Redox indicator
{{short description|Indicator which undergoes a definite color change at a specific electrode potential}}
{{refimprove|date=December 2009}}
A redox indicator (also called an oxidation-reduction indicator) is an indicator which undergoes a definite color change at a specific electrode potential.
The requirement for fast and reversible color change means that the oxidation-reduction equilibrium for an indicator redox system needs to be established very quickly. Therefore, only a few classes of organic redox systems can be used for indicator purposes.{{cite encyclopedia| encyclopedia = Ullmann's Encyclopedia of Industrial Chemistry|author=Ram W. Sabnis |author2=Erwin Ross |author3=Jutta Köthe |author4=Renate Naumann |author5=Wolfgang Fischer |author6=Wilhelm-Dietrich Mayer |author7=Gerhard Wieland |author8=Ernest J. Newman |author9=Charles M. Wilson |title=Indicator Reagents|year=2009|publisher=Wiley-VCH|place=Weinheim|doi=10.1002/14356007.a14_127.pub2|isbn=978-3-527-30673-2}}
There are two common classes of redox indicators:
- metal complexes of phenanthroline and bipyridine. In these systems, the metal changes oxidation state.
- organic redox systems such as methylene blue. In these systems, a proton participates in the redox reaction. Therefore, sometimes redox indicators are also divided into two general groups: independent or dependent on pH.
The most common redox indicator are organic compounds.
Redox Indicator example:
The molecule 2,2'- Bipyridine is a redox Indicator. In solution, it changes from light blue to red at an electrode potential of 0.97 V.
pH independent
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!Indicator !E0, V !Color of Oxidized form !Color of Reduced form |
2,2'-bipyridine (Ru complex)
|align=center| +1.33 |align=center bgcolor=white|colorless |align=center bgcolor=yellow|yellow |
Nitrophenanthroline (Fe complex)
|align=center| +1.25 |align=center bgcolor=cyan|cyan |align=center bgcolor=red|red |
N-Phenylanthranilic acid
|align=center| +1.08 |align=center bgcolor=violet|violet-red |align=center bgcolor=white|colorless |
1,10-Phenanthroline iron(II) sulfate complex (Ferroin)
|align=center| +1.06 |align=center bgcolor=cyan|cyan |align=center bgcolor=red|red |
N-Ethoxychrysoidine
|align=center| +1.00 |align=center bgcolor=red|red |align=center bgcolor=yellow|yellow |
2,2`-Bipyridine (Fe complex)
|align=center| +0.97 |align=center bgcolor=cyan|cyan |align=center bgcolor=red|red |
5,6-Dimethylphenanthroline (Fe complex)
| +0.97 |align=center bgcolor=#CCFF00|yellow-green |align=center bgcolor=cyan|cyan |
o-Dianisidine
|align=center| +0.85 |align=center bgcolor=red|red |align=center bgcolor=white|colorless |
Sodium diphenylamine sulfonate
|align=center| +0.84 |align=center bgcolor=#E41B9E|red-violet |align=center bgcolor=white|colorless |
Diphenylbenzidine
| +0.76 |align=center bgcolor=violet|violet |align=center bgcolor=white|colorless |
Diphenylamine
|align=center| +0.76 |align=center bgcolor=violet|violet |align=center bgcolor=white|colorless |
Viologen
|align=center| -0.43 |align=center bgcolor=white|colorless |align=center bgcolor=blue|blue |
pH dependent
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!Indicator !E0, V at pH=0 !E, V at pH=7 !Color of Oxidized form !Color of Reduced form |
Sodium 2,6-Dibromophenol-indophenol
or Sodium 2,6-Dichlorophenol-indophenol |align=center bgcolor=white| +0.64 |align=center bgcolor=white| +0.22 |align=center bgcolor=blue|blue |align=center bgcolor=white|colorless |
Sodium o-Cresol indophenol
|align=center bgcolor=white| +0.62 |align=center bgcolor=white| +0.19 |align=center bgcolor=blue|blue |align=center bgcolor=white|colorless |
Thionine (syn. Lauth's violet)
|align=center bgcolor=white| +0.56 |align=center bgcolor=white| +0.06 |align=center bgcolor=violet|violet |align=center bgcolor=white|colorless |
Methylene blue
|align=center bgcolor=white| +0.53 |align=center bgcolor=white| +0.01HEWITT, LF. "Oxidation-Reduction Potentials in Bacteriology and Biochemistry." Oxidation-Reduction Potentials in Bacteriology and Biochemistry. Edn 6 (1950). |align=center bgcolor=blue|blue |align=center bgcolor=white|colorless |
Indigotetrasulfonic acid
|align=center bgcolor=white| +0.37 |align=center bgcolor=white| -0.05 |align=center bgcolor=blue|blue |align=center bgcolor=white|colorless |
Indigotrisulfonic acid
|align=center bgcolor=white| +0.33 |align=center bgcolor=white| -0.08 |align=center bgcolor=blue|blue |align=center bgcolor=white|colorless |
Indigo carmine
(syn. Indigodisulfonic acid |align=center bgcolor=white| +0.29 |align=center bgcolor=white| -0.13 |align=center bgcolor=blue|blue |align=center bgcolor=white|colorless |
Indigomono sulfonic acid
|align=center bgcolor=white| +0.26 |align=center bgcolor=white| -0.16 |align=center bgcolor=blue|blue |align=center bgcolor=white|colorless |
Phenosafranin
|align=center bgcolor=white| +0.28 |align=center bgcolor=white| -0.25 |align=center bgcolor=red|red |align=center bgcolor=white|colorless |
Safranin T
|align=center bgcolor=white| +0.24 |align=center bgcolor=white| -0.29 |align=center bgcolor=#E41B9E|red-violet |align=center bgcolor=white|colorless |
Neutral red
|align=center bgcolor=white| +0.24 |align=center bgcolor=white| -0.33 |align=center bgcolor=red|red |align=center bgcolor=white|colorless |
See also
References
{{Reflist}}
External links
- [http://old.iupac.org/publications/pac/1978/pdf/5005x0463.pdf Redox Indicators. Characteristics And Applications]
{{DEFAULTSORT:Redox Indicator}}