PHOTOSTIMULATED INTERACTIONS OF BIPYRIDINIUM-AZOBENZENE WITH A BETA-AMINOCYCLODEXTRIN MONOLAYER-FUNCTIONALIZED ELECTRODE - AN OPTOELECTRONIC ASSEMBLY FOR THE AMPEROMETRIC TRANSDUCTION OF RECORDED OPTICAL SIGNALS
M. Lahav et al., PHOTOSTIMULATED INTERACTIONS OF BIPYRIDINIUM-AZOBENZENE WITH A BETA-AMINOCYCLODEXTRIN MONOLAYER-FUNCTIONALIZED ELECTRODE - AN OPTOELECTRONIC ASSEMBLY FOR THE AMPEROMETRIC TRANSDUCTION OF RECORDED OPTICAL SIGNALS, Israel Journal of Chemistry, 37(2-3), 1997, pp. 185-195
An amino-functionalized beta-cyclodextrin is covalently linked to a th
iopropionic acid-active ester monolayer associated with a Au electrode
to yield a cyclodextrin monolayer electrode. The photoisomerizable el
ectron acceptor trans or cis ridinium-4-(4'-N'-methylenepyridinium)-az
obenzene, It or Ic, respectively, exhibit different binding affinities
for the beta-cyclodextrin-receptor-monolayer. The photoisomer It has
a high affinity for the cyclodextrin monolayer while Ic exhibits low b
inding interactions to the monolayer interface. The photostimulated bi
nding and dissociation of It or Ic to and from the monolayer are trans
duced electrochemically. The association and dissociation of the photo
isomerizable substrate to and from the monolayer are confirmed by micr
ogravimetric, quartz-crystal-microbalance experiments.