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Journal articles on the topic 'Electrogenerated'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Forster, Robert J., Paolo Bertoncello, and Tia E. Keyes. "Electrogenerated Chemiluminescence." Annual Review of Analytical Chemistry 2, no. 1 (July 19, 2009): 359–85. http://dx.doi.org/10.1146/annurev-anchem-060908-155305.

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2

Ouyang, Jiangbo, and Allen J. Bard. "Electrogenerated chemiluminescence." Journal of Electroanalytical Chemistry and Interfacial Electrochemistry 222, no. 1-2 (May 1987): 331–42. http://dx.doi.org/10.1016/0022-0728(87)80297-8.

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3

Brina, Rossella, and Allen J. Bard. "Electrogenerated chemiluminescence." Journal of Electroanalytical Chemistry and Interfacial Electrochemistry 238, no. 1-2 (December 1987): 277–95. http://dx.doi.org/10.1016/0022-0728(87)85180-x.

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4

Lee, Chi-Woo, Jiangbo Ouyang, and Allen J. Bard. "Electrogenerated chemiluminescence." Journal of Electroanalytical Chemistry and Interfacial Electrochemistry 244, no. 1-2 (April 1988): 319–24. http://dx.doi.org/10.1016/0022-0728(88)80115-3.

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5

McCord, Paul, and Allen J. Bard. "Electrogenerated chemiluminescence." Journal of Electroanalytical Chemistry and Interfacial Electrochemistry 318, no. 1-2 (November 1991): 91–99. http://dx.doi.org/10.1016/0022-0728(91)85296-2.

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6

Fiorani, Andrea, Giovanni Valenti, Irkham, Francesco Paolucci, and Yasuaki Einaga. "Quantification of electrogenerated chemiluminescence from tris(bipyridine)ruthenium(ii) and hydroxyl ions." Physical Chemistry Chemical Physics 22, no. 27 (2020): 15413–17. http://dx.doi.org/10.1039/d0cp02005b.

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In this work, we quantify the electrogenerated chemiluminescence arising from the reaction of electrogenerated tris(bipyridine)ruthenium(iii) with hydroxyl ions, in terms of emission intensity and reaction rate.

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7

Yaschenko, N. N., S. V. Zhitar, and E. G. Zinovjeva. "Determination of phenolic compounds in medicinal preparations by galvanostatic coulometry." Chimica Techno Acta 8, no. 1 (April 13, 2021): 20218110. http://dx.doi.org/10.15826/chimtech.2021.8.1.10.

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In this work, the possibility of using reactions of electrogenerated titrants with phenolic compounds was studied and a method for their coulometric determination in medicaments by galvanostatic coulometry was developed. The research objects were: rutin, salicylic acid and drugs containing phenolic compounds such as «Ascorutin», «Salicylic Paste» and «Salicylic Ointment» of Russian manufacture. Electrogenerated halogens (Cl2, Br2 and I2) and hexacyanoferrate(III)-ions were used as titrants. It was found that for the quantitative determination of phenolic acids, the optimal reagent is electrogenerated bromine, for rutin - electrogenerated bromine and iodine, and for ascorbic acid - any of the studied electrogenerated titrants (Cl2, Br2, I2 and [Fe(CN)6]3-). The correct definition was checked by the «entered-found» method, the error does not exceed 2%. As experimental studies have shown, our method of coulometric titration with electrogenated bromine and iodine is characterized by good reproducibility of results, expression, accuracy and can be used to determine phenolic compounds in drugs, for example, «Ascorutin» tablets. It should be noted that by our procedure it is possible to determine the spectrum of phenol-containing compounds (rutin, ascorbic and salicylic acids) in drugs without their preliminary separation. Therefore, the coulometric method using electrogenerated titrants can be recommended for the determination of salicylic, ascorbic acids and rutin in dosage forms. The proposed method is accurate and eliminates the experiment error in comparison with the Pharmacopoeic method.

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8

Qi, Honglan, and Chengxiao Zhang. "Electrogenerated Chemiluminescence Biosensing." Analytical Chemistry 92, no. 1 (December 2, 2019): 524–34. http://dx.doi.org/10.1021/acs.analchem.9b03425.

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9

Suzuki, Shohei, Mitsuko Kato, and Shoichi Nakajima. "Application of electrogenerated triphenylmethyl anion as a base for alkylation of arylacetic esters and arylacetonitriles and isomerization of allylbenzenes." Canadian Journal of Chemistry 72, no. 2 (February 1, 1994): 357–61. http://dx.doi.org/10.1139/v94-055.

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Phenylacetic esters and phenylacetonitriles were alkylated with alkyl halides, at the position α to an ester or nitrile, either at room temperature (20 °C) or at −78 °C, by making use of electrogenerated triphenylmethyl anion (trityl anion). Double-bond isomerization of allylbenzenes was also effectively accomplished by use of this electrogenerated base (EGB).

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10

Richter, Mark M., and Allen J. Bard. "Electrogenerated Chemiluminescence. 58. Ligand-Sensitized Electrogenerated Chemiluminescence in Europium Labels." Analytical Chemistry 68, no. 15 (January 1996): 2641–50. http://dx.doi.org/10.1021/ac960211f.

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11

S. de Lima, Renata, Alex A. C. de Carvalho, Josealdo Tonholo, Phabyanno R. Lima, and Carmem L. P. S. Zanta. "The Oxidation Efficiency of Commercial, Electrogenerated and Electrogenerated In Situ Hypochlorite." Revista Virtual de Química 10, no. 4 (2018): 851–62. http://dx.doi.org/10.21577/1984-6835.20180062.

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12

Bollo, Soledad, Luis Núñez-Vergara, and Juan A. Squella. "Electrogenerated Nitro Radical Anions." Journal of The Electrochemical Society 151, no. 10 (2004): E322. http://dx.doi.org/10.1149/1.1786076.

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13

Ichia, Laila Sheeney-Haj, Eugenii Katz, Julian Wasserman, and Itamar Willner. "Magneto-switchable electrogenerated biochemiluminescence." Chemical Communications, no. 2 (December 20, 2001): 158–59. http://dx.doi.org/10.1039/b109782m.

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14

Quickenden, T. I., and K. Hansongnern. "Electrogenerated chemiluminescence from violanthrone." Journal of Bioluminescence and Chemiluminescence 10, no. 2 (March 1995): 103–6. http://dx.doi.org/10.1002/bio.1170100206.

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15

Choi, Jai-Pil, and Allen J. Bard. "Electrogenerated chemiluminescence (ECL) 79." Analytica Chimica Acta 541, no. 1-2 (June 2005): 141–48. http://dx.doi.org/10.1016/j.aca.2004.11.075.

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16

Debad, Jeff D., Sang Kwon Lee, Xiaoxin Qiao, Robert A. Pascal, Jr., Allen J. Bard, George W. Francis, József Szúnyog, and Bengt Långström. "Electrogenerated Chemiluminescence. 60. Spectroscopic Properties and Electrogenerated Chemiluminescence of Decaphenylanthracene and Octaphenylnaphthalene." Acta Chemica Scandinavica 52 (1998): 45–50. http://dx.doi.org/10.3891/acta.chem.scand.52-0045.

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17

Fuhrmann, B., and U. Spohn. "A PC-based titrator for flow gradient titrations." Journal of Automatic Chemistry 15, no. 6 (1993): 209–16. http://dx.doi.org/10.1155/s1463924693000276.

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This paper describes a PC (personal computer) based titrator which was developed for gradient flow titrations. Concentration gradients were generated electrolytically or volumetrically in small tubes. Complete titration curves can be recorded on-line and evaluated automatically. The titrator can be used with all liquid flow detectors with low axial dispersion. The titrator was evaluated for the titration of thiosulphate with electrogenerated triiodide and for the titration of ammonia with electrogenerated hypobromite after continuous gas dialytic separation of ammonia from the sample solution.

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18

Muthuraman, G., AG Ramu, YH Cho, EJ McAdam, and IS Moon. "Electrochemically generated bimetallic reductive mediator Cu1+[Ni2+(CN)4]1− for the degradation of CF4 to ethanol by electro-scrubbing." Waste Management & Research: The Journal for a Sustainable Circular Economy 36, no. 11 (October 10, 2018): 1043–48. http://dx.doi.org/10.1177/0734242x18804642.

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Remediation of electronic gas CF4 using commercially available technologies results in another kind of greenhouse gas and corrosive side products. This investigation aimed to develop CF4 removal at room temperature with formation of useful product by attempting an electrogenerated Cu1+[Ni2+(CN)4]1− mediator. The initial electrolysis of the bimetallic complex at the anodized Ti cathode demonstrated Cu1+[Ni2+(CN)4]1− formation, which was confirmed by additional electron spin resonance results. The degradation of CF4 followed mediated electrochemical reduction by electrogenerated Cu1+[Ni2+(CN)4]1−. The removal efficiency of CF4 of 95% was achieved by this electroscrubbing process at room temperature. The spectral results of online and offline Fourier transform infrared analyzer, either in gas or in solution phase, demonstrated that the product formed during the removal of CF4 by electrogenerated Cu1+[Ni2+(CN)4]1− by electroscrubbing was ethanol (CH3CH2OH), with a small amount of trifluoroethane (CF3CH3) intermediate.

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19

Martín-Yerga, Daniel, and Agustín Costa-García. "Stabilization of electrogenerated copper species on electrodes modified with quantum dots." Physical Chemistry Chemical Physics 19, no. 7 (2017): 5018–27. http://dx.doi.org/10.1039/c6cp07957a.

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20

Chen, Ming-Ming, Wei Zhao, Meng-Jiao Zhu, Xiang-Ling Li, Cong-Hui Xu, Hong-Yuan Chen, and Jing-Juan Xu. "Spatiotemporal imaging of electrocatalytic activity on single 2D gold nanoplates via electrogenerated chemiluminescence microscopy." Chemical Science 10, no. 15 (2019): 4141–47. http://dx.doi.org/10.1039/c9sc00889f.

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21

Lai, Rebecca Y., James J. Fleming, Brad L. Merner, Rudolf J. Vermeij, Graham J. Bodwell, and Allen J. Bard. "Electrogenerated Chemiluminescence. 74. Photophysical, Electrochemical, and Electrogenerated Chemiluminescent Studies of Selected Nonplanar Pyrenophanes." Journal of Physical Chemistry A 108, no. 3 (January 2004): 376–83. http://dx.doi.org/10.1021/jp0367981.

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22

Ouyang, Jiangbo, and Allen J. Bard. "Electrogenerated Chemiluminescence. 50. Electrochemistry and Electrogenerated Chemiluminescence of Micelle Solubilized Os(bpy)32+." Bulletin of the Chemical Society of Japan 61, no. 1 (January 1988): 17–24. http://dx.doi.org/10.1246/bcsj.61.17.

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23

Lai, Rebecca Y., and Allen J. Bard. "Electrogenerated Chemiluminescence 71. Photophysical, Electrochemical, and Electrogenerated Chemiluminescent Properties of Selected Dipyrromethene−BF2Dyes." Journal of Physical Chemistry B 107, no. 21 (May 2003): 5036–42. http://dx.doi.org/10.1021/jp034578h.

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24

Zhao, Ying, Qiang Zhang, Ke Chen, Hongfang Gao, Honglan Qi, Xianying Shi, Yajun Han, Junfa Wei, and Chengxiao Zhang. "Triphenothiazinyl triazacoronenes: donor–acceptor molecular graphene exhibiting multiple fluorescence and electrogenerated chemiluminescence emissions." Journal of Materials Chemistry C 5, no. 17 (2017): 4293–301. http://dx.doi.org/10.1039/c7tc00314e.

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25

Liu, Tongjun, and Zhenglong Li. "An electrogenerated base for the alkaline oxidative pretreatment of lignocellulosic biomass to produce bioethanol." RSC Adv. 7, no. 75 (2017): 47456–63. http://dx.doi.org/10.1039/c7ra08101d.

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26

Zhou, Jigang, Jun Zhu, Jack Brzezinski, and Zhifeng Ding. "Tunable electrogenerated chemiluminescence from CdSe nanocrystals." Canadian Journal of Chemistry 87, no. 1 (January 1, 2009): 386–91. http://dx.doi.org/10.1139/v08-180.

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Electrochemical behavior and related optoelectronic properties of CdSe nanocrystals (NCs) in aprotic solutions have been investigated. NCs of 2.50 ± 0.50 nm diameter were synthesized using a modified procedure in which the temperatures at the time of Se precursor injection and NC growth were controlled. The electrochemical band gap was found to agree with those determined by UV–vis absorption spectroscopy and by the tunneling current-voltage spectrum in the literature. Electrogenerated chemiluminescence of the NCs with peak maxima at 1.90 eV (red, 653 nm) and 2.55 eV (blue, 486 nm) can be generated and altered by scanning the voltage between –1.60 and –1.80 V and between –2.00 and –2.20 V, respectively. The results demonstrate the potential capability of the NCs for light emission tuned by the applied potential.Key words: CdSe nanocrystals, electrochemistry, electrogenerated chemiluminescence, UV–vis spectroscopy, photoluminescence.

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27

Galván-Miranda, Elizabeth K., Hiram M. Castro-Cruz, J. Arturo Arias-Orea, Matteo Iurlo, Giovanni Valenti, Massimo Marcaccio, and Norma A. Macías-Ruvalcaba. "Synthesis, photophysical, electrochemical and electrochemiluminescence properties of A2B2 zinc porphyrins: the effect of π-extended conjugation." Physical Chemistry Chemical Physics 18, no. 22 (2016): 15025–38. http://dx.doi.org/10.1039/c6cp01926a.

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28

Zhao, Ying, Dong Xue, Honglan Qi, and Chengxiao Zhang. "Twisted configuration pyrene derivative: exhibiting pure blue monomer photoluminescence and electrogenerated chemiluminescence emissions in non-aqueous media." RSC Advances 7, no. 37 (2017): 22882–91. http://dx.doi.org/10.1039/c7ra01586k.

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29

Shin, Sangbaie, Yun Sung Park, Sunghwan Cho, Insang You, In Seok Kang, Hong Chul Moon, and Unyong Jeong. "Effect of ion migration in electro-generated chemiluminescence depending on the luminophore types and operating conditions." Chemical Science 9, no. 9 (2018): 2480–88. http://dx.doi.org/10.1039/c7sc03996d.

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30

Morales, Daniela V., Catalina N. Astudillo, Veronica Anastasoaie, Baptiste Dautreppe, Bruno F. Urbano, Bernabé L. Rivas, Chantal Gondran, et al. "A cobalt oxide–polypyrrole nanocomposite as an efficient and stable electrode material for electrocatalytic water oxidation." Sustainable Energy & Fuels 5, no. 18 (2021): 4710–23. http://dx.doi.org/10.1039/d1se00363a.

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31

Soulsby, Lachlan C., David J. Hayne, Egan H. Doeven, David J. D. Wilson, Johnny Agugiaro, Timothy U. Connell, Lifen Chen, et al. "Mixed annihilation electrogenerated chemiluminescence of iridium(iii) complexes." Physical Chemistry Chemical Physics 20, no. 28 (2018): 18995–9006. http://dx.doi.org/10.1039/c8cp01737a.

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32

Gu, Jianmin, Jingxiao Wu, Yahui Gao, Tianhui Wu, Qing Li, Aixue Li, Jian-Yao Zheng, Bin Wen, and Faming Gao. "Electrogenerated chemiluminescence logic gate operations based on molecule-responsive organic microwires." Nanoscale 9, no. 29 (2017): 10397–403. http://dx.doi.org/10.1039/c7nr02347b.

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33

Chen, Xiaojiao, Yao He, Youyu Zhang, Meiling Liu, Yang Liu, and Jinghong Li. "Ultrasensitive detection of cancer cells and glycan expression profiling based on a multivalent recognition and alkaline phosphatase-responsive electrogenerated chemiluminescence biosensor." Nanoscale 6, no. 19 (2014): 11196–203. http://dx.doi.org/10.1039/c4nr03053b.

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34

Kerr, Emily, Egan H. Doeven, David J. D. Wilson, Conor F. Hogan, and Paul S. Francis. "Considering the chemical energy requirements of the tri-n-propylamine co-reactant pathways for the judicious design of new electrogenerated chemiluminescence detection systems." Analyst 141, no. 1 (2016): 62–69. http://dx.doi.org/10.1039/c5an01462j.

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35

Kirschbaum-Harriman, Stefanie, Axel Duerkop, and Antje J. Baeumner. "Improving ruthenium-based ECL through nonionic surfactants and tertiary amines." Analyst 142, no. 14 (2017): 2648–53. http://dx.doi.org/10.1039/c7an00197e.

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36

Zholudov, Yuriy, Natalia Lysak, Dmytro Snizhko, Olena Reshetniak, and Guobao Xu. "Electrochemiluminescence analysis of tryptophan in aqueous solutions based on its reaction with tetraphenylborate anions." Analyst 145, no. 9 (2020): 3364–69. http://dx.doi.org/10.1039/d0an00229a.

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37

Fang, Yi-Min, Jing Song, Juan Li, Yi-Wei Wang, Huang-Hao Yang, Jian-Jun Sun, and Guo-Nan Chen. "Electrogenerated chemiluminescence from Au nanoclusters." Chem. Commun. 47, no. 8 (2011): 2369–71. http://dx.doi.org/10.1039/c0cc04180g.

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38

Shan, Kun, Ping Zhou, Jiqing Cai, Renke Kang, Kang Shi, and Dongming Guo. "Electrogenerated chemical polishing of copper." Precision Engineering 39 (January 2015): 161–66. http://dx.doi.org/10.1016/j.precisioneng.2014.08.004.

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39

Gao, Wenyue, Stéphane Jeanneret, Dajing Yuan, Thomas Cherubini, Lu Wang, Xiaojiang Xie, and Eric Bakker. "Electrogenerated Chemiluminescence for Chronopotentiometric Sensors." Analytical Chemistry 91, no. 7 (March 5, 2019): 4889–95. http://dx.doi.org/10.1021/acs.analchem.9b00787.

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40

Kariv-Miller, Essie, Vesna Svetličić, and Phillip B. Lawin. "Electrogenerated R4N(Hg)5 films." Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases 83, no. 4 (1987): 1169. http://dx.doi.org/10.1039/f19878301169.

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41

Richter, Mark M., Jeff D. Debad, Durwin R. Striplin, G. A. Crosby, and Allen J. Bard. "Electrogenerated Chemiluminescence. 59. Rhenium Complexes." Analytical Chemistry 68, no. 24 (January 1996): 4370–76. http://dx.doi.org/10.1021/ac9606160.

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42

Maus, Russell G., and R. Mark Wightman. "Microscopic Imaging with Electrogenerated Chemiluminescence." Analytical Chemistry 73, no. 16 (August 2001): 3993–98. http://dx.doi.org/10.1021/ac010128e.

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43

VENKATACHALAM, S. "Electrogenerated Gas Bubbles in Flotation." Mineral Processing and Extractive Metallurgy Review 8, no. 1-4 (February 1992): 47–55. http://dx.doi.org/10.1080/08827509208952677.

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44

Booker, Christina, Xin Wang, Samar Haroun, Jigang Zhou, Michael Jennings, Brian L Pagenkopf, and Zhifeng Ding. "Tuning of Electrogenerated Silole Chemiluminescence." Angewandte Chemie 120, no. 40 (September 22, 2008): 7845–49. http://dx.doi.org/10.1002/ange.200802034.

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45

Booker, Christina, Xin Wang, Samar Haroun, Jigang Zhou, Michael Jennings, Brian L Pagenkopf, and Zhifeng Ding. "Tuning of Electrogenerated Silole Chemiluminescence." Angewandte Chemie International Edition 47, no. 40 (September 22, 2008): 7731–35. http://dx.doi.org/10.1002/anie.200802034.

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46

Crespo, Gastón A., Günter Mistlberger, and Eric Bakker. "Electrogenerated Chemiluminescence for Potentiometric Sensors." Journal of the American Chemical Society 134, no. 1 (December 21, 2011): 205–7. http://dx.doi.org/10.1021/ja210600k.

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47

Myung, Noseung, Zhifeng Ding, and Allen J. Bard. "Electrogenerated Chemiluminescence of CdSe Nanocrystals." Nano Letters 2, no. 11 (November 2002): 1315–19. http://dx.doi.org/10.1021/nl0257824.

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48

Myung, Noseung, Xianmao Lu, Keith P. Johnston, and Allen J. Bard. "Electrogenerated Chemiluminescence of Ge Nanocrystals." Nano Letters 4, no. 1 (January 2004): 183–85. http://dx.doi.org/10.1021/nl0349810.

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49

Petrosyan, V. A., A. A. Fainzil'berg, M. E. Niyazymbetov, and V. N. Solkan. "Synthesis based on electrogenerated carbenes." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 38, no. 5 (May 1989): 985–89. http://dx.doi.org/10.1007/bf00955430.

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50

Niyazymbetov, M. E., V. A. Petrosyan, A. A. Fainzil'berg, S. A. Shevelev, and V. V. Semenov. "Syntheses based on electrogenerated carbenes." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 38, no. 5 (May 1989): 991–95. http://dx.doi.org/10.1007/bf00955431.

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