42
2 MET-Type Bioelectrocatalysis
Table 2.2
(continued)
Compound
E°
/V versus SHE
pH
Conditions
References
chloraphine
−0.115
7
[91, 97]
indigo disulfonate
−0.116
7
*
[112]
−0.125
7
[91, 97]
−0.188
9.3
*
[113]
−0.100
7
15 °C
[108]
nile blue
−0.120
8
0.5 M phosphate
[114]
indigocarmine
−0.125
8
0.5 M phosphate
[114]
9-phenylisoalloxazine
−0.126
7
[91, 101]
2-hydroxy-1,4-naphthoquinone
−0.139
7
[91, 97]
−0.153
7.5
0.1 M phosphate
[95]
thioglycolic acid
−0.14
7
[91, 101]
2-amino-N-methylphenazine methosulfate
−0.145
7
[91, 97]
azure A
−0.153
8
0.5 M phosphate
[114]
indigo monosulfonate
−0.157
7
[91, 97]
anthraquinone-1,5-disulfonate
−0.170
7
*
[115]
alloxazine
−0.170
7
[91, 97]
brilliant alizarin blue
−0.173
7
[91, 97]
crystal violet
−0.176
7.5
15 °C
[108]
2-methyl-3-hydroxy-1,4-naphthoquinone
−0.180
7
[91, 97]
patent blue
−0.180
8
0.5 M phosphate
[114]
9-methylisoalloxazine
−0.183
7
[91, 97]
(continued)
2 MET-Type Bioelectrocatalysis
Table 2.2
(continued)
Compound
E°
/V versus SHE
pH
Conditions
References
chloraphine
−0.115
7
[91, 97]
indigo disulfonate
−0.116
7
*
[112]
−0.125
7
[91, 97]
−0.188
9.3
*
[113]
−0.100
7
15 °C
[108]
nile blue
−0.120
8
0.5 M phosphate
[114]
indigocarmine
−0.125
8
0.5 M phosphate
[114]
9-phenylisoalloxazine
−0.126
7
[91, 101]
2-hydroxy-1,4-naphthoquinone
−0.139
7
[91, 97]
−0.153
7.5
0.1 M phosphate
[95]
thioglycolic acid
−0.14
7
[91, 101]
2-amino-N-methylphenazine methosulfate
−0.145
7
[91, 97]
azure A
−0.153
8
0.5 M phosphate
[114]
indigo monosulfonate
−0.157
7
[91, 97]
anthraquinone-1,5-disulfonate
−0.170
7
*
[115]
alloxazine
−0.170
7
[91, 97]
brilliant alizarin blue
−0.173
7
[91, 97]
crystal violet
−0.176
7.5
15 °C
[108]
2-methyl-3-hydroxy-1,4-naphthoquinone
−0.180
7
[91, 97]
patent blue
−0.180
8
0.5 M phosphate
[114]
9-methylisoalloxazine
−0.183
7
[91, 97]
(continued)
