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Formation,Structure and In Vitro Antitumour Activity of a Novel Binuclear Organotin Complex

Formation, Structure and In Vitro Antitumour Activity of a Novel Binuclear Organotin Complex
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摘要 A 1:1 reaction of triphenyltin chloride with potassium N-[(3,5-dibromo-2-hydroxylphenyl)methylene]valinate in benzene led to the formation of a novel mixed organotin dinuclear complex, (HL)SnPh3oPh2SnL [L=2-O-3,5-Br2C6H3CH=NCH(i-Pr)COO], by means of a facile phenyl-tin bond cleavage process. In the complex, there are two distinct types of carboxylate moieties and a trans-O2SnC2N and a trans-O2SnC3 in distorted trigonal bipyramidal geometries were bridged by a carboxylate group. In vitro antitumor activity of the complex against three human tumour cell lines (HeLa, CoLo205 and MCF-7) was found to be much higher than cis-platin used in clinic. A 1:1 reaction of triphenyltin chloride with potassium N-[(3,5-dibromo-2-hydroxylphenyl)methylene]valinate in benzene led to the formation of a novel mixed organotin dinuclear complex, (HL)SnPh3oPh2SnL [L=2-O-3,5-Br2C6H3CH=NCH(i-Pr)COO], by means of a facile phenyl-tin bond cleavage process. In the complex, there are two distinct types of carboxylate moieties and a trans-O2SnC2N and a trans-O2SnC3 in distorted trigonal bipyramidal geometries were bridged by a carboxylate group. In vitro antitumor activity of the complex against three human tumour cell lines (HeLa, CoLo205 and MCF-7) was found to be much higher than cis-platin used in clinic.
出处 《Chinese Chemical Letters》 SCIE CAS CSCD 2005年第12期1584-1586,共3页 中国化学快报(英文版)
基金 supported by the Natural Science Foundation of Shandong Province(No.Z2002F01)and Qufu Normal Universiy
关键词 Binuclear tin complex organotin carboxylate antitumor activity crystal structure Binuclear tin complex,organotin carboxylate,antitumor activity,crystal structure
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  • 6[6]2 is a yellow crystal with m.p. 172-173 ℃ and yield is 63%. Intensity data of the complex were collected at 295 K on a Bruker Smart Apex CCD diffractometer. The crystal parameters were as follows: C54H48Br4N2O6Sn2, Mr = 1377.96, orthorhombic, space group P212121, a = 11.7776(9), b =18.0548(14), c = 26.039(2)A, V = 5537.0(8)A3, Z = 4,μ =3.836 mm-1, R1 = 0.0515, wR2= 0.0942. Flack x is 0.001(8). The elemental analysis, IR, NMR(1H and 13C) spectra and the final coordinates, bond lengths and angles of 2 have been deposited in the editorial office of CCL.
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