Sn. Port et al., FTIR STUDY OF REDOX SWITCHING OF PI-INTERACTIONS AND REORIENTATION OFADSORBED UBIQUINONE-10 ON GOLD, Langmuir, 11(11), 1995, pp. 4577-4582
The reduction of ubiquinone-10 adsorbed onto a gold electrode in borax
and sodium hydroxide solutions has been studied by subtractively norm
alized interfacial Fourier transform infrared spectroscopy (SNIFTIRS).
A reorientation of the adsorbed ubiquinone molecule on reduction coul
d be observed. The SNIFTIRS spectra show that the molecule is anchored
to the electrode surface through the isoprenoid groups, with the quin
one ring away from the surface. Upon reduction, the aromatic ring form
ed is adsorbed by pi interactions with the metal surface and is aligne
d flat to the surface, slightly lifting the isoprenoid chains.