scholarly journals Robust Synthesis of Gold Nanotriangles and their Self‐Assembly into Vertical Arrays

ChemistryOpen ◽  
2019 ◽  
Vol 8 (6) ◽  
pp. 705-711 ◽  
Author(s):  
Piotr Szustakiewicz ◽  
Guillermo González‐Rubio ◽  
Leonardo Scarabelli ◽  
Wiktor Lewandowski
2019 ◽  
Vol 14 (1) ◽  
Author(s):  
Jun Dong ◽  
Xing Zhao ◽  
Wei Gao ◽  
Qingyan Han ◽  
Jianxia Qi ◽  
...  

2010 ◽  
Vol 09 (05) ◽  
pp. 543-547 ◽  
Author(s):  
JUN WANG ◽  
SHIHE CAO ◽  
SIHUA XIA ◽  
NING GAN

Chain-like nickel arrays assembled from magnetic Ni spheres were successfully prepared through a facile hydrothermal process at 200°C under a 0.25 T external magnetic field. The external magnetic field is strongly believed to be the driving force of the self-assembly. The sample was highly crystalline as confirmed by the X-ray diffraction (XRD) patterns. The scanning electron microscope (SEM) and transmission electron microscope (TEM) images show that all Ni spheres are closely interconnected to form chains, with ~ 950 nm in diameter and ~ 1 cm in length, which arrange into vertical arrays on the silicon substrate. The coercivity and remnant magnetization ratio of the sample, 670 Oe and 0.612, respectively, are substantially higher than for the sample prepared without an applied external magnetic field (68 Oe and 0.336). Such enhancements can be attributed to their novel superstructure, shape anisotropy, reduced demagnetization factor, etc. This process can be used to fabricate large arrays of uniform chains of magnetic materials and modulate their magnetic properties.


Nanomaterials ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 581 ◽  
Author(s):  
Guoqing Wang ◽  
Yao Zhang ◽  
Xingguo Liang ◽  
Tohru Takarada ◽  
Mizuo Maeda

As a class of emerging nanoparticles, gold nanotriangles (AuNTs) are characterized by unique structural anisotropy and plasmonic properties. The organization of AuNTs into well-defined architecture potentially promises collective properties that are difficult to produce by individual AuNTs. To date, however, the orientation-controlled self-assembly of AuNTs has been achieved with limited success. Here, we describe an effective and straightforward approach to induce directed self-assembly of AuNTs. By taking advantage of the uneven chemical reactivity of AuNT surfaces, we implement regioselective modification of the edges and the top/bottom surfaces with two different double-stranded DNA (dsDNA) sequences. By means of terminal single base pairing/unpairing, controlled assembly of the dsDNA-modified AuNTs evolves in a face-to-face or edge-to-edge manner based on blunt-end stacking interaction on an intentional region of the AuNTs, along with entropic repulsion by unpaired terminal nucleobases on the other region. This approach could be useful for achieving directed self-assembly of other anisotropic nanoparticles.


Small ◽  
2011 ◽  
Vol 7 (6) ◽  
pp. 781-787 ◽  
Author(s):  
Benjamin D. Smith ◽  
David J. Kirby ◽  
Christine D. Keating

ACS Nano ◽  
2014 ◽  
Vol 8 (6) ◽  
pp. 5833-5842 ◽  
Author(s):  
Leonardo Scarabelli ◽  
Marc Coronado-Puchau ◽  
Juan J. Giner-Casares ◽  
Judith Langer ◽  
Luis M. Liz-Marzán

Author(s):  
D. Reis ◽  
B. Vian ◽  
J. C. Roland

Wall morphogenesis in higher plants is a problem still open to controversy. Until now the possibility of a transmembrane control and the involvement of microtubules were mostly envisaged. Self-assembly processes have been observed in the case of walls of Chlamydomonas and bacteria. Spontaneous gelling interactions between xanthan and galactomannan from Ceratonia have been analyzed very recently. The present work provides indications that some processes of spontaneous aggregation could occur in higher plants during the formation and expansion of cell wall.Observations were performed on hypocotyl of mung bean (Phaseolus aureus) for which growth characteristics and wall composition have been previously defined.In situ, the walls of actively growing cells (primary walls) show an ordered three-dimensional organization (fig. 1). The wall is typically polylamellate with multifibrillar layers alternately transverse and longitudinal. Between these layers intermediate strata exist in which the orientation of microfibrils progressively rotates. Thus a progressive change in the morphogenetic activity occurs.


Author(s):  
M. Kessel ◽  
R. MacColl

The major protein of the blue-green algae is the biliprotein, C-phycocyanin (Amax = 620 nm), which is presumed to exist in the cell in the form of distinct aggregates called phycobilisomes. The self-assembly of C-phycocyanin from monomer to hexamer has been extensively studied, but the proposed next step in the assembly of a phycobilisome, the formation of 19s subunits, is completely unknown. We have used electron microscopy and analytical ultracentrifugation in combination with a method for rapid and gentle extraction of phycocyanin to study its subunit structure and assembly.To establish the existence of phycobilisomes, cells of P. boryanum in the log phase of growth, growing at a light intensity of 200 foot candles, were fixed in 2% glutaraldehyde in 0.1M cacodylate buffer, pH 7.0, for 3 hours at 4°C. The cells were post-fixed in 1% OsO4 in the same buffer overnight. Material was stained for 1 hour in uranyl acetate (1%), dehydrated and embedded in araldite and examined in thin sections.


Author(s):  
Alan S. Rudolph ◽  
Ronald R. Price

We have employed cryoelectron microscopy to visualize events that occur during the freeze-drying of artificial membranes by employing real time video capture techniques. Artificial membranes or liposomes which are spherical structures within internal aqueous space are stabilized by water which provides the driving force for spontaneous self-assembly of these structures. Previous assays of damage to these structures which are induced by freeze drying reveal that the two principal deleterious events that occur are 1) fusion of liposomes and 2) leakage of contents trapped within the liposome [1]. In the past the only way to access these events was to examine the liposomes following the dehydration event. This technique allows the event to be monitored in real time as the liposomes destabilize and as water is sublimed at cryo temperatures in the vacuum of the microscope. The method by which liposomes are compromised by freeze-drying are largely unknown. This technique has shown that cryo-protectants such as glycerol and carbohydrates are able to maintain liposomal structure throughout the drying process.


Author(s):  
M. Sarikaya ◽  
J. T. Staley ◽  
I. A. Aksay

Biomimetics is an area of research in which the analysis of structures and functions of natural materials provide a source of inspiration for design and processing concepts for novel synthetic materials. Through biomimetics, it may be possible to establish structural control on a continuous length scale, resulting in superior structures able to withstand the requirements placed upon advanced materials. It is well recognized that biological systems efficiently produce complex and hierarchical structures on the molecular, micrometer, and macro scales with unique properties, and with greater structural control than is possible with synthetic materials. The dynamism of these systems allows the collection and transport of constituents; the nucleation, configuration, and growth of new structures by self-assembly; and the repair and replacement of old and damaged components. These materials include all-organic components such as spider webs and insect cuticles (Fig. 1); inorganic-organic composites, such as seashells (Fig. 2) and bones; all-ceramic composites, such as sea urchin teeth, spines, and other skeletal units (Fig. 3); and inorganic ultrafine magnetic and semiconducting particles produced by bacteria and algae, respectively (Fig. 4).


Author(s):  
Xiaorong Zhu ◽  
Richard McVeigh ◽  
Bijan K. Ghosh

A mutant of Bacillus licheniformis 749/C, NM 105 exhibits some notable properties, e.g., arrest of alkaline phosphatase secretion and overexpression and hypersecretion of RS protein. Although RS is known to be widely distributed in many microbes, it is rarely found, with a few exceptions, in laboratory cultures of microorganisms. RS protein is a structural protein and has the unusual properties to form aggregate. This characteristic may have been responsible for the self assembly of RS into regular tetragonal structures. Another uncommon characteristic of RS is that enhanced synthesis and secretion which occurs when the cells cease to grow. Assembled RS protein with a tetragonal structure is not seen inside cells at any stage of cell growth including cells in the stationary phase of growth. Gel electrophoresis of the culture supernatant shows a very large amount of RS protein in the stationary culture of the B. licheniformis. It seems, Therefore, that the RS protein is cotranslationally secreted and self assembled on the envelope surface.


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