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Polymeric coordination compound of zinc with a new ligand prepared by condensation, exhibiting antifungal and antibacterial activity

机译:锌与通过缩合制备的新配体的聚合配位化合物,具有抗真菌和抗菌活性

摘要

The invention relates to chemistry and medicine, namely to a new compound of the type of one-dimensional coordination polymer of zinc(II) comprising the residue of (E)-2,2'-(4,4'-dioxo-2,2'-dithioxo-2H,2'H-[5,5'-dithiazoliden]-3,3'(4H,4'H)-diyl)diacetic acid as a ligand, as well as to a process for its preparation, and the compound can be used as an antifungal and antibacterial drug.According to the invention, a polymeric coordination compound of zinc (II) of the formula [Zn(5,5'-Rda-Rda)(dmf)2(H2O)2]n is claimed, where 5,5'-Rda-Rda is the residue of (E)-2,2'-(4,4'-dioxo-2,2'-dithioxo-2H,2'H-[5,5'-dithiazoliden]-3,3'(4H,4'H)-diyl)diacetic acid; dmf - dimethylformamide. The claimed compound exhibits antifungal and antibacterial properties.The process, according to the invention, consists in that zinc tetrafluoroborate monohydrate and 2-(4-oxo-2-thioxothiazolidin-3-yl)acetic acid are dissolved in a mixture of solvents consisting of water, methanol and dimethylformamide, the resulting solution is stirred at 40°C, slowly evaporated to obtain a compound of the formula [Zn(5,5'-Rda-Rda)(dmf)2(H2O)2]n, comprising a new bridging ligand, representing a residue of (E)-2,2'-(4,4'-dioxo-2,2'-dithioxo-2H,2'H-[5,5'-dithiazoliden]-3,3'(4H,4'H)-diyl)diacetic acid, obtained as a result of condensation reaction of 2-(4-oxo-2-thioxothiazolidin-3-yl)acetic acid.
机译:本发明涉及化学和医学,即涉及一种具有(E)-2,2'-(4,4'-dioxo-2)残基的锌(II)的一维配位聚合物类型的新化合物,作为配体的2'-二硫代-2H,2'H- [5,5'-二噻唑啉] -3,3'(4H,4'H)-二基)二乙酸及其制备方法,根据本发明,式[Zn(5,5'-Rda-Rda)(dmf)2(H 2 O)2的锌(II)的聚合配位化合物。要求保护] n,其中5,5'-Rda-Rda是(E)-2,2'-(4,4'-dioxo-2,2'-dithioxo-2H,2'H- [5 ,5'-二噻唑啉] -3,3'(4H,4'H)-二基)二乙酸; dmf-二甲基甲酰胺。所要求保护的化合物表现出抗真菌和抗菌性能。根据本发明的方法包括将四氟硼酸锌一水合物和2-(4-氧代-2-硫代噻唑并恶唑烷-3-基)乙酸溶解在由以下组成的溶剂混合物中:在水,甲醇和二甲基甲酰胺中,在40°C下搅拌所得溶液,缓慢蒸发,得到式[Zn(5,5'-Rda-Rda)(dmf)2(H2O)2] n的化合物,其中新的桥接配体,代表(E)-2,2'-(4,4'-dioxo-2,2'-dithioxo-2H,2'H- [5,5'-dithiazoliden] -3,3的残基通过(2-(4-氧代-2-硫代噻唑并恶唑烷-3-基)乙酸的缩合反应获得'((4H,4'H)-二基)二乙酸。

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