ANM
2010
3rd
International Conference on Advanced Nano Materials
12-15 September 2010 - Agadir, Morocco
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Abstract
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ANMM302 |
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CHIRAL RECOGNITION ON 2D PATTERNED SURFACES: FROM
SINGLE MOLECULE TRACKING TO 3D CRYSTALS |
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M. Lingenfelder(1,3), G.
Tomba(2), G. Costantini(1), Y. Wang(1), Maarten van der Meijden(4),
Richard Kellogg(4), A. De Vita(2), D. Amabilino(3) and K. Kern(1) |
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(1) Max-Planck-Institute for Solid State Research,
Heisenbergstr. 1 D-70569 Stuttgart, Germany
(2) Physics Department, King's College London, Strand, London WC2R 2LS,
United Kingdom
(3) Institut de Ciència de Materials de Barcelona (CSIC) Campus
Universitari 08193-Bellaterra, Spain
(4) Syncom BV Kadijk 3 9747 AT Groningen 9704 CE Groningen, The
Netherlands |
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The
emergence of homochirality in biomolecular systems is one of the most
intriguing open questions of Nature. The self-assembly and
amplification of chiral subunits into higher-order species is crucial
in understanding the development of homochirality in biological
function. Apart from being related to the very first organic molecules
synthesized on earth, understanding the basics of chiral recognition
and discrimination is of high technological relevance. In fact, the
chemistry and technology of production and separation of enantiomers
has evolved into a branch of materials science under the name of
Chirotechnology.
In this scenario, our work aims to get an insight into the fundamental
aspects of chiral recognition, under the main inspiring question: How
does chiral recognition take place at the single molecule level? and
secondly: How can we tune the expression of chirality on a 2D template
to achieve stereoselectivity for the growth of 3D crystals?
By tracking the conformational dynamics of adsorbed dipeptides on
Cu(110) by scanning tunneling microscopy (STM) we have recently shown
that chiral recognition takes place at the single-molecule level via
the general “induced fit” mechanism developed by Pauling
and Koshland more than 50 years ago . Moreover, we can now show that
fully patterned biomolecular chiral surfaces can be created by two
novel methods: tuning the expression of supramolecular chirality by
molecular engineering of chiral adsorption sites (footprint engineering
of aminoacids) and 2D co-crystallization (mixed phases of achiral and
chiral molecules) under ultra high vacuum conditions. Recent
developments on diasteromeric recognition and selective crystallization
at the solid/liquid interface will also be presented.
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