The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.14098-44-3, Name is Benzo-15-crown-5, molecular formula is C14H20O5. In a Article£¬once mentioned of 14098-44-3, SDS of cas: 14098-44-3
On the facilitating effect of neutral macrocyclic ligands on the ion transfer across the interface between aqueous and organic solutions – Part III. Competitive facilitated ion-transfer
A theoretical equation of the reversible current-potential curves is derived for the competitive ion-transfer of two kinds of cations present in an aqueous (w) phase simultaneously facilitated by a macrocyclic ligand (L) present in an organic (o) phase. Especially, for the two limiting cases, i.e. case (A): c*Mj (j = 1, 2)?c*L and case (B): c*L?c*Mj (where c*Mj and c*L denote the bulk concentrations of cation Mj in the w-phase and of L in the o-phase, respectively), simple explicit expressions are derived and a method analyzing the facilitated waves is presented. Furthermore, the main part of the theoretical predictions obtained is verified experimentally at 25C by using the ion-transfer-polarographic method with the electrolyte dropping electrode, for the following four combinations: (i) competitive cations: protonated alanine and H+, L: benzo-18-crown-6 ether; (ii) Na+ and Li+, benzo-15-crown-5 ether; (iii) K+ and Na+, dibenzo-18-crown-6 ether; and (iv) Na+ and Ba2+, dibenzo-24-crown-8 ether.
Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.SDS of cas: 14098-44-3, you can also check out more blogs about14098-44-3
Reference£º
Chiral Catalysts,
Chiral catalysts – SlideShare