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Journal articles on the topic 'Oxazine dyes'

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Author: Grafiati

Published: 18 May 2024

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1

Luangdilok, W., and T. Panswad. "Effect of chemical structures of reactive dyes on color removal by an anaerobic-aerobic process." Water Science and Technology 42, no. 3-4 (August 1, 2000): 377–82. http://dx.doi.org/10.2166/wst.2000.0406.

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An Anaerobic/Aerobic SBR system was used to treat a synthetic wastewater with glucose and acetic acid (1000 mg/l COD) as carbon sources together with 20 and 100 mg/l of four different reactive dyes: disazo vinylsulphonyl, anthraquinone vinylsulphonyl, anthraquinone monochlorotriazinyle and oxazine. The decolorization efficiencies of the first three dyes at the 20 mg/l dye concentration were 63, 64 and 66%, respectively, and at the 100 mg/l dye concentration were 58, 32 and 41%, respectively. For the disazo dye, two color removal rates were evident, with the initial rate in the first two hours of the anaerobic stage higher than the latter. For the two anthraquinone dyes, only one rate of color removal was seen. For the oxazine dye, a high decolorization was observed in the reactor, but when disturbed, the color re-appeared for unexplainable reasons. The phosphorus removal efficiencies were 78, 52, 41 and 96% for the four dyes of 20 mg/l, respectively, while the corresponding numbers for the 100 mg/lcondition were 48, 48, 48 and 42%, respectively, and different types of dyes had different impacts on the phosphorus removal performance. COD and TKN removals were very high, i.e., 90–99 percent. The disazo reactive dye was decolorized by the reductive reaction, which resulted in the cleavage of the azo bond. Meanwhile, the decolorization of anthraquinone dyes is believed to be through the direct adsorption of dyes on to the floc materials.

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2

Urrutia, María N., and Cristina S. Ortiz. "Novel oxazine and oxazone dyes: aggregation behavior and physicochemical properties." New Journal of Chemistry 40, no. 12 (2016): 10161–71. http://dx.doi.org/10.1039/c6nj02053d.

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3

Blanchard, G. J. "An MNDO calculational study of selected oxazine, thiazine and oxazone dyes." Chemical Physics 138, no. 2-3 (November 1989): 365–75. http://dx.doi.org/10.1016/0301-0104(89)87142-3.

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4

Fleming, Scott, Andrew Mills, and Tell Tuttle. "Predicting the UV–vis spectra of oxazine dyes." Beilstein Journal of Organic Chemistry 7 (April 15, 2011): 432–41. http://dx.doi.org/10.3762/bjoc.7.56.

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In the current work we have investigated the ability of time-dependent density functional theory (TD-DFT) to predict the absorption spectra of a series of oxazine dyes and the effect of solvent on the accuracy of these predictions. Based on the results of this study, it is clear that for the series of oxazine dyes an accurate prediction of the excitation energy requires the inclusion of solvent. Implicit solvent included via a polarizable continuum approach was found to be sufficient in reproducing the excitation energies accurately in the majority of cases. Moreover, we found that the SMD solvent model, which is dependent on the full electron density of the solute without partitioning into partial charges, gave more reliable results for our systems relative to the conductor-like polarizable continuum model (CPCM), as implemented in Gaussian 09. In all cases the inclusion of solvent reduces the error in the predicted excitation energy to <0.3 eV and in the majority of cases to <0.1 eV.

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5

Miluski, Piotr, Marcin Kochanowicz, Jacek Żmojda, and Dominik Dorosz. "Theoretical Investigation of Oxazine 170 Perchlorate Doped Polymeric Optical Fiber Amplifier." Mathematical Problems in Engineering 2017 (2017): 1–6. http://dx.doi.org/10.1155/2017/4024191.

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Optical signal amplification in the waveguiding structure of optical fibers can be used for optical telecommunication systems and new light sources constructions. Organic dyes doped materials are interesting for new applications in polymeric optical fibers technology due to their benefits (efficient fluorescence, high absorption cross section, and easy processing). This article presents a numerical simulation of gain in poly(methyl methacrylate) optical fiber doped by Oxazine 170 Perchlorate. The calculated gain characteristic for the used dye molar concentration (0.2·10-6–1.4·10-6) and pump power (1–10 kW) is presented. The fabricated fluorescent polymeric optical fiber is also shown. The presented analysis can be used for optical amplifier construction based on dye-doped polymeric optical fiber (POF).

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6

Kusinski, Matthew, Jayashree Nagesh, Margarita Gladkikh, Artur F. Izmaylov, and Rebecca A. Jockusch. "Deuterium isotope effect in fluorescence of gaseous oxazine dyes." Physical Chemistry Chemical Physics 21, no. 10 (2019): 5759–70. http://dx.doi.org/10.1039/c8cp05731a.

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7

Chen, Guangming, Nobuo Iyi, Ryo Sasai, Taketoshi Fujita, and Kenji Kitamura. "Intercalation of Rhodamine 6G and Oxazine 4 into Oriented Clay Films and Their Alignment." Journal of Materials Research 17, no. 5 (May 2002): 1035–40. http://dx.doi.org/10.1557/jmr.2002.0153.

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The cationic dyes rhodamine 6G (R6G) and oxazine 4 (Ox4) were intercalated into oriented lithium hectorite (LiHT, a synthetic fluor-mica) films by ion-exchange, and their orientation was studied by x-ray and polarized spectroscopy. Orientation of dyes was determined by basal spacing obtained by x-ray diffraction data, showing that angles of the long axis were 60° for R6G and 47° for Ox4 against the layer. Polarized ultraviolet-visible spectroscopy showed that the high-order H-aggregate of R6G and Ox4 were oriented at 64° and 52° against layers, respectively; other states of dyes were oriented at much lower angles. The interlayer distance was mostly determined by dimensions of the high-order H-aggregate.

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8

Nieckarz, Robert J., Jos Oomens, Giel Berden, Pavel Sagulenko, and Renato Zenobi. "Infrared multiple photon dissociation (IRMPD) spectroscopy of oxazine dyes." Physical Chemistry Chemical Physics 15, no. 14 (2013): 5049. http://dx.doi.org/10.1039/c3cp00158j.

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9

Nikolaev, S. V., V. V. Pozhar, and M. I. Dzyubenko. "EMISSION CHARACTERISTICS OF OXAZINE DYES INCORPORATED IN SOLID POLYURETHANE MATRICES." Telecommunications and Radio Engineering 70, no. 3 (2011): 269–82. http://dx.doi.org/10.1615/telecomradeng.v70.i3.60.

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10

Umarov, K. U., A. N. Nizamov, N. Nizamov, and M. O. Yunusova. "Spectral-fluorescent properties of oxazine dyes in water-soluble polymers." Journal of Applied Spectroscopy 59, no. 3-4 (September 1993): 743–45. http://dx.doi.org/10.1007/bf00661812.

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11

Basché, Th, B. Sauter, and Ch Bräuchle. "Optical High Resolution Studies of Adsorbed and Matrixdoped Oxazine Dyes." Berichte der Bunsengesellschaft für physikalische Chemie 93, no. 10 (October 1989): 1055–58. http://dx.doi.org/10.1002/bbpc.19890931003.

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12

Steinhurst, Daniel A., and Jeffrey C. Owrutsky. "Second Harmonic Generation from Oxazine Dyes at the Air/Water Interface." Journal of Physical Chemistry B 105, no. 15 (April 2001): 3062–72. http://dx.doi.org/10.1021/jp003893q.

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13

Kass, Lawrence. "A Selective Stain for Eosinophils Using Two Oxazine Dyes Applied Sequentially." Biotechnic & Histochemistry 70, no. 1 (January 1995): 19–23. http://dx.doi.org/10.3109/10520299509108311.

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14

Alekseev, N. N., A. Ya Gorelenko, V. A. Grozhik, I. I. Kalosha, A. A. Kovalev, L. S. Loĭko, and V. A. Tolkachev. "Derivatives of oxazine 17 as laser dyes for liquid-crystal matrices." Soviet Journal of Quantum Electronics 15, no. 10 (October 31, 1985): 1431–33. http://dx.doi.org/10.1070/qe1985v015n10abeh007944.

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15

Prostota, Yaroslav, and Paulo J. Coelho. "Cationic 3H-indolium dyes by ring-opening of benzo[1,3]oxazine." Dyes and Pigments 98, no. 1 (July 2013): 93–99. http://dx.doi.org/10.1016/j.dyepig.2013.02.001.

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16

Dalchenko, P. G., M. I. Dzyubenko, V. F. Pedash, and Yu F. Pedash. "Comparative Analysis of Singlet and Excited States of Xanthene and Oxazine Dyes." Telecommunications and Radio Engineering 65, no. 11 (2006): 1003–14. http://dx.doi.org/10.1615/telecomradeng.v65.i11.40.

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17

Grofcsik, A., M. Kubinyi, A. Ruzsinszky, T. Veszprémi, and W. J. Jones. "Quantum chemical studies on excited state intermolecular proton transfer of oxazine dyes." Journal of Molecular Structure 555, no. 1-3 (November 2000): 15–19. http://dx.doi.org/10.1016/s0022-2860(00)00583-4.

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18

Goryaeva, E. M., and A. V. Shablya. "Luminescence and phototransfer of a proton in solutions of oxazine-base dyes." Journal of Applied Spectroscopy 43, no. 5 (November 1985): 1221–26. http://dx.doi.org/10.1007/bf00662378.

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19

Steinhurst, Daniel A., Andrew P. Baronavski, and Jeffrey C. Owrutsky. "Transient Second Harmonic Generation from Oxazine Dyes at the Air/Water Interface." Journal of Physical Chemistry B 106, no. 12 (March 2002): 3160–65. http://dx.doi.org/10.1021/jp013360x.

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20

Pauff, Steven M., and Stephen C. Miller. "Synthesis of Near-IR Fluorescent Oxazine Dyes with Esterase-Labile Sulfonate Esters." Organic Letters 13, no. 23 (December 2, 2011): 6196–99. http://dx.doi.org/10.1021/ol202619f.

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21

Mohamed, Noor Zalikha Islam, M. Z. A. Malik, S. A. A. A. Nazri, M. T. Zainuddin, N. M. A. Aziz, and M. I. Khairuldin. "Photo Characterization of Spirooxazine and Naphthopyran Organic Dyes upon UV Irradiation." Advanced Materials Research 879 (January 2014): 96–101. http://dx.doi.org/10.4028/www.scientific.net/amr.879.96.

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Organic dyes namely 1,3,3-trimethylindolino-naphtospirooxazine (TINS) and 3,3-diphenyl-3H-napthol [2,1-pyran DNP) were used in studies of photochromic transformation in ethanol solution. The samples were exposed to UV light ranging from 5, 10 and 15s respectively. TINS absorbs UV light at 613nm for multiple exposure time. The absorption initiated the opening of oxazine spirostructure with formation of open merocyanine species. Irradiation of DNP with UV at 5, 10 and 15s absorbs at 413nm with formation of opening cyclicstucture of naphthopyran, namely allenyl-naphtol. The intensity peaks of TINS and DNP were increased with increasing the period of irradiation time. TINS and DNP dyes exhibit normal photochromic in the polar protic solvent by displaying color changes form transparent to color blue and light orange under exposed UV light. The photochromic activity of these compounds is due to the reversible light-induced cleavage of the C-O bond between the heterocyclic oxygen atom and the quaternary carbon.

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22

Bujdák, Juraj, and Nobuo Iyi. "Optical properties of molecular aggregates of oxazine dyes in dispersions of clay minerals." Colloid and Polymer Science 287, no. 2 (November 12, 2008): 157–65. http://dx.doi.org/10.1007/s00396-008-1959-y.

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23

Vogel, Martin, Wolfgang Rettig, U. Fiedeldei, and H. Baumgärtel. "Non-radiative deactivation via biradicaloid charge-transfer states in oxazine and thiazine dyes." Chemical Physics Letters 148, no. 4 (July 1988): 347–52. http://dx.doi.org/10.1016/0009-2614(88)87286-5.

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24

Peters, A. "2,3-dihydroanthra(1,2-b)(1,4)oxazine-7,12-diones. Dyes for synthetic polymer fibres." Dyes and Pigments 20, no. 4 (1992): 291–305. http://dx.doi.org/10.1016/0143-7208(92)87028-y.

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25

Raju, K. "Iron(II) titration of some metal ions, with oxazine dyes as redox indicators." Talanta 35, no. 6 (June 1988): 490–92. http://dx.doi.org/10.1016/0039-9140(88)80114-0.

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26

Vogelsang, J., T. Cordes, C. Forthmann, C. Steinhauer, and P. Tinnefeld. "Controlling the fluorescence of ordinary oxazine dyes for single-molecule switching and superresolution microscopy." Proceedings of the National Academy of Sciences 106, no. 20 (May 11, 2009): 8107–12. http://dx.doi.org/10.1073/pnas.0811875106.

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27

Liu, Qing-Hao, Jin-Chun Guo, Hong-Yu Lu, Yan-Nan Guo, Hai-Bin Wang, Zhi-Yong Hu, Hong-Yan Liu, Dong-Liang, and Li-Gong Chen. "Synthesis and Application of Water-Soluble Oxazine Dyes for Detection of PHAs-Producing Bacteria." Journal of Fluorescence 28, no. 6 (September 21, 2018): 1347–55. http://dx.doi.org/10.1007/s10895-018-2297-1.

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28

PETERS, A. T., and X. MA. "ChemInform Abstract: 2,3-Dihydroanthra(1,2b)(1,4)oxazine-7,12-diones. Dyes for Synthetic Polymer Fibres." ChemInform 25, no. 2 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199402239.

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29

Ibrayev, Niyazbek, Evgeniya Seliverstova, and Nazerke Zhumabay. "Plasmon-enhanced Förster energy transfer in Langmuir-Blodgett films based on organic dyes." Open Material Sciences 5, no. 1 (June 29, 2019): 1–6. http://dx.doi.org/10.1515/oms-2019-0003.

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AbstractThe effect of plasmon resonance of silver island films (SIF) on the interlayer Förster resonance energy transfer (FRET) between xanthene and oxazine dye molecules was studied. It has been shown that the enhancement of FRET can be controlled by changing in the distance between the donor-acceptor system and the SIF. The maximum increase in energy transfer efficiency (EET) by a factor of 2.6 was recorded at a distance of 6 nm from the SIF. The assumption was made that an increase in EET can be associated with both the direct appearance of a plasmon-enhanced rate constant of energy transfer and an increase in the quantum yield of the energy donor in direct contact with the SIF. The results can serve as a basis for studying of photoinduced processes in hybrid materials such as “organic dye-plasmon nanoparticles”, to increase the photosensitivity of solar cells in the visible region of the spectrum, and for the studying of photobiological processes, as well as to create materials with desired properties, sensors and light energy converters.

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30

Osman, A. M., Z. H. Khalil, A. I. M. Koraiem, R. M. Abu Elhamd, and R. M. El-Aal. "Heterocyclic halide moieties in the synthesis and study of some conjugated oxazine methine cyanine dyes." Proceedings / Indian Academy of Sciences 109, no. 2 (April 1997): 115–34. http://dx.doi.org/10.1007/bf02871157.

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31

Chakraborty, Amitabha, Ratan Adhikari, and Swapan K. Saha. "Molecular interaction of oxazine dyes in aqueous solution: Temperature dependent molecular disposition of the aggregates." Journal of Molecular Liquids 164, no. 3 (December 2011): 250–56. http://dx.doi.org/10.1016/j.molliq.2011.09.022.

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32

Ghanadzadeh, A., H. Tajalli, P. Zirack, and J. Shirdel. "On the photo-physical behavior and electro-optical effect of oxazine dyes in anisotropic host." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 60, no. 12 (October 2004): 2925–32. http://dx.doi.org/10.1016/j.saa.2004.02.003.

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33

Hannay, J. R. "The interaction between Metallic Copper and certain dyes of the Thiazine, Oxazine, and Azlne Series." Journal of the Society of Dyers and Colourists 31, no. 12 (October 22, 2008): 244–52. http://dx.doi.org/10.1111/j.1478-4408.1915.tb00857.x.

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34

Brown, Stephen M., Kenneth L. Busch, and R. J. Cotter. "Reversible reductions of oxazine dyes induced by primary particle bombardment in liquid secondary-ion mass spectrometry." Rapid Communications in Mass Spectrometry 2, no. 11 (November 1988): 256–59. http://dx.doi.org/10.1002/rcm.1290021112.

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35

Shapiro, Howard M., and Sandra Stephens. "Flow cytometry of DNA content using oxazine 750 or related laser dyes with 633 nm excitation." Cytometry 7, no. 1 (January 1986): 107–10. http://dx.doi.org/10.1002/cyto.990070118.

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36

Cresswell, Stephanie A., and Jack K. Steehler. "Factors Affecting Quantitative Studies of Surface Adsorbates Using Multiresonant Second-Order Nonlinear Spectroscopy." Applied Spectroscopy 41, no. 8 (November 1987): 1329–35. http://dx.doi.org/10.1366/0003702874447004.

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Fundamental quantitative studies of dyes (Nile Blue 690, Oxazine 725, Cresyl Violet 670) adsorbed to fused-silica surfaces were performed to determine the usefulness of multiresonant χ(2) spectroscopy as a surface-selective tool. Factors considered include laser-induced desorption, saturation of resonant transitions, choice of the most useful molecular resonances, molecular orientation, laser incidence angle, and laser polarization. In the most restrictive case (doubly resonant), elimination of desorption and saturation problems required laser power densities below 67 kW/cm2, while for a nonresonant case power densities of 2 GW/cm2 could be used. The resonant enhancement of χ(2) and limitations on usable power densities combine to yield similar detection limits for resonant and nonresonant studies. Detection limits of 0.037 to 0.17 monolayer were obtained for various multiresonant and nonresonant cases. The multiresonant case retains the important advantage of selecting a single mixture component for examination, as demonstrated by an initial study of an adsorbate mixture system.

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37

Periyasamy, Aravin Prince, Martina Vikova, and Michal Vik. "Photochromic Polypropylene Filaments: Impacts of Mechanical Properties on Kinetic Behaviour." Fibres and Textiles in Eastern Europe 27, no. 3(135) (June 30, 2019): 19–25. http://dx.doi.org/10.5604/01.3001.0013.0738.

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Spiro [2H-indole-2,3'-[3H]naphth[2,1-b][1,4]oxazine],1,3-dihydro-1,3,3-trimethyl-6'-(1-piperidinyl) was incorporated onto polypropylene and photochromic polypropylene multifilaments produced through the mass coloration technique. Subsequently the polypropylene (PP) filaments were doped with a different concentration of photochromic pigment, and after producing the filaments different drawing ratios were applied. The photochromic colour build was found to be maximum with the highest concentration of dyes as well as with the lowest drawing ratio. Also the colour differences for L*, a*, b* and ΔE* were analysed with respect to the different concentrations and drawing ratios of the filament. The filaments generally showed good stability of photocoloration during the colour measurement till five cycles. The results for the optical density were reduced by increasing the fineness of the filament. In this experimental work, the impact of the drawing ratio on the optical and mechanical properties of these multifilaments were investigated.

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38

Gilani, A. Ghanadzadeh, M. Moghadam, S. E. Hosseini, and M. S. Zakerhamidi. "A comparative study on the aggregate formation of two oxazine dyes in aqueous and aqueous urea solutions." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 83, no. 1 (December 2011): 100–105. http://dx.doi.org/10.1016/j.saa.2011.07.086.

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39

Seebacher, Christian, Christian Hellriegel, Christoph Bräuchle, Matthias Ganschow, and Dieter Wöhrle. "Orientational Behavior of Single Molecules in Molecular Sieves: A Study of Oxazine Dyes in AlPO4-5 Crystals." Journal of Physical Chemistry B 107, no. 23 (June 2003): 5445–52. http://dx.doi.org/10.1021/jp027434w.

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40

Gilani, A. Ghanadzadeh, and S. Shokri. "Spectral and aggregative properties of two oxazine dyes in aqueous solutions containing structure-breaking and multifunctional additives." Journal of Molecular Liquids 193 (May 2014): 194–203. http://dx.doi.org/10.1016/j.molliq.2013.12.020.

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41

Choi, Adam, and Stephen C. Miller. "Silicon Substitution in Oxazine Dyes Yields Near-Infrared Azasiline Fluorophores That Absorb and Emit beyond 700 nm." Organic Letters 20, no. 15 (July 17, 2018): 4482–85. http://dx.doi.org/10.1021/acs.orglett.8b01786.

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42

Schneider, Siegfried, Wolfgang Stammler, Rudolf Bierl, and Wighard Jäger. "Ultrafast photoinduced charge separation and recombination in weakly bound complexes between oxazine dyes and N,N-dimethylaniline." Chemical Physics Letters 219, no. 5-6 (March 1994): 433–39. http://dx.doi.org/10.1016/0009-2614(94)00107-3.

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43

Zakerhamidi, M. S., and Sh Golghasemi Sorkhabi. "Solvent effects on the molecular resonance structures and photo-physical properties of a group of oxazine dyes." Journal of Luminescence 157 (January 2015): 220–28. http://dx.doi.org/10.1016/j.jlumin.2014.08.062.

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44

Milanchian, K., H. Tajalli, A. Ghanadzadeh Gilani, and M. S. Zakerhamidi. "Nonlinear optical properties of two oxazine dyes in aqueous solution and polyacrylamide hydrogel using single beam Z-scan." Optical Materials 32, no. 1 (November 2009): 12–17. http://dx.doi.org/10.1016/j.optmat.2009.05.011.

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45

Mironov, L. Yu. "Influence of complexing ion on the fluorescence sensitization efficiency for oxazine dyes in nanoparticles of Sc, Eu, Sm, and Lu diketonates." Optics and Spectroscopy 121, no. 6 (December 2016): 867–73. http://dx.doi.org/10.1134/s0030400x16120171.

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46

Vinodgopal, K. "Environmental photochemistry: Electron transfer from excited humic acid to TiO2 colloids and semiconductor mediated reduction of oxazine dyes by humic acid." Research on Chemical Intermediates 20, no. 8 (January 1994): 825–33. http://dx.doi.org/10.1163/156856794x00577.

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47

Raju, K. Vijaya, G. Madhu Gautam, and G. Bangar Raju. "A new reductimetric reagent: Iron (II) in acetic acid medium and in presence of pyrophosphate. Spectrophotometric titration of some oxazine dyes." Mikrochimica Acta 108, no. 3-6 (May 1992): 265–73. http://dx.doi.org/10.1007/bf01242436.

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48

Ehrl, M., H. W. Kindervater, F. W. Deeg, C. Braeuchle, and R. Hoppe. "Optical spectroscopy of thiazine and oxazine dyes in the cages of hydrated and dehydrated faujasite-type zeolites: molecular dynamics in a nanostructured environment." Journal of Physical Chemistry 98, no. 45 (November 1994): 11756–63. http://dx.doi.org/10.1021/j100096a021.

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49

Mall, Chandrakanta, Shachi Tiwari, and Prem Prakash Solanki. "Studies of binding of oxazine and thiazine dyes with cetyltrimethylammonium bromide and tween 80 surfactant spectrophotometrically for the photogalvanic cell for solar energy conversion and storage." Surfaces and Interfaces 27 (December 2021): 101547. http://dx.doi.org/10.1016/j.surfin.2021.101547.

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50

Kubin, R. F., R. A. Henry, M. E. Pietrak, D. E. Bliss, and J. H. Hall. "Anionic and Zwitterionic Photophysical Effects in Some Pyridinium Oxazole Laser Dyes." Laser Chemistry 10, no. 4 (January 1, 1990): 247–58. http://dx.doi.org/10.1155/1990/12860.

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Kauffman and Bentley [Laser Chem. 8, 49-59 (1988)] have reported increased laser output by changing the anion of certain pyridinium oxazole dyes from the tosylate to the mesylate salt. Likewise, zwitterion variants of these dyes are also reported to have a significantly improved laser output. We find anion changes to be modest and, with one exception, all zwitterions tested were no better or not as good as the tosylate salt with respect to lasing output. However, both the mesylate salt and the zwitterion variants have greatly improved lifetimes if there is no fluorine auxochrome in the basic dye. These authors also report observation of bifurcated lasing output curves. We see no such phenomena.

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