Littérature scientifique sur le sujet « Thiazine dyes »
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Articles de revues sur le sujet "Thiazine dyes"
Lee, Soo-Keun, et Andrew Mills. « Luminescence ofLeuco-Thiazine Dyes ». Journal of Fluorescence 13, no 5 (septembre 2003) : 375–77. http://dx.doi.org/10.1023/a:1026341420942.
Texte intégralBelov, Sergey, et Grigoriy Naumchik. « The Application of Ozone to Reduce the Coloring Intensity of Aqueous Solutions of Dyes Used in the Textile Industry ». E3S Web of Conferences 212 (2020) : 01001. http://dx.doi.org/10.1051/e3sconf/202021201001.
Texte intégralAhmed, S., et S. K. Saha. « Electrochemical study of the reaction between progressively alkylated thiazine leucodyes and Fe(III) on a glassy carbon electrode ». Canadian Journal of Chemistry 74, no 10 (1 octobre 1996) : 1896–902. http://dx.doi.org/10.1139/v96-213.
Texte intégralChauhan, Ratna, Reena Kushwaha et Lal Bahadur. « Study of Light Harvesting Properties of Different Classes of Metal-Free Organic Dyes in TiO2Based Dye-Sensitized Solar Cells ». Journal of Energy 2014 (2014) : 1–10. http://dx.doi.org/10.1155/2014/517574.
Texte intégralChen, Shui-Lin, Rolf M. Rohner et Heinrich Zollinger. « Influence of Dye Size and Fiber Porosity on the Dyeing Kinetics and Time Lags in the Uptake of Cationic Dyes on Acrylic Fibers ». Textile Research Journal 58, no 5 (mai 1988) : 247–54. http://dx.doi.org/10.1177/004051758805800501.
Texte intégralBongard, R. D., M. P. Merker, R. Shundo, Y. Okamoto, D. L. Roerig, J. H. Linehan et C. A. Dawson. « Reduction of thiazine dyes by bovine pulmonary arterial endothelial cells in culture ». American Journal of Physiology-Lung Cellular and Molecular Physiology 269, no 1 (1 juillet 1995) : L78—L84. http://dx.doi.org/10.1152/ajplung.1995.269.1.l78.
Texte intégralKrishnan, K. Gokula, V. Saravanan, C. Udhaya Kumar et C. Ramalingan. « Fused Thiazine Tethered Metal-Free Dyes for Dye Sensitized Solar Cells : A Computational Investigation ». Asian Journal of Chemistry 33, no 10 (2021) : 2373–78. http://dx.doi.org/10.14233/ajchem.2021.23340.
Texte intégralSadigh, Mahsa Khadem, et Mohammad Sadegh Zakerhamidi. « The Roles of Solute-Solute and Solute-Solvent Interactions on the Nonlinearity of Aqueous Solutions of Ionic Dyes ». Zeitschrift für Naturforschung A 73, no 9 (25 septembre 2018) : 785–94. http://dx.doi.org/10.1515/zna-2018-0154.
Texte intégralVara, Jimena, et Cristina S. Ortiz. « Thiazine dyes : Evaluation of monomeric and aggregate forms ». Spectrochimica Acta Part A : Molecular and Biomolecular Spectroscopy 166 (septembre 2016) : 112–20. http://dx.doi.org/10.1016/j.saa.2016.05.005.
Texte intégralChakraborty, Amitabha, Shamsuzzaman Ahamed, Subrata Pal et Swapan K. Saha. « Cyclic Voltammetric Investigations of Thiazine Dyes on Modified Electrodes ». ISRN Electrochemistry 2013 (12 février 2013) : 1–7. http://dx.doi.org/10.1155/2013/959128.
Texte intégralThèses sur le sujet "Thiazine dyes"
Sunwar, Chandra Bahadur. « Interaction of some thiazine dyes with clay minerals ». Thesis, University of North Bengal, 1985. http://hdl.handle.net/123456789/847.
Texte intégralPal, Subrata. « Studies on physico - chemical characteristics of progressively alkylated thiazine dyes and their interaction with montmorillonite ». Thesis, University of North Bengal, 1992. http://hdl.handle.net/123456789/715.
Texte intégralBose, Himangshu Sekhar. « Metachromatic behaviour of some thiazine dyes in solution in presence of inorganic and organic electrolytes, surfactants, polyelectrolytes and clay minerals ». Thesis, University of North Bengal, 1986. http://hdl.handle.net/123456789/731.
Texte intégralCongdon, Erin Elizabeth. « Insights into the mechanism of Tau polymerization and the effects of small molecules ». The Ohio State University, 2007. http://rave.ohiolink.edu/etdc/view?acc_num=osu1185397658.
Texte intégral葉慶偉. « Synthesis of monoazo thiazole disperse dyes ». Thesis, 1986. http://ndltd.ncl.edu.tw/handle/47153164538243509509.
Texte intégralLiu, S. S., et 劉新新. « Synthesis and dyeing properties of Thiazole dyes ». Thesis, 2000. http://ndltd.ncl.edu.tw/handle/15298565427743601584.
Texte intégral國立臺灣科技大學
纖維及高分子工程研究所
88
ABSTRACT The investigations of this study were using thiourea and 1,3-disubstituted thiourea by the reaction with monochloro acetic acid or ethyl chloroacetate in alcohol to give thiazolone derivatives;and were using thiourea with chloro acetonitrile in alcohol to yield 2,4-diimino-1,3-thiazole intermediates. Then used aldehyde and diazonium salt with it to prepare methines and azo compounds, which are yellow — reddish brown in colour. Besides the compounds of 2- Imino-5-(4-substituted-benzylidene)-thiazolidin-4-one (7) were difficult to dye PET fabrics, and 2-Acetylimino-5-(4-substituted-benzylidene)-thiazolidin-4-one (10) their light & sublimation fastness were 3 and 3-4 grade, the other dyes the fastness all above 4 grade ,adapted to dye PET fabrics. In order to deep the colour , try using Vilsmeier reagent with 2-imino-thiazolone and using alkyl-acetoacetate with 2,4-diimino-thiazole to form conjugate thiazole and thiazole -pyridine ring ,further reacted with diazonium compounds to get azo dyes:2-(4-Diethylamino-phenyl azo)-7-substituted-thiazolo【4,5-b】pyridin-5-one (15) and 2-(4-Diethylamino-phenyl azo)-4-chloro-thiazole-5-carbaldehyde (16) , which are blue — purple in colour .Their light & sublimation fastness were above the range of 4-5 grade , and bright colored , are good dyestuffs to dye PET fabrics. Further used amine group with (16) to prepare schiff‘s base bridge compounds:2-(4-Diethylamino-phenyl azo)-4-chloro-5-(4-chloro-5-substituted-benzylidene amino) thia- zole (17) ,which λmax are longer 5-10 nm , molar absorptivity (ε) are raiser 2 —3 times than (16) .The light & sublimation fastness were the same as (16) ,the colour still brighted, are good disperse dyestuffs to dye PET fabrics.
YI, WU SHAN, et 吳珊儀. « Synthesis and Dyeing Properties of Nonazo thiazole Dyes ». Thesis, 1999. http://ndltd.ncl.edu.tw/handle/66262378701374278486.
Texte intégral國立臺灣科技大學
纖維及高分子工程研究所
87
The reaction of mecraptoacetic acid with appropriate cyano compounds in the pyridine to yield the corresponding 4-oxo-4,5-dihydro-2-(1-methylene-substitufed)-1,3-thiazole intermediates, which can be reaction with some aldehyde compounds in the presence of piperidine to afford a series of yellow to orange 4-hydroxy-[1-arylidene (or hetarylidene)-1-substitufed]-1,3-thiazole dyes.The molecule structure of all compounds were confirmed by elemental analyes and spectral methods (UV,IR,MS, and 1NMR).These dyes were applied to polyester and nylon ; and their dyeing properties were investigated.
He, Ming Jin, et 何明進. « Synthesis and dyeing properties of thiazole azo dyes ». Thesis, 1996. http://ndltd.ncl.edu.tw/handle/34206588455582380134.
Texte intégralHe, Ming-Jin, et 何明進. « Synthesis and Dyeing Properties of Thiazole Azo Dyes ». Thesis, 1996. http://ndltd.ncl.edu.tw/handle/78377944903851339221.
Texte intégralYang, Ming-Ruei, et 楊明叡. « Preparation and characterization of silica hybridized with thiazole containing active group dyes ». Thesis, 2013. http://ndltd.ncl.edu.tw/handle/11265027613141481610.
Texte intégral崑山科技大學
材料工程研究所
101
A series of some novel hybrid materials prepared via sol-gel process has been synthesized from silica and thiazole containing active group azo dyes. The start material thiazole was synthesized from acetophenone, thiourea and iodide to get a thiazole containing active group. The thiazole containing active group regards as diazo component were coupled with N,N-dimethyl aniline as coupling component at ice bath, to give the heteroaryl thiazole containing active group azo dyes. Tetraethoxysilane and methyltrimethoxysilane hybridized respectively with thiazole containing active group dyes were synthesized via sol-gel process with precursor system. Alternatively, the thiazole containing active group azo dyes processed with hydrolysis-condensation reaction by tetraethoxysilane and methyltrimethoxysilane combined with vinyltriethoxysilane in appropriate proportion under catalyst. The structures of these hybrid materials and morphology of processed fabrics were carried out by FT-IR, 1H-NMR, 29Si-NMR, EDS and SEM analysis. The water repellent properties and characteristics of dyed PTT and PET fabrics were evaluated.
Chapitres de livres sur le sujet "Thiazine dyes"
Van Thien, Tran. « Thiazine, Oxazine, and Phenazine Leuco Dyes ». Dans Chemistry and Applications of Leuco Dyes, 67–95. Boston, MA : Springer US, 2002. http://dx.doi.org/10.1007/0-306-46906-5_3.
Texte intégralBolton, R. « Phenazine, oxazine, thiazine and sulfur dyes ». Dans Second Supplements to the 2nd Edition of Rodd's Chemistry of Carbon Compounds, 173–201. Elsevier, 1991. http://dx.doi.org/10.1016/b978-044453347-0.50381-5.
Texte intégral« A COMPARATIVE STUDY OF METCHROMASY INDUCED BY THIAZINE DYES ». Dans Micro- and Nanostructured Polymer Systems, 309–22. Apple Academic Press, 2016. http://dx.doi.org/10.1201/b19859-22.
Texte intégralActes de conférences sur le sujet "Thiazine dyes"
Cheng, Jianqun, Ke Chen, Yan Wang et Mingju Huang. « Comparison of high-density holographic characteristics of photopolymers sensitized by two kinds of thiazine dyes ». Dans Eighth International Symposium on Optical Storage and 2008 International Workshop on Information Data Storage, sous la direction de Fuxi Gan. SPIE, 2008. http://dx.doi.org/10.1117/12.822045.
Texte intégralZhang, Weiyi, Gang Zhou et Zhong-Sheng Wang. « Thiazolo[5,4-d]thiazole-Based Organic Dyes for Quasi-Solid-State Dye-Sensitized Solar Cells ». Dans Advanced Optoelectronics for Energy and Environment. Washington, D.C. : OSA, 2013. http://dx.doi.org/10.1364/aoee.2013.asa3a.12.
Texte intégralMassey, Melissa, et W. Russ Algar. « Evaluation of thiazole intercalating dyes as acceptors for quantum dot donors in Förster resonance energy transfer ». Dans SPIE Sensing Technology + Applications, sous la direction de Brian M. Cullum et Eric S. McLamore. SPIE, 2014. http://dx.doi.org/10.1117/12.2053165.
Texte intégralIenco, Andrea, Lorenzo Zani, Gianna Reginato, Massimo Calamante, Alessandro Mordini, Cosimo Fortunato et Marina Mazzoni. « Plasmonic Au nanoparticles for thin thiazole-based cheap-and-safe dye-sensitized solar cells (DSSC) ». Dans Optical Instrumentation for Energy and Environmental Applications. Washington, D.C. : OSA, 2014. http://dx.doi.org/10.1364/e2.2014.jw6a.16.
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