1,7-Meta-dicarbadecaborane diformic acid-triphenyltin chloride complex, as well as preparation method and application thereof
A technology of triphenyltin dicarboxylate and meta-decaborane, which is applied in tin organic compounds, drug combinations, antineoplastic drugs, etc., to achieve low cost, high anticancer activity, and good fat solubility
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Embodiment 1
[0018] 0.1 mmol m-C 4 B 10 h 12 o 4 Dissolve in 15 mL CH 3 CH 2 OH, after 15 min, add 0.1 mmol Ph 3 SnCl, stirred and reacted for 8 h, then added 0.1 mmol 2,2'-bipyridine to the above mixed solution, and continued to stir for 4 h. After the reaction was completed, it was filtered to obtain a pale pink solution, and the filtrate was naturally volatilized at room temperature, and after three weeks, pink crystals of 1,7-m-dicarbocaboranedicarboxylic acid triphenyltin chloride complex were obtained. The melting point of the target product is 224℃, and the yield is 68.6%.
[0019] The 1,7-m-dicarbadecaboranedicarboxylic acid triphenyltin chloride complex of the present invention is analyzed by X-single crystal diffraction, and the crystallographic data are as follows: the compound belongs to the monoclinic crystal system, and the space group is P2 1 / n , the cell parameters are: a = 11.3716(13)?, b = 16.7078(16)?, c = 19.0121(18)?, α = 90°, β = 89.8640(10)°, gam...
Embodiment 2
[0022] 0.1 mmol m-C 4 B 10 h 12 o 4 Dissolve in 15 mL CH 3 CH 2 OH, add 0.1 mmol Ph 3SnCl, after stirring for 2 h, 0.1 mmol 2,2'-bipyridine was added to the above mixed solution, and the stirring was continued for 4 h. After the reaction was completed, it was filtered to obtain a light pink solution, and the filtrate was naturally volatilized at room temperature. After three weeks, pink crystals were obtained with a melting point of 224° C. and a yield of 52.1%.
Embodiment 3
[0024] 0.1 mmol m-C 4 B 10 h 12 o 4 Dissolve in 15 mL CH 3 CH 2 OH, add 0.1 mmol Ph 3 SnCl, after stirring for 4 h, add 0.1 mmol 2,2'-bipyridine to the above mixed solution, and continue stirring for 4 h. After the reaction was completed, it was filtered to obtain a pale pink solution. The filtrate was naturally volatilized at room temperature, and after three weeks, pink crystals were obtained with a melting point of 224° C. and a yield of 56.3%.
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