Relevant bibliographies by topics / -2-thione

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

Academic literature on the topic '-2-thione'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "-2-thione"

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Liu, YingChun, and XiaoYu Li. "Perhydrobenzimidazole-2-thione." Acta Crystallographica Section E Structure Reports Online 65, no. 2 (2009): o248. http://dx.doi.org/10.1107/s1600536808043894.

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Laknifli, A., M. Pierrot, F. Chanon, and M. Chanon. "5-tert-Butylthiazolidine-2-thione and 5-Phenylthiazolidine-2-thione." Acta Crystallographica Section C Crystal Structure Communications 52, no. 1 (1996): 215–18. http://dx.doi.org/10.1107/s0108270195010699.

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Sathyanarayana, D. N., and S. V. Kasmir Raja. "Molecular vibrations of pyridine-2-thione and pyrimidine-2-thione." Spectrochimica Acta Part A: Molecular Spectroscopy 41, no. 6 (1985): 809–13. http://dx.doi.org/10.1016/0584-8539(85)80026-x.

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Saithong, Saowanit, Chaveng Pakawatchai та Jonathan P. H. Charmant. "Poly[μ-1,3-thiazolidine-2-thione-κ2 S 2:S 2-μ-thiocyanato-κ2 S:N-copper(I)]". Acta Crystallographica Section E Structure Reports Online 63, № 3 (2007): m857—m858. http://dx.doi.org/10.1107/s1600536807007441.

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The title compound, [Cu(SCN)(C3H5NS2)] n , was prepared from the direct reaction between copper(I) thiocyanate and 1,3-thiazolidine-2-thione. The structure is an infinite two-dimensional polymer, parallel to the ac plane, with tetrahedrally distorted Cu atoms which are coordinated by the S and N atoms of the thiocyanate ions, and by the thione S atom of 1,3-thiazolidine-2-thione molecules.
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Friedrichs, Steffi, and Peter G. Jones. "Secondary Interactions in Gold(I) Complexes with Thione Ligands. 2. Three Ionic Camphorsulfonates with Z’ = 2 [1]." Zeitschrift für Naturforschung B 59, no. 7 (2004): 793–9. http://dx.doi.org/10.1515/znb-2004-0708.

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All three structures of the form bis(thione)gold(I) camphor-10-sulfonate [thione = imidazolidine-2-thione, 1; 1-methyl-imidazolidine-2-thione, 2; thiazolidine-2-thione, 3] crystallize in chiral space groups with Z′ = 2; local inversion symmetry of the cationic assemblies (less pronounced for 3) provides some rationalisation for this. The basic structural units are accounted for in terms of classical hydrogen bonds, leading to rings involving ion pairs for 1 and 2, but to infinite chains of anions and cations for 3. Neighbouring ion pairs in 1 are joined by further classical hydrogen bonds, in
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Stoyanov, Stefan, Ivan Petkov, Liudmil Antonov, Tatyana Stoyanova, Petros Karagiannidis, and Paraskevas Aslanidis. "Thione–thiol tautomerism and stability of 2- and 4-mercaptopyridines and 2-mercaptopyrimidines." Canadian Journal of Chemistry 68, no. 9 (1990): 1482–89. http://dx.doi.org/10.1139/v90-227.

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The possible thione–thiol tautomerism of 2- and 4-mercaptopyridines, 2-mercaptopyrimidine, and 4,6-dimethyl-2-mercaptopyrimidine in solution is studied by means of absorption (UV–VIS) spectroscopy. In accordance with earlier observations, polar solvents and self-association shift the apparent tautomeric equilibrium significantly towards the thione form. In dilute solutions of nonpolar solvents the thiol form predominates. On standing, significant changes are observed in the absorption spectra of these tautomeric compounds in ethanol, dioxane, and water. The time course of the tautomerization,
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Munshi, Parthapratim, and T. N. Guru Row. "2H-Chromene-2-thione." Acta Crystallographica Section E Structure Reports Online 57, no. 12 (2001): o1175—o1176. http://dx.doi.org/10.1107/s1600536801019067.

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Munshi, Parthapratim, and T. N. Guru Row. "2H-Thiochromene-2-thione." Acta Crystallographica Section E Structure Reports Online 60, no. 11 (2004): o2168—o2170. http://dx.doi.org/10.1107/s1600536804026984.

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Mietlarek-Kropidłowska, Anna, Jaroslaw Chojnacki, and Barbara Becker. "1,3-Dibenzylimidazolidine-2-thione." Acta Crystallographica Section E Structure Reports Online 68, no. 8 (2012): o2521. http://dx.doi.org/10.1107/s1600536812032655.

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In the title compound, C17H18N2S, the imidazolidine ring adopts a twisted conformation. In the crystal, molecules are linked by slipped π–π interactions between the benzene rings of neighbouring molecules [centroid-to-centroid distance = 3.903 (2) Å].
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Nishio, Takehiko, and Kiyoko Shiwa. "Acylation and Alkoxycarbony-lation of Benzoxazoline-2-thione and Benzothiazoline-2-thione." HETEROCYCLES 62, no. 1 (2004): 313. http://dx.doi.org/10.3987/com-03-s(p)10.

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Dissertations / Theses on the topic "-2-thione"

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Silva, Sandrina Ribeiro Martins da. "1,3-Oxazoline-2-thiones saccharidiques : synthèse et réactivité de structures bio-actives originales." Thesis, Orléans, 2009. http://www.theses.fr/2009ORLE2083.

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A nos jours, la résistance des microorganismes aux antibiotiques est l'un des plus gros problèmes de la santé publique. La recherche de nouvelles familles de composés naturelles ou synthétiques nous amène vers la découverte des méthodologies innovantes conduisant à de nouveaux antibiotiques. Dans le présent travail, nous vous invitons à plonger dans le "nouveau monde" de la synthèse, la réactivité et l'activité biologique de 1,3-oxazoline-2-thiones (OXTs). En effet, cet hétérocycle peu exploré est un facilement obtenu par condensation entre _-hydroxycarbonyle et l'acide thiocyanique. Lorsque l
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Spencer, Gavin Murray. "Organometallic compounds of the 1,3-dithiole-2-thione-4,5-dithiolate (DMIT) ligand." Thesis, University of Aberdeen, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.300910.

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Compounds of the form R<sub>2</sub>Sn(dmit) (H<sub>2</sub>dmit = dimercaptoisotrithione) (R = Me, Et, Bu, Oct, Ph, <I>o</I>-MeOC<sub>6</sub>H<sub>4</sub>. MeO<sub>2</sub>CCH<sub>2</sub>CH<sub>2</sub> and Pr<sup>i</sup>O<sub>2</sub>CCH<sub>2</sub>CH<sub>2</sub>) and RR'Sn(dmit) (R = Ph, R' = Me) were synthesised and characterised. Five of the compounds were further investigated using solid state <sup>13</sup>C and <sup>119</sup>Sn nmr and Mossbauer spectroscopy. The crystal structure of the compounds Et<sub>2</sub>Sn(dmit), (MeO<sub>2</sub>CCH<sub>2</sub>CH<sub>2</sub>)<sub>2</sub>Sn(dmit) and
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Chohan, Zahid H. "Co-ordination chemistry of the 1,3-dithiole-2-thione (DMIT) and 2-one-4,5-dithiolato (DMIO) compounds." Thesis, University of Aberdeen, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.244990.

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Various bis-dmio and -dmit zincate complexes, [Q]<SUB>2</SUB>[Zn(dmio)<SUB>2</SUB>] [Q = NEt<SUB>4</SUB>, 1,4-dmp, Ph<SUB>4</SUB>P and FcCH<SUB>2</SUB>NMe<SUB>3</SUB>] and [Q]<SUB>2</SUB>[Zn(dmit)<SUB>2</SUB>] [Q = FcCH<SUB>2</SUB>NMe<SUB>3</SUB>], have been prepared and characterised by IR, <SUP>1</SUP>H and <SUP>13</SUP>C-NMR spectral and elemental analysis data. The solid state structure of [FcCH<SUB>2</SUB>NMe<SUB>3</SUB>]<SUB>2</SUB>[Zn(dmio)<SUB>2</SUB>] was determined by X-ray crystallography. The complexes, [Q]<SUB>2</SUB>[Zn(dmio)<SUB>2</SUB>] and [Q]<SUB>2</SUB>[Zn(dmit)<SUB>2</SUB>]
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Allan, Gillian Margaret. "Organic and organometallic compounds of the 1,3-dithiole-2-thione-4,5-dithiolate (dmit) ligand." Thesis, University of Aberdeen, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.312355.

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Neutral diorganotin compounds of the 1,3-dithiole-2-thione-4,5-dithiolate ligand have been prepared. The syntheses of Me<sub>2</sub>Sndmit, Et<sub>2</sub>Sndmit, Bu<sub>2</sub>Sndmit, (C<sub>8</sub>H<sub>17</sub>)<sub>2</sub>Sndmit, (C<sub>10</sub>H<sub>21</sub>)<sub>2</sub>Sndmit and (C<sub>14</sub>H<sub>29</sub>)<sub>2</sub>Sndmit are described. For the purposes of indicating the formation of different structural phases, D.S.C. powder patterns are reported for initial and recrystallised samples of Me<sub>2</sub>Sndmit, Et<sub>2</sub>Sndmit and Bu<sub>2</sub>Sndmit. Since Et<sub>2</sub>Sndmit
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Koner, Abhishek [Verfasser]. "On the imidazole-2-thione-based route to tricyclic 1,4-diphosphinines: synthesis, structures and reactions / Abhishek Koner." Bonn : Universitäts- und Landesbibliothek Bonn, 2018. http://d-nb.info/1154485862/34.

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Pereira, Elaine. "Adição de enolatos de titanio derivados de N-acil-(4S)-4-isopropil-1,3-tiazolidin-2-tiona a ions N-aciliminios ciclicos : sintese assimetrica dos alcaloides (+)-isoretronecanol e (+)-5-epi-tashiromina." [s.n.], 2005. http://repositorio.unicamp.br/jspui/handle/REPOSIP/249250.

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Orientador: Ronaldo Aloise Pilli<br>Dissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Quimica<br>Made available in DSpace on 2018-08-04T15:31:59Z (GMT). No. of bitstreams: 1 Pereira_Elaine_M.pdf: 9380147 bytes, checksum: a608a978d005928c3df671eb93be3ed9 (MD5) Previous issue date: 2005<br>Mestrado<br>Quimica Organica<br>Mestre em Química
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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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Ciccolini, Cecilia. "Synthesis of Mono and Poly-Heterocycles starting from 1,2-Diaza-1,3-Dienes (or precursors) as Building Blocks." Doctoral thesis, Urbino, 2020. http://hdl.handle.net/11576/2674162.

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Nozdryn, Tomasz. "Nouveaux dérivés fluorés du tétrathiafulvalène (TTF) : synthèse, électrochimie, et conversion ou organisation en matériaux organiques." Angers, 1995. http://www.theses.fr/1995ANGE0004.

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La réduction sélective du 4-methyloxycarbonyl-2-thioxo-1,3-dithiole permet d'accéder à volonté soit à l'aldéhyde soit à l'alcool correspondant. De cet alcool on peut passer au sel de phosphonium dérivé qui, via des réactions de Wittig, peut conduire à de nouveaux analogues de TTF à grande extension spatiale avec de bons rendements. Divers dérivés fluorés en série TTF, symétriques et dissymétriques, dans lesquels le noyau TTF est substitué par un ou plusieurs groupements -ch#2f ou -s-(ch#2)#2-c#nf#2#n#+#1 (n = 6, 8), ont été synthétisés par couplage de dithiol-(thi)ones convenablement choisies.
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VALADE, FARGES LYDIE. "Conducteurs et supraconducteur moleculaires : complexes de metaux de transition a ligand soufre." Toulouse 3, 1987. http://www.theses.fr/1987TOU30008.

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Etude des proprietes electriques et structurales de deux series de composes a coordinat dmit : composes a etat d'oxydation fractionnaire (m(dmit)::(2))c::(x) et composes donneur-accepteur d(m(dmit)::(2))::(y) (avec m = zn,ni,pt,pd; c = nbu**(+)::(4) et asph**(+)::(4); d = ttf, tmttf, ttmttf, bedt-ttf et tmtsf; n dans (m(dmit)::(2))**(n-) etant egal a 2,1,x,0). Mise en evidence de la nature 2d des composes de la premiere serie et quasi 3d de ceux de la deuxieme; relations structure-conductivite. Mise en evicence de la supraconduction dans le cas du complexe ttf(ni(dmit)::(2))::(2), avec une tem
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Book chapters on the topic "-2-thione"

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with 1-hydroxy-2-pyridine-thione." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49202-4_251.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) chloro complex with 1-hydroxypyridin-2-thione." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_75.

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Bottomley, Peter, Richard A. Hoodless, and Nigel A. Smart. "Review of Methods for the Determination of Ethylenethiourea (Imidazolidine-2-Thione) Residues." In Residue Reviews. Springer New York, 1985. http://dx.doi.org/10.1007/978-1-4612-5132-3_2.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of iron(III) complex with 1-hydroxy-2-pyridine thione." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-45972-0_417.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of iron(II) complex with 1-hydroxy-2-pyridine-thione." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-45972-0_416.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) complex with 1-phenyl-4,6-dimethylpyrimidine-2-thione." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54234-7_146.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) complex with 1-phenyl-4,6-dimethylpyrimidine-2-thione." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54234-7_147.

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Raper, E. S., J. R. Creighton, B. R. Flynn, and M. Norton. "Complexes of 1,3-Dihydro-1-Methyl-2H -Imidazole-2-Thione with Cobalt(II)." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132548.ch33.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) complex with 2-thione-4,6-diamino-5-hydroxypyrimidine." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 6. Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65056-1_245.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of iron(III) complex with 2-thione-4,6-diamino-5-hydroxypyrimidine." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 6. Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65056-1_111.

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Conference papers on the topic "-2-thione"

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Kosmas, Agnie Mylona, Demetrios K. Papayannis, Theodore E. Simos, and George Maroulis. "Computational Studies on Dihalogen Complexes of N-methyl Imidazoline-2-thione and N-methyl Imidazolidine-2-thione." In COMPUTATIONAL METHODS IN SCIENCE AND ENGINEERING: Theory and Computation: Old Problems and New Challenges. Lectures Presented at the International Conference on Computational Methods in Science and Engineering 2007 (ICCMSE 2007): VOLUME 1. AIP, 2007. http://dx.doi.org/10.1063/1.2836193.

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Sapaev, B., I. B. Sapaev, F. E. Saitkulov, A. A. Tashniyazov, and D. Nazaraliev. "Synthesis of 2-methylquinazoline-4-thione with the purpose of alkylation of 3-propyl 2-methylquinazoline-4-thione with alkylating agents." In 2021 ASIA-PACIFIC CONFERENCE ON APPLIED MATHEMATICS AND STATISTICS. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0089924.

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Guliyeva, Lala, Muhammed Trawally, Kübra Demir-Yazıcı, Kerem Kaya, Atilla Akdemir, and Özlen Güzel-Akdemir. "Thione or Thiol: Sructural Confirmation of (E)-2-(1-(4-cyanophenyl)ethylidene)-N-(2-fluoro-4-sulfamoylphenyl)hydrazine-1-Carbothioamide and Carbonic Anhydrase Inhibition Studies." In 8th International Students Science Congress. ULUSLARARASI ÖĞRENCİ DERNEKLERİ FEDERASYONU (UDEF), 2024. https://doi.org/10.52460/issc.2024.060.

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Thiosemicarbazones are Schiff bases formed by condensing an aldehyde or ketone with thiosemicarbazide derivatives. TSCs exhibit various biological activities and act as precursors for key scaffolds, with keto-enol tautomerism commonly resulting in thione or thiol forms. This study focuses on synthesizing and confirming the structure of compound 1, (E)-2-(1-(4-cyanophenyl)ethylidene)-N-(2-fluoro-4-sulfamoylphenyl)hydrazine-1-carbothioamide, through a condensation reaction in methanol. Both theoretical and experimental IR and X-ray studies confirm the presence of the thione form and E isomerism.
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Marzec, K. M., B. Gawel, W. Lasocha, et al. "Vibrational Characterization of Binding Model of 4-thiazolidinone-2-thione with Pb[sub 2][sup 2+] species." In XXII INTERNATIONAL CONFERENCE ON RAMAN SPECTROSCOPY. AIP, 2010. http://dx.doi.org/10.1063/1.3482691.

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Shutalev, Anatoly D., and Anastasia A. Fesenko. "An Unexpected Result of Base-Promoted Rearrangement of 4a-Acetyl-8a-hydroxydecahydroquinazoline-2-thione." In ECSOC 2022. MDPI, 2022. http://dx.doi.org/10.3390/ecsoc-26-13568.

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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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Dotsenko, Victor. "Synthesis and Alkylation of 5-Benzoyl-3-cyano-6-phenylpyridine-2(1H)-thione." In The 16th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2012. http://dx.doi.org/10.3390/ecsoc-16-01091.

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AL-Hilfi, Jassim A. "A structural study of 2-thenoyltrifluoroacetone Schiff bases and their thione derivatives: Synthesis, NMR and IR." In INTERNATIONAL CONFERENCE OF NUMERICAL ANALYSIS AND APPLIED MATHEMATICS ICNAAM 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0027547.

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Toda, Hiroyuki, Carl M. Verber, and Daniel P. Campbell. "Use of Z-scan measurement technique to characterize nonlinear optical properties of imidazole-2-thiones." In OSA Annual Meeting. Optica Publishing Group, 1991. http://dx.doi.org/10.1364/oam.1991.mgg2.

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The Z-scan technique for measuring third-order optical nonlinearities has been proposed and demonstrated recently.1 Using this technique, we measured the optically induced index change Δn for derivatives of imidazole-2-thione at a wavelength of 532 nm. In these materials, which are optically clear, we detected a quadratic relationship between the index change and the intensity in a 30–100-MW/cm2 range, as opposed to the linear relationship we observed in absorptive materials. We also observed that the distance between peak and valley of the Z-scan data was less than predicted for third-order e
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Hartung, Jens, Markus Heubes, Rainer Kneuer, and Michaela Schwarz. "Dynamic Behaviour of Cyclic Thiohydroxamic Acid Derivatives Barrier to Rotation about N2O Bonds in 4-Substituted N-Isopropoxythiazole-2(3H)-thiones and N-Isopropoxypyridine-2(1H)-thione." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01931.

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Reports on the topic "-2-thione"

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Beno, M. A., A. M. Kini, and J. M. Williams. Structures of two precursors to organic charge-transfer salts: 1,3-dithiolo[4,5-b][1,4]dithlin-2-thione and 1,3-dithiolo[4.5-b] [1,4]dithilin-2-one. Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/10132894.

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