• Proceedings of the Korean Society of Applied Pharmacology
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• 1994.04a
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• pp.221-221
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• 1994

The cross-coupling reaction of organo tin reagents with a variety of organic halides, catalyzed by palladium, provides a novel method for generating a carbon-carbon bond. We use this method for antibacterial agents, and synthesis of new quinolone derivatives which have carbon-carbon bond at C-7 position of general quinolone moieties. Aryl tin, quinolone moieties, and palladium catalyst were refluxed in DMF to afford new quinolone derivatives. This palladium catalyzed coupling reactions have capacity for further synthetic elaboration.

• Bulletin of the Korean Chemical Society
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• v.22 no.4
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• pp.375-378
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• 2001

The palladium catalyzed dehalogenative homocoupling of haloarylsulfonates under reductive conditions has proceeded selectively depending on the type of the halogen. Thus, an iodo or a bromo leaving group of haloarylsulfonates was homocoupled to gi ve symmetrical biaryls in good yields with the sulfonate group intact, whereas a chloro leaving group gave no reaction under the conditions used. When the more reactive nickel catalyst was employed instead of the palladium catalyst in the reaction, both dehalogenative and desulfonative homocouplings of haloarylsulfonates occurred regardless of the type of the halogen used.

• Bulletin of the Korean Chemical Society
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• v.18 no.10
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• pp.1067-1070
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• 1997

The synthesis and characterization of the nitrile ligands 3,4,5-tridodecyloxy benzonitrile (7) and 3,4,5-trioctadecyloxy benzonitrile (8), and their corresponding palladium(Ⅱ) complexes are described. The nitrile ligands display only a crystalline phase and do not show liquid crystalline behavior, while their corresponding palladium(Ⅱ) complexes dispaly an enantiotropic columnar mesophase. The induction of the columnar mesophase is mainly due to dimerization through the palladium complexation of the half disk-like nitrile ligands giving rise to a trans square planar geometry.

• YAKHAK HOEJI
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• v.59 no.2
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• pp.66-69
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• 2015

A concise synthesis of flurbiprofen, a member of the non-steroidal anti-inflammatory 2-arylpropionic acids, has been accomplished. The key feature of this synthesis involves successive palladium-catalyzed cross coupling reactions. In particular, a 2-arylacylate intermediate, which easily converted to the key 2-arylpropionic acid scaffold, was afforded by a versatile palladium-catalyzed cross coupling reaction between diazopropanate and bisphenylboronic acid. This synthetic procedure would facilitate synthesis of the flurbiprofen and anti-inflammatory 2-arylpropionic acid derivatives.

• Journal of the Korean Chemical Society
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• v.30 no.6
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• pp.516-520
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• 1986

This study is related to reactivity of dioxygen bridged palladium complexes having ${\pi}$-allyl ligands. In this case, new dioxygen bridged palladium complexes were prepared using superoxide ion$(O_2^-)$ as an oxygen source. Reactions of the dioxygen palladium complexes prepared in the study were examined in order to clarify the nature of the coordinated dioxygen. Treatments of a solution of the dioxygen bridged palladium complexes in benzene by water, methanol and acetic acid gave hydrogen peroxide $(H_2O_2)$ as hydroxy-, methoxy-, and acetoxybridged palladium complexes, respectively. The dioxygen bridged palladium complexes reacted also with substitution phenols of salicylaldehyde, 8-hydroxyquinoline and active methylenes of acetylacetone, dimethyl malonate to afford mononuclear complexes of palladium and hydrogen peroxide. The results suggest that dioxygen is coordinated as peroxo $(O_2^{2-})$ in the complexes and behaves as a strong base.

• Journal of the Korean Chemical Society
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• v.37 no.10
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• pp.903-909
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• 1993

Reaction mechanism of palladium(0, II)-phosphines complexes catalyzed cyclocarbonylation for unsaturated carboxylic acid such as crotonic acid, methacrylic acid and 3-butenoic acid has been investigated by product analysis, molecular mechanics and extended Huckel molecular orbital method. Reaction of 3-butenoic acid with palladium(0, II)-phosphines catalyst gives palladium containing cycloester through intermediate palladium-olefin ${\pi}$ -complex in the catalytic carbonylation. Palladium(0, II)-phosphines complexes catalyze the cyclocarbonylation of 3-butenoic acid to give 3-methylsuccinic anhydride and glutaric anhydride. But ${\pi}$ -complexes with palladium(0, II)-phosphines and unsaturated carboxylic acids such as crotonic acid and methacrylic acid are not effective the catalytic cyclocarbonylation.

• Korean Journal of Metals and Materials
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• v.46 no.4
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• pp.233-240
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• 2008

The reductive precipitation of platinum and palladium in hydrochloric acid solution using hydrazine as a reducing agent was investigated. The reductive precipitation ratios of platinum and palladium increased when increasing the stoichiometric ratio for reducing agent, precipitation time, and pH. The precipitation ratio of platinum was much lower than that of palladium. This is the reason the reaction rate of $PtCl{_6}^{2-}{\rightarrow}PtCl{_4}^{2-}$ at the reduction reaction step of $PtCl{_6}^{2-}{\rightarrow}PtCl{_4}^{2-}{\rightarrow}Pt$ is very slow. The purity of platinum precipitated was very affected by metallic impurities, while it was possible to precipitate the high purity palladium since the precipitation rate of palladium was relatively fast. At the pH of 1.3, the precipitation temperature of $25^{\circ}C$, and the addition amounts of the hydrazine of 10 and 1.75 times the stoichiometric ratio, the reductive precipitation ratios of platinum and palladium from their hydrochloric acid solutions containing 2,000 ppm were 98.5% and 99.9% in 30 min, respectively.

• Bulletin of the Korean Chemical Society
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• v.22 no.8
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• pp.857-866
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• 2001

Efficient syntheses of PGI2 analogue 2a and its epimer 3 have been accomplished. Using aryl iodide 6 as the common intermediate, either radical or palladium-assisted tandem alkene insertion strategies have been employed for construction of the benzoprostacyclin framework.

• 한국지구물리탐사학회:학술대회논문집
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• 2003.11a
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• pp.642-647
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• 2003

Palladium is widely used for several applications and recovery of palladium from secondary sources becomes increasingly important since palladium is one of maldistributed platinum group metals. Electrochemical recovery of dense palladium metal sheet from Pd leaching solution is a simple and easily controlled method. The surface morphology of the recovered Pd metal was significantly affected by current density and temperature. Dense deposit morphology was in higher stress state regardless of preparation condition under $55^{\circ}C$. Rising temperature up to $70^{\circ}C$ had a stress releasing effect besides densification of Pd deposit.

• Proceedings of the Korean Society of Precision Engineering Conference
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• 2002.10a
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• pp.829-832
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• 2002

Deformation of the specimens was investigated on hydrogen absorption-desorption cycling. In order to study this problem, the cold rolled and the annealed palladium thin plate as specimens had been used. By using the electrochemical method, the palladium plate specimens were cyclically hydrogenated in the 0.1mol $H_2SO_4$ electrolyte. As results, it is noted that the thickness of the plate specimens gradually increased in increasing hydrogenation cycles whereas the width and the length decreased. Also, Deformation of the cold rolled palladium specimen was lager than the annealed palladium specimen. And grains in the plate specimen were greatly deformed after hydrogenation cycling. But hydrogen absorption rate scarcely changed.