Citation: Fu-Xing ZHANG, Xin DENG, Zhe-Hao YANG, Xin ZHANG, Kang-Xia FU, Liang-Bing SHENG, Xiao-Ming ZHU, Wu-Jiu JIANG, Jiang-Xi YU. Synthesis, structure, and anticancer activity of organotin 9-fluorenone-4-carboxylates[J]. Chinese Journal of Inorganic Chemistry, ;2023, 39(7): 1287-1294. doi: 10.11862/CJIC.2023.092 shu

Synthesis, structure, and anticancer activity of organotin 9-fluorenone-4-carboxylates

  • Corresponding author: Fu-Xing ZHANG, zfx8056@163.com
  • Received Date: 22 November 2022
    Revised Date: 31 March 2023

Figures(8)

  • Three organotin 9-fluorenone-4-carboxylate compounds, triphenyltin 9‑fluorenone‑4‑carboxylate [(C6H5)3Sn(C14H7O3)] (1), tricyclohexyltin 9-fluorenone-4-carboxylate [(C6H11)3Sn(C14H7O3)] (2), and tri(2-methyl-2-phenylpropyl) tin 9-fluorenone-4-carboxylate [(C6H5C(CH3)2CH2)3Sn(C14H7O3)] (3), were synthesized by the solvothermal method using methanol as a solvent. The compounds were characterized by elemental analysis, IR spectroscopy, NMR (1H, 13C, and 119Sn), and thermogravimetric analysis. The crystal structures of the compounds were determined by single-crystal X-ray diffraction. The compounds were studied by quantum chemical calculation and in vitro anticancer activity. The results show that compound 1 has a 1D chain structure and the central tin atom is a five-coordinated distorted trigonal bipyramid configuration; compounds 2 and 3 are single tin nuclear molecules and the tin atoms are four-coordinated distorted tetrahedron configurations. The compounds have good inhibitory activity on the human cervical carcinoma cell line (HeLa), human liver cancer cell line (HUH-7), human non-small cell lung cancer cell line (A549), human lung adenocarcinoma cell line (H1975) and breast cancer cell line (MCF-7).
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