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Secrets of a chiral gold nanocluster unveiled

27.05.2010

Researchers at the Department of Chemistry and Nanoscience Center (NSC) of the University of Jyväskylä (Dr Olga Lopez-Acevedo and Professor Hannu Häkkinen) have resolved the structural, electronic and optical properties of a chiral gold nanocluster that remained a mystery for ten years. The theoretical structure was confirmed via comparison to experimental results obtained by X-ray diffraction from powder samples of the pure cluster material. The theoretical work was done in collaboration with researchers at Kansas State University and the experimental part at Hokkaido University. The team is supported by the Academy of Finland and the CSC – the IT Center for Science.

The synthesis of organothiolate-protected gold clusters of 1 to 3 nm in size has been well known since the mid-1990s, but the detailed atomic structure of the most stable clusters remained a mystery until very recently. In 2007, the structure of the first cluster that contained 102 gold atoms was resolved at Stanford University using single-crystal X-ray crystallography. The cluster now resolved has exactly 38 gold atoms and 24 organothiolate molecules covering its surface and it is just about one nanometer (nanometer = one millionth of a millimeter) in size. The shape of the particle is prolate (cigar-like), and 15 out if its 38 gold atoms reside on the protective surface layer chemically bound with the thiolate molecules. The gold-thiolate layer has a chiral structure, which is responsible for the observed chiral properties. The chiral structure has two structural forms (enantiomers), the so-called right-handed and left-handed forms, in a way comparable to a twist in a DNA molecule or to a twist in the staircase structure of a block of flats.

 kuva häkkinen JACS

 

Figure.  Left: The theoretical structure of the Au38(SR)24 cluster with hexylthiolates (SR = SC6H13). Right: comparison of the X-ray diffraction function of the theoretical structure (red curve) to the measured data (black curve) from pure powder samples of Au38(SR)24  with dodecylthiolates (SR = SC12H25). The perfect match between the calculation and the experiment confirms the structural assignment. In the structural figure, the 23 Au atoms in the core of the particle are shown by large yellow spheres, 15 Au atoms covalently bound to the thiolates are small yellow spheres, sulfurs are shown by the small orange spheres and the hydrocarbon chains by sticks. The structure of the protecting Au15(SR)24 layer is chiral and yields the chiral properties of the cluster.

Chirality is a very common structural property of molecules in nature.  The chiral nature of gold clusters influences the way they respond to circularly polarised light. This effect was first reported in experiments by Professor Robert L. Whetten's team at Georgia Institute of Technology (Atlanta, USA) exactly ten years ago. “We observed that particularly the 38-atom cluster (for which no structural information was available) is very sensitive for the polarisation of light, and the now-resolved structure finally explains our observations,” comments Professor Whetten. In the future, chiral gold nanoclusters could be used as bio-compatible, enantioselective sensors, drug carriers or catalysts.

Professor Häkkinen's team at the University of Jyväskylä has played a world-leading role in theoretical structural determination and characterisation of thiolate-protected gold nanoclusters over the last few years. The team has collaborated with researchers at Stanford University, Georgia Institute of Technology, Kansas State University, the University of North Carolina, Chalmers University of Technology and Hokkaido University. 

More information

For more information please contact Professor Hannu Häkkinen,
email hannu.j.hakkinen at jyu.fi, tel. +358 (0)14 260 4719

The study was published in the Journal of the American Chemical Society May 25, 2010.
Chirality and electronic structure of the thiolate-protected Au38 nanocluster”, O. Lopez-Acevedo, H. Tsunoyama, T. Tsukuda, H. Häkkinen, C.M. Aikens, JACS ASAP article May 25, 2010.

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