Reduction Potentials of One-Electron Couples
Tab to Data Tables
- Reduction potentials of quinones
- Reduction potentials of nitroaryl compounds
- Reduction potentials of bipyridinium and related compounds
- Reduction potentials of miscellanious organic compounds
- Reduction potentials of phenoxyl radicals
- Reduction potentials of amine, indole, pyrimidine and purine radicals
- Aminobenzenes and phenylenediamines
- Indoles (IndH)
- Pyrimidines
- Purines
- Reduction potentials of phenothiazine radicals
- Reduction potentials of radicals from miscellanious organic compounds
- Reduction potentials of inorganic couples
Data Tables
6.1. Aminobenzenes and phenylenediamines
_530. - Aniline
_531. - N,N-Dimethylaniline
_532. - o-Phenylenediamine
_533. - p-Phenylenediamine
_534. - N,N,N',N'-Tetramethyl-p-phenylenediamine
6.2. Indoles (IndH)
_535. - Indole
(R1 = R2 = R3 = R5 = H)
_536. - 5-Hydroxyindole
(R1 = R2 = R3 = H, R5 = OH)
_537. - 1-Methylindole
(R1 = CH3, R2 = R3 = R5 =H)
_538. - 2-Methylindole
(R1 = R3 = R5 = H, R2 = CH3)
_539. - 3-Methylindole
(R1 = R2 = R5 = H, R3 = CH3)
_540. - Indole-3-acetic acid
(R1 = R2 = R5 = H, R3 = CH2CO2H)
_541. - 2,3-Dimethylindole
(R1 = H, R2 = R3 = CH3, R5 = H)
_542. - Tryptamine
(R1 = R2 = R5 = H, R3 = CH2CH2NH2)
_543. - Tryptophan
(R1 = R2 = R5 = H, R3 = CH2CH(NH2)CO2H)
_544. - 5-Hydroxytryptophan
(R3 = CH2CH(NH2)CO2H, R5 = OH)
_545. - DL-Tryptophanamide
(R3 = CH2CH(NH2)CONH2)
_546. - N-Acetyl-L-tryptophan
(R3 = CH2CH(NHCOCH3)CO2H)
_547. - L-Tryptophyl-L-alanine
(R3 = CH2CH(NH2)CONHCH(CH3)CO2H)
6.3. Pyrimidines
_548. - Uracil
(R1 = R5 = H)
_549. - 1-Methyluracil
(R1 = CH3, R5 = H)
_550. - Thymine
(R1 = H, R5 = CH3)
_551. - Barbituric acid
_552. - Isobarbituric acid
_553. - Cytosine
(R1 = H)
_554. - 1-Methylcytosine
(R1 = CH3)
6.4. Purines
_556. - Adenine
(R9 = H)
_557. - Adenosine
(R9 = beta-D-ribofuranosyl,
)
_558. - Guanine
(R9 = H)
_559. - Guanosine
(R9 = beta-D-ribofuranosyl,
)
_560. - Hypoxanthine
_561. - Xanthine
_562. - Uric acid
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