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Relevant bibliographies by topics / Thioindigoid

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Academic literature on the topic 'Thioindigoid'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Thioindigoid"

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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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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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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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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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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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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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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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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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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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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Dissertations / Theses on the topic "Thioindigoid"

1

Bradshaw, C. "Fast photochromic systems." Thesis, University of Salford, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.384122.

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Corval, Anne. "Spectroscopie des isomères cis et trans du thioindigo : dynamique des états excités." Grenoble 1, 1989. http://www.theses.fr/1989GRE10031.

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Etude spectroscopique detaillee des isomeres cis et trans du thioindigo, en relation avec la photoisometrisation reversible de ces composes. Mise en evidence de l'existence d'une relaxation ultrarapide du premier etat singulet excite de ce compose. Etude de l'influence d'un solvant protique sur la dynamique de l'etat s::(1)-trans. Relation entre la desactivation non radiative rapide de cet etat et la presence de liaisons hydrogene solute-solvant stabilisant l'isomere trans

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Dinescu, Liviu. "Photomodulation of the spontaneous polarization of ferroelectric liquid crystals using chiral thioindigo dopants." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp02/NQ27822.pdf.

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Ramirez, Alejandra. "A study of the interaction of thioindigo dye with several inorganic host materials." To access this resource online via ProQuest Dissertations and Theses @ UTEP, 2008. http://0-proquest.umi.com.lib.utep.edu/login?COPT=REJTPTU0YmImSU5UPTAmVkVSPTI=&clientId=2515.

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Graupner, Franziska Verfasser], and Wolfgang [Akademischer Betreuer] [Zinth. "Ultraschnelle Fluoreszenzspektroskopie zu Photostabilität und Photoreaktivität von Thioindigo- und Hemithioindigo-basierten Farbstoffmolekülen / Franziska Graupner ; Betreuer: Wolfgang Zinth." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2015. http://d-nb.info/1147681465/34.

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Saad, Bendaoud. "Étude expérimentale de la photoexcitation des colorants de type anthracène, azobenzène et thioindigo dans des matrices de cristaux liquides nématiques et smectiques." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape9/PQDD_0004/NQ43110.pdf.

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Rambaud, Christophe. "Etude, par spectroscopie optique, de la délocalisation quantique de protons dans des cristaux d'acide benzoi͏̈que." Grenoble 1, 1989. http://www.theses.fr/1989GRE10103.

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Les transitions optiques des molecules de thioindigo dopant des cristaux d'acide benzoique, sont sensibles au transfert des protons par effet tunnel le long des liaisons hydrogene intradimeres de la matrice. Mesure dans le cas d'un acide carboxylique des niveaux d'energie des protons delocalises et de l'element de matrice d'effet tunnel. Sensibilite du systeme a transfert de protons aux contraintes internes et externes. Deduction des vitesses de relaxation des protons delocalises, comparaison avec des calculs theoriques indiquant l'importance des processus a plusieurs phonons dans cette relaxa

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Boice, Geneviève Nicole. "New organic chromophores for metal complexation: investigations into the synthesis and photophysics of thioindigo diimines, azaDIMEs, and their metal complexes." Thesis, 2018. https://dspace.library.uvic.ca//handle/1828/9306.

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The synthesis and comprehensive characterization of diamine and diimine derivatives of thioindigo are reported. X-ray crystal structures demonstrate a planar structure for the diimine derivatives and a twisted conformation for the diamines. The diamine compounds absorb in the UV (λmax 324 nm - 328 nm), and exhibit moderate fluorescence (ΦF = 0.25, 0.045). A transient triplet state is observed in laser flash photolysis (LFP) experiments, with lifetimes an order of magnitude longer than those of the triplet state of thioindigo. The diimine compounds absorb at longer wavelengths than the diam

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Sousa, José Miguel Coelho de. "Derivados de tetrafenilporfirinas e de tioindigo para células fotosolares sensibilizadas por corante." Master's thesis, 2021. http://hdl.handle.net/10316/98099.

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Dissertação de Mestrado em Química apresentada à Faculdade de Ciências e Tecnologia<br>A procura de novas fontes de energia renovável tem uma prioridade significativa nos desafios futuros das sociedades. Uma das fontes renováveis é a radiação solar, para a qual existem múltiplas tecnologias com diferentes graus de aplicação e integração nas redes eléctricas. Neste trabalho é explorada a tecnologia de células solares sensibilizadas por corante, destacada das outras pelo seu baixo preço e flexibilidade de aplicação.Os corantes explorados para aplicação em células solares sensibilizadas por coran

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Books on the topic "Thioindigoid"

1

Puhlmann, Jürgen. Synthese löslicher Thioindigo- und gemischter Indigo-Thioindigo-Farbstoffe sowie Untersuchung ihres Dichroismus in Flüssigkristallen. 1985.

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Book chapters on the topic "Thioindigoid"

1

Gooch, Jan W. "Thioindigoid Maroons." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_11833.

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Mostoslavskii, M. A. "Photochromic Thioindigoid Dyes." In Organic Photochromes. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4615-8585-5_2.

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Gooch, Jan W. "Thioindigo Pigments." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_11834.

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Lemieux, Robert P., Liviu Dinescu, and Kenneth E. Maly. "Optical Switching of a Ferroelectric Liquid Crystal Spatial Light Modulator Using Chiral Thioindigo Dopants." In ACS Symposium Series. American Chemical Society, 2001. http://dx.doi.org/10.1021/bk-2001-0798.ch017.

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5

"Thioindigoid maroons." In Encyclopedic Dictionary of Polymers. Springer New York, 2007. http://dx.doi.org/10.1007/978-0-387-30160-0_11601.

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"Thioindigo pigments." In Encyclopedic Dictionary of Polymers. Springer New York, 2007. http://dx.doi.org/10.1007/978-0-387-30160-0_11602.

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7

"thioindigo, n." In Oxford English Dictionary, 3rd ed. Oxford University Press, 2023. http://dx.doi.org/10.1093/oed/8245601987.

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8

"Thioindigo and Related Dyes." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186565.ch3.

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Wable, Jaidip B., Cheryl Mascarenhas, Hemantkumar N. Akolkar, Nirmala R. Darekar, and Pradnya Prabhu. "Synthesis, Properties, and Biological Applications of Benzothiophene." In S-Heterocycles. Royal Society of Chemistry, 2024. http://dx.doi.org/10.1039/9781837674015-00352.

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Benzothiophene is a heterocyclic aromatic compound containing sulfur as a heteroatom in the five-membered ring, which is fused with benzene. Medicinal chemistry has shown a great deal of interest in benzothiophene, as it showed various pharmacological properties and structural versatility. The synthesis of benzothiophene derivatives involves multiple strategies, with researchers using a variety of synthetic methodologies. Benzothiophene compounds exhibit a broad range of biological activities, making them attractive candidates for drug development. In terms of their biological and physiologica

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Conference papers on the topic "Thioindigoid"

1

Dinescu, Liviu, and Robert P. Lemieux. "Photomodulating the spontaneous polarization of a ferroelectric liquid crystal phase using chiral thioindigo dopants." In Electronic Imaging '97, edited by Ranganathan Shashidhar. SPIE, 1997. http://dx.doi.org/10.1117/12.271398.

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2

Galstyan, T. V., B. Saad, L. Dinescu, and R. P. Lemieux. "Dynamic Holograms on Polarization Gratings in a Ferroelectric Liquid Crystal." In The European Conference on Lasers and Electro-Optics. Optica Publishing Group, 1998. http://dx.doi.org/10.1364/cleo_europe.1998.cme3.

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We report a new mechanism for dynamic hologram (DH) formation based on the photoinduced increase of spontaneous polarization (Ps) in a ferroelectric liquid crystal (FLC) doped with a chiral thioindigo dye [1], The application of a DC electric field (without light irradiation) produced a switch of the Ps of our cell. A subsequent decrease of the voltage brought the system back to its initial state while demonstrating a significant hysteresis behavior. The experiment was repeated with the sample cell under spatially uniform irradiation at 514.5 nm. This caused the hysteresis region to shift to l

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