Synthesis, structure and biological activity some rare earth element complexes containing quinoline sulfonate derivatives

Authors

  • Nguyen Thi Ngoc Vinh Hong Duc University, Thanh Hoa, Vietnam Author
  • Le Thi Hong Hai Faculty of Chemistry, Hanoi National University of Education Author

DOI:

https://doi.org/10.51316/jca.2021.040

Keywords:

Lanthanide complexes, 5-bromo-7-(carboxymethoxy)-6-hydroxy-1-methylquinolin-1-ium-3-sulfonate, antibacterial activity

Abstract

Five new lanthanide complexes [Ln2(MeQBr-2H)3(H2O)6]. nH2O (Ln = Y, La, Pr, Nd, Eu) were synthesized by interaction between lanthanide chloride and a derivative of quinoline, namely 5-bromo-7-(carboxymethoxy)-6-hydroxy-1-methylquinolin-1-ium-3-sulfonate. The molecular formulas and structures of the complexes were determined using combination of IR, EDX, ESI MS, 1H NMR spectra, thermal analysis and single-crystal X-ray diffraction of similar compound YQBr. The results of tested antimicrobial activity showed that the complexes exhibit high activities on Bacillus subtilis, Lactobacillus fermentum with low IC50 values, 0.56÷3.55 (µg/ml).

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References

A.R. Gholap, K.S. Toti, F. Shiraza, R. Kumari, M.K Bhat, M.V. Deshpande, K.V Srinivasan, Bioorganic & Medicinal Chemistry, 15 (2007) 6705-6715. https://doi.org/10.1016/j.bmc.2007.08.009.

S. Nijssen, A. Fluit, D. Vijver, J. Top, R. Willems, M.J.M. Bonten, Intensive Care Medicine, 36, 2010, 512 – 519. doi: 10.1007/s00134-009-1714-y

G.N. Lipunova, E.V. Nosova, V.N. Charushin, O.N. Chupakhin, Comments on Inorganic Chemistry, 34 (2014) 1-36. https://doi.org/10.1080/02603594.2014.959116

Y.C. Liu, Z.F. Chen, X.Y. Song, Y. Peng, Q.P. Qin, H. Liang, European Journal of Medicinal Chemistry, 59 (2013) 168-175. https://doi.org/10.1016/j.ejmech.2012.11.001

Y.C Liu, Z.Y. Yang, Journal of Inorganic Biochemistry, 103 (2009) 1014-1022. doi:10.1016/j.jinorgbio.2009.04.013

Q.P. Qin, Z.F Wang, M.X Tan, X.L Huang, H.H. Zou, B.Q Zou, B.B. Shi, S.H. Zhang, Metallomics, 11 (2019) 1005-1015. https://doi.org/10.1039/C9MT00037B

R. Jastrazab, M. Nowak, M. Skrobaska, A. Tolinska, M. Zabiszak, M. Gabryel, L. Marciniak, M.T. Kaczmarek., Coordination Chemistry Reviews, 382 (2019) 145–159. https://doi.org/10.1016/j.ccr.2018.12.018

N.H. Dinh, L.V. Co, N.M. Tuan, L.T.H. Hai, L.V Meervelt, Heterocycles, 85 (2012) 627-637. https://10.3987/COM-11-12416.

Nguyễn Thị Ngọc Vinh, Nguyễn Thị Việt Hà, Đinh Thị Hiền, Trần Thị Đà, Lê Thị Hồng Hải, Tạp chí Hoá học, 56, 6E2 (2018) 180-184.

Nguyễn Thị Ngọc Vinh, Trần Thị Đà, Nguyễn Văn Đức, Lê Thị Hồng Hải, Tạp chí Hoá học, 57, 6E12 (2019) 397-402.

M. Balouiri, M. Sadiki, S.K. Ibnsouda, Joural of Pharmaceutical Analysis, 6 (2016) 71-79. https://doi.org/10.1016/j.jpha.2015.11.005

Published

30-07-2021

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How to Cite

Synthesis, structure and biological activity some rare earth element complexes containing quinoline sulfonate derivatives. (2021). Vietnam Journal of Catalysis and Adsorption, 10(2), 119-124. https://doi.org/10.51316/jca.2021.040

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