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Journal articles on the topic 'Thioindigoid'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Bradley, W. "Alkali Colour Reactions of Indigoid and Thioindigoid Dyes." Journal of the Society of Dyers and Colourists 57, no. 1 (2008): 9–15. http://dx.doi.org/10.1111/j.1478-4408.1941.tb02119.x.

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2

R., K. UPADHYAY, AGARWAL N., and MISHRA G. "Synthesis of 5-(2-0xo-3-indolinylidine)-3-aryl-2-( ahydroxy) phenylketo-4-thiazolidinones as Dyes." Journal of Indian Chemical Society Vol. 72, Dec 1995 (1995): 849–52. https://doi.org/10.5281/zenodo.5900723.

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Department of Chemisby, N. R. E. C. College, Khulja-203 131 <em>Manuscript received 29 April 1993, revised 27 January 1994, accepted 25 April 1994</em> Thioindigoid thiazolidinones, 5-(2-oxo-3-indolinylidine)-3-aryl-2-(a-hydroxy)phenylketo-4-thiazolidinones, obtained by condensing 3-aryl-2-(α-hydroxy)phenylketo-4-thiazolidinones with isatin, indicated as multinary products, have been studied for dyeing properties with respect to silk, polyster and cotton fibres.

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3

Egerton, G. S., and F. Galil. "The State of Indigoid and Thioindigoid Dyes in Dyed Materials." Journal of the Society of Dyers and Colourists 78, no. 4 (2008): 167–76. http://dx.doi.org/10.1111/j.1478-4408.1962.tb02482.x.

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4

Rademacher, Paul, Klaus Kowski, Heinrich Hermann, and Wolfgang Lüttke. "Photoelectron Spectra and Electronic Structures of a Series of Vinylogous Thioindigoid Compounds." European Journal of Organic Chemistry 1999, no. 11 (1999): 3191–97. http://dx.doi.org/10.1002/(sici)1099-0690(199911)1999:11<3191::aid-ejoc3191>3.0.co;2-7.

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5

Christie, Robert, and Adrian Abel. "Carbonyl pigments: miscellaneous types." Physical Sciences Reviews 6, no. 7 (2021): 265–80. http://dx.doi.org/10.1515/psr-2020-0154.

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Abstract Carbonyl pigments are characterized by the presence of one or more carbonyl (C = O) groups in their structures, generally as a component of the chromophoric grouping and as part of an extended conjugated π-electron system. Structurally, they constitute a diverse group of pigments that offer a wide range of colors throughout the spectrum, and most of them provide high levels of technical performance. This paper provides a description of the historical development of thioindigoid, isoindoline, isoindolinone, and quinophthalone pigment types, and discusses their molecular and crystal str

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6

Hanna, M. A., M. M. Girges, and D. Rasala. "Synthesis and characterization of a novel class of basic thioindigoid dyestuffs as possible vat dyes and pigments." Pigment & Resin Technology 24, no. 1 (1995): 3–6. http://dx.doi.org/10.1108/eb043128.

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7

Rademacher, Paul, Klaus Kowski, Heinrich Hermann, and Wolfgang Luettke. "ChemInform Abstract: Photoelectron Spectra of Indigo Dyes. Part 3. Photoelectron Spectra and Electronic Structures of a Series of Vinylogous Thioindigoid Compounds (I)-(III)." ChemInform 31, no. 6 (2010): no. http://dx.doi.org/10.1002/chin.200006187.

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8

Alvarado, Manuel, Russell C. Chianelli, and Roy M. Arrowood. "Computational Study of the Structure of a Sepiolite/Thioindigo Mayan Pigment." Bioinorganic Chemistry and Applications 2012 (2012): 1–6. http://dx.doi.org/10.1155/2012/672562.

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The interaction of thioindigo and the phyllosilicate clay sepiolite is investigated using density functional theory (DFT) and molecular orbital theory (MO). The best fit to experimental UV/Vis spectra occurs when a single thioindigo molecule attaches via Van der Waals forces to a tetrahedrally coordinated cation with an additional nearby tetrahedrally coordinated also present. The thioindigo molecule distorts from its planar structure, a behavior consistent with a color change. Due to the weak interaction between thioindigo and sepiolite we conclude that the thioindigo molecule must be trapped

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9

Rahman, Shah Mohammad Fatah-Ur, Farah Shahjin, and Koushi Fukunishi. "Enhanced photocontrolled binding of Ag+ by thioindigo derivative containing oxyethylene chains with OH groups at the terminal positions." Journal of Bangladesh Academy of Sciences 37, no. 2 (2014): 219–29. http://dx.doi.org/10.3329/jbas.v37i2.17564.

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A novel thioindigo dye was synthesized, from 7, 7-bis-chlorocarbonyl thioindigo, containing OH groups at the terminal positions of the oxyethylene side chains. The resultant dye 7, 7-Bis[[2- [2-(2-hydroxyethoxy)ethoxy]ethoxycarbonyl]thioindigo (1) was characterized by 1H NMR, IR, and mass spectral studies. The thioindigo derivative (1), which possesses a molecular architecture, undergoes reversible photochromic reaction and capable of capturing different metal ions and transports them through liquid membrane. Enhancement of binding ability (i) by incorporating OH groups instead of large phen

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10

Uno, Hidemitsu, Kana Moriyama, Takayuki Ishikawa, Noboru Ono, and Hidenori Yahiro. "Thioindigo precursor: control of polymorph of thioindigo." Tetrahedron Letters 45, no. 49 (2004): 9083–86. http://dx.doi.org/10.1016/j.tetlet.2004.10.028.

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11

Bressler, David C., and Phillip M. Fedorak. "Purification, Stability, and Mineralization of 3-Hydroxy-2- Formylbenzothiophene, a Metabolite of Dibenzothiophene." Applied and Environmental Microbiology 67, no. 2 (2001): 821–26. http://dx.doi.org/10.1128/aem.67.2.821-826.2001.

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ABSTRACT 3-Hydroxy-2-formylbenzothiophene (HFBT) is a metabolite found in many bacterial cultures that degrade dibenzothiophene (DBT) via the Kodama pathway. The fate of HFBT in cultures and in the environment is unknown. In this study, HFBT was produced by a DBT-degrading bacterium and purified by sublimation. When stored in organic solvent or as a crystal, the HFBT slowly decomposed, yielding colored products. Two of these were identified as thioindigo and cis-thioindigo. The supernatant of the DBT-degrading culture contained thioindigo, which has not been reported previously as a product of

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12

Weisz, Adrian, Marianita Perez-Gonzalez, Jackson F. Wood, Clark D. Ridge, and Yoichiro Ito. "Identification, separation by spiral high-speed counter-current chromatography, and quantification of 7-chloro-5-methyl-2H-1,4-benzothiazin-3(4H)-one, an impurity in the thioindigoid color additive D&C Red No. 30 and its lakes." Journal of Chromatography A 1637 (January 2021): 461863. http://dx.doi.org/10.1016/j.chroma.2020.461863.

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13

Konarev, Dmitri V., Salavat S. Khasanov, Alexander F. Shestakov та ін. "cis-Thioindigo (TI) – a new ligand with accessible radical anion and dianion states. Strong magnetic coupling in the {[TI-(μ2-O),(μ-O)]Cp*Cr}2dimers". Dalton Trans. 46, № 41 (2017): 14365–72. http://dx.doi.org/10.1039/c7dt02878d.

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A coordination complex containing thioindigo (TI<sup>2−</sup>) dianions and Cr<sup>3+</sup>with a highS= 3/2 spin state and salt {cryptand[2,2,2](Na<sup>+</sup>)}(TI˙<sup>−</sup>) (2) with paramagnetic TI˙<sup>−</sup>radical anions have been studied for the first time.

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14

Pereira, Ricardo C., Marta Pineiro, Adelino M. Galvão, and J. Sérgio Seixas de Melo. "Thioindigo, and sulfonated thioindigo derivatives as solvent polarity dependent fluorescent on-off systems." Dyes and Pigments 158 (November 2018): 259–66. http://dx.doi.org/10.1016/j.dyepig.2018.05.049.

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15

Evans, Norman. "Thioindigo Colours in Calico Printing." Journal of the Society of Dyers and Colourists 29, no. 5 (2008): 144–50. http://dx.doi.org/10.1111/j.1478-4408.1913.tb00724.x.

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16

Schulz, Marvin, and Jens Christoffers. "New macrocyclic bistriazolophanes with thioindigo chromophore." Tetrahedron 69, no. 2 (2013): 802–9. http://dx.doi.org/10.1016/j.tet.2012.10.107.

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17

Corval, A., and H. P. Trommsdorff. "THE EXCITED STATE OF CIS-THIOINDIGO." Le Journal de Physique Colloques 46, no. C7 (1985): C7–447—C7–451. http://dx.doi.org/10.1051/jphyscol:1985779.

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18

Petersen, J., R. Strohmaier, B. Gompf, and W. Eisenmenger. "Monolayers of tetrachloro-thioindigo and thioindigo in the STM: orientational disorder and the absence of photochromism." Surface Science 389, no. 1-3 (1997): 329–37. http://dx.doi.org/10.1016/s0039-6028(97)00446-9.

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19

Hoepping, Alexander, and Roland Mayer. "EINE NEUE SYNTHESEVARIANTE ZUR DARSTELLUNG VON THIOINDIGOIDEN." Phosphorus, Sulfur, and Silicon and the Related Elements 107, no. 1-4 (1995): 285–88. http://dx.doi.org/10.1080/10426509508027945.

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20

Konarev, Dmitri V., Alexey V. Kuzmin, Mikhail S. Batov, et al. "Strong magnetic coupling of spins in Fe(ii) dimers with differently charged thioindigo ligands." Dalton Transactions 49, no. 23 (2020): 7692–96. http://dx.doi.org/10.1039/d0dt01262a.

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Coordination complex of iron(ii) with radical anion and dianion of thioindigo {[2.2.2]cryptand(K<sup>+</sup>)}<sub>2</sub>{Fe<sup>II</sup>(TI˙<sup>−</sup>)(TI<sup>2−</sup>)}<sub>2</sub>·2C<sub>6</sub>H<sub>4</sub>Cl<sub>2</sub> (1) is obtained. Complex has two high-spin Fe<sup>II</sup> centers separated by oxygen atoms, and two TI˙<sup>−</sup> radical anions coordinated to Fe<sup>II</sup>.

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21

Ibrahim, M., M. M. El-Nahass, M. A. Kamel, A. A. El-Barbary, B. D. Wagner, and M. A. M. El-Mansy. "On the spectroscopic analyses of thioindigo dye." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 113 (September 2013): 332–36. http://dx.doi.org/10.1016/j.saa.2013.05.014.

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22

Saika, Tetsuyuki, Tomokazu Iyoda, Kenichi Honda, and Takeo Shimidzu. "Emission control of a pyrene-thioindigo compound." Journal of the Chemical Society, Chemical Communications, no. 8 (1992): 591. http://dx.doi.org/10.1039/c39920000591.

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23

Fukushima, Kotaro, Kazumi Nakatsu, Ryuichi Takahashi, Hiroshi Yamamoto, Keigo Gohda, and Seiji Homma. "Crystal Structures and Photocarrier Generation of Thioindigo Derivatives." Journal of Physical Chemistry B 102, no. 31 (1998): 5985–90. http://dx.doi.org/10.1021/jp9814552.

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24

Vlahakis, Jason Z., Kenneth E. Maly, and Robert P. Lemieux. "Thioindigo-containing organosiloxane liquid crystals with electroclinic properties." Journal of Materials Chemistry 11, no. 10 (2001): 2459–64. http://dx.doi.org/10.1039/b103755m.

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25

Corval, A., and H. P. Trommsdorff. "Electronic spectra and the isomerization potential of thioindigo." Journal of Physical Chemistry 91, no. 6 (1987): 1317–24. http://dx.doi.org/10.1021/j100290a010.

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26

Bien, J. T., M. Shang, and B. D. Smith. "7,7'-Bis[(aza-18-crown-6)carbonyl]thioindigo." Acta Crystallographica Section C Crystal Structure Communications 52, no. 1 (1996): 183–86. http://dx.doi.org/10.1107/s0108270195012455.

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27

Fatah-ur Rahman, S. M., and Koushi Fukunishi. "Metal ion binding by photoresponsive thioindigo crown ethers." Journal of the Chemical Society, Chemical Communications, no. 8 (1994): 917. http://dx.doi.org/10.1039/c39940000917.

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28

Khusayfan, N. M., E. F. M. El-Zaidia, and M. M. El-Nahass. "Fabrication and Electrical Characteristics of Thioindigo/Silicon Heterojunction." Silicon 10, no. 6 (2018): 2519–26. http://dx.doi.org/10.1007/s12633-018-9786-3.

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29

Rahman, A. N. Abdel, and A. F. Mansour. "Trans-thioindigo as a possible dye for solar collectors." Journal of Physics D: Applied Physics 18, no. 6 (1985): L49—L52. http://dx.doi.org/10.1088/0022-3727/18/6/005.

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30

Jacquemin, Denis, Julien Preat, Valérie Wathelet, Michèle Fontaine, and Eric A. Perpète. "Thioindigo Dyes: Highly Accurate Visible Spectra with TD-DFT." Journal of the American Chemical Society 128, no. 6 (2006): 2072–83. http://dx.doi.org/10.1021/ja056676h.

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31

Boice, Geneviève, Brian O. Patrick, Robert McDonald, Cornelia Bohne, and Robin Hicks. "Synthesis and Photophysics of Thioindigo Diimines and Related Compounds." Journal of Organic Chemistry 79, no. 19 (2014): 9196–205. http://dx.doi.org/10.1021/jo501630f.

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32

Hoppe, Rainer, Guenter Schulz-Ekloff, Dieter Woehrle, Christine Kirschhock, and Hartmut Fuess. "Synthesis, Location, and Photoinduced Transformation of Zeolite-Encaged Thioindigo." Langmuir 10, no. 5 (1994): 1517–23. http://dx.doi.org/10.1021/la00017a032.

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33

Corval, A., and H. P. Trommsdorff. "Optical spectra and excited-state dynamics of cis-thioindigo." Journal of Physical Chemistry 93, no. 20 (1989): 7081–87. http://dx.doi.org/10.1021/j100357a014.

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34

Jacquemin, Denis, Julien Preat, Valérie Wathelet, and Eric A. Perpète. "Theoretical investigation of the absorption spectrum of thioindigo dyes." Journal of Molecular Structure: THEOCHEM 731, no. 1-3 (2005): 67–72. http://dx.doi.org/10.1016/j.theochem.2005.06.038.

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35

Rivalta, A., A. Giunchi, L. Pandolfi, et al. "Crystal alignment of surface stabilized polymorph in thioindigo films." Dyes and Pigments 172 (January 2020): 107847. http://dx.doi.org/10.1016/j.dyepig.2019.107847.

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36

Gompper, Rudolf, Karsten Hartmann, Robert Kellner, and Kurt Polborn. "Bis(dicyanmethylen)- und Bis(cyanimino)-Derivate des Indigos und Thioindigos." Angewandte Chemie 107, no. 4 (1995): 531–34. http://dx.doi.org/10.1002/ange.19951070429.

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37

Khusayfan, N., and M. El-Nahass. "Structural and optical characterizations of thin organic films of thioindigo." Ukrainian Journal of Physical Optics 17, no. 1 (2016): 10. http://dx.doi.org/10.3116/16091833/17/1/10/2016.

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38

Aqad, Emad, Arkady Ellern, Lev Shapiro, and Vladimir Khodorkovsky. "Tetrathiafulvalene-thioindigo annelated donor–acceptor system with intramolecular charge transfer." Tetrahedron Letters 41, no. 16 (2000): 2983–86. http://dx.doi.org/10.1016/s0040-4039(00)00287-2.

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39

Veniaminov, A. V., and G. I. Lashkov. "Photochemical isomerization of thioindigo derivatives embedded in poly(methyl methacrylate)." Polymer Science U.S.S.R. 28, no. 4 (1986): 963–71. http://dx.doi.org/10.1016/0032-3950(86)90237-6.

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40

Gompper, Rudolf, Karsten Hartmann, Robert Kellner, and Kurt Polborn. "Bis(dicyanomethylene) and Bis(cyanoimino) Derivatives of Indigo and Thioindigo." Angewandte Chemie International Edition in English 34, no. 4 (1995): 464–67. http://dx.doi.org/10.1002/anie.199504641.

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41

Dinescu, Liviu, and Robert P. Lemieux. "Modulating the spontaneous polarization of a ferroelectric liquid crystal via the photoisomerization of a chiral thioindigo dopant: (R,R)-6,6′-bis(1-methylheptyloxy) thioindigo." Liquid Crystals 20, no. 6 (1996): 741–49. http://dx.doi.org/10.1080/02678299608033167.

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42

Rahman, S. M. Fatah-ur, Koushi Fukunishi, Masaki Kuwabara, Hiroki Yamanaka, and Mototeru Nomura. "Photocontrolled Binding of Metal Ions with Thioindigo Derivatives Containing Oxyethylene Chains." Bulletin of the Chemical Society of Japan 66, no. 5 (1993): 1461–65. http://dx.doi.org/10.1246/bcsj.66.1461.

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43

Hosseinnezhad, Mozhgan, Siamak Moradian, and Kamaladin Gharanjig. "Novel organic dyes based on thioindigo for dye-sensitized solar cells." Dyes and Pigments 123 (December 2015): 147–53. http://dx.doi.org/10.1016/j.dyepig.2015.07.016.

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44

Mochizuki, Misato, Takatoshi Senju, and Jin Mizuguchi. "Evaluation of Intermolecular Forces in Thioindigo Derivatives by Energy Partition Analysis." NIP & Digital Fabrication Conference 16, no. 1 (2000): 145–48. http://dx.doi.org/10.2352/issn.2169-4451.2000.16.1.art00039_1.

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45

Aqad, Emad, Arkady Ellern, Lev Shapiro, and Vladimir Khodorkovsky. "ChemInform Abstract: Tetrathiafulvalene-thioindigo Anellated Donor-Acceptor System with Intramolecular Charge Transfer." ChemInform 31, no. 28 (2010): no. http://dx.doi.org/10.1002/chin.200028119.

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46

Ilie, Cornelia-Ioana, Angela Spoială, Ludmila Motelica, et al. "Decoration of a Glass Surface with AgNPs Using Thio-Derivates for Environmental Applications." Coatings 14, no. 1 (2024): 96. http://dx.doi.org/10.3390/coatings14010096.

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The aim of this study is to decorate a glass surface with silver nanoparticles (AgNPs) and further prove its efficiency in the removal of some thio-derivatives—potential pollutants from water. Therefore, grafting the surface of glass-based platforms with AgNPs will strongly influence their interaction with other substances or molecules. The most commonly used molecules for glass-based platform functionalization/modification are organosilanes. In this case, the main interest is in thioalkyl organosilanes because, after silanization, the thio (-SH) functional groups that have a high affinity for

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47

Kurata, Hiroyuki, Sang Kim, Kouzou Matsumoto, Takeshi Kawase, and Masaji Oda. "Photochemical and Redox Switching in a Ring-closed Isomer of Thioindigo-extended Quinone." Chemistry Letters 36, no. 3 (2007): 386–87. http://dx.doi.org/10.1246/cl.2007.386.

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48

Fukunishi, Koushi, Masahiko Tatsuma, S. M. Fatah Ur Rahman, Masaki Kuwabara, Hiroki Yamanaka, and Mototeru Nomura. "Cis/Trans Isomerization of Thioindigo Derivatives Adsorbed on Silica Gel Modified with Octadecyl Groups." Bulletin of the Chemical Society of Japan 63, no. 12 (1990): 3701–3. http://dx.doi.org/10.1246/bcsj.63.3701.

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49

Costa, Ana L., Ana C. Gomes, Ricardo C. Pereira, et al. "Interactions and Supramolecular Organization of Sulfonated Indigo and Thioindigo Dyes in Layered Hydroxide Hosts." Langmuir 34, no. 1 (2017): 453–64. http://dx.doi.org/10.1021/acs.langmuir.7b03735.

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50

Boice, Geneviève N., Sofia Garakyaraghi, Brian O. Patrick, Corey A. Sanz, Felix N. Castellano, and Robin G. Hicks. "Diastereomerically Differentiated Excited State Behavior in Ruthenium(II) Hexafluoroacetylacetonate Complexes of Diphenyl Thioindigo Diimine." Inorganic Chemistry 57, no. 3 (2018): 1386–97. http://dx.doi.org/10.1021/acs.inorgchem.7b02803.

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