Six diorganotin phenoxy acetic acid containing silicon were synthesized by the reaction of diorganotin oxides with phenoxy acetic acids;and their structures were characterized by IR,1HNMR,13CNMR,elemental analysis.The...Six diorganotin phenoxy acetic acid containing silicon were synthesized by the reaction of diorganotin oxides with phenoxy acetic acids;and their structures were characterized by IR,1HNMR,13CNMR,elemental analysis.The preliminary bioassay tests showed that(Me3SiCH2)2Sn(OCOCH2C6H4CH3-p)2 exhibited a good antitumour activity in vitro against lung tumour cells A549 and colorectal tumour cell SW480.展开更多
Dibenzyltin bis(dithiomorpholinocarbamate) was synthesized by the reaction of dibenzyltin dichloride with dithiomorpholinocarbamate. The compound was characterized by elemental analysis, IR, 1H NMR and MS. and the cry...Dibenzyltin bis(dithiomorpholinocarbamate) was synthesized by the reaction of dibenzyltin dichloride with dithiomorpholinocarbamate. The compound was characterized by elemental analysis, IR, 1H NMR and MS. and the crystal structure was determined by X ray single crystal diffraction. The crystal belongs to orthorhombic with space group Pca21, a=1.8327(3)nm, b= 0.65678(12)nm, c=2.2583(4)nm, Z=4, V=2.718 (9)nm3, Dx=1.528g·cm-3,μ=1.271mm-1, F(000)=1272, R1=0.0434, wR2=0.1152. In the crystals, the structures consist of discrete molecules containing six coordinate tin atoms in a distorted octahedron configuration.展开更多
文摘Six diorganotin phenoxy acetic acid containing silicon were synthesized by the reaction of diorganotin oxides with phenoxy acetic acids;and their structures were characterized by IR,1HNMR,13CNMR,elemental analysis.The preliminary bioassay tests showed that(Me3SiCH2)2Sn(OCOCH2C6H4CH3-p)2 exhibited a good antitumour activity in vitro against lung tumour cells A549 and colorectal tumour cell SW480.
文摘Dibenzyltin bis(dithiomorpholinocarbamate) was synthesized by the reaction of dibenzyltin dichloride with dithiomorpholinocarbamate. The compound was characterized by elemental analysis, IR, 1H NMR and MS. and the crystal structure was determined by X ray single crystal diffraction. The crystal belongs to orthorhombic with space group Pca21, a=1.8327(3)nm, b= 0.65678(12)nm, c=2.2583(4)nm, Z=4, V=2.718 (9)nm3, Dx=1.528g·cm-3,μ=1.271mm-1, F(000)=1272, R1=0.0434, wR2=0.1152. In the crystals, the structures consist of discrete molecules containing six coordinate tin atoms in a distorted octahedron configuration.
