Journal of Chemistry

Volume 2013 (2013), Article ID 780939, 4 pages

http://dx.doi.org/10.1155/2013/780939

Research Article

Protected Gold Nanoparticles with Thioethers and Amines As Surrogate Ligands

M. Rafiq H. Siddiqui

Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia

Received 1 February 2012; Revised 17 April 2012; Accepted 17 April 2012

Academic Editor: Concha Gimeno

Copyright © 2013 M. Rafiq H. Siddiqui. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Dodecyl sulfide, dodecyl amine, and hexylamine were shown to act as surrogate ligands (L) via metastable gold nanoparticles. By collating analytical and spectroscopic data obtained simultaneously, empirical formula Au₂₄L was assigned. These impurity-free nanoparticles obtained in near quantitative yields showing exceptional gold assays (up to 98%Au) were prepared by a modification of the two-phase method. Replacement reactions on the Au₂₄L showed that Au:L ratios may be increased (up to Au₅₅:L (L= (H₂₅C₁₂)₂S)) or decreased (Au₁₂:L (L= H₂NC₁₂H₂₅ and H₂NC₆H₁₃)) as desired. This work encompassing the role of analytical techniques used, that is, elemental analysis, variable temperature ¹H NMR, FAB mass spectrometry, UV-Vis spectroscopy, thin film X-ray diffraction, and high-resolution electron microscopy (HREM) has implications in the study of size control, purity, stability, and metal assays of gold nanoparticles.

1. Introduction

Nanoparticles are the building blocks for nanostructures that have applications ranging from corrosion science to molecular recognition and nanotechnology. The progress reported so far to derive maximum electronic function from nanoparticles appears to be impeded by limitations in controlling their size and sometimes difficulties in freeing them from impurities or instability.

Attempts are continuing from physicists, chemists, and biologists to use monolayer protected clusters [1] (MPCs, nanoparticles) as building blocks in sensor and other devices [1–4]. However, the composition and concomitant molecular electronic properties of MPCs seem difficult to control because of size distribution, the nature of self-assembly, differences in preparative techniques, and sometimes instability. Processes developed to make monodisperse or size-controlled gold nanoparticles have been outlined [5, 6]. Recently, the merits and potential of using ligands (L) such as thioether and amines [7, 8] were discussed, and comparisons with thiol-capped gold nanoparticles have been made. Progress in this direction seems to be limited by challenges in synthesizing the pure analogues and exploiting them due to instability [7–9]. Due to our continued interest in gold chemistry and specially its applications in catalysis [10–14], we have been studying methods of synthesizing and stabilizing gold nanoparticles. Herein, methods to obtain gold nanoparticles with high metal content and purity, using them as preparatively convenient but readily replaceable (surrogate) ligands, are described. The importance of concurrent spectroscopic, analytical, and structural studies is emphasized. On this basis empirical formulae Au₂₄(S(C₁₂H₂₅)₂), Au₂₄(NH₂C₁₂H₂₅), and Au₂₄(NH₂C₆H₁₃) were assigned. These nanoparticles were metastable, which could be converted into both particles of higher Au:L or lower Au:L ratios.

2. Experimental

2.1. Synthetic Procedure

The preparation of dodecyl sulphide-capped gold nanoparticles typifies the synthetic procedure. Addition of dodecyl sulfide (0.028 g, 0.075 mmol) to a red toluene solution (25 mL) from the phase transfer reaction between HAuCl₄·3H₂O (0.147 g, 0.373 mmol) and [N(C₈H₁₇)4]Br (0.245 g, 0.448 mmol) showed no visible change in colour. This was added dropwise (15 min) to a gently stirred freshly prepared aqueous (100 mL) solution of NaBH₄ (0.138 g, 3.732 mmol). From the first addition, a dense ruby red organic layer begins to form, and after 2 h, the aqueous phase was rejected. The organic layer was washed gently with water (2 × 50 mL) and dried over MgSO₄ (5 g) and the total volume reduced to 15 mL by evaporation at room temperature to give a fine black lustrous solid in 2 h. The colourless mother liquor was decanted and the product washed with EtOH (3 × 50 mL), decanted and dried in air. Yield 75 mg (95% based on gold).

Following the same procedure and using an 8-fold excess of hexylamine, Au₂₄(H₂NC₆H₁₃) was obtained only in 43% yield (22 mg) (i.e., [N(C₈H₁₇)₄][AuBr₄] (0.250 g, 0.254 mmol, in toluene, 20 mL; NH₂C₆H₁₃ 0.205 g, 0.28 mL, 2.03 mmol; NaBH₄ 0.1 g, 2.7 mmol, in water 200 mL)).

Au₃L (L= HSC₁₂H₂₅), the prototype gold nanoparticles were prepared by the two-phase method of Brust et al. [1]. Au₂₄L (L= (C₁₂H₂₅)₂S, H₂NC₁₂H₂₅ and H₂NC₆H₁₃) reported in this paper were prepared by a modification of the two-phase method. Au₂₄(S(C₁₂H₂₅)₂) and its derivatives, Aux(S(C₁₂H₂₅)₂) where X = 26, 30, 55 having empirical compositions of Au₂₆(S(C₁₂H₂₅)₂), Au₃₀(S(C₁₂H₂₅)₂) and Au₅₅(S(C₁₂H₂₅)₂) and its precursor, [N(C₈H₁₇)₄][AuBr₄], and dodecyl sulfide are described.

2.2. Analytical Techniques

¹H NMR spectra were recorded on a Bruker Avance 400 MHz spectrometer. 5 to 10 mg of sample of the gold nanoparticles dissolved in 0.7 mL of the appropriate solvent was examined using 5 mm NMR tubes. The spectra were recorded straight away or at intervals described. Mass spectra (FAB +ve) were obtained according to previously reported methods [15]. The sulfur content was determined on a spectrociros charged chip detector ICP atomic emission spectrometer. Carbon, hydrogen, and nitrogen were analyzed on Carlo Erba Instruments Co. elemental analyser (Model 1106). Gold analyses were carried out from samples digested in aqua regia and the metal estimated against a BDH standard by atomic absorption spectroscopy. The halogens were determined by potentiometric titrations using AgNO₃ solutions. Powder XRD patterns were obtained using a Siemens D5005 X-ray diffractometer. Data was collected in the 36–110 (2θ) range with a step scan of 2θ = 0.036 and a step size of 1 s. using Co Kα    radiation. Thin solid films were prepared from freshly made and analyzed samples of Au₂₄(S(C₁₂H₂₅)₂) and Au₂₄(H₂NC₁₂H₂₅), and a saturated solution in CHCl₃ containing 50 mg/mL and 25 mg/mL, respectively, was deposited with a micropipette on a transparent glass disc (dia. 16 mm) to obtain uniform translucent films. The red solution which on drying spontaneously leaves lustrous golden sheen was subjected to the X-rays immediately or periodically as required. In order to ensure that the nanoparticle aggregation was not influenced by the X-ray beam, thin films aged separately in air were also examined. The observed diffraction patterns correspond to fcc gold based on the bulk lattice constants (powder diffraction file 04-0784) for the type of radiation used (Co kα). A sample of gold dust (BDH) was also examined (48.7 nm) and used as a further reference. The size of the nanoparticles was calculated from the diffraction peak line-width broadening using the Scherrer equation. Samples for electron microscopy examination were dispersed in a dry state onto a holey carbon film supported on a 3.05 mm diameter Cu mesh grid. High-resolution electron microscopy (HREM) was performed in a JEOL 2000EX microscope operating at 200 kV.

3. Results and Discussion

All nanoparticles were formulated based on elemental analysis and FAB mass. The air-dried product for the dodecyl sulphide-, dodecyl amine-, and hexylamine-capped gold nanoparticles were analyzed immediately and simultaneously by ¹H NMR, elemental analysis and +ve FAB mass spectrometry to confirm total exclusion of free ligand [N(C₈H₁₇)₄]Br, halides and solvent(s). The elemental analysis data and FAB mass of various gold compounds are given below.

Analysis for Au₂₄(S(C₁₂H₂₅)₂) C: 5.8; H: 0.9; S: 0.6 and Au: 92.6% an average empirical formula of Au₂₄(S(C₁₂H₂₅)₂) would require C 5.65; H: 0.99; S 0.63 and Au: 92.73%. MS (70 eV) (FAB +ve): m/z(%) 371.4 (100) {S(C₁₂H₂₅)₂ + H]+, 369.4 (85%) [S(C₁₂H₂₅)₂–H]+.

Analysis for Au₂₄(H₂NC₁₂H₂₅) C: 3.01; H: 0.52; N: 0.26 and Au: 95.9%. Au₂₄(H₂NC₁₂H₂₅) would require C: 2.94; H: 0.55; N: 0.28 and Au: 96.22%. MS (70 eV): m/z(%): 186.2 (100) [C₁₂H₂₅N+ H₃], 184.2 (85%) [C₁₂H₂₅N+H₂–H].

Analysis for Au₂₄(H₂NC₆H₁₃) C: 1.39; H: 0.30, N: 0.28 and Au: 98.2% Au₂₄(H₂NC₆H₁₃) would require C: 1.49, H: 0.31, N: 0.29 and Au: 97.9%. Ms (70 eV): m/z(%): 102.1 (100) [C₆H₁₃N⁺H₃], 100.1 (20%) [C₆H₁₃N⁺H₂–H].

Analysis for Au₂₄(H₂NC₆H₁₃) C: 1.39; H: 0.30; N: 0.28 and Au: 98.2%. Au₂₄(H₂NC₆H₁₃) would require C: 1.49; H: 0.31; N: 0.29 and Au: 97.9%. MS (70 eV); m/z(%): 102.1 (100) [C₆H₁₃N+H₃], 100.1 (20%) [C₆H₁₃N+H₂–H].

The presence of MPCs was confirmed by the characteristic peak at 525 nm in the Uv-Vis spectra (shown in Figure 1) and that of the bound ligand was determined by the broad features in the ¹H NMR (CDCl₃ solution). Empirical formulae Au₂₄(S(C₁₂H₂₅)₂), Au₂₄(H₂NC₁₂H₂₅), and Au₂₄(H₂NC₆H₁₃) were based on reproducible analytical and spectroscopic data.

Figure 1: The Uv-Vis spectra of (a) Au₂₄(S(C₁₂H₂₅)₂) and (b) Au₂₄(₂HNC₁₂H₂₅) in toluene showing the peak at 525 nm.

The high-resolution electron microscopy (HREM) of Au₂₄(S(C₁₂H₂₅)₂) (Figure 2) showed that the nanoparticles were uniform in shape and have a size of 3–5 nm diameter.

Figure 2: The HREM micrograph of Au₂₄(S(C₁₂H₂₅)₂) nanoparticles.

3.1. Properties and Storage Techniques for Au₂₄L

Au₂₄(S(C₁₂H₂₅)₂), Au₂₄(H₂NC₁₂H₂₅), and Au₂₄(H₂NC₆H₁₃) are insoluble in water, acetonitrile, dichloromethane, ethanol, and acetone but soluble in hexane, benzene, toluene, and tetrahydrofuran and extremely soluble in chloroform to give intensely red solutions. Their saturated solutions (unlike the thiol-capped analogues) when evaporated on flat glass or metal surfaces spontaneously formed lustrous golden films. Figure 3 shows X-ray diffraction pattern of thin films of Au₂₄(S(C₁₂H₂₅)₂) nanoparticles measured fresh and after one hour. The crystallite sizes as calculated by the Scherrer equation were between 5–15 nm for different samples, which is in very good agreement with the microscopy data. All these MPCs can be kept unchanged in the solid state for few hours but aggregate irreversibly unless completely covered in ethanol and in this way can be stored for several months.

Figure 3: X-ray diffraction of thin film of Au₂₄(S(C₁₂H₂₅)₂) nanoparticles: (a) fresh, (b) after 1 h.

3.2. Chemistry of Metastable Gold Nanoparticles

The significance of selecting thioether and amines for ligand capping to gold cores has been outlined previously [16]. A modified two-phase method was employed here under extremely gentle conditions and using ratios of ligand (L = (C₁₂H₂₅)₂S, (C₆H₁₃)₂S, H₂NC₁₂H₂₅ and H₂NC₆H₁₃) and [N(C₈H₁₇)₄]Br to Au considerably smaller than is conventionally reported. The reduction process was conducted at the interphase by dropwise addition of AuIII and L containing reaction mixture in toluene into aqueous NaBH₄. Due to the relatively weaker coordinating ability of thioether and amine ligands in nanoparticles compared to thiols, it was found necessary to avoid vigorous stirring or any other mechanical stress that might cause ligand desorption, such as removal of solvent under reduced pressure (often at elevated temperatures), ultrasonication, vacuum drying, or centrifugation.

3.3. Reagent Stoichiometries and Ligand Strengths

From a range of stoichiometries studied using dodecyl sulfide, at only AuIII : [N(C₈H₁₇)₄]Br : S(C₁₂H₂₅)₂ :  NaBH₄ ratios 1 : 1.2 : 0.2 : 10 impurity-free gold nanoparticles were obtained in 95% yield (based on gold). For the amine-capped MPCs, [N(C₈H₁₇)₄][AuBr₄] was used as the precursor thus permitting lower AuIII:L [N(C₈H₁₇)₄] ratios as low as 1 : 1.

3.4. Thioether and Amines as Surrogate Ligands

Surrogacy of the thioether and amine ligands is clearly demonstrated by treatment of Au₂₄(S(C₁₂H₂₅)₂), Au₂₄(H₂NC₁₂H₂₅), and Au₂₄(H₂NC₆H₁₃) with an 8-fold excess of dodecanethiol. The thiol substituted products that were isolated showing no traces of the parent ligands in their ¹H NMR and FAB +ve spectra. This technique has applications in metal chemical vapour deposition (MCVD) techniques where molecular complexes are purified [17] selectively using the coordination strengths of ligands.

We were unable to obtain hexyl sulphide-capped gold nanoparticles by this method, and yields were roughly halved for hexylamine (43%) compared with dodecylamine (75%), indicating that they are weaker ligands. More work is required for a further understanding of ligand-exchange reactions from soluble metal cores. However, from experimental data available so far for the isolated nanoparticles, we see a stability trend emerging for capped gold MPCs depending upon the coordination strength and steric and inductive effects from the ligands following:

SC₁₂H₂₅ ≫ H₂NC₁₂H25 > S(C₁₂H₂₅)₂ > S(C₁₀H₂₁)₂ > H₂NC₆H₁₃ ≫ [N(C₈H₁₇)₄]Br ≫ S(C₆H₁₃)₂.

4. Conclusions

The formation chemistry and subsequent surface reactions studied give an indication of the nature and strength of bonding in ligand-capped gold nanoparticles, in particular, and may contribute towards further understanding of the dynamics of metal/ligand interactions in self-assembled monolayers in general. This work would open vistas to the role of thioether and amines as surrogate ligands or on their own to provide routes to impurity-free metal-rich, size-controlled and stable gold nanoparticles and for mixed ligand capping.

Acknowledgment

This work is supported by the Research Center, College of Science, King Saud University, Riyadh, Kingdom of Saudi Arabia.

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