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Title: Structure and properties of chiral modifiers (R)-(+)-1-(1-naphthyl)-ethylamine and (S)-(-)-1-(2-naphthyl)-ethylamine on Pd(1 1 1) using infrared spectroscopy
Award ID(s):
1855199
NSF-PAR ID:
10380346
Author(s) / Creator(s):
; ;
Date Published:
Journal Name:
Applied Surface Science
Volume:
607
Issue:
C
ISSN:
0169-4332
Page Range / eLocation ID:
154962
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
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  1. Abstract

    Chiral modifiers of heterogeneous catalysts can function as activity promotors to minimize the influence of unmodified sites on the enantiomeric excess to obtain highly enantioselective catalysts. However, the origin on this effect is not well understood. It is investigated using a model catalyst of R‐(+)‐1‐(1‐naphthyl)‐ethylamine (R‐1‐NEA)/Pd(111) for the hydrogenation of methyl pyruvate (MP) to methyl lactate (ML). The activity of the model catalyst remains constant for multiple turnovers. No rate enhancement is found for R‐1‐NEA coverages below ∼0.5 monolayer (ML), but a significant increase is found at R‐1‐NEA coverages of ∼0.75 ML, with a rate approximately twice that of the unmodified catalyst. This is investigated using infrared spectroscopy to distinguish between MP monomers and dimers. MP titration experiments with hydrogen show a half‐order hydrogen pressure dependence, with the monomer reacting at twice the rate as the dimer. It is found that the dimer is the most abundant species on clean Pd(111), but the ratio of monomers to dimers increases as the R‐1‐NEA coverage increases due to surface crowding. The monomeric species is also found to be more stable on the crowded surface than on clean Pd(111); the chiral modifier also serves to stabilize the reactant. Finally, this model nicely explains the unusual 1‐NEA‐covergae dependence of the reactivity.

     
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  2. null (Ed.)