One important area remaining to be explored is whether these preassembled AuNPs can be used as structure precursors for fabricating other even more complex Au

nanostructures when surface organics are controllably removed [15–25]. Herein, we devise a new synthetic protocol, which combines both surfactant-assisted assembly and heat-activated attachment, to generate interfacial polygonal patterning of self-assembled nanostructures [15]. In particular, we will use small AuNPs (2 to 5 nm in size) as starting units to fabricate several different kinds of complex gold nanostructures in polygonal patterning with a high morphological yield of 100%. Methods Synthesis of interfacial polygonal patterning via self-assembly of Au nanoparticles Thiol-capped Au seeds were prepared by Brust’s two-phase

method with some minor modifications (see Additional HSP cancer file 1 for the detailed synthesis selleck screening library procedure) [11, 16, 21, 22]. In a typical experiment, two standard units (denoted as STUs) of Au nanoparticles were redissolved in cyclohexane (2 mL for each STU), followed by the addition of PVP (1.25 mM, 0.5 mL in 2-propanol) and DDT (0.11 M, 22 mL in cyclohexane). The obtained mixture was then placed into a Teflon-lined stainless steel autoclave, and the solvothermal synthesis was conducted at 150°C to 210°C for 2 to 14 h in an electric oven. After the reactions, gold products were harvested by centrifuging and dissolved into Tucidinostat nmr ethanol solvent for their stabilization. Detailed preparative parameters adopted in the above experiments can be found in Additional file 1: SI-1. The as-prepared gold nanomaterial products were characterized with transmission electron

microscopy (TEM; JEM2010F, JEOL Ltd., Akishima-shi, Tokyo, Japan) and field-emission Cyclin-dependent kinase 3 scanning electron microscopy (FESEM; JSM-6700F, JEOL Ltd., Akishima-shi). Results and discussion Figure  1a shows an example of Au nanoparticles (2 to 3 nm) packed in hexagonal organization. As building units, AuNPs are organized into interfacial polygonal patterning for the first time, exhibiting a remarkable degree of long-range order. Intriguingly, a distribution of hexagon, pentagon, and complex patterns can be clearly observed (Figure  1b), which had typical lateral dimensions such as scale approximately 500 nm. (Isolated bubbles with radii mostly greater than 300 nm were stable over a period of a few months)Under high magnification (Figure  1c,d), it is more clear that AuNPs are assembled into solid laterals (e.g., thickness 5 to 20 nm) with higher concentrations of AuNP aggregations, while loose dispersed AuNPs are distributed within polygonal patterning. Surprisingly, the internal angles approximately equal to 120° (120° ±1°).