Time-Lapse STM Studies of Diastereomeric Cinchona Alkaloids on Platinum Metals

The adsorption of cinchonidine (CD) and cinchonine (CN) on Pt(111) and Pd(111) single crystals has been
investigated by means of scanning tunneling microscopy (STM) in an ultrahigh vacuum system. In time-lapse series the mobilities of different adsorption species have been determined on a single molecule basis
and with varying hydrogen background pressures in the system. The diastereomeric cinchona alkaloids, CD
and CN, which are widely used as chiral modifiers of platinum group metals in catalytic enantioselective
hydrogenation, showed similar adsorption modes and diffusion behavior on Pt(111), except that the flatly
adsorbed CN molecules which were free (not in a dimer/cluster) were significantly more mobile than their
CD analogues. CD adsorbed on Pd(111) showed similar adsorption modes as observed on Pt(111) but at
considerably higher mobility of the flatly absorbed species already in the low-pressure region. The observed
adsorption behaviors are discussed in the context of independent ATR−IR measurements and theoretical
calculations. Special emphasis is put on the nonlinear effect observed in hydrogenation reactions with CD/CN mixtures. Our observations corroborate that this effect is mainly a consequence of the different adsorption
strengths of CD and CN on Pt.