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Journal articles on the topic 'Chemiluminescent reactions'

Author: Grafiati

Published: 4 June 2021

Last updated: 13 February 2022

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1

Ibragimova, D. A., O. M. Kamil, T. V. Yankova, N. A. Yashtulov, and N. K. Zaitsev. "THE EFFECT OF SURFACTANTS ON THE CHEMILUMINESCENT REACTION OF LUMINOL WITH HYDROGEN PEROXIDE." Fine Chemical Technologies 12, no. 6 (December 28, 2017): 71–76. http://dx.doi.org/10.32362/2410-6593-2017-12-6-71-76.

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The luminol-hydrogen peroxide chemiluminescent system is widely used for the creation of diagnostic systems, for chemical analysis, for studying the kinetics and mechanisms of chemical reactions, for the creation of special and emergency light sources, and for monitoring living systems. However, the use of the luminol-hydrogen peroxide chemiluminescent system is limited by the fact that there are almost no ways of managing the reaction. The introduction of organized molecular systems into the luminol-hydrogen peroxide chemiluminescent system can create an additional channel for controlling chemiluminescent reactions. The luminol-hydrogen peroxide system was not previously studied in various classes of hydrocarbon and perfluorinated micellar solutions. This work was the first to study the effect of cationic, anionic and nonionic hydrocarbon surface-active substances (cetyltrimethylammonium bromide, sodium decyl sulfate, sodium dodecyl sulfate, triton X 100) and perfluorinated surface-active substances (FT-135 and FT-248) on the chemiluminescent systems luminol-hydrogen peroxide-potassium hexacyanoferrate(III) and luminol-hydrogen peroxide-copper(II) sulphate. The systems retain the ability to chemiluminescence in the presence of a surfactant. Cationic surfactants lower the intensity of chemiluminescence, and anionic surfactants increase the intensity of chemiluminescence. The introduction of a surfactant into the system allows increasing the range of dependence of the chemiluminescence intensity on the catalyst concentration. Kinetic curves of the growth and decay of chemiluminescence were measured in the systems. The rate constants of the chemiluminescence decay were measured in the framework of the first-order kinetics model.

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2

Fereja, Tadesse Haile, Ariaya Hymete, and Thirumurugan Gunasekaran. "A Recent Review on Chemiluminescence Reaction, Principle and Application on Pharmaceutical Analysis." ISRN Spectroscopy 2013 (November 26, 2013): 1–12. http://dx.doi.org/10.1155/2013/230858.

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This paper provides a general review on principle of chemiluminescent reactions and their recent applications in drug analysis. The structural requirements for chemiluminescent reactions and the different factors that affect the efficiency of analysis are included in the review. Chemiluminescence application in immunoassay is the new version for this review. Practical considerations are not included in the review since the main interest is to state, through the aforementioned applications, that chemiluminescence has been, is, and will be a versatile tool for pharmaceutical analysis in future years.

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3

Fethi, F., F. Poblete, E. Martinez, A. Gonzalez Urena, and G. Taieb. "Reaction Cross Sections of Ca (41S, 43P and 31D States) With Halogenated Compounds and Water." Laser Chemistry 16, no. 4 (January 1, 1996): 229–43. http://dx.doi.org/10.1155/1996/29359.

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By using two independent and different methods, absolute values of the reaction cross-sections have been determined for the following chemiluminescent reactions Ca(3P,1D)+Cl4C(CHBr3)→CaX*(A, B)(X=Cl, Br)+Cl3C(CHBr2) and Ca(1D)+H2O→CaOH*+H Both chemiluminescence and laser-induced fluorescence spectra are reported. A comparison with related types of reactions is also presented.

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4

Pranszke, B., P. Kierzkowski, and A. Kowalski. "A Search for Isotope Effects in Chemiluminescent Reactions of Metastable Ca*( 3Pj, 1D2 ) Atoms with CH3I and CD3I Molecules." Zeitschrift für Naturforschung A 54, no. 3-4 (April 1, 1999): 191–94. http://dx.doi.org/10.1515/zna-1999-3-406.

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Chemiluminescent reactions of calcium atoms in the metastable 3Pj and 1D2 states with CH3I and CD3I were studied in a beam-gas arrangement. Calcium monoiodide spectra associated with transitions from the electronic A 2Π, B 2Σ+ and C 2Π states to the X 2Σ+ ground state were recorded. Total collision and chemiluminescence cross sections were measured. It was found that isotopic substitution in the methyl group does not change the reaction cross sections and the chemiluminescence spectra.

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5

Peck, Evan M., Allen G. Oliver, and Bradley D. Smith. "Enhanced Squaraine Rotaxane Endoperoxide Chemiluminescence in Acidic Alcohols." Australian Journal of Chemistry 68, no. 9 (2015): 1359. http://dx.doi.org/10.1071/ch15196.

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Squaraine rotaxane endoperoxides (SREPs) are storable chemiluminescent compounds that undergo a clean cycloreversion reaction that releases singlet oxygen and emits near-infrared light when warmed to body temperature. This study examined the effect of solvent on SREP chemiluminescence intensity and found that acidic alcohols, such as 2,2,2-trifluoroethanol, α-(trifluoromethyl)benzyl alcohol, and 1,1,1,3,3,3-hexafluoroisopropanol, greatly increased chemiluminescence. In contrast, aprotic solvents, such as trifluoroethylmethyl ether, had no effect. The interlocked rotaxane structure was necessary as no chemiluminescence was observed when the experiments were conducted with samples containing a mixture of the two non-interlocked components (squaraine thread and macrocycle endoperoxide). Spectroscopic analyses of the enhanced SREP chemiluminescent reactions showed a mixture of products. In addition to the expected squaraine rotaxane product caused by cycloreversion of the endoperoxide, a diol derivative was isolated. The results are consistent with an endoperoxide O–O bond cleavage process that is promoted by the hydrogen bonding solvent and produces light emission from a squaraine excited state.

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6

Motoyoshiya, Jiro. "Chemiluminescence in Organic Reactions: Fundamental Investigation and Application of Peroxyoxalate Chemiluminescence and Related Chemiluminescent Reactions." Journal of Synthetic Organic Chemistry, Japan 70, no. 10 (2012): 1018–29. http://dx.doi.org/10.5059/yukigoseikyokaishi.70.1018.

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7

Mei, Zhenhua, Shuyu Mei, and Xu Hun. "Thermodynamic Study of Chemiluminescent Reactions." Asian Journal of Chemistry 25, no. 8 (2013): 4731–34. http://dx.doi.org/10.14233/ajchem.2013.14075.

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8

Shinkai, Seiji, Kaori Ueda, Osamu Manabe, Yasuhiro Tezuka, Takashi Harayama, and Fumio Yoneda. "Chemiluminescent reactions of "unmodified" flavins." CHEMICAL & PHARMACEUTICAL BULLETIN 34, no. 5 (1986): 2272–74. http://dx.doi.org/10.1248/cpb.34.2272.

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9

Cui, Hua, Zhi-Feng Zhang, and Ming-Juan Shi. "Chemiluminescent Reactions Induced by Gold Nanoparticles." Journal of Physical Chemistry B 109, no. 8 (March 2005): 3099–103. http://dx.doi.org/10.1021/jp045057c.

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10

Marquette, Christophe A., Agnès Degiuli, and Loïc J. Blum. "Fiberoptic Biosensors Based on Chemiluminescent Reactions." Applied Biochemistry and Biotechnology 89, no. 2-3 (2000): 107–16. http://dx.doi.org/10.1385/abab:89:2-3:107.

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11

Walker, C. C., R. J. Dinus, T. J. McDonough, and K. E. L. Eriksson. "Use of an Improved Chemiluminescence Assay for Non-Intrusive Measurement of Hydroxyl Radicals in a Biomimetic Pulp Bleaching Model System." Holzforschung 53, no. 2 (March 1, 1999): 181–87. http://dx.doi.org/10.1515/hf.1999.030.

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Summary A chemiluminescence assay was used to measure the production of hydroxyl radicals (·OH) in aqueous solutions of hydrogen peroxide and iron-containing catalysts. Preliminary experiments evaluating assay sensitivity revealed that one of the required reagents, phthalhydrazide (PtH), interfered with the studied reactions. In addition, undesirable degradation of the chemiluminescent form of PtH was observed. By removing PtH from reaction solutions and modifying the published procedures, a successful non-intrusive method for measurement of ·OH was obtained. The modified assay was used to compare the rate of ·OH generation in solutions of H2O2, either FeSO4 or Fe-EDTA and a substrate, lignosulfonate. This “biomimetic” pulp bleaching system is meant to simulate naturally occurring biological reactions utilized for degradation of lignins by wood-degrading fungi. Results from these experiments show that FeSO4 produced more ·OH than Fe-EDTA. The improved non-intrusive chemiluminescence assay has proven to be an excellent tool for investigating the role of the ·OH in biomimetic pulp bleaching and potentially other systems.

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12

Kricka, L. J. "Chemiluminescent and bioluminescent techniques." Clinical Chemistry 37, no. 9 (September 1, 1991): 1472–81. http://dx.doi.org/10.1093/clinchem/37.9.1472.

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Abstract Light-emitting chemical reactions (chemiluminescence, CL) and biological reactions (bioluminescence, BL) have a diverse range of analytical applications but relatively few have been adopted by routine clinical laboratories. Advantages of CL and BL assays include sensitivity (attomole and sub-attomole detection limits), speed (signal generated in a few seconds and in some cases stable for several hours), nonhazardous reagents, and simple procedures. The most promising clinical applications are in immunoassay, protein blotting, and DNA probe assays. Chemiluminescent molecules exploited as labels include luminol, isoluminol, acridinium esters, thioesters and sulfonamides, and phenanthridinium esters. Separation and nonseparation assays have been devised, based on isoluminol and acridinium ester labels. The combination of the amplification properties of an enzyme and a CL or BL detection reaction provides a highly sensitive analytical system. Since 1983, CL and BL methods have been developed for many enzyme labels, e.g., alkaline phosphatase, glucose-6-phosphate dehydrogenase, horseradish peroxidase, Renilla luciferase, and xanthine oxidase. Currently, the most successful enzyme assays are the enhanced CL method for a peroxidase label involving a mixture of luminol, hydrogen peroxide, and an enhancer (e.g., p-iodophenol) and the direct CL method for alkaline phosphatase, with an adamantyl 1,2-dioxetane phenyl phosphate as substrate. Both systems are very sensitive (the detection limit for alkaline phosphatase when using the dioxetane reagent is 0.001 amol) and produce long-lived light emission (greater than 30 min), which is ideal for membrane applications in which light emission is detected with photographic film or a charge-coupled device camera.

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13

Mestdagh, J. M., C. Alcaraz, J. Berlande, J. Cuvellier, T. Gustavsson, P. Meynadier, P. De Pujo, O. Sublemontier, and J. P. Visticot. "Reaction Dynamics of Electronically Excited Barium Atoms With Free Molecules and Molecular Clusters." Laser Chemistry 10, no. 5-6 (January 1, 1990): 389–403. http://dx.doi.org/10.1155/1990/36585.

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In this review article we describe some recent results obtained in our laboratory. The successful combination of crossed molecular beam techniques and various laser excitation schemes has been used to study chemiluminescent reactions of ground and excited electronic states of barium with free molecules and molecular clusters. Studies include the identification of reaction products in cases where many chemiluminescent reaction channels are opened. The case of Ba(6sp1P1,6s5d1D2,6s5d3Dj) reacting with H20, methanol, ethanol, propanol-1, propanol-2, methyl-2, propanol-2, butanol-l, allyl alcohol, dimethyl ether, diethyl ether and diallyl ether is examined. A reaction mechanism is proposed which accounts for all these reactions. Studies reported in this review also include the unravelling of reaction dynamics where various forms of energy are mixed (electronic and kinetic energy). This is shown in studies of Ba(1D2and1P1)+O2 reactions. Finally the role of molecular clusters as reactant is examined. Evidence is provided that clusters of N20, H20 and CO2, in collision with Ba(1S0and1P1)+O2, do not lead efficiently to both reactive and non reactive luminescent exit channels.

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14

Black, G., L. E. Jusinski, M. R. Taherian, T. G. Slanger, and D. L. Huestis. "Chemiluminescent reactions in photodissociated cyanogen-oxygen mixtures." Journal of Physical Chemistry 90, no. 26 (December 1986): 6842–48. http://dx.doi.org/10.1021/j100284a027.

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15

Oberlander, M. D., R. P. Kampf, and J. M. Parson. "Chemiluminescent reactions of Ca with hydrogen peroxide." Chemical Physics Letters 176, no. 3-4 (January 1991): 385–89. http://dx.doi.org/10.1016/0009-2614(91)90048-e.

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16

Malinin, V. S., V. S. Sharov, A. V. Putvinsky, A. N. Osipov, and Yu A. Vladimirov. "Chemiluminescent reactions of phagocytes induced by electroporation." Journal of Electroanalytical Chemistry and Interfacial Electrochemistry 276, no. 1 (August 1989): 37–44. http://dx.doi.org/10.1016/0022-0728(89)87251-1.

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17

Malinin, V. S., V. S. Sharov, A. V. Putvinsky, A. N. Osipov, and Yu A. Vladimirov. "Chemiluminescent reactions of phagocytes induced by electroporation." Bioelectrochemistry and Bioenergetics 22, no. 1 (August 1989): 37–44. http://dx.doi.org/10.1016/0302-4598(89)85028-7.

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18

Cheng-Yin, Wu, Chu Yan-Nan, and Cao De-Zhao. "Chemiluminescent Reactions of Fluorine Atoms with lodine Molecules." Acta Physico-Chimica Sinica 13, no. 10 (1997): 885–89. http://dx.doi.org/10.3866/pku.whxb19971005.

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19

Zhuravlev, A. I., and V. M. Trainin. "Chemiluminescent reactions in the Belousov-Zhabotinskii oscillating system." Journal of Bioluminescence and Chemiluminescence 5, no. 4 (October 1990): 227–34. http://dx.doi.org/10.1002/bio.1170050404.

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20

Rosano, W. J., and J. M. Parson. "Chemiluminescent reactions of the IVA elements: Dihalide formation." Journal of Chemical Physics 84, no. 11 (June 1986): 6250–60. http://dx.doi.org/10.1063/1.450769.

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21

Naik, P. D., U. B. Pavanaja, A. V. Sapre, K. V. S. Rama Rao, J. P. Mittal, R. M. Iyer, and P. N. Bajaj. "Chemiluminescent reactions of samarium with some chlorinated hydrocarbons." Journal of Photochemistry and Photobiology A: Chemistry 41, no. 3 (February 1988): 285–92. http://dx.doi.org/10.1016/1010-6030(88)87002-3.

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22

Khalil, Driss, Nicolas Billy, Ge´rard Goue´dard, and Jacques Vigue´. "Crossed-beam studies of some chemiluminescent reactions producing IF." Physical Chemistry Chemical Physics 2, no. 4 (2000): 729–36. http://dx.doi.org/10.1039/a907836c.

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23

Knudsen, Fernanda S., Carlos A. A. Penatti, Leandro O. Royer, Karine A. Bidart, Marcelo Christoff, Denise Ouchi, and Etelvino J. H. Bechara. "Chemiluminescent Aldehyde and β-Diketone Reactions Promoted by Peroxynitrite." Chemical Research in Toxicology 13, no. 5 (May 2000): 317–26. http://dx.doi.org/10.1021/tx990176i.

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24

Shultz, Loranelle L., and Timothy A. Nieman. "Stopped-flow analysis of Ru(bpy)33+chemiluminescent reactions." Journal of Bioluminescence and Chemiluminescence 13, no. 2 (December 4, 1998): 85–90. http://dx.doi.org/10.1002/(sici)1099-1271(199803/04)13:2<85::aid-bio470>3.0.co;2-w.

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25

Slawinska, Danuta, and Janusz Slawinski. "Hydroxycoumarins as sensitizers and reactants of chemiluminescent oxidative reactions." Journal of Bioluminescence and Chemiluminescence 4, no. 1 (July 1989): 226–30. http://dx.doi.org/10.1002/bio.1170040132.

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26

Kricka, Larry J., Xiaoying Ji, Osamu Nozaki, and Peter Wilding. "Imaging of chemiluminescent reactions in mesoscale silicon-glass microstructures." Journal of Bioluminescence and Chemiluminescence 9, no. 3 (May 1994): 135–38. http://dx.doi.org/10.1002/bio.1170090306.

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27

Park, Jason Y., Joshua Gunpat, Li Liu, Brooks Edwards, Alana Christie, Xian-Jin Xie, Larry J. Kricka, and Ralph P. Mason. "Red-shifted emission from 1,2-dioxetane-based chemiluminescent reactions." Luminescence 29, no. 6 (April 24, 2014): 553–58. http://dx.doi.org/10.1002/bio.2666.

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28

Park, Jason Y., Joshua Gunpat, Li Liu, Brooks Edwards, Alana Christie, Xian-Jin Xie, Larry J. Kricka, and Ralph P. Mason. "Red-shifted emission from 1,2-dioxetane-based chemiluminescent reactions." Luminescence 29, no. 6 (September 2014): ii. http://dx.doi.org/10.1002/bio.2746.

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29

Fujimori, Keiichi, Akihisa Tanimoto, Kazunari Takada, Yoshitomo Misaki, Shinichi Kimura, Takayo Moriuchi-Kawakami, and Yasuhiko Shibutani. "Chemiluminescent Emitter Based on the Reactions by Ce(IV)." Analytical Letters 41, no. 16 (November 18, 2008): 2954–62. http://dx.doi.org/10.1080/00032710802440608.

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30

Harteck, Paul, and Robert R. Reeves. "Chemiluminescent Reactions of Major Importance for the Upper Atmosphere." Bulletin des Sociétés Chimiques Belges 71, no. 11-12 (September 2, 2010): 682–87. http://dx.doi.org/10.1002/bscb.19620711112.

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31

Parson, J. M., J. H. Wang, C. C. Fang, and B. S. Cheong. "Chemiluminescent reactions of Sn2, Ge2 and Si2 with O2." Chemical Physics Letters 152, no. 4-5 (November 1988): 330–35. http://dx.doi.org/10.1016/0009-2614(88)80101-5.

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32

Kierzkowski, P., B. Pranszke, A. Kowalski, and M. Menzinger. "Electronic Energy Partitioning in the Reactions of Metastable Mg*(3PJ) Atoms with F2, Cl2, Br2, I2, ICl, IBr." Zeitschrift für Naturforschung A 55, no. 3-4 (April 1, 2000): 433–40. http://dx.doi.org/10.1515/zna-2000-3-409.

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Abstract Chemiluminescent reactions of metastable Mg*(3PJ) atoms with F2 , Cl2 , Br2 , I2 , IC1, IBr molecules were studied in a beam-gas experiment. For all homonuclear targets the MgX(A 2Π -X 2Σ+) emission was observed, but for IC1 and IBr reactants the Mgl(A-X) emission was absent and only MgCl(A-X) or MgBr(A-X) spectra were found. In addition, for the I2 , IBr, IC1, Br2 reactions, broad pseudocontinua extend from above 400 nm into the infrared. These pseudocontinua are ten-tatively attributed to the Mgl, MgBr (B' 2Σ+ -X2Σ+) transition. The total attenuation cross sections, chemiluminescence cross sections and quantum yields were measured. The quantum yields are all below 5%. The results are analyzed using information theory. The low yields for the Mg* + F2 system are explained by a barrier in the entrance channel. For other reactions the low yields are most probably caused by predissociation of the MgX*(A 2Π) products

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33

Verdasco, E., M. Menéndez, M. Garay, A. González Ureña, O. Benoist D'azy, F. J. Poblete, and G. Taïeb. "Reaction Dynamics of Electronically Excited Calcium Atom." Laser Chemistry 12, no. 1-2 (January 1, 1992): 123–36. http://dx.doi.org/10.1155/lc.12.123.

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Absolute values of the total chemiluminescence cross-section for the beam-gas Ca(3P, 1D) + Cl4C → CaCl(A, B) + Cl3C and Ca(3P, 1D) + SF6 → CaF(A, B) + SF5 reactions have been measured at low collision energy, ET = 0.15 and 0.14eV, respectively. Both metastable atomic calcium states Ca(3P, 1D) were produced under low voltage dc-discharge conditions. By changing the discharge conditions, different metastable concentrations were produced to measure the state-to-state cross-section for both 3P and 1D reactions. The following values for the total chemiluminescence cross-sections were obtained:σD1 = 1.77 Å and σP3 = 0.25 Å for the Ca(3P, 1D) + Cl4C → CaCl(A, B) + Cl3C reaction.σD1 = 0.59 Å2 and σP3 = 0.56 Å2 for the Ca(3P, 1D) + SF6 → CaF(A) + SF5 reaction.σD1 = 0.04 Å2 and σP3 = 0.12 Å for the Ca(3P, 1D) + SF6 → CaF(B) + SF5 reaction.In addition, beam-beam experiments were carried out at the same average low collision energy that of the beam-gas, and therefore, normalization between both experiments was possible. This procedure allowed us to obtain the excitation function of the Ca(1D) + SF6 reaction in absolute values over the 0.15–0.60eV collision energy range.On the other hand, by simulation, the ratio of CaCl(B-X/A-X) emissions intensities was found to be of 0.15. The variation of this ratio with the relative concentration of 1D/3P in a Broida oven leads to the conclusion that this state favours the formation of the B state in the chemiluminescent Ca(3P, 1D) + CH3CHCl2 → CaCl(A, B) + CH3CHCl reaction.

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34

Jansen, Eugène H. J. M., Carin A. F. Buskens, and Rijk H. van den Berg. "A sensitive CCD image system for detection of chemiluminescent reactions." Journal of Bioluminescence and Chemiluminescence 3, no. 2 (April 1989): 53–57. http://dx.doi.org/10.1002/bio.1170030204.

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35

Thorpe, G. H., and L. J. Kricka. "Incorporation of enhanced chemiluminescent reactions into fully automated enzyme immunoassays." Journal of Bioluminescence and Chemiluminescence 3, no. 2 (April 1989): 97–100. http://dx.doi.org/10.1002/bio.1170030213.

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36

Burgard, Daniel A., Juno Abraham, April Allen, Jacqueline Craft, Wynter Foley, Ja'terrica Robinson, Breian Wells, Chenxu Xu, and Donald H. Stedman. "Chemiluminescent Reactions of Nickel, Iron, and Cobalt Carbonyls with Ozone." Applied Spectroscopy 60, no. 1 (January 2006): 99–102. http://dx.doi.org/10.1366/000370206775382730.

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37

Lymarev, A. V., I. V. Yudin, S. L. Panasyuk, and V. V. Matyushkov. "Chemiluminescent reactions of radicals in cellulose and some model compounds." Polymer Science U.S.S.R. 27, no. 1 (January 1985): 65–73. http://dx.doi.org/10.1016/0032-3950(85)90097-8.

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38

Arora, Pawan K. "Chemiluminescent reactions of ozone with 2,5-dimethylfuran, furfural and pyrrole." Journal of Photochemistry 35, no. 3 (December 1986): 269–76. http://dx.doi.org/10.1016/0047-2670(86)87058-7.

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39

Perez-Tejeda, Pilar, Alberto Martínez-Delgado, Elia Grueso, and Rosa M. Giráldez-Pérez. "Measuring nanoparticle-induced resonance energy transfer effect by electrogenerated chemiluminescent reactions." RSC Advances 10, no. 7 (2020): 3861–71. http://dx.doi.org/10.1039/c9ra08857a.

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Electrogenerated chemiluminescence efficiencies, redox potentials, photoluminescent (quenching and coupling) effects, and AFM images for the [Ru(bpy)₃]²⁺/Au@tiopronin system were determined in aqueous solutions of the gold nanoparticles at pH 7.0.

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40

Nohira, Hiroyuki, and Toshiyuki Nohira. "Revisiting the von Neumann–Wigner noncrossing rule and validity of a dynamic correlation diagram method." Journal of Theoretical and Computational Chemistry 18, no. 02 (March 2019): 1950013. http://dx.doi.org/10.1142/s0219633619500135.

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The noncrossing rule for potential energy surfaces can be applied only, as originally postulated by von Neumann and Wigner, to slowly occurring changes; it has, however, over many years, been widely used to rationalize fast chemical reactions. Taking the conversion of Dewar benzene to benzene as an example, we demonstrate a reaction that has a timescale for which crossings are allowed. Since it is now established that elementary chemical reactions proceed over ca. 10–100[Formula: see text]fs, as revealed experimentally by Zewail, the noncrossing rule cannot any longer be said to be valid for most chemical reactions. We further demonstrate that the mechanism of the chemiluminescent conversion of Dewar benzene to benzene is explained by an electronic state diagram derived using a dynamic correlation diagram method which allows crossings, whereas the reaction is not explained by a conventional approach, applying the noncrossing rule using a static correlation diagram method.

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41

Gumenchuk, G. B., A. N. Ponomaryov, I. V. Khyzhniy, S. A. Uyutnov, E. V. Savchenko, and V. E. Bondybey. "Triggering of relaxation cascades in pre-irradiated RGS by chemiluminescent reactions." Physics Procedia 2, no. 2 (August 2009): 441–47. http://dx.doi.org/10.1016/j.phpro.2009.07.029.

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42

Perez-Tejeda, Pilar, Elia Grueso, Ana Marin-Gordillo, Concepcion Torres-Marquez, and Rosa M. Giráldez-Pérez. "Aqueous Gold Nanoparticle Solutions for Improved Efficiency in Electrogenerated Chemiluminescent Reactions." ACS Applied Nano Materials 1, no. 9 (August 21, 2018): 5307–15. http://dx.doi.org/10.1021/acsanm.8b01323.

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43

Johnson, Keith, John P. Simons, Peter A. Smith, and Kvaran Agust. "Energy and angular momentum disposal in chemiluminescent reactions of Xe (3PJ)." Journal de Chimie Physique 84 (1987): 371–79. http://dx.doi.org/10.1051/jcp/1987840371.

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44

Wang, J. H., B. S. Cheong, C. C. Fang, and J. M. Parson. "Chemiluminescent reactions of group IV A atoms with PCl5 and SnCl4." Journal of Chemical Physics 93, no. 11 (December 1990): 7830–35. http://dx.doi.org/10.1063/1.459364.

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Sadeghi, N., P. Kowalczyk, and D. W. Setser. "The Cu*(2D5/2 and 2D3/2) chemiluminescent reactions with ClF." Physical Chemistry Chemical Physics 5, no. 16 (2003): 3443. http://dx.doi.org/10.1039/b300287j.

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Karavaev, A. D., and V. P. Kazakov. "Chemiluminescent stages of Belousov-Zhabotinskii reactions in systems with ruthenium complexes." Theoretical and Experimental Chemistry 26, no. 5 (1991): 534–40. http://dx.doi.org/10.1007/bf00531906.

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WABAIDUR, S. M., MU NAUSHAD, and Z. A. ALOTHMAN. "Recent analytical applications of nanoparticle sensitized lucigenin and luminol chemiluminescent reactions." Bulletin of Materials Science 35, no. 1 (February 2012): 7–12. http://dx.doi.org/10.1007/s12034-011-0260-8.

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Mylona, A., J. Nikokavouras, and I. M. Takakis. "Chemiluminescent reactions of E-2-hydroxy-4′-substituted stilbenes with ozone." Journal of Photochemistry and Photobiology A: Chemistry 41, no. 1 (February 1987): 61–68. http://dx.doi.org/10.1016/1010-6030(87)80006-0.

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Girotti, S., E. Ferri, M. Musiani, D. Gibellini, M. Zerbini, A. Roda, G. Gentilomi, and S. Venturoli. "Detection of viral DNA in hybridization reactions using two chemiluminescent substrates." Clinica Chimica Acta 224, no. 1 (January 1994): 73–80. http://dx.doi.org/10.1016/0009-8981(94)90122-8.

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Girotti, S., M. Musiani, P. Pasini, E. Ferri, G. Gallinella, M. L. Zerbini, A. Roda, G. Gentilomi, and S. Venturoli. "Application of a low-light imaging device and chemiluminescent substrates for quantitative detection of viral DNA in hybridization reactions." Clinical Chemistry 41, no. 12 (December 1, 1995): 1693–97. http://dx.doi.org/10.1093/clinchem/41.12.1693.

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Abstract:

Abstract In this quantitative dot-blot hybridization assay for detecting B19 parvovirus DNA, we used three different chemiluminescent substrates [adamantyl-1,2-dioxetane phenyl phosphates (PPD and the new PPD-Plus) and the chloro-5-substituted adamantyl-1,2-dioxetane phosphate (CSPD) plus Emerald enhancer] and a high-performance, low-intensity-light imaging luminograph apparatus. The hybridization test uses digoxigenin-labeled DNA probes, which are immunoenzymatically revealed by anti-digoxigenin Fab fragments conjugated with alkaline phosphatase. All the detection systems with the various chemiluminescent substrates gave sensitive and reproducible results for calibrators and positive or negative reference clinical samples, with high reproducibility (CV 4-17%). The signal was measured after 45 min of incubation. The luminograph apparatus could detect 10 fg of homologous DNA with the PPD-Plus substrate, whereas the detection limit with the CSPD and PPD substrates was 20 fg and 20-50 fg, respectively. Analysis of 26 samples with the three substrates showed good sensitivity and specificity for viral detection.

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