Relevant bibliographies by topics / 1,3,4-thiadiazole

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  2. Dissertations / Theses
  3. Books
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Academic literature on the topic '1,3,4-thiadiazole'

Author: Grafiati
Published: 4 June 2021
Last updated: 12 February 2022

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Journal articles on the topic "1,3,4-thiadiazole"

1

Journal, Baghdad Science. "Synthesis of some Schiff's bases derivatives from aminoazo compounds." Baghdad Science Journal 4, no. 3 (September 2, 2007): 416–19. http://dx.doi.org/10.21123/bsj.4.3.416-419.

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Reaction of,2- [( 4- amio phenyl ) diazenyl] 1,3,4- thiadiazole -5- thiol (S1) with p- chlorobenzeldehyde,3,4 – dimethoxy benzaldehyde and pyrrol-2- carbonxaldehyde gave -5- [{4-(4-chlorobenzylidene amino) phenyl} diezenyl]-1,3,4- thiadiazole-2- thiol (S2),5-[{ 4-[(3,4- dimethoxybenzyldene )amino phenyl ] diazenyl)-1,3,4- thiadiazole-2-thiol,(S3) and -5- [4-(1,H – pyrrol -2- yl- methylene)amino phenyl] diazenyl)-1,3,4- thiadiazole-2- thiol (S4) respectively as schiff's bases compounds. On the same route-2-[(4-amino-1- naphthyl ) diazenyl] -1,3,4- thiadiazole -5- thiol (S5) reacts with –p- chloro benzaldehyde and –m- nitrobenzaldehyde to give the follwing schiff's bases -5-[{ 4-(4- chloro benzylidene ) amino -1- naphthyl} diazenyl] -1,3,4- thiadiazole -2- thiol (S6) and -5- ({ 4- [3- nitrobenzylidene) amino] -1- naphthyl({ diazenyl) -1,3,4 – thiadiazole-2- thiol (S7). Sn2 reaction was carried out by the reaction of compound (S6,S7) with bromo ethyl acetate to get ethyl[5{4-(4- chlorobenzylidene amino)-1- naphthyl} diazenyl] -1- 1,3,4- thiadiazole-2- yl- thio] acetate (S8) and ethyl [5-{4- (2- nitrobenzylidene amino)-1- naphthyl diazenyl] -1,3,4- thiadiazole -2-yl-acetate (S9).(Fig.1).
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2

Journal, Baghdad Science. "Preparation of some azo compounds by diazotization and coupling of 2- amino -5 – thiol -1,3,4- thiadizaole." Baghdad Science Journal 4, no. 2 (June 7, 2015): 271–75. http://dx.doi.org/10.21123/bsj.4.2.271-275.

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2- amino -5- thiol-1,3,4- thiadiazole (S1) was prepared by cyclic locking of thiosemicarbazide in the presence of anhydrous sodium carbonate and CS2. diazotization of (S1) compound gave diazonium salt (S2) that reacts with different activated aromatic compounds to get the following azo compounds ,2 [(4- aminophenyl) diazenyl ] 1,3,4- thiazdiazole-5- thiol (S3) ,2-[4-amino- 1-naphthyl diazenyl] -1,3,4 – thiazdiazole-5-thiol (S4) , 3-amino-4-[(5- mercapto -1,3,4- thiadiazole -2-yl) diazenyl ] phenol(S5) ,1-[(5-mercapto-1,3,4-thiadiazole-2-yl) diazenyl] -2-naphthol (S6) , 5-{[4-(dimethylamino) phenyl] diazenyl}-1,3,4-thiadiazole-2- thiol(S7) ,5-{[4-(diethylamino) phenyl] diazenyl}-1,3,4- thiadiazole-2- thiol(S8) ,2- amino-5-[(5-mercapto-1,3,4-thiadiazole-2-yl) diazenyl] phenol(S9) . All the prepared azo compounds have been characterized and identified through the study of their some physical, chemical and spectrometrical (U.V.I.R) properties.
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3

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-1,3,4-thiadiazole-2-thione (14) by sodium nitrite resulting in di-(5-amino-1,3,4-thiadiazol-2-yl) disulfide (19) is also reported. The preliminary in vitro evaluation of these newly synthesized compounds is discussed.
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Journal, Baghdad Science. "Synthesis and Characterization of Five, Sevene Heterocyclic Membered Rings." Baghdad Science Journal 10, no. 3 (September 1, 2013): 803–17. http://dx.doi.org/10.21123/bsj.10.3.803-817.

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New compounds containing heterocyclic units have been synthesized. These compounds include 2-amino 5- phenyl-1,3,4-thiadiazole (1) as starting material to prepare the Schiff bases 2N[3-nitrobenzylidene -2 hydroxy benzylidene and 4-N,N-dimethyl aminobenzylidene] -5-phenyl-1,3,4-thiadiazole (2abc) , 2N[3-nitrophenyl, 2-hydroxyphenyl or 4-N,N-dimethylaminophenyl] 3-]2-amino-5-phenyl-1,3,4-thiadiazole]-2,3-dihydro-[1,3]oxazepine-benzo-4,7-dione] (3abc), 2N[3-nitrophenyl,2-hydroxyphenyl,4-N,N-dimethylaminophenyl]-3-[2-amino-5-phenyl-1,3,4-thiadiazole-2-yl]-2,3-dihydro-[1,3]oxazepine-4,7-dione[(4abc), 2-N-[3-nitrophenyl, 2-hydroxyphenyl or 4-N,N-dimethylaminophenyl]-3-[2-amino-5-phenyl-1,3,4-thiadiazole-2yl]-1,2,3-trihydro-benzo-[1,2-e][1,3] diazepine-4,7-dione (5abc) ,2N[2-(3-nitrophenyl,2-hydroxyphenyl or 4-N,N-dimethylaminophenyl)]-4-oxo-1,3-thiazolidine-3-yl]-2-amino-5-phenyl-1,3,4-thiadiazole (6abc), 2-N-[5-(3-nitrophenyl,2-hydroxyphenyl or 4-N,N-dimethylaminophenyl)-tetrazolo-1-yl]-2-amino-5-phenyl-1,3,4-thiadiazole (7abc) , 2-N-[5-(3-nitrophenyl,2-hydroxyphenyl or 4-N,N-dimethylaminophenyl)-3-[2-amino-5-phenyl-1,3,4-thiadiazole-2-yl]-2,3-dihydro-[1,3]oxazepine-benzo-4,7-dithione (8abc) , 2-N-[5-(3-nitrophenyl,2-hydroxyphenyl or 4-N,N-dimethylaminophenyl)-3-[2-amino-5-phenyl-1,3,4-thiadiazole-2-yl]-2,3-dihydro-[1,3]oxazepine -4,7-dithione -5-ene (9abc) and 2-N-[5-(3-nitrophenyl,2-hydroxyphenyl or 4-N,N-dimethylaminophenyl)-3-[2-amino-5-phenyl-1,3,4-thiadiazole-2-yl] -1,2,3-trihydro-benzo-[1,2-e][1,3] diazepine -4,7-dithione - (10abc) . the structures of these compounds were characterized by FT-IR, 1H,13C-NMR,Uv/vis spectroscopy and the melting points were determined besides the evaluation of its biological activity.
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Plotnikova, M. D., A. B. Shein, M. G. Shcherban`, and A. D. Solovyev. "The study of thiadiazole derivatives as potential corrosion inhibitors of low-carbon steel in hydrochloric acid." Bulletin of the Karaganda University. "Chemistry" series 103, no. 3 (September 30, 2021): 93–102. http://dx.doi.org/10.31489/2021ch3/93-102.

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The inhibition effect of series of thiadiazole derivatives against the corrosion of mild steel in 15 % HCl was studied by weight-loss method and electrochemical measurements. The experiments were performed on steel St3 at 293 K, the exposure time of the samples in solution for weight-loss measurements was 24 h. Potentiodynamic polarization curves were obtained in a typical three electrode cell with the help of electrochemical measuring complex SOLARTRON 1280 C. A scan rate was 1 mV⋅s-1 and a measurement point was taken every 0.2 s. 2-aminothiazole, 5-amino-1,3,4-thiadiazole-2-thiol, 2-amino-1,3,4-thiadiazole, 2-amino-5-(furan-2-yl)- 1,3,4-thiadiazole, 1,3,4-thiadiazole-2-ylamide of acetic acid were studied as potential inhibitors. The maximal inhibition efficiency was obtained at concentration 0.10-0.20 g⋅L−1. The best result was demonstrated by 5-amino-1,3,4-thiadiazole-2-thiol (inhibition effect was more than 90 %). The minimal inhibition effect had 1,3,4-thiadiazole-2-ylamide acetic acid. The corrosion inhibition effect calculated from data of the corrosion current density and from the weight-loss measurements were in sufficiently good agreement. The effective activation energy of the corrosion of St3 increased significantly due the presence of the inhibitors (from 3.3 to 94.8 kJ⋅mol-1). The results point to promising of investigating of series of thiadiazole derivatives and inhibitory compositions based on thiadiazole as potential acid corrosion inhibitors.
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6

Tyutina, Marina A., Tatyana V. Kudayarova, and Elena A. Danilova. "PRODUCTS OF INTERACTION BETWEEN 2,5-DIAMINO- 1,3,4-THIADIAZOLE AND p-AMINOBENZALDEHYDE." IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENIY KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 59, no. 5 (July 12, 2018): 16. http://dx.doi.org/10.6060/tcct.20165905.5351.

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5-Amino-2N-benzylidene-4'-amino-1,3,4-thiadiazole and 2,5 bis (N-benzylidene-4'-amino) - 1,3,4-thiadiazole was synthesized by interaction between 2,5-diamino-1,3,4-thiadiazole and p –ami-nobenzaldehyde in ethanol environment. The structure was established on data of mass spectrometry, the elemental analysis, UV-Vis, IR, 1H NMR spectroscopy. An electronic and geometrical structure of the synthesized compounds was studied by methods of quantum chemistry.
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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 (March 4, 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 exhibited moderate to good activity against Gram-positive bacteria and the same compound exhibit low to moderate activity on most gram-negative bacteria under study. Finally, compound E and F had little or no effect organism.
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8

Schäfer, W., U. Rosenfeld, H. Zaschke, H. Stettin, and H. Kresse. "Kristallin-flüssige 1,3,4-Thiadiazole. II [1]. 1,3,4-Thiadiazole mit Cyclohexanstrukturfragmenten." Journal für Praktische Chemie 331, no. 4 (1989): 631–36. http://dx.doi.org/10.1002/prac.19893310413.

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Shi, Da-Hua, Hui-Long Zhu, Yu-Wei Liu, Zong-Ming Tang, Chen Lu, Xiao-Dong Ma, Xiao-Kai Song, Wei-Wei Liu, Tong Dong, and Meng-Qiu Song. "Synthesis and Evaluation of 5-Benzyl-1,3,4-Thiadiazole Derivatives as Acetylcholinesterase Inhibitors." Journal of Chemical Research 41, no. 11 (November 2017): 664–67. http://dx.doi.org/10.3184/174751917x15094552081242.

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Three novel 5-benzyl-1,3,4-thiadiazole derivatives were synthesised starting from phenylacetic acid derivatives. These compounds were characterised by NMR, HRMS and single-crystal X-ray diffraction analysis. 2-Pyrrolidyl-5-[2-(4-bromophenyl)methyl]-1,3,4-thiadiazole showed moderate acetylcholinesterase-inhibition activity with a 50% inhibitory concentration value of 33.16 μM. 2-Pyrrolidyl-5-[2-(4-bromophenyl)methyl]-1,3,4-thiadiazole and acetylcholinesterase docking was demonstrated using the Molecular Operating Environment program.
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10

Ila, Reshmi Dani, Surya Pratap Verma, and G. Krishnamoorthy. "The origin of the longer wavelength emission in 2-(4-fluorophenylamino)-5-(2,4-dihydroxybenzeno)-1,3,4-thiadiazole and its analogue 2-phenylamino-5-(2-hydroxybenzono)-1,3,4-thiadiazole." Photochemical & Photobiological Sciences 19, no. 6 (2020): 844–53. http://dx.doi.org/10.1039/c9pp00490d.

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Dissertations / Theses on the topic "1,3,4-thiadiazole"

1

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-dimethyl-1,3,4-thiadiazole s'est revelee plus complexe. Les conditions experimentales optimales ont ete determinees afin d'obtenir des rendements satisfaisants a partir des derives carbonyles et des sels d'iminium. Nous avons ainsi pu preparer des series de composes difonctionnels, analogues aux series precedentes. L'etude de la polyalkylation du 2,5-dimethyl-1,3,4-thiadiazole par polylithiation, puis action des derives halogenes, a permis de determiner le degre maximum de substitution qu'il etait possible d'atteindre : il s'agit de l'hexasubstitution dans le cas de l'iodure de methyle et de la tetrasubstitution symetrique dans les cas du chlorure de trimethylsilyle et du bromure de benzyle. Dans la troisieme partie, en vue d'etablir des comparaisons entre les types structuraux azole-c-c-aryle et azole-n-c-aryle au niveau des proprietes phytosanitaires, nous avons realise la synthese de plusieurs amides n-thiadiazoliques, avec d'excellents rendements. Parmi tous les produits prepares, trente six ont ete testes par la societe novartis en vue de determiner leur activite en tant que fongicides et/ou herbicides. Le 5-methyl-23-methyl-2-(4-morpholino)butyl-1,3,4-thiadiazole s'est montre le compose le plus interessant.
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Fürmeyer, Fabian [Verfasser]. "Fe(II) and Co(II) Spin Crossover Complexes using 1,3,4 Thiadiazole Bridging Ligands / Fabian Fürmeyer." Mainz : Universitätsbibliothek der Johannes Gutenberg-Universität Mainz, 2020. http://d-nb.info/1223054845/34.

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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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4

Ingner, Fredric. "Suzuki coupling of functionalized arylboronic acids to a 2-Amino-5-(4-bromophenyl)-1,3,4-thiadiazole scaffold." Thesis, Uppsala universitet, Institutionen för kemi - BMC, 2014. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-247573.

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Sutherland, Ian Thor. "APPLYING A LATE-STAGE LAWESSON’S CYCLIZATION STRATEGY TOWARDS THE SYNTHESIS OF 1,3,4-THIADIAZOLE-2-CARBOXYLATE THIOESTERS." Kent State University Honors College / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=ksuhonors1437100137.

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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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7

Copin, Chloé. "Exploration moléculaire en série imidazo[2, 1-b][1, 3, 4]thiadiazole : applications à la synthèse d'inhibiteurs de kinases impliqués dans les maladies neurodégénératives." Thesis, Orléans, 2013. http://www.theses.fr/2013ORLE2074.

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Depuis plus d’un siècle, la chimie hétérocyclique représente l’un des plus vastes domaines de recherche en chimie organique. En particulier, les hétérocycles bicycliques fusionnés à 5 chaînons, contenant à la fois des atomes de soufre et d’azote, présentent, de par leur rareté et leur potentiel biologique, un champ d’intérêt croissant pour les équipes de recherche et développement académiques ou des entreprises pharmaceutiques. Parmi les nombreux composés bicycliques [5-5], notre étude s’est focalisée sur le noyau imidazo[2,1-b][1,3,4]thiadiazole décrit sporadiquement dans la littérature et pour lequel les voies d’accès actuelles ne se limitent qu’à une seule méthode faisant intervenir une étape de cyclisation et des conditions drastiques. Ce verrou entraine inéluctablement une faible diversité fonctionnelle autour de cet hétérocycle, restreignant ainsi les domaines d’applications notamment biologiques. Afin de pallier à cette problématique, nous avons initié une étude de la réactivité de chacune des trois positions fonctionnalisables du bicycle imidazo[2,1-b][1,3,4]thiadiazole, développant ainsi diverses réactions pallado-catalysées (Suzuki-Miyaura, CH-arylation, Buchwald-Hartwig), de substitution nucléophile aromatique et de Pictet-Spengler. L’étude des propriétés biologiques des différents composés synthétisés et hautement valorisables durant ces travaux a abouti à la découverte de deux séries de molécules inhibant sélectivement les kinases DYRK-1A et CLK-1, deux protéines d’intérêt dans le traitement des affections du système nerveux central (neuropathies, Alzheimer…)
For more than a century, heterocyclic chemistry is one of the largest area in organic chemistry research. In particular, because of their rarity and their biological potential, [5-5] fused ring heterocycles containing both sulfur and nitrogen atoms are a large area of interest for both academic and industrial research and development teams. Among these numerous [5-5] bicycles, our study is focused on imidazo[2,1-b][1,3,4]thiadiazole scaffold, which is quite few described in the literature and whose pathways are limited to almost one method involving a cyclisation step and drastic conditions. This lock leads inevitably to low functional diversity around this heterocycle, thus restricting its applications, including biological. In order to overcome this problematic, we then initiated the reactivity study of each three positions of the bicycle imidazo[2,1-b][1,3,4]thiadiazole, developing thereby several palladium couplings (Suzuki-Miyaura, direct arylation, Buchwald-Hartwig), as well as aromatic nucleophilic substitution and Pictet-Spengler reaction. The study of the biological properties of the different compounds synthesized in this work and highly valuable led to the discovery of two series of molecules, inhibiting selectively DYRK-1A and CLK-1, two kinases of interest in the treatment of dysfunction of central nervous system (neuropathies, Alzheimer…)
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Seltmann, Jens. "Struktur-Eigenschaftsbeziehungen V-förmiger Mesogene zur Realisierung biaxial nematischer Mesophasen." Doctoral thesis, Universitätsbibliothek Chemnitz, 2011. http://nbn-resolving.de/urn:nbn:de:bsz:ch1-qucosa-67693.

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Die vorliegende Arbeit befasst sich mit der Synthese und der Untersuchung von Struktur-Eigenschaftsbeziehungen neuartiger V-förmiger, formstabiler Mesogene zur Realisierung biaxial nematischer Mesophasen (Nb). Alle synthetisierten Verbindungen besitzen ein formtreues Oligo(phenylenethinylen)-Grundgerüst, an welches laterale Alkyloxyketten und verschiedene terminale Substituenten (z. B. -CN, O(CH2)nCOOEt, Pyridyle) angebunden wurden. Durch dieses spezielle Design erhält man ausschließlich nematische und keine höher geordneten flüssigkristallinen Phasen. Durch den Einsatz verschiedener zentraler heterozyklischer Kernbausteine konnten erfolgreich Öffnungswinkel zwischen 108.9° und 160° realisiert werden. Dabei zeigen Thiadiazolderivate stets enantiotrope Mesophasen, wobei im Hochtemperaturbereich eine uniaxiale Phase mit biaxialen Aggregaten vorliegt. Beim Abkühlen konnte bei etwa 50 °C mittels Polarisationsmikroskopie und dielektrischer Spektroskopie ein Übergang in die Nb-Phase nachgewiesen werden. Die erstmalige Beobachtung eines direkten Übergangs von der isotropen Phase in die Nb-Phase gelang durch den Einsatz von Benzo[1,2-b:4,3-b]dithiophen als Kernbaustein.
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Jia, Huang Shing, and 黃信嘉. "Synthesis and Characteristics of 1,3,4-Thiadiazole Derivatives." Thesis, 2004. http://ndltd.ncl.edu.tw/handle/12191180337143130451.

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碩士
國立臺灣科技大學
高分子工程系
92
The investigation was prepared by the reaction with thiosemicarbazide, carbon disulfide, p-substiuented-benzoic acid in ethanol at refluxed to get 1,3,4-thiadiazole(3、5a~5d). Then 1,3,4-thiadiazole derivatives coupled with N-substiuented-pyridone derivatives(12a~12j) and pyroazolone derivatives(13a~13j). Furthermore, 1,3,4-thiadiazole intermediates were reacted with cyanuric chloride to give a reactive dyes (20), and these dyes condensed with hydrazine hydrate and 4-nitrobenzaldehyde in ethanol to obtain azo-methine dyes (26a~26b)。 Characterization of these dyes was carried out by spectral and elemental analysis. The solvent effect in the visible absorption spectra was also evaluated.
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10

Huang, Chi-Shuen, and 黃啟舜. "A novel discotic liquid crystal based on 1,3,4-thiadiazole." Thesis, 2006. http://ndltd.ncl.edu.tw/handle/91775315936438796932.

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碩士
國立中央大學
化學研究所
94
In the first series, the preparation, characterization and mesomorphic properties of palladium chloride and palladium bromide complexes derived from bis-(1,3,4-thiadiazole) derivatives are described. These compounds with a different number of alkoxy side chain exhibited various mesophases, which were studied and investigated by differential scanning calorimeter (DSC), polarized optical microscopy (POM) and powder X-ray diffraction (XRD). The formation of mesophases was found to be sensitive to the number of the alkoxy side chain, carbon length of the side chains, stereo geometry, and the coordination of metal centers. As light emittng materials, the physical properties by UV-Vis spectrophotometer, and photoluminescence (PL) were also studied and discussed. In the second series, a new type of metallomesogenic complexes structurally similar to the first series with a OH group added was prepared ane studied. Theses metal complexes were coordinated in different geometries from the first series. All compounds in the series existing intramolecular hydrogen bond and an ESIPT behavior, were investigated by FT-IR and UV-PL. In addition, in order to better understand the molecular arrangement in columnar mesophases, the molecular volume dilatomery and other parameters were also measured and discussed.
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Books on the topic "1,3,4-thiadiazole"

1

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

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Book chapters on the topic "1,3,4-thiadiazole"

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Demaison, J. "151 C2H2N2S 1,3,4-Thiadiazole." In Asymmetric Top Molecules. Part 1, 317. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-10371-1_153.

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Patil, Ajay M., Ravindra S. Shinde, B. R. Sharma, and Sunil R. Mirgane. "Green Synthesis, Characterization, and Biological Studies of 1,3,4-Thiadiazole Derived Schiff Base Complexes." In Green Chemistry and Sustainable Technology, 261–74. Includes bibliographical references and index.: Apple Academic Press, 2020. http://dx.doi.org/10.1201/9780367808310-11.

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Patil, Ajay M., Ravindra S. Shinde, and Sunil R. Mirgane. "Facile Synthesis of Some 1,3,4 Thiadiazole-Based Ligands and Their Metal Complexes as Potential Antimicrobial Agents." In Modern Green Chemistry and Heterocyclic Compounds, 145–57. Series statement: Innovations in physical chemistry: monographic series: Apple Academic Press, 2020. http://dx.doi.org/10.1201/9780367276942-6.

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Zhang, Wanjia, Zhiyong Gao, Runqing Liu, Haisheng Han, Pan Chen, Yue Yang, Lei Sun, et al. "A Novel Collector 5–(Butylthio)–1,3,4–Thiadiazole–2–Thiol: Synthesis and Improved Flotation of Galena and Sphalerite from Pyrite." In The Minerals, Metals & Materials Series, 633–49. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-37070-1_55.

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Varvaresou, Athanasia, Anna Tsantili-Kakoulidou, and Theodora Siatra-Papastaikoudi. "A Critical Appraisal of logP Calculation Procedures Using Experimental Octanol-Water and Cyclohexane-Water Partition Coefficients and HPLC Capacity Factors for a Series of Indole Containing Derivatives of 1,3,4-Thiadiazole and 1,2,4-Triazole." In Molecular Modeling and Prediction of Bioactivity, 493–94. Boston, MA: Springer US, 2000. http://dx.doi.org/10.1007/978-1-4615-4141-7_133.

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"*** 2-AMIN0-5-(5-NITR0-2-FURYL)-1,3,4-THIADIAZOLE." In Dangerous Properties of Industrial and Consumer Chemicals, 49–50. CRC Press, 1994. http://dx.doi.org/10.1201/9781482293500-18.

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Hudson, M. J., M. B. Hassan, and G. Tiravanti. "Extraction of Cadmium from Aqueous Solution Using 1,3,4-Thiadiazole-2,5-Dithiol." In Studies in Environmental Science, 529–35. Elsevier, 1986. http://dx.doi.org/10.1016/s0166-1116(08)70961-0.

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John, S. Abraham, Osamu Hatozaki, and Noboru Oyama. "Studies on the interaction between underpotentially deposited copper and 2.5-dimercapto-1,3,4-thiadiazole adsorbed on gold electrode." In Studies in Surface Science and Catalysis, 943–46. Elsevier, 2001. http://dx.doi.org/10.1016/s0167-2991(01)82242-4.

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Cailler, Lucie P., Alexander G. Martynov, Yulia G. Gorbunova, Aslan Yu Tsivadze, and Alexander B. Sorokin. "Carbene insertion to N–H bonds of 2-aminothiazole and 2-amino-1,3,4-thiadiazole derivatives catalyzed by iron phthalocyanine." In Porphyrin Science by Women, 1198–207. WORLD SCIENTIFIC, 2021. http://dx.doi.org/10.1142/9789811223556_0106.

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Conference papers on the topic "1,3,4-thiadiazole"

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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. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0134-1.

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Parra, M. L., E. Y. Elgueta, A. I. Sánchez, J. M. Vergara, P. I. Hidalgo, and J. A. Ulloa. "Liquid Crystals based on carboxylic acids, amines and nitro compounds derived from 1,3,4-thiadiazole." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0104-1.

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Zhu, Fangkun, Wenxiu Fan, Li Qu, and Hailing Hao. "Prepation and tribological investigation of a novel S-N style 1,3,4-thiadiazole-2-thione derivatives." In 2011 International Conference on Consumer Electronics, Communications and Networks (CECNet). IEEE, 2011. http://dx.doi.org/10.1109/cecnet.2011.5768657.

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Viprabha, K., and D. Udaya Kumar. "Amelioration of opto – electronic response of thiophene - Imidazo[2,1-b][1,3,4]thiadiazole based organic semiconductors." In PROCEEDINGS OF THE 3RD INTERNATIONAL CONFERENCE ON AUTOMOTIVE INNOVATION GREEN ENERGY VEHICLE: AIGEV 2018. Author(s), 2019. http://dx.doi.org/10.1063/1.5085601.

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You might also be interested in the extended bibliographies on the topic '1,3,4-thiadiazole' for particular source types:
Journal articles
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