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Journal articles on the topic 'Pyrrole derivative polymer'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Soganci, Tugba, Hakan Can Soyleyici, and Metin Ak. "A soluble and fluorescent new type thienylpyrrole based conjugated polymer: optical, electrical and electrochemical properties." Physical Chemistry Chemical Physics 18, no. 21 (2016): 14401–7. http://dx.doi.org/10.1039/c6cp02214f.

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Recently, increased attention has been focused on the synthesis of soluble and processable conducting polymers due to interest in their potential application. For this purpose a new type electroactive 2,5-di(2-thienyl)pyrrole derivative was synthesized and its novel solution-processable and fluorescent polymer, namely poly(N-(2,5-di(thiophen-2-yl)-1H-pyrrol-1-yl)-3,4,5-tris(dodecyloxy benzamide) (P(TPDOB)), was electrochemically synthesized.

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2

Su, Chang, Ling Min Wang, Li Huan Xu, Jun Lei Liu, Fang Yang, and Cheng Zhang. "Syntheses and Properties of Pyrrole Derivative as a Cathode Material for Li-Ion Batteries." Applied Mechanics and Materials 236-237 (November 2012): 731–35. http://dx.doi.org/10.4028/www.scientific.net/amm.236-237.731.

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A copolymer of 4-(1H-pyrrol-1-yl)phenol (PLPY) and pyrrole ( P(PLPY-co-Py) )was synthesized. And the chemical structure and battery performance of the prepared materials were characterized comparably by 1H NMR, FT-IR spectra and galvanostatic charge-discharge testing using simulant lithium ion half-cell method, respectively. The results shows that the introduction of the phenol group to the pyrrole as a rigid side chain could prevent the polymer from agglomeration and optimize the particle morphology of the resulting polymers, all of which made it demonstrate a significantly improved specific

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3

Xu, Li Huan, Fang Yang, Chang Su, and Cheng Zhang. "Research of Properties on Li-Ion Batteries Based on a Polypyrrole Derivative Bearing TEMPO as a Cathode Material." Advanced Materials Research 936 (June 2014): 447–51. http://dx.doi.org/10.4028/www.scientific.net/amr.936.447.

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4-(3-(Pyrrol-1-yl) butyric acid base)-2,2,6,6-tetramethylpiperidin (Py-B-TEMPO) was synthesized by etherification reaction of 4-hydroxy-2,2,6,6-tetramethylpiperidin-1-yloxy. And the polymer of its monomer was prepared by chemical oxidative polymerization and the chemical structure and battery performance of the prepared materials were characterized comparably by Mass spectrometry, 1H NMR, FT-IR spectra and galvanostatic charge-discharge testing using simulant lithium ion half-cell method, respectively. The results shows that the introduction of the TEMPO group to the pyrrole could prevent the

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4

Ouyang, Mi, Genghao Wang, and Cheng Zhang. "A novel electrochromic polymer containing triphenylamine derivative and pyrrole." Electrochimica Acta 56, no. 12 (2011): 4645–49. http://dx.doi.org/10.1016/j.electacta.2011.02.103.

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5

Yasuzawa, Mikito, Shigeru Inoue, and Shinji Imai. "Preparation of Glucose Sensor Using Polydimethylsiloxane / Polypyrrole Complex." International Journal of Modern Physics B 17, no. 08n09 (2003): 1217–22. http://dx.doi.org/10.1142/s0217979203018776.

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New glucose oxidase (GOD) immobilized glucose sensors were prepared by the electropolymerization of 1-(6-D-gluconamidohexyl) pyrrole (GHP) on the platinum wire electrode precoated with the mixture solution of pyrrole derivative GHP, polydimethylsiloxane (PDS) and Nafion. The addition of Nafion into the precoating mixture solution was essential to obtain suitable sensor sensitivity. However, the sensitivity was about the half of that of the electrode without PDS precoating. Although, the introduction of Nafion was effective to improve the long-term stability of the enzyme-immobilized electrode,

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6

Guerra, Silvia, Vincenzina Barbera, Alessandra Vitale, et al. "Edge Functionalized Graphene Layers for (Ultra) High Exfoliation in Carbon Papers and Aerogels in the Presence of Chitosan." Materials 13, no. 1 (2019): 39. http://dx.doi.org/10.3390/ma13010039.

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Ultra-high exfoliation in water of a nanosized graphite (HSAG) was obtained thanks to the synergy between a graphene layer edge functionalized with hydroxy groups and a polymer such as chitosan (CS). The edge functionalization of graphene layers was performed with a serinol derivative containing a pyrrole ring, serinol pyrrole (SP). The adduct between CS and HSAG functionalized with SP was formed simply with a mortar and pestle, then preparing water dispersions stable for months in the presence of acetic acid. Simple casting of such dispersions on a glass support led to carbon papers. Aerogels

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7

Munro, Orde Q., and Greville L. Camp. "Self-recognition in a flexible bis(pyrrole) Schiff base derivative: formation of a one-dimensional hydrogen-bonded polymer." Acta Crystallographica Section C Crystal Structure Communications 59, no. 12 (2003): o672—o675. http://dx.doi.org/10.1107/s0108270103023230.

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8

Nowik-Zajac, Anna, Iwona Zawierucha, and Cezary Kozlowski. "Selective Transport of Ag(I) through a Polymer Inclusion Membrane Containing a Calix[4]pyrrole Derivative from Nitrate Aqueous Solutions." International Journal of Molecular Sciences 21, no. 15 (2020): 5348. http://dx.doi.org/10.3390/ijms21155348.

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Cellulose-triacetate-based polymer inclusion membranes (PIMs) with different concentrations of a calixpyrrole ester derivative as the membrane carrier were studied to determine their ability to transport Ag(I) from aqueous nitrate solutions. The effects of the concentrations of ion carriers and metal ions, the pH of the source aqueous phase, and stripping agents on the effective transport of Ag(I) were assessed. All studied parameters were found to be important factors for the transport of Ag(I) metal ions. The initial fluxes were determined at different temperatures. The prepared membranes we

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9

Xuan, Duc Dau. "Recent Progress in the Synthesis of Pyrroles." Current Organic Chemistry 24, no. 6 (2020): 622–57. http://dx.doi.org/10.2174/1385272824666200228121627.

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: Pyrrole derivatives are nitrogen-containing heterocyclic compounds and widely distributed in a large number of natural and non-natural compounds. These compounds possess a broad spectrum of biological activities such as anti-infammatory, antiviral, antitumor, antifungal, and antibacterial activities. Besides their biological activity, pyrrole derivatives have also been applied in various areas such as dyes, conducting polymers, organic semiconductors. : Due to such a wide range of applicability, access to this class of compounds has attracted intensive research interest. Various established

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10

Azak, Hacer, Huseyin Bekir Yildiz, and Buket Bezgin Carbas. "Synthesis and characterization of a new poly(dithieno (3,2-b:2′, 3′-d) pyrrole) derivative conjugated polymer: Its electrochromic and biosensing applications." Polymer 134 (January 2018): 44–52. http://dx.doi.org/10.1016/j.polymer.2017.11.044.

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11

Agneeswari, Rajalingam, Insoo Shin, Vellaiappillai Tamilavan, et al. "Modulation of the properties of pyrrolo[3,4-c]pyrrole-1,4-dione based polymers containing 2,5-di(2-thienyl)pyrrole derivatives with different substitutions on the pyrrole unit." New Journal of Chemistry 39, no. 6 (2015): 4658–69. http://dx.doi.org/10.1039/c5nj00606f.

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12

Jarosz, Tomasz, and Przemyslaw Ledwon. "Electrochemically Produced Copolymers of Pyrrole and Its Derivatives: A Plentitude of Material Properties Using “Simple” Heterocyclic Co-Monomers." Materials 14, no. 2 (2021): 281. http://dx.doi.org/10.3390/ma14020281.

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Polypyrrole is a classical, well-known conjugated polymer that is produced from a simple heterocyclic system. Numerous pyrrole derivatives exhibit biological activity, and the repeat unit is a common building block present in the chemical structure of many polymeric materials, finding wide application, primarily in optoelectronics and sensing. In this work, we focus on the variety of copolymers and their material properties that can be produced electrochemically, even though all these systems are obtained from mixtures of the “simple” pyrrole monomer and its derivatives with different conjugat

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13

Jarosz, Tomasz, and Przemyslaw Ledwon. "Electrochemically Produced Copolymers of Pyrrole and Its Derivatives: A Plentitude of Material Properties Using “Simple” Heterocyclic Co-Monomers." Materials 14, no. 2 (2021): 281. http://dx.doi.org/10.3390/ma14020281.

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Polypyrrole is a classical, well-known conjugated polymer that is produced from a simple heterocyclic system. Numerous pyrrole derivatives exhibit biological activity, and the repeat unit is a common building block present in the chemical structure of many polymeric materials, finding wide application, primarily in optoelectronics and sensing. In this work, we focus on the variety of copolymers and their material properties that can be produced electrochemically, even though all these systems are obtained from mixtures of the “simple” pyrrole monomer and its derivatives with different conjugat

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14

Welterlich, Irina, Jörg-Martin Neudörfl, and Bernd Tieke. "Electrochemical polymerization of 1,3,4,6-tetraarylpyrrolo[3,2-b]pyrrole-2,5-dione (isoDPP) derivatives." Polymer Chemistry 6, no. 6 (2015): 1005–13. http://dx.doi.org/10.1039/c4py01315h.

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Electrochemical polymerization of tetraaryldiketopyrrolo[3,2-b]pyrrole (isoDPP) derivatives leads to deeply coloured low band gap polymers with reversible oxidation and reduction behaviour and electrochromic properties.

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15

Tsujimoto, Masaki, Kenichi Maruyama, Yuji Mishima, and Junko Motonaka. "Enzyme Biosensor Based on an Electropolymerized Osmium Redox Polymer." International Journal of Modern Physics B 17, no. 08n09 (2003): 1517–22. http://dx.doi.org/10.1142/s0217979203019253.

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Electrochemical polymerizations of metal complex as electron mediator in aqueous solution have been developed. The metal complexes as electron mediator of biosensor for practical application have a rapid electron transfer rate, a chemical stability, and an accessible manipulation. The electro-polymerized redox polymer relatively decreased the enzyme and catalytic activity, although these could be treated in organic solvent. In this work, the water-soluble osmium complex-modified pyrrole derivatives with long, flexible spacer chain were synthesized. The electro-polymerized redox polymer was gen

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16

Zhu, Yu, Kai Zhang, and Bernd Tieke. "Electrochemical Polymerization of Bis(3,4-ethylenedioxythiophene)-Substituted 1,4-Diketo-3,6-diphenyl-pyrrolo[3,4-c]pyrrole (DPP) Derivative." Macromolecular Chemistry and Physics 210, no. 6 (2009): 431–39. http://dx.doi.org/10.1002/macp.200800507.

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17

Agneeswari, Rajalingam, Insoo Shin, Vellaiappillai Tamilavan, et al. "Effects of the incorporation of an additional pyrrolo[3,4-c]pyrrole-1,3-dione unit on the repeating unit of highly efficient large band gap polymers containing benzodithiophene and pyrrolo[3,4-c]pyrrole-1,3-dione derivatives." Organic Electronics 30 (March 2016): 253–64. http://dx.doi.org/10.1016/j.orgel.2015.12.032.

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18

Zargar, N. D., and K. Z. Khan. "Interesting Mechanistic Approach for Nitrogen Heterocycles of Industrial Importance." International Journal of Advanced Chemistry 6, no. 1 (2018): 89. http://dx.doi.org/10.14419/ijac.v6i1.10382.

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Nitrogen heterocycles have played an important role in different industrial sectors.Porphyrins the macrocyclic compounds containing pyrrole rings provide an extremely versatile platform with desired peripheral functionality and metal complexes to form the self assembly under varying reaction conditions. Haemoglobin an iron complex is responsible for binding molecular oxygen and transporting it to different sites. Mechanistically interesting N-heterocycles, Arylidene-1,3-indandione adducts (6) and (7) synthesized frequently are of immense pharmaceutical importance showing fungicidal and bacteri

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19

Tamilavan, Vellaiappillai, Seungmin Kim, Rajalingam Agneeswari, et al. "Two new tercopolymers incorporating electron-rich benzodithiophene and electron-accepting pyrrolo[3,4-c]pyrrole-1,3-dione and difluorobenzothiadiazole derivatives for polymer solar cells." Polymer Bulletin 75, no. 1 (2017): 239–53. http://dx.doi.org/10.1007/s00289-017-2028-9.

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20

Ishii, Kanji, Kosuke Sato, Yuya Oaki, and Hiroaki Imai. "Highly porous polymer dendrites of pyrrole derivatives synthesized through rapid oxidative polymerization." Polymer Journal 51, no. 1 (2018): 11–18. http://dx.doi.org/10.1038/s41428-018-0115-x.

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21

Cosnier, Serge, and Michael Holzinger. "Design of carbon nanotube-polymer frameworks by electropolymerization of SWCNT-pyrrole derivatives." Electrochimica Acta 53, no. 11 (2008): 3948–54. http://dx.doi.org/10.1016/j.electacta.2007.10.027.

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22

Chen, Xuegang, Kai Guo, Fanchao Li, Li Zhou, and Hongbin Qiao. "Synthesis and properties of Zn2+/Cd2+-directed self-assembled metallo-supramolecular polymers based on 1,4-diketo-pyrrolo[3,4-c]pyrrole (DPP) derivatives." RSC Adv. 4, no. 101 (2014): 58027–35. http://dx.doi.org/10.1039/c4ra10685g.

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23

Mansour, Anissa, Yassin Belghith, Mohamed Salah Belkhiria, Anna Bujacz, Vincent Guérineau та Habib Nasri. "Synthesis, crystal structures and spectroscopic characterization of Co(II) bis(4,4′-bipyridine) with meso-porphyrins α,β,α,β-tetrakis(o-pivalamidophenyl) porphyrin (α,β,α,β-TpivPP) and tetraphenylporphyrin (TPP)". Journal of Porphyrins and Phthalocyanines 17, № 11 (2013): 1094–103. http://dx.doi.org/10.1142/s1088424613500843.

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The reaction of the starting materials [ Co II ( Porph )] (Porph = α,α,α,α-tetrakis(o-pivalamidophenyl)porphyrin (TpivPP) and the meso-tetraphenylporphyrin (TPP)) with an excess of 4,4′-bipyridine in chlorobenzene leads to the creation of two cobalt(II) derivatives: [ Co II (α,β,α,β- TpivPP )(4,4′- bpy )2]· C 6 H 5 Cl · C 6 H 14(1) and [ Co II ( TPP )(4,4′- bpy )2]·2 bpy (2). These compounds have been characterized by UV-vis, IR, 1 H NMR and MALDI-TOF spectroscopy. The proton NMR spectra of (1) and (2) clearly indicated that these derivatives are paramagnetic while the UV-vis data confirmed cr

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24

Yin, Yin, Li Chao Dong, Na Jin, Yan Guan, Jun Ge Zhi, and Wen Sheng Deng. "Synthesis and Aggregation-Induced Emission Feature of Series of Polysiloxanes Containing Triphenylpyrrole Side-Chain." Key Engineering Materials 842 (May 2020): 47–52. http://dx.doi.org/10.4028/www.scientific.net/kem.842.47.

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A series of aggregation-induced emission (AIE) active polysiloxanes (P7-1~P7-2, P29-1~P29-6) were prepared through hydrosilylation between polymethylhydrosiloxane (PMHS, DP=7 or 29) and AIE-active vinyl monomer 1-(4'-allyloxy-biphenyl)-2,5-diphenyl pyrrole (M-TPP), or with optical active monomer cholesteryl allyloxy ether (M-Chol*). Monomer M-TPP and all of the polymers exhibits aggeragation-induced emission enhancement properties. The fluorescence intensity of M-TPP in THF/H2O mixtures increases when the water fraction is higher than 60%, while is over 20% for polysiloxanes, which mainly beca

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25

Etaiw, Safaa Eldin H., Moustafa Sh Ibrahim, and Dina M. Abd El-Aziz. "Supramolecular host–guest systems constructed of pyrrole derivatives and 3D-coordination polymers." Journal of Materials Science 45, no. 9 (2010): 2474–83. http://dx.doi.org/10.1007/s10853-010-4219-8.

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26

Tamilavan, Vellaiappillai, Kyung Hwan Roh, Rajalingam Agneeswari, et al. "Benzodithiophene-Based Broad Absorbing Random Copolymers Incorporating Weak and Strong Electron Accepting Imide and Lactam Functionalized Pyrrolo[3,4-c]pyrrole Derivatives for Polymer Solar Cells." Macromolecular Chemistry and Physics 216, no. 9 (2015): 996–1007. http://dx.doi.org/10.1002/macp.201400614.

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27

Weiss, Zehava, Daniel Mandler, Galit Shustak, and Abraham J. Domb. "Pyrrole derivatives for electrochemical coating of metallic medical devices." Journal of Polymer Science Part A: Polymer Chemistry 42, no. 7 (2004): 1658–67. http://dx.doi.org/10.1002/pola.11097.

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28

Audebert, Pierre, and Gerard Bidan. "Synthesis and Electrochemical Behaviour of Some Polymers Issued From Halogenated Derivatives of Pyrrole." Molecular Crystals and Liquid Crystals 118, no. 1 (1985): 187–91. http://dx.doi.org/10.1080/00268948508076209.

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29

Ruggeri, G., M. Bianchi, G. Puncioni, and F. Ciardelli. "Molecular control of electric conductivity and structural properties of polymers of pyrrole derivatives." Pure and Applied Chemistry 69, no. 1 (1997): 143–50. http://dx.doi.org/10.1351/pac199769010143.

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30

Yang, Tianbao, Niu Tang, Qizhong Wan, Shuang-Feng Yin, and Renhua Qiu. "Recent Progress on Synthesis of N,N′-Chelate Organoboron Derivatives." Molecules 26, no. 5 (2021): 1401. http://dx.doi.org/10.3390/molecules26051401.

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N,N′-chelate organoboron compounds have been successfully applied in bioimaging, organic light-emitting diodes (OLEDs), functional polymer, photocatalyst, electroluminescent (EL) devices, and other science and technology areas. However, the concise and efficient synthetic methods become more and more significant for material science, biomedical research, or other practical science. Here, we summarized the organoboron-N,N′-chelate derivatives and showed the different routes of their syntheses. Traditional methods to synthesize N,N′-chelate organoboron compounds were mainly using bidentate ligan

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31

Heravi, Majid M., Afsaneh Feiz, and Ayoob Bazgir. "Recent Advances in the Chemistry and Synthesis of Thienopyrazine, Pyrrolopyrazine and Furopyrazine Derivatives." Current Organic Chemistry 23, no. 24 (2020): 2635–63. http://dx.doi.org/10.2174/1385272823666191106101954.

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Bicyclic compounds derived from pyrazine and aromatic five-membered heterocycles including thiophene, furan and pyrrole show various biological and pharmacological proBicyclic compounds derived from pyrazine and aromatic five-membered heterocycles including thiophene, furan and pyrrole show various biological and pharmacological properties, such as anti-inflammatory, antiviral, antitumor, antioxidant, antimycobacterial, and cytostatic activities. In many cases, it has been demonstrated that there are more potent cytostatic and cytotoxic agents against human tumor cell lines, leukemia, colon ca

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32

Okner, Regina, Abraham J. Domb, and Daniel Mandler. "Electrochemical Formation and Characterization of Copolymers Based onN-Pyrrole Derivatives." Biomacromolecules 8, no. 9 (2007): 2928–35. http://dx.doi.org/10.1021/bm7004752.

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33

Zhang, Kai, Bernd Tieke, John C. Forgie, and Peter J. Skabara. "Electrochemical Polymerisation ofN-Arylated andN-Alkylated EDOT-Substituted Pyrrolo[3,4-c]pyrrole-1,4-dione (DPP) Derivatives: Influence of Substitution Pattern on Optical and Electronic Properties." Macromolecular Rapid Communications 30, no. 21 (2009): 1834–40. http://dx.doi.org/10.1002/marc.200900442.

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34

Maas, Gerhard, Hans-Georg Herz, Elke Scheppach, Barbara Susanne, and Hans-Jörg Schneider. "Reactivity of Tetracyclic Iminium Salts of the Benzo[f]pyrido[2,1-a]- isoindole and Azepino[2,1-a]benzo[f]isoindole Type, with a Preliminary Analysis of their Interactions with Nucleic Acids*." Zeitschrift für Naturforschung B 59, no. 4 (2004): 486–97. http://dx.doi.org/10.1515/znb-2004-0417.

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AbstractHydride reduction of the tetracyclic isoindolium salt derivatives 2a - c yields the neutral isoindole derivatives 9-chloro-1,2,3,4,6,6a,7,12b-octahydrobenzo[ƒ]pyrido[2,1-a]isoindole (3a), 4,4a,5,7,8,9,10,10a-octahydropyrido[2,1-a]thieno[3,2-f]isoindole (3b), and 10-chloro- 2,3,4,5,7,7a,8,13b-octahydro-1H-azepino[ƒ]pyrido[2,1-a]isoindole (3c). Oxidation of 3a with selenium dioxide is accompanied by a ring transformation and yields 8-chloro-5,5a,6,12-tetrahydrobenzo[g]pyrrolo[1,2-b]isoquinolin-12-one (4). Deprotonation of isoindolium salt derivatives 2a,c,d yields cyclic enamines which u

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35

Han, GY, GQ Shi, LT Qu, JY Yuan, FE Chen, and PY Wu. "Electrochemical polymerization of chiral pyrrole derivatives in electrolytes containing chiral camphor sulfonic acid." Polymer International 53, no. 10 (2004): 1554–60. http://dx.doi.org/10.1002/pi.1597.

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36

Kotkar, Dilip, Vishwas Joshi, and Pushpito K. Ghosh. "Towards chiral metals. Synthesis of chiral conducting polymers from optically active thiophene and pyrrole derivatives." Journal of the Chemical Society, Chemical Communications, no. 14 (1988): 917. http://dx.doi.org/10.1039/c39880000917.

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37

Kim, Kyu-Sik, Kaname Katsuraya, Yoshihide Yachi, Kenichi Hatanaka, and Toshiyuki Uryu. "Synthesis of Lysine-Core Dendrimer Containing Long Pyrrole-Terminated Alkylene Derivative." FIBER 56, no. 12 (2000): 584–91. http://dx.doi.org/10.2115/fiber.56.584.

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38

Moon, Doo-Kyung, Anne Buyle Padias, H. K. Hall, Trey Huntoon, and Paul D. Calvert. "Electroactive Polymeric Materials for Battery Electrodes: Copolymers of Pyrrole and Pyrrole Derivatives with Oligo(ethyleneoxy) Chains at the 3-Position." Macromolecules 28, no. 18 (1995): 6205–10. http://dx.doi.org/10.1021/ma00122a030.

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39

Tarkuc, Simge, Metin Ak, Erdal Onurhan, and Levent Toppare. "Electrochromic Properties of ‘Trimeric' Thiophene‐pyrrole‐thiophene Derivative Grown from Electrodeposited 6‐(2,5‐di(thiophen‐2‐yl)‐1H‐pyrrol‐1‐yl)hexan‐1‐amine and its Copolymer." Journal of Macromolecular Science, Part A 45, no. 2 (2007): 164–71. http://dx.doi.org/10.1080/10601320701786976.

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40

Udum, Yasemin Arslan, Hüseyin Bekir Yıldız, Hacer Azak, et al. "Synthesis and spectroelectrochemistry of dithieno(3,2-b:2′,3′-d)pyrrole derivatives." Journal of Applied Polymer Science 131, no. 17 (2014): n/a. http://dx.doi.org/10.1002/app.40701.

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41

Green, Joshua P., Haojie Dai, Filip Aniés, and Martin Heeney. "Functional 4H-Dithieno[3,2-b:2′,3′-d]pyrrole Derivatives in Base-Dopable Conjugated Polymers and Oligomers." Macromolecules 53, no. 15 (2020): 6649–55. http://dx.doi.org/10.1021/acs.macromol.0c01071.

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42

Ledwon, Przemyslaw, Alina Brzeczek, Sandra Pluczyk, et al. "Synthesis and electrochemical properties of novel, donor–acceptor pyrrole derivatives with 1,8-naphthalimide units and their polymers." Electrochimica Acta 128 (May 2014): 420–29. http://dx.doi.org/10.1016/j.electacta.2013.10.163.

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43

Ren, Fei, Zhiqi Liu, Yunxiang Lei, et al. "Coumarin-substituted pyrrole derivatives with aggregation-enhanced emission characteristics for detecting the glass transition temperature of polymers." Dyes and Pigments 188 (April 2021): 109222. http://dx.doi.org/10.1016/j.dyepig.2021.109222.

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44

Cetiner, Suat, Fatma Kalaoglu, Hale Karakas, and A. Sezai Sarac. "Characterization of conductive poly(acrylonitrile-co-vinyl acetate) composites: Matrix polymerization of pyrrole derivatives." Fibers and Polymers 12, no. 2 (2011): 151–58. http://dx.doi.org/10.1007/s12221-011-0151-z.

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45

Mourato, Ana, Ana S. Viana, Franz-Peter Montforts, and Luisa Maria Abrantes. "Polypyrrole on self-assembled monolayers of a pyrrolyl lipoic acid derivative—electrosynthesis and polymer film characterization." Journal of Solid State Electrochemistry 14, no. 11 (2010): 1985–95. http://dx.doi.org/10.1007/s10008-010-1036-6.

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46

Tamilavan, Vellaiappillai, Jihoon Lee, Rajalingam Agneeswari, et al. "Photocurrent enhancement of an efficient large band gap polymer incorporating benzodithiophene and weak electron accepting pyrrolo[3,4−c]pyrrole−1,3−dione derivatives via the insertion of a strong electron accepting thieno[3,4−b]thiophene unit." Polymer 80 (December 2015): 95–103. http://dx.doi.org/10.1016/j.polymer.2015.10.054.

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Deng, Zhiping, and David C. Stone. "Characterization of Polymer Films of Pyrrole Derivatives for Chemical Sensing by Cyclic Voltammetry, X-ray Photoelectron Spectroscopy and Vapour Sorption Studies." Analyst 122, no. 10 (1997): 1129–38. http://dx.doi.org/10.1039/a703165c.

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Coche-Guerente, L., S. Cosnier, C. Innocent, and P. Mailley. "Development of amperometric biosensors based on the immobilization of enzymes in polymer films electrogenerated from a series of amphiphilic pyrrole derivatives." Analytica Chimica Acta 311, no. 1 (1995): 23–30. http://dx.doi.org/10.1016/0003-2670(95)00178-3.

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Paul, Sanjay, and Asish R. Das. "A new application of polymer supported, homogeneous and reusable catalyst PEG–SO3H in the synthesis of coumarin and uracil fused pyrrole derivatives." Catalysis Science & Technology 2, no. 6 (2012): 1130. http://dx.doi.org/10.1039/c2cy20117h.

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Warnan, Julien, Clément Cabanetos, Romain Bude, Abdulrahman El Labban, Liang Li, and Pierre M. Beaujuge. "Electron-Deficient N-Alkyloyl Derivatives of Thieno[3,4-c]pyrrole-4,6-dione Yield Efficient Polymer Solar Cells with Open-Circuit Voltages > 1 V." Chemistry of Materials 26, no. 9 (2014): 2829–35. http://dx.doi.org/10.1021/cm5002303.

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