Relevant bibliographies by topics / Thiophene polymer

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Thiophene polymer'

Author: Grafiati
Published: 4 June 2021
Last updated: 17 February 2022

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Journal articles on the topic "Thiophene polymer"

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Muangrat, Worawut, Rungroj Maolanon, Sirapat Pratontep, Supanit Porntheeraphat, and Winadda Wongwiriyapan. "Polymer-Coated Single-Walled Carbon Nanotubes for Ethanol and Dichloromethane Discrimination." Advanced Materials Research 802 (September 2013): 267–72. http://dx.doi.org/10.4028/www.scientific.net/amr.802.267.

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Sensor response and pattern recognition of polymer-coated single-walled carbon nanotubes (SWNTs) were investigated. Printed circuit board (PCB) with Cu/Au interdigitated electrode was used as sensor platform. SWNTs network was firstly formed on PCB by drop-casting. For polymer-coated SWNTs preparation, poly(methyl methacrylate) (PMMA) and thiophene were employed as polymers to coat on SWNTs by spin coating; PMMA/SWNTs and thiophene/SWNTs. Raman spectra showed no obvious structure changes of SWNTs after polymer coating. Next, gas sensing test was conducted. Pristine SWNTs, PMMA/SWNTs and thioph
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Chan, Eddie Wai Chi, Paul Baek, David Barker, and Jadranka Travas-Sejdic. "Highly functionalisable polythiophene phenylenes." Polymer Chemistry 6, no. 43 (2015): 7618–29. http://dx.doi.org/10.1039/c5py01033k.

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Jiang, Zhenhua, Cailing Ni, Yubing Zhou, and Yuancheng Qin. "Exploring the Effect of the Number of Characteristic Groups in Melaminebased Polymers on the Photocatalytic Performance." Current Chinese Science 1, no. 1 (2020): 141–50. http://dx.doi.org/10.2174/2210298101999200716191729.

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: Three polymers containing different numbers of thiophene groups were constructed. Degradation experiments on the aqueous solutions of tetracycline and norfloxacin revealed that the polymer with three thiophene groups in the monomer indicated the best degradation efficiency of 73.7% for tetracycline and 56.9% for norfloxacin. Moreover, this polymer had a relatively stronger ability to separate and transport photocharging carriers under visible light. Therefore, the photocatalytic performance of conjugated polymers could be regulated by changing the number of characteristic groups. Background:
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Li, Guangtao, Tianyu Wang, Andrea Schulz, et al. "Porphyrin–acetylene–thiophene polymer wires." Chem. Commun., no. 5 (2004): 552–53. http://dx.doi.org/10.1039/b313415f.

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Chen, Wei Xing, Su Yan Zhang, Ai Jie Ma, and Qi Guan Wang. "The Synthesis and Characterization of Thiophene Derivative Polymers." Advanced Materials Research 284-286 (July 2011): 1846–49. http://dx.doi.org/10.4028/www.scientific.net/amr.284-286.1846.

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Thiophene derivative polymer is an important kind of conductive polymers. They often have good electrochemical activity, environment stability and ease of processing. Here, 3-bromothiophene and 3-thiophenezoic acid as monomers, using chemical oxidation approach, the poly (3-thiophenezoic acid) (PTPA), the copolymer of 3-bromine thiophene (BTP) and 3-thiophenezoic acid (TPA) are synthesized in the media of chloroform or methanol. The structures of both polymers are characterized with FT IR, NMR and UV-vis. The results showed that the reactivity of TPA can be improved after alkalizing. The copol
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Xie, Xiao Hua, Wei Shen, Rong Xing He, and Ming Li. "A Class of Semiconducting Polymers as Potential Materials for Polymer Solar Cells." Advanced Materials Research 716 (July 2013): 177–84. http://dx.doi.org/10.4028/www.scientific.net/amr.716.177.

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In this work, fifteen polymers have been studied to test their potential as donors for polymer solar cells by density functional theory. Those polymers contained five homopolymers based on pyridazine, [1,2,thiadiazolo [3,4-pyridazine, [1,2,oxadiazole [3,4-pyridazine, isothiazolo [3,4-pyridazine and isoxazolo [3,4-pyridazine, and ten copolymers composed of the above compounds and thiophene incorporated with 1:1 and 1:2 ratios. The fifteen polymers have been examined in terms of the abilities of absorbing sunlight, stabilities in the environment, and photovoltaic properties. The results suggest
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Chao, Ying-Chieh, Jhe-Han Chen, Yi-Jie Chiou, et al. "Design of Thienothiophene-Based Copolymers with Various Side Chain-End Groups for Efficient Polymer Solar Cells." Polymers 12, no. 12 (2020): 2964. http://dx.doi.org/10.3390/polym12122964.

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Three two-dimensional donor–acceptor conjugated copolymers consisting of a benzo[1,2-b:4,5-b′]dithiophene derivative and thieno[3,2-b]thiophene with a conjugated side chain were designed and synthesized for use in bulk heterojunction (BHJ) or nonfullerene polymer solar cells (PSCs). Through attaching various acceptor end groups to the conjugated side chain on the thieno[3,2-b]thiophene moiety, the electronic, photophysical, and morphological properties of these copolymers were significantly affected. It was found that the intermolecular charge transfer interactions were enhanced with the incre
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Yin, Xiaodong, Yali Qiao, Matthew R. Gadinski, Qing Wang, and Chuanbing Tang. "Flexible thiophene polymers: a concerted macromolecular architecture for dielectrics." Polymer Chemistry 7, no. 17 (2016): 2929–33. http://dx.doi.org/10.1039/c6py00233a.

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Highly flexible and transparent free-standing films can be readily obtained from oligothiophene-containing norbornene polymers and their hydrogenated derivatives prepared by ROMP. The rigidness/softness of the polymer backbone and polar side chains dictate dielectric properties.
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LI, YUNING, and BENG S. ONG. "HIGH MOBILITY CONJUGATED POLYMER SEMICONDUCTORS FOR ORGANIC THIN FILM TRANSISTORS." COSMOS 05, no. 01 (2009): 59–77. http://dx.doi.org/10.1142/s0219607709000427.

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Organic thin film transistors (OTFTs) are promising candidates as alternatives to silicon TFTs for applications where light weight, large area and flexibility are required. OTFTs have shown potential for cost effective fabrication using solution deposition techniques under mild conditions. However, two major issues must be addressed prior to the commercialization of OTFT-based electronics: (i) low charge mobilities and (ii) insufficient air stability. This article reviews recent progress in the design and development of thiophene-based polymer semiconductors as channel materials for OTFTs. To
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Huang, Hongyan, Meng Qiu, Quan Li, et al. "Donor–acceptor conjugated polymers based on thieno[3,2-b]indole (TI) and 2,1,3-benzothiadiazole (BT) for high efficiency polymer solar cells." Journal of Materials Chemistry C 4, no. 23 (2016): 5448–60. http://dx.doi.org/10.1039/c6tc00929h.

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Three conjugated polymers based on the thieno[3,2-b]indole (TI) unit as electron-donor block and benzothiadiazole (BT) as electron-accepting block and thiophene rings as spacers. Their photovoltaic performance were finely tuned by thiophene spacers.
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Dissertations / Theses on the topic "Thiophene polymer"

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Unsal, Gungor Elif Mufide. "The Effect Of Potassium Hydroxide On The Polymerization Of Trichlorophenol, Pyrrole And Thiophene By Microwave Initiation." Phd thesis, METU, 2008. http://etd.lib.metu.edu.tr/upload/3/12609670/index.pdf.

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The synthesis of black conducting polymer (CP) and/or crosslinked polymers (CLP) and/or radical ion polymer (RIP) and/or white polymers (WP) and/or orange polymer (OP) were achieved by using KOH with TCP, pyrrole and thiophene via microwave energy in a very short time interval. Polymerizations were carried out by constant microwave energy with different time intervals varying from 1 to 25 min<br>or at constant time intervals with variation of microwave energy from 90 to 900 watt<br>or varying the water content from 0, 0.5 to 5 ml at constant time intervals and microwave energy, or at constant
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Rebourt, Eymard. "Vers des polymères conducteurs tridimensionnels : préparation et caractérisation de poly(n-octyl-3-thiophènes) réticulés totalement conjugués." Université Joseph Fourier (Grenoble), 1994. http://www.theses.fr/1994GRE10182.

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Il nous a paru interessant de jouer sur la dimensionnalite des polymeres conducteurs electroniques afin d'obtenir des materiaux dont les proprietes (notamment la conductivite) seraient particulieres. D'ou l'idee de preparer des structures totalement conjuguees de dimension fractale voire tridimensionnelles. Pour obtenir ces structures, nous avons reticule des chaines de poly(n-octyl-3-thiophene) avec quatre types de trithienylbenzenes prealablement prepares et caracterises: le tri(thienyl-2)-1,3,5-benzene, le tri(thienyl-2)-1,2,4-benzene, le tri(thienyl-3)-1,3,5-benzene et le tri(thienyl-3)-1,
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Konkol, Kristine Louise. "Synthesis and Design of Thiophene Materials: Effects of Ring Fusion and Metal Coordination." Diss., North Dakota State University, 2019. https://hdl.handle.net/10365/31608.

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Conjugated organic materials comprise a field of materials chemistry focused on the development of semiconducting organic plastics, popular applications of which are plastic solar cells and display technologies. One of the reasons these materials have gained so much attention is that their optical and electronic properties can be tuned through engineering at the molecular level. Thiophene, an aromatic heterocycle, is a popular building block in the synthesis of many conjugated materials, prized for both the ease in which it can be synthetically functionalized and its ability to form highly con
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Banks, Surya R. "Organometallic Materials: Ferroceno[c]thiophenes and 1,2-Bisthienylmetallocenes." UKnowledge, 2016. http://uknowledge.uky.edu/chemistry_etds/68.

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Development of synthetic routes toward two general organometallic frameworks was undertaken. The first project involved synthetic attempts of substituted and unsubstituted ferroceno[c]thiophene while the second one was the synthesis of 1,2-dithienylmetallocenes. The long-term goal of this work is to lay the foundations for study of electronic, electrochromic, redox, and optical properties of thiophene-based materials integrated with organometallic systems such as ferrocene, ruthenocene and cymantrene. The synthetic pathway for the target molecule in the first project involved converting 1,2-bi
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Palma, Cando Alex Uriel [Verfasser]. "Electrogenerated Films of Carbazole- and Thiophene-Based Microporous Polymer Networks / Alex Uriel Palma Cando." Wuppertal : Universitätsbibliothek Wuppertal, 2017. http://d-nb.info/1128844540/34.

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Turkarslan, Ozlem. "Synthesis, Characterization And Electrochromic Properties Of Conducting Copolymers Of Terephthalic Acid Bis-(thiophen-3-ylmethyl)thioester With Thiophene And Pyrrole And Conducting Polymer Of 1-(4-fluorophenyl)-2,5-di(thiophen-2-yl)-1h-pyrrole." Master's thesis, METU, 2006. http://etd.lib.metu.edu.tr/upload/12607169/index.pdf.

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Terephthalic acid bis-(thiophen-3-ylmethyl)thioester (TTMT) was synthesized via the reaction of thiophen-3-ylmethanethiol with terephthaloyl dichloride. Nuclear magnetic resonance (1H-NMR) and Fourier transform infrared (FTIR) spectroscopies were utilized for the characterization of the monomer. This 3-functionalized thiophene monomer was polymerized in the presence of thiophene (Th) and pyrrole (Py) upon constant potential application in acetonitrile/tetrabutylammonium tetrafluoroborate (TBAFB). The resulting copolymers were characterized via cyclic voltammetry (CV), FTIR, differential scanni
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Marque, Pascal. "Proprietes spectroelectrochimiques des couches minces de polythiophenes : application electrochromique." Paris 6, 1988. http://www.theses.fr/1988PA066396.

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Preparation par polymerisation electrolytique de couches minces de polythiophene; les conditions de reaction determinent les proprietes optiques et electrochimiques par action sur notamment la longueur moyenne de conjugaison. Etude du mecanisme d'insertion ionique accompagnant l'oxydoreduction et de la thermodynamique de la reaction, permettant d'etablir les compromis structuraux et fonctionnels pour l'optimisation des performances
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Enee, Véronique. "Synthèse d'oligo(3-octylthiophènes) régioréguliers : briques moléculaires pour l'élaboration de polymères conjugués incluant des complexes de métaux de transition." Université Joseph Fourier (Grenoble), 1997. http://www.theses.fr/1997GRE10012.

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Le but de ce travail consiste en la synthese d'un polymere conjugue a complexes organometalliques, afin de creer un materiau original jouissant des proprietes du polymere et du complexe organometallique. Ainsi, selon la longueur des bras espaceurs conjugues de la matrice polymere, un couplage entre sites metalliques voisins pourra se produire ou non. De plus, (et cela constitue notre objectif majeur), les proprietes intrinseques du polymere pourraient se coupler a celles du complexe: il serait alors possible de modifier les proprietes du polymere, en agissant sur celles du metal (ou inversemen
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Roncali, Jean. "Polymères organiques conducteurs fonctionnalisés." Paris 13, 1989. http://www.theses.fr/1989PA132014.

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Etude de la cinétique de la polymérisation électrolytique de dérivés du chiophène et amélioration de son efficacité et de sa sélectivité en vue d'obtenir la meilleure conductivité électrique possible; relation entre la conductivité et les propriétés spectroscopiques et électrochimiques des polymères. Modification des polythiophènes par voie électrochimique et greffage covalent de groupes fonctionnels sur le monomère; étude des facteurs stériques et électroniques associés aux differents substituants en vue de conserver les propriétés conductrices du polymère. Préparation électrochimique de poly
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Brisset, Hugues. "La rigidification : une nouvelle stratégie de contrôle des propriétés électroniques des systèmes conjugués linéaires." Angers, 1996. http://www.theses.fr/1996ANGE0029.

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Ce travail porte sur l'élaboration de nouveaux systèmes conjugués linéaires à faible bande interdite au moyen d'une stratégie originale basée sur la rigidification du système conjugué. Apres un premier chapitre consacre à un bref rappel des différentes approches de la synthèse de polymères conjugues à faible bande interdite, le second chapitre est consacré à l'élaboration de nouveaux polymères conjugués obtenus par électropolymérisation de précurseurs synthétisés à partir de deux structures de bases: le cyclopentadithiophène et le 6,6'-bis(4,5-dihydro-6h-cyclopentabthienylidene). L'analyse str
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Books on the topic "Thiophene polymer"

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F, Perepichka Dmitrii, ed. Handbook of thiophene-based materials. Wiley, 2009.

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Book chapters on the topic "Thiophene polymer"

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Livi, Francesco, Jon E. Carlé, and Eva Bundgaard. "Thiophene in Conducting Polymers: Synthesis of Poly(thiophene)s and Other Conjugated Polymers Containing Thiophenes, for Application in Polymer Solar Cells." In Topics in Heterocyclic Chemistry. Springer International Publishing, 2014. http://dx.doi.org/10.1007/7081_2014_128.

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Taliani, C., G. Ruani, R. Zamboni, L. Yang, R. Dorsinville, and R. R. Alfano. "Nonlinear Optical Properties of Thiophene Based Conjugated Polymers." In Frontiers of Polymer Research. Springer US, 1991. http://dx.doi.org/10.1007/978-1-4615-3856-1_10.

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Bridges, C. R., and D. S. Seferos. "Chapter 2. Controlled Chain-growth Synthesis of Conjugated Polymers: Moving Beyond Thiophene." In Polymer Chemistry Series. Royal Society of Chemistry, 2016. http://dx.doi.org/10.1039/9781782624004-00038.

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Sarkar, Abhijit, Leong L. San, Hardy S. O. Chan, and Siu C. Ng. "A Soluble and Electrically Conducting Polymer System Incorporating Thiophene and Acetylenic Moeities." In Polymers and Other Advanced Materials. Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-0502-4_36.

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Ruani, G., A. J. Pal, R. Zamboni, C. Taliani, and F. Kajzar. "Photoinduced Absorption and Nonlinear Optical Response in a Polycondensed Thiophene-Based Polymer (PTT)." In Conjugated Polymeric Materials: Opportunities in Electronics, Optoelectronics, and Molecular Electronics. Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-2041-5_33.

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Taliani, C., R. Zamboni, G. Ruani, et al. "Design and Optical Properties of a Low Energy Gap Conjugated Polymer: Polydithieno(3,4-b:3’,4’-d)Thiophene." In Nonlinear Optical Effects in Organic Polymers. Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-2295-2_13.

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Barnes, George, Chin Pang Yau, and Martin Heeney. "Poly(thiophene)s." In Encyclopedia of Polymeric Nanomaterials. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-29648-2_120.

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Barnes, George, and Chin Pang Yau. "Poly(thiophene)s." In Encyclopedia of Polymeric Nanomaterials. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-36199-9_120-1.

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Fave, J. L. "Excitons in Chains of Thiophene Rings." In Electronic Properties of Polymers. Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-84705-9_11.

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Siekierski, M., J. Plocharski, M. Catellani, and S. Destri. "Electrochemical Synthesis of Poly(dithieno thiophene)." In Electronic Properties of Polymers. Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-84705-9_62.

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Conference papers on the topic "Thiophene polymer"

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Anquetil, Patrick A., Hsiao-hua Yu, John D. Madden, Peter G. Madden, Timothy M. Swager, and Ian W. Hunter. "Thiophene-based conducting polymer molecular actuators." In SPIE's 9th Annual International Symposium on Smart Structures and Materials, edited by Yoseph Bar-Cohen. SPIE, 2002. http://dx.doi.org/10.1117/12.475194.

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Cheylan, S., A. Fraleoni-Morgera, J. Puigdollers, et al. "Comprehensive study of a novel thiophene-based polymer." In Optics & Photonics 2005, edited by Zakya H. Kafafi and Paul A. Lane. SPIE, 2005. http://dx.doi.org/10.1117/12.617190.

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Chandrashekara, G. K., M. G. Murali, Arun D. Rao, and Praveen C. Ramamurthy. "Influence of thiophene spacer on conjugated polymer for organic photovoltaics." In 2016 IEEE 43rd Photovoltaic Specialists Conference (PVSC). IEEE, 2016. http://dx.doi.org/10.1109/pvsc.2016.7749900.

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Sunitha, M. S., A. V. Adhikari, K. A. Vishnumurthy, et al. "Nonlinear Optical Properties of a Newly Synthesized Thiophene Based Conjugated Polymer." In OPTICS: PHENOMENA, MATERIALS, DEVICES, AND CHARACTERIZATION: OPTICS 2011: International Conference on Light. AIP, 2011. http://dx.doi.org/10.1063/1.3643655.

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Jiang, Xuezhong, He Yan, Eric H. Klingenberg, and Delwin L. Elder. "Enhanced lifetime of polymer light-emitting diodes using poly(thieno[3,4-b]thiophene)-based conductive polymers." In SPIE Optics + Photonics, edited by Zakya H. Kafafi and Franky So. SPIE, 2006. http://dx.doi.org/10.1117/12.682742.

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Do, Lee Mi, Do Hoon Hwang, Kang Hoon Choi, et al. "Polymer light-emitting diodes of poly(m-phenylene-thiophene) derivative and tris(8-hydroxyquinoline) aluminum heterostructure." In Optical Science, Engineering and Instrumentation '97, edited by Zakya H. Kafafi. SPIE, 1997. http://dx.doi.org/10.1117/12.295543.

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Chotpattananont, Datchanee, and Anuvat Sirivat. "Electrorheological Properties of Suspensions Prepared From Polythiophene Conductive Polymer." In ASME 2005 International Mechanical Engineering Congress and Exposition. ASMEDC, 2005. http://dx.doi.org/10.1115/imece2005-79491.

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Electrorheological (ER) fluids are typically composed of polarizable particles dispersed in a non-conducting fluid. Upon the application of an electric field, chain-like or fibrillar aggregates of the suspended particles are oriented along the direction of the electric field, thereby inducing viscoelasticity and a drastic increase in viscosity. In our study, Poly(3-thiophene acetic acid), PTAA, has been developed for using as ER material. The rheological properties of this PTAA suspension upon the application of electric field were investigated under various deformations; oscillatory shear flo
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Vishnumurthy, K. A., A. Vasudeva Adhikari, M. S. Sunitha, et al. "Synthesis and Characterization of a New Conjugated Polymer Bearing Pyrazole and Thiophene Moieties as Potent NLO Material." In OPTICS: PHENOMENA, MATERIALS, DEVICES, AND CHARACTERIZATION: OPTICS 2011: International Conference on Light. AIP, 2011. http://dx.doi.org/10.1063/1.3643638.

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Fallon, Kealan, Nilushi Wijeyasinghe, Eric Manley, Tobin Marks, Thomas D. Anthopoulos, and Hugo A. Bronstein. "Indolo-naphthyridine-6,13-dione thiophene building block for conjugated polymer electronics: Molecular origin of ultrahigh n-type mobility (Conference Presentation)." In Organic Field-Effect Transistors XVI, edited by Oana D. Jurchescu and Iain McCulloch. SPIE, 2017. http://dx.doi.org/10.1117/12.2273880.

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R, Prashanth Kumar K., Udayakumar D, Siji Narendran N. K, and Chandrasekharan K. "Synthesis and evaluation of optical and electrochemical properties of a new conjugated polymer containing substituted thiophene and non-conjugation linkers." In LIGHT AND ITS INTERACTIONS WITH MATTER. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4898268.

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