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Journal articles on the topic 'Tetrasulfures'

Author: Grafiati

Published: 4 June 2021

Last updated: 4 February 2022

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1

Rejmak, Paweł. "Computational refinement of the puzzling red tetrasulfur chromophore in ultramarine pigments." Physical Chemistry Chemical Physics 22, no. 39 (2020): 22684–98. http://dx.doi.org/10.1039/d0cp03019h.

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2

Zhang, Ru Liang, Li Fen Zhao, Yu Dong Huang, and Li Liu. "Effect of silane coupling agent on the mechanical properties of nitrile butadiene rubber (NBR)/organophilic montmorillonite (OMMT) nanocomposites." Science and Engineering of Composite Materials 23, no. 3 (2016): 277–82. http://dx.doi.org/10.1515/secm-2013-0108.

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AbstractThe effect of coupling agents on the mechanical properties of nitrile butadiene rubber (NBR)/organophilic montmorillonite (OMMT) clay nanocomposites was studied using three different types of silane coupling agents, which were γ-(aminopropyl)triethoxysilane, γ-(mercaptopropyl) triethoxy silane, and bis-[(γ-triethoxy silane)proply] tetrasulfur. The NBR/OMMT nanocomposites were prepared via the melt compounding with OMMT clay. The effect of silane coupling agents on the dispersion of OMMT in the polymer matrix was studied by X-ray diffraction. Dynamic mechanical analysis was employed to

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3

Konarev, D. V., R. N. Lyubovskaga, O. S. Roshchupkina, B. P. Tarasov, and Yu M. Shulga. "Molecular complexes of C60 with tetrasulfur tetranitride." Russian Chemical Bulletin 46, no. 1 (1997): 32–35. http://dx.doi.org/10.1007/bf02495342.

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4

Thewalt, Ulf, Maria Burger, Regina Mausser, and Konrad Holl. "NH4+FeBr4- • S4N4, eine Einschlußverbindung von ungeladenem S4N4 in eine ionische Wirtsverbindung." Zeitschrift für Naturforschung B 40, no. 7 (1985): 861–63. http://dx.doi.org/10.1515/znb-1985-0701.

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Abstract S4N4 reacts with NH4+FeBr4- in benzene to give the 1:1 inclusion compound NH4+FeBr4- • S4N4. The dark red crystals are monoclinic, space group Cc with Z = 4 and lattice constants a = 6.430(1), b = 17.644(4), c = 12.180(2) Å , and β = 90.77(3)°. An X-ray analysis shows that the geometry of the S4N4 group is almost identical to that of crystalline tetrasulfur tetranitride. The S4N4 molecule is surrounded by ionic neigbors in such a way that the S atoms form close contacts to Br atoms of the FeBr4- anions and the N atoms are close to the NH4+ cations.

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5

Bock, Hans, Bahman Solouki, and Herbert W. Roesky. "Gas-phase reactions. 52. Pyrolysis of tetrasulfur tetranitride." Inorganic Chemistry 24, no. 25 (1985): 4425–27. http://dx.doi.org/10.1021/ic00219a046.

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6

Bing, Yan, Pan Shou-Fu, and Yu Jun-Hua. "Electron impact excitation of tetrasulfur S 4 molecule." Chinese Physics 16, no. 7 (2007): 1956–58. http://dx.doi.org/10.1088/1009-1963/16/7/025.

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7

Isobe, Kiyoshi. "Chemistry of Tetrasulfur Including Mysterious Rectangular S4Metal Complexes." Chemistry Letters 40, no. 10 (2011): 1060–66. http://dx.doi.org/10.1246/cl.2011.1060.

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8

Rakitin, Oleg A. "Recent Developments in the Synthesis of 1,2,5-Thiadiazoles and 2,1,3-Benzothiadiazoles." Synthesis 51, no. 23 (2019): 4338–47. http://dx.doi.org/10.1055/s-0039-1690679.

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The fast-growing interest in 1,2,5-thiadiazoles and their fused analogues including 2,1,3-benzothiadiazoles in recent years as important compounds in materials science and biomedicine has led to great progress in the synthesis of these heterocyclic systems. In this short review, the development of known procedures together with novel reactions is covered. New starting materials, unknown and unexpected transformations for the construction of the thiadiazole ring are emphasized.1 Introduction2 Synthesis of Monocyclic 1,2,5-Thiadiazoles2.1 From 1,2-Diamines, vic-Dioximes and Related Compounds2.2

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9

Gregson, David, Gerhard Klebe, and Hartmut Fuess. "Charge density distribution in tetrasulfur tetraimide (S4(NH)4)." Journal of the American Chemical Society 110, no. 25 (1988): 8488–93. http://dx.doi.org/10.1021/ja00233a027.

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10

Pritchina, Elena A., Nina P. Gritsan, Andrey V. Zibarev, and Thomas Bally. "Photochemical Study on the Reactivity of Tetrasulfur Tetranitride, S4N4." Inorganic Chemistry 48, no. 9 (2009): 4075–82. http://dx.doi.org/10.1021/ic802145x.

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11

KONAREV, D. V., R. N. LYUBOVSKAYA, O. S. ROSHCHUPKINA, B. P. TARASOV, and YU M. SHUL'GA. "ChemInform Abstract: Molecular Complexes of C60 with Tetrasulfur Tetranitride." ChemInform 28, no. 29 (2010): no. http://dx.doi.org/10.1002/chin.199729093.

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12

McCarthy, M. C., S. Thorwirth, C. A. Gottlieb, and P. Thaddeus. "Tetrasulfur, S4: Rotational spectrum, interchange tunneling, and geometrical structure." Journal of Chemical Physics 121, no. 2 (2004): 632–35. http://dx.doi.org/10.1063/1.1769372.

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13

Sormova, Hanka, Roberto Linguerri, Pavel Rosmus, Jürgen Fabian, and Najia Komiha. "On the Electronic States of S4+ and S4- Isomers." Collection of Czechoslovak Chemical Communications 72, no. 1 (2007): 83–99. http://dx.doi.org/10.1135/cccc20070083.

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For three energetically most stable structures of tetrasulfur, S4, S4+ and S4- (cis-chain, rectangular, and trans-chain forms), equilibrium geometries, harmonic wavenumbers, ionization energies, electron affinities, electronic vertical and adiabatic excitation energies, and electronic transition moments were calculated by ab initio methods. It was found that similarly to the ground state of S4, the S4+ cis-isomer could interconvert, perturbed, however, by vibronic coupling with a very close-lying excited state and large-amplitude vibrations. Moreover, the cis- and rectangular minima are calcul

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14

Pritchina, Elena A., Daria S. Terpilovskaya, Yuri P. Tsentalovich, Matthew S. Platz, and Nina P. Gritsan. "Photochemistry of Tetrasulfur Tetranitride: Laser Flash Photolysis and Quantum Chemical Study." Inorganic Chemistry 51, no. 8 (2012): 4747–55. http://dx.doi.org/10.1021/ic3000153.

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15

Chung, Gyusung, and Duckhwan Lee. "Tetrasulfur tetranitride and its selenium analogs: ab initio and DFT calculations." Journal of Molecular Structure: THEOCHEM 582, no. 1-3 (2002): 85–90. http://dx.doi.org/10.1016/s0166-1280(01)00769-2.

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16

Wong, Ming Wah, and Ralf Steudel. "Structure and spectra of tetrasulfur S4 – an ab initio MO study." Chemical Physics Letters 379, no. 1-2 (2003): 162–69. http://dx.doi.org/10.1016/j.cplett.2003.08.026.

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17

Matus, Myrna H., David A. Dixon, Kirk A. Peterson, John A. W. Harkless, and Joseph S. Francisco. "Coupled-cluster study of the electronic structure and energetics of tetrasulfur, S4." Journal of Chemical Physics 127, no. 17 (2007): 174305. http://dx.doi.org/10.1063/1.2774973.

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18

Irsen, Stephan H., Philipp Jacobs, and Richard Dronskowski. "ChemInform Abstract: Tetrasulfur Tetranitride: Phase Transition and Crystal Structure at Elevated Temperature." ChemInform 32, no. 18 (2001): no. http://dx.doi.org/10.1002/chin.200118008.

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19

Harkless, John A. W., and Joseph S. Francisco. "Bond Dissocation and Conformational Energetics of Tetrasulfur: A Quantum Monte Carlo Study†." Journal of Physical Chemistry A 112, no. 10 (2008): 2088–92. http://dx.doi.org/10.1021/jp076376h.

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20

Pritchina, Elena A., Daria S. Terpilovskaya, Yuri P. Tsentalovich, Matthew S. Platz, and Nina P. Gritsan. "ChemInform Abstract: Photochemistry of Tetrasulfur Tetranitride: Laser Flash Photolysis and Quantum Chemical Study." ChemInform 43, no. 28 (2012): no. http://dx.doi.org/10.1002/chin.201228008.

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21

Ramírez-Solís, A., Franck Jolibois, and Laurent Maron. "Ab Initio Molecular Dynamics Studies of Tetrasulfur. Dynamics Coupling theC2vOpen andD2hClosed Forms of S4." Journal of Physical Chemistry A 114, no. 47 (2010): 12378–83. http://dx.doi.org/10.1021/jp107994k.

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22

Mataka, Shuntaro, Kazufumi Takahashi, and Masashi Tashiro. "3-ARYL-1,2,5-THIADIAZOLES FROM THE REACTION OF TETRASULFUR TETRANITRIDE WITH ARYL METHYL KETONES." Organic Preparations and Procedures International 17, no. 2 (1985): 152–54. http://dx.doi.org/10.1080/00304948509355490.

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23

Quelch, Geoffrey E., Henry F. Schaefer, and Colin J. Marsden. "Resolution of a long-standing problem in elemental sulfur chemistry: a theoretical study of tetrasulfur." Journal of the American Chemical Society 112, no. 24 (1990): 8719–33. http://dx.doi.org/10.1021/ja00180a012.

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24

Wright, L. L., R. C. Haltiwanger, J. Noordik, and M. Rakowski DuBois. "Expansion of the molybdenum coordination sphere in dinuclear tetrasulfur-bridged complexes with the Cp2Mo2S4 core." Journal of the American Chemical Society 109, no. 1 (1987): 282–83. http://dx.doi.org/10.1021/ja00235a048.

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25

Kim, Kyongtae, and Jaeeock Cho. "Reactions of Monohalomethyl Aryl Ketoximes with Tetrasulfur Tetranitride: Much Improved Synthesis of 3-Aryl-1,2,5-thiadiazoles." HETEROCYCLES 38, no. 8 (1994): 1859. http://dx.doi.org/10.3987/com-94-6755.

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26

Scherer, Wolfgang, Michael Spiegler, Bjørn Pedersen, et al. "Molecular recognition in the solid state: topology of experimental and theoretical charge densities for tetrasulfur tetranitride." Chemical Communications, no. 7 (2000): 635–36. http://dx.doi.org/10.1039/a910209o.

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27

Xu, Yuning, Tianlv Xu, Dong Jiajun, Steven R. Kirk, and Samantha Jenkins. "A QTAIM and stress tensor perspective of large-amplitude motions of the tetrasulfur tetranitride S4N4molecular graph." International Journal of Quantum Chemistry 116, no. 13 (2016): 1025–39. http://dx.doi.org/10.1002/qua.25122.

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28

Irsen, Stephan H., Peter Kroll, Richard Dronskowski, Thomas E. Weirich, and Matthias Epple. "Chemical Reactivity of Tetrasulfur Tetranitride: Synthesis, Physical Properties, and Structural Characterization of the Amorphous Phase Cu7S4N4." Zeitschrift für anorganische und allgemeine Chemie 629, no. 10 (2003): 1751–59. http://dx.doi.org/10.1002/zaac.200300123.

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29

González-Montiel, Simplicio, César Ignacio Sandoval-Chávez, Oscar Muñoz-Granados, et al. "C–H ⋯Pd interactions in palladium complexes derived from tetrasulfur-difluorinated ligands. Experimental, computational and catalytic studies." Polyhedron 173 (November 2019): 114115. http://dx.doi.org/10.1016/j.poly.2019.114115.

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30

QUELCH, G. E., H. F. III SCHAEFER, and C. J. MARSDEN. "ChemInform Abstract: Resolution of a Long-Standing Problem in Elemental Sulfur Chemistry: A Theoretical Study of Tetrasulfur." ChemInform 22, no. 6 (2010): no. http://dx.doi.org/10.1002/chin.199106002.

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31

Ghilardi, Carlo A., Stefano Midollini, Simonetta Moneti та Annabella Orlandini. "Reactivity of tetrasulfur tetranitride towards d10 phosphine complexes. Crystal structure of (PPh3)Pt(μ-S2N2)2Pt(PPh3)". Journal of Organometallic Chemistry 286, № 3 (1985): 419–26. http://dx.doi.org/10.1016/0022-328x(85)80055-3.

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32

Kanti Si, Mrinal, та Bishwajit Ganguly. "Exploring the origin and magnitude of tetrasulfur tetranitrogen interaction with π-ring systems using first principle calculations". Chemical Physics Letters 713 (грудень 2018): 160–65. http://dx.doi.org/10.1016/j.cplett.2018.10.026.

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33

Kong, Yung Cheol, and Kyongtae Kim. "Reactions of arylglyoxals with tetrasulfur tetranitrides (S4N4): Formation of 2-aroyl-5-arylimidazoles and 2-aroyl-5-aryloxazoles." Journal of Heterocyclic Chemistry 36, no. 4 (1999): 911–15. http://dx.doi.org/10.1002/jhet.5570360414.

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34

Cho, Jaeeock, and Kyongtae Kim. "Reactions of tetrasulfur tetranitride with bromomethyl ketones. One pot synthesis of 3,5-diaroyl- and 3,5-diacyl-1,2,4-thiadiazoles." Journal of Heterocyclic Chemistry 29, no. 6 (1992): 1433–39. http://dx.doi.org/10.1002/jhet.5570290611.

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35

KIM, K., and J. CHO. "ChemInform Abstract: Reactions of Monohaloethyl Aryl Ketoximes with Tetrasulfur Tetranitride: Much Improved Synthesis of 3-Aryl-1,2,5-thiadiazoles." ChemInform 25, no. 46 (2010): no. http://dx.doi.org/10.1002/chin.199446155.

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36

Mistry, F., F. G. Herring, A. Haas, and F. Aubke. "Radical formation during the reaction of bis(fluorosulfuryl)peroxide, S2O6F2, with tetrasulfur tetranitride, S4N4, and elemental sulfur, S8." Journal of Fluorine Chemistry 66, no. 2 (1994): 147–52. http://dx.doi.org/10.1016/0022-1139(93)03011-a.

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37

Besenyei, Elizabeth, Guenter K. Eigendorf, and David C. Frost. "Mass spectral studies on the thermal decomposition of tetrasulfur tetranitride and the mechanism for formation of polymeric sulfur nitride." Inorganic Chemistry 25, no. 24 (1986): 4404–8. http://dx.doi.org/10.1021/ic00244a025.

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38

Cho, Jaeeock, and Kyongtae Kim. "Reactions of tetrasulfur tetranitride with alkyl aryl ketoximes: synthesis of 3-aryl- and 3-alkyl-4-aryl-1,2,5-thiadiazoles." Journal of the Chemical Society, Perkin Transactions 1, no. 19 (1993): 2345. http://dx.doi.org/10.1039/p19930002345.

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39

CHO, J., and K. KIM. "ChemInform Abstract: Reactions of Tetrasulfur Tetranitride with Bromomethyl Ketones. One- Pot Synthesis of 3,5-Diaroyl- and 3,5-Diacyl-1,2,4-thiadiazoles." ChemInform 24, no. 17 (2010): no. http://dx.doi.org/10.1002/chin.199317172.

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40

Kong, Yung Cheol, and Kyongtae Kim. "ChemInform Abstract: Reactions of Arylglyoxals with Tetrasulfur Tetranitride (S4N4): Formation of 2-Aroyl-5-arylimidazoles and 2-Aroyl-5-aryloxazoles." ChemInform 31, no. 4 (2010): no. http://dx.doi.org/10.1002/chin.200004049.

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41

Kim, Kyongtae, Jaeeock Cho, and Sung Cheol Yoon. "Reactions of tetrasulfur tetranitride with aryl dibromomethyl ketones: one-pot synthesis of 3-aroylformamido-4-aryl-1,2,5-thiadiazoles and their reactions." Journal of the Chemical Society, Perkin Transactions 1, no. 3 (1995): 253. http://dx.doi.org/10.1039/p19950000253.

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42

CHO, J., and K. KIM. "ChemInform Abstract: Reactions of Tetrasulfur Tetranitride with Alkyl Aryl Ketoximes: Synthesis of 3-Aryl- and 3-Alkyl-4-aryl-1,2,5-thiadiazoles." ChemInform 25, no. 4 (2010): no. http://dx.doi.org/10.1002/chin.199404161.

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43

Kong, Yung Cheol, Kyongtae Kim, and Yung Ja Park. "Reactions of (Aryl)(chloro)methyl p-Tolyl Sulfoxides with Tetrasulfur Tetranitride (S4N4): Formation and Characterization of 3,5-Diaryl-1,2,4,6-thiatriazine 1-Oxides." Tetrahedron 56, no. 37 (2000): 7153–61. http://dx.doi.org/10.1016/s0040-4020(00)00632-3.

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44

KIM, K., J. CHO, and S. C. YOON. "ChemInform Abstract: Reactions of Tetrasulfur Tetranitride with Aryl Dibromomethyl Ketones: One-Pot Synthesis of 3-Aroylformamido-4-aryl-1,2,5-thiadiazoles and Their Reactions." ChemInform 26, no. 26 (2010): no. http://dx.doi.org/10.1002/chin.199526142.

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45

Kong, Yung Cheol, Kyongtae Kim, and Yung Ja Park. "ChemInform Abstract: Reactions of (Aryl)(chloro)methyl p-Tolyl Sulfoxides with Tetrasulfur Tetranitride (S4N4): Formation and Characterization of 3,5-Diaryl-1,2,4,6-thiatriazine 1-Oxides." ChemInform 31, no. 51 (2000): no. http://dx.doi.org/10.1002/chin.200051149.

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46

Yoon, Sung Cheol, Jaeeock Cho, and Kyongtae Kim. "Reactions of 1-aryl-2,2-dihalogenoethanone oximes with tetrasulfur tetranitride (S4N4): a general method for the synthesis of 3-aryl-4-halogeno-1,2,5-thiadiazoles." Journal of the Chemical Society, Perkin Transactions 1, no. 1 (1998): 109–16. http://dx.doi.org/10.1039/a704408i.

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47

Gillespie, Ronald J., James P. Kent, and Jeffery F. Sawyer. "Reactions of tetrasulfur tetranitride and trichlorotrithiatriazene with selenium chlorides. The preparations and crystal structures of SeS2N2Cl2, (S5N5)(SeCl5), and the disordered materials (SexS3-xN2Cl)(SbCl6)." Inorganic Chemistry 29, no. 6 (1990): 1251–59. http://dx.doi.org/10.1021/ic00331a028.

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48

Casewit, Carla J., and M. Rakowski DuBois. "Absorption and EPR spectral characterization of tetrasulfur-bridged mixed-valence dimers of molybdenum(III/IV). EPR evidence for tight ion pair formation in anionic systems." Inorganic Chemistry 25, no. 1 (1986): 74–80. http://dx.doi.org/10.1021/ic00221a019.

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49

YOON, S. C., J. CHO, and K. KIM. "ChemInform Abstract: Reactions of 1-Aryl-2,2-dihalogenoethanone Oximes with Tetrasulfur Tetranitride (S4N4): A General Method for the Synthesis of 3-Aryl-4-halogeno-1,2,5-thiadiazoles." ChemInform 29, no. 23 (2010): no. http://dx.doi.org/10.1002/chin.199823134.

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50

Kim, Kil-Joong, Hyi-Seung Lee, and Kyongtae Kim. "Reactions of 1-aryl-2,2,2-trifluoroethanone oximes with tetrasulfur tetranitride: Novel synthesis of 5-aryl-5-trifluoromethyl-4H-1,3,2,4,6-dithiatriazines and 1-aryl-2,2,2-trifluoro-ethanonylidenaminosulfenamides." Journal of Heterocyclic Chemistry 33, no. 2 (1996): 295–302. http://dx.doi.org/10.1002/jhet.5570330214.

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