Polymer Science, Series C最新文献

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Molecular Switch Based on a Linear Macromolecule Inserted in a Second-Generation Dendron Brush 基于二代树突刷插入线性大分子的分子开关
IF 2.2 4区 化学
Polymer Science, Series C Pub Date : 2022-08-31 DOI: 10.1134/S1811238222700114
A. A. Polotsky, T. M. Birshtein
{"title":"Molecular Switch Based on a Linear Macromolecule Inserted in a Second-Generation Dendron Brush","authors":"A. A. Polotsky,&nbsp;T. M. Birshtein","doi":"10.1134/S1811238222700114","DOIUrl":"10.1134/S1811238222700114","url":null,"abstract":"<p>The behavior of a single linear chain inserted in a planar polymer brush made of second-generation dendrons grafted via their focal point has been theoretically studied using the Scheutjens–Fleer self-consistent field method. It has been shown that the linear macromolecule can undergo a conformational transition from the state of a “coil” located inside the brush to the state of a “flower” consisting of a strongly stretched stem immersed in the brush and a head located above the brush. This transition has features of a first-order phase transition. It can be provoked by increasing the length of the linear macromolecule, by increasing the grafting density, or by improving the quality of the solvent in which the brush is immersed. An increase the linear chain length lowers the height of the energy barrier separating the “coil” and “flower” states, but the transition itself occurs in a solvent of poorer quality. A new state of the linear chain under the poor solvent conditions, “flower in the brush,” when both the stem and the head of the flower are inside the brush, was discovered.</p>","PeriodicalId":740,"journal":{"name":"Polymer Science, Series C","volume":"64 2","pages":"256 - 270"},"PeriodicalIF":2.2,"publicationDate":"2022-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"5176826","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Polyvinylidene Fluoride Copolymers with Grafted Polyethyl Methacrylate Chains: Synthesis and Thermal and Dielectric Properties 接枝聚甲基丙烯酸乙酯链聚偏氟乙烯共聚物的合成及其热介电性能
IF 2.2 4区 化学
Polymer Science, Series C Pub Date : 2022-08-31 DOI: 10.1134/S1811238222700138
E. A. Kleimyuk, A.I. Kosyakova, A. I. Buzin, V. G. Shevchenko, Yu. N. Luponosov, S. A. Ponomarenko
{"title":"Polyvinylidene Fluoride Copolymers with Grafted Polyethyl Methacrylate Chains: Synthesis and Thermal and Dielectric Properties","authors":"E. A. Kleimyuk,&nbsp;A.I. Kosyakova,&nbsp;A. I. Buzin,&nbsp;V. G. Shevchenko,&nbsp;Yu. N. Luponosov,&nbsp;S. A. Ponomarenko","doi":"10.1134/S1811238222700138","DOIUrl":"10.1134/S1811238222700138","url":null,"abstract":"<p>Polyvinylidene fluoride copolymers with grafted polyethyl methacrylate chains have been synthesized for the first time via photoinduced reversible deactivation radical polymerization. Binary and ternary copolymers of vinylidene fluoride with chlorotrifluoroethylene and trifluoroethylene were used as initial polymer chains for modification. The effect of the content of grafted chains on the thermal and dielectric properties of the copolymers has been studied. It has been shown that an increase in the content of grafted chains leads to a decrease in the degradation temperature, dielectric permittivity, and dielectric losses of the copolymers, but it significantly improves their film-forming properties due to a decrease in the degree of crystallinity.</p>","PeriodicalId":740,"journal":{"name":"Polymer Science, Series C","volume":"64 2","pages":"200 - 210"},"PeriodicalIF":2.2,"publicationDate":"2022-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"4046831","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Ferrocenyl-Containing Oligosiloxanes and Polysiloxanes: Synthesis, Properties, and Application 含二茂铁的低聚硅氧烷和聚硅氧烷:合成、性能和应用
IF 2.2 4区 化学
Polymer Science, Series C Pub Date : 2022-08-31 DOI: 10.1134/S1811238222700096
K. V. Deriabin, R. M. Islamova
{"title":"Ferrocenyl-Containing Oligosiloxanes and Polysiloxanes: Synthesis, Properties, and Application","authors":"K. V. Deriabin,&nbsp;R. M. Islamova","doi":"10.1134/S1811238222700096","DOIUrl":"10.1134/S1811238222700096","url":null,"abstract":"<p>This review addresses the systematization and analysis of methods for the synthesis of ferrocenyl-containing oligo- and (co)polysiloxanes and the potential application areas of these compounds. Various ways to introduce a ferrocenyl moiety into the structure of oligo- and (co)polysiloxanes are considered. Methods of synthesizing ferrocenyl-containing oligo-, cyclo-, silsesquio-, and (co)polysiloxanes via the reactions of catalytic hydrosilylation, dehydrocoupling, azide-alkyne cycloaddition, hydrothiolation, and ring-opening polymerization and polycondensation are demonstrated. It is shown that ferrocenyl-containing oligo- and (co)polysiloxanes feature the redox behavior and are of interest for molecular electronics, chemical modification of electrodes, and design of electrochemical sensors, and as materials for charge dissipation and neuronal implants. Oligo- and (co)polysiloxanes with chiral ferrocenyl substituents can be used in asymmetric catalysis and manufacture of liquid crystals for nonlinear optical systems.</p>","PeriodicalId":740,"journal":{"name":"Polymer Science, Series C","volume":"64 2","pages":"95 - 109"},"PeriodicalIF":2.2,"publicationDate":"2022-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"5170522","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Self-assembly of Polyfluorene Molecular Brushes with Poly(methacrylic acid) Side Chains in Ethanol and Water 带聚甲基丙烯酸侧链的聚芴分子刷在乙醇和水中的自组装
IF 2.2 4区 化学
Polymer Science, Series C Pub Date : 2022-08-31 DOI: 10.1134/S181123822270014X
M. A. Simonova, D. M. Ilgach, K. I. Kaskevich, M. I. Nepomnyashaya, L. S. Litvinova, A. P. Filippov, A. V. Yakimansky
{"title":"Self-assembly of Polyfluorene Molecular Brushes with Poly(methacrylic acid) Side Chains in Ethanol and Water","authors":"M. A. Simonova,&nbsp;D. M. Ilgach,&nbsp;K. I. Kaskevich,&nbsp;M. I. Nepomnyashaya,&nbsp;L. S. Litvinova,&nbsp;A. P. Filippov,&nbsp;A. V. Yakimansky","doi":"10.1134/S181123822270014X","DOIUrl":"10.1134/S181123822270014X","url":null,"abstract":"<p>Graft copolymers with the polyfluorene backbone and poly(<i>tert</i>-butyl methacrylate) and poly(methacrylic acid) side chains are synthesized by atom transfer radical polymerization. The behavior of the synthesized brushes in chloroform, ethanol, and water solutions is studied by molecular hydrodynamics and optics. The graft copolymers are characterized by a high grafting density. The brushes with poly(methacrylic acid) side chains form unimolecular micelles capable of encapsulating curcumin in aqueous solutions. The grafting density of side chain affects the properties of brush complexes with curcumin.</p>","PeriodicalId":740,"journal":{"name":"Polymer Science, Series C","volume":"64 2","pages":"189 - 199"},"PeriodicalIF":2.2,"publicationDate":"2022-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"5175095","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effect of the Structure of Arms and Way of Their Attachment to Calix[4]arene on Self-Assembly Processes in Aqueous Solutions of Thermoresponsive Star-Shaped Poly(2-alkyl-2-oxazolines) and Poly(2-alkyl-2-oxazines) 臂的结构及其与 Calix[4]arene 的连接方式对热致伸缩性星形聚(2-烷基-2-恶唑啉)和聚(2-烷基-2-恶嗪)水溶液中自组装过程的影响
IF 2.2 4区 化学
Polymer Science, Series C Pub Date : 2022-08-31 DOI: 10.1134/S1811238222700102
T. Yu. Kirila, A. B. Razina, A. V. Ten’kovtsev, A. P. Filippov
{"title":"Effect of the Structure of Arms and Way of Their Attachment to Calix[4]arene on Self-Assembly Processes in Aqueous Solutions of Thermoresponsive Star-Shaped Poly(2-alkyl-2-oxazolines) and Poly(2-alkyl-2-oxazines)","authors":"T. Yu. Kirila,&nbsp;A. B. Razina,&nbsp;A. V. Ten’kovtsev,&nbsp;A. P. Filippov","doi":"10.1134/S1811238222700102","DOIUrl":"10.1134/S1811238222700102","url":null,"abstract":"<p>The aqueous solutions of star-shaped four-arm poly(2-alkyl-2-oxazolines) and poly(2-alkyl-2-oxazines), in which the upper rim-functionalized calix[4]arene acts as a branching center, are studied by static and dynamic light scattering and turbidimetry. It is shown that at low temperatures in aqueous solutions of these polymer stars aggregates are formed as a result of interaction of hydrophobic calix[4]arene cores and formation of hydrogen bonds between dehydrated monomer units of arms. The process of aggregation dominates upon heating of the solutions. Varying the mode of arm attachment to a core causes a change in its configuration. The values of the phase transition temperature decrease when comparing polymers with the lower rim-functionalized core with polymers in which arms are attached to the upper rim of calix[4]arene.</p>","PeriodicalId":740,"journal":{"name":"Polymer Science, Series C","volume":"64 2","pages":"211 - 218"},"PeriodicalIF":2.2,"publicationDate":"2022-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"5172747","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effect of Annealing at High Temperatures on the Morphology of Aqueous Solutions of Star-Shaped Poly(2-Isopropyl-2-Oxazoline) and Linear Poly(2-Ethyl-5,6-Dihydrooxazine) 高温退火对星形聚(2-异丙基-2-恶唑啉)和线型聚(2-乙基-5,6-二氢恶嗪)水溶液形貌的影响
IF 2.2 4区 化学
Polymer Science, Series C Pub Date : 2022-07-08 DOI: 10.1134/S1811238222700072
A. V. Smirnova, A. V. Tenkovtsev, A. P. Filippov
{"title":"Effect of Annealing at High Temperatures on the Morphology of Aqueous Solutions of Star-Shaped Poly(2-Isopropyl-2-Oxazoline) and Linear Poly(2-Ethyl-5,6-Dihydrooxazine)","authors":"A. V. Smirnova,&nbsp;A. V. Tenkovtsev,&nbsp;A. P. Filippov","doi":"10.1134/S1811238222700072","DOIUrl":"10.1134/S1811238222700072","url":null,"abstract":"<p>Aqueous solutions of linear poly(2-ethyl-5,6-dihydrooxazine) and eight-armed star-shaped poly(2-isopropyl-2-oxazoline) have been studied by light scattering and turbidimetry. The influence of the duration of annealing at temperatures above the phase separation temperature on the behavior of the solutions has been analyzed. It has been shown that the characteristics of linear polymer solutions do not vary in the studied annealing time interval. The cloud point of star polymer solutions also does not depend on the annealing time. However, significant changes have been observed at the microscopic level, namely, irreversible aggregation due to the interaction of hydrophobic segments of poly(2-isopropyl-2-oxazoline) arms formed during annealing at a high temperature.</p>","PeriodicalId":740,"journal":{"name":"Polymer Science, Series C","volume":"64 2","pages":"154 - 160"},"PeriodicalIF":2.2,"publicationDate":"2022-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"4345421","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Synthesis and Properties of Polymer Photonic Crystals Based on Core–Shell Particles 基于核壳粒子的聚合物光子晶体的合成与性能研究
IF 2.2 4区 化学
Polymer Science, Series C Pub Date : 2022-07-08 DOI: 10.1134/S1811238222700084
N. N. Shevchenko, B. M. Shabsel’s, D. I. Iurasova, Yu. O. Skurkis
{"title":"Synthesis and Properties of Polymer Photonic Crystals Based on Core–Shell Particles","authors":"N. N. Shevchenko,&nbsp;B. M. Shabsel’s,&nbsp;D. I. Iurasova,&nbsp;Yu. O. Skurkis","doi":"10.1134/S1811238222700084","DOIUrl":"10.1134/S1811238222700084","url":null,"abstract":"<p>This review addresses recent achievements in the field of producing photonic-crystalline structures from polymer core/shell particles. The synthesis of polymer particles, in which a core is formed by hard crosslinked polymers and a shell is based on thermoplastic polymers or elastomers, offers the way to create the so-called stimuli-responsive (or “smart”) photonic crystals. Main principles underlying the self-assembly of polymer particles into periodic colloidal structures are considered. Elastic large-area 3D structures can be formed by the self-organization of core/shell particles under their compression at high temperatures. Prospects for the application of smart photonic-crystalline films are also highlighted.</p>","PeriodicalId":740,"journal":{"name":"Polymer Science, Series C","volume":"64 2","pages":"245 - 255"},"PeriodicalIF":2.2,"publicationDate":"2022-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"4341627","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Polymerization of Micelle-Forming Monomers 胶束形成单体的聚合
IF 2.2 4区 化学
Polymer Science, Series C Pub Date : 2022-07-08 DOI: 10.1134/S1811238222700060
I. M. Zorin, N. A. Zorina, P. A. Fetin
{"title":"Polymerization of Micelle-Forming Monomers","authors":"I. M. Zorin,&nbsp;N. A. Zorina,&nbsp;P. A. Fetin","doi":"10.1134/S1811238222700060","DOIUrl":"10.1134/S1811238222700060","url":null,"abstract":"<p>Studies on free-radical micellar polymerization of ionogenic amphiphilic monomers have been analyzed. Major types of the monomers and features of their polymerization in the micellar state have been described. Approaches to the analysis of kinetic features and mechanism of micellar polymerization have been considered; the applicability of the Morgan–Kaler microemulsion model to the description of quantitative features of micellar polymerization has been shown.</p>","PeriodicalId":740,"journal":{"name":"Polymer Science, Series C","volume":"64 2","pages":"123 - 134"},"PeriodicalIF":2.2,"publicationDate":"2022-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"4339829","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Amphiphilic ABA-Type Block–Graft Molecular Brushes Based on Polyimide 基于聚酰亚胺的两亲aba型嵌段接枝分子刷
IF 2.2 4区 化学
Polymer Science, Series C Pub Date : 2022-06-29 DOI: 10.1134/S1811238222700047
I. V. Ivanov, A. V. Kashina, N. V. Kukarkina, A. V. Yakimansky
{"title":"Amphiphilic ABA-Type Block–Graft Molecular Brushes Based on Polyimide","authors":"I. V. Ivanov,&nbsp;A. V. Kashina,&nbsp;N. V. Kukarkina,&nbsp;A. V. Yakimansky","doi":"10.1134/S1811238222700047","DOIUrl":"10.1134/S1811238222700047","url":null,"abstract":"<p>New amphiphilic ABA-type molecular brushes of mixed block–graft topology, where the central block B is a molecular brush with a hydrophobic polyimide backbone and hydrophilic side chains of poly(methacrylic acid) and A blocks are peripheral hydrophobic chains of poly(methyl methacrylate), have been synthesized. For the synthesis of the copolymers, an approach based on a combination of atom transfer radical polymerization (ATRP) and click chemistry in the variant of Cu(I)-catalyzed azide–alkyne cycloaddition was proposed. To implement the proposed approach, a procedure was developed for the synthesis of heterofunctional polyimide macroinitiators containing ATRP-initiating groups in each unit and terminal alkynyl groups capable of participating in the “click” reaction. Further, the synthesis of well-defined block–graft ABA molecular brushes was carried out using such initiators. First, peripheral poly(methyl methacrylate) chains were synthesized in a controlled mode using ATRP, followed by their functionalization with azide groups. Then, using the click chemistry approach, these chains were grafted to the terminal alkynyl groups of the heterofunctional initiator. The hydrophilic side chains were introduced into block B using the “grafting from” ATRP method in several steps through the intermediate formation of a regularly grafted prepolymer with poly(<i>tert</i>-butyl methacrylate) side chains. At the last step, as a result of selective acid hydrolysis of the side-chain ester groups in block B, amphiphilic multicomponent brushes with hydrophilic poly(methacrylic acid) units in the side chains were obtained. The possibility of sequential and simultaneous ATRP and click reaction has been examined.</p>","PeriodicalId":740,"journal":{"name":"Polymer Science, Series C","volume":"64 2","pages":"219 - 231"},"PeriodicalIF":2.2,"publicationDate":"2022-06-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"5121631","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Attempts to Optimizing the Synthesis of Hypercrosslinked Polystyrene. 1. Crosslinking with Monochlorodimethyl Ether 超交联聚苯乙烯合成工艺优化的尝试。与一氯二甲醚交联
IF 2.2 4区 化学
Polymer Science, Series C Pub Date : 2022-06-29 DOI: 10.1134/S1811238222700059
M. P. Tsyurupa, Z. K. Blinnikova, Yu. A. Davidovich, M. M. Ilyin, V. A. Davankov
{"title":"Attempts to Optimizing the Synthesis of Hypercrosslinked Polystyrene. 1. Crosslinking with Monochlorodimethyl Ether","authors":"M. P. Tsyurupa,&nbsp;Z. K. Blinnikova,&nbsp;Yu. A. Davidovich,&nbsp;M. M. Ilyin,&nbsp;V. A. Davankov","doi":"10.1134/S1811238222700059","DOIUrl":"10.1134/S1811238222700059","url":null,"abstract":"<p>This contribution was focused on the developing of an improved method for preparing hypercrosslinked polystyrene by bridging styrene-0.5% DVB copolymer with monochlorodimethyl ether (MCDE) up to 100, 150, 200 and 300% via Fidel–Crafts reaction. The modification comprises both the reduction in the consumption of the catalyst, SnCl<sub>4</sub>, and the complete substitution of SnCl<sub>4</sub> with the more active and less expensive catalyst, FeCl<sub>3</sub>. Reducing the SnCl<sub>4</sub> quantity from 1.0 to 0.1 mol per one mole of the ether leads to the formation of hypercrosslinked networks which exhibit a quite good swelling in non-solvents, rater low apparent density, and a noticeable pore volume, but, surprisingly, to a dramatic reduction in the measured inner surface area. The latter finding could be explained by the formation in the networks with very narrow pores which remain inaccessible to the testing argon atoms. The situation changes cardinally if the reaction mixture is additionally provided with oxalyl chloride (0.5 mol per mol of the ether) which reacts with methanol at the moment of its formation during the reaction of the ether with polystyrene. The latter reaction proceeds so violently that it is possible to reduce the amount of SnCl<sub>4</sub> by a factor of at least 13 or diminish the essential portion of FeCl<sub>3</sub> by a factor of 30, compared to the recommended previously 0.3 mol FeCl<sub>3</sub> per one mole of the MCDE.</p>","PeriodicalId":740,"journal":{"name":"Polymer Science, Series C","volume":"64 2","pages":"75 - 81"},"PeriodicalIF":2.2,"publicationDate":"2022-06-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"5121048","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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