Pm. Schmidt et al., INCLUSION COMPLEXATION OF TETRATHIAFULVALENE IN CYCLODEXTRINS AND BIOELECTROANALYSIS OF THE GLUCOSE-GLUCOSE OXIDASE REACTION, Chemical Engineering Science, 50(12), 1995, pp. 1867-1876
Tetrathiafulvalene (TTF) forms water-soluble inclusion complexes with
alpha-, hp-beta- and gamma-cyclodextrin (CD). Cyclic voltammetry (CV)
has been performed at a stationary electrode to characterize these TTF
:CD inclusion complexes. The CV analysis yielded average peak separati
ons of 63 mV and diffusion limited currents, indicating completely rev
ersible electron transfer. The half-wave potential (E(1/2)) of the com
plex shifted to more positive values with increasing CD concentration,
permitting use of a modified Nernst equation to estimate the complexa
tion ratio and the equilibrium formation constant (K-form) of the comp
lexes. The complexation ratio was determined as 1:2, 1:1 and 1:1 for T
TF with alpha-CD, hp-beta-CD and gamma-CD, respectively. The K-form fo
r these complexes was then estimated to be 5.44 x 10(3) m(6)/kmol(2),
5.40 x 10(3) m(3)/kmol and 0.141 x 10(3) m(3)/kmol. The diffusion coef
ficients (Do) for 1 mol/m(3) TTF in alpha-CD varied from 4.44 x 10(-11
) to 0.76 x 10(-11) m(2)/s as the alpha-CD concentration increased fro
m 3 to 50 mol/m(3). The D-0 values for hp-beta-CD varied from 12.9 x 1
0(-11) to 4.03 x 10(-11) m(2)/s over the same cyclodextrin range where
as those of gamma-CD ranged from 2.20 x 10(-12) to 1.75 x 10(-12) m(2)
/s. CV curves for TTF:hp-beta-CD in the presence of glucose and GOx sh
owed a large anodic current with no discernible peaks, indicating bioe
lectrocatalysis. The ratio of this current to the diffusion limited cu
rrent was used to determine the second-order homogeneous rate constant
k(s) for the reaction with GOx, which demonstrated the efficiency of
the inclusion complex as a mediator. The k(s) value for 1 mol/m(3) TTF
decreased from 3.84 x 10(5) to 1.04 x 10(5) m(3)/kmols with an increa
se in hp-beta-CD concentration from 3 to 15 mol/m(3). Extremely high d
iffusion and kinetic parameters in 3 mol/m(3) CD solutions were due to
insolubility of TTF at low CD concentrations, and indicated that the
CD concentration must be maintained above this level.