Redox indicator: Difference between revisions
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{{short description|Indicator which undergoes a definite color change at a specific electrode potential}} |
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{{refimprove|date=December 2009}} |
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A '''redox indicator''' (also called an '''oxidation-reduction indicator''') is an indicator |
A '''redox indicator''' (also called an '''oxidation-reduction indicator''') is an indicator which undergoes a definite color change at a specific [[electrode potential]]. |
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The requirement for fast and reversible color change means that the oxidation-reduction [[Chemical equilibrium|equilibrium]] for an indicator [[redox system]] needs to be established very |
The requirement for fast and reversible color change means that the oxidation-reduction [[Chemical equilibrium|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.<ref>{{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}}</ref> |
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There are two common |
There are two common classes of redox indicators: |
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* metal |
* [[metal complex]]es of [[phenanthroline]] and [[bipyridine]]. In these systems, the metal changes oxidation state. |
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⚫ | |||
* true [[organic redox system]]s (Ex. [[Methylene blue]]) |
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Sometimes colored inorganic [[oxidant]]s or [[reductant]]s (Ex. [[Potassium manganate]], [[Potassium dichromate]]) are also ''incorrectly'' called redox indicators. They can’t be classified as '''true''' redox indicators because of their '''irreversibility'''. |
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The most common redox indicator are [[organic compounds]]. |
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⚫ | |||
Redox Indicator example: |
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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. |
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==pH independent |
==pH independent== |
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{| border="1" |
{| border="1" |
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!Indicator |
!Indicator |
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|[[2,2'-bipyridine]] (Ru complex) |
|[[2,2'-bipyridine]] (Ru complex) |
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|align=center| +1.33 |
|align=center| +1.33 |
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|align=center bgcolor=white|colorless |
|align=center bgcolor=white|colorless |
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|align=center bgcolor=yellow|yellow |
|align=center bgcolor=yellow|yellow |
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|- |
|- |
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|Nitro[[phenanthroline]] (Fe complex) |
|Nitro[[phenanthroline]] (Fe complex) |
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|align=center| +1.25 |
|align=center| +1.25 |
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|align=center bgcolor=cyan|cyan |
|align=center bgcolor=cyan|cyan |
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|align=center bgcolor=red|red |
|align=center bgcolor=red|red |
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|- |
|- |
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|N-[[Phenylanthranilic acid]] |
|N-[[Phenylanthranilic acid]] |
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|align=center| +1.08 |
|align=center| +1.08 |
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|align=center bgcolor=violet|violet-red |
|align=center bgcolor=violet|violet-red |
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|align=center bgcolor=white|colorless |
|align=center bgcolor=white|colorless |
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|- |
|- |
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|1,10- |
|1,10-Phenanthroline iron(II) sulfate complex ([[Ferroin]]) |
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|align=center| +1.06 |
|align=center| +1.06 |
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|align=center bgcolor=cyan|cyan |
|align=center bgcolor=cyan|cyan |
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|align=center bgcolor=red|red |
|align=center bgcolor=red|red |
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|- |
|- |
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|N-[[Ethoxychrysoidine]] |
|N-[[Ethoxychrysoidine]] |
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|align=center| +1.00 |
|align=center| +1.00 |
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|align=center bgcolor=red|red |
|align=center bgcolor=red|red |
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|align=center bgcolor=yellow|yellow |
|align=center bgcolor=yellow|yellow |
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|- |
|- |
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|2,2`-[[Bipyridine]] (Fe complex) |
|2,2`-[[Bipyridine]] (Fe complex) |
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|align=center| +0.97 |
|align=center| +0.97 |
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|align=center bgcolor=cyan|cyan |
|align=center bgcolor=cyan|cyan |
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|align=center bgcolor=red|red |
|align=center bgcolor=red|red |
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|- |
|- |
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|5,6-Dimethyl[[phenanthroline]] (Fe complex) |
|5,6-Dimethyl[[phenanthroline]] (Fe complex) |
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| +0.97 |
| +0.97 |
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|align=center bgcolor=#CCFF00|yellow-green |
|align=center bgcolor=#CCFF00|yellow-green |
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|align=center bgcolor= |
|align=center bgcolor=cyan|cyan |
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|- |
|- |
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| |
|[[o-Dianisidine]] |
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|align=center| +0.85 |
|align=center| +0.85 |
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|align=center bgcolor=red|red |
|align=center bgcolor=red|red |
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|align=center bgcolor=white|colorless |
|align=center bgcolor=white|colorless |
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|- |
|- |
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|Sodium [[diphenylamine sulfonate]] |
|Sodium [[diphenylamine sulfonate]] |
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|align=center| +0.84 |
|align=center| +0.84 |
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|align=center bgcolor=#E41B9E|red-violet |
|align=center bgcolor=#E41B9E|red-violet |
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|align=center bgcolor=white|colorless |
|align=center bgcolor=white|colorless |
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|- |
|- |
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|[[Diphenylbenzidine]] |
|[[Diphenylbenzidine]] |
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| +0.76 |
| +0.76 |
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|align=center bgcolor=violet|violet |
|align=center bgcolor=violet|violet |
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|align=center bgcolor=white|colorless |
|align=center bgcolor=white|colorless |
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|- |
|- |
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|[[Diphenylamine]] |
|[[Diphenylamine]] |
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|align=center| +0.76 |
|align=center| +0.76 |
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|align=center bgcolor=violet|violet |
|align=center bgcolor=violet|violet |
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|align=center bgcolor=white|colorless |
|align=center bgcolor=white|colorless |
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|- |
|- |
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|[[Viologen]] |
|[[Viologen]] |
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|align=center| -0.43 |
|align=center| -0.43 |
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|align=center bgcolor=white|colorless |
|align=center bgcolor=white|colorless |
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|align=center bgcolor=blue|blue |
|align=center bgcolor=blue|blue |
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|} |
|} |
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==pH dependent |
==pH dependent== |
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{| border="1" |
{| border="1" |
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!Indicator |
!Indicator |
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!E<sup>0</sup>, V |
!E<sup>0</sup>, V |
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at pH=0 |
at pH=0 |
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!E |
!E, V |
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at pH=7 |
at pH=7 |
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!Color of |
!Color of |
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|Sodium 2,6-Dibromophenol-indophenol |
|Sodium 2,6-Dibromophenol-indophenol |
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or Sodium [[DCPIP|2,6-Dichlorophenol-indophenol]] |
or Sodium [[DCPIP|2,6-Dichlorophenol-indophenol]] |
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|align=center bgcolor=white| +0.64 |
|align=center bgcolor=white| +0.64 |
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|align=center bgcolor=white| +0.22 |
|align=center bgcolor=white| +0.22 |
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|align=center bgcolor=blue|blue |
|align=center bgcolor=blue|blue |
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|align=center bgcolor=white|colorless |
|align=center bgcolor=white|colorless |
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|- |
|- |
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|Sodium o-Cresol [[indophenol]] |
|Sodium o-Cresol [[indophenol]] |
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|align=center bgcolor=white| +0.62 |
|align=center bgcolor=white| +0.62 |
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|align=center bgcolor=white| +0.19 |
|align=center bgcolor=white| +0.19 |
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|align=center bgcolor=blue|blue |
|align=center bgcolor=blue|blue |
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|align=center bgcolor=white|colorless |
|align=center bgcolor=white|colorless |
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|- |
|- |
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|[[Thionine]] (syn. [[Lauth's violet]]) |
|[[Thionine]] (syn. [[Lauth's violet]]) |
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|align=center bgcolor=white| +0.56 |
|align=center bgcolor=white| +0.56 |
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|align=center bgcolor=white| +0.06 |
|align=center bgcolor=white| +0.06 |
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|align=center bgcolor=violet|violet |
|align=center bgcolor=violet|violet |
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|align=center bgcolor=white|colorless |
|align=center bgcolor=white|colorless |
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|- |
|- |
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|[[Methylene blue]] |
|[[Methylene blue]] |
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|align=center bgcolor=white| +0.53 |
|align=center bgcolor=white| +0.53 |
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|align=center bgcolor=white| +0.01<ref>HEWITT, LF. "Oxidation-Reduction Potentials in Bacteriology and Biochemistry." Oxidation-Reduction Potentials in Bacteriology and Biochemistry. Edn 6 (1950).</ref> |
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|align=center bgcolor=white| +0.01 V |
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|align=center bgcolor=blue|blue |
|align=center bgcolor=blue|blue |
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|align=center bgcolor=white|colorless |
|align=center bgcolor=white|colorless |
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|- |
|- |
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|Indigotetra[[sulfonic acid]] |
|Indigotetra[[sulfonic acid]] |
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|align=center bgcolor=white| +0.37 |
|align=center bgcolor=white| +0.37 |
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|align=center bgcolor=white| -0.05 |
|align=center bgcolor=white| -0.05 |
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|align=center bgcolor=blue|blue |
|align=center bgcolor=blue|blue |
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|align=center bgcolor=white|colorless |
|align=center bgcolor=white|colorless |
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|- |
|- |
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|Indigotri[[sulfonic acid]] |
|Indigotri[[sulfonic acid]] |
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|align=center bgcolor=white| +0.33 |
|align=center bgcolor=white| +0.33 |
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|align=center bgcolor=white| -0.08 |
|align=center bgcolor=white| -0.08 |
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|align=center bgcolor=blue|blue |
|align=center bgcolor=blue|blue |
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|align=center bgcolor=white|colorless |
|align=center bgcolor=white|colorless |
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|[[Indigo carmine]] |
|[[Indigo carmine]] |
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(syn. Indigodi[[sulfonic acid]] |
(syn. Indigodi[[sulfonic acid]] |
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|align=center bgcolor=white| +0.29 |
|align=center bgcolor=white| +0.29 |
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|align=center bgcolor=white| -0.13 |
|align=center bgcolor=white| -0.13 |
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|align=center bgcolor=blue|blue |
|align=center bgcolor=blue|blue |
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|align=center bgcolor=white|colorless |
|align=center bgcolor=white|colorless |
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|- |
|- |
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|[[Indigo]]mono [[sulfonic acid]] |
|[[Indigo]]mono [[sulfonic acid]] |
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|align=center bgcolor=white| +0.26 |
|align=center bgcolor=white| +0.26 |
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|align=center bgcolor=white| -0.16 |
|align=center bgcolor=white| -0.16 |
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|align=center bgcolor=blue|blue |
|align=center bgcolor=blue|blue |
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|align=center bgcolor=white|colorless |
|align=center bgcolor=white|colorless |
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|- |
|- |
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|[[Phenosafranin]] |
|[[Phenosafranin]] |
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|align=center bgcolor=white| +0.28 |
|align=center bgcolor=white| +0.28 |
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|align=center bgcolor=white| -0.25 |
|align=center bgcolor=white| -0.25 |
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|align=center bgcolor=red|red |
|align=center bgcolor=red|red |
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|align=center bgcolor=white|colorless |
|align=center bgcolor=white|colorless |
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|- |
|- |
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|[[Safranin |
|[[Safranin|Safranin '''T''']] |
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|align=center bgcolor=white| +0.24 |
|align=center bgcolor=white| +0.24 |
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|align=center bgcolor=white| -0.29 |
|align=center bgcolor=white| -0.29 |
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|align=center bgcolor=#E41B9E|red-violet |
|align=center bgcolor=#E41B9E|red-violet |
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|align=center bgcolor=white|colorless |
|align=center bgcolor=white|colorless |
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|- |
|- |
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|[[Neutral red]] |
|[[Neutral red]] |
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|align=center bgcolor=white| +0.24 |
|align=center bgcolor=white| +0.24 |
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|align=center bgcolor=white| -0.33 |
|align=center bgcolor=white| -0.33 |
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|align=center bgcolor=red|red |
|align=center bgcolor=red|red |
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|align=center bgcolor=white|colorless |
|align=center bgcolor=white|colorless |
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==See also== |
==See also== |
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*[[Analytical chemistry|Chemical analysis]] |
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*[[pH indicator]] |
*[[pH indicator]] |
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*[[Complexometric indicator]] |
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⚫ | |||
==References== |
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{{Reflist}} |
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==External links== |
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⚫ | |||
{{DEFAULTSORT:Redox Indicator}} |
{{DEFAULTSORT:Redox Indicator}} |
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[[Category:Redox indicators |
[[Category:Redox indicators]] |
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[[Category:Physical chemistry]] |
[[Category:Physical chemistry]] |
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[[it:Indicatore (chimica)#Indicatori di ossido-riduzione]] |
Latest revision as of 14:59, 28 September 2023
This article needs additional citations for verification. (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.[1]
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
[edit]Indicator | E0, V | Color of Oxidized form | Color of Reduced form |
---|---|---|---|
2,2'-bipyridine (Ru complex) | +1.33 | colorless | yellow |
Nitrophenanthroline (Fe complex) | +1.25 | cyan | red |
N-Phenylanthranilic acid | +1.08 | violet-red | colorless |
1,10-Phenanthroline iron(II) sulfate complex (Ferroin) | +1.06 | cyan | red |
N-Ethoxychrysoidine | +1.00 | red | yellow |
2,2`-Bipyridine (Fe complex) | +0.97 | cyan | red |
5,6-Dimethylphenanthroline (Fe complex) | +0.97 | yellow-green | cyan |
o-Dianisidine | +0.85 | red | colorless |
Sodium diphenylamine sulfonate | +0.84 | red-violet | colorless |
Diphenylbenzidine | +0.76 | violet | colorless |
Diphenylamine | +0.76 | violet | colorless |
Viologen | -0.43 | colorless | blue |
pH dependent
[edit]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 |
+0.64 | +0.22 | blue | colorless |
Sodium o-Cresol indophenol | +0.62 | +0.19 | blue | colorless |
Thionine (syn. Lauth's violet) | +0.56 | +0.06 | violet | colorless |
Methylene blue | +0.53 | +0.01[2] | blue | colorless |
Indigotetrasulfonic acid | +0.37 | -0.05 | blue | colorless |
Indigotrisulfonic acid | +0.33 | -0.08 | blue | colorless |
Indigo carmine
(syn. Indigodisulfonic acid |
+0.29 | -0.13 | blue | colorless |
Indigomono sulfonic acid | +0.26 | -0.16 | blue | colorless |
Phenosafranin | +0.28 | -0.25 | red | colorless |
Safranin T | +0.24 | -0.29 | red-violet | colorless |
Neutral red | +0.24 | -0.33 | red | colorless |
See also
[edit]References
[edit]- ^ Ram W. Sabnis; Erwin Ross; Jutta Köthe; Renate Naumann; Wolfgang Fischer; Wilhelm-Dietrich Mayer; Gerhard Wieland; Ernest J. Newman; Charles M. Wilson (2009). "Indicator Reagents". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a14_127.pub2. ISBN 978-3-527-30673-2.
- ^ HEWITT, LF. "Oxidation-Reduction Potentials in Bacteriology and Biochemistry." Oxidation-Reduction Potentials in Bacteriology and Biochemistry. Edn 6 (1950).