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Comparative study of p-nitrophenyl picolinate hydrolysis catalyzed by Bis(O,O'-di(2-phenylalkyl)dithiophosphate) nickel(II)

机译:双(O,O'-DI(2-苯基烷基)二硫代磷酸盐(II)催化对硝基苯基吡啶基水解水解的对比研究

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The hydrolysis of p-nitrophenyl picolinate (PNPP) catalyzed by two nickel (II) complexes (bis(O,O'-di(2-phenylmethyl) dithiophosphate) nickel(II) (NiR~1) and bis(O,O'-di(2-phenylethyl) dithiophosphate) nickel(II) (NiR~2)) was investigated kinetically in this work. The results indicate that both metal complexes accelerate the hydrolysis of PNPP dramatically and the NiR~1 exhibits higher catalytic function on PNPP hydrolysis in the buffered solution with relatively low pH values, while NiR~2 shows slightly more efficacy on hydrolysis of PNPP in relatively high pH buffered solutions. This variance is ascribed to the synergism effect of space hindrance of the complexes and the nucleophilic attack of metal-hydroxy species generated by the complexes.
机译:用两种镍(II)配合物催化的对硝基苯基吡啶基吡啶基(PNPP)的水解(双(O,O'-DI(2-苯基甲基)二硫代磷酸镍)镍(II)(NIR〜1)和双(O,O') -DI(2-苯基乙基)二硫代磷酸磷酸二硫代磷酸镍(II)(II)(NIR〜2)在这项工作中进行了研究。结果表明,两种金属复合物显着加速PNPP的水解,并且NIR〜1在具有相对低的pH值的缓冲溶液中对PNPP水解的催化功能较高,而NIR〜2在相对高的PNPP水解稍微略微效果pH缓冲解决方案。这种方差归因于复合物的空间阻力的协同作用和复合物产生的金属 - 羟基物种的亲核侵蚀。

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