Relevant bibliographies by topics / Thianthrene

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

Academic literature on the topic 'Thianthrene'

Author: Grafiati
Published: 11 December 2022
Last updated: 31 July 2025

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Journal articles on the topic "Thianthrene"

1

May, Bonnie L., Henry Yee, and Donald G. Lee. "Oxygen transfer reactions. 2. A comparison of the reactions of ruthenium tetroxide, chromyl chloride, and permanganate with thianthrene 5-oxide." Canadian Journal of Chemistry 72, no. 11 (1994): 2249–54. http://dx.doi.org/10.1139/v94-286.

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Products obtained from the oxidation of thianthrene 5-oxide, SSO, have been used to compare oxygen transfer mechanisms for three high-valent transition metals. Oxidation of SSO by benzyltriethylammonium permanganate in methylene chloride gives the corresponding sulfone, thianthrene 5,5-dioxide (SSO2), as the exclusive product. Oxidation of SSO by ruthenium tetroxide also gives SSO2 as the predominant product along with minor amounts of the disulfoxide, thianthrene 5,10-dioxide (SOSO). However, the converse is observed when chromyl chloride is used as the oxidant; SOSO is the major product. It
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Zhao, Wenyi, and Henry J. Shine. "Primary and secondary 5-(alkyloxy)thianthrenium perchlorates. Characterization with 1H NMR spectroscopy, reactions with iodide and bromide ion, and thermal decomposition in solution." Canadian Journal of Chemistry 76, no. 6 (1998): 695–702. http://dx.doi.org/10.1139/v98-010.

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A series of 5-(alkyloxy)thianthrenium perchlorates has been made in which the alkyl group is primary (1a-1p) and secondary (2a-2g). Preparations were carried out by reaction of the corresponding alkanol with thianthrene cation radical perchlorate in CH2Cl2 solution followed by precipitation of the perchlorate salt with dry ether. 1H NMR spectroscopy reveals that the presence of a stereogenic center in the alkyl group causes inequivalence in the ordinarily paired protons (e.g., H-4, H-6) of the thianthrenium ring. Reaction of iodide and bromide ion with primary alkyl-group compounds (e.g., meth
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Ueda, Masafumi, Moe Isozaki, and Yasuhiro Mazaki. "Synthesis, Structure, and Characterization of Thiacalix[4]-2,8-thianthrene." Molecules 28, no. 14 (2023): 5462. http://dx.doi.org/10.3390/molecules28145462.

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Sulfur-containing macrocycles have attracted substantial interest because they exhibit unique characteristics due to their polygonal ring-shaped skeleton. In this study, a thianthrene-based cyclic tetramer with the sulfur linker, thiacalix[4]-2,8-thianthrene (TC[4]TT), was successfully prepared from a cyclo-p-phenylenesulfide derivative using acid-induced intramolecular condensation. Single crystal X-ray diffraction revealed that TC[4]TT adopts an alternative octagonal form recessed to the inner side. Its internal cavity included small solvents, such as chloroform and carbon disulfide. Due to
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Swager, Timothy, Wen Ong, Federico Bertani, and Enrico Dalcanale. "Redox Switchable Thianthrene Cavitands." Synthesis 50, no. 23 (2018): 4697. http://dx.doi.org/10.1055/s-0037-1610833.

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Swager, Timothy, Wen Ong, Federico Bertani, and Enrico Dalcanale. "Redox Switchable Thianthrene Cavitands." Synthesis 49, no. 02 (2016): 358–64. http://dx.doi.org/10.1055/s-0036-1588659.

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Beck, Johannes, Thomas Bredow, and Rachmat Triandi Tjahjanto. "Thianthrene Radical Cation Hexafluorophosphate." Zeitschrift für Naturforschung B 64, no. 2 (2009): 145–52. http://dx.doi.org/10.1515/znb-2009-0201.

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In the presence of [NBu4][PF6] as the electrolyte, thianthrene (TA) is transformed by electrochemical oxidation to thianthrenium hexafluorophosphate containing the TA•+ radical cation. The reactions were performed in CH2Cl2, H3CCN, and liquid SO2 as solvents. In CH2Cl2, TA[PF6] is sparingly soluble and is deposited directly in crystalline form on the platinum electrode. In H3CCN and liquid SO2, TA[PF6] is highly soluble and gives dark blue solutions from which it can be crystallized upon concentration of the solutions. The air sensitive crystals are black with bronze metallic luster. They belo
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Plater, M. John, and William T. A. Harrison. "Chiral Thianthrenes." International Journal of Molecular Sciences 25, no. 8 (2024): 4311. http://dx.doi.org/10.3390/ijms25084311.

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The absolute configuration and stability of two thianthrene chiral sulfoxides has been determined by means of X-ray single-crystal structure determinations. The analyses and configurations allow verification that the diastereomeric sulfoxides are stable in solution and are not interconverting, which has been suggested in some studies of sulfoxides. The two thianthrene sulfoxides have slightly different Rf values, which allowed their separation using flash chromatography on silica. The spots run back-to-back, which posed a challenge for their separation. The pure, separated compounds in solutio
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WOO, H. G., S. Y. KIM, L. Y. HONG, H. G. KANG, H. S. HAM, and W. G. KIM. "ChemInform Abstract: Thianthrene. Cationic Polymerization of Vinyl Monomers Initiated by Thianthrene Cation Radical." ChemInform 27, no. 8 (2010): no. http://dx.doi.org/10.1002/chin.199608047.

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Liu, Haichao, Yu Gao, Jungang Cao, et al. "Efficient room-temperature phosphorescence based on a pure organic sulfur-containing heterocycle: folding-induced spin–orbit coupling enhancement." Materials Chemistry Frontiers 2, no. 10 (2018): 1853–58. http://dx.doi.org/10.1039/c8qm00320c.

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Yamashita, Masataka, Hironobu Hayashi, Mitsuharu Suzuki, et al. "Bisanthra-thianthrene: synthesis, structure and oxidation properties." RSC Advances 6, no. 74 (2016): 70700–70703. http://dx.doi.org/10.1039/c6ra13036d.

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Dissertations / Theses on the topic "Thianthrene"

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Herranz-Lancho, Coral. "Synthesis and characterization of molecules for electronic devices." Thesis, Strasbourg, 2013. http://www.theses.fr/2013STRAE037.

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La miniaturisation toujours plus poussée des composants électroniques a atteint une limite en arrivant à l’échelle atomique. Afin de fabriquer des circuits à cette échelle, il est nécessaire de intéresser aux plus petits composants pouvant être intégrés : les molécules individuelles et les groupes d’atomes. Dans cette optique, les molécules de 1,4-bis(pyridin-4-ylethynyl) benzène (BPEB), Dibenzo[a,h]thianthrene (DBTH), de Bis{82,92,152,162,222,232- hexa-(2,4,6-trifluorophenoxy)[g,l,q]-5,10,15,20-tetraazaporphyrino)}[b,e]-benzene (H4Pc2) ont été conçues, synthétisées et caractérisées afin d’en
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Tjahjanto, Rachmat Triandi [Verfasser]. "Thianthrene and related heterocycles : metal complexes, radical cation salts and semiconductors / vorgelegt von Rachmat Triandi Tjahjanto." 2009. http://d-nb.info/1000614646/34.

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Dar, Tajwar. "Thermal studies of chlorinated thiophenols." Thesis, 2016. http://hdl.handle.net/1959.13/1321950.

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Research Doctorate - Doctor of Philosophy (PhD)<br>The formation of toxic pollutants formed during the thermal decomposition of chlorinated thiophenol and its related compounds (thiophenes and thioxane) have been investigated using combined combustion experiments and quantum chemical calculations. Computational calculations elucidated the kinetic and mechanistic aspects for the formation of two main pollutants, polychlorinated dibenzothiophene and polychlorinated thianthrene. In order to gain better understanding of thermal decomposition of chlorinated thiophenols, thermochemical parameters of
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Books on the topic "Thianthrene"

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Lovell, James M. Synthesis of potentially conducting tetrathiafulvalene and thianthrene containing compounds. University of Manchester, 1995.

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Book chapters on the topic "Thianthrene"

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Johnson, Randy A., and Lon J. Mathias. "Thianthrene-Containing Polymers: Polyimides, Aramids, and Polybenzoxazoles." In Step-Growth Polymers for High-Performance Materials. American Chemical Society, 1996. http://dx.doi.org/10.1021/bk-1996-0624.ch026.

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Koek, J. H., E. W. J. M. Kohlen, L. vd Wolf, and K. Hissink. "Thianthrene Oxide as a Mechanistic Probe for Bleach Ingredients." In The Activation of Dioxygen and Homogeneous Catalytic Oxidation. Springer US, 1993. http://dx.doi.org/10.1007/978-1-4615-3000-8_55.

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Andrews, M. D. "Reaction of Thianthrene 5-Oxides with Organolithiums." In Fused Five-Membered Hetarenes with One Heteroatom. Georg Thieme Verlag KG, 2001. http://dx.doi.org/10.1055/sos-sd-010-00318.

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SHINE, HENRY J. "EPR AND THE HISTORY OF THE THIANTHRENE CATION RADICAL." In Foundations of Modern EPR. WORLD SCIENTIFIC, 1998. http://dx.doi.org/10.1142/9789812816764_0018.

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Joule, John A. "Thianthrenes." In Advances in Heterocyclic Chemistry Volume 48. Elsevier, 1990. http://dx.doi.org/10.1016/s0065-2725(08)60341-4.

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Conference papers on the topic "Thianthrene"

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Hoerhold, Hans-Heinrich, Hartwig Tillmann, Cornelia Bader, Elisabeth Klemm, Wolfgang Holzer, and Alfons Penzkofer. "MEH-PPV and thianthrene-containing PPV-derivatives as efficient polymeric materials for solid-state lasers." In International Symposium on Optical Science and Technology, edited by Zakya H. Kafafi. SPIE, 2002. http://dx.doi.org/10.1117/12.457491.

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Reports on the topic "Thianthrene"

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Steele, W. V., R. D. Chirico, S. E. Knipmeyer, and A. Nguyen. The thermodynamic properties of thianthrene and phenoxathiin. Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/10141162.

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Steele, W. V., R. D. Chirico, S. E. Knipmeyer, and A. Nguyen. The thermodynamic properties of thianthrene and phenoxathiin. Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/6673493.

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