra are obtained accurately by using α-d-styrene in the place of styrene and by measuring the spectra on the copolymer in o-dichlorobenzene at 170°C. The relative intensities of three peaks of the splitting signal for the methoxy protons in the nonalternating copolymers obtained by the use of benzoyl peroxide in the absence of metal halides agree well with the cotacticity distribution calculated theoretically by the Lewis-Mayo mechanism with the stereoregulation following Bernoullian statistics. The splitting signals in the 1H- and 13C-NMR spectra of the alternating copolymers prepared in the presence of metal halides cannot be explained by the same mechanism. The relative intensities of three peaks of the splitting signals for the methoxy protons and for the carbonyl carbon in the methyl methacrylate unit (the contents of cotactic triads centered by the methyl methacrylate unit) are not equal to those for the aromatic C1 carbon in the styrene unit (the contents of cotactic triads centered by styrene unit). The value of f2Y - 4fxfz is not equal to zero, where fx, fy, and fz are the cosyndiotactic, coheterotactic, and coisotactic triad contents, respectively, in the alternating copolymer. Copolymers obtained in the presence of zinc chloride are not exactly equimolar alternating but always contain a methyl methacrylate unit in excess, and the relative intensities of the three peaks for the aromatic C1 carbon change with the copolymer composition. These results are explained by a proposed mechanism: the alternating copolymerization proceeds through the homopolymerization of a ternary molecular complex composed of a metal halide, methyl methacrylate, and styrene, accompanied with the stereoregulation following first-order Markovian statistics; the increase of methyl methacrylate content in the copolymer prepared in the presence of zinc chloride is caused by the participation of the binary molecular complex composed of a metal halide and methyl methacrylate in addition to the ternary molecular complex.  相似文献   

6.
Syndiotactic polystyrene graft copolymers, including syndiotactic-polystyrene-graft-poly(methyl methacrylate) and syndiotactic-polystyrene-graft-atactic-polystyrene, were synthesized by atom transfer radical polymerization (ATRP) using bromoacetylated syndiotactic polystyrene as macroinitiator and copper bromide combined with 2,2′-bipyridine as catalyst. The macroinitiator was prepared from the acid-catalyzed halogenation reaction of partially acetylated syndiotactic polystyrene, which was synthesized in a heterogeneous process with acetyl chloride and anhydrous aluminum chloride in carbon disulfide. The graft copolymers were characterized by 1H- and 13C-NMR spectra.  相似文献   

7.
2-Methacryloxyethyl phenyl phosphate/methyl methacrylate (MEPP/MMA) copolymers were synthesized by the bulk polymerization of MMA in the presence of various amounts of MEPP. MEPP was prepared by the esterification of phenyl dichlorophosphate with 2-hydroxyethyl methacrylate, followed by hydrolysis. Structural and compositional details of MEPP were obtained by Fourier transform infrared spectroscopy, 1H nuclear magnetic resonance, 13C nuclear magnetic resonance, 31P nuclear magnetic resonance, and mass spectrometer, as well as by elemental analysis. The monomer reactivity ratios of MEPP/MMA system were calculated by the methods of Fineman-Ross, Kelen-Tüdös, and Joshi-Joshi. The thermal degradation temperature of the MEPP/MMA copolymers was considerably enhanced by only a slight decrease in Tg, as determined by differential scanning calorimetry and thermogravimetric analysis experiments. The fire-retardant properties of MEPP/MMA copolymers were also studied by LOI and UL-94 tests, indicating that an MEPP/MMA copolymer with only 2.17 wt% phosphorus can effectively inhibit burning.  相似文献   

8.
Plasma-polymerized methyl methacrylate (PPMMA) film was produced by a radio-frequency glow discharge of methyl methacrylate (MMA) gas with argon. PPMMA deposited under a plasma of mild energy was separated into a soluble fraction (sol-PPMMA) and an insoluble matrix (insol-PPMMA), which is highly crosslinked, by solvent-extraction and filtration. The chemical structure of the sol-PPMMA was determined by pyrolysis/gas chromatography, IR spectroscopy, 1H-NMR, 13C-NMR, and elemental analysis techniques. On the other hand, the structure of the insol-PPMMA was examined with IR spectroscopy, 13C-NMR with CP/MAS method, and elemental analysis. The crosslinking mechanism in the plasma polymerization of MMA is discussed on the basis of product analyses of the sol-PPMMA and the insol-PPMMA.  相似文献   

9.
Copolymers of methyl methacrylate (MMA) with 2,3,5,6‐tetrafluorophenyl methacrylate (TFPMA), pentafluorophenyl methacrylate (PFPMA), and 4‐trifluoromethyl‐2,3,5,6‐tetrafluorophenyl methacrylate (TFMPMA) were investigated. All the three systems showed a random copolymerization character. The composition, glass transition temperature (Tg), and refractive index of the copolymers obtained were studied. Tgs of TFPMA/MMA and PFPMA/MMA copolymers were found to deviate positively from the Gordon–Taylor equation. However, Tgs of TFMPMA/MMA copolymers were well fit with the Gordon–Taylor equation. These results indicated the existence of interaction between MMA and either TFPMA or PFPMA units in copolymers. This interaction resulted in the enhancement of the Tg of MMA polymers through the copolymerization with TFPMA and PFPMA. The refractive index and the light transmittance of copolymers were close to those of PMMA. Copyright © 2007 John Wiley & Sons, Ltd.  相似文献   

10.
The methacrylate monomer, 2-[(5-methylisoxazol-3-yl)amino]-2-oxo-ethyl methacrylate (IAOEMA), was synthesized by reacting 2-chloro-N-(5-methylisoxazol)acetamide dissolved in acetonitrile with sodium methacrylate in the presence of triethylbenzylammoniumchloride (TEBAC). The free-radical-initiated copolymerization of IAOEMA, with styrene (ST) and methyl methacrylate (MMA) was carried out in dimethylsulphoxide (DMSO) solution at 65 °C using 2,2-azobisisobutyronitrile (AIBN) as an initiator with different monomer-to-monomer ratios in the feed. The monomer (IAOEMA) and copolymers were characterized by FTIR, 1H- and 13C-NMR spectral studies. The copolymer composition was evaluated by nitrogen content in polymers led to the determination of reactivity ratios. The reactivity ratios of the monomers were determined by the application of Fineman-Ross and Kelen-Tüdös methods. The analysis of reactivity ratios revealed that ST and MMA are more reactive than IAOEMA, and copolymers formed are statisticalle in nature. The molecular weights (Mw and Mn) and polydispersity index of the polymers were determined using gel permeation chromagtography. Glass transition temperatures of the copolymers were found to increase with an increase in the mole fraction of IAOEMA in the copolymers. The apparent thermal decomposition activation energies (Ed) were calculated by Ozawa method using the SETARAM Labsys TGA thermobalance.  相似文献   

11.
Well-defined AB(BA), ABA, and BAB block copolymers of tert-butyl methacrylate (tBMA) (A) and ethylene oxide (EO) (B) have been prepared by sequential living anionic polymerization of the two comonomers, irrespective of their addition order. Diphenyl methyl potassium and naphthalene potassium have been successfully used as mono- and difunctional initiators, respectively. In all cases, molecular weight and composition of the block copolymers can be predicted on the basis of the monomer over initiator molar ratio, and the molecular weight distribution is relatively narrow. Size exclusion chromatography, selective extractions of homopolymers, and 1H- and 13C-NMR spectroscopy support that block copolymerization proceeds without homopolymer formation nor side reactions, e.g., transesterification reactions. The PtBMA blocks have been quantitatively hydrolyzed into polyacid ones with formation of polyacid-b-polyether block copolymers as supported by titration, 1H-NMR, and IR analysis. © 1992 John Wiley & Sons, Inc.  相似文献   

12.
A new monomer, 2-methylene-7-oxabicyclo[2.2.1]heptane ( IV ) was synthesized via four steps. Its structure was confirmed by IR, 1H-NMR, and 13C-NMR spectra as well as elementary analysis. Free radical polymerization and copolymerization of IV were investigated. No homopolymer was obtained due to the effect of allyl inhibition. When IV copolymerized with electron-donor monomers, such as vinyl acetate and stvrene, IV acted as inhibitor for the polymerization of vinyl acetate, but could not inhibit the polymerization of styrene. However, the copolymers of IV with electron-accepting monomers, such as methyl methacrylate, acrylonitrile, or maleic anhydride (MA) were obtained. The contents of IV in the copolymers increased as e values of electron-accepting monomers increased. Strictly alternating copolymer was obtained only in the case of MA and IV . The thermal properties of copolymers were investigated. © 1995 John Wiley & Sons, Inc.  相似文献   

13.
The acrylonitrile/methyl methacrylate copolymers of different monomer concentration were prepared by photo polymerization using uranyl ion as initiator. The carbon 13 and proton spectra of these copolymers are overlapping and complex. The complete spectral assignment of the 13C- and 1H-NMR spectra were done with the help of Distortionless Enhancement by Polarization Transfer (DEPT) and two dimensional 13C–1H Heteronuclear Single Quantum Correlation (HSQC) experiments. The methylene, methine and the methyl carbon resonances show both stereochemical (triad level) and compositional (dyad, triad, tetrad, pentad and hexad level) sensitivity. 2D Double Quantum Filtered Correlated Spectroscopy (DQFCOSY) experiment was used to ascertain the various geminal couplings between the methylene protons. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 1081–1092, 1998  相似文献   

14.
A new methacrylate monomer 2-(4-nitrophenyl)-2-oxoethyl-2-methacrylate (NFM) was synthesized and its radical copolymerization with glycidyl methacrylate (GMA) was studied in 1,4-dioxane solution at 65°C using 2,2′-azobisisobutyronitrile as an initiator. The synthesized monomer and copolymers were characterized by FTIR, 1H and 13C-NMR spectroscopy. The analysis of reactivity ratios revealed that NFM is less reactive than GMA, and copolymers formed are statistically in nature. Thermogravimetric analysis of the polymers reveals that the thermal stability of the copolymers increases with an increasing in the mole fraction of NFM in the copolymers. Glass transition temperatures of the copolymers decreased with an increasing of NFM molar fraction in copolymers. In addition, according to the results obtained from the contact angle and zeta potential measurements the hydrophobic character of the polymer decreases (it means surface free energy increases) and its zeta potential becomes more negative with increase of NFM ratio in the copolymer. Polymers with carbonyl functional groups have been particularly interesting because of their use as photoresists.  相似文献   

15.
Copolymers containing N-vinylcarbazole (V) and butyl methacrylate (B) units of different compositions were synthesized and their compositions were determined from quantitative 13C{1H} NMR spectroscopy. The reactivity ratios of the comonomers were estimated using the Kelen-Tudos and non-linear error in variable methods. The complete spectral assignment in terms of compositional and configurational sequences of the overlapping 1H and 13C{1H} spectra of the copolymers were done with the help of distortionless enhancement by polarization transfer, 2D heteronuclear single quantum correlation and total correlated spectroscopy experiments.  相似文献   

16.
By the use of various metal halides methyl methacrylate and styrene were copolymerized to produce equimolar alternating sequences and different cotacticities. The 13C-NMR spectra of these copolymers were simple in comparison to those of random copolymers because of the fixed monomer sequence which yielded sharply split triplets for carbonyl, methoxy, and quaternary carbons. The relative intensities in these split peaks varied according to the metal halide used. A comparison of the intensities made it possible to obtain clear-cut and quantitative information on the methyl methacrylate-centered triad cotacticity of the copolymers. The spectral assignment with respect to the methoxy carbon was definitely justified by the combined use of partly relaxed Fourier transform and selective decoupling techniques. The spectrum of aromatic C1 carbon in styrene units also split into three main peaks. From their relative intensities the splitting was attributed to styrene-centered triad cotacticity. The assignment of this carbon was compared with two other assignments made for random copolymers of methyl methacrylate with styrene; they were contradictory, however. Furthermore, an apparent discrepancy was observed between methyl methacrylate-and styrene-centered tactic triads of these alternating copolymers. The origin of this discrepancy suggests a close relationship with the copolymerization mechanism.  相似文献   

17.
Pure isotactic and enriched syndiotactic poly(tributyltin methacrylate) were synthesized by the reaction of the respective poly(methacrylic acid) with tributyltin oxide. The heterotactic polymer was prepared in a similar manner and from free radical initiated (AIBN or BPO) polymerization of tributyltin methacrylate. In each case, polymer configuration was confirmed by 1H-NMR of the hydrolyzed/esterfied product. The relatively large 119Sn-NMR linewidth of the isotactic tributyltin containing polymer suggests an intra-molecular exchange of the pendant tin groups. Tg, Td, and M v data are also reported. Poly(tributyltinmethacrylate-co-styrene) was prepared by free radical polymerization and reactivity ratios [r(styrene) = 0.51, r(TBTM) = 0.49] and Q-e values for TBTM (0.78, 0.38) were determined.  相似文献   

18.
Atom transfer radical polymerization conditions with copper(I) bromide/2,2-bipyridine (Cu/2,2-bpy) as the catalyst system were employed for the homopolymerization and random copolymerization of 1-phenoxycarbonyl ethyl methacrylate (PCMA) with methyl methacrylate (MMA). Temperature studies indicated that the polymerizations occurred smoothly in bulk at 110 °C. Poly(PCMA)(polydispersity index=1.27) homopolymer was characterized and then used as macroinitiator for increasing its molecular weight. The homopolymerization of PCMA was also carried out under free radical conditions using 2,2-azobisisobutyronitrile as an initiator.The monomer and polymers were characterized by FT-IR and 1H and 13C-NMR techniques. The glass transition temperatures, the solubility parameters and average-molecular weights of the polymers were determined. Thermal stabilities of the polymers were given as compared with each other by using TGA curves. Thermal degradation products of poly(PCMA)s obtained by ATRP and free radical polymerization were compared with each other by using 1H-NMR technique.  相似文献   

19.
Copolymerization of acrylonitrile and ethyl methacrylate using atom transfer radical polymerization (ATRP) at ambient temperature was carried out under optimized reaction conditions using 2‐bromopropionitrile as initiator and CuBr/2,2′‐bipyridine as the catalyst system. The copolymer composition, obtained from 1H NMR spectra, were used to determine the monomer reactivity ratios (rA = 0.68 and rE = 1.75) involved in ATRP. Two‐dimensional NMR (heteronuclear single quantum correlation and total correlated spectroscopy) experiments were employed to resolve the highly overlapping and complex 1H and 13C{1H} NMR spectra of copolymers. The complete spectral assignments of the quaternary carbons viz. carbonyl and nitrile carbons were done with the help of heteronuclear multiple bond correlation spectra. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 2955–2971, 2006  相似文献   

20.
Copolymers of 2-ethylacrylic acid (EAA) and methacrylic acid (MAA) were prepared in bulk and in N,N-dimethylformamide (DMF). Although precipitation of the copolymers was observed in bulk, the reaction mixtures remained apparently homogeneous in DMF. Best-fit terminal-model reactivity ratios were determined by a nonlinear least squares technique to be rMAA = 1.14 and rEAA = 0.23 in bulk, and rMAA = 1.91 and rEAA = 0.09 in 50% DMF solution. Examination of 13C-NMR spectra provided convincing evidence for the formation of statistical copolymers. Copolymerizations richer in MAA provided copolymers of higher molecular weights.  相似文献   

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