Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

A facile synthesis of asymmetric hybrid colloidal particles.

ABSTRACT: This paper describes a simple approach to the synthesis of asymmetric, hybrid colloidal particles by precipitation polymerization. The key is to introduce Au or Ag colloids 2 min after (rather than before) starting the polymerization. The hybrid particles were uniform in size, and each one of them only contained one Au (or Ag) nanoparticle in its surface. Due to the simplicity of this procedure, it should be possible to use it for large-scale production. This method can be extended to metal nanoparticles other than Au and Ag and with a range of sizes, as long as they have appropriate stabilizers on the surface.

SUBMITTER: Ohnuma A

PROVIDER: S-EPMC2640490 | biostudies-literature | 2009 Feb

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

A facile synthesis of asymmetric hybrid colloidal particles.

Ohnuma Akira A Cho Eun Chul EC Camargo Pedro H C PH Au Leslie L Ohtani Bunsho B Xia Younan Y

Journal of the American Chemical Society 20090201 4

This paper describes a simple approach to the synthesis of asymmetric, hybrid colloidal particles by precipitation polymerization. The key is to introduce Au or Ag colloids 2 min after (rather than before) starting the polymerization. The hybrid particles were uniform in size, and each one of them only contained one Au (or Ag) nanoparticle in its surface. Due to the simplicity of this procedure, it should be possible to use it for large-scale production. This method can be extended to metal nano ...[more]

PMID: 19140763

Similar Datasets

Laser Fragmentation Synthesis of Colloidal Bismuth Ferrite Particles.

Project description:Laser fragmentation of colloidal submicron-sized bismuth ferrite particles was performed by irradiating a liquid jet to synthesize bismuth ferrite nanoparticles. This treatment achieved a size reduction from 450 nm to below 10 nm. A circular and an elliptical fluid jet were compared to control the energy distribution within the fluid jet and thereby the product size distribution and educt decomposition. The resulting colloids were analysed via UV-VIS, XRD and TEM. All methods were used to gain information on size distribution, material morphology and composition. It was found that using an elliptical liquid jet during the laser fragmentation leads to a slightly smaller and narrower size distribution of the resulting product compared to the circular jet.

| S-EPMC7075302 | biostudies-literature

Synthesis method of asymmetric gold particles.

Project description:Asymmetric particles can exhibit unique properties. However, reported synthesis methods for asymmetric particles hinder their application because these methods have a limited scale and lack the ability to afford particles of varied shapes. Herein, we report a novel synthetic method which has the potential to produce large quantities of asymmetric particles. Asymmetric rose-shaped gold particles were fabricated as a proof of concept experiment. First, silica nanoparticles (NPs) were bound to a hydrophobic micro-sized polymer containing 2-chlorotritylchloride linkers (2-CTC resin). Then, half-planar gold particles with rose-shaped and polyhedral structures were prepared on the silica particles on the 2-CTC resin. Particle size was controlled by the concentration of the gold source. The asymmetric particles were easily cleaved from the resin without aggregation. We confirmed that gold was grown on the silica NPs. This facile method for synthesizing asymmetric particles has great potential for materials science.

| S-EPMC5462826 | biostudies-literature

Like-charge interactions between colloidal particles are asymmetric with respect to sign.

Project description:Two-dimensional dispersions of colloidal particles with a range of surface chemistries and electrostatic potentials are characterized under a series of solution ionic strengths. A combination of optical imaging techniques are employed to monitor both the colloid structure and the electrostatic surface potential of individual particles in situ. We find that like-charge multiparticle interactions can be tuned from exclusively repulsive to long-range attractive by changing the particle surface composition. This behavior is strongly asymmetric with respect to the sign of the surface potential. Collective long-range attractive interactions are only observed among negatively charged particles.

| S-EPMC4161288 | biostudies-literature

Facile self-assembly of colloidal diamond from tetrahedral patchy particles via ring selection.

Project description:Diamond-structured crystals, particularly those with cubic symmetry, have long been attractive targets for the programmed self-assembly of colloidal particles, due to their applications as photonic crystals that can control the flow of visible light. While spherical particles decorated with four patches in a tetrahedral arrangement-tetrahedral patchy particles-should be an ideal building block for this endeavor, their self-assembly into colloidal diamond has proved elusive. The kinetics of self-assembly pose a major challenge, with competition from an amorphous glassy phase, as well as clathrate crystals, leaving a narrow widow of patch widths where tetrahedral patchy particles can self-assemble into diamond crystals. Here we demonstrate that a two-component system of tetrahedral patchy particles, where bonding is allowed only between particles of different types to select even-member rings, undergoes crystallization into diamond crystals over a significantly wider range of patch widths conducive for experimental fabrication. We show that the crystallization in the two-component system is both thermodynamically and kinetically enhanced, as compared to the one-component system. Although our bottom-up route does not lead to the selection of the cubic polytype exclusively, we find that the cubicity of the self-assembled crystals increases with increasing patch width. Our designer system not only promises a scalable bottom-up route for colloidal diamond but also offers fundamental insight into crystallization into open lattices.

| S-EPMC8640719 | biostudies-literature

Purposefully Designed Surfactants for Facile and Controllable Gold Colloidal Nanocrystal Synthesis.

Project description:Three new cationic surfactants-N-cetyl-bis(2-dimethylaminoethyl)ether bromide (CBDEB), N-dodecyl-bis(2-dimethylaminoethyl)ether bromide (DBDEB), and N-hexyl-bis(2-dimethylaminoethyl)ether bromide (HBDEB)-have been designed herein using a simple and tailorable synthesis route. CBDEB and DBDEB, the 16- and 12-carbon chain surfactants, demonstrate facile, rapid, and controllable aqueous syntheses of gold nanoparticles (AuNPs) as dual-action reducing and capping agents. The synthesis strategy, using only surfactant and HAuCl4 salt, and 4 min of heating at 80 °C, results in spherical AuNPs (average diameters of 13.4 ± 3.8 nm for CBDEB and 12.0 ± 3.8 nm for DBDEB). Microwave irradiation was also investigated as a heating method and produces AuNPs in as little as 30 s. Control over the size and shape of AuNPs was proven to be feasible (toward populations of Euclidean shapes) by appropriately tuning reaction parameters, such as the molar ratio of surfactant to Au3+, temperature, incorporation of a time delay before heating, or shape control agents, such as Cu2+. Frustratingly, the cytotoxicity of CBDEB is similar to that of cetyltrimethylammonium bromide (CTAB), a popular 16-carbon chain cationic surfactant. Notably, while the shorter HBDEB (6-carbon chain) does not produce AuNPs under the applied conditions, it does appear to improve cell viability upon cytotoxicity evaluation and may be favorable as a new biological surfactant.

| S-EPMC10633875 | biostudies-literature

A facile synthesis of dynamic, shape-changing polymer particles.

Project description:We herein report a new facile strategy to ellipsoidal block copolymer nanoparticles that exhibit a pH-triggered anistropic swelling profile. In a first step, elongated particles with an axially stacked lamellae structure are selectively prepared by utilizing functional surfactants to control the phase separation of symmetric polystyrene-b-poly(2-vinylpyridine) (PS-b-P2VP) in dispersed droplets. In a second step, the dynamic shape change is realized by cross-linking the P2VP domains, thereby connecting glassy PS discs with pH-sensitive hydrogel actuators.

| S-EPMC4074252 | biostudies-literature

Hybrid hollow silica particles: synthesis and comparison of properties with pristine particles.

Project description:In the past decade, interest in hollow silica particles has grown tremendously because of their applications in diverse fields such as thermal insulation, drug delivery, battery cathodes, catalysis, and functional coatings. Herein, we demonstrate a strategy to synthesize hybrid hollow silica particles having shells made of either polymer-silica or carbon-silica. Hybrid shells were characterized using electron microscopy. The effect of hybrid shell type on particle properties such as thermal and moisture absorption was also investigated.

| S-EPMC9054576 | biostudies-literature

Merging gold and organocatalysis: a facile asymmetric synthesis of annulated pyrroles.

Project description:The combination of cinchona-alkaloid-derived primary amine and Au(I) -phosphine catalysts allowed the selective C-H functionalization of two adjacent carbon atoms of pyrroles under mild reaction conditions. This sequential dual activation provides seven-membered-ring-annulated pyrrole derivatives in excellent yields and enantioselectivities.

| S-EPMC4238261 | biostudies-literature

Facile Synthesis of Asymmetric aza-Boron Dipyrromethene Analogues Bearing Quinoxaline Moiety.

Project description:An asymmetric aza-BODIPY analogue bearing quinoxaline moiety was synthesized via a titanium tetrachloride-mediated Schiff-base-forming reaction of 6,7-dimethyl-1,4-dihydroquinoxaline-2,3-dione and benzo[d]thiazol-2-amine. This novel aza-BODIPY analogue forms a complementary hydrogen-bonded dimer due to the quinoxaline moiety in the crystal structure. It also shows intense absorption and fluorescence, with fluorescence quantum yields close to unity. The electrochemical measurements and the DFT calculations revealed the presence of the low-lying HOMO, which benefits their potential applications as an electron-transporting material.

| S-EPMC10745853 | biostudies-literature

Colloidal spherical stibnite particles <i>via</i> high-temperature metallo-organic synthesis.

Project description:Antimony trisulfide (Sb2S3) is an emerging semiconductor with a high absorption coefficient and a bandgap in the visible range. This makes it a promising material for various electronic and optoelectronic applications. However, one of the main challenges is still the synthesis of the material, as it is usually obtained either as a nanomaterial in its amorphous form with inferior optical properties or in crystalline rod-like structures in the micrometer or sub-micrometer range, which leads to application-related difficulties such as clogging in inkjet printing or spraying processes or highly porous layers in film applications. In this study, a one-pot synthesis of highly crystalline, spherical Sb2S3 sub-micron particles is presented. The particles are growing encapsulated in a removable, wax-like matrix that is formed together with an intermediate from the precursors SbCl3 and l-cysteine. Both substances are insoluble in the reaction mixture but well-dispersable in the solvent 1-octadecene (ODE). The intermediate forms a complex crosslinked architecture whose basic building block consists of an Sb atom attached to three cysteine molecules via Sb-S bonds. Embedded in the matrix consisting of excess cysteine, ODE, and chlorine, the intermediate decomposes into amorphous Sb2S3 particles that crystallize as the reaction proceeds at 240 °C. The final particles are highly crystalline, spherical, and in the sub-micron range (420 ± 100 nm), making them ideal for further processing. The encapsulation method could not only provide a way to extend the size range of colloidal particles, but in the case of Sb2S3, this method circumvents the risk of carbonization of ligands or insufficient crystallization during the annealing of amorphous material.

| S-EPMC11334972 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data