• Title/Summary/Keyword: CATION

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Solvation in Mixed Solvents (IV). Solvolysis of Adamantyl Derivatives in Methanol-Acetonitrile Mixtures

  • Lee, Ik-Choon;Lee, Byung-Choon;Lee, Bon-su;Sohn, Se-Chul
    • Bulletin of the Korean Chemical Society
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    • v.6 no.1
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    • pp.19-23
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    • 1985
  • Solvolysis of 1-adamantyl chloride, -bromide and -tosylate have been studied in methanol-acetonitrile mixtures. Rate maxima were found for 1-adamantyl bromide and tosylate at 80-90 % methanol mixtures. The rate maximum observed was interpreted as a result of cooperative enhancement of cation and anion solvation. 1-Adamantyl tosylate had small cation solvation but had extensive anion solvation. It was concluded that the Y scale based on adamantyl tosylate is superior to others since it varies in a wide range especially for weakly ionizing medium.

Heterogeneous Catalysis of Iso-Octane over Cation Exchanged Mordenite Surfaces

  • Chong, Paul-Joe
    • Bulletin of the Korean Chemical Society
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    • v.5 no.2
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    • pp.79-82
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    • 1984
  • This study concerns about catalyic cracking of iso-octane over cation ($Cd^{2+},\;Ca^{2+}\;and\;La^{3+}$) exchange mordenites. It deals with mordenite shape selectivity and with kinetics of this catalytic reaction. The striking feature was that over the region of cracking temperature investigated, 523-665K, the yield of isobutene was predominant, relative to that of larger or smaller carbon chain(s). This permits kinetic analysis of the heterogeneous catalytic system in terms of the modified pulse-version microcatalytic chromatography. The observed activation energy ($E_a,\;KJ\;mol^{-1}$) was found to be 46 for Cd-M, 57 for Ca-M and 59 for La-M, respectively.

Density Functional Theory Study of Vibrational Spectra of Anthracene Neutral and Radical Cation

  • 이상연;부봉현
    • Bulletin of the Korean Chemical Society
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    • v.17 no.8
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    • pp.754-759
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    • 1996
  • Ab initio Hartree-Fock and Becke 3-Lee-Yang-Parr (B3LYP) density functional theory calculations using 6-31G* basis set were carried out to study the vibrational spectra of anthracene neutral (h10 and d10) and radical cation (h10). We report results of the fundamental vibrational frequencies obtained on the basis of the calculations. The assignments of fundamentals show a one-to-one correspondence between the observed and calculated fundamentals.

2-Benzothiazolylhydrazones with Cation Radicals in Nitrile Solvents. Formations of 1,2,4-Triazoles and Triazolo[3,4-b]benzothiazoles

  • Park, Gun Ha;Jeon, Geon;O, Si Hwa
    • Bulletin of the Korean Chemical Society
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    • v.21 no.4
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    • pp.425-428
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    • 2000
  • Arenealdehyde 2-benzothiazolylhydrazone in thianthrene cation radicalafforded triazolo[3,4-b]benzothiazoles and 1,2,4-triazoles as major and minor product, respectively. On the contrary the similar reaction in tris(2,4-dibromophenyl)aminium hexachloroantimonate gave 1,2,4-triazoles and triazolo[3,4-b]benzothiazoles as ma-jor and minor product, respectively.

A $^{13}C$ NMR Study of 7-Norbornadienyl Cation by Modified Hammett-Brown Equation

  • 박정규;신정휴
    • Bulletin of the Korean Chemical Society
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    • v.20 no.6
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    • pp.667-671
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    • 1999
  • A series of the para-substituted 7-aryl-norbornadienyl cation (3) was prepared in FSO3H/SO2ClF solution at -100℃ and their 13C NMR shifts were measured at -80℃. The plots of the chemical shifts (changes in chemical shifts) of cationic carbon, ΔδC+, aganist our calculated new substituent constant, σc+s, gave an excellent correlation (r=0.994), with a ρc+ value of 12.63. These results indicate that the new substituent constants, σc+s, can be successfully employed to compare the relative charge demand of the carbonium ion by π-and πσ-participation.

A New Substituent Constant $σ^{c+}4_s$;a Fit for π-Participation in Modified Hammett-Brown Equation

  • 조정호;신정휴
    • Bulletin of the Korean Chemical Society
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    • v.17 no.4
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    • pp.347-348
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    • 1996
  • A set of substituent constants, σc+, has been widely used comparing the stability of carbocation in super acid condition. Plotting of 13C chemical shifts of cationic carbon (Δδc+) against σc+ constants yields an excellent correlation with a good correlation coefficient (r=0.999) for a cyclopentyl cation system. But these σc+ constants show poor linearity in norbornenyl cations that well known to show homoallylic stabilization in a cationic condition. We calculated the new substituent constant, σc+π, and found that the new substituent constants give an excellent correlation in π- and πσ-participating cation systems.

Reactions of Thianthrene Cation Radical Perchlorate with Azo-bis-2-phenoxy-2-propane and Azo-bis-2-(p-nitrophenoxy)-2-propane

  • Lee, Jae-Moon;Kim, Kyong-Tae;Shin, Jyng-Hyu
    • Bulletin of the Korean Chemical Society
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    • v.6 no.6
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    • pp.358-361
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    • 1985
  • Thianthrene cation radical perchlorate (1) reacted with azo-bis-2-phenoxy-2-propane (6) to give thianthrene (2), cisthianthrene-5,10-dioxide, 5-(p-hydroxyphenyl) thianthrenium perchlorate (10), acetone, phenol, and 5-(2-propenyl) thianthrenium perchlorate (11) when the mole trtio of 1 to 6 was 1:1. Among the products, 11 was a new compound. However, when the corresponding mole ratio was 5:1, 11 was not formed. Similar result was obtained for azo-bis-2-(p-nitrophenoxy)-2-propane.

Preparation of Cation Exchange Membrane using Polybenzimidazole and Its Characteristic (폴리벤지미다졸(PBI)을 이용한 양이온교환막의 제조 및 특성)

  • Kim, Joeng-Geun;Lee, Sang-Ho;Ryu, Cheol-Hwi;Hwang, Gab-Jin
    • Membrane Journal
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    • v.22 no.4
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    • pp.265-271
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    • 2012
  • Polybenzimidazole (PBI) was prepared by condensation polymerization using diaminobenzidine (DAB) and isophtalic acid (IPAc). The cation exchange membrane was prepared by introduce the ion exchange group in the PBI polymer. It was confirmed from FT-IR analysis that the prepared PBI powder had same peak compared with commercial PBI power. The ionic conductivity of PBI film was $0.1{\sim}0.9{\times}10^{-2}$ S/cm. The ionic conductivity of prepared SPBI cation exchange membrane showed $3.7{\sim}4.7{\times}10^{-2}$ S/cm and had higher than Nafion117 ($2.0{\times}10^{-2}$ S/cm).

A Study on the Transition Characteristics of Precipitation Components in Dangjin and Anmyon-do Area (唐津과 安眠島地域 降水 成分의 變化特性에 關한 硏究)

  • Chung, Jin-Do;Lee, Choun-Ho
    • Journal of Korean Society for Atmospheric Environment
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    • v.20 no.5
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    • pp.593-601
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    • 2004
  • In this study, we are going to compare the chemical composition of the precipitation that falls in the Dangjin and Anmyon-do areas by analyzing the water soluble components (anion and cation). We also examined the effects of seasonal change and regional difference in those data sets. The [$NO_3\;^- \;+\;SO_4\;^{2-}$] at 49.2${\mu}$eq/l is 67% of the total anion of 73.1${\mu}$eq/l, while that of [$NH_4\;^+\;+\;Ca^{2+}$] at 37.7${\mu}$eq/l is 62% of the cation in Dangjin area. Also, the [$NO_3\;^-\;+\;SO_4\;^{2-}$] concentration of 151.8 (${\mu}$eq/l) is 62% for the total anion of 143.5 (${\mu}$eq/l), and the [$NH_4\;^+\;+\;Ca^{2+}$] concentration of 119.7 (${\mu}$eq/l) is 47% for the cation of 254.3 (${\mu}$eq/l) in Anmyon-do area. The ion composition ratio is shown for the order by 22% of $SO_4\;^{2-}$, 20.8% of $NH_4\;^+$ and 15.4% of $Cl^-$ that is the sum of 58.7% for the total ion composition in Dangjin area, and is the order by 33.8% of $NH_4\;^+$, 16.3% of $SO_4\;^{2-}$ and 11.1% of $Cl^-$ in Anmyon-do area. Furthermore, We predicted that even areas which were previously clean will get acid rain if there is large scale construction there or nearby.