Log in

Relevant bibliographies by topics / Thianthrene / Journal articles

To see the other types of publications on this topic, follow the link: Thianthrene.

Journal articles on the topic 'Thianthrene'

Author: Grafiati

Published: 11 December 2022

Last updated: 31 July 2025

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 50 journal articles for your research on the topic 'Thianthrene.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

2

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

3

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

4

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

7

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

8

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

11

MITCHELL, S. C., and R. H. WARING. "Fate of thianthrene in rat." Xenobiotica 28, no. 1 (1998): 93–101. http://dx.doi.org/10.1080/004982598239786.

Full text

APA, Harvard, Vancouver, ISO, and other styles

12

Speer, Martin E., Martin Kolek, Jean Jacques Jassoy, et al. "Thianthrene-functionalized polynorbornenes as high-voltage materials for organic cathode-based dual-ion batteries." Chemical Communications 51, no. 83 (2015): 15261–64. http://dx.doi.org/10.1039/c5cc04932f.

Full text

APA, Harvard, Vancouver, ISO, and other styles

13

Schaefer, Ted, Rudy Sebastian, and Christian Beaulieu. "Molecular orbital and 1H nuclear magnetic resonance studies of the inversion potentials of thianthrene and thioxanthene." Canadian Journal of Chemistry 69, no. 6 (1991): 927–33. http://dx.doi.org/10.1139/v91-137.

Full text

Abstract:

The inversion potentials, obtained from STO-3G, STO-3G(*), 3-21G, 3-21G(*), and 4-31G basis sets, are reported for thianthrene and thioxanthene, molecules in which both or only one of the methylene groups have been replaced by sulfur in 9,10-dihydroanthracene. Comparison with the available experimental data suggests that the split-valence bases lead to an overestimate, possibly by about 10 kJ/mol, of the inversion barrier in the crystal, whereas the STO-3G and STO-3G* basis sets underestimate this barrier. It appears that the inversion barrier for thianthrene is much lower in solution than in

APA, Harvard, Vancouver, ISO, and other styles

14

Chen, Xiao-Yue, Xiao-Xue Nie, Yichen Wu, and Peng Wang. "para-Selective arylation and alkenylation of monosubstituted arenes using thianthrene S-oxide as a transient mediator." Chemical Communications 56, no. 37 (2020): 5058–61. http://dx.doi.org/10.1039/d0cc00641f.

Full text

Abstract:

Using thianthrene S-oxide (TTSO) as a transient mediator, para-arylation and alkenylation of mono-substituted arenes have been demonstrated via a para-selective thianthrenation/Pd-catalyzed thio-Suzuki–Miyaura coupling sequence under mild conditions.

APA, Harvard, Vancouver, ISO, and other styles

15

Bock, H., B. Hierholzer, and P. Rittmeyer. "Radikalionen, 81. ENDOR-spektroskopische Untersuchungen an Radikalkationen aromatischer Organoschwefel-Verbindungen / Radical Ions, 81. ENDOR Spectroscopic Investigations of Radical Cations of Aromatic Organosulfur Compounds." Zeitschrift für Naturforschung B 44, no. 2 (1989): 187–204. http://dx.doi.org/10.1515/znb-1989-0216.

Full text

Abstract:

Conditions for ENDOR measurem ents of organosulfur radical cations are discussed and tested. The one electron oxidation of a variety of aromatic sulfur com pounds comprising benzene-1,2-dithiole, 1,4-dithiine, thianthrene and diphenylsulfide derivatives as well as 33S isotope-marked bis(2,5-dimethoxyphenyl)disulfide is accomplished using the oxygen-free, powerful and selective AlCl3/H2CCl2 reagent. Partly with substantial structural changes, paramagnetic M⊕ species of 1,2-benzodithiete, 1,4-dithiine, thianthrene and diphenyl sulfide result. Their temperature-dependent ENDOR signal patterns pro

APA, Harvard, Vancouver, ISO, and other styles

16

Fujita, Tomoyuki, Tetsuo Maeda, Byung Ju Kim, et al. "Photolytic aziridination by thianthrene sulfilimine derivatives." Journal of Sulfur Chemistry 29, no. 5 (2008): 459–65. http://dx.doi.org/10.1080/17415990802183868.

Full text

APA, Harvard, Vancouver, ISO, and other styles

17

Mitchell, Steve C., and Rosemary H. Waring. "Fate of thianthrene in biological systems." Xenobiotica 47, no. 8 (2016): 731–40. http://dx.doi.org/10.1080/00498254.2016.1222107.

Full text

APA, Harvard, Vancouver, ISO, and other styles

18

González-Núñez, María Elena, Rossella Mello, Jorge Royo, et al. "Conformational Mobility of Thianthrene-5-oxide." Journal of Organic Chemistry 70, no. 9 (2005): 3450–57. http://dx.doi.org/10.1021/jo048802q.

Full text

APA, Harvard, Vancouver, ISO, and other styles

19

Lynch, V. M., S. H. Simonsen, B. E. Davis, et al. "1,4,6,9-Tetraazathianthrene: a planar thianthrene, C8H4N4S2." Acta Crystallographica Section C Crystal Structure Communications 50, no. 9 (1994): 1470–72. http://dx.doi.org/10.1107/s0108270194002234.

Full text

APA, Harvard, Vancouver, ISO, and other styles

20

Holzer, W., A. Penzkofer, A. Lux, H. H. Hörhold, and E. B. Kley. "Photo-physical and lasing characterisation of neat films of a thianthrene-substituted distyrylbenzene dye (Thianthrene-DSB)." Synthetic Metals 145, no. 2-3 (2004): 119–27. http://dx.doi.org/10.1016/j.synthmet.2004.04.027.

Full text

APA, Harvard, Vancouver, ISO, and other styles

21

Dötze, Marc, Hendrik Czepat, Jens Kudnig, and Günter Klar. "Elementorganische Verbindungen mit o-Phenylenresten, XXXI [1]. Charge-transfer-Komplexe von 2,3,7,8-Tetrakis(methylthio)chalkogenanthrenen mit 7,7,8,8-Tetracyanchinodimethan und Tetracyanethen / Organometalloidal Compounds with o-Phenylene Substituents, Part XXXI [1]. Charge-transfer Complexes of 2,3,7,8-Tetrakis(methylthio)chalkogenanthrenes with 7,7,8,8-Tetracyanoquinodimethane and Tetracyanoethene." Zeitschrift für Naturforschung B 53, no. 11 (1998): 1316–22. http://dx.doi.org/10.1515/znb-1998-1114.

Full text

Abstract:

The title compounds are prepared by slow evaporation of dilute solutions of the components. 2,3,7,8-Tetrakis(methylthio)thianthrene and -selenanthrene give isostructural 2:1 complexes with 7,7,8,8-tetracyanoquinodimethane (TCNQ) built up by donor/acceptor/donor units in which the TCNQ molecule is inserted into the cavity formed by two of the folded, oppositely arranged chalcogenanthrene molecules. These units are connected to chains by S -S contacts via the methylthio groups. From 2,3,7,8-tetrakis(methylthio)thianthrene and tetracyanoethene again a 2:1 complex is obtained, however, with a colu

APA, Harvard, Vancouver, ISO, and other styles

22

Triandi, Rachmat, and Johannes Beck. "Synthesis and Crystal Structures of Silver Thianthrene Complexes with Weakly Coordinating Anions." Zeitschrift für Naturforschung B 62, no. 10 (2007): 1291–97. http://dx.doi.org/10.1515/znb-2007-1010.

Full text

Abstract:

Two novel silver complexes with thianthrene (TA) as a ligand have been synthesized in the poorly coordinating solvent liquid sulfur dioxide, using silver salts with weakly coordinating anions [BF4]− and [SbF6]−. Both colorless compounds contain discrete molecular entities and SO2 molecules included in the crystal structure. Selection of crystals and the diffraction data collection were performed at low temperatures (123 K). The tris(μ-thianthrene-κ2S)disilver(I) bis(hexafluoroantimonate) sulfur dioxide solvate [Ag2(TA)3][SbF6]2·5SO2 (1) (monoclinic, P21/c, a = 21.644(3), b = 12.4216(4), c = 21

APA, Harvard, Vancouver, ISO, and other styles

23

Hinrichs, Winfried, Peer Berges, and Günter Klar. "Elementorganische Verbindungen mit ö-Phenylenresten, XI [1] 3:l-Komplexe von Hexachlor-dibenzo-p-dioxin-2,3-chinon mit 2,3,7,8-Tetramethoxythianthren und -selenanthren / Organometallic Compounds with o-Phenylene Substituents, Part XI [1] 3:1 Complexes of Hexachloro-dibenzo-p-dioxin-2,3-quinone with 2,3,7,8-Tetram ethoxythianthrene and Selenanthrene." Zeitschrift für Naturforschung B 41, no. 9 (1986): 1133–41. http://dx.doi.org/10.1515/znb-1986-0913.

Full text

Abstract:

Abstract The title com pounds can be isolated from concentrated solutions of 2,3,7,8-tetramethoxy thianthrene or selenanthrene and tetrachloro-o-benzoquinone as dark blue crystals. Bond distances and bond and folding angles of the components indicate these com pounds to be charge transfer complexes in which the tetramethoxy thianthrene or selenanthrene molecules act as donors (D), the hexachloro-dibenzo-p-dioxin-2,3-quinone molecules as acceptors (A). In the asymmetric units of the two isostructural complexes an acceptor, a donor and another acceptor molecule are arranged parallel to each othe

APA, Harvard, Vancouver, ISO, and other styles

24

Świst, Agnieszka, Jadwiga Sołoducho, Przemysław Data, and Mieczysław Łapkowski. "Thianthrene-based oligomers as hole transporting materials." Arkivoc 2012, no. 3 (2012): 193–209. http://dx.doi.org/10.3998/ark.5550190.0013.315.

Full text

APA, Harvard, Vancouver, ISO, and other styles

25

Bizzarri, Paolo Costa, and Carlo Delia Casa. "Synthesis and Conductivity of Thianthrene-Type Polymers." Molecular Crystals and Liquid Crystals 118, no. 1 (1985): 245–48. http://dx.doi.org/10.1080/00268948508076218.

Full text

APA, Harvard, Vancouver, ISO, and other styles

26

Boduszek, Bogdan, and Henry J. Shine. "Preparation of solid thianthrene cation radical tetrafluoroborate." Journal of Organic Chemistry 53, no. 21 (1988): 5142–43. http://dx.doi.org/10.1021/jo00256a042.

Full text

APA, Harvard, Vancouver, ISO, and other styles

27

Nakai, Takeo, Masatoshi Kozaki, Kazunobu Sato, et al. "Exchange Interaction of Some Thianthrene-Derived Dications." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 334, no. 1 (1999): 139–48. http://dx.doi.org/10.1080/10587259908023311.

Full text

APA, Harvard, Vancouver, ISO, and other styles

28

Sabbah, Raphaël, and Lahcen El Watik. "Etude thermodynamique de la molecule de thianthrene." Thermochimica Acta 138, no. 2 (1989): 241–47. http://dx.doi.org/10.1016/0040-6031(89)87260-0.

Full text

APA, Harvard, Vancouver, ISO, and other styles

29

Johnson, Randy A., and Lon J. Mathias. "Synthesis and Characterization of Thianthrene-Based Polyamides." Macromolecules 28, no. 1 (1995): 79–85. http://dx.doi.org/10.1021/ma00105a009.

Full text

APA, Harvard, Vancouver, ISO, and other styles

30

Shin, Seung Rim, and Henry J. Shine. "Reactions of phenols with thianthrene cation radical." Journal of Organic Chemistry 57, no. 9 (1992): 2706–10. http://dx.doi.org/10.1021/jo00035a031.

Full text

APA, Harvard, Vancouver, ISO, and other styles

31

Steele, W. V., R. D. Chirico, S. E. Knipmeyer, and A. Nguyen. "The thermodynamic properties of thianthrene and phenoxathiin." Journal of Chemical Thermodynamics 25, no. 8 (1993): 965–92. http://dx.doi.org/10.1006/jcht.1993.1093.

Full text

APA, Harvard, Vancouver, ISO, and other styles

32

Sugimoto, Yukihiro, Francis J. Derbyshire, and Alan W. Scaroni. "The effect of sulfur evolution on the properties of high-temperature carbons—I. Thianthrene and thianthrene-anthracene precursors." Carbon 23, no. 4 (1985): 411–16. http://dx.doi.org/10.1016/0008-6223(85)90034-x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

33

Edson, Joseph B., and Daniel M. Knauss. "Thianthrene as an activating group for the synthesis of poly(aryl ether thianthrene)s by nucleophilic aromatic substitution." Journal of Polymer Science Part A: Polymer Chemistry 42, no. 24 (2004): 6353–63. http://dx.doi.org/10.1002/pola.20464.

Full text

APA, Harvard, Vancouver, ISO, and other styles

34

Hoque, A. K. M. M., Henry J. Shine, and T. Krishnan Venkatachalam. "Reaction of Thianthrene Cation Radical with Diarylmercurials. Search for Single Electron Transfer Is Elusive." Collection of Czechoslovak Chemical Communications 58, no. 1 (1993): 82–88. http://dx.doi.org/10.1135/cccc19930082.

Full text

Abstract:

Diarylmercurials (Ar2Hg) with Ar = p-tolyl Ib, o-tolyl Ic, p-anisyl Id and 2-allyloxy-4,5-dimethylphenyl Ie, reacted with thianthrene cation radical perchlorate (Th.+ClO4-) in two stoichiometric ratios: 2 : 1 and 4 : 1 (Th.+ClO4-/Ar2Hg). In the 2 : 1 ratio the products were the 5-arylthianthreniumyl perchlorates IIb - IIe, thianthrene (Th) and ArHg+ClO4- (assayed as ArHgCl, III) in quantitative yields. In the 4 : 1 ratio reaction with ArHg+ occurred, too, and the products were IIb - IIe, Th, the complex Th3Hg(ClO4)2 and HgO (after workup). In contrast, Ph2Hg (Ia) did not react beyond the 2 : 1

APA, Harvard, Vancouver, ISO, and other styles

35

Liu, Meng, Zhiqiang Yang, Zhe Feng, et al. "Combining Functional Units to Design Organic Materials with Dynamic Room-Temperature Phosphorescence under Continuous Ultraviolet Irradiation." Molecules 29, no. 11 (2024): 2621. http://dx.doi.org/10.3390/molecules29112621.

Full text

Abstract:

Developing materials with dynamic room-temperature phosphorescence (RTP) properties is crucial for expanding the applications of organic light-emitting materials. In this study, we designed and synthesized two novel RTP molecules by combining functional units, incorporating the folded unit thianthrene into the classic luminescent cores thioxanthone or anthraquinone to construct TASO and TA2O. In this combination, the TA unit contributes to the enhancement of spin–orbit coupling (SOC), while the luminescent core governs the triplet energy level. After the strategic manipulation of SOC using the

APA, Harvard, Vancouver, ISO, and other styles

36

Okamura, Haruyuki, Ryosuke Matsumori, and Masamitsu Shirai. "I-Line Sensitive Photoacid Generators Having Thianthrene Skeleton." Journal of Photopolymer Science and Technology 17, no. 1 (2004): 131–34. http://dx.doi.org/10.2494/photopolymer.17.131.

Full text

APA, Harvard, Vancouver, ISO, and other styles

37

Ternay, A. L., Bobbie E. South, R. Mckellar, and W. W. Lam. "RING FLATTENING IN THIANTHRENE SULFONIUM BIS(CARBOMETHOXY)METHYLIDES." Phosphorus, Sulfur, and Silicon and the Related Elements 73, no. 1-4 (1992): 63–66. http://dx.doi.org/10.1080/10426509208034432.

Full text

APA, Harvard, Vancouver, ISO, and other styles

38

Shine, Henry J., and Wang Yueh. "Reaction of thianthrene cation radical with alcohols: Cyclohexanols." Tetrahedron Letters 33, no. 44 (1992): 6583–86. http://dx.doi.org/10.1016/s0040-4039(00)60991-7.

Full text

APA, Harvard, Vancouver, ISO, and other styles

39

Soroka, Miroslaw, and Henry J. Shine. "Reaction of thianthrene cation radical with grignard reagents." Tetrahedron 42, no. 22 (1986): 6111–21. http://dx.doi.org/10.1016/s0040-4020(01)88071-6.

Full text

APA, Harvard, Vancouver, ISO, and other styles

40

Ahmad, Abrar, Ashok Kumar Chauhan, Saleem Javed, and Ashwani Kumar. "Desulfurization of thianthrene by a Gordonia sp. IITR100." Biotechnology Letters 36, no. 11 (2014): 2209–14. http://dx.doi.org/10.1007/s10529-014-1606-2.

Full text

APA, Harvard, Vancouver, ISO, and other styles

41

Sheikh, Md, Toshiaki Yoshimura, Hiroyuki Morita, et al. "Synthesis of Thianthrene Derivatives Linked by Carbon Chains." Synthesis 46, no. 01 (2013): 42–48. http://dx.doi.org/10.1055/s-0033-1338550.

Full text

APA, Harvard, Vancouver, ISO, and other styles

42

Prema, S., and M. Srinivasan. "Preparation and properties of polyamides containing thianthrene units." European Polymer Journal 23, no. 11 (1987): 897–903. http://dx.doi.org/10.1016/0014-3057(87)90065-6.

Full text

APA, Harvard, Vancouver, ISO, and other styles

43

Friedrich, Reiner, Silvia Janietz, and Armin Wedel. "Synthesis and characterization of new thianthrene-containing polymers." Macromolecular Chemistry and Physics 200, no. 4 (1999): 731–38. http://dx.doi.org/10.1002/(sici)1521-3935(19990401)200:4<731::aid-macp731>3.0.co;2-a.

Full text

APA, Harvard, Vancouver, ISO, and other styles

44

LYNCH, V. M., S. H. SIMONSEN, B. E. DAVIS, et al. "ChemInform Abstract: 1,4,6,9-Tetraazathianthrene: A Planar Thianthrene, C8H4N4S2." ChemInform 26, no. 11 (2010): no. http://dx.doi.org/10.1002/chin.199511055.

Full text

APA, Harvard, Vancouver, ISO, and other styles

45

Schreiner, Roger P., S. Edward Stevens, and Ming Tien. "Oxidation of Thianthrene by the Ligninase of Phanerochaete chrysosporium." Applied and Environmental Microbiology 54, no. 7 (1988): 1858–60. http://dx.doi.org/10.1128/aem.54.7.1858-1860.1988.

Full text

APA, Harvard, Vancouver, ISO, and other styles

46

Abboud, K. A., V. M. Lynch, S. H. Simonsen, A. Piórko та R. G. Sutherland. "Structure of (η5-cyclopentadienyl)(η6-thianthrene)iron(II) hexafluorophosphate". Acta Crystallographica Section C Crystal Structure Communications 46, № 6 (1990): 1018–22. http://dx.doi.org/10.1107/s0108270189010437.

Full text

APA, Harvard, Vancouver, ISO, and other styles

47

Shine, Henry J. "Oxygen Transfer From Alcohols to the Thianthrene Cation Radical." Phosphorus, Sulfur, and Silicon and the Related Elements 95, no. 1-4 (1994): 429–30. http://dx.doi.org/10.1080/10426509408034264.

Full text

APA, Harvard, Vancouver, ISO, and other styles

48

Yus, Miguel, Francisco Foubelo, and José V. Ferrández. "Thianthrene as a source of the 1,2-benzene dianion." Tetrahedron Letters 43, no. 40 (2002): 7205–7. http://dx.doi.org/10.1016/s0040-4039(02)01661-1.

Full text

APA, Harvard, Vancouver, ISO, and other styles

49

Yang, L., J. Fang, N. Meichin, K. Tanaka, H. Kita, and K. Okamoto. "Gas permeation properties of thianthrene-5,5,10,10-tetraoxide-containing polyimides." Polymer 42, no. 5 (2001): 2021–29. http://dx.doi.org/10.1016/s0032-3861(00)00500-0.

Full text

APA, Harvard, Vancouver, ISO, and other styles

50

Du, Naiying, Gilles P. Robertson, Ingo Pinnau, and Michael D. Guiver. "Polymers of Intrinsic Microporosity with Dinaphthyl and Thianthrene Segments†." Macromolecules 43, no. 20 (2010): 8580–87. http://dx.doi.org/10.1021/ma101930x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!