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Journal articles on the topic 'Polymers Esters'

Author: Grafiati

Published: 4 June 2021

Last updated: 2 February 2022

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1

Popovic, Ivanka, and Lynne Katsikas. "The thermal degradation of some polymeric di-alkyl esters of itaconic acid." Journal of the Serbian Chemical Society 78, no. 12 (2013): 2179–200. http://dx.doi.org/10.2298/jsc131214154p.

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One group of polymers that may help relieve the dependence on crude oil is based on itaconic acid, the biotechnological production of which has become feasible. Itaconic acid and its derivatives can easily be incorporated into polymers and may serve as a substitute for petrochemically derived acrylate or methacrylate monomers. The applications of polymers based on itaconic di-esters depend largely on their thermal stability. The thermal stability of poly(di-itaconates) is dependent, not only on the general structure of the monomer repeating unit, but also on the structure of the ester substitu

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2

Ryu, Ji Hyun, Gyeong Jin Lee, Yu-Ru V. Shih, Tae-il Kim, and Shyni Varghese. "Phenylboronic Acid-polymers for Biomedical Applications." Current Medicinal Chemistry 26, no. 37 (2019): 6797–816. http://dx.doi.org/10.2174/0929867325666181008144436.

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Background: Phenylboronic acid-polymers (PBA-polymers) have attracted tremendous attention as potential stimuli-responsive materials with applications in drug-delivery depots, scaffolds for tissue engineering, HIV barriers, and biomolecule-detecting/sensing platforms. The unique aspect of PBA-polymers is their interactions with diols, which result in reversible, covalent bond formation. This very nature of reversible bonding between boronic acids and diols has been fundamental to their applications in the biomedical area. Methods: We have searched peer-reviewed articles including reviews from

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3

Dessain, Edison C., and Dennis Anderson. "A Study of the Interaction of Phthalate Esters with Chlorine-Containing Polymers." Applied Spectroscopy 46, no. 1 (1992): 152–55. http://dx.doi.org/10.1366/0003702924444281.

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The infrared spectra of blends of various ortho-phthalate esters with polyvinyl chloride) and vinylidene chloride/(20%)acrylonitrile copolymer were recorded. The data indicate that the lowering of the ester carbonyl absorption frequency is due to a dipole-dipole/complex type interaction between the carbonyl of the ester and the chlorine of the polymer in addition to hydrogen bonding with acidic hydrogens. The lowering of the absorption frequence increases with an increase in the amount of chlorine in the polymer chain.

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4

Fila, Karolina, Beata Podkościelna, and Maciej Podgórski. "Cross-Linked Polythiomethacrylate Esters Based on Naphthalene—Synthesis, Properties and Reprocessing." Materials 13, no. 13 (2020): 3021. http://dx.doi.org/10.3390/ma13133021.

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Two structurally different aromatic dithioesters were synthesized from two dithiols and methacryloyl chloride. The polymer networks based on methyl methacrylate and/or styrene and the new dimethacrylates were subsequently prepared. The polymerization yields of copolymers were in the range of 95–99%. The thermal and mechanical properties of the copolymers were determined by means of differential scanning calorimetry (DSC), thermogravimetric analysis (TG/DTG), and Shore D hardness. The addition of dithioesters—1,5-NAF-S-Met (or 1,4(1,5)-NAF-CH2S-Met) (from 0.5% to 5%) to MMA- or ST-based polymer

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5

Romano, Angelo, Ignazio Roppolo, Elisabeth Rossegger, Sandra Schlögl, and Marco Sangermano. "Recent Trends in Applying Ortho-Nitrobenzyl Esters for the Design of Photo-Responsive Polymer Networks." Materials 13, no. 12 (2020): 2777. http://dx.doi.org/10.3390/ma13122777.

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Polymers with light-responsive groups have gained increased attention in the design of functional materials, as they allow changes in polymers properties, on demand, and simply by light exposure. For the synthesis of polymers and polymer networks with photolabile properties, the introduction o-nitrobenzyl alcohol (o-NB) derivatives as light-responsive chromophores has become a convenient and powerful route. Although o-NB groups were successfully exploited in numerous applications, this review pays particular attention to the studies in which they were included as photo-responsive moieties in t

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6

Fainleib, A. M. "Copolymers and interpenetrating polymer networks of thermoreactive nitrogen-containing resins. Mini review." Polymer journal 42, no. 4 (2020): 245–53. http://dx.doi.org/10.15407/polymerj.42.04.245.

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In a short review the effective methods of optimization of structure and properties of high-performance polymers obtained from thermoreactive nitrogen-containing resins such as benzoxazines, bismaleimides, cyanate esters have been analysed. High crosslinked density copolymer thermosets are synthesized through chemical interactions between reactive functional groups, which belong to the monomers/oligomers used. The different possible processes such as copolymerization or formation of interpenetrating polymer networks are discussed. The high-performance polymers and composites from thermoreactiv

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7

Howell, Bob A., Kendahl L. Oberdorfer, and Eric A. Ostrander. "Phosphorus Flame Retardants for Polymeric Materials from Gallic Acid and Other Naturally Occurring Multihydroxybenzoic Acids." International Journal of Polymer Science 2018 (December 24, 2018): 1–12. http://dx.doi.org/10.1155/2018/7237236.

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The development of polymer and polymer additives from renewable biosources is becoming increasingly prominent. This reflects increasing concerns about sustainability, environmental quality, and human health. Bioproducts produced in nature are generally inexpensive and benign in the environment. Moreover, degradation of derivatives does not yield toxic products. Gallic acid (3,4,5-trihydroxybenzoic acid) is found widely in nature and has long been touted for its medicinal qualities. 3,5-Dihydroxybenzoic acid is also produced by several plants, most notably buckwheat. Both compounds, as the anil

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8

Barde, Mehul, Charles Warren Edmunds, Nicole Labbé, and Maria Lujan Auad. "Fast pyrolysis bio-oil from lignocellulosic biomass for the development of bio-based cyanate esters and cross-linked networks." High Performance Polymers 31, no. 9-10 (2019): 1140–52. http://dx.doi.org/10.1177/0954008319829517.

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Fast pyrolysis of pine wood was carried out to yield a liquid bio-oil mixture that was separated into organic and aqueous phases. The organic phase (ORG-bio-oil) was characterized by gas chromatography–mass spectroscopy, 31P-nuclear magnetic resonance spectroscopy, and Fourier transform infrared (FTIR) spectroscopy. It was further used as a raw material for producing a mixture of biphenolic compounds (ORG-biphenol). ORG-bio-oil, ORG-biphenol, and bisphenol-A were reacted with cyanogen bromide to yield cyanate ester monomers. Cyanate esters were characterized using FTIR spectroscopy and were th

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9

YAMAMOTO, Tohei. "Readical Polymerizations and Polymers ov Vinyl Esters." Kobunshi 45, no. 3 (1996): 132–35. http://dx.doi.org/10.1295/kobunshi.45.132.

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10

Chang, Y., J. Noriyan, D. R. Lloyd, and J. W. Barlow. "Polymer sorbents for phosphorus esters: I. Selection of polymers by analog calorimetry." Polymer Engineering and Science 27, no. 10 (1987): 693–702. http://dx.doi.org/10.1002/pen.760271002.

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11

KONDO, TSUNEO, KAZUHIKO MIZUNO, and TADASHI KATO. "CELL WALL-BOUND p-COUMARIC AND FERULIC ACIDS IN ITALIAN RYEGRASS." Canadian Journal of Plant Science 70, no. 2 (1990): 495–99. http://dx.doi.org/10.4141/cjps90-058.

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Cell wall-bound p-coumaric and ferulic acids were determined for stems of Italian ryegrass (Lolium multiflorum Lam.) sampled at different stages of growth. The greater part of the detected p-coumaric acid was linked to cell wall polymers through ester linkages. No definite relationship was found between the accumulation of p-coumaric acid esters and plant maturation. Some part of the detected ferulic acid was simultaneously esterified and etherified to cell wall polymers. Such ester- and ether-linked ferulic acid augmented with increasing maturity, suggesting that the number of ferulic acid cr

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12

Soydan, Ali Murat, and Recep Akdeniz. "Polymer Electrolytes Based on Borane/Poly(ethylene glycol) Methyl Ether for Lithium Batteries." Journal of Chemistry 2017 (2017): 1–6. http://dx.doi.org/10.1155/2017/4839410.

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This work presents a different approach to preparing polymer electrolytes having borate ester groups for lithium ion batteries. The polymers were synthesized by reaction between poly(ethylene glycol) methyl ether (PEGME) and BH3-THF complex. Molecular weight of PEGMEs was changed with different chain lengths. Then the polymer electrolytes comprising boron were prepared by doping of the matrices with CF3SO3Li at various molar ratios with respect to EO to Li and they are abbreviated as PEGMEX-B-Y. The identification of the PEGME-borate esters was carried out by FTIR and 1H NMR spectroscopy. Ther

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13

Buchanan, Charles M., Norma L. Buchanan, John S. Debenham, et al. "Preparation and characterization of arabinoxylan esters and arabinoxylan ester/cellulose ester polymer blends." Carbohydrate Polymers 52, no. 4 (2003): 345–57. http://dx.doi.org/10.1016/s0144-8617(02)00290-4.

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14

Pujari, N. S., J. Trivedi, G. C. Ingavle, and S. Ponrathnam. "Novel beaded polymers from telechelic methacrylic ether esters." Reactive and Functional Polymers 66, no. 10 (2006): 1087–96. http://dx.doi.org/10.1016/j.reactfunctpolym.2006.01.020.

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15

Ioelovich, Michael. "Adjustment of Hydrophobic Properties of Cellulose Materials." Polymers 13, no. 8 (2021): 1241. http://dx.doi.org/10.3390/polym13081241.

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In this study, physicochemical and chemical methods of cellulose modification were used to increase the hydrophobicity of this natural semicrystalline biopolymer. It has been shown that acid hydrolysis of the initial cellulose increases its crystallinity, which improves hydrophobicity, but only to a small extent. A more significant hydrophobization effect was observed after chemical modification by esterification, when polar hydroxyl groups of cellulose were replaced by non-polar substituents. The esterification process was accompanied by the disruption of the crystalline structure of cellulos

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16

Cuthbert, Julia, Saigopalakrishna S. Yerneni, Mingkang Sun, Travis Fu, and Krzysztof Matyjaszewski. "Degradable Polymer Stars Based on Tannic Acid Cores by ATRP." Polymers 11, no. 5 (2019): 752. http://dx.doi.org/10.3390/polym11050752.

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Degradable polymers are crucial in order to reduce plastic environmental pollution and waste accumulation. In this paper, a natural product, tannic acid was modified to be used as a polymer star core. The tannic acid was modified with atom transfer radical polymerization (ATRP) initiators and characterized by 1H NMR, FT-IR, and XPS. Twenty-five arm polymer stars were prepared by photoinduced ATRP of poly(methyl methacrylate) (PMMA) or poly(oligo(ethylene oxide) methacrylate) (molar mass Mw = 300 g/mol) (P(OEO300MA)). The polymer stars were degraded by cleaving the polymer star arms attached to

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17

Fox, S. Carter, and Kevin J. Edgar. "Synthesis of regioselectively brominated cellulose esters and 6-cyano-6-deoxycellulose esters." Cellulose 18, no. 5 (2011): 1305–14. http://dx.doi.org/10.1007/s10570-011-9574-3.

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18

Ding, Jian Jun, Wen Yan Zhao, Hong Yan Guan, Xuan Li, and Yi Fei Mei. "Composition Analysis of an Unknown Redispersible Powder." Key Engineering Materials 726 (January 2017): 55–59. http://dx.doi.org/10.4028/www.scientific.net/kem.726.55.

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As an important type of additive, the redispersible powder is widely applied in cement-based and gyp-based materials, so as to improve the cementing strength, impermeability, workability, hydrophobicity and so on. However, the chemical composition of the redispersible powders determines its applicability, as well as the degree of improvement to the matrix materials. In this paper, the chemical composition of an unknown redispersible powder was analyzed by several instruments. Firstly, Fourier transform infrared spectroscopy (FTIR) analysis indicated that the polymer was polymerized with monome

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19

Minei, Pierpaolo, Giuseppe Iasilli, Giacomo Ruggeri, and Andrea Pucci. "Luminescent Solar Concentrators from Waterborne Polymer Coatings." Coatings 10, no. 7 (2020): 655. http://dx.doi.org/10.3390/coatings10070655.

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This study reports for the first time the use of waterborne polymers as host matrices for luminescent solar concentrators (LSCs). Notably, three types of waterborne polymer dispersions based either on acrylic acid esters and styrene (Polidisp® 7602), acrylic and methacrylic acid esters (Polidisp® 7788) or aliphatic polyester-based polyurethane (Tecfin P40) were selected as amorphous coatings over glass substrates. Water soluble Basic Yellow 40 (BY40) and Disperse Red 277 (DR277) were utilized as fluorophores and the derived thin polymer films (100 μm) were found homogeneous within the dye rang

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20

Yu, Haoyang, Shaohui Lin, Daniel Sun, and Qinmin Pan. "Synthesis of norbornene derivatives and their polymers via ROMP of norbornene derivatives." High Performance Polymers 32, no. 6 (2020): 729–37. http://dx.doi.org/10.1177/0954008319900536.

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Dicyclopentadiene (DCPD) is a by-product resulting from the ethylene industry, which is high yield and underused in China. A technical route of producing valuable products—norbornene derivatives and their polymers from DCPD—was proposed and studied in this research. 5-Norbornene-2,3-dicarboxylic anhydride, a downstream product of DCPD, was employed as starting material to synthesize norbornene derivatives. Norbornene derivatives, 5-norbornene-2,3-dicarboxylic acid dimethyl ester and 5-norbornene-2,3-dicarboxylic acid diphenylethyl esters, as well as their polymers have broad application prospe

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21

Iqbal, Muhammad, Remco Knigge, Hero Heeres, Antonius Broekhuis, and Francesco Picchioni. "Diels–Alder-Crosslinked Polymers Derived from Jatropha Oil." Polymers 10, no. 10 (2018): 1177. http://dx.doi.org/10.3390/polym10101177.

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Methyl oleate, methyl linoleate, and jatropha oil were fully epoxidized using in situ-generated performic acid. The epoxidized compounds were further reacted with furfurylamine in a solvent-free reaction to obtain furan-functionalized fatty esters which, then, functioned as oligomers for a network preparation. Thermoreversible crosslinking was obtained through a (retro) Diels–Alder reaction with bismaleimide, resulting in the formation of a brittle network for furan-functionalized methyl linoleate and jatropha oil. The furan-functionalized fatty esters were mixed with alternating (1,4)-polyket

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22

WANG, Jiang-feng, Ying LU, Jing-bin HUANG, Hao ZOU, He ZHANG та Yan-qiang ZHONG. "Polymers poly(β-amino esters) nanoparticles for gene delivery". Academic Journal of Second Military Medical University 31, № 5 (2011): 473–76. http://dx.doi.org/10.3724/sp.j.1008.2011.00473.

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23

Gangadhara and Kaushal Kishore. "Novel photocrosslinkable liquid-crystalline polymers: poly[bis(benzylidene)] esters." Macromolecules 26, no. 12 (1993): 2995–3003. http://dx.doi.org/10.1021/ma00064a001.

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24

Shaban, H., M. A. Al-Sarawi, A. Behbehane, and J. Mathew. "Thermotropic polymers: synthesis and kinetic analysis of homopoly(esters)." European Polymer Journal 37, no. 6 (2001): 1115–21. http://dx.doi.org/10.1016/s0014-3057(00)00222-6.

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25

Roth, Peter J., Kerstin T. Wiss, Rudolf Zentel, and Patrick Theato. "Synthesis of Reactive Telechelic Polymers Based on Pentafluorophenyl Esters." Macromolecules 41, no. 22 (2008): 8513–19. http://dx.doi.org/10.1021/ma801681b.

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26

Andrzejewska, Ewa, Peter Kusch, and Maciej Andrzejewski. "Thermal decomposition of crosslinked polymers of some dimethacrylate esters." Polymer Degradation and Stability 40, no. 1 (1993): 27–30. http://dx.doi.org/10.1016/0141-3910(93)90186-m.

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27

Salomon, G., C. J. Schooneveldt-van der Kloes, and J. H. L. Zwiers. "Infrared spectra of some methacrylic esters and their polymers." Recueil des Travaux Chimiques des Pays-Bas 79, no. 3 (2010): 313–29. http://dx.doi.org/10.1002/recl.19600790311.

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28

Mbiada, A. A. Younyia, S. Musa, O. Richter, A. Kneer, and S. Barbe. "Controlling Surface Hydrophobicity of Cellulose-Lignin Composite Coatings." Polymers from Renewable Resources 9, no. 2 (2018): 51–58. http://dx.doi.org/10.1177/204124791800900201.

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In the first part of this study, lignin esters were prepared by acylating lignin with organic acid anhydrides containing short saturated chains of various lengths (C2 to C4). The prepared esters were then mixed at different ratios with cellulose acetate in order to produce hydrophilic cellulose-lignin composite coatings. The impact of the chain length and the ratio of lignin ester on the surface hydrophobicity of the coatings were determined by measuring contact angles with deionized water. The second part of this contribution was dedicated to the development of hydrophobic cellulose-lignin co

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29

Wang, Danrong, Defa Hou, Zhiwei Chen, Hanbing Ma, Chundi Huang, and Lu Yang. "Effects of trace phenolic hydroxyl groups on the cure behaviours and properties of cyanate esters." High Performance Polymers 32, no. 7 (2020): 775–83. http://dx.doi.org/10.1177/0954008319900787.

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To improve the curing properties of cyanate esters and retain their heat resistance, dielectric properties and adhesion properties, modified cyanate copolymers were prepared by blending bisphenol A cyanate (BADCy) ester with phenol, hydroquinone (HO), resorcinol and phloroglucinol (LO). Differential scanning calorimetry analysis (DSC) and Fourier transform infrared spectroscopy were used to investigate the cure behaviours of the prepared compounds. The prepared materials were compared with the BADCy ester containing trace of cobalt acetylacetonate (CoAt). The CoAt/BADCy blend modified by HO ex

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30

Nakayama, Yuushou, Kazumasa Watanabe, Ryo Tanaka та ін. "Synthesis, Properties, and Biodegradation of Sequential Poly(Ester Amide)s Containing γ-Aminobutyric Acid". International Journal of Molecular Sciences 21, № 10 (2020): 3674. http://dx.doi.org/10.3390/ijms21103674.

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Poly(ester amide)s are attracting attention because they potentially have excellent thermal and mechanical properties as well as biodegradability. In this study, we synthesized a series of novel poly(ester amide)s by introducing γ-aminobutyric acid (GABA) regularly into polyesters, and investigated their properties and biodegradabilities. GABA is the monomer unit of biodegradable polyamide 4 (PA4). The new poly(ester amide)s were synthesized from the reaction of ammonium tosylate derivatives of alkylene bis(γ-aminobutylate) and p-nitrophenyl esters of dicarboxylic acids. All the obtained polym

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31

Didier, Benoit, Mark F. Mohamed, Elizabeth Csaszar, Kate G. Colizza, Alexei A. Neverov, and R. Stan Brown. "Methanolysis of organophosphorus esters promoted by an M2+ catalyst supported on polystyrene-based copolymers." Canadian Journal of Chemistry 86, no. 2 (2008): 91–100. http://dx.doi.org/10.1139/v07-099.

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The methanolysis of three neutral organophosphorus esters (a phosphonate, a phosphonothioate, and a phosphorothionate) promoted by several polymer-supported Zn(II) or Cu(II) containing catalysts was studied. The catalysts consist of a Zn(II) or Cu(II) complex with 1,5,9-triazacyclododecane or phenanthroline attached to a porous polystyrene resin. In each case, the polymer supported catalyst showed activity at near neutral sspH in methanol (8.38) and ambient temperature and provided accelerations of up to a factor of 2.9 × 106 relative to the background reaction at sspH 9.05. The solid material

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32

Meijs, Gordon F., and Ezio Rizzardo. "Thiohydroxamic esters." Polymer Bulletin 26, no. 3 (1991): 291–95. http://dx.doi.org/10.1007/bf00587972.

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33

DAWSON, A. M., and A. JOHNSON. "The Chemistry of Esters of Leuco Vat Dyes VI-The Supposed Production of Semiquinone Esters." Journal of the Society of Dyers and Colourists 82, no. 2 (2008): 49–53. http://dx.doi.org/10.1111/j.1478-4408.1966.tb02697.x.

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van Nuland, Youri M., Gerrit Eggink та Ruud A. Weusthuis. "Application of AlkBGT and AlkL from Pseudomonas putida GPo1 for Selective Alkyl Ester ω-Oxyfunctionalization in Escherichia coli". Applied and Environmental Microbiology 82, № 13 (2016): 3801–7. http://dx.doi.org/10.1128/aem.00822-16.

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ABSTRACTThe enzyme system AlkBGT fromPseudomonas putidaGPo1 can efficiently ω-functionalize fatty acid methyl esters. Outer membrane protein AlkL boosts this ω-functionalization. In this report, it is shown that whole cells ofEscherichia coliexpressing the AlkBGT system can also ω-oxidize ethyl nonanoate (NAEE). Coexpression of AlkBGT and AlkL resulted in 1.7-fold-higher ω-oxidation activity on NAEE. With this strain, initial activity on NAEE was 70 U/g (dry weight) of cells (gcdw), 67% of the initial activity on methyl nonanoate. In time-lapse conversions with 5 mM NAEE the main product was 9

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35

Zhang, Chao, Meng Li, Hai-Yan Lu, and Chuan-Feng Chen. "Synthesis, chiroptical properties, and self-assembled nanoparticles of chiral conjugated polymers based on optically stable helical aromatic esters." RSC Advances 8, no. 2 (2018): 1014–21. http://dx.doi.org/10.1039/c7ra12652b.

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Buchanan, Charles M., Debra D. Dorschel, Robert M. Gardner, Ron J. Komarek, and Alan W. White. "Biodegradation of Cellulose Esters: Composting of Cellulose Ester-Diluent Mixtures." Journal of Macromolecular Science, Part A 32, no. 4 (1995): 683–97. http://dx.doi.org/10.1080/10601329508010281.

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Demirdirek, Bahar, and Kathryn E. Uhrich. "Physically crosslinked salicylate-based poly (N-isopropylacrylamide-co-acrylic acid) hydrogels for protein delivery." Journal of Bioactive and Compatible Polymers 33, no. 2 (2017): 224–36. http://dx.doi.org/10.1177/0883911517721070.

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Physically crosslinked hydrogels were developed via solvent casting methods using a temperature-sensitive polymer, poly( N-isopropylacrylamide- co-acrylic acid), and a therapeutic polymer, salicylate-based poly(anhydride-esters), to concurrently release salicylic acid and bovine serum albumin in a sustained manner. The physical interactions between the two polymer systems were confirmed using Fourier transform infrared spectroscopy. The crosslinked polymers were porous, thus able to encapsulate bovine serum albumin (23 wt%) and then released the protein in a sustained fashion over 96 h. Concur

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38

Mooring, Lyndsey, Scott Thompson, Stephen A. Hall, et al. "‘Phoenix polymers’: fire induced nanohardness in fibril-forming aromatic cyanate esters." RSC Advances 8, no. 63 (2018): 36264–71. http://dx.doi.org/10.1039/c8ra07449f.

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39

Hamerton, Ian, and John N. Hay. "Recent Technological Developments in Cyanate Ester Resins." High Performance Polymers 10, no. 2 (1998): 163–74. http://dx.doi.org/10.1088/0954-0083/10/2/001.

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Although they are relative newcomers to the composites industry, cyanate ester (CE) resins are enjoying unprecedented success in certain applications. Several major space and radome manufacturers have qualified CE resins despite the extensive database on epoxies and the inherently conservative nature of the industry. Increasing demands on the materials used in these areas have stimulated the use of CE resins over other more conventional polymers. The aim of this review is to bring to the reader’s attention the more recent developments in the processing, toughening, properties and applications

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40

Thayanukul, Parinda, Futoshi Kurisu, Ikuro Kasuga, and Hiroaki Furumai. "Characterization of bacterial isolates from water reclamation systems on the basis of substrate utilization patterns and regrowth potential in reclaimed water." Water Science and Technology 68, no. 7 (2013): 1556–65. http://dx.doi.org/10.2166/wst.2013.395.

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Microbial regrowth causes problems during water reuse. Comprehensive understanding of the microorganisms that can regrow in reclaimed water and their substrate requirements are necessary. In this study, potential regrowth organisms were isolated from seven water reclamation plants in Japan. Based on 16S rDNA analysis, the isolates were grouped into 34 operational taxonomic units, belonging to Alphaproteobacteria, Betaproteobacteria, Gammaproteobacteria, Actinobacteria, Bacteroidetes, and Firmicutes. Substrate utilization profiling using Biolog microplate™ classified the isolates into four grou

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41

Simocko, Chester, Thomas C. Young, and Kenneth B. Wagener. "ADMET Polymers Containing Precisely Spaced Pendant Boronic Acids and Esters." Macromolecules 48, no. 16 (2015): 5470–73. http://dx.doi.org/10.1021/acs.macromol.5b01410.

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42

Cheng, Jing, Ran Ji, Shi-Juan Gao, Fu-Sheng Du, and Zi-Chen Li. "Facile Synthesis of Acid-Labile Polymers with Pendent Ortho Esters." Biomacromolecules 13, no. 1 (2011): 173–79. http://dx.doi.org/10.1021/bm201410c.

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43

Mello, Renata S., Elisa S. Orth, Watson Loh, Haidi D. Fiedler, and Faruk Nome. "Polymers Containing Hydroxamate Groups: Nanoreactors for Hydrolysis of Phosphoryl Esters." Langmuir 27, no. 24 (2011): 15112–19. http://dx.doi.org/10.1021/la203437j.

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Giusti, Luciano A., Michelle Medeiros, Natasha Londero Ferreira, José R. Mora, and Haidi D. Fiedler. "Polymers containing imidazole groups as nanoreactors for hydrolysis of esters." Journal of Physical Organic Chemistry 27, no. 4 (2014): 297–302. http://dx.doi.org/10.1002/poc.3263.

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García, Nuria, Julio Guzmán, and Evaristo Riande. "Migration Phenomena in Methacrylic Esters and Polymers Derived from Glycerol." Macromolecular Chemistry and Physics 203, no. 15 (2002): 2225–31. http://dx.doi.org/10.1002/1521-3935(200211)203:15<2225::aid-macp2225>3.0.co;2-7.

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De Ruijter, C., J. Bos, H. Boerstoel, and T. J. Dingemans. "Novel thermotropic esters-based polymers with broad nematic processing windows." Journal of Polymer Science Part A: Polymer Chemistry 46, no. 19 (2008): 6565–74. http://dx.doi.org/10.1002/pola.22967.

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Shigetomi, Yasumasa, Takehiro Kojima, and Naruhito Ono. "Allylic polymers. I. Copolymerization of allyl esters with vinyl acetate." Journal of Polymer Science Part A: Polymer Chemistry 28, no. 12 (1990): 3317–25. http://dx.doi.org/10.1002/pola.1990.080281211.

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Cabasso, Israel, Johannes Smid, and Suresh K. Sahni. "Radiopaque polymers based on acrylated phosphonate esters derived from polyols." Journal of Applied Polymer Science 41, no. 1112 (1990): 3025–42. http://dx.doi.org/10.1002/app.1990.070411136.

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Gumbley, Patricia, Damla Koylu, and Samuel W. Thomas. "Photoresponsive Polymers Containing Nitrobenzyl Esters via Ring-Opening Metathesis Polymerization." Macromolecules 44, no. 20 (2011): 7956–61. http://dx.doi.org/10.1021/ma2015529.

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Mukhitdinova, B. A., E. E. Ergozhin, G. S. Polimbetova, and A. K. Borangazieva. "The Synthesis of Organophosphorus Compounds from Phosphine and Alcohols in the Presence of Quinones and Redox Polymers on their Basis." Eurasian Chemico-Technological Journal 14, no. 3 (2012): 191. http://dx.doi.org/10.18321/ectj114.

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Abstract:

<p>This article presents the synthesis of phosphoric acid esters from phosphoric hydrogen РН3 and aliphatic alcohols. The process is based on the oxidation of phosphine by quinones and redox polymers on the basis of mono- and disubstituted quinoid derivatives of monoethanolamine vinyl ether. Molecular iodine is used as a catalyst. Two-, three-, four- and multicomp onent systems are studied in order to determine optimal conditions of the oxidation of phosphine quinones and repoxpolymers on their basis. The rate and selectivity of reaction were monitored by the absorption of РН<sub>3

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