Kolthoff I M, Yamashita K
Proc Natl Acad Sci U S A. 1975 Aug;72(8):2863-7. doi: 10.1073/pnas.72.8.2863.
Tetraethyl-, tetrapropyl-, and tetrabutylammonium ions are capillary-active on the interface water-mercury. In the adsorbed state they increase Brdicka and presodium currents. These currents drop sharply at potentials where tetrabutylammonium ions are desorbed, these potentials being -1.60, -1.66, -1.72, and -1.79 V versus the saturated calomel electrode (SCE) at tetrabutyla-mmonium concentrations of 0.1, 0.25, 1, and 5 mM, respectively. Indications are that tetraethylammonium ions at a concentration of 50 mM are desorbed at a potential of the order of -1.9 V (versus SCE). The increase of Brdicka currents is attributed--at least in part--to a decrease in the rate of electroreduction of cobalt(II). In the desorbed state the effect--if any--of tetrabutylammonium ions on Brdicka and presodium currents is very small. Tetrabutylammonium ions also greatly increase Brdicka currents observed with cysteine, the effect disappearing after these ions attain their desorption potential. The effect of tetraphenylarsonium on Brdicka currents is very similar to that of tetrabutylammonium, while that of diphenylguanidine is similar to that of tetraethylammonium ions.
四乙铵离子、四丙铵离子和四丁铵离子在水-汞界面具有毛细管活性。在吸附状态下,它们会增加布迪卡电流和预钠电流。在四丁铵离子解吸的电位下,这些电流会急剧下降,在四丁铵浓度分别为0.1、0.25、1和5 mM时,相对于饱和甘汞电极(SCE),这些电位分别为-1.60、-1.66、-1.72和-1.79 V。有迹象表明,浓度为50 mM的四乙铵离子在约-1.9 V(相对于SCE)的电位下解吸。布迪卡电流的增加至少部分归因于钴(II)电还原速率的降低。在解吸状态下,四丁铵离子对布迪卡电流和预钠电流的影响(如果有的话)非常小。四丁铵离子也会显著增加用半胱氨酸观察到的布迪卡电流,在这些离子达到其解吸电位后,这种影响消失。四苯砷离子对布迪卡电流的影响与四丁铵离子非常相似,而二苯基胍的影响与四乙铵离子相似。