• Title/Summary/Keyword: Tetramethylammonium bromide

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Liquid Chromatography of Aromatic Sulfonic Acids by Tetramethylammonium Bromide (Tetramethylammonium Bromide를 이용한 방향족 술폰산들의 액체크로마토그래피)

  • Oh, Hae-Beom
    • Journal of the Korean Chemical Society
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    • v.37 no.9
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    • pp.793-799
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    • 1993
  • Ion-pair model was predominated over ion-interaction model in the retention mechanism of analytes when tetramethylammonium bromide (TMAB) was used as a counter-ion in the investigation of aromatic sulfonic acids on the reversed-phase liquid chromatography by $C_{18}$ column as a stationary phase. The capacity factors of analytes were influenced by the type and concentration of counter-ions, concentrations of methanol and co-anion, types and position of functional group, and the pH mobile phase. Components of analyte mixture could be separated under the optimum conditions by this method.

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Oxidative Cyclisation Based One-Pot Synthesis of 3-Substituted[1,2,4]triazolo[4,3-b]pyridazines Using Me4NBr/Oxone

  • Ruso, Jayaraman Sembian;Nagappan, Rajendiran;Kumaran, Rajendran Senthil
    • Journal of the Korean Chemical Society
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    • v.57 no.5
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    • pp.606-611
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    • 2013
  • A facile one-pot syhthesis of 3-substituted triazolopyridazine and thieno-triazolopyridazine derivatives is described. This protocol involves the preparation of heteroaryl hydrazone from the aldehyde and pyridazinohydrazine derivative followed by subjecting the intermediate directly to oxidative cyclization to assemble the desired 1,2,4-triazloe moiety by employing the mixture of Me4NBr and oxone. This condition is efficient and is able to tolerate wide range of functional groups.