Citation: KUANG Dai-Zhi, YU Jiang-Xi, FENG Yong-Lan, ZHANG Fu-Xing, JIANG Wu-Jiu, ZHU Xiao-Ming. Syntheses, Structures, Anti-tumor Activity of Tri(n-butyl)tin Carboxylates with Hydrogen-Bonded Network[J]. Chinese Journal of Inorganic Chemistry, ;2015, (6): 1112-1118. doi: 10.11862/CJIC.2015.067
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Two tri(n-butyl)tin carboxylates (n-Bu)3SnO2CR(H2O) (R: C(OH)Ph2 (1), C5NH3Cl (2)) were synthesized by the reactions of bis[tri(n-butyl)tin] oxide with benzilic acid and 2-chloronicotinic acid under microwave irradia-tion, respectively. Their structures were characterized by IR, 1H and 13C NMR, elemental analysis and X-ray single crystal diffraction. Both of the complexes belong to orthorhombic system, but their space groups are different. One is Pbca and the other is P212121. For each of them, the central tin atom is aberrant trigonal bipyramid with five-coordination. In their crystal structures, there are multi-hydrogen bonds, resulting in the formation of a 2D structure of 1 and a 3D supermolecular network of 2. The preliminary tests showed that both of which displayed strong in vitro anti-tumor activity against five human tumor cell lines, Colo205, HepG2, MCF-7, Hela and NCI-H460, and especially for the later three, the complexes were much stronger than carboplatin, but the activity order was 1>2.
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