LeSuer Robert J, Buttolph Catherine, Geiger William E
Department of Chemistry, The University of Vermont, Burlington, Vermont 05405, USA.
Anal Chem. 2004 Nov 1;76(21):6395-401. doi: 10.1021/ac040087x.
Cyclic voltammetry experiments at minielectrodes exhibit less ohmic error for lower polarity solvents when the supporting electrolyte anion is B(C(6)F(5))(4) rather than one of the smaller traditional anions such as BF(4), PF(6), or ClO(4). Conductance measurements have been performed for [NBu(4)][B(C(6)F(5))(4)] in tetrahydrofuran, dichloromethane, benzotrifluoride, and acetonitrile and compared with results for NBu(4) salts of several traditional anions in the same solvents. In solvents with dielectric constants of 10 or less, ion association constants, K(A), are as much as 2 orders of magnitude lower with B(C(6)F(5))(4), TFAB, as the electrolyte anion and the degree of this lowering is related to the acceptor property of the solvent. Analyses carried out on the basis of a Fuoss model attribute this fact to differences in concentrations of contact ion pairs rather than of solvent-separated ion pairs. The greater dissociation of the TFAB ion is attributed to its highly delocalized charge.
当支持电解质阴离子为[B(C₆F₅)₄]⁻而非较小的传统阴离子如[BF₄]⁻、[PF₆]⁻或[ClO₄]⁻时,在微电极上进行的循环伏安实验对于较低极性溶剂表现出较小的欧姆误差。已对四氢呋喃、二氯甲烷、三氟甲苯和乙腈中的[NBu₄][B(C₆F₅)₄]进行了电导率测量,并与相同溶剂中几种传统阴离子的[NBu₄]⁺盐的结果进行了比较。在介电常数为10或更低的溶剂中,以[B(C₆F₅)₄]⁻(TFAB)作为电解质阴离子时,离子缔合常数K(A)低至2个数量级,且这种降低程度与溶剂的受体性质有关。基于福斯模型进行的分析将这一事实归因于接触离子对浓度的差异,而非溶剂分隔离子对浓度的差异。TFAB离子更大的离解归因于其高度离域的电荷。