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Journal articles on the topic 'Dihydroacridine'

Author: Grafiati

Published: 4 June 2021

Last updated: 16 February 2022

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1

Suzuki, Ryota, Reiki Tada, Takumi Hosoda, Youhei Miura, and Naoki Yoshioka. "Synthesis of ester-substituted dihydroacridine derivatives and their spectroscopic properties." New Journal of Chemistry 40, no. 3 (2016): 2920–26. http://dx.doi.org/10.1039/c5nj02839f.

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2

Liu, Xiang-Yang, Feng Liang, Yi Yuan, Zuo-Quan Jiang, and Liang-Sheng Liao. "Utilizing 9,10-dihydroacridine and pyrazine-containing donor–acceptor host materials for highly efficient red phosphorescent organic light-emitting diodes." Journal of Materials Chemistry C 4, no. 33 (2016): 7869–74. http://dx.doi.org/10.1039/c6tc02180h.

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3

LaFortune, James H. W., Julia M. Bayne, Timothy C. Johnstone, Louie Fan, and Douglas W. Stephan. "Catalytic double hydroarylation of alkynes to 9,9-disubstituted 9,10-dihydroacridine derivatives by an electrophilic phenoxyphosphonium dication." Chemical Communications 53, no. 100 (2017): 13312–15. http://dx.doi.org/10.1039/c7cc08037a.

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4

Singh, Palwinder, Arun Kumar, Sukhmeet Kaur, Amrinder Singh, Muskan Gupta, and Gurcharan Kaur. "Stitching of tyrosine and 10H-acridin-9-one: turn-ON fluorescence in the narrow pH range 7.4–8.5 and intracellular labelling of cancer cells." MedChemComm 7, no. 4 (2016): 632–35. http://dx.doi.org/10.1039/c5md00534e.

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5

Cho, An-Na, Nallan Chakravarthi, Kakaraparthi Kranthiraja, et al. "Acridine-based novel hole transporting material for high efficiency perovskite solar cells." Journal of Materials Chemistry A 5, no. 16 (2017): 7603–11. http://dx.doi.org/10.1039/c7ta01248a.

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The cost-effective hole transporting material ACR-TPA based on a 9,9-dimethyl-9,10-dihydroacridine core is synthesized and found to be a promising alternative to spiro-MeOTAD because of its comparable photovoltaic performance.

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6

Kupka, A., C. Schauerte, and K. Merz. "Isostructural Crystallization Behavior of Dihydroanthracene and Dihydroacridine." Crystal Growth & Design 14, no. 6 (2014): 2985–89. http://dx.doi.org/10.1021/cg5002623.

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7

Duan, Yanbing, Haifeng Sun, Peng Guo, and Min Ji. "S-4-Chlorophenyl 9,10-dihydroacridine-9-carbothioate." Acta Crystallographica Section E Structure Reports Online 65, no. 3 (2009): o446. http://dx.doi.org/10.1107/s1600536809003468.

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8

Baker, L. J., G. R. Clark, B. R. Copp, R. P. Hansen, and C. J. Squire. "2-Ethylthio-9-methyl-1,4-dihydroacridine-1,4-dione and 9-methyl-2-(4-tolylthio)-1,4-dihydroacridine-1,4-dione." Acta Crystallographica Section C Crystal Structure Communications 55, no. 4 (1999): 634–36. http://dx.doi.org/10.1107/s0108270198014929.

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9

Seo, Jeong-A., Sang Kyu Jeon, Myoung Seon Gong, Jun Yeob Lee, Chang Ho Noh, and Sung Han Kim. "Long lifetime blue phosphorescent organic light-emitting diodes with an exciton blocking layer." Journal of Materials Chemistry C 3, no. 18 (2015): 4640–45. http://dx.doi.org/10.1039/c5tc00640f.

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An acridine derived compound, 9,9-dimethyl-10-(9-phenyl-9H-carbazol-3-yl)-9,10-dihydroacridine (PCZAC), was newly designed as a hole transport type high triplet energy material for application as a hole transport type exciton blocking layer of blue phosphorescent organic light-emitting diodes.

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10

Sourdon, V., G. Boyer, and J. P. Galy. "Crystal structure of 4,9-dimethyl-9,10-dihydroacridine, C15H15N." Zeitschrift für Kristallographie - New Crystal Structures 216, no. 1-4 (2001): 679–80. http://dx.doi.org/10.1524/ncrs.2001.216.14.679.

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11

Friebolin, Heike, та Christoph Rüchardt. "Bimolecular formation of radicals by hydrogen transfer, 9. Uncatalyzed transfer hydrogenation of α-methylstyrene by 9,10-dihydroacridine andN-methyl-9,10-dihydroacridine". Liebigs Annalen 1995, № 7 (1995): 1339–41. http://dx.doi.org/10.1002/jlac.1995199507177.

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12

Patel, Jully, Karunamay Majee, Ejaz Ahmạd, Koji Tanaka, and Sumanta Kumar Padhi. "[RuV(NCN-Me)(bpy)(O)]3+ Mediates efficient C–H bond oxidation from NADH analogs in aqueous media rather than water oxidation." Dalton Transactions 44, no. 3 (2015): 920–23. http://dx.doi.org/10.1039/c4dt02827a.

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The [Ru<sup>V</sup>O]<sup>3+</sup> and [Ru<sup>VI</sup>O]<sup>4+</sup> generated from [Ru<sup>II</sup>(NCN-Me)(bpy)(H<sub>2</sub>O)](PF<sub>6</sub>)<sub>2</sub> play the selective role in C–H bond oxidation of 2-(pyridin-2-yl)-9,10-dihydroacridine (PADHH) and water splitting, respectively, are reported.

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13

Seino, M., Y. Akui, T. Ishida, and T. Nogami. "Magnetic properties of 9,9-disubstituted 9,10-dihydroacridine-10-yloxyls." Synthetic Metals 133-134 (March 2003): 581–83. http://dx.doi.org/10.1016/s0379-6779(02)00353-3.

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14

Alipour, Mousa, Mehdi M. Baradarani, and John A. Joule. "Spiro[4H -pyran-3,3′-oxindoles] Derived from 9,10-dihydroacridine." Journal of Heterocyclic Chemistry 54, no. 4 (2017): 2223–27. http://dx.doi.org/10.1002/jhet.2809.

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15

Charbit, Jean Jacques, Anne Marie Galy, Jean Pierre Galy, and Jacques Barbe. "Preparation of some new N-substituted 9,10-dihydroacridine derivatives." Journal of Chemical & Engineering Data 34, no. 1 (1989): 136–37. http://dx.doi.org/10.1021/je00055a038.

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16

Iwasaki, Kousuke, Yamazaki Yudai, and Hiroaki Gotoh. "Evaluation of Nitroxide Radical Catalyst Activity in C-H Activation Step of the Oxidative Coupling between 9,10-Dihydroacridine and Nitromethane." Asian Journal of Chemistry 31, no. 9 (2019): 2107–10. http://dx.doi.org/10.14233/ajchem.2019.22034.

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Organocatalysts have been the subject of intense research effort because of their low toxicity, facile handling, and eco-friendly characteristics. Recently, the development of C-H activation reaction using organocatalysts has also been studied. Herein, we report the studies on the oxidative coupling of 9,10-dihydroacridine and nitromethane using a series of stable radicals. tert-Butyl(10-phenyl-9-anthryl)nitroxide was found to be an optimal catalyst for the coupling reaction.

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17

FRIEBOLIN, H., та C. RUECHARDT. "ChemInform Abstract: Bimolecular Formation of Radicals by Hydrogen Transfer. Part 9. Uncatalyzed Transfer Hydrogenation of α-Methylstyrene by 9,10- Dihydroacridine and N-Methyl-9,10-dihydroacridine". ChemInform 26, № 42 (2010): no. http://dx.doi.org/10.1002/chin.199542069.

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18

Yunnikova, L. P., T. V. Makhova, A. L. Yunnikov, and V. Yu Gorokhov. "Features of reactions of 10-methyl-9,10-dihydroacridine heteroanalogs with imines." Russian Journal of Organic Chemistry 45, no. 5 (2009): 735–39. http://dx.doi.org/10.1134/s1070428009050157.

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19

Grubert, Lutz, and Werner Abraham. "Photoswitchable calix[4]arenes bearing dihydroacridine substituents at the upper rim." Tetrahedron 63, no. 44 (2007): 10778–87. http://dx.doi.org/10.1016/j.tet.2007.06.126.

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20

Wilson, Robert, Hashem Akhavan-Tafti, Renuka DeSilva, and A. Paul Schaap. "Electrochemiluminescence of 2′,6′-difluorophenyl 10-methyl-9,10-dihydroacridine-9-carboxylate." Chemical Communications, no. 20 (2000): 2067–68. http://dx.doi.org/10.1039/b003158p.

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21

AHLUWALIA, V. K., R. SAHAY, and DAS U. DAS. U. "ChemInform Abstract: One-Pot Facile Synthesis of Some New 9,10-Dihydroacridine Derivatives." ChemInform 28, no. 6 (2010): no. http://dx.doi.org/10.1002/chin.199706140.

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22

Jung, Jieun, Kei Ohkubo, David P. Goldberg, and Shunichi Fukuzumi. "Photocatalytic Oxygenation of 10-Methyl-9,10-dihydroacridine by O2 with Manganese Porphyrins." Journal of Physical Chemistry A 118, no. 32 (2014): 6223–29. http://dx.doi.org/10.1021/jp505860f.

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23

Freitas, Vera L. S., José R. B. Gomes, Joel F. Liebman, and Maria D. M. C. Ribeiro da Silva. "Energetic and reactivity properties of 9,10-dihydroacridine and diphenylamine: A comparative overview." Journal of Chemical Thermodynamics 115 (December 2017): 276–84. http://dx.doi.org/10.1016/j.jct.2017.08.001.

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24

Ferenc, Tomasz, Ewa Janik-Spiechowicz, Wanda Bratkowska, et al. "Genotoxicity assessment of new synthesized acridine derivative — 3,6-diamino-10-methyl-9,10-dihydroacridine." Mutation Research/Genetic Toxicology and Environmental Mutagenesis 444, no. 2 (1999): 463–70. http://dx.doi.org/10.1016/s1383-5718(99)00112-6.

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25

Boisvert, Guy, and Richard Giasson. "Induction of radical cyclizations with the 10-methyl-9,10-dihydroacridine / NaBH4 photocatalytic system." Tetrahedron Letters 33, no. 44 (1992): 6587–90. http://dx.doi.org/10.1016/s0040-4039(00)60992-9.

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26

Jiang, Hong, You-Cheng Liu, Jing Li, et al. "Novel photo-induced coupling reaction of 9-fluorenylidenemalononitrile with 10-methyl-9,10-dihydroacridine." Chemical Communications, no. 8 (March 22, 2002): 882–83. http://dx.doi.org/10.1039/b201239a.

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27

Li, Jianqing, Zeyan Zhuang, Xiangyu Zhu, Zujin Zhao, and Ben Zhong Tang. "9,9-Dimethyl-9,10-dihydroacridine functionalized phosphoindole oxides with AIE property for OLED application." Journal of Information Display 21, no. 3 (2020): 139–47. http://dx.doi.org/10.1080/15980316.2020.1784805.

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28

Yang, Xin, Janitha Walpita, Dapeng Zhou, et al. "Toward Organic Photohydrides: Excited-State Behavior of 10-Methyl-9-phenyl-9,10-dihydroacridine." Journal of Physical Chemistry B 117, no. 49 (2013): 15290–96. http://dx.doi.org/10.1021/jp401770e.

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29

Carloni, Patricia, Lucedio Greci, Alexander Mar'in, and Pierluigi Stipa. "Aromatic secondary amines as antioxidants for polyolefins: Part 1—9,10-dihydroacridine (acridan) derivatives." Polymer Degradation and Stability 44, no. 2 (1994): 201–9. http://dx.doi.org/10.1016/0141-3910(94)90165-1.

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30

Masimukku, Naveen, Dalius Gudeika, Oleksandr Bezvikonnyi, et al. "Aryl-substituted acridanes as hosts for TADF-based OLEDs." Beilstein Journal of Organic Chemistry 16 (May 13, 2020): 989–1000. http://dx.doi.org/10.3762/bjoc.16.88.

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Four aryl-substituted acridan derivatives were designed, synthesized and characterized as electroactive materials for organic light emitting diodes based on emitters exhibiting thermally activated delayed fluorescence. These compounds possessed relatively high thermal stability with glass-transition temperatures being in the range of 79–97 °C. The compounds showed oxidation bands arising from acridanyl groups in the range of 0.31–038 V. Ionization potentials of the solid films ranged from 5.39 to 5.62 eV. The developed materials were characterized by triplet energies higher than 2.5 eV. The la

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31

Berná, J., P. Kristian, J. Imrich, et al. "New Type of Spiro Heterocycles. A Convenient Synthesis of Spiro[dihydroacridine 9(10H), 4′-Thiazolines]." Synthetic Communications 25, no. 24 (1995): 3973–79. http://dx.doi.org/10.1080/00397919508011473.

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32

Jiang, Hong, You-Cheng Liu, Jing Li, et al. "ChemInform Abstract: Novel Photo-induced Coupling Reaction of 9-Fluorenylidenemalononitrile with 10-Methyl-9,10-dihydroacridine." ChemInform 33, no. 30 (2010): no. http://dx.doi.org/10.1002/chin.200230185.

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33

BOISVERT, G., and R. GIASSON. "ChemInform Abstract: Induction of Radical Cyclizations with the 10-Methyl-9,10- dihydroacridine/NaBH4 Photocatalytic System." ChemInform 24, no. 12 (2010): no. http://dx.doi.org/10.1002/chin.199312079.

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34

Fukuzumi, Shunichi, Tomoyoshi Suenobu, Shuichiro Kawamura, Akito Ishida, and Koichi Mikami. "Selective two-electron reduction of C60 by 10-methyl-9,10-dihydroacridine via photoinduced electron transfer." Chemical Communications, no. 3 (1997): 291–92. http://dx.doi.org/10.1039/a607417k.

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35

Li, Zhi-heng, Rui Liu, Zheng-li Tan, Lan He, Zhong-lin Lu, and Bing Gong. "Aromatization of 9,10-Dihydroacridine Derivatives: Discovering a Highly Selective and Rapid-Responding Fluorescent Probe for Peroxynitrite." ACS Sensors 2, no. 4 (2017): 501–5. http://dx.doi.org/10.1021/acssensors.7b00139.

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36

Liu, Yiming, Qi Chen, Yujie Tong, and Yuguo Ma. "9,9-Dimethyl Dihydroacridine-Based Organic Photocatalyst for Atom Transfer Radical Polymerization from Modifying “Unstable” Electron Donor." Macromolecules 53, no. 16 (2020): 7053–62. http://dx.doi.org/10.1021/acs.macromol.0c00377.

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37

Cheng, Dandan, Defang Xu, Ying Wang, et al. "9,9-Dimethyl-9,10-dihydroacridine-based donor–acceptor cruciform luminophores: Envident aggregation-induced emission and remarkable mechanofluorochromism." Dyes and Pigments 173 (February 2020): 107937. http://dx.doi.org/10.1016/j.dyepig.2019.107937.

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38

BERNAT, J., P. KRISTIAN, J. IMRICH, et al. "ChemInform Abstract: New Type of Spiro Heterocycles. A Convenient Synthesis of Spiro( dihydroacridine 9(10H),4′-thiazolines)." ChemInform 27, no. 16 (2010): no. http://dx.doi.org/10.1002/chin.199616175.

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39

Zhou, Dapeng, Renat Khatmullin, Janitha Walpita, et al. "Mechanistic Study of the Photochemical Hydroxide Ion Release from 9-Hydroxy-10-methyl-9-phenyl-9,10-dihydroacridine." Journal of the American Chemical Society 134, no. 28 (2012): 11301–3. http://dx.doi.org/10.1021/ja3031888.

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40

Cheng, Dandan, Defang Xu, Ying Wang, et al. "High contrast mechanochromic luminescence of aggregation-induced emission (AIE)-based 9,9-dimethyl-9,10-dihydroacridine-containing cruciform luminophores." Dyes and Pigments 173 (February 2020): 107934. http://dx.doi.org/10.1016/j.dyepig.2019.107934.

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41

Chen, Cui-Cui, Yi-Qi Zhang, Dong-Xiao Zhong, et al. "The study of 9,10-dihydroacridine derivatives as a new and effective molecular scaffold for antibacterial agent development." Biochemical and Biophysical Research Communications 546 (March 2021): 40–45. http://dx.doi.org/10.1016/j.bbrc.2021.01.096.

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42

Zhao, Bo, Yanqin Miao, Zhongqiang Wang, et al. "High efficiency and low roll-off green OLEDs with simple structure by utilizing thermally activated delayed fluorescence material as the universal host." Nanophotonics 6, no. 5 (2016): 1133–40. http://dx.doi.org/10.1515/nanoph-2016-0177.

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AbstractWe achieved high-efficiency and low-roll-off green fluorescent and phosphorescent organic light-emitting diodes (OLEDs) simultaneously by adopting the thermally activated delayed fluorescence material of bis[4-(9,9-dimethyl-9,10-dihydroacridine)phenyl]sulfone as the universal host. At a luminance of 1000 cd/m2, fluorescent OLEDs based on C545T get a current efficiency, power efficiency, and external quantum efficiency (EQE) of 31.8 cd/A, 25.0 lm/W, and 9.26%, respectively. This is almost the highest efficiency based on C545T at the luminance of 1000 cd/m2 to date. On the other hand, ph

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43

Griffiths, John, and Russell Cox. "Colour and halochromic properties of azo dyes derived from 10-methyl-9-methylene-9,10-dihydroacridine as coupling component." Dyes and Pigments 47, no. 1-2 (2000): 65–71. http://dx.doi.org/10.1016/s0143-7208(00)00064-4.

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44

He, Xin, Shenghong Ren, Hui Liu, et al. "Efficient Nondoped Pure Blue Organic Light‐Emitting Diodes Based on an Anthracene and 9,9‐Diphenyl‐9,10‐dihydroacridine Derivative." Chemistry – An Asian Journal 15, no. 1 (2019): 163–68. http://dx.doi.org/10.1002/asia.201901376.

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45

Zhang, Xiaguang, Wei Shen, Dongmei Zhang, Yongzhen Zheng, Rongxing He, and Ming Li. "Theoretical investigation of dihydroacridine and diphenylsulphone derivatives as thermally activated delayed fluorescence emitters for organic light-emitting diodes." RSC Advances 5, no. 64 (2015): 51586–91. http://dx.doi.org/10.1039/c5ra04929f.

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46

Fukuzumi, Shunichi, and Yoshihiro Tokuda. "Efficient Six-Electron Photoreduction of Nitrobenzene Derivatives by 10-Methyl-9,10-dihydroacridine in the Presence of Perchloric Acid." Bulletin of the Chemical Society of Japan 65, no. 3 (1992): 831–36. http://dx.doi.org/10.1246/bcsj.65.831.

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47

Cui, Xu, Zhenjun Si, Yanhui Li, and Qian Duan. "Synthesis of telechelic PNIPAM ended with 9,10-dihydroacridine group as a recyclable and specific Fe3+ detection fluorescent sensor." Dyes and Pigments 173 (February 2020): 107873. http://dx.doi.org/10.1016/j.dyepig.2019.107873.

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48

Fukuzumi, Shunichi, Shunsuke Fujita, Tomoyoshi Suenobu, Hiroshi Imahori, Yasuyuki Araki, and Osamu Ito. "Dehydrogenation vs Oxygenation in Photosensitized Oxidation of 9-Substituted 10-Methyl-9,10-dihydroacridine in the Presence of Scandium Ion." Journal of Physical Chemistry A 106, no. 7 (2002): 1465–72. http://dx.doi.org/10.1021/jp0128729.

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49

Sandjo, Louis P., Victor Kuete, and Maique W. Biavatti. "Pyridinoacridine alkaloids of marine origin: NMR and MS spectral data, synthesis, biosynthesis and biological activity." Beilstein Journal of Organic Chemistry 11 (September 18, 2015): 1667–99. http://dx.doi.org/10.3762/bjoc.11.183.

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This review focuses on pyridoacridine-related metabolites as one biologically interesting group of alkaloids identified from marine sources. They are produced by marine sponges, ascidians and tunicates, and they are structurally comprised of four to eight fused rings including heterocycles. Acridine, acridone, dihydroacridine, and quinolone cores are features regularly found in these alkaloid skeletons. The lack of hydrogen atoms next to quaternary carbon atoms for two or three rings makes the chemical shift assignment a difficult task. In this regard, one of the aims of this review is the com

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50

Kristian, Pavol, Juraj Bernát, Igor Chomca, Kalevi Pihlaja, Karel Douglas Klika, and Ján Imrich. "A Convenient Synthesis of Polyfunctionally Substituted 2',2'-Bis(ethoxycarbonyl)methylene-5'-methoxycarbonyl(cyano)spiro[dihydroacridine-9(10H),4'-thiazolidines]." HETEROCYCLES 51, no. 1 (1999): 137. http://dx.doi.org/10.3987/com-98-8308.

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