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Synthesis, crystal structures, and antitumor activity of three new organotin carboxylates

✍ Scribed by Adama Moussa Sakho; Dafeng Du; Wenjie Li; Shuangshuang Liu; Dongsheng Zhu; Lin Xu


Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
559 KB
Volume
21
Category
Article
ISSN
1042-7163

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✦ Synopsis


Abstract

Three new organotin(IV) carboxylates of composition [(R)~2~Sn(O~2~CC~6~H~4~C‐OC~6~H~4~CH~3~)~2~] 1, [(R)~2~Sn(O~2~CC~6~H~4~COC~6~H~4~‐C~2~H~5~)~2~]~2~ 2, and R~3~SnO~2~ CC~6~H~4~COC~6~H~4~CH~3~ 3, were obtained by reactions of (R)~2~SnO [R = o‐tolyl] with 2‐(4‐methyl benzoyl) benzoic acid and 2‐(4‐ethyl benzoyl) benzoic acid, and reaction of Cy~3~SnOH [Cy = cyclohexyl] with 2‐(4‐methyl benzoyl) benzoic acid, respectively. The complexes 1, 2 and 3 have been characterized by elemental analysis, infrared (IR), ^1^HNMR, and X‐ray crystallography diffraction analyses. The complex 1 has two folded symmetrical structure; the tin atom in 1 is found to adopt a distorted toward skew‐trapezoidal bipyramidal geometry. Molecular structure of the complex 2 is centrosymmetric, and the internal tin atom is five‐coordinated and is in distorted trigonal bipyramidal geometry. The crystal structure of the complex 3 is found to exhibit distorted tetrahedral geometry. Pilot studies have indicated that the complexes 1 and 2 have shown good antitumor activities. Β© 2010 Wiley Periodicals, Inc. Heteroatom Chem 21:304–313, 2010; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20614


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