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首页> 外文期刊>Journal of Dispersion Science and Technology >Phosphate Diester Cleavage Promoted by the Metallomicelles of Ce(III) Complexes of Aza-Crown Ether with Different Numbers of Nitrogen Atoms
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Phosphate Diester Cleavage Promoted by the Metallomicelles of Ce(III) Complexes of Aza-Crown Ether with Different Numbers of Nitrogen Atoms

机译:不同氮原子数的氮杂冠醚Ce(III)配合物的金属硅化物促进磷酸酯的裂解

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The design of artificial hydrolase has attracted extensive attention due to their scientific significance and potential application in the field of gene medicine and molecular biology. This work reports the catalytic activation of two aza-crown ether Ce(III) complexes and their metallomicelles as artificial hydrolase in bis(4-nitrophenyl) phosphate ester (BNPP) hydrolysis. The chemical composition of two complexes was determined by the fluorescence spectra and the mole ratio method for electronic absorption spectra. The bonding effect of BNPP and solubilizing effect of the complexes were proved by a method of fluorescence spectroscopy. The catalytic activity of different catalytic systems in BNPP hydrolysis was measured with UV-vis spectrophotometric method. These catalytic systems showed high catalytic activity for promoting BNPP hydrolysis at the almost physiological conditions. BNPP hydrolysis rate in these catalytic system is about 10(7) - to 10(9)-fold faster than that of the BNPP spontaneous hydrolysis in aqueous solution at the same conditions. The metallomicelle systems exhibited higher catalytic activity compared with the complex solution systems in BNPP hydrolysis, and hexadecyltrimethyl ammonium bromide micelle provides a useful catalytic environment for reaction. The acid effect of the catalytic system is ascribed to the formation of metal-bound hydroxide serving as a better kind of nucleophile.
机译:人工水解酶的设计由于其科学意义和在基因医学和分子生物学领域的潜在应用而受到广泛关注。这项工作报告了双(4-硝基苯基)磷酸酯(BNPP)水解中作为人工水解酶的两个氮杂-冠醚Ce(III)配合物及其金属硅化物的催化活化。通过荧光光谱和电子吸收光谱的摩尔比方法确定了两种配合物的化学组成。通过荧光光谱法证明了BNPP的键合作用和配合物的增溶作用。采用紫外可见分光光度法测定了不同催化体系在BNPP水解中的催化活性。这些催化体系在几乎生理条件下具有促进BNPP水解的高催化活性。在相同条件下,这些催化体系中BNPP的水解速率比BNPP在水溶液中自发水解的速率快约10(7)-10(9)倍。与BNPP水解中的复杂溶液系统相比,金属硅油体系显示出更高的催化活性,十六烷基三甲基溴化铵胶束为反应提供了有用的催化环境。催化体系的酸作用归因于形成金属结合的氢氧化物,它是一种更好的亲核试剂。

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