Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.597766
Title: Enantioselective properties of the intrinsically chiral Cu{531} surface
Author: Clegg, M. L.
Awarding Body: University of Cambridge
Current Institution: University of Cambridge
Date of Award: 2010
Availability of Full Text:
Full text unavailable from EThOS.
Please contact the current institution’s library for further details.
Abstract:
The focus of this study is to gain an improved understanding of enantioselective heterogeneous catalysis, by investigating the adsorption of both reactants and possible products on a well-defined chiral surface. This has been achieved by employing a selection of surface science techniques, principally Reflection-Absorption Infrared Spectroscopy (RAIRS) and Scanning Tunnelling Microscopy (STM). STM images of the clean substrate clearly show that the Cu{531} surface strongly departs from the bulk-terminated structure, instead exhibiting marked roughness. The surface can be considered a frozen lattice gas, where all atoms are on lattice sites. In order to fully understand surface reactions it is important to gain insight into how individual reactants interact with the surface. Therefore, the adsorption of pyruvic acid and ammonia, chosen with a view to producing alanine, were studied individually. At 300 K, pyruvic acid adsorption results in the formation of pyruvate species having two distinct adsorption geometries depending on coverage, whereas it was found that ammonia adsorbs intact below room temperature. Pyruvic acid exposure to an ammonia pre-covered surface at 100 K results in the formation of the pyruvate ion, the enol tautomer of pyruvate, and glyoxylic acid. No infrared bands observed in this system are assigned to nitrogen-containing species, indicating that ammonia is acting, not as a reactant, but as a catalyst on the surface. Dosing pyruvic acid on an ammonia pre-covered surface at 300 K results in the formation of two nitrogen-containing species: iminoacetic acid and aminoacrylic acid. However, no clear evidence of alanine, the target molecule, was observed. STM images of single enantiomer adsorption of alanine show massive restructuring of the surface, forming distinctly different facets depending on the chirality of the adsorbate. RAIRS experiments using racemic alanine revealed no preferential adsorption of a single handedness, indicating that Cu{531} is not able to perform enantiospecific separation of alanine.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.597766  DOI: Not available
Share: