Photoluminescent Lanthanide(III) Complexes Based on 2-[((4-Chlorophenyl)amino)methylene]-5,5-dimethylcyclohexane-1,3-dione

封面

如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅存取

详细

Five coordination compounds of the general formula [LnL2(NO3)3]n (Ln3+ = Eu (I), Sm (II), Tb(III), Dy (IV), and Gd (V)) are synthesized from 2-[((4-chlorophenyl)amino)methylene]-5,5-dimethylcyclohexane-1,3-dione (L). The crystal structures of the ligand and complex III are determined by X-ray diffraction (XRD) of single crystals (CIF files CCDC nos. 2298715 (L) and 2298716 (III)). Complex III is polymeric due to the bidentate-bridging coordination of the ligand by the oxygen atoms of the cyclohexanedione fragment, and the coordination number of the central atom is ten. According to the phase XRD data, all synthesized polycrystalline compounds are isostructural to the single crystals of complex III. The photoluminescence properties of the ligand and coordination compounds in the polycrystalline state are studied. The energy transfer from the ligand to lanthanide(III) ion is shown to proceed via the “antenna” mechanism in the case of the europium(III), samarium(III), and terbium(III) compounds. Among the series of the complexes, the highest quantum yield is observed for compound I (21.9%), and the sensibilization efficiency of the europium(III) complex is 43.5%.

全文:

受限制的访问

作者简介

K. Smirnova

Nikolaev Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences

Email: lisalider@gmail.com
俄罗斯联邦, Novosibirsk

E. Sanzhenakova

Nikolaev Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences

Email: lisalider@gmail.com
俄罗斯联邦, Novosibirsk

I. Eltsov

Novosibirsk National Research State University

Email: lisalider@gmail.com
俄罗斯联邦, Novosibirsk

I. Pozdnyakov

Voevodsky Institute of Chemical Kinetics and Consumption, Siberian Branch, Russian Academy of Sciences

Email: lisalider@gmail.com
俄罗斯联邦, Novosibirsk

A. Russkikh

Kuban State University

Email: lisalider@gmail.com
俄罗斯联邦, Krasnodar

V. Dotsenko

Kuban State University

Email: lisalider@gmail.com
俄罗斯联邦, Krasnodar

E. Lider

Nikolaev Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences

编辑信件的主要联系方式.
Email: lisalider@gmail.com
俄罗斯联邦, Novosibirsk

参考

  1. Bunzli, J.C.G., Chem. Rev., 2010, vol. 110, no. 5, p. 2729.
  2. Aspinall, H.C., Chem. Rev., 2002, vol. 102, no. 6, p. 1807.
  3. Hasegawa, Y., Kitagawa, Y., and Nakanishi, T., NPG Asia Mater., 2018, vol. 10, no. 4, p. 52.
  4. Bao, G., Wen, S., Lin, G., et al., Coord. Chem. Rev., 2021, vol. 429, p. 213642.
  5. Wei, C., Ma, L., Wei, H.B., et al., Sci. China Technol. Sci., 2018, vol. 61, no. 9, p. 1265.
  6. Armelao, L., and Quici, S., Coord. Chem. Rev., 2010, vol. 254, nos. 5–6, p. 48705.
  7. Bryleva, Y.A., Komarov, V.Y., Glinskaya, L.A., et al., New J. Chem., 2023, vol. 47, no. 21, p. 10446.
  8. Bryleva, Y.A., Artemʹev, A.V., Glinskaya, L.A., et al., J. Struct. Chem., 2021, vol. 62, no. 2, p. 265.
  9. Bryleva, Y.A., Artemʹev, A.V., Glinskaya, L.A., et al., Inorg. Chim. Acta, 2021, vol. 516.
  10. Artemʹev, A.V., Gusarova, N.K., Malysheva, S.F., et al., Mendeleev Commun., 2012, vol. 22, no. 6, p. 294.
  11. Crosby, G.A., Whan, R.E., and Freeman, J.J., J. Phys. Chem., 1962, vol. 6, no. 12, p. 2493.
  12. Rao, V.S. and Sauve, G., Comprehensive Organic Functional Group Transformations, 1995, vol. 2, p. 737.
  13. Chiara, J.L., Comprehensive Organic Functional Group Transformations II, 2005, p. 709.
  14. Lue, P., and Greenhill, J.V., Adv. Heterocycl. Chem., 1996, vol. 67, p. 207.
  15. Aly, A.A., and Hassan, A.A., Adv. Heterocycl. Chem., 2014, vol. 112, p. 145.
  16. Ebenezer, W.J. and Wight, P., ChemInform, 1996, p. 20576.
  17. Liu, T., Wan, J.P., and Liu, Y., Chem. Commun., 2021, vol. 57, no. 72, p. 9112.
  18. Yu, T., Ji, F., Huang, D., et al., Org. Chem. Front., 2021, vol. 8, no. 20, p. 5716.
  19. Wan, J.P., Cao, S., and Liu, Y., Org. Lett., 2016, vol. 18, no. 23, p. 6034.
  20. Stanovnik, B., Eur. J. Org. Chem., 2019, vol. 2019, no. 31–32, p. 5120.
  21. Gao, Y., Liu, Y., and Wan, J.P., Org. Chem., 2019, vol. 84, no. 4, p. 2243.
  22. Edafiogho, I.O. and Kombian, S.B., J. Pharm. Sci., 2007, vol. 96, no. 10, p. 2509.
  23. Bimoussa, A., Oubella, A., Hachim, M.E., et al., J. Mol. Struct., 2021, vol. 1241, 130622.
  24. Masaret, G.S., ChemistrySelect, 2021, vol. 6, no. 5, p. 974.
  25. Eddington, N.D., Cox, D.S., Khurana, M., et al., Eur. J. Med. Chem., 2003, vol. 38, no. 1, p. 49.
  26. Anderson, A.J., Nicholson, J.M., Bakare, O., et al., Bioorg. Med. Chem., 2006, vol. 14, no. 4, p. 997.
  27. Amaye, I.J., Harper, T.L., and Jackson-Ayotunde, P., J. Fluorine Chem., 2021, vol. 251, p. 109886.
  28. Li, H., Shu, H., Wang, X., et al., Org. Mater., 2020, vol. 02, no. 1, p. 033.
  29. Li, H., Shu, H., Liu, Y., et al., Adv. Opt. Mater., 2019, vol. 7, no. 8, p. 1801719.
  30. Smirnova, K.S., Ivanova, E.A., Sukhikh, T.S., et al., Inorg. Chim. Acta, 2021, vol. 525, p. 120490.
  31. Smirnova, K.S., Ivanova, E.A., Eltsov, I.V., et al., Polyhedron, 2022, vol. 227, p. 116122.
  32. Smirnova, K.S., Ivanova, E.A., Pozdnyakov, I.P., et al., Inorganica Chim. Acta, 2022, vol. 542, p. 121107.
  33. Jiang, H., Li, Y., Sun, M., et al., Arkivoc. Arkat., 2020, vol. 2020, no. 6, p. 1.
  34. Mohareb, R.M., Manhi, F.M., Mahmoud, M.A.A., et al., Med. Chem. Res., 2020, vol. 29, no. 8, p. 1536.
  35. Van Tinh, D., Fischer, M., and Stadlbauer, W., J. Heterocycl. Chem., 1996, vol. 33, no. 3, p. 905.
  36. Rather, M.A., Lone, A.M., Teli, B., et al., Medchemcomm, 2017, vol. 8, no. 11, p. 2133.
  37. Wang, J.M., Asami, T., Che, F.S., et al., J. Agric. Food Chem., 1997, vol. 45, no. 7, p. 2728.
  38. Wolfbeis, O.S. and Erich Ziegler, E.Z., Z. Naturforsch., A: Phys. Sci., 1976, vol. 31, no. 11, p. 1519.
  39. Zacharias, G., Wolfbeis, O.S., and Junek, H., Monatsh. Chem., 1974, vol. 105, no. 6, p. 1283.
  40. Fossa, P., Menozzi, G., Dorigo, P., et al., Bioorg. Med. Chem., 2003, vol. 11, no. 22, p. 4749.
  41. Frolov, K.A., Dotsenko, V.V., and Krivokolysko, S.G., Chem. Heterocycl. Compd., 2013, vol. 49, no. 9, p. 1301.
  42. Komkov, A.V., Prezent, M.A., Ignatenko, A.V., et al., Russ. Chem. Bull., 2006, vol. 55, no. 11, p. 2085.
  43. Dotsenko, V.V., Krivokolysko, S.G., Chernega, A.N., et al., Russ. Chem. Bull., 2002, vol. 51, no. 8, p. 1556.
  44. Dotsenko, V.V. and Krivokolysko, S.G., Chem. Heterocycl. Compd., 2013, vol. 48, no. 10, p. 1568.
  45. Dotsenko, V.V., Frolov, K.A., Krivokolysko, S.G., et al., Chem. Heterocycl. Compd., 2013, vol. 49, no. 3, p. 440.
  46. Grannik, V.G., Shanazarov, A.K., Solovʹeva, N.P., et al., Chem. Heterocycl. Compd., 1987, vol. 23, no. 11, p. 1171.
  47. Qin, J.H. and Han, X.D., Z. Krist. New Cryst. Struct., 2012, vol. 227, no. 1, p. 7.
  48. Eremina, Y.A., Ermakova, E.A., Sukhikh, T.S., et al., J. Struct. Chem., 2021, vol. 62, no. 2, p. 309.
  49. Yang, L.W., Liu, S., Rettig, S.J., et al., Inorg. Chem., 1995, vol. 34, no. 19, p. 4921.
  50. CrysAlisPro 1.171.38.46, The Woodlands: Rigaku Oxford Diffraction, 2015.
  51. APEX2 (version 2.0), SAINT (version 8.18c) and SADABS (version 2.11), Madison: Bruker Advanced X-ray Solutions, 2000–2012.
  52. Sheldrick, G.M., Acta Crystallogr., Sect. A: Found. Adv., 2015, vol. 71, p. 3.
  53. Sheldrick, G.M., Acta Crystallogr, Sect. C: Struct. Chem., 2015, vol. 71, p. 3.
  54. Dolomanov, O.V., Bourhis, L.J., Gildea, R.J., et al., J. Appl. Crystallogr., 2009, vol. 42, no. 2, p. 339.
  55. Werts, M.H.V., Jukes, R.T.F., and Verhoeven, J.W., Phys. Chem. Chem. Phys., 2002, vol. 4, no. 9, p. 1542.
  56. Werts, M.H.V., Luminescent Lanthanide Complexes: Visible Light Sensitised Red and Near-Infrared Luminescence, Univ. of Amsterdam, 2000.
  57. Andres, J. and Chauvin, A.-S., Encycl. Inorg. Bioinorg. Chem., 2012, p. 1.
  58. Klink, S.I., Hebbink, G.A., Grave, L., et al., J. Phys. Chem. A, 2002, vol. 106, no. 15, p. 3681.
  59. Bunzli, J.-C.G. and Eliseeva, S.V., Lanthanide Luminescence, Hanninen, P. and Harma, H. (Eds), 2010, vol. 7, p. 1.

补充文件

附件文件
动作
1. JATS XML
2. Scheme 1. Possible routes for the synthesis of 2-[((4-chlorophenyl)amino)methylene]-5,5-dimethyl-cyclohexane-1,3-dione

下载 (178KB)
3. Scheme 2. Structural formula of 2-[((4-chlorophenyl)amino)methylene]-5,5-dimethyl-cyclohexane-1,3-dione (L) and correlation of the ligand bands from NMR spectroscopy data

下载 (103KB)
4. Scheme 3. Scheme of synthesis of complexes I-V

下载 (162KB)
5. Fig. 1. Calculated from single crystal structure (orange line) and experimental powder diffractograms of the complexes [LnL2(NO3)3]n

下载 (391KB)
6. Fig. 2. Ligand structure and C(H)-C-N-C(H) torsion angle (φt) in L

下载 (94KB)
7. Fig. 3. Coordination unit of the [TbL2(NO3)3]n (III) complex (a) and the polymer layered structure (b). Hydrogen atoms are not shown

下载 (208KB)
8. Fig. 4. Overlay of crystal structures of the complexes [TbL2(NO3)3]n (III, purple colour) and [Tb(Lʹ)2(NO3)3]n (KBSD, turquoise colour)

下载 (177KB)
9. Fig. 5. Diffuse reflectance (dashed lines), luminescence excitation and emission spectra for ligand and complexes I-II. Emission spectra were recorded at λvozb = 370 nm and luminescence excitation spectra at λisl = 460 nm for L, λisl = 613 nm for the europium(III) complex, λisl = 594 nm for the samarium(III) complex and λisl = 545 nm for the terbium(III) complex

下载 (252KB)
10. Fig. 6. Kinetic luminescence curves of the ligand and complexes: the kinetic curve of L is indicated in red at λvozb = 375 nm and λisl = 470 nm, the biexponential approximation in blue with lifetimes of 0.6 ns (52%) and 1. 7 ns (48%), instrument response function in black (a); the kinetic curve of the europium(III) complex is in blue at λvozb = 370 nm and λisl = 615 nm, the approximation is in red with characteristic times of 1. 17 ms (b); the kinetic curve of the samarium(III) complex is in blue at λvozb = 370 nm and λisl = 595 nm, the approximation is in red with a characteristic time of 0.034 ms (c)

下载 (295KB)
11. Fig. 7. Phosphorescence spectrum of complex V at 77 K and decomposition of the spectrum into Gaussian components

下载 (243KB)
12. Fig. 8. CIE1931 colour space reflecting the emission colour of the ligand and complexes I and II

下载 (138KB)

版权所有 © Российская академия наук, 2024