AB INITIO Simulations of Desorption and Reactivity of Glycine at a Water-Pyrite Interface at ``Iron-Sulfur World'' Prebiotic Conditions

Details AB INITIO Simulations of Desorption and Reactivity of Glycine at a Water-Pyrite Interface at ``Iron-Sulfur World'' Prebiotic Conditions AB INITIO Simulations of Desorption and Reactivity of Glycine at a Water-Pyrite Interface at ``Iron-Sulfur World'' Prebiotic Conditions

Aug 2006

adsabs.harvard.edu/cgi-bin/nph-data_query?bibcode=2006oleb...36..363p&link_type=abstract

Origins of Life and Evolution of Biospheres, Volume 36, Issue 4, pp.363-379

Physics

1

Amino Acids, Car-Parrinello Molecular Dynamics, Hydrogen Bonds, Origins Of Life, Pyrite Surface

Scientific paper

Glycine at the interface of a pyrite surface (001) FeS2, and bulk water at high pressure and temperature conditions relevant to the “iron-sulfur world” scenario of the origin of life is investigated by theoretical means. Car-Parrinello molecular dynamics is used in order to study the desorption process of the zwitterionic form of this amino acid using two different adsorption modes, where either only one or both oxygens of the carboxylate group are anchored to surface iron atoms. It is found that the formation of stabilizing hydrogen bonds plays a key role in the detachment process, leading to longer retention times for the bidentate adsorption mode. In addition, the chemical reactivity of this heterogeneous system is probed by calculating the Fukui functions as site-specific reactivity indices. The most prominent targets for both nucleophilic and electrophilic reactions to occur are surface atoms, whereas the reactivity of glycine is only slightly affected upon anchoring.

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