Relevant bibliographies by topics / Selenophene

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

Academic literature on the topic 'Selenophene'

Author: Grafiati
Published: 4 June 2021
Last updated: 18 February 2022

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Journal articles on the topic "Selenophene"

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Skhiri, Aymen, Ridha Ben Salem, Jean-François Soulé, and Henri Doucet. "Reactivity of bromoselenophenes in palladium-catalyzed direct arylations." Beilstein Journal of Organic Chemistry 13 (December 22, 2017): 2862–68. http://dx.doi.org/10.3762/bjoc.13.278.

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The reactivity of 2-bromo- and 2,5-dibromoselenophenes in Pd-catalyzed direct heteroarylation was investigated. From 2-bromoselenophene, only the most reactive heteroarenes could be employed to prepare 2-heteroarylated selenophenes; whereas, 2,5-dibromoselenophene generally gave 2,5-di(heteroarylated) selenophenes in high yields using both thiazole and thiophene derivatives. Moreover, sequential catalytic C2 heteroarylation, bromination, catalytic C5 arylation reactions allowed the synthesis of unsymmetrical 2,5-di(hetero)arylated selenophene derivatives in three steps from selenophene.
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Hollinger, Jon, Dong Gao, and Dwight S. Seferos. "Selenophene Electronics." Israel Journal of Chemistry 54, no. 5-6 (April 3, 2014): 440–53. http://dx.doi.org/10.1002/ijch.201400011.

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Hellwig, Paola S., Thiago J. Peglow, Filipe Penteado, Luana Bagnoli, Gelson Perin, and Eder J. Lenardão. "Recent Advances in the Synthesis of Selenophenes and Their Derivatives." Molecules 25, no. 24 (December 13, 2020): 5907. http://dx.doi.org/10.3390/molecules25245907.

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The selenophene derivatives are an important class of selenium-based heterocyclics. These compounds play an important role in prospecting new drugs, as well as in the development of new light-emitting materials. During the last years, several methods have been emerging to access the selenophene scaffold, employing a diversity of cyclization-based synthetic strategies, involving specific reaction partners and particularities. This review presents a comprehensive discussion on the recent advances in the synthesis of selenophene-based compounds, starting from different precursors, highlighting the main differences, the advantages, and limitations among them.
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Alakhras, Fadi. "Electrochemical behavior and conductivity measurements of electropolymerized selenophene-based copolymers." Materials Science-Poland 33, no. 1 (March 1, 2015): 25–35. http://dx.doi.org/10.1515/msp-2015-0007.

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AbstractElectrochemical copolymerization of selenophene and thiophene was performed at a constant electrode potential. The obtained homopolymer films and copolymers were studied and characterized with cyclic voltammetry and conductivity measurements, from which conductivity values around 13.35 S · cm-1 were determined. The influence of the applied electropolymerization potential and the monomer feed ratio of selenophene and thiophene on the copolymers properties was investigated. The obtained copolymers showed good stability of the redox activity in an acetonitrile-based electrolyte solution. At higher polymerization potentials and at higher concentrations of thiophene in the feed, more thiophene units were incorporated into the copolymer chain. The conductivities of the copolymers were between those of homopolymers, implying that oxidation of both monomers was possible and the copolymer chains might accordingly be composed of both selenophene and thiophene units.
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Hollinger, Jon, Dong Gao, and Dwight S. Seferos. "ChemInform Abstract: Selenophene Electronics." ChemInform 45, no. 37 (August 28, 2014): no. http://dx.doi.org/10.1002/chin.201437245.

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Prediger, Patrícia, Ricardo Brandão, Cristina W. Nogueira, and Gilson Zeni. "Palladium-Catalyzed Carbonylation of 2-Haloselenophenes: Synthesis of Selenophene-2-carboxamides, Selenophene-2,5-dicarboxamides andN,N′-Bridged Selenophene-2-carboxamides." European Journal of Organic Chemistry 2007, no. 32 (November 2007): 5422–28. http://dx.doi.org/10.1002/ejoc.200700599.

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Le Gal, Yann, Thierry Roisnel, Frédéric Barrière, Takehiko Mori, and Dominique Lorcy. "Diselenolene proligands: reactivity and comparison with their dithiolene congeners." New Journal of Chemistry 45, no. 20 (2021): 8971–77. http://dx.doi.org/10.1039/d1nj01335a.

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Wang, Sheng Tao, Bao Yang Lu, Jing Kun Xu, and Wei Qiang Zhou. "Electrosyntheses of Poly(selenophene-co-3-methylthiophene) with Improved Thermoelectric Property in Boron Trifluoride Diethyl Etherate." Advanced Materials Research 937 (May 2014): 17–22. http://dx.doi.org/10.4028/www.scientific.net/amr.937.17.

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Novel poly (selenophene-co-3-methylthiophene) was successfully achieved by directly electrochemical oxidation of the monomer mixtures of selenophene and 3-methylthiophene (3MeT) in boron trifluoride diethyl etherate. The effect of monomer concentration ratios on the copolymerization were investigated by cyclic voltammetry. The structures of as-prepared copolymers were characterized by UV-vis and infrared spectroscopy. The conductivity and thermoelectric measurements revealed the incorporation of 3MeT into the polyselenophene (PSe) chain improved significantly the conductivity and thermoelectric property of PSe.
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Hasegawa, Masashi, Shiori Haga, Tohru Nishinaga, and Yasuhiro Mazaki. "Selenacalix[4]selenophene: Synthesis, Structure, and Gel Formation of Cyclic Selenoether of Selenophene." Organic Letters 22, no. 10 (April 2, 2020): 3755–58. http://dx.doi.org/10.1021/acs.orglett.0c00839.

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Nakayama, Juzo, Takashi Umezawa, Tomoki Matsui, Yoshiaki Sugihara, and Akihiko Ishii. "Thermolysis of Selenophene 1,1-Dioxides." HETEROCYCLES 48, no. 1 (1998): 61. http://dx.doi.org/10.3987/com-97-8000.

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Dissertations / Theses on the topic "Selenophene"

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Aydemir, Kadir. "Electrochromism With Selenophene Derivatives." Master's thesis, METU, 2008. http://etd.lib.metu.edu.tr/upload/12609341/index.pdf.

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SELENOPHENE DERIVATIVES FOR ELECTROCHROMIC APPLICATIONS Aydemir, Kadir M.S., Department of Chemistry Supervisor: Prof. Dr. Levent Toppare February 2008, 60 pages A novel selenophene-based monomer
1,4-di(selenophen-2-yl) benzene (DSB), synthesized via Stille coupling reaction of 1,4 dibromobenzene and tributyl (2-selenophenyl) stannane and corresponding conducting homopolymer (Poly (DSB)) was electrochemically synthesized in the presence of tetrabutylammoniumhexafluorophosphate (TBAPF6) as the supporting electrolyte in dichloromethane. The resulting conducting polymer was characterized by Cyclic Voltammetry (CV), Fourier Transform Infra Red Spectrometry (FTIR) and Ultraviolet&ndash
Visible Spectrometry (UV-Vis Spectrometry). Spectroelectrochemistry analysis and kinetic studies of Poly (DSB) revealed &ndash
* transition (max) at 340 nm with almost zero percent transmittance (T%) concurrently with striking and rapid (0.6 s) absorbance change at near infrared region (1250 nm) with 35% percent transmittance, indicating that Poly (DSB) is a very suitable near infrared electrochromic material. Copolymer of selenophene with ethylenedioxythiophene (EDOT) was potentiostatically synthesized. Poly (selenophene-co-EDOT) was characterized by Cyclic Voltammetry, FTIR and UV-Vis Spectrometry. During spectroelectrochemistry studies, &ndash
* transition (max) was observed at 555 nm with a switching time of 1.4 s and 39% transmittance. Polaron and bipolaron bands were observed at 851 nm and 1299 nm, respectively. Switching time at 1299 nm was 1.8 s with a percent transmittance of 72. Copolymer of DSB with EDOT (Poly (DSB-co-EDOT)) was synthesized and characterized. max, polaron and bipolaron bands were observed at 457 nm, 696 nm and 1251 nm, respectively. A rapid switching time (0.2 s) with 12% transmittance was observed at 696 nm. At the near infrared region (1251 nm), satisfactory percent transmittance (35%) and a moderate switching time (1.75 s) were observed.
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McCarthy-Ward, Thomas. "Novel selenophene-containing conjugated materials." Thesis, Imperial College London, 2013. http://hdl.handle.net/10044/1/30166.

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This thesis is an exploration of the synthesis and characterisation of novel selenophene-containing conjugated materials. Conjugated materials containing thiophene units are well-known and offer many exciting applications in OPV, OTFT, and flexible-electronics devices. Theory and some studies suggest that replacing thiophene units with selenophene could potentially improve optical and electronic properties of interest to device performance. This thesis comprises: • An introduction detailing the potential interest in selenophene-containing materials and the state of current research. • An investigation into the Stille polymerization process on a known thiophene-based polymer, PBTTT, testing the limits of Stille polymerization's effectiveness and the extent to which Stille polymerization can be optimized, as well as investigating the effect of alkyl chain length on the properties of a known polymer. • A systematic investigation into the effects of replacing thiophene with selenophene on the backbone of a known thiophene-based polymer, poly(terthiophene), and also selenium-bearing analogues of other well-studied polymers, showing how increasing selenophene incorporation affects properties relevant to device performance. • The synthesis and characterisation of a novel high-performance low-bandgap polyselenophene featuring DPP units, including a discussion on the synthesis of DPP-functionalised selenophene. Approaches for developing novel fused selenophene-containing materials including issues with functionalising selenophenes, the synthesis of several potentially useful intermediates, the use of a new selenium-transfer reagent, and the successful synthesis and characterisation of three novel fused selenophene-containing systems.
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MERLET, NADINE. "Le polymethyl-3 selenophene : synthese et caracterisation electrochimiques." Paris 6, 1989. http://www.theses.fr/1989PA066347.

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Ce travail est consacre a l'etude electrochimique du polymethyl-3selenophene. Lors de la synthese de ce polymere, nous avons pu mettre en evidence un phenomene de germination tridimensionnel progressif. La caracterisation du depot obtenu a ete effectuee notamment par methodes a echelons de potentiel et a surtout ete abordee en terme de coefficient de diffusion. L'importance de l'epaisseur intervient sur la stabilite electrochimique du film, sur les temps de reponse ainsi que sur son comportement en tant qu'electrode modifiee. Les perturbations capacitives du polymethyl-3selenophene ont pu etre extraites et une approche de modelisation obtenue
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Ardahan, Gulben. "A New P And N Dopable Selenophene Derivative And Its Electrochromic Properties." Master's thesis, METU, 2005. http://etd.lib.metu.edu.tr/upload/3/12609595/index.pdf.

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A novel electrically conducting polymer, poly(2-dodecyl-4,7-di(selenophen-2-yl)benzotriazole) (Poly(SBT)), containing selenophene as a strong donor and benzotriazole as a strong acceptor group was synthesized by electrochemical polymerization. Homopolymerization and copolymerization ( in the presence of 3,4-ethylenedioxythiophene (EDOT) ) was achieved in acetonitrile/ dichloromethane(95/5 v/v) with 0.1M tetrabutylammonium hexafluorophosphate (TBAPF6). The electrochemical and optical properties of homopolymer and copolymer were investigated by Cyclic voltammetry, UV-Vis, near IR Spectroscopy. Cyclic voltammetry and spectroelectrochemistry studies demonstrated that homopolymer can be reversibly reduced and oxidized (both n- and p-doped) between -1.9 V and 1.4 V, at a scan rate of 100 mV/s. Optical contrast was calculated as 32% and 56% with a switching time of 2.4 s and 0.4 s at 511 and 1200 nm respectively. Poly(SBT) exhibits a &
#955
max value of 511nm and a band gap of 1.67eV.
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MAHATSEKAKE, CLEMENT. "Synthese et etude electrochimique de polymeres derives du thiophene et du selenophene." Caen, 1992. http://www.theses.fr/1992CAEN2055.

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Au cours de ce travail, nous avons synthetise un certain nombre de polymeres en serie heterocyclique. La synthese des monomeres precurseurs est decrite dans le chapitre i. Trois series de composes sont decrites: - les 3-alkyl-thiophenes; - les 3-alkylchalcogeno-thiophenes; - les 3-alkyl-selenophenes. Dans tous les cas, la chaine alkyle est lineaire et possede un a douze atomes de carbone. Dans le chapitre ii nous decrivons: - l'analyse detaillee des conditions de polymerisation par voie electrochimique, en particulier la determination des potentiels anodiques et cathodique des monomeres; la polymerisation proprement dite: elle conduit a des materiaux conducteurs a l'etat dope. Ceux-ci ont ete ensuite etudies a l'aide de leurs voltamogrammes et de techniques physiques telles que i. R. , exafs, xanes
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JARKAS, NACHWA Kirsch Gilbert. "SYNTHESE D'ANALOGUES BIHETEROCYCLIQUES DE PYRIDOCARBAZOLES A PARTIR DE 3-OXOBENZOB FURANNE, SELENOPHENE ET THIOPHENE /." [S.l.] : [s.n.], 1997. ftp://ftp.scd.univ-metz.fr/pub/Theses/1997/Jarkas.Nachwa.SMZ9716.pdf.

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Haid, Stefan [Verfasser]. "Functionalized selenophene oligomers and co-oligomers and their application in organic solar cells / Stefan Haid." Ulm : Universität Ulm. Fakultät für Naturwissenschaften, 2012. http://d-nb.info/1028055110/34.

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Epik, Bugra. "The Synthesis Of Donor-acceptor Type Electroactive Monomers Bearing Pyrrole And Selenophene As The Donor Moieties And Their Polymers." Master's thesis, METU, 2010. http://etd.lib.metu.edu.tr/upload/2/12611341/index.pdf.

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Synthesis of new electroactive monomers are highly desired since these compounds can be utilized as active layers in many device applications such as ECDs, LEDs and solar cells. Pyrrole and selenophene bearing polymers were also proven to be excellent candidates as electrochromic materials. Benzothiodiazole can be coupled to to pyrrole and selenophene yield materials that can be polymerized to give donor acceptor type polymers. These donor-acceptor type materials
Poly(4,7-di(1H-pyrrol-2-yl)benzo[c][1,2,5]thiadiazole P(PYBTPY) and poly(4,7-di(selenophen-2-yl)benzo[c][1,2,5]thiadiazole P(SEBTSE) were synthesized via bromination, stannylation and Stille coupling reactions. Electrochemical and electrochromic properties of the polymers were examined in detail.
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DEPRETS, STEPHANIE Kirsch Gilbert. "FONCTIONNALISATION DES 3-OXO-BENZOBFURANE, -THIOPHENE, -SELENOPHENE ET DE L'INDOXYLE POUR DES REACTIONS DE COUPLAGE CATALYSEES PAR LE PALLADIUM. APPLICATION A LA SYNTHESE DE SYSTEMES TETRACYCLIQUES /." [S.l.] : [s.n.], 1998. ftp://ftp.scd.univ-metz.fr/pub/Theses/1998/Deprets.Stephanie.SMZ9850.pdf.

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Wilhelm, Ethel Antunes. "Efeito hepatoprotetor causado pelo 3-alquinil selenofeno contra o dano oxidativo induzido por agentes químicos em ratos." Universidade Federal de Santa Maria, 2009. http://repositorio.ufsm.br/handle/1/11099.

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Conselho Nacional de Desenvolvimento Científico e Tecnológico
The liver presents extraordinary functional diversity, particularly in the control of energy production, immune defense and volemic reserve. The human being is exposed occupationally and in the environment to a variety of hepatotoxic compounds, such as the use of paints and their derivatives (2-nitropropane, 2-NP), chemical reagents (carbon tetrachloride, CCl4) and exposure to cigarette (2-NP). Therefore, it is interesting the study of therapies to prevent or even reverse the poisoning caused by these compounds. Considering that reactive oxygen species (ROS) have an important role in various diseases, especially in liver diseases, the use of antioxidant therapies should be considered. In this context, the heterocyclic compounds containing selenium in their structures have attracted the attention of researchers. Thus, this study investigated the antioxidant activity of 3-alkynyl selenophenes in models of oxidative damage in vitro and ex vivo in rats (Wistar, male, weighing 200-300g). A class of 3-alkynyl selenophene compounds with different substitutions was tested, with the objective to assess their antioxidant profile and their possible toxic effect in vitro. As a result, 3-alkynyl selenophenes had antioxidant activity, but this activity was dependent on the presence of terminal alkynes in the molecule or easy conversion to it. The possible toxic effect of 3-alkynyl selenophenes was evaluated through the activity of the enzyme δ-aminolevulinate dehydratase (δ-ALA-D) in vitro. The results showed that none of 3-alkynyl selenophenes inhibited the activity of this enzyme, suggesting that this class of compound did not present toxicity on this enzyme. From these results, selenophene h (compound that had the best antioxidant activity in vitro) was selected for the evaluation of its protective effect against oxidative damage induced by 2-NP and CCl4 (ex vivo). Selenophene h (25 mg/kg) protected against the increase of markers of liver damage (aspartate aminotransferase (AST) and alanine aminotransferase (ALT) activities) and oxidative stress induced by administration of 2-NP in rats. 2-NP induced microscopic changes, evaluated by histopathological inspections, that were protected by this compound. Selenophene h showed a protective effect against the increase of lipid peroxidation and inhibition of activity of δ-ALA-D in animals treated with 2-NP. Selenophene h protected against oxidative damage induced by CCl4 in rats. A single dose of CCl4 caused significant hepatotoxicity, evidenced by elevated plasma enzyme activity of AST and ALT, increased incidence of histopathological lesions, increased lipid peroxidation levels and the activity of Glutathione-S-transferase (GST), decreased levels of ascorbic acid and the activity of catalase and δ-ALA-D. In conclusion, 3-alkynyl selenophene protected from all these changes, confirming its hepatoprotective effect. Considering the results, we suggest that 3-alkynyl selenophene, an antioxidant, may be a useful therapy for the oxidative damage induced by 2-NP or CCl4 .
O fígado apresenta extraordinária pluralidade funcional, destacando-se no controle de produção de energia, defesa imunológica e reserva volêmica. No meio ambiente e ocupacionalmente, o ser humano está exposto a uma variedade de compostos hepatotóxicos, como por exemplo, no uso de tintas e seus derivados (2-nitropropano, 2- NP), reagentes químicos (tetracloreto de carbono, CCl4) e na exposição ao cigarro (2-NP). Portanto, é interessante o estudo de terapias que previnam ou até mesmo revertam a intoxicação causada por estes compostos. Considerando que as espécies reativas de oxigênio (EROs) apresentam importante papel sobre diversas patologias, em especial nas doenças hepáticas, o uso de terapias antioxidantes deve ser considerada. Neste contexto, destacam-se os compostos heterocíclicos contendo selênio em sua estrutura. Deste modo, neste estudo investigou-se a atividade antioxidante de 3-alquinil selenofenos em modelos de dano oxidativo in vitro e ex vivo em ratos (Wistar, machos, pesando entre 200 300 g). Para esse fim, testou-se uma classe de compostos 3-alquinil selenofeno, com diferentes substituições na estrutura química, com o objetivo de avaliar o perfil antioxidante e seu possível efeito tóxico in vitro em ratos. Como resultado, 3- alquinil selenofenos tiveram atividade antioxidante, porém esta atividade foi dependente da presença de um alquino terminal na molécula ou da fácil conversão da molécula a um alquino terminal. Além disso, o possível efeito tóxico dos 3-alquinil selenofenos foi avaliado através da atividade da enzima δ-aminolevulinato desidratase (δ-ALA-D) in vitro. Os resultados obtidos demonstraram que nenhum dos 3-alquinil selenofenos testados inibiu a atividade desta enzima, sugerindo que esta classe de compostos não apresentou toxicidade sobre a atividade da δ-ALA-D. A partir destes resultados, selecionou-se o selenofeno h (que obteve melhor atividade antioxidante in vitro) para a avaliação do seu efeito protetor contra o dano oxidativo induzido por 2-NP e CCl4 em ratos (ex vivo). O selenofeno h (25 mg/kg) protegeu contra o aumento dos marcadores de dano hepático (aspartato aminotranferase (AST) e alanina aminotransferase (ALT)) e de estresse oxidativo induzidos pela administração do 2-NP. O 2-NP induziu alterações microscópicas avaliadas por inspeções histopatológicas as quais foram protegidas pelo composto. O selenofeno h demonstrou efeito protetor contra o aumento da peroxidação lipídica e inibição da atividade da δ-ALA-D nos animais tratados com 2-NP. Além disso, o selenofeno h protegeu contra o dano oxidativo induzido pelo CCl4 em ratos. Uma única dose de CCl4 causou significante hepatotoxicidade, evidenciada por elevação da atividade plasmática das enzimas AST e ALT, aumento da incidência de lesões histopatológicas, aumento dos níveis de peroxidação lipídica e da atividade da enzima glutationa-S-transferase (GST), bem como diminuição dos níveis de ácido ascórbico e da atividade das enzimas catalase e δ-ALA-D. A partir dos resultados demonstrados, verificou-se que o selenofeno h protegeu contra todas estas alterações, confirmando o seu efeito hepatoprotetor. Considerando os resultados obtidos, pode-se sugerir que o selenofeno h, uma molécula com atividade antioxidante, pode ser uma útil terapia contra o dano oxidativo induzido pelos hepatotoxicantes: 2-NP e CCl4.
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Books on the topic "Selenophene"

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Moeller, Tara. Selenophile. DreamPunk Press, 2018.

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Book chapters on the topic "Selenophene"

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Wohlfarth, Ch. "Second virial coefficient of poly[(selenophene-2-yl)methyl methacrylate]." In Polymer Solutions, 1106. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-02890-8_672.

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Abdallah, Hassan H., and Ponnadurai Ramasami. "First Principle Study of the Anti– and Syn–Conformers of Thiophene–2–Carbonyl Fluoride and Selenophene–2–Carbonyl Fluoride in the Gas and Solution Phases." In Lecture Notes in Computer Science, 114–21. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01973-9_13.

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Kirsch, G., E. Perspicace, and S. Hesse. "Synthesis and Transformations of 2- and 3-hydroxy-Selenophenes and 2- and 3-Amino-Selenophenes." In Selenium and Tellurium Chemistry, 239–50. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-20699-3_10.

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"Selenophene, Tetrahydroselenophene, Tellurophene, and Tetrahydrotellurophen." In Chemistry of Heterocyclic Compounds: A Series Of Monographs, 479–93. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186527.ch16.

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"Condensed Selenophene and Tellurophene Systems." In Chemistry of Heterocyclic Compounds: A Series Of Monographs, 447–61. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186565.ch9.

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Murphy, P. J. "By Formylation of a Benzo[]selenophene and Cyclization." In Fused Five-Membered Hetarenes with One Heteroatom, 1. Georg Thieme Verlag KG, 2001. http://dx.doi.org/10.1055/sos-sd-010-00450.

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Murphy, P. J. "Benzo[]selenophene-1(3)-thione by Reaction of Benzo[]selenophen-1(3)-imine with Hydrogen Sulfide." In Fused Five-Membered Hetarenes with One Heteroatom, 1. Georg Thieme Verlag KG, 2001. http://dx.doi.org/10.1055/sos-sd-010-00428.

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Pfeiffer, W. D. "From 2-(Methylselanyl)thiophene-3-carbaldehyde or 2-(Methylselanyl)selenophene-3-carbaldehyde." In Five-Membered Hetarenes with One Chalcogen and One Additional Heteroatom, 1. Georg Thieme Verlag KG, 2002. http://dx.doi.org/10.1055/sos-sd-011-01192.

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Ranu, Brindaban C., Tubai Ghosh, Laksmikanta Adak, and Subir Panja. "Synthesis and Reactivity of Selenophene and Their Benzo- and Other Carbocyclic-Fused Derivatives." In Reference Module in Chemistry, Molecular Sciences and Chemical Engineering. Elsevier, 2019. http://dx.doi.org/10.1016/b978-0-12-409547-2.14776-6.

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Pelkey, E. T. "Selenophenes." In Comprehensive Heterocyclic Chemistry III, 975–1006. Elsevier, 2008. http://dx.doi.org/10.1016/b978-008044992-0.00313-8.

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Conference papers on the topic "Selenophene"

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Rampon, Daniel S., Ludger A. Wessjohann, and Paulo H. Schneider. "Palladium-Catalyzed Direct Arylation of Selenophene." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013915174110.

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Dey, Somnath, Yang Han, Siham Y. Al-Qaradawi, Hassan S. Bazzi, Martin Heeney, and Mohammed Al-Hashimi. "Synthesis and Characterization of Soluble Thiophene-, Selenophene- and Tellurophene-Vinylene Copolymers." In Qatar Foundation Annual Research Conference Proceedings. Hamad bin Khalifa University Press (HBKU Press), 2016. http://dx.doi.org/10.5339/qfarc.2016.eepp1934.

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Chen, Yih-wen, Jang-yang Chang, and Kai-Ming Chou. "Abstract 3813: DNA polymerase eta and a novel anticancer selenophene compound." In Proceedings: AACR 103rd Annual Meeting 2012‐‐ Mar 31‐Apr 4, 2012; Chicago, IL. American Association for Cancer Research, 2012. http://dx.doi.org/10.1158/1538-7445.am2012-3813.

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Rietz, Anne, Yih-wen Chen, and Kai-Ming Chou. "Abstract 2029: Interactions between a selenophene compound and DNA polymerase eta." In Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1538-7445.am2013-2029.

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Newby, Josh, and Tiara Sivells. "WEAK HYDROGEN BONDING IN COMPLEXES OF SELENOPHENE AND WATER: A MATRIX ISOLATION FTIR AND COMPUTATIONAL STUDY." In 2020 International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2020. http://dx.doi.org/10.15278/isms.2020.tb08.

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Yang, Yung‐Ning, Wen‐Yu Pan, Ssu‐Ching Yeh, Tsui‐Chun Tsou, Li‐Tzong Chen, and Jang‐Yang Chang. "Abstract B69: Enhancement of nonhomologous end joining DNA repair capacity confers cancer cells resistant to novel selenophene compound D‐501036." In Abstracts: AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics--Nov 15-19, 2009; Boston, MA. American Association for Cancer Research, 2009. http://dx.doi.org/10.1158/1535-7163.targ-09-b69.

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Dhole, Samyak, Rajan Singh, and Roy Paily. "The effects of backbone fluorination on photovoltaic properties of polymers of thiophene, selenophene and tellurophene and their hexyl derivatives: A DFT study." In 2017 Devices for Integrated Circuit (DevIC). IEEE, 2017. http://dx.doi.org/10.1109/devic.2017.8074001.

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Rampon, Daniel S., Aloir A. Merlo, and Paulo H. Schneider. "Synthesis of New Liquid-Crystalline Selenophenes via Electrophilic Cyclization of (Z)-Selenoenynes." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0011-1.

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Stein, André L., Alisson R. Rosário, Filipe N. Bilheri, Cristina W. Nogueira, and Gilson Zeni. "FeCl3-Diorganoyl Dichalcogenides Promoted Cyclization to Fused 4-Substituted selenophenes[2,3-b]thiophenes." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0355-1.

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Reports on the topic "Selenophene"

1

White, Carter James. Selenophene transition metal complexes. Office of Scientific and Technical Information (OSTI), July 1994. http://dx.doi.org/10.2172/10190649.

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2

Sanger, Michael J. Dynamic NMR studies of restricted arene rotation in the chromiu tricarbonyl thiophene and selenophene complexes. Office of Scientific and Technical Information (OSTI), May 1994. http://dx.doi.org/10.2172/10190002.

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You might also be interested in the extended bibliographies on the topic 'Selenophene' for particular source types:
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