1968
DOI: 10.1016/0039-9140(68)80157-2
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Iron (III) complexation with 2,3-pyridinediol

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Cited by 12 publications
(3 citation statements)
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“…TLC plates were developed in solvent system A (benzene‐acetone‐acetic acid, 50:50:1), and compounds were visualized by observation under UV light and by spraying with 2% (w/v) ferric chloride (FeCl 3 ·6H 2 O) solution in ethanol. Iron (III) complexes with 2,3‐pyridinediol and forms a blue to purple‐red product, depending on the acidity [11]. The products were isolated by extracting TLC scrapings with acetone.…”
Section: Methodsmentioning
confidence: 99%
“…TLC plates were developed in solvent system A (benzene‐acetone‐acetic acid, 50:50:1), and compounds were visualized by observation under UV light and by spraying with 2% (w/v) ferric chloride (FeCl 3 ·6H 2 O) solution in ethanol. Iron (III) complexes with 2,3‐pyridinediol and forms a blue to purple‐red product, depending on the acidity [11]. The products were isolated by extracting TLC scrapings with acetone.…”
Section: Methodsmentioning
confidence: 99%
“…After 4 d 22.9% of the initial radioactivity was recovered as 14 CO 2 , 54.2% remained in the medium, and 2.3% remained in biomass. [2,[6][7][8][9][10][11][12][13][14] C]TCP was decomposed rapidly upon UV irradiation with a half-life of approximately 25 min, and 25.1% of the initial radioactivity was recovered as 14 CO 2 . This result was in agreement with the finding of Smith [1], who reported that 25% of 14 C-TCP was decomposed to 14 CO 2 .…”
Section: Metabolism Of Photodegradation Products By Tcp-degrading Bacmentioning
confidence: 99%
“…Iron(III) forms a 1:2 complex with 2,-3-pyridinediol at pH 5 (282). A sensitive reagent for molybdenum (VI) but which does not react with tungsten is 7-iodo-8-quinolinol-5-sulfonic acid (75).…”
mentioning
confidence: 99%