E. Karivmiller et al., N-METHYLQUINUCLIDINIUM-MERCURY COMPOUND - ELECTRODEPOSITION AND CATALYSIS, Journal of the Electrochemical Society, 142(10), 1995, pp. 3386-3392
We have explored the formation of an R(4)N-metal derived from n-methyl
quinuclidinium (MQ(+)) and mercury cathode. For each MQ(+) cation, 5 H
g atoms are consumed and the stoichiometric composition of electrodepo
sited MQ-mercury is MQ(Hg-5). The early stages of an MQ(Hg-5) depositi
on were investigated by cyclic voltammetry and potential step chronoam
perometry. The first process is the deposition of an initial layer whi
ch is controlled by two-dimensional nucleation and growth kinetics. De
position of the bulk phase is initiated by a three-dimensional nucleat
ion and growth controlled by diffusion of MQ(+) from the solution. A s
ignificant difference in the catalytic properties of the initial layer
and the bulk phase is identified showing that the initial layer trans
fers electrons to organic substrates more efficiently and is a better
catalyst.