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{{short description|Indicator which undergoes a definite color change at a specific electrode potential}}
{{Unreferenced|date=December 2009}}
{{refimprove|date=December 2009}}
A '''redox indicator''' (also called an '''oxidation-reduction indicator''') is an indicator that undergoes a definite color change at a specific [[electrode potential]].
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 [[Chemical equilibrium|equilibrium]] for an indicator [[redox system]] needs to be established very fast. Therefore only a few classes of organic redox systems can be used for indicator purposes.
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>


There are two common type of redox indicators:
There are two common classes of redox indicators:
* metal-organic complexes (Ex. [[phenanthroline]])
* [[metal complex]]es of [[phenanthroline]] and [[bipyridine]]. In these systems, the metal changes oxidation state.
* [[organic redox system]]s 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]].
* true [[organic redox system]]s (Ex. [[Methylene blue]])
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'''.


The most common redox indicator are [[organic compounds]].
Almost all redox indicators with true [[organic redox system]]s involve a proton as a participant in their electrochemical reaction. Therefore sometimes redox indicators are also divided into two general groups: independent or dependent on [[pH]].
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 redox indicators==
==pH independent==
{| border="1"
{| border="1"
!Indicator
!Indicator
Line 20: Line 21:
|-
|-
|[[2,2'-bipyridine]] (Ru complex)
|[[2,2'-bipyridine]] (Ru complex)
|align=center| +1.33 V
|align=center| +1.33
|align=center bgcolor=white|colorless
|align=center bgcolor=white|colorless
|align=center bgcolor=yellow|yellow
|align=center bgcolor=yellow|yellow
|-
|-
|Nitro[[phenanthroline]] (Fe complex)
|Nitro[[phenanthroline]] (Fe complex)
|align=center| +1.25 V
|align=center| +1.25
|align=center bgcolor=cyan|cyan
|align=center bgcolor=cyan|cyan
|align=center bgcolor=red|red
|align=center bgcolor=red|red
|-
|-
|N-[[Phenylanthranilic acid]]
|N-[[Phenylanthranilic acid]]
|align=center| +1.08 V
|align=center| +1.08
|align=center bgcolor=violet|violet-red
|align=center bgcolor=violet|violet-red
|align=center bgcolor=white|colorless
|align=center bgcolor=white|colorless
|-
|-
|1,10-[[Phenanthroline]] (Fe complex)
|1,10-Phenanthroline iron(II) sulfate complex ([[Ferroin]])
|align=center| +1.06 V
|align=center| +1.06
|align=center bgcolor=cyan|cyan
|align=center bgcolor=cyan|cyan
|align=center bgcolor=red|red
|align=center bgcolor=red|red
|-
|-
|N-[[Ethoxychrysoidine]]
|N-[[Ethoxychrysoidine]]
|align=center| +1.00 V
|align=center| +1.00
|align=center bgcolor=red|red
|align=center bgcolor=red|red
|align=center bgcolor=yellow|yellow
|align=center bgcolor=yellow|yellow
|-
|-
|2,2`-[[Bipyridine]] (Fe complex)
|2,2`-[[Bipyridine]] (Fe complex)
|align=center| +0.97 V
|align=center| +0.97
|align=center bgcolor=cyan|cyan
|align=center bgcolor=cyan|cyan
|align=center bgcolor=red|red
|align=center bgcolor=red|red
|-
|-
|5,6-Dimethyl[[phenanthroline]] (Fe complex)
|5,6-Dimethyl[[phenanthroline]] (Fe complex)
| +0.97 V
| +0.97
|align=center bgcolor=#CCFF00|yellow-green
|align=center bgcolor=#CCFF00|yellow-green
|align=center bgcolor=red|red
|align=center bgcolor=cyan|cyan
|-
|-
|o-[[Dianisidine]]
|[[o-Dianisidine]]
|align=center| +0.85 V
|align=center| +0.85
|align=center bgcolor=red|red
|align=center bgcolor=red|red
|align=center bgcolor=white|colorless
|align=center bgcolor=white|colorless
|-
|-
|Sodium [[diphenylamine sulfonate]]
|Sodium [[diphenylamine sulfonate]]
|align=center| +0.84 V
|align=center| +0.84
|align=center bgcolor=#E41B9E|red-violet
|align=center bgcolor=#E41B9E|red-violet
|align=center bgcolor=white|colorless
|align=center bgcolor=white|colorless
|-
|-
|[[Diphenylbenzidine]]
|[[Diphenylbenzidine]]
| +0.76 V
| +0.76
|align=center bgcolor=violet|violet
|align=center bgcolor=violet|violet
|align=center bgcolor=white|colorless
|align=center bgcolor=white|colorless
|-
|-
|[[Diphenylamine]]
|[[Diphenylamine]]
|align=center| +0.76 V
|align=center| +0.76
|align=center bgcolor=violet|violet
|align=center bgcolor=violet|violet
|align=center bgcolor=white|colorless
|align=center bgcolor=white|colorless
|-
|-
|[[Viologen]]
|[[Viologen]]
|align=center| -0.43 V
|align=center| -0.43
|align=center bgcolor=white|colorless
|align=center bgcolor=white|colorless
|align=center bgcolor=blue|blue
|align=center bgcolor=blue|blue
|}
|}


==pH dependent redox indicators==
==pH dependent==
{| border="1"
{| border="1"
!Indicator
!Indicator
!E<sup>0</sup>, V
!E<sup>0</sup>, V
at pH=0
at pH=0
!E<sup>0</sup>, V
!E, V
at pH=7
at pH=7
!Color of
!Color of
Line 94: Line 95:
|Sodium 2,6-Dibromophenol-indophenol
|Sodium 2,6-Dibromophenol-indophenol
or Sodium [[DCPIP|2,6-Dichlorophenol-indophenol]]
or Sodium [[DCPIP|2,6-Dichlorophenol-indophenol]]
|align=center bgcolor=white| +0.64 V
|align=center bgcolor=white| +0.64
|align=center bgcolor=white| +0.22 V
|align=center bgcolor=white| +0.22
|align=center bgcolor=blue|blue
|align=center bgcolor=blue|blue
|align=center bgcolor=white|colorless
|align=center bgcolor=white|colorless
|-
|-
|Sodium o-Cresol [[indophenol]]
|Sodium o-Cresol [[indophenol]]
|align=center bgcolor=white| +0.62 V
|align=center bgcolor=white| +0.62
|align=center bgcolor=white| +0.19 V
|align=center bgcolor=white| +0.19
|align=center bgcolor=blue|blue
|align=center bgcolor=blue|blue
|align=center bgcolor=white|colorless
|align=center bgcolor=white|colorless
|-
|-
|[[Thionine]] (syn. [[Lauth's violet]])
|[[Thionine]] (syn. [[Lauth's violet]])
|align=center bgcolor=white| +0.56 V
|align=center bgcolor=white| +0.56
|align=center bgcolor=white| +0.06 V
|align=center bgcolor=white| +0.06
|align=center bgcolor=violet|violet
|align=center bgcolor=violet|violet
|align=center bgcolor=white|colorless
|align=center bgcolor=white|colorless
|-
|-
|[[Methylene blue]]
|[[Methylene blue]]
|align=center bgcolor=white| +0.53 V
|align=center bgcolor=white| +0.53
|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>
|align=center bgcolor=white| +0.01 V
|align=center bgcolor=blue|blue
|align=center bgcolor=blue|blue
|align=center bgcolor=white|colorless
|align=center bgcolor=white|colorless
|-
|-
|Indigotetra[[sulfonic acid]]
|Indigotetra[[sulfonic acid]]
|align=center bgcolor=white| +0.37 V
|align=center bgcolor=white| +0.37
|align=center bgcolor=white| -0.05 V
|align=center bgcolor=white| -0.05
|align=center bgcolor=blue|blue
|align=center bgcolor=blue|blue
|align=center bgcolor=white|colorless
|align=center bgcolor=white|colorless
|-
|-
|Indigotri[[sulfonic acid]]
|Indigotri[[sulfonic acid]]
|align=center bgcolor=white| +0.33 V
|align=center bgcolor=white| +0.33
|align=center bgcolor=white| -0.08 V
|align=center bgcolor=white| -0.08
|align=center bgcolor=blue|blue
|align=center bgcolor=blue|blue
|align=center bgcolor=white|colorless
|align=center bgcolor=white|colorless
Line 131: Line 132:
|[[Indigo carmine]]
|[[Indigo carmine]]
(syn. Indigodi[[sulfonic acid]]
(syn. Indigodi[[sulfonic acid]]
|align=center bgcolor=white| +0.29 V
|align=center bgcolor=white| +0.29
|align=center bgcolor=white| -0.13 V
|align=center bgcolor=white| -0.13
|align=center bgcolor=blue|blue
|align=center bgcolor=blue|blue
|align=center bgcolor=white|colorless
|align=center bgcolor=white|colorless
|-
|-
|[[Indigo]]mono [[sulfonic acid]]
|[[Indigo]]mono [[sulfonic acid]]
|align=center bgcolor=white| +0.26 V
|align=center bgcolor=white| +0.26
|align=center bgcolor=white| -0.16 V
|align=center bgcolor=white| -0.16
|align=center bgcolor=blue|blue
|align=center bgcolor=blue|blue
|align=center bgcolor=white|colorless
|align=center bgcolor=white|colorless
|-
|-
|[[Phenosafranin]]
|[[Phenosafranin]]
|align=center bgcolor=white| +0.28 V
|align=center bgcolor=white| +0.28
|align=center bgcolor=white| -0.25 V
|align=center bgcolor=white| -0.25
|align=center bgcolor=red|red
|align=center bgcolor=red|red
|align=center bgcolor=white|colorless
|align=center bgcolor=white|colorless
|-
|-
|[[Safranin]] '''T'''
|[[Safranin|Safranin '''T''']]
|align=center bgcolor=white| +0.24 V
|align=center bgcolor=white| +0.24
|align=center bgcolor=white| -0.29 V
|align=center bgcolor=white| -0.29
|align=center bgcolor=#E41B9E|red-violet
|align=center bgcolor=#E41B9E|red-violet
|align=center bgcolor=white|colorless
|align=center bgcolor=white|colorless
|-
|-
|[[Neutral red]]
|[[Neutral red]]
|align=center bgcolor=white| +0.24 V
|align=center bgcolor=white| +0.24
|align=center bgcolor=white| -0.33 V
|align=center bgcolor=white| -0.33
|align=center bgcolor=red|red
|align=center bgcolor=red|red
|align=center bgcolor=white|colorless
|align=center bgcolor=white|colorless
|-
|-
|}
|}



==See also==
==See also==
*[[Analytical chemistry|Chemical analysis]]
*[[pH indicator]]
*[[pH indicator]]
*[[Complexometric indicator]]
*[http://pac.iupac.org/publications/pac/pdf/1978/pdf/5005x0463.pdf Redox Indicators. Characteristics And Applications]

==References==
{{Reflist}}

==External links==
*[http://old.iupac.org/publications/pac/1978/pdf/5005x0463.pdf Redox Indicators. Characteristics And Applications]

{{DEFAULTSORT:Redox Indicator}}
{{DEFAULTSORT:Redox Indicator}}
[[Category:Redox indicators| ]]
[[Category:Redox indicators]]
[[Category:Physical chemistry]]
[[Category:Physical chemistry]]

[[it:Indicatore (chimica)#Indicatori di ossido-riduzione]]

Latest revision as of 14:59, 28 September 2023

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:

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]
  1. ^ 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.
  2. ^ HEWITT, LF. "Oxidation-Reduction Potentials in Bacteriology and Biochemistry." Oxidation-Reduction Potentials in Bacteriology and Biochemistry. Edn 6 (1950).
[edit]