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Mendeleev Communications, 2008, Volume 18, Issue 6, Pages 302–304
DOI: https://doi.org/10.1016/j.mencom.2008.11.004
(Mi mendc3335)
 

This article is cited in 6 scientific papers (total in 6 papers)

Synthesis and photochromic properties of 11-phenoxy-2-phenylnaphth[2,3-f]indole-5,10-dione

E. A. Kolodinaa, M. S. Shvartsberga, N. P. Gritsanab

a V.V. Voevodsky Institute of Chemical Kinetics and Combustion, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation
b Novosibirsk State University, Novosibirsk, Russian Federation
Full-text PDF (324 kB) Citations (6)
Abstract: 11-Phenoxy-2-phenylnaphth[2,3-f]indole-5,10-dione has been synthesized, its photochromic properties have been studied, and photoinduced 10-phenoxy-2-phenylnaphth[2,3-f]indole-5,11-dione has been isolated.
Document Type: Article
Language: English


Citation: E. A. Kolodina, M. S. Shvartsberg, N. P. Gritsan, “Synthesis and photochromic properties of 11-phenoxy-2-phenylnaphth[2,3-f]indole-5,10-dione”, Mendeleev Commun., 18:6 (2008), 302–304
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  • https://www.mathnet.ru/eng/mendc/v18/i6/p302
  • This publication is cited in the following 6 articles:
    1. Olga Kargina, Elena Pritchina, Olga Fominykh, Leonid Gornostaev, III INTERNATIONAL SCIENTIFIC AND PRACTICAL SYMPOSIUM “MATERIALS SCIENCE AND TECHNOLOGY” (MST-III-2023), 3154, III INTERNATIONAL SCIENTIFIC AND PRACTICAL SYMPOSIUM “MATERIALS SCIENCE AND TECHNOLOGY” (MST-III-2023), 2024, 020003  crossref
    2. Andrey G. Lvov, Lyubov S. Klimenko, Vasily N. Bykov, Stefan Hecht, “Revisiting Peri‐Aryloxyquinones: From a Forgotten Photochromic System to a Promising Tool for Emerging Applications”, Chemistry A European J, 30:11 (2024)  crossref
    3. V. A. Litvinova, A. S. Tikhomirov, A. E. Shchekotikhin, “Methods for functionalization of anthraquinones”, Russian Chem. Reviews, 93:10 (2024), RCR5141  mathnet  mathnet  crossref
    4. S. F. Vasilevskii, A. A. Stepanov, “Acetylene derivatives of quinones and their transformation products: synthesis, reactivity and applied aspects”, Russian Chem. Reviews, 91:1 (2022), RCR5020  mathnet  mathnet  crossref  isi  scopus
    5. D. S. Baranov, Yu. V. Gatilov, “Cyclization of 2-(3-R-prop-2-ynyloxy)-4-phenyliminonaphthalen- 1(4H)-ones into 2-R-methylidene-6-phenylamino-2,3-dihydronaphtho[2,1-b]-1,4-dioxines”, Mendeleev Commun., 26:4 (2016), 282–284  mathnet  crossref
    6. Ekaterina A. Kolodina, Mark S. Shvartsberg, Nina P. Gritsan, “ChemInform Abstract: Synthesis and Photochromic Properties of 11‐Phenoxy‐2‐phenylnaphth[2,3‐f]indole‐5,10‐dione.”, ChemInform, 40:16 (2009)  crossref
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