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首页> 外文期刊>Analytical Sciences >Effects of Electrolytes on the Configuration Change of Cobalt(II)-Halide Complexes in Chloroform/Water Reverse Micelle Systems
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Effects of Electrolytes on the Configuration Change of Cobalt(II)-Halide Complexes in Chloroform/Water Reverse Micelle Systems

机译:电解质对氯仿/水反胶束体系中钴(II)-卤化物配合物构型变化的影响

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摘要

The effects of various salts and HClO4 on the configuration change of cobalt(II)-halide complexes in CHCl3/CTAC or CTAB/H2O reverse micelle systems were examined at 25°C by means of spectrophotometry, where CTAC and CTAB represent cetyltrimethylammonium chloride and bromide, respectively. The formation of the [CoCl4]2- or [CoBr4]2- species of the tetrahedral configuration from [Co(H2O)6]2+ of the octahedral configuration in the reverse micelles was greatly promoted not only by a decrease in the W value (W = [H2O]/[surfactant]), but also, at a constant W value (e.g., W = 2.0), by the addition of relatively low concentrations of salts or the acid (e.g., 4.0 mol dm-3 in the aqueous phase or 4.0 × 10-2 mol dm-3 in the whole reverse micelle system). The effects of perchlorate salts increased as Na+ ≤ Li+ ∼ H+ Sr2+ Ca2+ Mg2+. Non-metallic salts, various tetraalkylammonium (R4N+) salts at lower concentrations, gave minor effects. The enhanced effects of metal salts on the configuration change of the cobalt(II)-halide complexes were interpreted by a further distortion of the hydrogen-bonded structure of the water in a “water pool” in the presence of salts of even relatively low concentrations. A conformation change with increasing temperature was also attributed to a further distortion of the water structure. An almost completed formation of [CoBr4]2- as well as [CoCl4]2- was attained in the reverse micelles at a low W value of 0.69 containing LiClO4 or HClO4. A partial transfer of the [CoX4]2- species from a “water pool” into the CHCl3 phase by the addition of the metal salts may be suspected. An examination of cobalt(II)-bromide complexes in dichloromethane/CTAB/H2O at W = 1.3 - 5.55 justified all the arguments concerning the chloroform systems. The Raman spectra of D2O containing concentrated LiBr and LiClO4 have supplied conclusive evidence that the hydrogen-bonded structure of the bulk water is completely distorted by extremely concentrated salts.
机译:在25°C下通过分光光度法检查了各种盐和HClO4对CHCl3 / CTAC或CTAB / H2O反胶束系统中卤化钴(II)配合物构型变化的影响,其中CTAC和CTAB代表十六烷基三甲基氯化铵和溴化物。 , 分别。在逆胶束中由八面体构型的[Co(H2O)6] 2+形成四面体构型的[CoCl4] 2-或[CoBr4] 2-种类,不仅通过W值的降低而得到了极大的促进。 (W = [H2O] / [表面活性剂]),但在恒定的W值(例如W = 2.0)下,通过添加相对较低浓度的盐或酸(例如4.0 mol dm-3)水相或整个反胶束系统中的4.0×10-2 mol dm-3)。当Na +≤Li +〜H +

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