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α-和γ-[S2W18O62]4-以及α-、β-和γ-[SiW12O40]4-的伏安还原:利用新型溶解和传统溶液相过程获得的数据研究多金属氧酸盐阴离子可逆电位的异构体依赖性

Voltammetric Reduction of alpha- and gamma-[S2W18O62]4- and alpha-, beta-, and gamma-[SiW12O40]4-: isomeric dependence of reversible potentials of polyoxometalate anions using data obtained by novel dissolution and conventional solution-phase processes.

作者信息

Zhang Jie, Bond Alan M, Richardt Peter J S, Wedd Anthony G

机构信息

School of Chemistry, Monash University, Clayton, Victoria 3800, Australia.

出版信息

Inorg Chem. 2004 Dec 27;43(26):8263-71. doi: 10.1021/ic049043x.

Abstract

Comparative studies on the voltammetric reduction of the alpha and gamma isomers of Dawson S(2)W(18)O(62)(-) and alpha, beta, and gamma forms of Keggin SiW(12)O(40)(-) polyoxometalate anions have been undertaken. For the six reversible one-electron S(2)W(18)O(62)(-)(/5)(-)(/6)(-)(/7)(-)(/8)(-)(/9)(-)(/10)(-) processes in acetonitrile, reversible potentials (E(0)(')) were found to be independent of isomeric form within experimental error (+/-5 mV). However, because both the alpha and gamma* isomers of Bu(4)N[S(2)W(18)O(62)] are insoluble in water, solid-state voltammetric studies with microcrystals adhered to electrode surfaces in contact with aqueous Et(4)NCl and Bu(4)NCl electrolyte media were also possible. Although no isomeric distinction was again detected in the solid-state studies, it was found that reduction of adhered solid by four or more electron equivalents led to rapid dissolution. When Et(4)NCl was the electrolyte, this dissolution process coupled with potential cycling experiments enabled conventional solution-phase data to be obtained in water for the analogous six one-electron reduction steps previously detected in acetonitrile. A strong medium effect attributed to Lewis acidity effects was apparent upon comparison with E(0)(') data obtained in water and acetonitrile. In contrast, with the SiW(12)O(40)(-) system, E(0)(') values for the SiW(12)O(40)(-)(/5)(-)(/6)(-)(/7)(-) processes in acetonitrile exhibited a larger (about 70 mV) dependence on isomeric form, and the isomerization step, gamma-SiW(12)O(40)(-)--> alpha-SiW(12)O(40)(-), was detected on the voltammetric time scale. The influence of isomeric form on reversible potential data is considered in terms of structural and charge density differences exhibited in the S(2)W(18)O(62)(-) and SiW(12)O(40)(-) systems studied in this paper and published data available on the alpha, beta, gamma, and gamma isomers of As(2)W(18)O(62)(-) and P(2)W(18)O(62)(-) Dawson anions and Keggin systems.

摘要

已对道森结构S(2)W(18)O(62)(-)的α和γ异构体以及凯gin结构SiW(12)O(40)(-)多金属氧酸盐阴离子的α、β和γ形式进行了伏安还原的比较研究。对于在乙腈中的六个可逆单电子S(2)W(18)O(62)(-)(/5)(-)(/6)(-)(/7)(-)(/8)(-)(/9)(-)(/10)(-)过程,在实验误差(±5 mV)范围内,发现可逆电位(E(0)('))与异构体形式无关。然而,由于Bu(4)N[S(2)W(18)O(62)]的α和γ*异构体都不溶于水,因此也可以对附着在电极表面并与Et(4)NCl和Bu(4)NCl水性电解质介质接触的微晶进行固态伏安研究。尽管在固态研究中再次未检测到异构体差异,但发现附着固体被四个或更多电子当量还原会导致快速溶解。当Et(4)NCl为电解质时,这种溶解过程与电位循环实验相结合,使得能够在水中获得与先前在乙腈中检测到的类似的六个单电子还原步骤的常规溶液相数据。与在水和乙腈中获得的E(0)(')数据相比,明显存在归因于路易斯酸性效应的强烈介质效应。相比之下,对于SiW(12)O(40)(-)体系,SiW(12)O(40)(-)(/5)(-)(/6)(-)(/7)(-)过程在乙腈中的E(0)(')值对异构体形式的依赖性更大(约70 mV),并且在伏安时间尺度上检测到异构化步骤γ-SiW(12)O(40)(-)→α-SiW(12)O(40)(-)。本文根据所研究SiW(12)O(40)(-)体系中显示的结构和电荷密度差异以及已发表的关于As(2)W(18)O(62)(-)和P(2)W(18)O(62)(-)道森阴离子和凯gin体系的α、β、γ和γ异构体的数据,考虑了异构体形式对可逆电位数据的影响。

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