2D Ising Model for Enantiomer Adsorption on Achiral Surfaces: L- and D-Aspartic Acid on Cu(111).

The 2D Ising model is well-formulated to address problems in adsorption thermodynamics. It is particularly well-suited to describing the adsorption isotherms predicting the surface enantiomeric excess, ees, observed during competitive co-adsorption of enantiomers onto achiral surfaces. Herein, we make the direct one-to-one correspondence between the 2D Ising model Hamiltonian and the Hamiltonian used to describe competitive enantiomer adsorption on achiral surfaces.

2D Ising Model for Adsorption-induced Enantiopurification of Racemates.

Mechanisms for the spontaneous transformation of achiral chemical systems into states of enantiomeric purity have important ramifications in modern pharmacology and potential relevance to the origins of homochirality in life on Earth. Such mechanisms for enantiopurification are needed for production of chiral pharmaceuticals and other bioactive compounds. Previously proposed chemical mechanisms leading from achiral systems to near homochirality are initiated by a symmetry-breaking step resulting in a minor excess of one enantiomer via statistical fluctuations in enantiomer concentrations.

Enantiospecific equilibrium adsorption and chemistry of d-/l-proline mixtures on chiral and achiral Cu surfaces.

A fundamental understanding of the enantiospecific interactions between chiral adsorbates and understanding of their interactions with chiral surfaces is key to unlocking the origins of enantiospecific surface chemistry. Herein, the adsorption and decomposition of the amino acid proline (Pro) have been studied on the achiral Cu(110) and Cu(111) surfaces and on the chiral Cu(643) surfaces. Isotopically labelled 1- C-l-Pro has been used to probe the Pro decomposition mechanism and to allow mass spectrometric discrimination of d-Pro and 1- C-l-Pro when adsorbed as mixtures.

Enantiospecific Adsorption and Decomposition of D- and L-Asp Mixtures on Cu(643).

The study of molecular chirality is essential to understanding the fundamentals of enantiospecific chemical interactions that are ubiquitous in the biochemistry of life on Earth. At a molecular level, there is insufficient understanding of chiral recognition and enantiomer-enantiomer interaction (aggregation) of chiral molecules adsorbed on surfaces. Here, using enantiospecific isotopic labelling and surface sensitive techniques, we show that when the two enantiomers of chiral aspartic acid (Asp) are adsorbed on the naturally chiral Cu(643)R&S surfaces, they decompose enantiospecifically depending on the chirality of the surface.

Enantiomer surface chemistry: conglomerate versus racemate formation on surfaces.

Research on surface chirality is motivated by the need to develop functional chiral surfaces for enantiospecific applications. While molecular chirality in 3D has been the subject of study for almost two centuries, many aspects of 2D chiral surface chemistry have yet to be addressed. In 3D, racemic mixtures of chiral molecules tend to aggregate into racemate (molecularly heterochiral) crystals much more frequently than conglomerate (molecularly homochiral) crystals.