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Novel class of Bi(iii) hydroxamato complexes: synthesis, urease inhibitory activity and activity against H. pylori.

机译:新型的Bi(iii)羟肟基配合物:合成,脲酶抑制活性和针对幽门螺杆菌的活性。

摘要

Reaction of Bi(NO3)3 with benzohydroxamic acid (Bha) and salicylhydroxamic acid (Sha) gives the novel Bi(iii) complexes [Bi2(Bha-1H)2(μ-Bha-1H)2(η(2)-NO3)2] () and [Bi6(CH3OH)2(η(1)-NO3)2(η(2)-NO3)(OH2)2(Sha-1H)12](NO3)2 (). X-ray crystal structure of reveals two hydroxamato coordination modes; bidentate bridging (O, Ou27) and bidentate non-bridging (O, Ou27) and of reveals one coordination mode; bidentate bridging (O, Ou27). , specifically designed to and demonstrated to inhibit the activity of urease, exhibits excellent antibacterial activity against three strains of Helicobacter pylori with MIC ≥ 16 μg mL(-1).
机译:Bi(NO3)3与苯并异羟肟酸(Bha)和水杨基异羟肟酸(Sha)的反应产生了新型Bi(iii)络合物[Bi2(Bha-1H)2(μ-Bha-1H)2(η(2)-NO3 )2]()和[Bi6(CH3OH)2(η(1)-NO3)2(η(2)-NO3)(OH2)2(Sha-1H)12](NO3)2()。的X射线晶体结构揭示了两种异羟肟酸酯配位模式;双齿桥接(O,O u27)和双齿非桥接(O,O u27),并且揭示了一种协调模式;双齿桥接(O,O u27)。专门设计用于抑制尿素酶的活性,并证明对三株幽门螺杆菌(MIC≥16μgmL(-1))具有优异的抗菌活性。

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