Near-monodisperse tetrahedral rhodium nanoparticles on charcoal: the shape-dependent catalytic hydrogenation of arenes.
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Biomedical subjects
Publications and source records attributed to Seung Uk Son.
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Cubic-phase InSe nanowires were synthesized. Obtaining an appropriate high reaction temperature for formation of nanocrystals using poor solubility of Se powder in oleylamine induced the generation of unusual cubic phase of InSe to form nanowires. In comparison, hexagonal-phase nanoplates were formed by dissolving Se powder in oleylamine before increase of reaction temperature. The diameter of highly monodisperse wires was controlled by varying the amount of Se.
Heterogeneous self-supported organometallic nanocatalysts (ONs) were synthesized by treatment of the eta6-pi-hydroquinone rhodium complex [(1,4-hydroquinone)Rh(COD)]+ with Al(Oi-Pr)3. The organometallic nanocatalysts, the size of which can be controlled by alteration of the reaction conditions, show high catalytic activities in the stereoselective polymerization of phenylacetylene to produce cis-poly(phenylacetylene). A key feature of the ON catalyst synthesis is a facile eta6 to eta4 hapticity change occurring in the quinonoid ring, which is triggered by deprotonation of the -OH groups by Al(Oi-Pr)3, with concomitant coordination of the quinone oxygen atoms to the aluminum.
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Coordination of the carbocyclic ring of hydroquinones to electrophilic transition-metal fragments such as Mn(CO)3+ and Rh(COD)+ produces stable pi-bonded eta6-complexes that are activated to facile reversible deprotonation of the -OH groups. The deprotonations are accompanied by electron transfer to the transition metal, which acts as an internal oxidizing agent or electron sink. With manganese as the metal, the resulting eta5-semiquinone and eta4-quinone complexes have been used to synthesize one- two- and three-dimensional polymeric metal-organometallic coordination networks. With rhodium as the metal, the pi-quinonoid complexes have been demonstrated to play a unique role in multifunctional C-C coupling catalysis and in the synthesis of new organolithium reagents. Both classes of pi-quinonoid complexes appear to have significant applications in nanochemistry by providing an excellent vehicle for templating the directed self-assembly of nanoparticles into functional materials.
The ionic complexes [(1,4- and 1,3-hydroquinone)Rh(P(OPh)3)2]BF4 form porous organometallic structures dictated by charge assisted hydrogen bonding.
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The pi-bonded rhodium quinonoid complex, K+[(1,4-benzoquinone)Rh(COD)]-, functions as a good catalyst for the coupling of arylboronic acid and aldehydes to afford diaryl alcohols. The catalysis is heterobimetallic in that both the transition metal and concomitant alkali metal counterion play an integral part in the reaction. In addition, the anionic quinonoid catalyst itself plays a bifunctional role by acting as a ligand to the boronic acid and as a Lewis acid receptor site for the transferring aryl group.
We successfully synthesized monodisperse chromium nanoparticles from the thermolysis of a Fischer carbene complex.
Novel complexes 1 and 2 based on N-heterocyclic carbenes, which are analogous to Ru(bpy)(3)(2+) and Ru(terpy)(2)(2+), respectively, were synthesized. The complex, which is analogous to Ru(terpy)(2)(2+), exhibited promising photoluminescence properties with a long lifetime of 820 ns in acetonitrile and 3100 ns in water at room temperature, respectively. In addition, ab initio calculations were carried out.
We synthesized Ni/Pd core/shell nanoparticles from the consecutive thermal decomposition of metal-surfactant complexes. The nanoparticle catalyst was atom-economically applied for various Sonogashira coupling reactions.
We synthesized uniform Cu2O coated Cu nanoparticles from the thermal decomposition of copper acetylacetonate followed by air oxidation and used these nanoparticles as catalysts for Ullmann type amination coupling reactions of aryl chlorides
A novel coordination polymer containing Co(NCS)2 and a rigid ligand, 2,5-bis(4-pyridylethynyl)-thiophene showing unusual flexibility was synthesized.
[reaction: see text] A very efficient method for the synthesis of benz[f]indenone derivatives was developed. This method allows the introduction of a variety of substituents to a molecule. The first zirconocene compound of benz[f]indene was synthesized.
Heterobimetallic Ru/Co nanoparticles, immobilized on charcoal, were synthesized and used as catalysts in the Pauson-Khand-type reaction in the presence of pyridylmethyl formate instead of carbon monoxide; the catalysts were effective for intra- and intermolecular reactions and easily reused without loss of catalytic activity.
A new azophenol-based colorimetric sensor shows a selective detection for pyrophosphate in aqueous solution.
[reaction: see text] Palladium and cobalt nanoparticles immobilized on silica have been used as catalyst in a sequential allylic alkylation and Pauson-Khand reaction to form bicyclic enones.
[formula: see text] Dispersions of nanometer-sized cobalt particles with very high stability were prepared in charcoal and analyzed by electron microscopy and X-ray analysis. The resulting cobalt nanoparticles on charcoal (CNC) were successfully used as a catalyst for the carbonylative cycloaddition of alkyne, alkene, and carbon monoxide (Pauson-Khand reaction), hydrogenation, and the reductive Pauson-Khand reaction.