Gotowa bibliografia na temat „Thiazine dyes”
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Artykuły w czasopismach na temat "Thiazine dyes"
Lee, Soo-Keun, i Andrew Mills. "Luminescence ofLeuco-Thiazine Dyes". Journal of Fluorescence 13, nr 5 (wrzesień 2003): 375–77. http://dx.doi.org/10.1023/a:1026341420942.
Pełny tekst źródłaBelov, Sergey, i 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.
Pełny tekst źródłaAhmed, S., i 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, nr 10 (1.10.1996): 1896–902. http://dx.doi.org/10.1139/v96-213.
Pełny tekst źródłaChauhan, Ratna, Reena Kushwaha i 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.
Pełny tekst źródłaChen, Shui-Lin, Rolf M. Rohner i 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, nr 5 (maj 1988): 247–54. http://dx.doi.org/10.1177/004051758805800501.
Pełny tekst źródłaBongard, R. D., M. P. Merker, R. Shundo, Y. Okamoto, D. L. Roerig, J. H. Linehan i 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, nr 1 (1.07.1995): L78—L84. http://dx.doi.org/10.1152/ajplung.1995.269.1.l78.
Pełny tekst źródłaKrishnan, K. Gokula, V. Saravanan, C. Udhaya Kumar i C. Ramalingan. "Fused Thiazine Tethered Metal-Free Dyes for Dye Sensitized Solar Cells: A Computational Investigation". Asian Journal of Chemistry 33, nr 10 (2021): 2373–78. http://dx.doi.org/10.14233/ajchem.2021.23340.
Pełny tekst źródłaSadigh, Mahsa Khadem, i 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, nr 9 (25.09.2018): 785–94. http://dx.doi.org/10.1515/zna-2018-0154.
Pełny tekst źródłaVara, Jimena, i Cristina S. Ortiz. "Thiazine dyes: Evaluation of monomeric and aggregate forms". Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 166 (wrzesień 2016): 112–20. http://dx.doi.org/10.1016/j.saa.2016.05.005.
Pełny tekst źródłaChakraborty, Amitabha, Shamsuzzaman Ahamed, Subrata Pal i Swapan K. Saha. "Cyclic Voltammetric Investigations of Thiazine Dyes on Modified Electrodes". ISRN Electrochemistry 2013 (12.02.2013): 1–7. http://dx.doi.org/10.1155/2013/959128.
Pełny tekst źródłaRozprawy doktorskie na temat "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.
Pełny tekst źródłaPal, 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.
Pełny tekst źródłaBose, 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.
Pełny tekst źródłaCongdon, 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.
Pełny tekst źródła葉慶偉. "Synthesis of monoazo thiazole disperse dyes". Thesis, 1986. http://ndltd.ncl.edu.tw/handle/47153164538243509509.
Pełny tekst źródłaLiu, S. S., i 劉新新. "Synthesis and dyeing properties of Thiazole dyes". Thesis, 2000. http://ndltd.ncl.edu.tw/handle/15298565427743601584.
Pełny tekst źródła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, i 吳珊儀. "Synthesis and Dyeing Properties of Nonazo thiazole Dyes". Thesis, 1999. http://ndltd.ncl.edu.tw/handle/66262378701374278486.
Pełny tekst źródła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, i 何明進. "Synthesis and dyeing properties of thiazole azo dyes". Thesis, 1996. http://ndltd.ncl.edu.tw/handle/34206588455582380134.
Pełny tekst źródłaHe, Ming-Jin, i 何明進. "Synthesis and Dyeing Properties of Thiazole Azo Dyes". Thesis, 1996. http://ndltd.ncl.edu.tw/handle/78377944903851339221.
Pełny tekst źródłaYang, Ming-Ruei, i 楊明叡. "Preparation and characterization of silica hybridized with thiazole containing active group dyes". Thesis, 2013. http://ndltd.ncl.edu.tw/handle/11265027613141481610.
Pełny tekst źródła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.
Części książek na temat "Thiazine dyes"
Van Thien, Tran. "Thiazine, Oxazine, and Phenazine Leuco Dyes". W Chemistry and Applications of Leuco Dyes, 67–95. Boston, MA: Springer US, 2002. http://dx.doi.org/10.1007/0-306-46906-5_3.
Pełny tekst źródłaBolton, R. "Phenazine, oxazine, thiazine and sulfur dyes". W 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.
Pełny tekst źródła"A COMPARATIVE STUDY OF METCHROMASY INDUCED BY THIAZINE DYES". W Micro- and Nanostructured Polymer Systems, 309–22. Apple Academic Press, 2016. http://dx.doi.org/10.1201/b19859-22.
Pełny tekst źródłaStreszczenia konferencji na temat "Thiazine dyes"
Cheng, Jianqun, Ke Chen, Yan Wang i Mingju Huang. "Comparison of high-density holographic characteristics of photopolymers sensitized by two kinds of thiazine dyes". W Eighth International Symposium on Optical Storage and 2008 International Workshop on Information Data Storage, redaktor Fuxi Gan. SPIE, 2008. http://dx.doi.org/10.1117/12.822045.
Pełny tekst źródłaZhang, Weiyi, Gang Zhou i Zhong-Sheng Wang. "Thiazolo[5,4-d]thiazole-Based Organic Dyes for Quasi-Solid-State Dye-Sensitized Solar Cells". W Advanced Optoelectronics for Energy and Environment. Washington, D.C.: OSA, 2013. http://dx.doi.org/10.1364/aoee.2013.asa3a.12.
Pełny tekst źródłaMassey, Melissa, i W. Russ Algar. "Evaluation of thiazole intercalating dyes as acceptors for quantum dot donors in Förster resonance energy transfer". W SPIE Sensing Technology + Applications, redaktorzy Brian M. Cullum i Eric S. McLamore. SPIE, 2014. http://dx.doi.org/10.1117/12.2053165.
Pełny tekst źródłaIenco, Andrea, Lorenzo Zani, Gianna Reginato, Massimo Calamante, Alessandro Mordini, Cosimo Fortunato i Marina Mazzoni. "Plasmonic Au nanoparticles for thin thiazole-based cheap-and-safe dye-sensitized solar cells (DSSC)". W 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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