Relevant bibliographies by topics / Dithiole

Contents

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

Academic literature on the topic 'Dithiole'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Dithiole"

1

Jourdain, I. V., and F. Guyon. "Syntheses and electrochemical characterization of heteroleptic cyclopentadienyl-bis(dithiolene) complexes of niobium and tantalum." Canadian Journal of Chemistry 78, no. 12 (2000): 1570–74. http://dx.doi.org/10.1139/v00-144.

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Diamagnetic niobium and tantalum complexes of general formula [M(η5-C5Me5)(dithiolene)2] have been prepared (M = Nb, dithiolene = dddt2– (5,6-dihydro-1,4dithiine-2,3-dithiolate) (1); M = Ta, dithiolene = dddt2– (2); M = Nb, dithiolene = dddt2– and dmit2– (1,3-dithiole-2-thione-4,5-dithiolate) (3)). All these complexes exhibit temperature-dependent 1H NMR spectra which result from a fluxional behavior of the dithiolene ligands. Their redox properties have been investigated by cyclic voltammetry and reversible oxidation processes involving the dithiolene ligands have been evidenced for the compl
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Chen, Xuan-Rong, Yun-Xia Sui, Lu Zhai, Wei-Hua Ning, and Xiao-Ming Ren. "Influence of the molecular structures of dithiolate ligands on crystal packing modes and magnetic properties in salts (Bz-Et3N)[Ni(dmit)x(mnt)2−x] (x = 0–2)." CrystEngComm 16, no. 37 (2014): 8717–25. http://dx.doi.org/10.1039/c4ce01168f.

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Nickel-bis-dithiolene salts, (Bz-Et<sub>3</sub>N)[Ni(dmit)<sub>x</sub>(mnt)<sub>2−x</sub>] (x = 0–2 for 1–3 and mnt<sup>2−</sup> = maleonitriledithiolate, dmit<sup>2−</sup> = 2-thioxo-1,3-dithiole-4,5-dithiolate), have been prepared and characterized.
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Silva, Rafaela A. L., Bruno J. C. Vieira, Marta M. Andrade, et al. "TTFs nonsymmetrically fused with alkylthiophenic moieties." Beilstein Journal of Organic Chemistry 11 (May 5, 2015): 628–37. http://dx.doi.org/10.3762/bjoc.11.71.

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Two new dithiolene ligand precursors, containing fused TTF and alkyl thiophenic moieties 3,3'-{[2-(5-(tert-butyl)thieno[2,3-d][1,3]dithiol-2-ylidene)-1,3-dithiole-4,5-diyl]bis[sulfanediyl]}dipropanenitrile (α-tbtdt, 1), and 3,3'-{[2-(5-methylthieno[2,3-d][1,3]dithiol-2-ylidene)-1,3-dithiole-4,5-diyl]bis[sulfanediyl]}dipropanenitrile (α-mtdt, 2), were synthesized and characterized. The electrochemical properties of these electronic donors were studied by cyclic voltammetry (CV) in dichloromethane. Both compounds show two quasi-reversible oxidation processes, versus Ag/AgCl, typical of TTF donor
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Stachel, Hans-Dietrich, Thomas Zoukas, Manfred Hußlein, Julyane Nienaber, and Matthias Schorp. "Kondensierte Dithiole, III. Synthese von 1,2-Dithiolo-furanen." Liebigs Annalen der Chemie 1993, no. 3 (1993): 305–11. http://dx.doi.org/10.1002/jlac.199319930151.

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Oliveira, Sandrina, Dulce Belo, Isabel Cordeiro Santos, Sandra Rabaça, and Manuel Almeida. "Synthesis and characterization of the cyanobenzene-ethylenedithio-TTF donor." Beilstein Journal of Organic Chemistry 11 (June 3, 2015): 951–56. http://dx.doi.org/10.3762/bjoc.11.106.

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A dissymmetric TTF-type electron donor, cyanobenzene-ethylenedithio-tetrathiafulvalene (CNB-EDT-TTF), was obtained in high yield, by a cross-coupling reaction with triethyl phosphite between 2-thioxobenzo[d][1,3]dithiole-5-carbonitrile and 5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-one. This new donor was characterized namely by single crystal X-ray diffraction, cyclic voltammetry, NMR, UV-visible and IR spectroscopy.
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Stachel, Hans-Dietrich, Matthias Schorp, and Thomas Zoukas. "Kondensierte 1,2-Dithiole, II. Synthese von Thieno-1,2-dithiolen." Liebigs Annalen der Chemie 1992, no. 10 (1992): 1039–44. http://dx.doi.org/10.1002/jlac.1992199201171.

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Zang, Shuang-Quan, Yang Su, and Ruo-Jie Tao. "N-(4-Nitrobenzyl)quinolinium bis(2-thioxo-1,3-dithiole-4,5-dithiolato)palladium(III) acetone solvate." Acta Crystallographica Section E Structure Reports Online 62, no. 5 (2006): m1002—m1003. http://dx.doi.org/10.1107/s1600536806012049.

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In the title ion-pair compound, (C16H13N2O2)[Pd(C3S5)2]·C3H6O, the PdIII atom exhibits square-planar coordination geometry involving four S atoms of two 2-thioxo-1,3-dithiole-4,5-dithiolate (dmit) ligands. Some weak S...S interactions and hydrogen bonds are found, resulting in a three-dimensional supramolecular network structure.
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Zeller, Matthias, and Vladimir A. Azov. "2-(1,3-Dithiol-2-ylidene)-1,3-dithiole-4-carbaldehyde." Acta Crystallographica Section E Structure Reports Online 69, no. 7 (2013): o1157. http://dx.doi.org/10.1107/s160053681301711x.

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Pedersen, Carl Th. "1,2-Dithiole-3-Thiones and 1,2-Dithiol-3-Ones." Sulfur reports 16, no. 2 (1995): 173–216. http://dx.doi.org/10.1080/01961779508048738.

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Fabian, Jürgen, and Peter Birner. "A theoretical study of the disulfide/dithione valence isomerism." Collection of Czechoslovak Chemical Communications 53, no. 9 (1988): 2096–115. http://dx.doi.org/10.1135/cccc19882096.

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According to MNDO calculations on 1,2-dithiete (IIIa), 1,2-dithiin (IVa) and 3,4-dimethylene-1,2-dithiane (Va) the closed-ring compounds are thermodynamically more stable than the open-chain compounds whereas the reverse holds for 4-methylene-1,2-dithiole (VIa). Substitution of the exocyclic CH2 group of VIa by O, S, NH, and OH+ stabilizes its cyclic mesoionic structure. The low triplet state energy of VIa and of some derivatives relative to the lowest singlet state energy signalizes the biradicaloid nature of these electronic structures. Replacement of hydrogen of the methine groups adjacent
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Dissertations / Theses on the topic "Dithiole"

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Saidi, Mokhtar. "Comportement électrochimique de quelques dithiole-1,2 thiones-3, dithiole-1,2 ones-3 et cations méthylthio-3 dithiole-1,2 ylium." Grenoble 2 : ANRT, 1988. http://catalogue.bnf.fr/ark:/12148/cb376183935.

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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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De, La Motte Anita Margaret. "New 1,2-dithiole chemistry." Thesis, Imperial College London, 1991. http://hdl.handle.net/10044/1/46741.

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Saidi, Mokhtar. "Comportement electrochimique de quelques dithiole-1. 2 thiones-3, dithiole-1. 2 ones-3 et cations methylthio-3 dithiole-1. 2 yluim." Rennes 1, 1988. http://www.theses.fr/1988REN10061.

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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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Bona, Meriem. "Détermination du logP eau/n-octanol de 1,2-dithiole-3-thiones et de 1,2-dithiole-3-ones : règles de calcul." Rennes 1, 1995. http://www.theses.fr/1995REN1S005.

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Green, Andrew. "Functionalised 1,3-dithiole derivatives exhibiting intramolecular donor-acceptor properties." Thesis, Durham University, 1997. http://etheses.dur.ac.uk/5066/.

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A variety of functionalised 1,3-dithiole derived donor-π-acceptor systems linked by an alkenic bridge have been synthesised, the acceptor units being dicyanomethylene and cyanoimine. They exhibit intramolecular electron transfer from the electron donor moiety to the electron acceptor moiety. The presence of electron donating substituents on the 1,3-dithiole ring increases the degree of overall charge transfer; this process has been studied by UV-VIS spectroscopy and X-ray crystallography. The latter technique indicates a significant amount of intramolecular electron transfer in the ground stat
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Coffin, Malcolm Andrew. "The synthesis and redox properties of new 1,3-dithiole systems." Thesis, Durham University, 1992. http://etheses.dur.ac.uk/6124/.

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The theory of conductivity in organic metals and a review of organic π-electron donors is introduced in Chapter One, outlining some of die many variations that have been made to the tetrathiafulvalene (TTF) molecule, the donor component in the first true organic metal. A range of new' alkylseleno-substituted ethanediylidene-2,2’-bis(l,3-dithiole) donors have been efficiently synthesised. These compounds form semi-conducting charge- transfer complexes with 7,7,8,8-tetracyano-p-quinodimethane (TCNQ). The synthesis, electrochemistry. X-ray crystal structure and magnetic properties are presented (
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Guio, Laurence V. Y. "Polynuclear clusters in desulfurisation reactions of 1,3-dithiole-2-thiones." Thesis, University of Sheffield, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.275037.

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CHOLLET, MARYLENE. "Contribution a l'etude des effets electroniques des restes 4 ou 5-1,2-dithiole-3-thione-yl et 4 ou 5-1,2-dithiole-3-one-yl." Rennes 1, 1997. http://www.theses.fr/1997REN10079.

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L'etude du sens et de l'intensite des effets electroniques des restes 5-1,2-dithiole-3-thione(one)-yl et 4-1,2-dithiole-3-thione(one)-yl fait l'objet de cette these. Elle a ete realisee en suivant deux voies de recherche. La premiere a consiste a determiner les valeurs de pka, en milieu aqueux par spectrophotometrie u. V. -visible, de plusieurs 4 ou 5-aminophenyldithiolethiones(ones) et de la 4-p-hydroxyphenyldithiolethione. Les resultats obtenus, entres dans des correlations de type hammett, permettent d'affirmer que : - les restes 5-1,2-dithiole-3-thione(one)-yl sont fortement attracteurs pa
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Books on the topic "Dithiole"

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Stiefel, Edward I., ed. Dithiolene Chemistry. John Wiley & Sons, Inc., 2003. http://dx.doi.org/10.1002/0471471933.

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Ashcroft, Martin John. Quinoxaline-2,3-dithiolate and its metal complexes. University of Manchester, 1994.

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Wilson, Clare Rosemary. Studies of metal dithiolene complexes related to the redox properties of Moco. University of Manchester, 1997.

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Ball, C. P. The development of a fibre-optic heavy metal ion sensor based on immobilised dithizone. UMIST, 1993.

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Occupational Medicine and Hygiene Laboratory. Lead and inorganic compounds of lead in air: Colorimetric field method using sym-diphenyl-thiocarbazone (dithizone). Health and Safety Executive, 1987.

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Karlin, Kenneth D., and Edward I. Stiefel. Dithiolene Chemistry: Synthesis, Properties, and Applications. Wiley & Sons, Incorporated, John, 2010.

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Dithiolene chemistry: Synthesis, properties, and applications. Interscience, 2004.

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Biothiols Part A Monothiols and Dithiols, Protein Thiols, and Thiyl Radicals. Elsevier, 1995. http://dx.doi.org/10.1016/s0076-6879(00)x0154-1.

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Karlin, Kenneth D., and Edward I. Stiefel. Dithiolene Chemistry Vol. 52: Synthesis, Properties, and Applications. Wiley & Sons, Incorporated, John, 2004.

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(Editor), John N. Abelson, Melvin I. Simon (Editor), and Helmut Sies (Editor), eds. Biothiols, Part A: Monothiols and Dithiols, Protein Thiols, and Thiyl Radicals (Methods in Enzymology). Academic Press, 1995.

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Book chapters on the topic "Dithiole"

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Hamilton, R. D., and E. Campaigns. "Dithiole and Dithiolium Systems." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187005.ch5.

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Kensler, T. W., J. D. Groopman, B. D. Roebuck, and T. J. Curphey. "Chemoprotection by l,2-Dithiole-3-thiones." In ACS Symposium Series. American Chemical Society, 1993. http://dx.doi.org/10.1021/bk-1994-0546.ch011.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of bis(pentamethylcyclopentadienyl)-iron(III)tris(4, 5-dimercapto-1, 3-dithiole-2-thionatotungsten(V)." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_58.

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Meyer, David J., Brian Coles, Jonathan Harris, et al. "Induction of Rat Liver GSH Transferases by 1,2-Dithiole-3-Thione Illustrates Both Anticarcinogenic and Tumor-Promoting Properties." In Antimutagenesis and Anticarcinogenesis Mechanisms III. Springer US, 1993. http://dx.doi.org/10.1007/978-1-4615-2984-2_16.

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Abashev, G. G., E. V. Shklyaeva, A. G. Tenishev, A. B. Sheremetev, and I. L. Yudin. "2-Cyanoethylthio-1,3-Dithiole-2-Selone—New Precusors in Tetrathiafulvalene Synthesis. Tetrathiafulvalenes, Incorporating 1,3,4-Oxadiazole and Cyanoethyl Moieties." In Molecular Low Dimensional and Nanostructured Materials for Advanced Applications. Springer Netherlands, 2002. http://dx.doi.org/10.1007/978-94-010-0349-0_28.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of bis(pentamethylcyclopentadienyl)-iron(III)tris(4, 5-dimercapto-1, 3-dithiole-2-thionato)-molybdenum(V)." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_59.

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Kuhlman, Thomas Scheby. "Dithiane." In Springer Theses. Springer International Publishing, 2013. http://dx.doi.org/10.1007/978-3-319-00386-3_9.

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Schomburg, Dietmar, and Dörte Stephan. "Thiosulfate-dithiol sulfurtransferase." In Enzyme Handbook. Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/978-3-642-59025-2_167.

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Shimizu, Y., T. Uemiya, N. Yoshie, et al. "Crystal Structures of a New Organic Second Order Nonlinear Optical Material [Cyano(ethoxycarbonyl)methylene]-2-ylidene-4,5-dimethyl-1,3-dithiole." In Springer Proceedings in Physics. Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-93426-1_31.

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Schomburg, Dietmar, Margit Salzmann, and Dörte Stephan. "D-Proline reductase (dithiol)." In Enzyme Handbook. Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-58051-2_181.

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Conference papers on the topic "Dithiole"

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Couto, Marcos, Mauricio Cabrera, Gustavo A. Echeverría, Oscar E. Piro, Mercedes González, and Hugo Cerecetto. "3H-1,2-dithiole-3-thione to (E)-3-[1-(alkylthio)alkylidene]-3H-1,2- dithiole transformation: theoretical and experimental studies." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_20139111275.

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Iwasawa, Yasuhiro, and Yukio Furukawa. "Bis(1,2,5-thiadiazolo)-p-quinobis(1,3-dithiole) (BTQBT) templating effect on structure and performance of organic solar cells." In PADJADJARAN INTERNATIONAL PHYSICS SYMPOSIUM 2013 (PIPS-2013): Contribution of Physics on Environmental and Energy Conservations. AIP, 2013. http://dx.doi.org/10.1063/1.4820280.

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Andreu, R., M. J. Blesa, S. Franco, et al. "Ab Initio HF and DFT Calculation of the Second Order NLO Response of Tetrathiafulvalene and 1,3-Dithiole Derivatives." 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/10.1063/1.2836075.

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Paz, Manuel. "The Reactions of Mitomycin C with Dithiols II. Formation of Dithiol Cross-Links." In The 14th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2010. http://dx.doi.org/10.3390/ecsoc-14-00483.

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Sahraoui, Bouchta, I. V. Kityk, Isabelle N. Ledoux-Rak, Tan T. Nguyen, M. Salle, and A. Gorgues. "Electronic structure and electro-optical coefficients in push-pull chromophores incorporating the 1,3-dithiole-2-ylidene moiety as electron-donating part." In 2000 International Topical Meeting on Optics in Computing (OC2000), edited by Roger A. Lessard and Tigran V. Galstian. SPIE, 2000. http://dx.doi.org/10.1117/12.386779.

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Li, Tingbin, Yali Hu, Chunlin Ma, Guofang He, Dong Xu, and Quan Ren. "The relationship between the hybrid form of center metal-atom and the third order nonlinear optical property of 1,3-dithiole-2-thione-4,5-dithiolato-S, S' (dmit) bis-chelate transition metal complexes study by z-scan." In Photonics Asia 2007, edited by Yiping Cui, Qihuang Gong, and Yuen-Ron Shen. SPIE, 2007. http://dx.doi.org/10.1117/12.755351.

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Tae-Wook Kim, Gunuk Wang, and Takhee Lee. "Comparisons of charge transport through alkane- monothiols and dithiols." In 2006 IEEE Nanotechnology Materials and Devices Conference. IEEE, 2006. http://dx.doi.org/10.1109/nmdc.2006.4388764.

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Fukaya, Toshio, Masagi Mizuno, Shigeo Murata, and Akihiro Mito. "THG properties of metal-dithiolene complexes." In OE/LASE '92, edited by Robert A. Fisher and John F. Reintjes. SPIE, 1992. http://dx.doi.org/10.1117/12.58089.

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Paz, Manuel. "The Reactions of Mitomycin C with Dithiols I. Reductive Activation." In The 14th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2010. http://dx.doi.org/10.3390/ecsoc-14-00482.

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Paz, Manuel M. "The Reactions of Mitomycin C with Dithiols III. Mysterious Reactions." In The 14th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2010. http://dx.doi.org/10.3390/ecsoc-14-00484.

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Reports on the topic "Dithiole"

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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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Jenkins, C. W., R. B. King, and I. Bresinska. Synthesis of Polystyrene-Supported Dithizone Analogues for Use as Chemical Sensors for Heavy Metals. Office of Scientific and Technical Information (OSTI), 1998. http://dx.doi.org/10.2172/656434.

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Eisenberg, R. Photochemistry of dithiolate complexes of the platinum group elements. Progress report, May 1, 1993--April 30, 1994. Office of Scientific and Technical Information (OSTI), 1994. http://dx.doi.org/10.2172/10141031.

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Grdina, D. J., J. L. Schwartz, and N. Shigematsu. Protection against radiation-induced mutations at the hprt locus by spermine and N,N{double_prime}-(dithiodi-2,1-ethanediyl)bis-1,3-propanediamine (WR-33278). Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/10184595.

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Grdina, D. J., N. Shigematsu, and J. L. Schwartz. Protection against radiation-induced mutations at the hprt locus by spermine and N,N{double_prime}-(dithiodi-2,1-ethanediyl)bis-1,3-propanediamine (WR-33278). WR-33278 and spermine protect against mutation induction. Office of Scientific and Technical Information (OSTI), 1994. http://dx.doi.org/10.2172/10172494.

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Corsello, S. Computer-aided design and modeling of nickel dithiolene near-infrared dyes. 1998 summer research program for high school juniors at the University of Rochester`s Laboratory for Laser Energetics: Student research reports. Office of Scientific and Technical Information (OSTI), 1999. http://dx.doi.org/10.2172/362522.

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Lippa, I. Synthesis and analysis of nickel dithiolene dyes in a nematic liquid crystal host. 1998 summer research program for high school juniors at the University of Rochester`s Laboratory for Laser Energetics: Student research reports. Office of Scientific and Technical Information (OSTI), 1999. http://dx.doi.org/10.2172/362527.

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