• Title/Summary/Keyword: Chemical products

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Concomitant Addition and Acetalization of α,β-Unsaturated Aldehydes with Diols

  • Jeon, Kyu-Ok;Yu, Ji-Sook;Lee, Chang-Kiu
    • Bulletin of the Korean Chemical Society
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    • v.25 no.11
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    • pp.1653-1656
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    • 2004
  • ${\alpha},{\beta}$-Unsaturated aldehydes such as acrolein and crotonaldehyde were reacted with diols in the presence of conc. sulfuric acid to give products of which concomitant addition to C-C double bond and acetalization took place. Boron trifluoride etherate and titanium tetrachloride gave only acetalization products.

Photolysis of Aqueous Ammonia in the Absence and the Presence of O₂

  • 박형련;김희정;성아영
    • Bulletin of the Korean Chemical Society
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    • v.17 no.9
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    • pp.798-802
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    • 1996
  • The photochemical decomposition of aqueous ammonia in the absence (saturated with argon) and the presence of O2 (saturated with air or oxygen) has been investigated using 184.9 nm UV light. The decomposition of ammonia depended on the concentration of oxygen in the solution. With increasing the concentration of oxygen, the decomposition of ammonia diminishes. Hydrazine is found the major product from the irradiation. In the presence of oxygen, hydrogenperoxide was also produced. The product yields depended also on the concentration of oxygen in the solution. The initial quantum yield of the products and of the ammonia decomposed were determined. Probable reaction mechanisms for the reaction were presented from the products analysis.

Theoretical Study on the Regioselectivity of Tetrazolylimines with Alkyl Grignard Reagents

  • 유성은;공영대;김수경
    • Bulletin of the Korean Chemical Society
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    • v.20 no.4
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    • pp.441-444
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    • 1999
  • The alkyl Grignard addition reaction on 1-benzyltetrazolylimine proceeds to give N-alkylated products (azophilic addition) and, in contrast, the same reaction on 2-benzyltetrazolylimine produced predominantly C-alkylated products (carbophilic addition). In this report we described theoretical explanations for this experimental finding on the basis of the frontier molecular orbitals and the electrostatic nature of the reactants and the reaction intermediates.

Photoaddition Reaction of 5,7-Dimethoxycoumarin with Adenosine

  • Cho, Tae-Heung;Shim, Hyun-Kwan;Shim, Sang-Chul
    • Bulletin of the Korean Chemical Society
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    • v.8 no.3
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    • pp.206-211
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    • 1987
  • The photoreaction of 5,7-dimethoxycoumarin with adenosine has been carried out in a dry film state. The mixture of DMC and adenosine was irradiated with 350 nm UV light and two major products were isolated. The structure was determined by various spectroscopic measurements involving $^{13}C$ nuclear magnetic resonance and fast atom bombardment mass spectrometry. These addition products were produced by covalent bond formation between the pyrone ring at carbon 3 or 4 and the sugar ring moiety of adenosine at carbon 5'.

Formation of Tetra-Chlorinated Dibenzo-p-dioxins and Their Thermal Decomposition Products from Pyrolysis Reaction of Tri-Chlorophenates

  • 홍종기;박종세;김강진
    • Bulletin of the Korean Chemical Society
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    • v.17 no.4
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    • pp.334-338
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    • 1996
  • Tetra-chlorodibenzo-p-dioxins (tetra-CDDs) were prepared by microscale pyrolysis of trichlorophenates. During the pyrolysis reaction, tri-, di-, and mono-CDDs were also formed by the thermolysis of tetra-CDDs. The dechlorination pathways of tetra-CDDs were suggested for this reaction. The identification of these products was performed with capillary column gas chromatography-mass spectrometry.

Studies on the Different Reaction Pathways between 3-Acetyl-5-benzoyl-6-methyl-2-phenyl-4H-pyran-4-one and Alkylamines

  • Genc, Hasan;Tan, Meltem;Gumus, Selcuk;Menges, Nurettin;Bildirici, Ishak;Sener, Ahmet
    • Bulletin of the Korean Chemical Society
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    • v.31 no.9
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    • pp.2633-2636
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    • 2010
  • 3-Acetyl-5-benzoyl-6-methyl-2-phenyl-4H-pyran-4-one has been subjected to condensation with a series of primary amines (ethylamine - octylamine) to clarify the proposed mechanism in our previous study. The reactions of the shorter amines of the series (ethylamine - butylamine) yielded unsymmetric pyridinone products, whereas the other amines (pentylamine - octylamine) yielded symmetrical pyridinones. The starting material and the products as well as the intermediates have been subjected to theoretical analysis by quantum chemical calculations at B3LYP/6-31G(d,p) level, which provided supporting data for the experimental findings.

HYDROLYZED GINSENG-SAPONIN QUATERNARY; A NOVEL CONDITIONING AGENT FOR HAIR CARE PRODUCTS

  • Kim, Young-Dae;Kim, Chang-Kew;Lee, Chung-Nam;Ha, Byung-Jo
    • Journal of the Society of Cosmetic Scientists of Korea
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    • v.14 no.1
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    • pp.16-37
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    • 1988
  • A new quaternary ammonium compound, hydrolyzed ginseng-sapoin quaternary (HGSQ), from hydrolyzed Korean ginseng-saponin and 2, 3-epoxypropyltrimethyl ammonium chloride has been developed as a conditioning agent for hair care products. This structure has the hydrophilic group from the introduced cationic and the hydrophobic group from the aglycone of ginseng saponin. Its properties: surface tension, conductivity, critical micelle concentration, eye irritation, sorption onto hair, force reduction (%) for 20% extension and moisture retention effect comparing with the commercial standards. Also half-head tests of HGSQ-containing shampoo were carried out to compare the conditioning effects in shampoos.

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Chemical Modification of Wood with Alkylene Oxides, Vinylpirrolidinone and Furans:Effects on Dimensional Stabilization

  • Guevara, R.;Moslemi, A.A.
    • Journal of the Korean Wood Science and Technology
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    • v.10 no.4
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    • pp.38-52
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    • 1982
  • The effect of propylene oxide, butylene oxide, furan resin, and vinylpyrrolidinone in controlling wood dimensional stability have been examined. Wood in the green or ovendry condition was treated with various chemical treatments using a vacuum-pressure procedure, and treated specimens were tested for tangential sweelling, moisture gain, and changes in sorption hysteresis. Results' indicate that propylene oxide, and butylene oxide enhanced with the crosslin king agent trimethylol propane trimethacrylate and applied to ovendry wood were the most efficient chemical treatments in controlling tangential sweeling caused by liquid water or water vapor, and in reducing water vapor adsorption. The sorption behavior of treated wood as depicted by the ratios of sorption was "very favorable" in most instances. In the particular case of furan resin treatments, ratios of sorption were improved from 25 to 100 percent as compared to those of untreated wood.

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Evaluation of the Basic Properties for the Korean Major Domestic Wood Species I. Korean Red Pine (Pinus densiflora) in Pyeongchang-gun, Gangwon-do

  • Yonggun PARK;Chul-ki KIM;Hanseob JEONG;Hyun Mi LEE;Kwang-Mo KIM;In-Hwan LEE;Min-Ji KIM;Gyu Bin KWON;Nayoung YOON;Namhee LEE
    • Journal of the Korean Wood Science and Technology
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    • v.52 no.1
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    • pp.87-100
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    • 2024
  • Wood has different properties depending on the species or growth area. Therefore, in order to use wood efficiently, it is necessary to have a proper understanding of the characteristics of wood depending on the species and the appropriate use for them. In particular, in order to effectively use more than 1,000 species of woody plants in South Korea as wood, it is necessary to evaluate the characteristics of various Korean domestic woods and make a database of them. In this study, the anatomical properties (length and width of tracheid, cell wall thickness), physical properties (specific gravity and shrinkage), mechanical properties (bending strength, compressive strength, tensile strength, shear strength, hardness), and chemical composition (ash, extract, lignin, total sugar content) of Korean red pine which was grown in Pyeongchang-gun, Gangwon-do, South Korea were evaluated.