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2.
B. Prathab T. M. Aminabhavi R. Parthasarathi V. Subramanian 《Theoretical chemistry accounts》2007,117(1):167-169
Molecular dynamics simulations have been carried out on different perfluoroalkyl methacrylates to predict their densities. Density calculations on selected perfluoroalkyl methacrylates have been performed using molecular dynamics in the NPT ensemble by employing COMPASS force field. The calculated density values compared quite well with the experimental data reported in the literature. 相似文献
3.
D. M. Petrović-Djakov J. M. Filipović Lj. P. Vrhovac J. S. Veličković 《Journal of Thermal Analysis and Calorimetry》1996,46(6):1681-1686
The kinetics of the AIBN-initiated free radical bulk polymerization of fiveo-alkylphenyl methacrylates was studied by means of DSC in the temperature range 353–373 K, and the enthalpy of polymerization, the overall reaction rate constant and the activation energy were determined. The results were compared with those published recently on correspondingp-alkylaryl methacrylates. All measured reaction rate constants were found to increase with increasing temperature and to decrease with increasingo-alkyl substituent mass and size. It was shown thato-substituents influence the rates of polymerization to a greater extent thanp-substituents. At about 373 K, all differences in rate, most probably resulting from steric hindrance caused by the alkyl groups, disappear in both series, a phenomenon earlier observed for dimethyl phenyl methacrylates.This work was supported by the Ministry of Science of the Republic of Serbia. 相似文献
4.
Duygu Avci Selim H. Kseflu Robert D. Thompson Lon J. Mathias 《Journal of polymer science. Part A, Polymer chemistry》1994,32(15):2937-2945
New ester derivatives of ethyl α-hydroxymethylacrylate were synthesized using acid chlorides (traditional solution reactions), sodium salts of acids (with phase transfer catalysis), and trifluoroacetic anhydride (trifluoroacetate). The interfacial process gave high yields of clean products under very mild conditions. Derivatives obtained include the formate, acetate, hexanoate, stearate, benzoate, trifluoroacetate, and adamantanoate. Bulk polymerizations with 2,2′-azobis (isobutyronitrile) gave high molecular weight polymers with intrinsic viscosities of over 2 dL/g and molecular weights of several million [based on size-exclusion chromatography (SEC) comparison to polystyrene standards]. These high molecular weights were the result of autoacceleration in the bulk as shown by monitoring molecular weight with respect to conversion. Solution polymerization in benzene gave more typical polymer, e.g., the acetate derivative showed an SEC molecular weight of 52,000. Glass transition temperatures for the n-alkyl esters decreased from the formate (77°C) to the hexanoate (15°C); the stearate showed a side-chain melting point of 40°C but no Tg. Glass transitions were observed for the trifluoroacetate, benzoate, and adamantanoate polymers at 69, 130, and 214°C, respectively. Solution 13C-NMR showed evidence of tacticity information for the formate and acetate derivatives with appaent preference for syndiotactic polymer formation similar to that of methyl methacrylate. FTIR and solid-state 13C-NMR analysis gave spectra with functional group peaks and chemical shift values expected based on composition. The stearate monomer and polymer gave solid-state 13C chemical shifts of 34 and 33 ppm, respectively, for the central CH2 units consistent with monoclinic and orthorhombic crystal packing. © 1994 John Wiley & Sons, Inc. 相似文献
5.
Guillermina Burillo Takeshi Ogawa Jimmy S. Hwang 《Journal of polymer science. Part A, Polymer chemistry》1992,30(10):2159-2164
A number of diacetylene containing acrylate and methacrylates have been synthesized and the interaction between their propagating radicals and the diacetylene groups was studied by ESR spectroscopy. In the case of polymerization at 70°C using AIBN as an initiator, the propagating radicals of methacrylates are temporarily trapped with the diacetylenes with rapid exchange of the electron, thus showing strong signals of the propagating radicals. Gamma irradiation of the frozen state produces a blue color in samples, and the ESR signals were found to be those of uninteracted acrylate and methacrylates. From a comparison of spectral widths, there seems to exist an intramolecular interaction between the radicals and the diacetylene group at the frozen state. © 1992 John Wiley & Sons, Inc. 相似文献
6.
S. D. Smith T. E. Long J. E. Mcgrath 《Journal of polymer science. Part A, Polymer chemistry》1994,32(9):1747-1753
The thermal stabilities of various poly(alkyl methacrylate) homopolymers and poly(methyl methacrylate-g-dimethyl siloxane) (PMMA-g-PSX) graft copolymers have been determined by thermogravimetric analysis (TGA). As expected, the thermal stabilities of poly(alkyl methacrylates) were a function of the ester alkyl group, and polymerization mechanism. In particular, thermally labile linkages, which result from termination during free radical or nonliving polymerization mechanisms, decrease the ultimate thermal stabilities of the polymers. However, graft copolymers, which were prepared by the macromonomer technique with free radical initiators, exhibited enhanced thermal stability compared to homopolymer controls. A more complex free radical polymerization mechanism for the macromonomer modified polymerization may account for this result. © 1994 John Wiley & Sons, Inc. 相似文献
7.
Farnesene (Far) is a bio‐based terpene monomer that is similar in structure to commercially used dienes like butadiene and isoprene. Nitroxide‐mediated polymerization (NMP) is adept for the polymerization of dienes, but not particularly effective at controlling the polymerization of methacrylates using commercial nitroxides. In this study, Far is statistically copolymerized with a functional methacrylate, glycidyl methacrylate (GMA), by NMP using N‐succinimidyl modified commercial BlocBuilder (NHS‐BB) initiator. Reactivity ratios are determined to be r Far = 0.54 ± 0.04 and r GMA = 0.24 ± 0.02. The ability of the poly(Far‐stat‐GMA) chains to reinitiate for chain extension with styrene showed a clear shift in molecular weight and monomodal distribution. Copolymerizations using a new alkoxyamine, Dispolreg 007 (D7), is explored as it is shown to homopolymerize methacrylates, but not yet reported for statistical copolymerizations. Bimodal molecular weight distributions are observed when an equimolar ratio of Far and GMA is copolymerized with D7 due to slow decomposition of the initiator, but chain ends are active as shown by successful chain extension with styrene. Both NHS‐BB and D7 initiators are used to synthesize poly[Far‐b‐(GMA‐stat‐Far)] and poly(Far‐b‐GMA) diblock copolymers. While the NHS‐BB initiated polymer chains have lower dispersity, D7 exhibits more linear polymerization kinetics and maintains more active chain ends. 相似文献
8.
Copolymers of pentafluorophenylhexafluoroisopropyl methacrylate (FPPMA) with trifluoroethyl methacrylate (TFEMA) were prepared in THF solution and in bulk using azobisisobutyronitrile as a free radical initiator. The monomer reactivity ratios of TFEMA (M1) and FPPMA (M2) were calculated as r1 = 0.55 and r2 = 0.07. The refractive indices of poly(TFEMA) and poly(FPPMA) are very similar as 1.435 and 1.430, respectively, at 532 nm, and the copolymer films were transparent. The glass transition temperatures (Tg) of the copolymers were in the range of 80–90°C and showed a negative deviation from the Gordon–Taylor equation. The thermal decomposition temperature (Td) was increased with the content of FPPMA in copolymers. Low water absorption for 1:1 FPPMA/TFEMA copolymer was detected. Copolymers of FPPMA with hexafluoroisopropyl methacrylate (HFPMA) were also prepared. The monomer reactivity ratios of HFPMA (M1) and FPPMA (M2) were calculated as r1 = 0.43 and r2 = 0.10. The Tgs of the copolymers were in the range of 88–95°C and showed also a negative deviation from the Gordon–Taylor equation. Tg and Td of the copolymers were increased with the content of FPPMA. The refractive index of poly(HFPMA) (1.384 at 532 nm) is much lower than that of FPPMA homopolymer, but copolymer films obtained were clear and transparent. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
9.
Duygu Avci Lon J. Mathias Kevin Thigpen 《Journal of polymer science. Part A, Polymer chemistry》1996,34(15):3191-3201
Several new benzoate ester derivatives of ethyl α-hydroxymethylacrylate were synthesized using phase transfer catalysis and found to display unexpectedly rapid photopolymerization; i.e., from 2 to 8 times faster than MMA. New derivatives described here include the 4-fluoro-, 4-trifluoromethyl-, 4-methyl-, 2-hydroxy-, 4-nitro-, 4-methoxy-, 4-cyano-, and 3,4,5-trimethoxybenzoate esters along with the parent benzoate ester. Relative reactivities of these monomers in photopolymerizations were compared with those of the nonaromatic formate, acetate, hexanoate, and stearate derivatives. Reactivities of the nonaromatic ester derivatives increased with the length of the side chain while for the more reactive aromatic esters, rates increased in the order 4-methyl-, 4-fluoro- and benzoate < 4-trifluoromethyl- and 2-hydroxy- < 4-cyano- < 4-methoxy- < 3,4,5-trimethoxybenzoate. Tgs of the benzoate polymers ranged from 125°C for the 4-fluoro to 163°C for the 4-cyanobenzoate while those of the alkyl ester derivatives ranged from 15 to 78°C. Number average molecular weights of photoinitiated polymers (ca 10,000–20,000) were lower than those found for bulk and solution polymers (20,000—708,000) consistent with higher radical concentrations from photoinitiation. These materials greatly expand the number of candidates available for rapid photocure in thin film and coating applications, especially because their physical properties are those of linear rather than highly crosslinked structures formed from multifunctional systems. © 1996 John Wiley & Sons, Inc. 相似文献
10.
Angelika Macior Izabela Zaborniak Pawe Chmielarz Joanna Smenda Karol Wolski Ewa Ciszkowicz Katarzyna Lecka-Szlachta 《Molecules (Basel, Switzerland)》2022,27(3)
The article presents the modification of ash wood via surface initiated activators regenerated by electron transfer atom transfer radical polymerization mediated by elemental silver (Ag0 SI-ARGET ATRP) at a diminished catalyst concentration. Ash wood is functionalized with poly(methyl methacrylate) (PMMA) and poly(2-(dimethylamino)ethyl methacrylate) (PDMAEMA) to yield wood grafted with PMMA-b-PDMAEMA-Br copolymers with hydrophobic and antibacterial properties. Fourier transform infrared (FT-IR) spectroscopy confirmed the covalent incorporation of functional ATRP initiation sites and polymer chains into the wood structure. The polymerization kinetics was followed by the analysis of the polymer grown in solution from the sacrificial initiator by proton nuclear magnetic resonance (1H NMR) and gel permeation chromatography (GPC). The polymer layer covalently attached to the wood surface was observed by scanning electron microscopy (SEM). The hydrophobic properties of hybrid materials were confirmed by water contact angle measurements. Water and sodium chloride salt aqueous solution uptake tests confirmed a significant improvement in resistance to the absorption of wood samples after modification with polymers. Antibacterial tests revealed that wood-QPDMAEMA-Br, as well as wood-PMMA-b-QPDMAEMA-Br, exhibited higher antibacterial activity against Gram-positive bacteria (Staphylococcus aureus) in comparison with Gram-negative bacteria (Escherichia coli). The paper presents an economic concept with ecological aspects of improving wood properties, which gives great opportunities to use the proposed approach in the production of functional hybrid materials for industry and high quality sports equipment, and in furniture production. 相似文献