1956
DOI: 10.1021/ac60113a010
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Spectrophotometric Determination of Iron in Strong Alkali Media 4,7-Dihydroxy-1,10-phenanthroline as Iron(II) Organic Chelation Report

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Cited by 33 publications
(8 citation statements)
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“…The absorption spectra between 350 and 650 nm. of the iron(II) and iron(III) compounds are shown in Figure VIII-2.The wavelength of maximum absorbance of the iron(II) compound, 520 nm., and molar absorptivity, e = l4,800 liter-mole"^-cm"^, found were the same as reported earlier by Schilt and co workers(60). These workers showed that the molar absorptivity of the iron(II) compound is independent of the concentration of alkali; in the present study this was shown to be true also in ammonia buffers as dilute as 0.2 M NH4OH plus 0.1 M NH4CI (pH = 9.1).…”
supporting
confidence: 90%
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“…The absorption spectra between 350 and 650 nm. of the iron(II) and iron(III) compounds are shown in Figure VIII-2.The wavelength of maximum absorbance of the iron(II) compound, 520 nm., and molar absorptivity, e = l4,800 liter-mole"^-cm"^, found were the same as reported earlier by Schilt and co workers(60). These workers showed that the molar absorptivity of the iron(II) compound is independent of the concentration of alkali; in the present study this was shown to be true also in ammonia buffers as dilute as 0.2 M NH4OH plus 0.1 M NH4CI (pH = 9.1).…”
supporting
confidence: 90%
“…Of the compounds listed in Table II A -synthesis; B -colorlmetrlc study; C -reduction potential; D -formation constant of Iron compound; E -pH markers In Isoelectric focusing; F -NMR spectrum; G -infrared spectrum; H -determination of copper; I -determination of iron; J -acid dissociation constants; K -Mossbauer spectrum; L -decomposition of metal derivatives by acid or base; M -catalyst; N -kinetics of oxidation of ferrous derivative with peroxydisulfate; 0 -mixed-llgand compounds; P -solubility of perchlorate. A (14,66); B (26); C (31); E (52); G (29,65); I (29,60); J (42); K (18); L (11,13); M (17,57); N (11); 0 (68); P (12) A (14,54,66) A (14,66) to determine the reduction potentials of the iron (III,II) couples. Mixed-ligand compounds such as these, and the simple tris-chelated iron derivatives of other hydroxyphenanthrolines should provide a host of indicators with reduction potentials lower than 0.8 volt.…”
Section: And Of Hydroxy-ljlo-phenanthrolinesmentioning
confidence: 99%
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“…Reduction of iron(III) with hydrogen proceeds slowly at room temperature, but the rate is considerably increased at 100 °C. After the purification procedure (without removal of dissolved palladium) was carried out on solutions initially containing 7 X 10"5 M iron(III), the iron which remained in solution was estimated spectrophotometrically using 4,7-dihydroxy-l,10-phenanthroline (7) with 10-cm cells. Figure 1 shows absorbance as a function of time and temperature.…”
Section: Resultsmentioning
confidence: 99%
“…In (25,41,42,45,46). Actually, phenanthroline has already been used in studies of redox modifications of Na ϩ /Ca 2ϩ exchange activity in mammalian heart sarcolemmal vesicles (41).…”
Section: The Effect Of Peroxynitrite On External Na-dependentmentioning
confidence: 99%