Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Chirality transfer from gold nanocluster to adsorbate evidenced by vibrational circular dichroism

Abstract

The transfer of chirality from one set of molecules to another is fundamental for applications in chiral technology and has likely played a crucial role for establishing homochirality on earth. Here we show that an intrinsically chiral gold cluster can transfer its handedness to an achiral molecule adsorbed on its surface. Solutions of chiral Au38(2-PET)24 (2-PET=2-phenylethylthiolate) cluster enantiomers show strong vibrational circular dichroism (VCD) signals in vibrations of the achiral adsorbate. Density functional theory (DFT) calculations reveal that 2-PET molecules adopt a chiral conformation. Chirality transfer from the cluster to the achiral adsorbate is responsible for the preference of one of the two mirror images. Intermolecular interactions between the adsorbed molecules on the crowded cluster surface seem to play a dominant role for the phenomena. Such chirality transfer from metals to adsorbates likely plays an important role in heterogeneous enantioselective catalysis.

Introduction

Chirality plays a prominent role in nature and has tremendous impact on biology, medicine and pharmaceutical sciences. While the origin of homochirality on earth is still unclear it is a fact that many biological macromolecules are made from chiral building blocks. In contrast, metals are highly symmetric in their bulk. However, it became clear in the last decade that the situation may change at the nanoscale1,2,3,4. In fact, metal nanoparticles or clusters covered by thiolates bear chirality as evidenced by the observation of circular dichroism (CD) activity in electronic transitions that are localized mainly in the metal part. Whetten and coworkers5 observed prominent CD activity for gold clusters covered by glutathione, a chiral cysteine-containing tri-peptide. Other examples of gold nanoparticles or clusters of different size and covered by different chiral thiolates were reported later6,7,8,9,10,11,12. Furthemore, it emerges from X-ray crystal structure studies that gold clusters are composed of a dense symmetric core covered by monomeric SR–Au–SR or dimeric SR–Au–SR–Au–SR staple motifs (SR: thiolate)11,13,14,15,16. Interestingly, these staple motifs are arranged in a chiral fashion on the surface of the metal core. This has been found for example in the case of Au102(PMBA)44 (PMBA=para-mercaptobenzoic acid)13, but also for Au38(2-PET)24 (2-PET=2-phenylethylthiolate)14. The Au38(2-PET)24 cluster consists of a face-fused bi-icosahedral Au23 core protected by six dimeric and three monomeric staple motifs. The latter are found along the equator of the prolate core, whereas the long units form two triblade fans at its ends. The two fans at the poles of the cluster have the same handedness, giving rise to chirality. We have shown before that the enantiomers of the Au38(2-PET)24 cluster, denoted C and A (clockwise/anticlockwise) for the right- and left-handed enantiomers, respectively, can be separated by chiral high-performance liquid chromatography (HPLC)15. Similarly, enantiomers of Au40(2-PET)24 (ref. 16) and Au28(TBBT)20 (TBBT=4-tert-butylbenzenethiolate)11 were separated by chiral HPLC. Furthermore, the enantiomers of the Au102(PMBA)44 were enriched by phase transfer using a chiral ammonium salt as phase transfer agent17.

Research on gold clusters has mainly focused on their structure and electronic properties18 and on the nature and reactivity of the Au–S interface19,20,21,22. Not much attention has been paid to the structure (conformation) of the adsorbed thiolates, despite its importance for the chemical behaviour of the clusters and applications in sensing or recognition23. One reason for this lack of knowledge is the difficulty to study the conformation of adsorbed molecules in solution. One powerful technique to probe the conformation of chiral molecules is vibrational CD (VCD)24, that is, the differential absorption of left- and right-circularly polarized light by a chiral sample. VCD is sensitive to the absolute configuration but also to the conformation of a chiral molecule in solution. Indeed, the technique has already been applied to study the conformation of chiral thiolates on gold particles and clusters9,25,26,27. Achiral molecules or racemic samples do not show VCD activity. Achiral molecules can adopt chiral conformations (they are transiently chiral)28,29. In the absence of a chiral environment the two enantiomeric forms of the chiral conformation are equally abundant and therefore no VCD signal can be observed.

In this contribution, we demonstrate that an achiral thiolate adsorbed on a well-defined chiral gold cluster shows significant VCD signals. The thiolates adopt a chiral conformation and for each metal cluster enantiomer, one enantiomeric form is preferred over the other. This shows that the metal cluster can transfer its chirality to the adsorbed molecule. The type of chirality transfer evidenced in this contribution is suspected to play an important role in enantioselective processes such as chiral catalysis.

Results

Preparation and general considerations

We have prepared Au38(2-PET)24 clusters and separated the enantiomers using chiral chromatography as described in the methods section and in more detail in the Supplementary information. Characterization of the cluster is in agreement with previous reports (see Supplementary Figs 1–3)15. We then measured and analysed its infrared and VCD spectra in solution.

The vibrational spectrum of a compound depends on its structure. In fact, VCD spectra are very sensitive to the conformation of a molecule. The conformational analysis of the entire Au38(2-PET)24 cluster in solution is complex considering the enormous number of possible conformers. Each thiolate can be oriented in two ways with respect to the staple plane (cistrans isomerism, see also Supplementary Fig. 4). In addition, for each thiolate, several conformers can be obtained by rotation around the S–C (3 possibilities) and CH2–CH2 bonds (3 possibilities) giving rise to (2 × 3 × 3=) 18 principle conformers per adsorbed thiolate (see Fig. 1). For the whole cluster this amounts to 1824 conformers. Of course many of these possibilities are not feasible due to steric constraints, but a systematic conformational analysis is out of reach. To understand vibrational spectra of the cluster we therefore performed density functional theory (DFT) calculation on the free 2-phenylethylthiol and on a cyclic Au4(2-PET)4 structure, which serves as a model for the staple motifs.

Figure 1: Structure of the Au38(2-PET)24 cluster.
figure1

The 2-PET ligand is omitted for clarity except for one dimeric staple motif. For one 2-PET ligand the bonds relevant for the discussion of the 2-PET conformation are marked (S–C1–C2–C3–C4). Within the staple shown the centre 2-PET molecule adopts an anti conformation around the C1–C2 bond, whereas the other two molecules are in gauche conformation. Colour code: core Au atoms: orange, staple Au atoms: ochre, sulfur: green, carbon: blue, hydrogen: grey. The structure is extracted from the reported crystal structure of the cluster14.

Infrared spectrum of 2-phenylethylthiol

We first consider infrared spectra of neat 2-phenylethylthiol and of the Au38(2-PET)24 cluster in Fig. 2. In the reported spectral range (1,200–1,700 cm−1) two principle types of vibrations are observed: Vibrations associated with the phenyl moiety (ring vibrations) and vibrations located in the CH2–CH2 part of the molecule (CH2 scissoring, twisting and wagging). Supported by the calculations the most prominent bands in the spectrum of neat 2-phenylethylthiol can be assigned to in-plane phenyl ring vibrations (1,603, 1,583 and 1,495 cm−1), CH2 scissoring (1,454 and 1,429 cm−1), phenyl in-plane C–H bending (1,322 cm−1) and CH2 wagging (1,278 cm−1 and 1,235 cm−1). A detailed assignment is given in the Supplementary Table 1. Note that the vibrations involving Au–S bonds are found below 400 cm−1 and are thus not accessible in the current experiment30.

Figure 2: Infrared spectra of 2-phenylethylthiol and of gold cluster.
figure2

Infrared spectra of 2-phenylethylthiol (b) and Au38(2-PET)24 cluster (a). The experimental spectra are shown in black. Calculated spectra are also shown (red and blue). Red (blue) spectra are associated with 2-PET and 2-phenylethylthiol, respectively, adopting gauche (anti) conformation. For the calculation of the top spectra a Au4(2-PET)4 cyclic structure was used as a model for the staple motifs found on the Au38(2-PET)24 cluster. For the red (blue) spectrum all the 2-PET molecules within the Au4(2-PET)4 structure adopt gauche (anti) conformation. Green dotted lines mark wagging modes that are sensitive to conformation.

The infrared spectra of neat 2-phenylethylthiol as well as of 2-PET within the staple depend on conformation. Figure 2 shows that the CH2 wagging mode is particularly sensitive to conformation. For neat 2-phenylethylthiol the calculations predict a strong mode around 1,280 cm−1 for the gauche conformer, whereas the corresponding mode is predicted at 1,232 cm−1 for the anti conformer. Comparison with the experimental spectrum (bottom black spectrum in Fig. 2) reveals that in the neat 2-phenylethylthiol liquid both conformers are abundant with bands of about equal intensity. Note that the anti conformer is slightly more stable, according to the calculations, however, this is compensated by the fact that the two gauche conformers exist (gauche+and gauche −), with positive and negative S–C1–C2–C3 dihedral angles, respectively (see Fig. 1). The two conformers are mirror images to each other, show identical infrared spectra and are of course equally abundant in the 2-phenylethylthiol liquid. Comparison between the calculated spectra of 2-phenylethylthiol and of Au4(2-PET)4 in Fig. 2 shows that the spectra of the free 2-phenylethylthiol and bound 2-PET are similar for the corresponding conformers (compare red and blue spectra, respectively). However, the experimental spectrum of the cluster resembles mostly the spectrum of 2-phenylethylthiol in gauche conformation, indicating that the latter plays an important role for the cluster dissolved in CD2Cl2. With this information we turn our attention to the vibrational optical activity.

VCD spectra of Au38(2-PET)24

VCD spectra of the cluster enantiomers are shown in Fig. 3, together with the infrared spectrum of A-Au38(2-PET)24. The infrared spectrum of the other cluster enantiomer C-Au38(2-PET)24 is identical (see Supplementary Fig. 2). Note that the enantiomer eluting first on the HPLC (enantiomer 1) was assigned to A-Au38(2-PET)24 before, based on the comparison between experimental and calculated CD spectra15. The VCD spectra of A- and C-Au38(2-PET)24 show prominent bands associated with the achiral 2-PET ligand. Both the absolute strength of the VCD signals (on the order 10−4) and the anisotropy factors (Δɛ/ɛ=ΔA/A, up to 10−3) are comparable to the ones typically observed for chiral organic molecules, despite the fact that they arise from achiral 2-PET. The significant VCD signals of achiral 2-PET indicate that, once adsorbed on the chiral cluster, the molecule adopts a chiral conformation.

Figure 3: Infrared and VCD spectra of Au38(2-PET)24.
figure3

Infrared spectrum of A-Au38(2-PET)24 (black) and VCD spectra of enantiomer 1 (A-Au38(2-PET)24, red) and of enantiomer 2 (C-Au38(2-PET)24, blue).

The intense bands in the VCD spectra of the cluster at 1,454 and 1,418 cm−1, respectively, are associated with CH2 scissoring coupled to the in-plane phenyl ring vibrations and pure CH2 scissoring modes, respectively. The latter has a particularly high anisotropy factor, that is, it is strong in the VCD but only weak in the infrared spectrum. In contrast, the pure in-plane phenyl ring vibration at 1,495 cm−1 that gives a prominent infrared signal is silent in the VCD. The very intense band at 1,263 cm−1 in the infrared, which shows a prominent VCD signal, is associated with a CH2 wagging/twisting mode, where the CH2 attached to the sulfur is wagging, whereas the other CH2 group is twisting. Note that for 2-PET in the anti conformation the corresponding modes are pure wagging modes. From the analysis it emerges that strong VCD signatures are mainly associated with the CH2 modes.

Comparison with calculated spectra

Using DFT calculations we have systematically investigated the effect of different conformational elements on the VCD spectra of 2-PET using the Au4(2-PET)4 model. The corresponding calculated VCD spectra are shown in Fig. 4. When all four 2-PET molecules adopt anti conformation the calculated VCD signals vanish (not shown). In contrast, when the 2-PET molecules adopt gauche conformation significant VCD signals are apparent, particularly in vibrations associated with the CH2 modes mentioned above. This indicates that the most important conformational degree of freedom for the VCD spectra is the dihedral angle around the CH2–CH2 bond (S–C1–C2–C3 dihedral angle, see definition in Fig. 1). The conformational degree of freedom around the S–C bond (dihedral angle around the S–C bond) has only a minor effect on the VCD spectra. This is underlined by a comparison between calculated VCD spectra (a) and (b) in Fig. 4, of two different Au4(2-PET)4 structures that differ in the dihedral angles around the S–C bonds. The influence of the orientation of the phenyl ring (with respect to the CH2–CH2 group, dihedral angle C1–C2–C3–C4) on the VCD spectra is more difficult to assess. In free 2-phenylethylthiol there is only one minimum on the potential energy surface of this degree of freedom and the C1–C2–C3–C4 dihedral angle (see Fig. 1) is 90° for the anti conformer and close to 100° for the gauche conformer. However, the potential energy surface in this coordinate is shallow and therefore the orientation of the phenyl ring with respect to the CH2–CH2 group is sensitive to intermolecular interactions between neighbouring 2-PET molecules, which certainly play an important role due to the high density of thiolates on the cluster surface. In our Au4(2-PET)4 model the intermolecular interactions play a less prominent role. For example in structure (b) in Fig. 4, the corresponding dihedral angles are between 100° and 110°. To investigate the influence of this structural parameter on the VCD spectra the C1–C2–C3–C4 dihedral angles were fixed at 120° (structure (c)) and 60° (structure (d)), respectively. All other coordinates were relaxed and the VCD spectra calculated. The VCD spectra of structures (b) and (c) are hardly distinguishable. For structure (d), where the phenyl ring is tilted in opposite direction with respect to the CH2–CH2 bond, the VCD spectrum changes. Particularly the weak in-plane ring vibrations slightly above 1,600 cm−1 and the intense wagging/twisting mode around 1,263 cm−1 change sign. Importantly, the pure scissoring modes around 1,418 cm−1 stays positive in the calculated VCD spectrum, showing that the sign of this mode depends solely on the S–C1–C2–C3 dihedral angle.

Figure 4: VCD spectra of calculated structures.
figure4

Experimental VCD spectrum of A-Au38(2-PET)24 compared with calculated VCD spectra of Au4(2-PET)4 in different conformations (ad). The corresponding structures are also shown. Structures a and b differ in some of the dihedral angles around the S–C bond. Structures b, c and d differ in the orientation of the phenyl ring (C1–C2–C3–C4 dihedral angle, see Fig. 1). See text for more information.

Discussion

Both infrared and VCD spectra of the cluster show that a significant fraction of the adsorbed 2-PET molecules adopts gauche conformation in solution. VCD furthermore clearly shows that the abundance of the two possible forms of gauche conformations (gauche+and gauche−; positive or negative S–C1–C2–C3 dihedral angle) is unbalanced. For the free thiol the two forms are equally abundant (and interconvert fast) and no VCD signal can be observed (the molecule is achiral). However, the VCD of the transiently chiral gauche conformers of the free thiol can be calculated (see Supplementary Fig. 5) and the spectra resemble the ones calculated for Au4(2-PET)4. Once adsorbed on the cluster the latter transfers its chirality to the molecule and one of the two gauche conformers becomes more stable than the other. Figure 5 shows qualitative good agreement between the experimental VCD spectrum of enantiomer 1 (A-Au38(2-PET)24) and a superposition of the calculated VCD spectra of structures (a), (c) and (d) (with relative weights 6, 75 and 19%). This shows that the left-handed cluster ((A-Au38(2-PET)24) induces a positive S–C1–C2–C3 dihedral angle (gauche +) in the 2-PET.

Figure 5: Comparison between experimental and calculated VCD spectra.
figure5

Comparison between the experimental VCD spectrum of A-Au38(2-PET)24 and a spectrum that was obtained from a linear combination of calculated VCD spectra of structures (a), (c) and (d) (with relative weights 6, 75 and 19%). A structure of A-Au38(2-PET)24 is also shown (core Au atoms: orange, staple Au atoms: orange, sulfur: green, 2-PET is omitted for clarity). The preferred gauche conformation of 2-PET on A-Au38(2-PET)24 is shown at the top of the Fig. It should be noted that whereas the Au–S framework is chiral for the Au38(2-PET)24 cluster it is achiral for the Au4(2-PET)4 model used for the calculation. However, the Au–S vibrations are very low in energy and therefore large contributions from that chirality are not expected in the spectral range considered here.

It is important to note that the conformational analysis done here refers to the solution structure of the cluster. In fact, the infrared spectra provide clear evidence that solution and solid-state structures are different with respect to the conformation of the 2-PET ligand. In the solution spectrum of the cluster the strong band at 1,263 cm−1 indicates a predominance of gauche conformers. In contrast, in the solid state of the racemic mixture strong bands at 1,220 and 1,310 cm−1 indicate a much larger fraction of anti conformers (Supplementary Fig. 6). Interestingly, in the solid of the enantiopure sample the fraction of gauche to anti conformers is again different (Supplementary Fig. 6). This shows that packing forces in the solid-state influence the conformation of the 2-PET ligand.

In summary, VCD measurements reveal a chirality transfer from an intrinsically chiral metal particle or cluster to the adsorbed achiral molecules. This is the first direct observation of chirality transfer of this kind. Chirality transfer via hydrogen bonding and other intermolecular interactions has been evidenced before31,32 and is an issue in many important fields of modern chemistry ranging from supramolecular chemistry33 to catalysis34. Note that in vibrational optical activity the term ‘chirality transfer’ is used if an achiral structure shows optical activity due to its interaction with a chiral environment31,32. The optical activity observed in our case arises due to a mirror symmetry breaking, which favours one enantiomer of a transiently chiral molecule. Interestingly, in coordination chemistry organic ligands with defined configuration are used to transfer the chiral information to the metal centre35. In the system studied here it is in contrast the metal particle that transfers its chirality to the organic molecule.

Methods

Isolation, characterization and enantioseparation of Au38(2-PET)24

The Au38(2-PET)24 cluster was prepared and purified according to previously reported protocols36,37. In brief, tetrachloroauric acid and L-glutathione were dissolved in acetone and reduced by sodium borohydride. The resulting clusters were then dissolved in water and a mixture of ethanol and toluene and 2-phenylethylthiol was added. Heating to 80 °C gave a mixture of Aun(2-PET)m (n: 25–144, m=18–60) containing Au38(2-PET)24 as major cluster. Excess thiol was removed by extensive methanol washing and the crude clusters were size-selected by size exclusion chromatography. For more details see Supplementary Methods.

The pure Au38(2-PET)24 clusters were characterized by matrix-assisted laser desorption/ionization mass spectrometry and ultraviolet–visible spectroscopy (see Supplementary Fig. 1), which showed the characteristic mass and optical transitions of the cluster. Enantiomers of the cluster were then separated on a chiral cellulose-based semi-preparative column using n-hexane/i-propanol (80/20) as eluent. The two enantiomers of the cluster were collected in several HPLC runs. CD spectra of the separated clusters (Supplementary Fig. 3) are identical to the ones reported before15.

Infrared and VCD of Au38(2-PET)24

For infrared and VCD experiments the clusters (anticlockwise and clockwise versions of Au38(2-PET)24, respectively) were dissolved in CD2Cl2 at a concentration of 10 mg in 180 microliter and measured in a sealed transmission cell equipped with CaF2 windows and 200 μm metal spacer at room temperature. For comparison the infrared spectrum of neat 2-phenylethylthiol was also measured in a sealed NaCl cell. Infrared and VCD spectra of the cluster were recorded on a Bruker PMA 50 accessory coupled to a Tensor 27 Fourier transform infrared spectrometer.

DFT calculations

The geometry optimizations, vibrational frequencies, infrared absorption and VCD intensities were performed by DFT. For the gold atoms an effective core potential was used. The calculations were performed using the b3pw91 functional and a LanL2DZ basis set for Au and a 6-31G(d,p) basis set for all other atoms.

Additional Information

How to cite this article: Dolamic, I. et al. Chirality transfer from gold nanocluster to adsorbate evidenced by vibrational circular dichroism. Nat. Commun. 6:7117 doi: 10.1038/ncomms8117 (2015).

References

  1. 1

    Garzón, I. L. et al. Chirality in bare and passivated gold nanoclusters. Phys. Rev. B 66, 073403 (2002).

    Article  ADS  Google Scholar 

  2. 2

    Gautier, C. & Burgi, T. Chiral gold nanoparticles. Chem. Phys. Chem. 10, 483–492 (2009).

    CAS  Article  Google Scholar 

  3. 3

    Knoppe, S. & Burgi, T. Chirality in thiolate-protected gold clusters. Acc. Chem. Res. 47, 1318–1326 (2014).

    CAS  Article  Google Scholar 

  4. 4

    Noguez, C. & Garzon, I. L. Optically active metal nanoparticles. Chem. Soc. Rev. 38, 757–771 (2009).

    CAS  Article  Google Scholar 

  5. 5

    Schaaff, T. G. & Whetten, R. L. Giant gold-glutathione cluster compounds: intense optical activity in metal-based transitions. J. Phys. Chem. B 104, 2630–2641 (2000).

    CAS  Article  Google Scholar 

  6. 6

    Yao, H., Fukui, T. & Kimura, K. Chiroptical responses of D-/L-penicillamine-capped gold clusters under perturbations of temperature change and phase transfer. J. Phys. Chem. C 111, 14968–14976 (2007).

    CAS  Article  Google Scholar 

  7. 7

    Yao, H., Miki, K., Nishida, N., Sasaki, A. & Kimura, K. Large optical activity of gold nanocluster enantiomers induced by a pair of optically active penicillamines. J. Am. Chem. Soc. 127, 15536–15543 (2005).

    CAS  Article  Google Scholar 

  8. 8

    Gautier, C. & Bürgi, T. Chiral inversion of gold nanoparticles. J. Am. Chem. Soc. 130, 7078–7084 (2008).

    Article  Google Scholar 

  9. 9

    Gautier, C. & Burgi, T. Chiral N-isobutyryl-cysteine protected gold nanoparticles: preparation, size selection, and optical activity in the UV–vis and infrared. J. Am. Chem. Soc. 128, 11079–11087 (2006).

    CAS  Article  Google Scholar 

  10. 10

    Xu, Q. et al. Chiral 38-gold-atom nanoclusters: synthesis and chiroptical properties. Small 10, 1008–1014 (2013).

    Article  Google Scholar 

  11. 11

    Zeng, C., Li, T., Das, A., Rosi, N. L. & Jin, R. Chiral structure of thiolate-protected 28-gold-atom nanocluster determined by X-ray crystallography. J. Am. Chem. Soc. 135, 10011–10013 (2013).

    CAS  Article  Google Scholar 

  12. 12

    Zhu, M. et al. Chiral Au nanospheres and nanorods: synthesis and insight into the origin of chirality. Nano Lett. 11, 3963–3969 (2011).

    CAS  Article  ADS  Google Scholar 

  13. 13

    Jadzinsky, P. D., Calero, G., Ackerson, C. J., Bushnell, D. A. & Kornberg, R. D. Structure of a thiol monolayer-protected gold nanoparticle at 1.1A resolution. Science 318, 430–433 (2007).

    CAS  Article  ADS  Google Scholar 

  14. 14

    Qian, H., Eckenhoff, W. T., Zhu, Y., Pintauer, T. & Jin, R. Total structure determination of thiolate-protected Au38 nanoparticles. J. Am. Chem. Soc. 132, 8280–8281 (2010).

    CAS  Article  Google Scholar 

  15. 15

    Dolamic, I., Knoppe, S., Dass, A. & Bürgi, T. First enantioseparation and circular dichroism spectra of Au38 clusters protected by achiral ligands. Nat. Commun. 3, 798 (2012).

    Article  ADS  Google Scholar 

  16. 16

    Knoppe, S., Dolamic, I., Dass, A. & Burgi, T. Separation of enantiomers and CD spectra of Au40(SCH2CH2Ph)24: spectroscopic evidence for intrinsic chirality. Angew. Chem. Int. Edit. 51, 7589–7591 (2012).

    CAS  Article  Google Scholar 

  17. 17

    Knoppe, S. et al. Chiral phase transfer and enantioenrichment of thiolate-protected Au-102 clusters. J. Am. Chem. Soc. 136, 4129–4132 (2014).

    CAS  Article  Google Scholar 

  18. 18

    Walter, M. et al. A unified view of ligand-protected gold clusters as superatom complexes. Proc. Natl Acad. Sci. 105, 9157–9162 (2008).

    CAS  Article  ADS  Google Scholar 

  19. 19

    Hakkinen, H. The gold-sulfur interface at the nanoscale. Nat. Chem. 4, 443–455 (2012).

    Article  Google Scholar 

  20. 20

    Hakkinen, H., Walter, M. & Gronbeck, H. Divide and protect: capping gold nanoclusters with molecular gold-thiolate rings. J. Phys. Chem. B 110, 9927–9931 (2006).

    Article  Google Scholar 

  21. 21

    Hostetler, M. J., Templeton, A. C. & Murray, R. W. Dynamics of place-exchange reactions on monolayer-protected gold cluster molecules. Langmuir 15, 3782–3789 (1999).

    CAS  Article  Google Scholar 

  22. 22

    Lee, D., Donkers, R. L., Wang, G. L., Harper, A. S. & Murray, R. W. Electrochemistry and optical absorbance and luminescence of molecule-like Au-38 nanoparticles. J. Am. Chem. Soc. 126, 6193–6199 (2004).

    CAS  Article  Google Scholar 

  23. 23

    Jans, H. & Huo, Q. Gold nanoparticle-enabled biological and chemical detection and analysis. Chem. Soc. Rev. 41, 2849–2866 (2012).

    CAS  Article  Google Scholar 

  24. 24

    Nafie, L. A., Keiderling, T. A. & Stephens, P. J. Vibrational circular dichroism. J. Am. Chem. Soc. 98, 2715–2723 (1976).

    CAS  Article  Google Scholar 

  25. 25

    Gautier, C. & Burgi, T. Vibrational circular dichroism ofN-acetyl-l-cysteine protected gold nanoparticles. Chem. Commun. 5393–5395 (2005).

  26. 26

    Gautier, C. & Burgi, T. Vibrational circular dichroism of adsorbed molecules: BINAS on gold nanoparticles. J. Phys. Chem. C 114, 15897–15902 (2010).

    CAS  Article  Google Scholar 

  27. 27

    Yao, H., Nishida, N. & Kimura, K. Conformational study of chiral penicillamine ligand on optically active silver nanoclusters with IR and VCD spectroscopy. Chem. Phys. 368, 28–37 (2010).

    CAS  Article  Google Scholar 

  28. 28

    Borho, N. & Xu, Y. J. Lock-and-key principle on a microscopic scale: the case of the propylene oxide - ethanol complex. Angew. Chem. Int. Edit. 46, 2276–2279 (2007).

    CAS  Article  Google Scholar 

  29. 29

    Zehnacker, A. & Suhm, M. A. Chirality recognition between neutral molecules in the gas phase. Angew. Chem. Int. Edit. 47, 6970–6992 (2008).

    CAS  Article  Google Scholar 

  30. 30

    Dolamic, I., Varnholt, B. & Burgi, T. Far-infrared spectra of well-defined thiolate-protected gold clusters. Phys. Chem. Chem. Phys. 15, 19561–19565 (2013).

    CAS  Article  Google Scholar 

  31. 31

    Sadlej, J., Dobrowolski, J. C. & Rode, J. E. VCD spectroscopy as a novel probe for chirality transfer in molecular interactions. Chem. Soc. Rev. 39, 1478–1488 (2010).

    CAS  Article  Google Scholar 

  32. 32

    Merten, C. & Xu, Y. J. Chirality transfer in a methyl lactate-ammonia complex observed by matrix-isolation vibrational circular dichroism spectroscopy. Angew. Chem. Int. Edit. 52, 2073–2076 (2013).

    CAS  Article  Google Scholar 

  33. 33

    Hembury, G. A., Borovkov, V. V. & Inoue, Y. Chirality-sensing supramolecular systems. Chem. Rev. 108, 1–73 (2008).

    CAS  Article  Google Scholar 

  34. 34

    Sengupta, S. & Shi, X. D. Recent advances in asymmetric gold catalysis. Chem. Cat. Chem. 2, 609–619 (2010).

    CAS  Google Scholar 

  35. 35

    Crassous, J. Chiral transfer in coordination complexes: towards molecular materials. Chem. Soc. Rev. 38, 830–845 (2009).

    CAS  Article  Google Scholar 

  36. 36

    Knoppe, S., Dharmaratne, A. C., Schreiner, E., Dass, A. & Burgi, T. Ligand exchange reactions on Au(38) and Au(40) clusters: a combined circular dichroism and mass spectrometry study. J. Am. Chem. Soc. 132, 16783–16789 (2010).

    CAS  Article  Google Scholar 

  37. 37

    Knoppe, S., Boudon, J., Dolamic, I., Dass, A. & Burgi, T. Size exclusion chromatography for semipreparative scale separation of Au38(SR)24 and Au40(SR)24 and larger clusters. Anal. Chem. 83, 5056–5061 (2011).

    CAS  Article  Google Scholar 

Download references

Acknowledgements

We gratefully acknowledge the financial support from the University of Geneva and the Swiss National Science Foundation (grant numbers 200021_135349/1, 200020_152596).

Author information

Affiliations

Authors

Contributions

B.V. prepared the clusters. I.D. separated the clusters and performed the VCD measurement. T.B. designed the concept of the work and performed the calculations. All the authors contributed to the writing of the manuscript. The project was supervised by T.B.

Corresponding author

Correspondence to Thomas Bürgi.

Ethics declarations

Competing interests

The authors declare no competing financial interests.

Supplementary information

Supplementary Information

Supplementary Figures 1-6, Supplementary Table 1, Supplementary Methods and Supplementary References (PDF 576 kb)

Rights and permissions

This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Dolamic, I., Varnholt, B. & Bürgi, T. Chirality transfer from gold nanocluster to adsorbate evidenced by vibrational circular dichroism. Nat Commun 6, 7117 (2015). https://doi.org/10.1038/ncomms8117

Download citation

Further reading

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing