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Journal articles on the topic 'Phenothiazine dyes'

Author: Grafiati

Published: 4 June 2021

Last updated: 9 February 2022

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1

Kafafy, Hany, Hongwei Wu, Ming Peng, et al. "Steric and Solvent Effect in Dye-Sensitized Solar Cells Utilizing Phenothiazine-Based Dyes." International Journal of Photoenergy 2014 (2014): 1–9. http://dx.doi.org/10.1155/2014/548914.

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Three phenothiazine-based dyes have been prepared and utilized as dye-sensitized solar cells (DSSCs). The effects of dye-adsorption solvent on the performances of dye-sensitized solar cells based on phenothiazine dyes were investigated in this study. The highest conversion efficiency of 3.78% was obtained using ethanol (EtOH) and 2.53% for tetrahydrofuran (THF), respectively, as dye-adsorption solvents. Cell performance using EtOH as a dye-adsorption solvent showed relatively higher performance than that using THF. Electrochemical and photochemical tests of phenothiazine dyes in solution and a

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2

Buene, Audun Formo, Mats Christensen, and Bård Helge Hoff. "Effect of Auxiliary Donors on 3,8-Phenothiazine Dyes for Dye-Sensitized Solar Cells." Molecules 24, no. 24 (2019): 4485. http://dx.doi.org/10.3390/molecules24244485.

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Phenothiazines are one of the more common dye scaffolds for dye-sensitized solar cells. However, these sensitizers are exclusively based on a 3,7-substitution pattern. Herein, we have synthesized and characterized novel 3,8-substituted phenothiazine dyes in order to evaluate the effect of auxiliary donor groups on the performance of this new dye class. The power conversion efficiency increased by 7%–10% upon insertion of an auxiliary donor in position 8 of the phenothiazine, but the structure of the auxiliary donor (phenyl, naphthyl, pyrene) had a low impact when electrodes were stained with c

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3

Chen, Yung-Chung, Yuan-Tsung Kuo, and Chia-Jung Liang. "Numbers of cyanovinyl substitutes and their effect on phenothiazine based organic dyes for dye-sensitized solar cells." RSC Advances 8, no. 18 (2018): 9783–89. http://dx.doi.org/10.1039/c7ra13751f.

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Phenothiazine based dyes (OMS1–3), comprising different conjugation lengths, numbers of electron deficient (cyanovinyl) moieties have been synthesized. OMS3 dye has two cyanovinyl moieties between phenothiazine core exhibits the best cell performance at 4.00%.

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4

Buene, Audun Formo, Nanna Boholm, Anders Hagfeldt та Bård Helge Hoff. "Effect of furan π-spacer and triethylene oxide methyl ether substituents on performance of phenothiazine sensitizers in dye-sensitized solar cells". New Journal of Chemistry 43, № 24 (2019): 9403–10. http://dx.doi.org/10.1039/c9nj01720h.

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5

Watanabe, Motonori, Hidehisa Hagiwara, Aoi Iribe, et al. "Spacer effects in metal-free organic dyes for visible-light-driven dye-sensitized photocatalytic hydrogen production." J. Mater. Chem. A 2, no. 32 (2014): 12952–61. http://dx.doi.org/10.1039/c4ta02720e.

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6

Huang, Zu-Sheng, Herbert Meier, and Derong Cao. "Correction: Phenothiazine-based dyes for efficient dye-sensitized solar cells." Journal of Materials Chemistry C 4, no. 16 (2016): 3662. http://dx.doi.org/10.1039/c6tc90068b.

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7

Qian, Xing, Lin Lu, Yi-Zhou Zhu, Huan-Huan Gao, and Jian-Yu Zheng. "Phenothiazine-functionalized push–pull Zn porphyrin photosensitizers for efficient dye-sensitized solar cells." RSC Advances 6, no. 11 (2016): 9057–65. http://dx.doi.org/10.1039/c5ra26754d.

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8

Huang, Zu-Sheng, Herbert Meier, and Derong Cao. "Phenothiazine-based dyes for efficient dye-sensitized solar cells." Journal of Materials Chemistry C 4, no. 13 (2016): 2404–26. http://dx.doi.org/10.1039/c5tc04418a.

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Due to their structure features, 10H-phenothiazine-based dyes show high photovoltaic performance and have great potential for future technical applications in dye-sensitized solar cells (DSSCs). The recent significant scientific progress of the dyes and their DSSCs is reviewed, and the relationship between the molecular structure and the photoelectric conversion properties is especially discussed.

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9

Okafor, Charles O. "New phenothiazine dyes and pigments." Dyes and Pigments 6, no. 6 (1985): 405–15. http://dx.doi.org/10.1016/0143-7208(85)80022-x.

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10

Chiykowski, Valerie A., Brian Lam, Chuan Du, and Curtis P. Berlinguette. "Comparative analysis of triarylamine and phenothiazine sensitizer donor units in dye-sensitized solar cells." Chemical Communications 53, no. 15 (2017): 2367–70. http://dx.doi.org/10.1039/c6cc09178d.

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11

Yang, Jie, Hua Wang, Yun Yang, Jiapeng Wu, Pengfei Hu, and Lin Guo. "Pseudocapacitive-dye-molecule-based high-performance flexible supercapacitors." Nanoscale 9, no. 28 (2017): 9879–85. http://dx.doi.org/10.1039/c7nr03385k.

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Two kinds of widely used dye molecules including anthraquinone derivatives and phenothiazine dyes with intrinsic redox centers can be effectively decolorized and resource utilized as pseudocapacitive energy-storage materials. A new type of flexible supercapacitor based on dye wastewater has been successfully fabricated.

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12

Jia, Hai-Lang, Zhi-Jie Peng, Yu-Chao Chen, Cheng-Yan Huang, and Ming-Yun Guan. "Highly efficient stereoscopic phenothiazine dyes with different anchors for dye-sensitized solar cells." New Journal of Chemistry 42, no. 23 (2018): 18702–7. http://dx.doi.org/10.1039/c8nj04164d.

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13

Molnar, Eva, Emese Gal, Luiza Gaina, et al. "Novel Phenothiazine-Bridged Porphyrin-(Hetero)aryl dyads: Synthesis, Optical Properties, In Vitro Cytotoxicity and Staining of Human Ovarian Tumor Cell Lines." International Journal of Molecular Sciences 21, no. 9 (2020): 3178. http://dx.doi.org/10.3390/ijms21093178.

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We report here the synthetic procedure applied for the preparation of new AB3-type and trans-A2B2 type meso-halogenophenothiazinyl-phenyl-porphyrin derivatives, their metal core complexation and their peripheral modification using Suzuki–Miyaura cross coupling reactions with various (hetero)aryl (phenothiazinyl, 7-formyl-phenothiazinyl, (9-carbazolyl)-phenyl and 4-formyl-phenyl, phenyl) boronic acid derivatives. The meso-phenothiazinyl-phenyl-porphyrin (MPP) dyes family was thus extended by a series of novel phenothiazine-bridged porphyrin-(hetero)aryl dyads characterized by UV–Vis absorption/

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14

Ouared, Ihssène, Mâammar Rekhis, and Mohamed Trari. "Theoretical Study of Phenothiazine Organic Dyes with Different Spacers for Dye-Sensitised Solar Cells." Australian Journal of Chemistry 72, no. 4 (2019): 244. http://dx.doi.org/10.1071/ch18449.

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In this paper, six organic dyes have been studied by density functional theory (DFT). The electron-acceptor group is the cyanoacrylic acid unit for all sensitisers, and the electron-donor unit is a phenothiazine (PTZ) fragment substituted by an ethynyl-pyrene unit; the π-linker was varied, and the influence was investigated. The dye bearing the divinylthiophene linker showed the highest absorption maximum. The theoretical photovoltaic properties revealed that the overall efficiency of the solar cell could be remarkably improved using the designed dyes. The results indicated that all of the stu

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15

Gao, Hongqiang, Pengchong Xue, Jiang Peng, et al. "Red-emitting dyes based on phenothiazine-modified 2-hydroxychalcone analogues: mechanofluorochromism and gelation-induced emission enhancement." New Journal of Chemistry 43, no. 1 (2019): 77–84. http://dx.doi.org/10.1039/c8nj05212c.

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16

Chang, Yuan Jay, Po-Ting Chou, Yan-Zuo Lin, et al. "Organic dyes containing oligo-phenothiazine for dye-sensitized solar cells." Journal of Materials Chemistry 22, no. 40 (2012): 21704. http://dx.doi.org/10.1039/c2jm35556f.

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17

Slodek, Aneta, Dawid Zych, Sylwia Golba, Sylwia Zimosz, Paweł Gnida, and Ewa Schab-Balcerzak. "Dyes based on the D/A-acetylene linker-phenothiazine system for developing efficient dye-sensitized solar cells." Journal of Materials Chemistry C 7, no. 19 (2019): 5830–40. http://dx.doi.org/10.1039/c9tc01727e.

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18

Nagarajan, Bhanumathi, Suman Kushwaha, Ramachandran Elumalai, Sudip Mandal, Kothandaraman Ramanujam, and Dhamodharan Raghavachari. "Novel ethynyl-pyrene substituted phenothiazine based metal free organic dyes in DSSC with 12% conversion efficiency." Journal of Materials Chemistry A 5, no. 21 (2017): 10289–300. http://dx.doi.org/10.1039/c7ta01744h.

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19

Usacheva, Marina N., Matthew C. Teichert, and Merrill A. Biel. "The interaction of lipopolysaccharides with phenothiazine dyes." Lasers in Surgery and Medicine 33, no. 5 (2003): 311–19. http://dx.doi.org/10.1002/lsm.10226.

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20

Koochana, Prashanth Kumar, Abhinav Mohanty, Biswamaitree Subhadarshanee, et al. "Phenothiazines and phenoxazines: as electron transfer mediators for ferritin iron release." Dalton Transactions 48, no. 10 (2019): 3314–26. http://dx.doi.org/10.1039/c8dt04383c.

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21

Lin, Yan-Duo, Bo-Yu Ke, Yuan Jay Chang, et al. "Pyridomethene–BF2 complex/phenothiazine hybrid sensitizer with high molar extinction coefficient for efficient, sensitized solar cells." Journal of Materials Chemistry A 3, no. 32 (2015): 16831–42. http://dx.doi.org/10.1039/c5ta03807c.

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22

Hua, Yong, Lawrence Tien Lin Lee, Caishun Zhang, et al. "Co-sensitization of 3D bulky phenothiazine-cored photosensitizers with planar squaraine dyes for efficient dye-sensitized solar cells." Journal of Materials Chemistry A 3, no. 26 (2015): 13848–55. http://dx.doi.org/10.1039/c5ta01665g.

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23

Xie, ZhiBin, Anupam Midya, Kian Ping Loh, et al. "Highly efficient dye-sensitized solar cells using phenothiazine derivative organic dyes." Progress in Photovoltaics: Research and Applications 18, no. 8 (2010): 573–81. http://dx.doi.org/10.1002/pip.980.

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24

Luo, Jun-Sheng, Zhong-Quan Wan, and Chun-Yang Jia. "Recent advances in phenothiazine-based dyes for dye-sensitized solar cells." Chinese Chemical Letters 27, no. 8 (2016): 1304–18. http://dx.doi.org/10.1016/j.cclet.2016.07.002.

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25

Ding, Yongjie, Jianhua Li, Shuaishuai Liu, et al. "New phenothiazine dyes containing benzothiadiazole-acceptor for dye-sensitized solar cells." Dyes and Pigments 194 (October 2021): 109664. http://dx.doi.org/10.1016/j.dyepig.2021.109664.

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26

Slodek, Aneta, Dawid Zych, Grażyna Szafraniec-Gorol, Paweł Gnida, Marharyta Vasylieva, and Ewa Schab-Balcerzak. "Investigations of New Phenothiazine-Based Compounds for Dye-Sensitized Solar Cells with Theoretical Insight." Materials 13, no. 10 (2020): 2292. http://dx.doi.org/10.3390/ma13102292.

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New D-π-D-π-A low-molecular-weight compounds, based on a phenothiazine scaffold linked via an acetylene unit with various donor moiety and cyanoacrylic acid anchoring groups, respectively, were successfully synthesized. The prepared phenothiazine dyes were entirely characterized using nuclear magnetic resonance (NMR) spectroscopy and elemental analysis. The compounds were designed to study the relationship between end-capping donor groups’ structure on their optoelectronic and thermal properties as well as the dye-sensitized solar cells’ performance. The effect of π-conjugation enlargement by

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27

Wang, Gang, Yingying Wu, Wenhui Ding та ін. "Photovoltaic performance of long-chain poly(triphenylamine-phenothiazine) dyes with a tunable π-bridge for dye-sensitized solar cells". Journal of Materials Chemistry A 3, № 27 (2015): 14217–27. http://dx.doi.org/10.1039/c5ta03425f.

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28

Chiykowski, Valerie A., Brian Lam, Chuan Du, and Curtis P. Berlinguette. "On how electron density affects the redox stability of phenothiazine sensitizers on semiconducting surfaces." Chemical Communications 53, no. 17 (2017): 2547–50. http://dx.doi.org/10.1039/c6cc09992k.

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29

Onoabedje, Efeturi Abraham, Obioma Chinwe Chinwuko, Benjamin Ebere Ezema, and Mercy Amarachukwu Ezeokonkwo. "Synthesis of polycyclic mixed phenothiazine-phenoxazine organic dyes." Phosphorus, Sulfur, and Silicon and the Related Elements 193, no. 7 (2018): 437–42. http://dx.doi.org/10.1080/10426507.2018.1436545.

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30

Liu, Hu, Xingrong Liao, Xiaoyu Li, et al. "Molecular design of new organic sensitizers based on thieno[1,4]benzothiazine for dye-sensitized solar cells." RSC Advances 5, no. 70 (2015): 56865–71. http://dx.doi.org/10.1039/c5ra07785k.

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A novel thieno[1,4]benzothiazine donor has been developed for the first time to construct metal-free organic sensitizers, which exhibit more dramatically red-shifted absorptions than phenothiazine-based dyes.

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31

Bhuin, Shouvik, Sayantan Halder, Subit Kumar Saha, and Manab Chakravarty. "Binding interactions and FRET between bovine serum albumin and various phenothiazine-/anthracene-based dyes: a structure–property relationship." RSC Advances 11, no. 3 (2021): 1679–93. http://dx.doi.org/10.1039/d0ra09580j.

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The present study demonstrates binding interactions and Förster resonance energy transfer (FRET) between bovine serum albumin (BSA) and a series of structurally and electronically diverse phenothiazine (PTZ) and anthracene (ANT) dyes.

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32

Jin, Xingyi, Libo Sun, Dongyuan Li, Cheng-Long Wang та Fu-Quan Bai. "Efficiency difference between furan- and thiophene-based D–π–A dyes in DSSCs explained by theoretical calculations". RSC Advances 8, № 52 (2018): 29917–23. http://dx.doi.org/10.1039/c8ra04450c.

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33

Shen, Xiao-Feng, Motonori Watanabe, Atsushi Takagaki, Jun Tae Song, and Tatsumi Ishihara. "Pyridyl-Anchored Type BODIPY Sensitizer-TiO2 Photocatalyst for Enhanced Visible Light-Driven Photocatalytic Hydrogen Production." Catalysts 10, no. 5 (2020): 535. http://dx.doi.org/10.3390/catal10050535.

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Dye-sensitized photocatalytic hydrogen production using a boron-dipyrromethene (BODIPY) organic material having a pyridyl group at the anchor site was investigated. Phenyl, carbazole, and phenothiazine derivatives were introduced into BODIPY dyes, and their photocatalytic activities were examined. Identification was performed by nuclear magnetic resonance (NMR), infrared (IR), mass (MS) spectra, and absorption spectra, and catalyst evaluation was performed by using visible-light irradiation and photocatalytic hydrogen production and photocurrent. These dyes have strong absorption at 600–700 nm

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34

Han, Feng, Lina Chi, Wenting Wu, Xiaofen Liang, Meiyan Fu, and Jianzhang Zhao. "Environment sensitive phenothiazine dyes strongly fluorescence in protic solvents." Journal of Photochemistry and Photobiology A: Chemistry 196, no. 1 (2008): 10–23. http://dx.doi.org/10.1016/j.jphotochem.2007.11.007.

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35

Lee, Chongmok, Yoo Wha Sung, and Joon Woo Park. "Multiple Equilibria of Phenothiazine Dyes in Aqueous Cyclodextrin Solutions†." Journal of Physical Chemistry B 103, no. 5 (1999): 893–98. http://dx.doi.org/10.1021/jp983767a.

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36

Tuite, Eimer M., and Bengt Nordén. "Structural Heterogeneity in Polynucleotide-Facilitated Assembly of Phenothiazine Dyes." Journal of Physical Chemistry B 122, no. 11 (2018): 2891–99. http://dx.doi.org/10.1021/acs.jpcb.7b12835.

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37

Wagner, Stephen J. "Virus inactivation in blood components by photoactive phenothiazine dyes." Transfusion Medicine Reviews 16, no. 1 (2002): 61–66. http://dx.doi.org/10.1053/tmrv.2002.29405.

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38

Onoabedje, Efeturi A., Uchechukwu C. Okoro, and David W. Knight. "Rapid Access to New Angular Phenothiazine and Phenoxazine Dyes." Journal of Heterocyclic Chemistry 54, no. 1 (2015): 206–14. http://dx.doi.org/10.1002/jhet.2569.

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39

Czímerová, Adriana, Alexander Čeklovský, and Juraj Bujdák. "Interaction of montmorillonite with phenothiazine dyes and pyronin in aqueous dispersions: A visible spectroscopy study." Open Chemistry 7, no. 3 (2009): 343–53. http://dx.doi.org/10.2478/s11532-009-0035-x.

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AbstractLayer charge is one of the key parameters used for the characterisation of expandable clay minerals, smectites. It determines most significant properties of the material which are important from the industrial application point of view. This work is related to a novel method introduced to characterize the layer charge of smectites, based on using cationic organic dyes as molecular sensors. One xanthene and four phenothiazine cationic dyes were tested using reduced charge montmorillonites (RCMs) and compared with methylene blue, which has been used most frequently. The characterization

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40

Ahmed, Shahnaz, Smiti Rani Bora, Tridip Chutia, and Dhruba Jyoti Kalita. "Structural modulation of phenothiazine and coumarin based derivatives for high performance dye sensitized solar cells: a theoretical study." Physical Chemistry Chemical Physics 23, no. 23 (2021): 13190–203. http://dx.doi.org/10.1039/d1cp00036e.

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41

Muenmart, D., N. Prachumrak, R. Tarsang та ін. "New D–D–π–A type organic dyes having carbazol-N-yl phenothiazine moiety as a donor (D–D) unit for efficient dye-sensitized solar cells: experimental and theoretical studies". RSC Advances 6, № 44 (2016): 38481–93. http://dx.doi.org/10.1039/c6ra06220b.

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DSSCs using novel organic dyes (CPhTnPA, n = 0–2) with carbazol-N-yl phenothiazine moiety as a donor (D–D) unit as the sensitizers exhibited efficiency as high as 7.78% which reached 95% with respect to that of the reference N719-based device (8.20%).

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42

Pan, Bina, Yi-Zhou Zhu, Changjuana Qiu, Binga Wang, and Jian-Yu Zheng. "Synthesis of Phenothiazine Dyes Featuring Benzothiadiazole Unit for Efficient Dye-sensitized Solar Cells." Acta Chimica Sinica 76, no. 3 (2018): 215. http://dx.doi.org/10.6023/a17120543.

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43

Hua, Yong, Shuai Chang, Dandan Huang, et al. "Significant Improvement of Dye-Sensitized Solar Cell Performance Using Simple Phenothiazine-Based Dyes." Chemistry of Materials 25, no. 10 (2013): 2146–53. http://dx.doi.org/10.1021/cm400800h.

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44

Zhang, Xiaofeng, Faliang Gou, Dongning Zhao та ін. "π-Spacer effect in dithiafulvenyl-π-phenothiazine dyes for dye-sensitized solar cells". Journal of Power Sources 324 (серпень 2016): 484–91. http://dx.doi.org/10.1016/j.jpowsour.2016.05.120.

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45

Gao, Huan-Huan, Xing Qian, Wen-Ying Chang, Shan-Shan Wang, Yi-Zhou Zhu та Jian-Yu Zheng. "Oligothiophene-linked D–π–A type phenothiazine dyes for dye-sensitized solar cells". Journal of Power Sources 307 (березень 2016): 866–74. http://dx.doi.org/10.1016/j.jpowsour.2016.01.055.

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46

Chiu, Kuo Yuan, Zong-Liang Tseng, Lung-Chien Chen та ін. "D-π-A Type Phenothiazine Organic Dyes for Dye-Sensitized TiO2 Solar Cells". Science of Advanced Materials 10, № 6 (2018): 801–7. http://dx.doi.org/10.1166/sam.2018.3249.

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47

Gnida, Paweł, Paweł Jarka, Pavel Chulkin, et al. "Impact of TiO2 Nanostructures on Dye-Sensitized Solar Cells Performance." Materials 14, no. 7 (2021): 1633. http://dx.doi.org/10.3390/ma14071633.

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The effect of TiO2 nanostructures such as nanoparticles, nanowires, nanotubes on photoanode properties, and dye-sensitized solar cells photovoltaic parameters were studied. The series of dye-sensitized solar cells based on two dyes, that is, commercially N719 and synthesized 3,7′-bis(2-cyano-1-acrylic acid)-10-ethyl-phenothiazine were tested. Additionally, the devices containing a mixture of this sensitizer and chenodeoxycholic acid as co-adsorbent were fabricated. The amount of adsorbed dye molecules to TiO2 was evaluated. The prepared photoanodes with different TiO2 nanostructures were inves

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48

Mohr, Harald, Barbara Bachmann, Anette Klein-Struckmeier, and Bernd Lambrecht. "Virus Inactivation of Blood Products by Phenothiazine Dyes and Light." Photochemistry and Photobiology 65, no. 3 (1997): 441–45. http://dx.doi.org/10.1111/j.1751-1097.1997.tb08586.x.

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49

Wagner, Stephen J., Andrey Skripchenko, Daniel Robinette, James W. Foley, and Louis Cincotta. "Factors Affecting Virus Photoinactivation by a Series of Phenothiazine Dyes." Photochemistry and Photobiology 67, no. 3 (1998): 343–49. http://dx.doi.org/10.1111/j.1751-1097.1998.tb05208.x.

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50

Figueiredo, Rômulo Aguiar, Lilian Costa Anami, Isabel Mello, Erica dos Santos Carvalho, Sandra Márcia Habitante, and Denise Pontes Raldi. "Tooth Discoloration Induced by Endodontic Phenothiazine Dyes in Photodynamic Therapy." Photomedicine and Laser Surgery 32, no. 8 (2014): 458–62. http://dx.doi.org/10.1089/pho.2014.3722.

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