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Relevant bibliographies by topics / Thiophen Derivatives

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Academic literature on the topic 'Thiophen Derivatives'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Thiophen Derivatives"

1

Vu Quoc, Trung, Duong Tran Thi Thuy, Thuan Dang Thanh, et al. "Some chalcones derived from thiophene-3-carbaldehyde: synthesis and crystal structures." Acta Crystallographica Section E Crystallographic Communications 75, no. 7 (2019): 957–63. http://dx.doi.org/10.1107/s2056989019007503.

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The synthesis, spectroscopic data and crystal and molecular structures of four 3-(3-phenylprop-1-ene-3-one-1-yl)thiophene derivatives, namely 1-(4-hydroxyphenyl)-3-(thiophen-3-yl)prop-1-en-3-one, C13H10O2S, (1), 1-(4-methoxyphenyl)-3-(thiophen-3-yl)prop-1-en-3-one, C14H12O2S, (2), 1-(4-ethoxyphenyl)-3-(thiophen-3-yl)prop-1-en-3-one, C15H14O2S, (3), and 1-(4-bromophenyl)-3-(thiophen-3-yl)prop-1-en-3-one, C13H9BrOS, (4), are described. The four chalcones have been synthesized by reaction of thiophene-3-carbaldehyde with an acetophenone derivative in an absolute ethanol solution containing potass

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Clark, Peter D., Nicholas M. Irvine, and Pratibha Sarkar. "The synthesis of 3H-naphthol[1,8-bc]thiophene derivatives." Canadian Journal of Chemistry 69, no. 6 (1991): 1011–16. http://dx.doi.org/10.1139/v91-148.

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Methods for the synthesis of keto derivatives of the little studied naphtho[1,8-bc]thiophene system have been developed. Using the readily available benzothiophene derivative 6,7-dihydrobenzo[b]thiophen-4(5H)-one 4, a 3-keto-naphtho[1,8-bc]thiophene 14 was synthesized by a tin(IV) chloride catalyzed cyclization of the acid chloride derivative of the saturated acid 13b. The bicyclic ketone 4 was also used to prepare the keto-sulfoxide 7, which was cyclized to the 4-keto-naphtho[1,8-bc]thiophene system 9 in a Pummerer-type rearrangement. Key words: synthesis, organosulfur, naphtho[1,8-bc]thiophe

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Arrousse, N., Y. Fernine, Nabil Al-Zaqri, et al. "Thiophene derivatives as corrosion inhibitors for 2024-T3 aluminum alloy in hydrochloric acid medium." RSC Advances 12, no. 17 (2022): 10321–35. http://dx.doi.org/10.1039/d2ra00185c.

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Thiophene derivatives: thiophene-2-carbaldehyde oxime (OXM) and 5-(thiophen-2-yl)-1H-tetrazole (TET), were synthesized and characterized. Furthermore, their inhibitory property for AA2024-T3 in 1 M HCl solution was investigated via electrochemical and with theoretical study.

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Salbeck, Josef, and Erhard Günther. "Elektrochemische und spektroelektrochemische Untersuchungen neuer S-heterochinoider Elektronenakzeptoren, N-Cyanimin-substituierte Thieno[3,2-b]thiophen-2,5-dione / Electrochemical and Spectroelectrochemical Investigations of New S-Heteroquinoid Electron Acceptors, N-Cyanimine Substituted Thieno[3,2-b]thiophene-2,5-diones." Zeitschrift für Naturforschung B 46, no. 3 (1991): 353–60. http://dx.doi.org/10.1515/znb-1991-0315.

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Wang, Qing Xiu, Li Jie Duan, Bo Yang Qu, Juan Wang, and Fu De Liu. "Synthesis and Optical/Electrochemical Properties of Conjugated Polymers with Diphenyl and Thiophene in Main Chain." Advanced Materials Research 1035 (October 2014): 497–501. http://dx.doi.org/10.4028/www.scientific.net/amr.1035.497.

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Two thiophene derivatives 4,4'-di (thiophen-2-yl) biphenyl and 4,4'-di (thiophen-2-yl) -2-nitrobiphenyl ,which were used as monomers for preparing poly (4,4'-di (thiophen-2-yl) biphenyl) (DPBT) and poly (4,4'-di (thiophen-2-yl)-2-nitrobiphenyl) (DPNT) by ferric chloride oxidation polymerization, were synthesized via Suzuki reaction with 4,4'-dibromobiphenyl as the raw material. UV-vis absorption spectra, fluorescence spectra, photoluminescence spectra and electrochemical properties of the polymers were recorded and used for calculating the band-gap (Eg), HOMO orbital energy (EHOMO) and LUMO or

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Lahsasni, Siham, Dunya A. M. Al-Hemyari, Hazem A. Ghabbour, et al. "Synthesis, Characterization, and Antibacterial and Anti-Inflammatory Activities of New Pyrimidine and Thiophene Derivatives." Journal of Chemistry 2018 (August 1, 2018): 1–11. http://dx.doi.org/10.1155/2018/8536063.

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Substituted[4,5]thieno[2,3-d]thiazolo[3,2-a]pyrimidin-5-one (3a–b) and pyrimidin-5(6H)-imine (3c–e) were synthesized via reaction of the starting compounds, ethyl 2-amino-substituted[b]thiophene-3-carboxylate (2a–c) and 2-amino-substituted [b]thiophene-3-carbonitrile (2d–f), respectively, with 2-bromothiazole. Synthesis of (bromo-substituted[b]thiophen-2-yl)alkanamide derivatives (4a–e) and thieno[2,3-d][1,3]oxazin-4-imine derivative (5) was accomplished via reaction of the starting compounds with bromoalkyl chloride through nucleophilic substitution; however, for the synthesis of compound 5,

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Cherniawski, Benjamin P., Steven A. Lopez, Edmund K. Burnett, et al. "The effect of hexyl side chains on molecular conformations, crystal packing, and charge transport of oligothiophenes." Journal of Materials Chemistry C 5, no. 3 (2017): 582–88. http://dx.doi.org/10.1039/c6tc04612f.

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Wojciechowski, Krzysztof, and Michał Nowacki. "Synthesis of [1]Benzothieno[2,3-b]quinolines via Transition-Metal-Free [3+3] Annulation of Nitroarenes and Benzo[b]thiophen-3-ylacetonitrile or 3-(Phenylsulfonylmethyl)benzo[b]thiophene Carbanions." Synthesis 49, no. 16 (2017): 3794–800. http://dx.doi.org/10.1055/s-0036-1588426.

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Benzo[b]thiophen-3-ylacetonitriles or 3-(phenylsulfonylmethyl)benzo[b]thiophenes react with nitrobenzene derivatives in the presence of potassium tert-butoxide and chlorotrimethylsilane to form, in good yields, 11-cyano- or 11-(phenylsulfonyl)[1]benzothieno[2,3-b]quinolines, respectively.

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Ryu, Seunghyup, Chaeyoung Yun, Soomin Ryu, Jihae Ahn, Choongik Kim, and Sungyong Seo. "Characterization of [1]Benzothieno[3,2-b]benzothiophene (BTBT) Derivatives with End-Capping Groups as Solution-Processable Organic Semiconductors for Organic Field-Effect Transistors." Coatings 13, no. 1 (2023): 181. http://dx.doi.org/10.3390/coatings13010181.

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Solution-processable [1]benzothieno[3,2-b]benzothiophene (BTBT) derivatives with various end-capping groups, 2-(phenylethynyl)benzo[b]benzo[4,5]thieno[2,3-d]thiophene (Compound 1), 2-octyl-7-(5-(phenylethynyl)thiophen-2-yl)benzo[b]benzo[4,5]thieno[2,3-d]thiophene (Compound 2), and triisopropyl((5-(7-octylbenzo[b]benzo[4,5]thieno[2,3-d]thiophen-2-yl)thiophen-2-yl)ethynyl)silane (Compound 3), have been synthesized and characterized as active layers for organic field-effect transistors (OFETs). Thermal, optical, and electrochemical properties of the newly synthesized compounds were characterized

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Al-Refai, Mahmoud, Basem F. Ali, Ala'a B. Said, Armin Geyer, Michael Marsch, and Klaus Harms. "Synthesis, characterization, crystal structure and supramolecularity of ethyl (E)-2-cyano-3-(3-methylthiophen-2-yl)acrylate and a new polymorph of ethyl (E)-2-cyano-3-(thiophen-2-yl)acrylate." Acta Crystallographica Section E Crystallographic Communications 75, no. 9 (2019): 1357–61. http://dx.doi.org/10.1107/s2056989019011435.

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The synthesis, crystal structure and structural motif of two thiophene-based cyanoacrylate derivatives, namely, ethyl (E)-2-cyano-3-(3-methylthiophen-2-yl)acrylate (1), C11H11NO2S, and ethyl (E)-2-cyano-3-(thiophen-2-yl)acrylate (2), C10H9NO2S, are reported. Derivative 1 crystallized with two independent molecules in the asymmetric unit, and derivative 2 represents a new monoclinic (C2/m) polymorph. The molecular conformations of 1 and the two polymorphs of 2 are very similar, as all non-H atoms are planar except for the methyl of the ethyl groups. The intermolecular interactions and crystal p

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Dissertations / Theses on the topic "Thiophen Derivatives"

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Thomas, Mary Solly. "Complexes of thiophene derivatives as potential metallomesogens." Thesis, Pretoria : [s.n.], 2006. http://upetd.up.ac.za/thesis/available/etd-12072006-171634.

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Weddell, Derek Alexander. "Synthesis, structure determination and mechanism in thiophene derivatives." Thesis, Nottingham Trent University, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.343542.

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Alaviuhkola, T. (Terhi). "Aromatic borate anions and thiophene derivatives for sensor applications." Doctoral thesis, University of Oulu, 2007. http://urn.fi/urn:isbn:9789514286575.

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Abstract This study was part of a project targeted at developing chemical sensors for organic cations and metal ions by exploiting the interactions between cations and anionic borate derivatives. As well, the chemical synthesis of thiophene monomers with charged or neutral ion-recognition sites was investigated. The primary task in the first part of the work was to prepare anionic receptor molecules based on synthesized borate derivatives and study their complexation with N-heteroaromatic and tropylium cations. The complexation was studied in solution by 1H NMR and ESIMS techniques and in so

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Cannon, Benjamin Tyree. "Thiophene and Derivatives for Use in Pyridazines and Thiapentalenes." TopSCHOLAR®, 2015. http://digitalcommons.wku.edu/theses/1476.

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This thesis introduces the idea of Band Theory and how it can be used to describe a solid-state materials ability to carry an electrical charge. Next, this thesis defines what makes a material a conductor, semiconductor, or insulator. Semiconductors are attracting interest in chemistry, as well as in the manufacturing of consumer electronics, because of their ability to carry a charge, without the risk of short-circuiting like traditional conductors.1,4 Organic semiconductors, which behave differently than traditional semiconductors, are of particular interest because they offer mechanical fle

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Tirkes, Seha. "Synthesis, Characterization, And Polymerization Of Polyether Bridged Thiophene And Aniline Derivatives." Phd thesis, METU, 2008. http://etd.lib.metu.edu.tr/upload/3/12609399/index.pdf.

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New compounds consisting of 3-thienyl and aniline units linked by polyether bridges have been synthesized and their electrochemical polymerization was performed via constant potential electrolysis and cyclic voltammetry. In the case of 3-thienyl derivatives two compounds, 1,12-di-3-thienyl-2,5,8,11-tetraoxadodecane (MI) and 1,15-di-3-thienyl-2,5,8,11,14-pentaoxapentadecane (MII) were synthesized utilizing literature methods and their corresponding polymers, poly(I) and poly(II) were prepared in an electrolytic solution containing 0.1 M terabutylammonium hexafluorophosphate (TBAPF6) dissolved i

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Soucy-Breau, Chantal. "Synthesis of naturally occurring phototoxic thiophenes and their derivatives." Thesis, University of Ottawa (Canada), 1990. http://hdl.handle.net/10393/5712.

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Analogues and derivatives of naturally occurring $\alpha$-terthienyl 3 have been synthesized by using the nickel-catalyzed Grignard-Wurtz cross-coupling reaction. This method has proven useful for the introduction of non-polar substituents on 2-bromothiophene which upon subsequent cross-coupling with 5-iodo-$\alpha$-dithienyl 185 led to a successful variety of 5-substituted $\alpha$-terthienyls. Derivatives of $\alpha$-terthienyl bearing polar functional groups were synthesized either by: (1) introduction of electron-withdrawing and electron-donating at C-5 and C-5$\sp{\prime\prime}$; or (2) c

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Hunziker, Christoph. "Crystalline thiophene and phenolic polyene derivatives for organic electronic and photonic applications /." Zürich : ETH, 2008. http://e-collection.ethbib.ethz.ch/show?type=diss&nr=18032.

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Asil, Demet. "A Glow In The Dark: Synthesis And Electropolymerization Of Chemiluminescent Thiophene Derivatives." Master's thesis, METU, 2008. http://etd.lib.metu.edu.tr/upload/3/12609863/index.pdf.

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ABSTRACT A GLOW IN THE DARK: SYNTHESIS AND ELECTROPOLYMERIZATION OF CHEMILUMINESCENT THIOPHENE DERIVATIVES Asil, Demet M.Sc., Department of Chemistry Supervisor : Prof. Dr. Ahmet M. &Ouml<br>nal Co-Supervisor: Assist. Prof. Dr. Atilla Cihaner September 2008, 63 Pages Two novel chemiluminescent monomers, 2,3-dihydrothieno(3,4-d)pyridazine-1,4-dione (T-Lum) and 5,7-di-thiophen-2-yl-2,3-dihydro-thieno[3,4-d]pyridazine-1,4-dione (TTT-Lum), were synthesized. The reaction between T-Lum and TTT-Lum in alkaline solution with H2O2 gave chemiluminescence which can be catalyzed using Fe(III)

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Dang, Xuan Dung. "Electrosynthesis and characterization of thin copolymer films based on pyrrole and thiophene derivatives." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2005. http://nbn-resolving.de/urn:nbn:de:swb:14-1125491701029-31683.

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Die Copolymerisation wurde mit dem Ziel untersucht, polymere Materialien zu synthetisieren, die die individuellen Eigenschaften der entsprechenden Homopolymere kombinieren. Die Dissertation konzentrierte sich auf die Elektrosynthese und Charakterisierung von leitfähigen Copolymerfilmen auf Basis von Pyrrol- und Thiophenderivaten. Mit einer Reihe von elektrochemischen, spektroskopischen und mikroskopischen Untersuchungsmethoden (Zyklovoltammetrie, elektrochemische Impedanz-spektroskopie, photoelektrochemische Spektroskopie, Elektrospray- Ionisations-Massenspektroskopie, Festkörper- NMR, Raman-S

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Aslan, Evren. "Characterization Of Conducting Polymers Of Ester Linkage Containing Thiophene Derivatives Via Mass Spectroscopy." Master's thesis, METU, 2004. http://etd.lib.metu.edu.tr/upload/12605704/index.pdf.

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ABSTRACT CHARACTERIZATION OF CONDUCTING POLYMERS OF ESTER LINKAGE CONTAINING THIOPHENE DERIVATIVES VIA MASS SPECTROSCOPY Aslan, Evren M.Sc., Department of Chemistry Supervisor: Prof. Dr. Levent Toppare Co-Supervisor: Prof.Dr. Jale Hacaloglu December 2004, 86 pages In order to investigate the thermal and structural characteristics of terepthalic acid bis-(2-thiophen-3-yl-ethyl)ester (TATE), decanedioic acid bis-(2-thiophen-3-yl- ethyl) ester (DATE) and octanoic acid 2-thiophen-3-yl-ethyl ester (OTE), their corresponding homopolymers, copolymers with thiophene and polythiophene, pyroly

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Books on the topic "Thiophen Derivatives"

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1928-, Gronowitz Salo, ed. Thiophene and its derivatives. Wiley, 1985.

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1928-, Gronowitz Salo, ed. Thiophene and its derivatives. Wiley, 1992.

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1928-, Gronowitz Salo, ed. Thiophene and its derivatives. Wiley, 1986.

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1928-, Gronowitz Salo, ed. Thiophene and its derivatives. Wiley, 1986.

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Salo, Gronowitz, ed. Thiophene and its derivatives. Wiley, 1985.

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Hartough, Howard D. Thiophene and Its Derivatives. Wiley & Sons, Incorporated, John, 2009.

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1928-, Gronowitz Salo, ed. Thiophene and its derivatives. Wiley, 1991.

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Hartough, Howard D. Thiophene and Its Derivatives. Wiley & Sons, Incorporated, John, 2008.

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Gronowitz, Salo. Thiophene and Its Derivatives, Part 3. Wiley & Sons, Incorporated, John, 2009.

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Gronowitz, Salo. Thiophene and Its Derivatives, Part 4. Wiley & Sons, Incorporated, John, 2009.

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Book chapters on the topic "Thiophen Derivatives"

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Frank, J. Howard, J. Howard Frank, Michael C. Thomas, et al. "Polyacetylenes (and Their Thiophene Derivatives)." In Encyclopedia of Entomology. Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6359-6_3033.

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Gronowitz, Salo, and Anna-Britta Hornfeldt. "Physical Properties of Thiophene Derivatives." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187265.ch1.

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Spinelli, Domenico, Giovanni Consiglio, Carlo Dell'Erba, and Marino Novi. "Nucleophilic Substitution of Thiophene Derivatives." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187265.ch2.

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Li, Jie Jack. "Hinsberg synthesis of thiophene derivatives." In Name Reactions. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_125.

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Frejd, Torbjörn. "Organometallic Derivatives of Thiophenes." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187272.ch2.

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Press, Jeffery B. "Pharmacologically Active Compounds and other Thiophene Derivatives." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187234.ch5.

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Taylor, Roger. "Electrophilic Substitution of Thiophene and its Derivatives." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187241.ch1.

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Press, Jeffery B. "Biologically Active Thiophene Derivatives Revisited: 1983-1988." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187265.ch3.

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Derhaeg, L., C. Samyn, and A. Persoons. "EFISH-Studies of Stilbene- and Thiophene-Derivatives." In Organic Molecules for Nonlinear Optics and Photonics. Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-011-3370-8_12.

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Palupanuri, Naveena, Swathi Konda, Lavanya Sara, and B. Nikitha. "Synthesis and Biological Evaluation of Substituted Thiophene Derivatives." In GeNeDis 2020. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-78787-5_23.

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Conference papers on the topic "Thiophen Derivatives"

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Hubbard, Arthur T., and James H. White. "Surface Spectroscopy: LEED, EELS and AES." In CORROSION 1991. NACE International, 1991. https://doi.org/10.5006/c1991-91264.

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Abstract Applications of low energy electron diffraction (LEED), Auger electron spectroscopy (AES), and electron energy loss spectroscopy (EELS) in the study of corrosion processes and corrosion inhibitor films are described. Studies in our laboratories of surface phemomena related to the depassivation, electrodissolution and corrosion of Fe-Ni-Cr alloys and the formation of polymer films on well- defined electrode surfaces will be presented to illustrate techniques and applications. For example, exposure of clean Fe-Cr-Ni(111) and Fe-Cr-Ni(111) to aqueous electrolytes forms an amorphous, hydr

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Kawate, Kenji, Ken-ichi Ohkura, Mikio Yamazaki, Masami Kuroda, and Osamu Nabeta. "Organic electroluminescent devices with thiophene derivatives." In IS&T/SPIE 1994 International Symposium on Electronic Imaging: Science and Technology, edited by Peter S. Friedman. SPIE, 1994. http://dx.doi.org/10.1117/12.172145.

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Юлия Александровна, Айзина,, та Ткачук, Дарья Олеговна. "THE METHOD OPTIMIZATION OBTAINING 4,5,9,10-TETRAHYDROTIENO[3/,4,5,6]CYCLOOCT[1,2-С]-THIOPHENE". У Перспективные научные исследования молодых ученых: сборник статей всероссийской научной конференции (Северодвинск, Ноябрь 2022). Crossref, 2022. http://dx.doi.org/10.37539/221123.2022.89.55.004.

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Проведена оптимизация метода получения труднодоступного 3,4-дизамещенного производного тиофена - 4,5,9,10-тетрагидротиено[3/,4,5,6]циклоокта[1,2-с]-тиофена. The method for obtaining a hard-to-reach 3,4-disubstituted thiophene derivative, 4,5,9,10-tetrahydrothieno[3/,4,5,6]cycloocta[1,2-c]-thiophene, has been optimized.

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Wang Dejun, Li Tiejin, H. Segawa, Wu Feipeng, and T. Shimidzu. "The rectifying characteristics of the electropolymerized ultro-thin films of thiophene and thiophene derivatives." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.834851.

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Kuroda, Masami, Kenji Kawate, Osamu Nabeta, and N. Furusho. "Electrophotographic properties of thiophene derivatives as charge transport material." In Printing Technologies for Images, Gray Scale, and Color, edited by Derek B. Dove, Takao Abe, and Joachim L. Heinzl. SPIE, 1991. http://dx.doi.org/10.1117/12.46349.

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Jen, Alex K.-Y., Varanasi Pushkara Rao, Tian-An Chen, et al. "High Performance Chromophores and Polymers for E-O Applications." In Organic Thin Films for Photonic Applications. Optica Publishing Group, 1995. http://dx.doi.org/10.1364/otfa.1995.tud.3.

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Although tricyanovinylated thiophene derivatives have been demonstrated to possess large molecular nonlinearities, their use in practical electro-optic devices utilizing high temperature processing conditions is somewhat limited by the low thermal stability (Td ≈ 250 °C) of the tricyanovinyl group. Furthermore, the tricyanovinyl group is very sensitive to many polar solvents which are commonly employed in the curing and processing of polyimide based electro-optic materials. For this reason, we modified some of the highly active tricyanovinyl derivatives with the objective of achieving tradeoff

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Leclerc, Mario, Pierre-Luc T. Boudreault, Reda Badrou Aich, Anne-Catherine Breton, and Ye Tao. "Copolymers Based on 2,7-Carbazole With Alkylated and Perfluoroalkylated Thiophene Derivatives." In 2009 MRS Fall Meetin. Materials Research Society, 2009. http://dx.doi.org/10.1557/proc-1270-ii09-02.

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MOURA, R. O., R. S. A. DE ARAÚJO, F. F. RIBEIRO, et al. "Synthesis and Citotoxicity Evaluation of 3-Cyano-2-aminocycloalkyl[ b]thiophene derivatives." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0288-2.

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Popczyk, A., J. Mysliwiec, and B. Sahraoui. "Influence of the Acceptor Moiety on Nonlinear Optical Properties of Thiophene Derivatives." In 2020 22nd International Conference on Transparent Optical Networks (ICTON). IEEE, 2020. http://dx.doi.org/10.1109/icton51198.2020.9203297.

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Mochizuki, H., and H. Tachibana. "Photoelectronic Properties of Thiophene-Vinylene Derivatives with Phthalimide Groups in Both Terminals." In 2017 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2017. http://dx.doi.org/10.7567/ssdm.2017.ps-10-05.

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