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Wahl M, von Arx M, Jung TA, et al. Time-lapse STM studies of diastereomeric cinchona alkaloids on platinum metals. J Phys Chem B. 2006;110(43):21777-82doi: 10.1021/jp0628941.
Wahl, M., von Arx, M., Jung, T. A., & Baiker, A. (2006). Time-lapse STM studies of diastereomeric cinchona alkaloids on platinum metals. The journal of physical chemistry. B, 110(43), 21777-82. https://doi.org/10.1021/jp0628941
Wahl, Markus, et al. "Time-lapse STM studies of diastereomeric cinchona alkaloids on platinum metals." The journal of physical chemistry. B vol. 110,43 (2006): 21777-82. doi: https://doi.org/10.1021/jp0628941
Wahl M, von Arx M, Jung TA, Baiker A. Time-lapse STM studies of diastereomeric cinchona alkaloids on platinum metals. J Phys Chem B. 2006 Nov 02;110(43):21777-82. doi: 10.1021/jp0628941. PMID: 17064139.
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J Phys Chem B. 2006 Nov 02;110(43):21777-82. doi: 10.1021/jp0628941.

Time-lapse STM studies of diastereomeric cinchona alkaloids on platinum metals.

The journal of physical chemistry. B

Markus Wahl, Matthias von Arx, Thomas A Jung, Alfons Baiker

Affiliations

  1. Institut für Physik der Universität Basel, Klingelbergstrasse 82, CH-4056 Basel, Switzerland. [email protected]

PMID: 17064139 DOI: 10.1021/jp0628941

Abstract

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.

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