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用台式计算机处理电子吸收光谱 - II:分光光度滴定法计算稳定常数。

Handling of electronic absorption spectra with a desk-top computer-II: calculation of stability constants from spectrophotometric titrations.

机构信息

Institute of Inorganic Chemistry, University of Basel, CH-4056 Basel, Switzerland.

出版信息

Talanta. 1979 Dec;26(12):1111-8. doi: 10.1016/0039-9140(79)80026-0.

Abstract

A fully automatic system for combined spectrophotometric and pH titrations was described in Part I. Its performance in the titration of weak acids and metal complexes is discussed, along with a computer program for numerical treatment of the data, based on Marquardt's modification of the Newton-Gauss non-linear least-squares method. The deprotonation of p-nitrophenol at concentrations of 4 x 10(-5) and 4 x 10(-6)M was studied in order to test the sensitivity. Results identical within the reproducibility of the pH-meter were obtained: pK(H) = 7.00 +/- 0.01 and 7.02 +/- 0.01, respectively. Three complexation reactions were studied: (1) the interaction of SCN(-) with the Co(2+) complex of 1,4,8,11-tetramethyl-1,4,8,11-tetra-azacyclotetradecane (TMC); five independent experiments gave pK [CoTMC (SCN)(+) right harpoon over left harpoon CoTMC(2+) + SCN(-)] = 3.099 +/- 0.003: (2) the deprotonation of the Cu(2+) complex of 3,7-diazanonanediamide (DANA); five experiments gave pK (CuDANA(2+) right harpoon over left harpoon CuDANAH(+)(-1) + H(+)) = 7.14 +/- 0.01 and pK (CuDANAH(+)(-1) right harpoon over left harpoon CuDANAH(-2) + H(+)) = 8.38 +/- 0.01: (3) for the reaction of Cu(2+) with 1,3,7-triazacyclodecane (L), data from different ligand: metal ratios had to be combined to obtain pK (CuL(2+) right harpoon over left harpoon Cu(2+) + L) = 16.19 +/- 0.01, pK (CuL(2+)(2) right harpoon over left harpoon CuL(2+) + L) = 10.30 +/- 0.01, and pK (Cu(2)L(2) (OH)(2+)(2) right harpoon over left harpoon 2 CuL(2+) + 2 OH(-)) = 14.58 +/- 0.03. Titration curves with a total change in absorbance of as little as 0.03 units could be analysed satisfactorily, extending considerably the useful range of concentrations for spectrophotometric titrations. In combined spectrophotometric/pH titrations the accuracy of the glass electrode is normally the limiting factor. Other equilibrium constants can easily be reproduced with standard errors of less than 0.01 log unit.

摘要

第一部分描述了一种用于分光光度法和 pH 滴定的全自动系统。讨论了其在弱酸和金属络合物滴定中的性能,以及一种基于 Marquardt 对牛顿-高斯非线性最小二乘法的修正的用于数据数值处理的计算机程序。研究了 p-硝基苯酚在 4×10(-5)和 4×10(-6)M 浓度下的去质子化作用,以检验其灵敏度。得到了在 pH 计的重现性内相同的结果:pK(H) = 7.00 ± 0.01 和 7.02 ± 0.01。研究了三个络合反应:(1)SCN(-)与 Co(2+)络合物 1,4,8,11-四甲基-1,4,8,11-四氮杂环十四烷(TMC)的相互作用;五个独立的实验给出了 pK [CoTMC(SCN)(+) 右箭头 over 左箭头 CoTMC(2+) + SCN(-)] = 3.099 ± 0.003:(2)Cu(2+)与 3,7-二氮杂壬二酰胺(DANA)络合物的去质子化作用;五个实验给出了 pK (CuDANA(2+) 右箭头 over 左箭头 CuDANAH(+)(-1) + H(+)) = 7.14 ± 0.01 和 pK (CuDANAH(+)(-1) 右箭头 over 左箭头 CuDANAH(-2) + H(+)) = 8.38 ± 0.01:(3)对于 Cu(2+)与 1,3,7-三氮杂环十二烷(L)的反应,必须结合来自不同配体:金属比的数据才能得到 pK (CuL(2+) 右箭头 over 左箭头 Cu(2+) + L) = 16.19 ± 0.01,pK (CuL(2+)(2) 右箭头 over 左箭头 CuL(2+) + L) = 10.30 ± 0.01,和 pK (Cu(2)L(2)(OH)(2+)(2) 右箭头 over 左箭头 2 CuL(2+) + 2 OH(-)) = 14.58 ± 0.03。可以满意地分析总吸光度变化小至 0.03 个单位的滴定曲线,大大扩展了分光光度滴定的有用浓度范围。在分光光度法和 pH 滴定的组合中,玻璃电极的精度通常是限制因素。其他平衡常数可以很容易地以小于 0.01 个对数单位的标准误差重现。

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