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Journal ArticleDOI

Electrochemical Studies of Enantioselectivity at Chiral Metal Surfaces

Gary Anthony Attard
- 20 Mar 2001 - 
- Vol. 105, Iss: 16, pp 3158-3167
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TLDR
In this article, a brief resume of the relevant electrochemical and heterogeneous catalysis literature is expounded together with an analysis of the problem of chirality in two dimensions in order to show that, by utilizing an electrochemical surface science ap...
Abstract
The combination of electrochemical methods with the use of well-defined kinked metal surfaces allows the experimentalist to examine many fundamental aspects of asymmetric reactions at solid surfaces in a new and detailed manner. For example, by systematically changing both the stereogenic center on a particular chemisorbing molecule and also the molecular architecture of the metal surface, relationships between adsorption geometry and reactive sites on the metal surface may be deduced. In addition, by measuring the differential rate of chemisorption of chiral auxiliaries on R and S metal surfaces insights in to the mechanism of the so-called “Orito” reaction (whereby enantioselective hydrogenation of α-ketoesters is observed) may be deduced. In the present article, a brief resume of the relevant electrochemical and heterogeneous catalysis literature is expounded together with an analysis of the problem of chirality in two dimensions in order to show that, by utilizing an electrochemical surface science ap...

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Journal ArticleDOI

Complex organic molecules at metal surfaces: bonding, organisation and chirality

TL;DR: In this article, the authors present a review of the available literature for complex carboxylic acids, amino acids, anhydrides and ring systems, all deposited under controlled conditions onto defined metal surfaces.
Journal ArticleDOI

Asymmetric heterogeneous catalysis.

TL;DR: This Review shows that highly ordered metal-organic catalysts that might allow a rational design, synthesis, and the unequivocal structural characterization to give tailor-made catalysts have more to them than facile separation or recycling.
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Platinum Metal Catalysts of High-Index Surfaces: From Single-Crystal Planes to Electrochemically Shape-Controlled Nanoparticles

TL;DR: The Natural Science Foundation of China as discussed by the authors [20673091, 20433060, 20503023, 20873113, 20833005], Mnistry of Science and Technology of China [2009CB220102, 2007DFA40890]
Journal ArticleDOI

Chiral selection on inorganic crystalline surfaces

TL;DR: Experimental and theoretical approaches to chiral selection on inorganic crystalline surfaces are reviewed — research that is poised to open this new frontier in understanding and exploiting surface-molecule interactions.
References
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Journal ArticleDOI

Enantioselective Epoxidation of Unfunctionalized Olefins Catalyzed by (salen)Manganese Complexes

TL;DR: The FTIR spectrum properties of compound IIIA,B are consistent with the presence of SO3groups attached to the aromatic rings of polysemiquinone polyaniline.
Journal ArticleDOI

The oxidation of small organic molecules: A survey of recent fuel cell related research

TL;DR: In this paper, a review of recent electrochemical literature concerning the oxidation of small organic molecules as potential fuels for fuel cells is presented, and the nature of poisoning species and reaction intermediates are discussed.
Journal ArticleDOI

Oxygen reduction of platinum low-index single-crystal surfaces in alkaline solution: Rotating ring disk{sub Pt(hkl)} studies

TL;DR: In this article, the first results of a study of the oxygen reduction reaction on a rotating ring-disk electrode using single-crystal Pt disk electrodes in alkaline solution were presented.
Journal ArticleDOI

Progress in asymmetric heterogeneous catalysis: Design of novel chirally modified platinum metal catalysts

TL;DR: Heterogeneous asymmetric catalysis on chirally modified supported platinum catalysts has undergone significant development recently based on the knowledge gained on the mechanism of the asymmetric hydrogenation of α-ketoesters, catalyzed by platinum modified with cinchona alkaloids.
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