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首页> 外文期刊>Electroanalysis >Spectroelectrochemical Investigation of TPPMn(III/II)-Driven Liquid | Liquid | Electrode Triple Phase Boundary Anion Transfer into 4-(3-Phenylpropyl)-Pyridine: ClO _4 -, CO _3H -, Cl -, and F -
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Spectroelectrochemical Investigation of TPPMn(III/II)-Driven Liquid | Liquid | Electrode Triple Phase Boundary Anion Transfer into 4-(3-Phenylpropyl)-Pyridine: ClO _4 -, CO _3H -, Cl -, and F -

机译:TPPMn(III / II)驱动液体的光谱电化学研究液体|电极三相边界阴离子转移到4-(3-苯基丙基)-吡啶中:ClO _4-,CO _3H-,Cl-和F-

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摘要

The triple phase boundary transfer of anions from the aqueous into an organic phase can be driven electrochemically here with the tetraphenylporphyrinato-Mn(III/II) (or TPPMn) redox system in 4-(3-phenylpropyl)-pyridine) (or PPP). Anions investigated are perchlorate, chloride, fluoride, and bicarbonate. The bicarbonate and fluoride transfer processes are shown to be chemically more complex compared to the perchlorate and chloride cases with UV-vis-spectroelectrochemical measurements indicating a combination of HCO _3 -/CO _3 ~(2-) transfer processes and association of fluoride with TPPMn(III) +, respectively. In situ spectroelectrochemistry is developed for ion-transfer voltammetry into sub-microliter organic phase regions on mesoporous ITO conducting film electrodes.
机译:阴离子从水相到有机相的三相边界转移可以在此处通过四苯基卟啉-Mn(III / II)(或TPPMn)氧化还原体系在4-(3-苯基丙基)-吡啶)(或PPP)中进行电化学驱动。研究的阴离子为高氯酸根,氯离子,氟离子和碳酸氢根。与高氯酸盐和氯化物的情况相比,碳酸氢盐和氟化物的转移过程在化学上更复杂,并且具有紫外可见光谱电化学测量,表明HCO _3-/ CO _3〜(2-)转移过程以及氟化物与TPPMn的缔合(III)+。原位光谱电化学被开发用于离子转移伏安法到中孔ITO导电膜电极上的亚微升有机相区域。

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