Academic literature on the topic 'Thiadiazol'

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Journal articles on the topic "Thiadiazol"

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Singh, S., and Amandeep Kaur. "SYNTHESIS AND ANTICANCER ACTIVITY OF NOVEL 2-BENZYL-6- (SUBSTITUTED PHENYL)-IMIDAZO[2,1-B] [1,3,4] THIADIAZOLE DERIVATIVES." INDIAN DRUGS 56, no. 04 (2019): 13–20. http://dx.doi.org/10.53879/id.56.04.11454.

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A new series of 2-benzyl-6-(substituted phenyl)-imidazo[2,1-b][1,3,4] thiadiazoles (S1-S8) was synthesized as potential anti-cancer agents. These compounds were evaluated for their anticancer activity against various cancer cell lines. The anticancer activity data reveals that the compounds S1 (2-benzyl- 6-phenylimidazo[2,1-b][1,3,4]thiadiazole) showed maximum growth inhibition against CNS cancer cell lines while the compounds S2 (2-benzyl-6-(4-chlorophenyl) imidazo[2,1-b][1,3,4] thiadiazole) and S3 (2-benzyl-6-(2,4-dichlorophenyl)imidazo[2,1-b][1,3,4] thiadiazole) showed maximum inhibition ag
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C., S. ANDOTRA, C. LANGER T., and KOTHA AMRITA. "Synthesis and Antifungal Activity of some Substituted 1,3,4-Thiadiazolo[3,2-a]-s-triazin-5-phenyl-7-thiones and Imidazo-[2, 1-b ]-1,3,4-thiadiazol-5-ones." Journal of Indian Chemical Society Vol. 74, Feb 1997 (1997): 125–27. https://doi.org/10.5281/zenodo.5875250.

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Department of Chemistry. University of Jammu, Jammu-180 004 <em>Manuscript&nbsp;received 25 October !994. revised 4 July 1995, accepted 4 August 1995</em> 2-Amino-5-aryl-substituted-1,3,4-thiadiazoles (1) have been refluxed with benzoyllsothiocyanate to get N-[5-aryl-substituted-1,3,4- thiadiazol-2-yl)-<em>N</em>-benzoyl thlonreas (1a). These on refluxing with PCI<sub>5</sub> and POCI<sub>3</sub> give 2-aryl-substituted-1,3,4-thiadiazolo[3,2-<em>a</em>]-<em>s</em>- triazin-5-phenyl-7-thiones (3). Compound 1&nbsp;on refluxing with chloroacetic acid and anhydrous sodium acetate gives 2-substitut
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Zhao, Yuxiang, Peter J. McCarthy, and Cyril Párkányi. "Synthesis and In Vitro Evaluation of Novel Acyclic and Cyclic Nucleoside Analogs with a Thiadiazole Ring." ISRN Organic Chemistry 2013 (March 5, 2013): 1–10. http://dx.doi.org/10.1155/2013/159164.

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The synthesis of six thiadiazole nucleoside analogs is reported: 5-diacetylamino-1,2,4-thiadiazol-3-one (1), 5-amino-2- (tetrahydrofuran-2-yl)-1,2,4-thiadiazol-3-one (2), 5-amino-3-[(2′-hydroxyethoxy)methyl]-1,3,4-thiadiazol-2-one (3), 5-amino-3-(4′-hydroxy-2′-hydroxymethyl-butyl)-1,3,4-thiadiazole-2-thione (4), (R)-5-amino-3-(2′,3′-dihydroxypropyl)-1,3,4-thiadiazole-2-thione (5), and (S)-5-amino-3-(2′,3′-dihydroxypropyl)-1,3,4-thiadiazole-2-thione (6). The synthesis, characterization, and properties of these new synthesized thiadiazole derivatives are discussed. A dimerization of 5-amino-3H-1
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A. Ameen, Husam, and Ahlam J. Qasir. "Synthesis and Preliminary Antimicrobial Study of 2-Amino-5-Mercapto-1,3,4-Thiadiazole Derivatives." Iraqi Journal of Pharmaceutical Sciences ( P-ISSN 1683 - 3597 E-ISSN 2521 - 3512) 21, no. 1 (2017): 98–104. http://dx.doi.org/10.31351/vol21iss1pp98-104.

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Nitrogen heterocycles are of a special interest because they constitute an important class of natural and non natural products, many of which exhibit useful biological activities.Among these nitrogen heterocycles are 1, 3, 4-thiadiazole containing compounds. The therapeutic effects of these derivatives have been well studied for a number of pathological conditions including inflammation, pain, or hypertension. Moreover, synthesis of thiadiazoles has attracted wide-spread attention due to their diverse applications as antibacterial, anticancer, antifungal anti-inflammatory and antidepressant ag
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Rakhmonov, R., Sh Sharipov, M. Odilzoda, B. Safarov, A. Kobilzoda, and A. Abdurakhmonov. "SYNTHESIS AND FUNCTIONALIZATION OF SOME PARA-R-PHENYLIMIDAZO[2,1-B][1,3,4]- THIADIAZOLE DERIVATIVES." East European Scientific Journal 1, no. 4(68) (2021): 54–61. http://dx.doi.org/10.31618/essa.2782-1994.2021.1.68.15.

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The article describes the synthesis of new modifications of derivatives of 6-phenyl-, 6-piodophenyl- and 6-p-bromophenylimidazo[2,1-b][1,3,4]-thiadiazoles - N -((6-(4-iodophenyl)-2-R-imidazo[2,1-b][1,3,4]-thiadiazol-5-yl)methyl)-alkyl/ heterylamine based on the Mannich reaction, bromination 2((ethylsulfonyl)methyl)-6-phenylimidazo[2,1-b][1,3,4]-thiadiazole and the structure of the resulting compounds was established on the basis of IR spectroscopy. It was shown that the presence of substituents at the 2-nd position of the thiadiazole fragment and substituents at the 5th and 6th positions of th
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Ardan, Bohdan, Vasyl Kinzhybalo, Yurii Slyvka, et al. "Ligand-forced dimerization of copper(I)–olefin complexes bearing a 1,3,4-thiadiazole core." Acta Crystallographica Section C Structural Chemistry 73, no. 1 (2017): 36–46. http://dx.doi.org/10.1107/s2053229616018751.

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As an important class of heterocyclic compounds, 1,3,4-thiadiazoles have a broad range of potential applications in medicine, agriculture and materials chemistry, and were found to be excellent precursors for the crystal engineering of organometallic materials. The coordinating behaviour of allyl derivatives of 1,3,4-thiadiazoles with respect to transition metal ions has been little studied. Five new crystalline copper(I) π-complexes have been obtained by means of an alternating current electrochemical technique and have been characterized by single-crystal X-ray diffraction and IR spectroscop
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Zain Alabdeen, Khalid. "The Activity of 1,3,4 Thiadiazole Derivatives on the Soluble Oils." Journal of Petroleum Research and Studies 2, no. 1 (2021): 59–88. http://dx.doi.org/10.52716/jprs.v2i1.34.

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That Thiadiazoles derivative is biologically active as antimicrobial agents in cooling fluids.&#x0D; Derivatives of 1, 3, 4- thiadiazole have prepared:&#x0D; &#x0D; 2-amino-3-[(2-amino-1, 3, 4-thiadiazol-5-yl) dithio] propanoic acid.&#x0D; 2-(2-Carbethoxyamino-1, 3, 4-thiadiazol-5-yl)-thio acetic acid.&#x0D; [(5-amino-1,3,4-thiadiazol-2-yl) dithio] acetic acid&#x0D; &#x0D; The synthesized compounds have been used as antimicrobial against the microorganisms which have been found in the cooling fluid of industrial&#x0D; purposes by using media culture the results showed that the compounds 1 and
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Pavlova, V. V., P. V. Zadorozhnii, V. V. Kiselev, A. V. Kharchenko, and O. V. Okhtina. "Modeling of new potential inhibitors of dihydrofolate reductase based on 1,3,4-thiadiazole amidoalkyl derivatives." Voprosy Khimii i Khimicheskoi Tekhnologii, no. 5 (October 2023): 91–97. http://dx.doi.org/10.32434/0321-4095-2023-150-5-91-97.

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Derivatives of 1,3,4-thiadiazole are very important for medical chemistry and pharmacy as potential drug substances. In this work, we carried out molecular docking studies of amidoalkyl derivatives of 1,3,4-thiadiazole: N-(2,2,2-trichloro-1-((5-aryl-1,3,4-thiadiazol-2-yl)amino)ethyl)carboxamides and N-(2,2,2-trichloro-1-((5-(arylamino)-1,3,4-thiadiazol-2-yl)amino)ethyl)carboxamides with dihydrofolate reductase (DHFR). The AutoDock Vina program based on the PyRx 0.8 platform was used for docking. Before docking, the enzyme structure (PDB ID: 1DLS) was prepared using the Chimera 1.14 program, an
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Shein, Anatoliy B., Mariya D. Plotnikova, and Alexander E. Rubtsov. "PROTECTIVE PROPERTIES OF SOME THIADIAZOLE DERIVATIVES IN SULFURIC ACID SOLUTIONS." IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENII KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 62, no. 7 (2019): 123–29. http://dx.doi.org/10.6060/ivkkt.20196207.5968.

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The work presents the results of the study of some thiadiazole derivatives as corrosion inhibitors for mild steel in 5-20% H2SO4. Gravimetric tests and electrochemical studies were performed on low-carbon steel St3 at ambient temperature. The exposure time of the samples was 24 h. Polarization curves were obtained by potentiodynamic method (v = 1 mV/s) in a three-electrode cell, using the SOLARTRON 1280 C electrochemical measuring complex. The following thiadiazole derivatives were studied: (E)-N,N-dimethyl-4-{[(5-phenyl-1,3,4-thiadiazol-2-yl)imino]methyl}aniline, (E)-5-{[4-(dimethylamino)benz
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Journal, Baghdad Science. "SYNTHESIS AND ANTIMICROBIAL ACTIVITY OF SOME (2-AMINO-5-THIOL-1, 3, 4-THIADIAZOLE DERIVATIVES." Baghdad Science Journal 4, no. 1 (2007): 89–94. http://dx.doi.org/10.21123/bsj.4.1.89-94.

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Five derivatives of thiadiazole were prepared with aldehydes and alkyl halides, compoundA: 2-amino-5-thiol-1,3,4- thiadiazole, compound B :2-(o-hydroxybenzylidine)amino-5-thiol-1,3,4-thiadiazole, compoundC: 2(2-butan-lidine)amino-5-thiol-1,3,4-thiadiazole, compound E: 2- amino-5-(2-Propanylthio)-1,3,4-thiadiazol) and compound F:2(o-chlorobenzylamino)-5-(2-propanyl thio)-1,3,4 thiadiazol. All prepared compounds were diagnosed by (IR) and (UV) Spectroscopy. All of those compounds were screened for their anti-microbial activity in vitro. The results show that most of the compounds A, B, C exhibit
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Dissertations / Theses on the topic "Thiadiazol"

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Hipler, Frank. "Chemie gegen Reibung und Verschleiss: Untersuchung molekularer Wirkungsmechanismen von Thiadiazol-Schmierstoffadditiven." [S.l. : s.n.], 2003. http://deposit.ddb.de/cgi-bin/dokserv?idn=968939511.

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Gorris, Friederieke Erika Sophie [Verfasser], and Horst [Akademischer Betreuer] Weller. "Ladungstransporteigenschaften von thiadiazol-funktionalisierten Kupferindiumselenidnanokristalldünnschichten / Friederieke Erika Sophie Gorris ; Betreuer: Horst Weller." Hamburg : Staats- und Universitätsbibliothek Hamburg, 2019. http://d-nb.info/1188818759/34.

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Schüttler, Christian [Verfasser], and Zezschwitz Paultheo [Akademischer Betreuer] von. "Flexible Synthese enantiomerenreiner 1,2-Diamine und 2,3-Diaminocarbonsäuren aus 1,2,5-Thiadiazol-1,1-dioxiden / Christian Schüttler. Betreuer: Paultheo von Zezschwitz." Marburg : Philipps-Universität Marburg, 2015. http://d-nb.info/1076865763/34.

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AMIEL, PASCALE. "Tautomerie et dithioalkylations du 2,5-dimercapto-1,3,4-thiadiazole : synthese de nouveaux heterocycles : 2-thione-n(3)-acridinyl-5-alkyltio-1,3,4-thiadiazoles : activites antiparasitaires et anticancereuses de quelques derives thiadiazoles." Aix-Marseille 2, 1994. http://www.theses.fr/1994AIX22955.

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Changtong, Chuchawin. "Synthesis and photochemistry of phenyl subtituted-1,2,4-thiadiazoles; 15N-labeling studies." Link to electronic thesis, 2005. http://www.wpi.edu/Pubs/ETD/Available/etd-050505-090309/.

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Nakamura, Ana Paula Rizzato. "Síntese e caracterização de sílica gel funcionalizada com 2-aminotiazol e 5-amino-1,3,4-tiadiazol-2-tiol para aplicações adsortivas e voltamétricas /." Ilha Solteira, 2018. http://hdl.handle.net/11449/153058.

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Orientador: Newton Luiz Dias Filho<br>Resumo: No presente trabalho, a 3-cloropropil sílica gel (SG) foi preparada e organofuncionalizada com dois grupos funcionais, 2-aminotiazol (SATZ) e 5-amino-1,3,4-tiadiazol-2-tiol (SATT). Com o objetivo de produzir novos materiais através da modificação química da superfície da sílica gel, com aplicabilidade na remoção de íons metálicos em meio etanólico, tendo a possibilidade de serem aplicados na remoção de metais pesados em combustível etanol e aguardente. Esses novos materiais também podem ser trabalhados como novos eletrodos quimicamente modificados
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Deckert, Christoph [Verfasser]. "Modellkomplexe zur Sauerstoffaktivierung auf Basis des 1,3,4-Thiadiazols / Christoph Deckert." Mainz : Universitätsbibliothek Mainz, 2015. http://d-nb.info/1072395371/34.

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Cousin, Pascal. "2,5-diméthyl-1,3,4-thiadiazole : fonctionnalisation par voie organolithienne et applications." Poitiers, 1998. http://www.theses.fr/1998POIT2284.

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Dans la premiere partie, la monofonctionnalisation du 2,5-dimethyl-1,3,4-thiadiazole a pu etre obtenue aisement par formation du monolithien a l'aide du diisopropylamidure de lithium, suivie d'une reaction d'addition aux composes a liaison c=o ou de substitution avec les sels d'iminium et des derives halogenes de structure variee. Cette reaction a conduit a des series organisees de composes thiadiazoliques : alcools secondaires ou tertiaires, cetones, oximes et amines tertiaires. Dans la seconde partie, la realisation dans de bonnes conditions de la difonctionnalisation symetrique du 2,5-dimet
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Gauduchon, Emmanuelle. "Fonctionnalisation régiosélective en position 4 ou 5 ducycle 1,2,3-thiadiazole et applications." Poitiers, 1998. http://www.theses.fr/1998POIT2333.

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Dans la premiere partie de ce travail, nous avons rationalise la preparation de matieres premieres 1,2,3-thiadiazoliques monofonctionnalisees en position 4 ou 5. Nous avons ainsi obtenu des esters, acides, derives d'acide et amines qui nous ont permis de realiser la synthese deux series d'amides n-substitues (n-arylthiadiazolylcarboxamides et n-thiadiazolylbenzamides) et une serie d'aldimines conjuguees (n-thiadiazolylbenzaldimines). Dans la seconde partie, nous avons prepare trois carbures 1,2,3-thiadiazoliques et transforme les amines primaires 1,2,3-thiadiazoliques en derives halogenes. Nou
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Schmidt, Michael Joseph. "A New Late-Stage Lawesson's Cyclization Strategy Towards the Synthesis of Aryl 1,3,4-Thiadiazole-2-Carboxylate Esters." Kent State University Honors College / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=ksuhonors1373911614.

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Books on the topic "Thiadiazol"

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Bakulev, Vasiliy A., and Wim Dehaen. The Chemistry of 1,2,3-Thiadiazoles. John Wiley & Sons, Inc., 2004. http://dx.doi.org/10.1002/0471656992.

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W, Dehaen, ed. The chemistry of 1,2,3-Thiadiazoles. John Wiley & Sons, 2004.

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Ben, Robert N. Synthesis of 2-carboxyethyl-5-methyl-1,3,4-oxadiazole and thiadiazole. Laurentian University, 1990.

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Kats, Eynav. חקר המנגנון ואופטימיזציה של תהליכי הסינתזה של פירימידינים ות. אוניברסיטת בן גוריון בנגב, 2006.

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Lüdtke, Eberhard. Antithrombotische thiazol- und thiadiazol- n-nitrosimine. 1992.

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Knecht, Dagmar. Synthesen neuer Molekülsysteme mit 1,2,5-Thiadiazol-, 1,2,5-Selenadiazol- und 1,2,5-Telluradiazolstruktur: Reaktionen und Eigenschaften. 1987.

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Bakulev, Vasiliy A., Edward C. Taylor, Peter Wipf, and Wim Dehaen. Chemistry Of 1,2,3-Thiadiazoles. Wiley & Sons, Incorporated, John, 2004.

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Thiadiazoles: Advances in Research and Applications. Nova Science Publishers, Incorporated, 2020.

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Cohen, Alberto. Thiadiazoles: Advances in Research and Applications. Nova Science Publishers, Incorporated, 2020.

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Bakulev, Vasiliy A., Edward C. Taylor, Peter Wipf, and Wim Dehaen. Chemistry of Heterocyclic Compounds, the Chemistry of 1,2,3-Thiadiazoles. Wiley & Sons, Incorporated, John, 2004.

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Book chapters on the topic "Thiadiazol"

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Kaur, Navjeet. "Thiadiazole Synthesis." In Lawesson’s Reagent in Heterocycle Synthesis. Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-4655-3_4.

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Chiacchio, Ugo, and Giovanni Romeo. "Thiadiazoles." In Modern Heterocyclic Chemistry. Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527637737.ch14.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with (1R, 2R)-1,2-bis-(5-amino-1,3,4-thiadiazol-2-yl)ethane-1,2-diol." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 7. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65895-6_342.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) complex with (1R, 2R)-1,2-bis-(5-amino-1,3,4-thiadiazol-2-yl)ethane-1,2-diol." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 7. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65895-6_255.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of cobalt(II) complex with (1R, 2R)-1,2-bis-(5-amino-1,3,4-thiadiazol-2-yl)ethane-1,2-diol." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 7. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65895-6_187.

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Demaison, J. "150 C2H2N2S 1,2,5-Thiadiazole." In Asymmetric Top Molecules. Part 1. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-10371-1_152.

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Demaison, J. "151 C2H2N2S 1,3,4-Thiadiazole." In Asymmetric Top Molecules. Part 1. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-10371-1_153.

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Pace, Andrea, Antonio Palumbo Piccionello, Ivana Pibiri, Silvestre Buscemi, and Nicolò Vivona. "Chemistry of Fluorinated Oxadiazoles and Thiadiazoles." In Fluorine in Heterocyclic Chemistry Volume 1. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-04346-3_9.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of manganese(II) complex with thiadiazole." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_406.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of iron(II) complex with thiadiazole." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_85.

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Conference papers on the topic "Thiadiazol"

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Li, Hsin, Xiao-Feng Shen, Ying-Sheng Lin та ін. "Sensitizers D-A1-A2-π-A Include 10'H-Spiro[fluorene-9,9’-Phenanthren].Benzo[c] and -10‘-one.[ 1, 2, 5]Thiadiazole for Photocatalytic Hydrogen Production and Dye-Sensitized Solar Cells". У 2024 31st International Workshop on Active-Matrix Flatpanel Displays and Devices (AM-FPD). IEEE, 2024. http://dx.doi.org/10.23919/am-fpd61635.2024.10615532.

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Fuzi, Siti Aishah Ahmad, Mohammad Hafizuddin Hj Jumali, and Bandar Ali Abdulqader Al-Asbahi. "Enhanced optophysical properties of poly[(9,9-di-n-octylfluorenyl-2,7-diyl)-alt-(benzo[2,1,3]thiadiazol-4,8-diyl)] via addition of TiO2 nanoparticles." In THE 2015 UKM FST POSTGRADUATE COLLOQUIUM: Proceedings of the Universiti Kebangsaan Malaysia, Faculty of Science and Technology 2015 Postgraduate Colloquium. AIP Publishing LLC, 2015. http://dx.doi.org/10.1063/1.4931266.

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Nikalje, Anna Pratima, Shailee Tiwari, Sumaiya Siddiqui, and Julio Seijas Vázquez. "Microwave-assisted Facile Synthesis And Anticancer Evaluation Of N-((5-(substituted Methylene Amino)- 1,3,4-thiadiazol-2-yl)methyl) Benzamide Derivatives." In The 20th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-a010.

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Pavlova, Valeriia V., Pavlo V. Zadorozhnii, Vadym V. Kiselev, and Aleksandr V. Kharchenko. "Synthesis, Spectral Characteristics, and Molecular Docking Studies of 2,4-Dichloro-N-(2,2,2-trichloro-1-((5-(phenylamino)-1,3,4-thiadiazol-2-yl)amino)ethyl)benzamide." In ECSOC 2022. MDPI, 2022. http://dx.doi.org/10.3390/ecsoc-26-13642.

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Marquez-Lucero, Alfredo. "Thiadiazole derivatives with nonlinear optical properties." In Integrated Optoelectronic Devices 2005, edited by James G. Grote, Toshikuni Kaino, and Francois Kajzar. SPIE, 2005. http://dx.doi.org/10.1117/12.582050.

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Elgueta, E. Y., M. L. Parra, and J. A. Ulloa. "Novel Polycatenar Mesogens Containing 1,3,4-thiadiazole." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0134-1.

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Ananda, S., V. Keerthikumara, H. Kumar Keshav, et al. "Structural, DFT and nonlinear optical studies of hemihydrate thiadiazole derivative." In 66TH DAE SOLID STATE PHYSICS SYMPOSIUM. AIP Publishing, 2024. http://dx.doi.org/10.1063/5.0178379.

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Abood, Zeid Hassan, Amani Nadhim Kadhim та Husham Attallah Suhail. "Microwave assisted synthesis of new β-Lactams bearing thiadiazole moiety". У 4TH INTERNATIONAL SCIENTIFIC CONFERENCE OF ENGINEERING SCIENCES AND ADVANCES TECHNOLOGIES. AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0157220.

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Liu, Y., X. H. Zhang, W. J. Ding, and X. X. Sun. "Synthesis of 4-Carbazole -7- Thiophen[1,2,5] Thiadiazolo [3,4-C]Pyridine." In The International Workshop on Materials, Chemistry and Engineering. SCITEPRESS - Science and Technology Publications, 2018. http://dx.doi.org/10.5220/0007435401220126.

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Falzirolli, Hugo, Fábio Vandresen, Francieli Furlan, and Cleuza Conceição da Silva. "Multicomponent synthesis of R-(+)-limonene-based 1,3,4-thiadiazoles." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013821151948.

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