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Journal articles on the topic 'Organic chemistry|Chemistry|Polymers'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Serpe, Michael J., and Stephen L. Craig. "Physical Organic Chemistry of Supramolecular Polymers." Langmuir 23, no. 4 (2007): 1626–34. http://dx.doi.org/10.1021/la0621416.

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2

Wolfbeis, O. S. "Organic Conductive Polymers in Analytical Chemistry." Microchimica Acta 143, no. 2-3 (2003): 73. http://dx.doi.org/10.1007/s00604-003-0076-3.

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3

Maji, Tapas Kumar, and Susumu Kitagawa. "Chemistry of porous coordination polymers." Pure and Applied Chemistry 79, no. 12 (2007): 2155–77. http://dx.doi.org/10.1351/pac200779122155.

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Remarkable advances in the recent development of porous compounds based upon coordination polymers have paved the way toward functional chemistry having potential applications such as gas storage, separation, and catalysis. From the synthetic point of view, the advantage is a designable framework, which can readily be constructed from building blocks, the so-called bottom-up assembly. Compared with conventional porous materials such as zeolites and activated carbons, porous inorganic-organic hybrid frameworks have higher potential for adsorption of small molecules because of their designabilit

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4

Jablonský, Michal, Andrea Škulcová, and Jozef Šima. "Use of Deep Eutectic Solvents in Polymer Chemistry–A Review." Molecules 24, no. 21 (2019): 3978. http://dx.doi.org/10.3390/molecules24213978.

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This review deals with two overlapping issues, namely polymer chemistry and deep eutectic solvents (DESs). With regard to polymers, specific aspects of synthetic polymers, polymerization processes producing such polymers, and natural cellulose-based nanopolymers are evaluated. As for DESs, their compliance with green chemistry requirements, their basic properties and involvement in polymer chemistry are discussed. In addition to reviewing the state-of-the-art for selected kinds of polymers, the paper reveals further possibilities in the employment of DESs in polymer chemistry. As an example, t

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5

Shuttleworth, Stephen J., Steven M. Allin, Richard D. Wilson, and Daniel Nasturica. "Functionalised Polymers in Organic Chemistry; Part 2." Synthesis 2000, no. 08 (2000): 1035–74. http://dx.doi.org/10.1055/s-2000-6310.

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6

Bates, Joshua I., Julien Dugal-Tessier, and Derek P. Gates. "Phospha-organic chemistry: from molecules to polymers." Dalton Trans. 39, no. 13 (2010): 3151–59. http://dx.doi.org/10.1039/b918938f.

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7

Lubetkin, S. D. "Colloid chemistry of polymers." Polymer 30, no. 8 (1989): 1565. http://dx.doi.org/10.1016/0032-3861(89)90236-x.

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8

Feldman, D. "Polymers chemistry. An Introduction." Journal of Polymer Science Part A: Polymer Chemistry 30, no. 8 (1992): 1778. http://dx.doi.org/10.1002/pola.1992.080300838.

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9

Rotello, Vincent M. "Organic chemistry meets polymers, nanoscience, therapeutics and diagnostics." Beilstein Journal of Organic Chemistry 12 (August 2, 2016): 1638–46. http://dx.doi.org/10.3762/bjoc.12.161.

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The atom-by-atom control provided by synthetic organic chemistry presents a means of generating new functional nanomaterials with great precision. Bringing together these two very disparate skill sets is, however, quite uncommon. This autobiographical review provides some insight into how my program evolved, as well as giving some idea of where we are going.

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10

Wang, Shuguang, Zhongwu Wang, Jie Li, Liqiang Li, and Wenping Hu. "Surface-grafting polymers: from chemistry to organic electronics." Materials Chemistry Frontiers 4, no. 3 (2020): 692–714. http://dx.doi.org/10.1039/c9qm00450e.

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This review comprehensively summarizes the recent progress in surface-grafting polymers, including their formation process and the utilization of surface-grafting polymers as functional materials of insulators, conductors and semiconductors in versatile organic electronic devices.

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11

Marrocchi, Assunta, Antonio Facchetti, Daniela Lanari, Stefano Santoro та Luigi Vaccaro. "Click-chemistry approaches to π-conjugated polymers for organic electronics applications". Chemical Science 7, № 10 (2016): 6298–308. http://dx.doi.org/10.1039/c6sc01832g.

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12

Bahry, Teseer, Zhenpeng Cui, Ariane Deniset-Besseau, et al. "An alternative radiolytic route for synthesizing conducting polymers in an organic solvent." New Journal of Chemistry 42, no. 11 (2018): 8704–16. http://dx.doi.org/10.1039/c8nj01041b.

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13

Varfolomeyev, Sergey, Elena Efremenko, Irina P. Beletskaya, et al. "Postgenomic chemistry (IUPAC Technical Report)." Pure and Applied Chemistry 77, no. 9 (2005): 1641–54. http://dx.doi.org/10.1351/pac200577091641.

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Numerous areas of chemistry can benefit from the ongoing genomic revolution. Here, we discuss and highlight trends in chemistry in the postgenomic era. The areas of interest include combinatorial approaches in organic chemistry; design and analysis of proteins containing unnatural amino acids; trace element-containing proteins; design and characterization of new enzyme types; applications of postgenomic chemistry in drug design; identification of lipid networks and global characterization of lipid molecular species; development of recombinant and self-proliferating polymers; and applications i

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14

Soloducho, Jadwiga, Dorota Zajac, and Joanna Cabaj. "Semiconducting Polymers - A Novel Trend in Organic Electronic Chemistry." Current Organic Synthesis 13, no. 6 (2016): 861–75. http://dx.doi.org/10.2174/1570179413666160624085533.

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15

Bates, Joshua I., Julien Dugal-Tessier, and Derek P. Gates. "ChemInform Abstract: Phospha-Organic Chemistry: From Molecules to Polymers." ChemInform 41, no. 30 (2010): no. http://dx.doi.org/10.1002/chin.201030250.

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16

Shuttleworth, Stephen J., Steven M. Allin, Richard D. Wilson, and Daniel Nasturica. "ChemInform Abstract: Functionalized Polymers in Organic Chemistry. Part 2." ChemInform 31, no. 39 (2000): no. http://dx.doi.org/10.1002/chin.200039270.

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17

Bee, Timothy G., Elisa M. Cross, Anthony J. Dias, Kang-Wook Lee, Molly S. Shoichet, and Thomas J. McCarthy. "Control of wettability of polymers using organic surface chemistry." Journal of Adhesion Science and Technology 6, no. 6 (1992): 719–31. http://dx.doi.org/10.1163/156856192x01060.

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18

Morin, Jean-François. "Recent advances in the chemistry of vat dyes for organic electronics." Journal of Materials Chemistry C 5, no. 47 (2017): 12298–307. http://dx.doi.org/10.1039/c7tc03926c.

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19

Blatt, Celso. "Professor Remolo Ciola, a Master and a Genius." Brazilian Journal of Analytical Chemistry 8, no. 10Years (2021): 16–21. http://dx.doi.org/10.30744/brjac.2179-3425.letter-cblatt.

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Professor Remolo Ciola has always impressed me with his knowledge of basic chemistry, organic chemistry, synthesis, polymers and catalysis. In addition, he was very good at designing and creating technological solutions to solve problems.

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20

Alahakoon, Sampath B., Shashini D. Diwakara, Christina M. Thompson, and Ronald A. Smaldone. "Supramolecular design in 2D covalent organic frameworks." Chemical Society Reviews 49, no. 5 (2020): 1344–56. http://dx.doi.org/10.1039/c9cs00884e.

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2D covalent organic frameworks (COFs) are a class of porous polymers with crystalline structures. This tutorial review discusses how the concepts of supramolecular chemistry are used to add form and function to COFs through their non-covalent bonds.

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21

Wu, Yingjie, Qihan Zhang, He Wang, and Mingfeng Wang. "Multiscale engineering of functional organic polymer interfaces for neuronal stimulation and recording." Materials Chemistry Frontiers 4, no. 12 (2020): 3444–71. http://dx.doi.org/10.1039/d0qm00279h.

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This review summarizes recent progress on chemistry and engineering techniques of organic polymers across a range of electrically insulating polymers, semiconducting polymers and conducting polymers for neural interfacing, stimulation and recording.

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22

Chassaing, S., V. Bénéteau, and P. Pale. "When CuAAC 'Click Chemistry' goes heterogeneous." Catalysis Science & Technology 6, no. 4 (2016): 923–57. http://dx.doi.org/10.1039/c5cy01847a.

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Within the green chemistry context, heterogeneous catalysis is more and more applied to organic synthesis. The well known ‘click chemistry’ and especially its flagship, the copper-catalyzed azide–alkyne cycloaddition reaction (CuAAC), is now catch up by such heterogenisation process and copper ions or metals have been grafted or deposited on or into various solids, such as (bio)polymers, charcoal, silica, zeolites, POM or MOF.

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23

Orowitz, Tirza Ecclesia, Patria Pari Agnes Ago Ana Sombo, Driyanti Rahayu, and Aliya Nur Hasanah. "Microsphere Polymers in Molecular Imprinting: Current and Future Perspectives." Molecules 25, no. 14 (2020): 3256. http://dx.doi.org/10.3390/molecules25143256.

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Molecularly imprinted polymers (MIPs) are specific crosslinked polymers that exhibit binding sites for template molecules. MIPs have been developed in various application areas of biology and chemistry; however, MIPs have some problems, including an irregular material shape. In recent years, studies have been conducted to overcome this drawback, with the synthesis of uniform microsphere MIPs or molecularly imprinted microspheres (MIMs). The polymer microsphere is limited to a minimum size of 5 nm and a molecular weight of 10,000 Da. This review describes the methods used to produce MIMs, such

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24

Zhao, Xiaoning, Shuangshuang Zhang, Tengfei Miao, et al. "The implementation of the catalytic Staudinger–Vilarrasa reaction in polymer chemistry as a highly efficient chemistry strategy." Polymer Chemistry 9, no. 34 (2018): 4413–21. http://dx.doi.org/10.1039/c8py00884a.

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A versatile and highly efficient chemistry strategy, the catalytic S–V reaction of acids with azides, was firstly implemented in polymer chemistry for the construction of various amide-containing polymers.

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25

Whitesides, George M. "Organic Materials Science." MRS Bulletin 27, no. 1 (2002): 56–65. http://dx.doi.org/10.1557/mrs2002.22.

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AbstractThe following article is based on the presentation given by George M. Whitesides, recipient of the 2000 MRS Von Hippel Award, the Materials Research Society's highest honor, at the 2000 MRS Fall Meeting in Boston on November 29, 2000. Whitesides was cited for “bringing fundamental concepts of organic chemistry and biology into materials science and engineering, through his pioneering research on surface modification, self-assembly, and soft lithography.” The article focuses on the growing role of organic chemistry in materials science. Historically, that role has been to provide organi

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26

Ward, I. M. "High pressure chemistry and physics of polymers." Polymer 35, no. 19 (1994): 4254. http://dx.doi.org/10.1016/0032-3861(94)90607-6.

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27

Liebman, S. A., R. A. Pesce-Rodriguez, and C. N. Matthews. "Organic analysis of hydrogen cyanide polymers: Prebiotic and extraterrestrial chemistry." Advances in Space Research 15, no. 3 (1995): 71–80. http://dx.doi.org/10.1016/s0273-1177(99)80066-0.

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28

Davidescu, Corneliu-Mircea. "15th International Conference on Polymers and Organic Chemistry (POC-2014)." Pure and Applied Chemistry 86, no. 11 (2014): 1619. http://dx.doi.org/10.1515/pac-2014-5054.

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29

Jiang, Donglin. "Covalent Organic Frameworks: An Amazing Chemistry Platform for Designing Polymers." Chem 6, no. 10 (2020): 2461–83. http://dx.doi.org/10.1016/j.chempr.2020.08.024.

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30

Rossin, Andrea. "Editorial for Special Issue “Functional Coordination Polymers and Metal–Organic Frameworks”." Inorganics 9, no. 5 (2021): 33. http://dx.doi.org/10.3390/inorganics9050033.

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Metal–Organic Frameworks (MOFs) and Coordination Polymers (CPs) are at the forefront of contemporary coordination chemistry research, as witnessed by the impressive (and ever-growing) number of publications appearing in the literature on this topic in the last 20 years (Figure 1), reaching almost 4000 papers in 2020 [...]

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31

George, Steven M., Byunghoon Yoon, and Arrelaine A. Dameron. "Surface Chemistry for Molecular Layer Deposition of Organic and Hybrid Organic−Inorganic Polymers." Accounts of Chemical Research 42, no. 4 (2009): 498–508. http://dx.doi.org/10.1021/ar800105q.

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32

Kramer, Søren, Niklas R. Bennedsen, and Søren Kegnæs. "Porous Organic Polymers Containing Active Metal Centers as Catalysts for Synthetic Organic Chemistry." ACS Catalysis 8, no. 8 (2018): 6961–82. http://dx.doi.org/10.1021/acscatal.8b01167.

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33

Haino, Takeharu. "Supramolecular Chemistry: From Host-guest Complexes to Supramolecular Polymers." Journal of Synthetic Organic Chemistry, Japan 71, no. 11 (2013): 1172–81. http://dx.doi.org/10.5059/yukigoseikyokaishi.71.1172.

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34

Pearce, Eli M. "Polymers: Chemistry and physics of modern materials." Journal of Polymer Science Part A: Polymer Chemistry 30, no. 8 (1992): 1777. http://dx.doi.org/10.1002/pola.1992.080300836.

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35

Housecroft, Catherine E. "Coordination Polymers and Metal-Organic Frameworks: Structures and Applications—A Themed Issue in Honor of Professor Christoph Janiak on the Occasion of His 60th Birthday." Chemistry 3, no. 3 (2021): 831–33. http://dx.doi.org/10.3390/chemistry3030060.

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This themed issue of Chemistry is in honor of Professor Christoph Janiak on the occasion of his 60th birthday, and celebrates his innovative contributions to the fields of supramolecular chemistry, coordination polymers, networks and metal-organic frameworks, inorganic/organic hybrid materials and inorganic materials from ionic liquids [...]

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36

Burmeister, David, Lukas Ahrens, Andreas Opitz, et al. "Utilizing Diels–Alder “click” chemistry to functionalize the organic–organic interface of semiconducting polymers." Journal of Materials Chemistry C 8, no. 10 (2020): 3302–7. http://dx.doi.org/10.1039/c9tc06180k.

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An all-solution-based modular functionalization of a cross-linked polymer semiconductor interface is presented. The thus covalently introduced moieties can be utilised for tailor-made organic–organic interfaces in organic optoelectronic devices.

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37

Jung, Ji-Hye, Yeong-Gweon Lim, Kyung-Hee Lee, and Bon Tak Koo. "Synthesis of glycidyl triazolyl polymers using click chemistry." Tetrahedron Letters 48, no. 37 (2007): 6442–48. http://dx.doi.org/10.1016/j.tetlet.2007.07.096.

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38

Li, J., and Q. Zhang. "To achieve ferromagnetism in organic polymers by doping: quantum chemistry studies." IEEE Transactions on Magnetics 27, no. 6 (1991): 5384–86. http://dx.doi.org/10.1109/20.278846.

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39

Shuttleworth, Stephen J., Allin, and Pradeep K. Sharma. "Functionalised Polymers: Recent Developments and New Applications in Synthetic Organic Chemistry." Synthesis 1997, no. 11 (1997): 1217–39. http://dx.doi.org/10.1055/s-1997-1358.

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40

Vasilevskaya, Elena, and Viktor Khvalyuk. "CHEMISTRY IN THE NEW GENERATION OF UNIVERSITY EDUCATION STANDARDS IN BELARUS." GAMTAMOKSLINIS UGDYMAS / NATURAL SCIENCE EDUCATION 6, no. 3 (2009): 24–28. http://dx.doi.org/10.48127/gu-nse/09.6.24b.

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The article presents the structure and content of a new generation of post-secondary education standards in Belarus. New educational standards consist of four units: a social science core, a natural science core, a core of professional disciplines, and a selection of special courses. We discuss the place and role of chemistry in new curriculums for students of natural sciences, engineering and humanities. For chemistry students, the natural science core includes such disciplines as Higher Mathemat-ics, Physics, Ecology, Introduction to Information Technology, Information Technology in Chemistr

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41

Maier, W. F., G. Kirsten, M. Orschel, P. A. Weiß, A. Holzwarth, and J. Klein. "Combinatorial chemistry of materials, polymers and catalysts." Macromolecular Symposia 165, no. 1 (2001): 1–2. http://dx.doi.org/10.1002/1521-3900(200103)165:1<1::aid-masy1>3.0.co;2-z.

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42

Xu, Heng, and Dmitry M. Rudkevich. "Reversible Chemistry of CO2in the Preparation of Fluorescent Supramolecular Polymers." Journal of Organic Chemistry 69, no. 25 (2004): 8609–17. http://dx.doi.org/10.1021/jo0488210.

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43

Goldmann, Anja S., Mathias Glassner, Andrew J. Inglis, and Christopher Barner-Kowollik. "Post-Functionalization of Polymers via Orthogonal Ligation Chemistry." Macromolecular Rapid Communications 34, no. 10 (2013): 810–49. http://dx.doi.org/10.1002/marc.201300017.

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44

Bonardi, Aude-Héloise, Frédéric Dumur, Guillaume Noirbent, Jacques Lalevée, and Didier Gigmes. "Organometallic vs organic photoredox catalysts for photocuring reactions in the visible region." Beilstein Journal of Organic Chemistry 14 (December 12, 2018): 3025–46. http://dx.doi.org/10.3762/bjoc.14.282.

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Recent progresses achieved in terms of synthetic procedures allow now the access to polymers of well-defined composition, molecular weight and architecture. Thanks to these recent progresses in polymer engineering, the scope of applications of polymers is far wider than that of any other class of material, ranging from adhesives, coatings, packaging materials, inks, paints, optics, 3D printing, microelectronics or textiles. From a synthetic viewpoint, photoredox catalysis, originally developed for organic chemistry, has recently been applied to the polymer synthesis, constituting a major break

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45

Giraud, Lauriane, Stéphane Grelier, Etienne Grau та ін. "Upgrading the chemistry of π-conjugated polymers toward more sustainable materials". Journal of Materials Chemistry C 8, № 29 (2020): 9792–810. http://dx.doi.org/10.1039/d0tc01645d.

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46

Corriu, Robert J. P., Philippe Gerbier, Christian Guerin, Bernard J. L. Henner, Alain Jean, and P. Hubert Mutin. "Organosilicon polymers: pyrolysis chemistry of poly[(dimethylsilylene)diacetylene]." Organometallics 11, no. 7 (1992): 2507–13. http://dx.doi.org/10.1021/om00043a038.

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47

Musgrave, Rebecca A., Andrew D. Russell, Paul R. Gamm, et al. "Redox Chemistry of Nickelocene-Based Monomers and Polymers." Organometallics 40, no. 12 (2021): 1945–55. http://dx.doi.org/10.1021/acs.organomet.1c00247.

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48

Arslan, Mehmet, Gokhan Acik, and Mehmet Atilla Tasdelen. "The emerging applications of click chemistry reactions in the modification of industrial polymers." Polymer Chemistry 10, no. 28 (2019): 3806–21. http://dx.doi.org/10.1039/c9py00510b.

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49

Miroshnikov, Mikhail, Kizhmuri P. Divya, Ganguli Babu, et al. "Power from nature: designing green battery materials from electroactive quinone derivatives and organic polymers." Journal of Materials Chemistry A 4, no. 32 (2016): 12370–86. http://dx.doi.org/10.1039/c6ta03166h.

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50

Cowie, J. M. G. "New trends in physics and physical chemistry of polymers." Polymer 32, no. 4 (1991): 764. http://dx.doi.org/10.1016/0032-3861(91)90494-4.

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