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Speciation in oxovanadium(IV)-carnosine system

机译:氧钒(IV)-肌肽系统的形态

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The complex species formed in aqueous solution (25degreesC, I=0.15 mol dm(-3) KCl ionic medium) between VO2+ cation and carnosine (HL) have been studied potentiometrically and spectrophotometrically. The application of the least-squares computer program LETAGROP to the experimental emf and UV-Vis data, taking into account the hydrolytic species of VO2+ ion, indicates that under the employed experimental conditions (carnosine-oxovanadium(IV) ratios ranging from 6/1 to 25/1; pH range 2.5-5 and 7-9) only the species in the ligand-metal ratio 2: 1, [VO(H3L)(H2L)](5+), [VO(H2L)(2)](4+) and [VO(H2L)(HL)](3+) (acid zone, pH 2.5-5), and [VO(HL)L](+), [VOL2] and [VOL2H-1](-) (basic zone, pH 7-9), are formed in significant amounts. At pH 5-7 VO(OH)(2) precipitates. With ratio ligand-metal greater than or equal to 60:1, the hydrolysis is repressed and precipitation is not observed. In the pH range 2.5-9, the same species and moreover the species [VO(HL)(2)](2+) is also found. This model is confirmed at 25degreesC and I=1.5 mol dm(-3) ionic medium. The stability constants and ionization constants of the complexes formed were determined. The species distribution diagrams as a function of pH and electronic spectra are jointly discussed. Theoretical calculations of protonation constants of carnosine have also been made using PALLAs 3.0 program. (C) 2002 Elsevier Science Ltd. All rights reserved. [References: 56]
机译:电位和分光光度法研究了在VO2 +阳离子和肌肽(HL)之间在水溶液中(25°C,I = 0.15 mol dm(-3)KCl离子介质)形成的复杂物质。考虑到VO2 +离子的水解种类,最小二乘计算机程序LETAGROP在实验电动势和UV-Vis数据中的应用表明,在所采用的实验条件下(肌肽-氧钒(IV)的比率范围为6/1到25/1; pH范围2.5-5和7-9)只有配体与金属之比为2的物种:1,[VO(H3L)(H2L)](5 +),[VO(H2L)(2) ](4+)和[VO(H2L)(HL)](3 +)(酸区,pH 2.5-5)和[VO(HL)L](+),[VOL2]和[VOL2H-1] (-)(碱性区域,pH 7-9)大量形成。在pH 5-7时,VO(OH)(2)沉淀。当配体金属比大于或等于60:1时,水解被抑制并且没有观察到沉淀。在pH值2.5-9范围内,还发现了相同的物种,此外还有[VO(HL)(2)](2+)。该模型在25°C和I = 1.5 mol dm(-3)离子介质中得到证实。测定所形成的配合物的稳定性常数和电离常数。共同讨论了随pH和电子光谱变化的物种分布图。还使用PALLAs 3.0程序对肌肽的质子化常数进行了理论计算。 (C)2002 Elsevier ScienceLtd。保留所有权利。 [参考:56]

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