Abstract
The review is devoted to analysis of photo- and electroluminescent properties of metal complexes (Al, Be, Mg, Ga, In, Zn, and B) based on substituted quinoline derivatives. Literature data shows that changing the substituents in quinoline ligands and the metal complexing agent can affect the color and intensity of photoluminescence in the corresponding metal complexes. OLED devices fabricated based on these complexes have exhibited high brightness and efficient electroluminescence across a broad spectral range from red to blue. Furthermore, these compounds possess excellent electron-transport properties, enabling their utilization as conductive layers in OLEDs.
REFERENCES
Tang, C.W. and Van Slyke, S.A., Organic Electroluminescent Diodes, Appl. Phys. Lett., 1987, vol. 51, p. 913.
Che, C.-M., Kwok, C.-C., Lai, S.-W., et al., Chem.-Eur. J., 2010, vol. 16, p. 233.
Yang, X., Yao, C., and Zhou, G., Platinum Met. Rev., 2013, vol. 57, p. 2.
Kalinowski, J., Fattori, V., Cocchib, M., and Gareth Williams, J.A., Coord. Chem. Rev., 2011, vol. 255, p. 2401.
Tung, Y.-L., Wu, P.-C., Liu, C.-S., et al., Organometallics, 2004, vol. 23, p. 3745.
Lee, T.-C., Hung, J.-Y., Chi, Y., et al., Adv. Funct. Mater., 2009, vol. 19, p. 2639.
Liu, T.-H. and Chen, C.H., J. Appl. Phys., 2006, vol. 100, no. 9, p. 094508.
Kappaun, S., Slugovc, C., and List, E.J.W., Int. J. Mol. Sci., 2008, vol. 9, no. 8, p. 1527.
Dumur, F., Bertin, D., and Gigmes, D., Int. J. Nanotechnol., 2012, vol. 9, p. 377.
Hu, T., He, L., Duan, L., and Qiu, Y., J. Mater. Chem., 2012, vol. 22, p. 4206.
Costa, R.D., Orti, E., Bolink, H.J., et al., Angew. Chem. Int. Ed., 2012, vol. 51, p. 8178.
Dumur, F., Lepeltier, M., Zamani Siboni, H., et al., Adv. Opt. Mater., 2014, vol. 2, p. 262.
Sano, T., Nishio, Y., Hamada, Y., et al., J. Mater. Chem., 2000, vol. 10, p. 157.
Perez-Bolivar, C., Montes, V.A., and Anzenbacher, P., Inorg. Chem. 2006, vol. 45, p. 9610.
Yakushchenko, I.K., Kaplunov, M.G., Krasnikova, S.S., and Efimov, O.N., RF Patent 2265040, 2005.
Sharma, A., Singh, D., Makrandi, J.K., et al., Mater. Lett., 2007, vol. 61, p. 4614.
Jang, S.-H. and Park, J.-W., Mol. Cryst. Liq. Cryst., 2007, vol. 471, p. 269.
Ghedini, M., La Deda, M., Aiello, I., and Grisolia, A., Inorg. Chim. Acta, 2004, vol. 357, p. 33.
Ghedini, M., La Deda, M., Aiello, I., and Grisolia, A., Synth. Met., 2003, vol. 138, p. 189.
Huang, Q., Cui, J., Yan, H., et al., Appl. Phys. Lett. 2002, vol. 81, p. 3528.
Kim, J.J., Kim, K.S., Baek, S., et al., J. Polym. Sci., Part A: Polym. Chem., 2002, vol. 40, p. 1173.
Li, Z.H., Wong, M.S., Fukutani, H., and Tao, Y., Org. Lett., 2006, vol. 8, p. 4271.
Huang, T.H., Lin, J.T., Chen, L.Y., et al., Adv. Mater., 2006, vol. 18, p. 602.
Lane, P.A., Kushto, G.P., and Kafafi, Z.H., Appl. Phys. Lett., 2007, vol. 90, p. 023511.
Tse, S.C., Tsung, K.K., and So, S.K., Appl. Phys. Lett., 2007, vol. 90, p. 213502.
Aubouya, L., Gerbier, P., Guerin, C., et al., Synth. Met., 2007, vol. 157, nos. 2–3, p. 91.
Zeng, H.-P., Wang, G.-R., Zeng, G.-C., and Li, J., Dyes and Pigments, 2009, vol. 83, p. 155.
Xie, J., Fan, L., Su, J., and Tian, H., Dyes and Pigments, 2003, vol. 59, p. 153.
Tao, X.T., Suzuki, H., Wada, T., et al., J. Am. Chem. Soc., 1999, vol. 121, p. 9447.
Wang, T.T., Zeng, G.C., Zeng, H.P., et al., Tetrahedron, 2009, vol. 65, p. 6325.
Rai, V.K., Srivastava, R., Chauhan, G., et al., Mater. Lett., 2008, vol. 62, p. 2561.
Kumar, A., Palai, A.K., Srivastava, R., et al., J. Organomet. Chem., 2014, vol. 756, p. 38.
Kaplunov, M.G., Nikitenko, S.N., and Krasnikova, S.S., in Organic Light Emitting Devices, Singh J., Ed., In Tech, 2012. Chapter 7.
Kim, D.-E., Kim, W.-S., Kim, B.-S., et al., Colloids Surf. A, 2008, vols. 313–314, p. 320.
Kim, B.-S., Kim, D.-E., Choi, G.-C., et al., J. Electr. Eng. Technol., 2009, vol. 4, p. 418.
Jang, Y.-K., Kim, D.-E., Kwon, O.-K., et al., J. Korean Phys. Soc., 2006, vol. 49, p. 1057.
Qiu, L., Jiang, P., He, W., et al., Inorg. Chim. Acta, 2007, vol. 360, p. 431.
Yakushchenko, I.K., Kaplunov, M.G., and Krasnikova, S.S., Patent RF 2310676, 2007.
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This study was supported by the Ministry of Science and Higher Education of the Russian Federation (state assignment for scientific activity of 2023, no. FENW-2023-0014).
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The review article “Photoluminescence and electroluminescence of metal complexes of quinoline derivatives” is a translation of Chapter 6.1 of the monograph by A.S. Burlov, V.G. Vlasenko, D.A. Garnovskiy, A.I. Uraev, E.I. Maltsev, D.A. Lypenko, and A.V. Vannikov, Electroluminescent Organic Light-Emitting Diodes Based on Metal Coordination Compounds, Rostov-on-Don: Yuzhn. Fed. Univ., 2015; ISBN 978-5-9275-1469-4. This chapter discusses complexes of metals (Al, Be, Mg, Ga, In, Zn, and B) with 8-substituted quinoline ligands, which were used as electroluminescent and electron-transport layers in OLED devices. The photoluminescence and electroluminescence properties of metal complexes are systematically categorized based on the nature of the metal complexing agent and the modification of ligand systems using 8-substituted quinolines. The review encompasses publications up to 2015.
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Burlov, A.S., Vlasenko, V.G., Garnovskii, D.A. et al. Photoluminescence and Electroluminescence of Metal Complexes of Quinoline Derivatives. Russ J Coord Chem 49 (Suppl 1), S29–S37 (2023). https://doi.org/10.1134/S1070328423600821
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DOI: https://doi.org/10.1134/S1070328423600821