Environmentally-friendly Oxidation

In recent years, organic synthesis has improved to the points of being environmentally-friendly. Many excellent methodologies have been devised for green chemistry and environmentally-friendly manufacturing. Oxidation reactions employing atmospheric oxygen or molecular oxygen as oxidant is one of the methodologies of green chemistry. The earth is filled with air, and about 20% of air is oxygen. If oxygen could be utilized as the oxidant, this would provide a method that is not only economically prudent, but also environmentally clean. However, the oxidation capability of atmospheric oxygen and molecular oxygen is not powerful enough when used alone. Therefore, there is much active R&D underway to make improvements in the oxidation capability with the presence of transition metal complex catalysts and radical producing catalysts. For example, Markó and co-workers have reported that tetrapropylammonium perruthenate (TPAP) can be used for the oxidation of alcohols to aldehydes and ketones using molecular oxygen as the oxidant.1) Similarly, Uemura and co-workers have demonstrated that palladium(II) diacetate is also a catalyst for the same type of oxidations.2) Katsuki and co-workers reported that the oxidation method of alcohols using (nitrosyl)Ru-Salen complex as a catalyst.3) This catalyst is activated by photo-irradiation and can be used to oxidize primary alcohols to aldehydes selectively. Fukuzumi and co-workers reported that the oxygenation using 9-aromatic substituted acridinium derivatives as effective electron-transfer photocatalysts.4) Ishii and his group have reported a catalytic carbon radical formation method using N-hydroxyphthalimide (NHPI).5) In this method, the hydrogen atom of the hydroxyimino group in NHPI is pulled off by molecular oxygen, thereby producing a phthalimide N-oxyl (PINO) radical. The PINO radical then pulls hydrogen atoms from carbon-hydrogen bonds such as alkanes and alcohols to furnish the corresponding carbon radicals. The resulting carbon radicals readily react with different types of molecules, thereby producing oxygen-containing compounds such as carboxylic acids under an oxygen atmosphere.
Typical transition metal complex catalysts and carbon radical producing catalysts for oxidation using molecular oxygen are as follows.

Transition Metal Complexes

Radical Producing Catalysts

Redox Catalysts

Ligands

Transition Metal Complexes

C0373 C0373 M0042 M0042 V0016 V0016
T0746 T0746 C1944 C1944 A1424 A1424
T1559 T1559 I0079 I0079 D1997 D1997
C0373 Bis(2,4-pentanedionato)cobalt(II) Dihydrate
M0042 Bis(2,4-pentanedionato)manganese(II) Dihydrate
V0016 Bis(2,4-pentanedionato)vanadium(IV) Oxide
T0746 Bis(trifluoro-2,4-pentanedionato)cobalt(II) Hydrate
C1944 Chloronitrosyl[N,N'-bis(3,5-di-tert-butylsalicylidene)-1,1,2,2-tetramethylethylenediaminato]ruthenium(IV)
A1424 Palladium(II) Acetate
T1559 Tetrapropylammonium Perruthenate
I0079 Tris(2,4-pentanedionato)iron(III)
D1997 Tris(triphenylphosphine)ruthenium(II) Dichloride

Radical Producing Catalysts

M1775 M1775 D3428 D3428 D3429 D3429
B2897 B2897 M1774 M1774 M2072 M2072
H1036 H1036 H0395 H0395
M1775 10-Methyl-9-phenylacridinium Perchlorate
D3428 9-(2,5-Dimethylphenyl)-10-methylacridinium Perchlorate
D3429 9-(2,6-Dimethylphenyl)-10-methylacridinium Perchlorate
B2897 9-(2-Biphenylyl)-10-methylacridinium Perchlorate
M1774 9-Mesityl-10-methylacridinium Perchlorate
M2072 9-Mesityl-2,7,10-trimethylacridinium Perchlorate
H1036 N-Hydroxy-4-nitrophthalimide
H0395 N-Hydroxyphthalimide

Redox Catalysts

T1560 T1560 H0186 H0186
T1560 2,2,6,6-Tetramethylpiperidine 1-Oxyl Free Radical
H0186 Hydroquinone

Ligands

P0221 P0221 P0879 P0879 B1733 B1733
P0160 P0160 A0869 A0869 M1132 M1132
P1297 P1297 T1438 T1438 P0052 P0052
B0989 B0989 D1678 D1678 T1359 T1359
T0434 T0434 T0519 T0519
P0221 1,10-Phenanthroline Monohydrate
P0879 1,10-Phenanthroline Monohydrate
B1733 1,3-Bis(4-methoxyphenyl)-1,3-propanedione
P0160 1-Phenyl-1,3-butanedione
A0869 2-Acetylcyclopentanone
M1132 3-Methyl-2,4-pentanedione
P1297 3-Phenyl-2,4-pentanedione
T1438 5,10,15,20-Tetrakis(2,6-dichlorophenyl)porphyrin
P0052 Acetylacetone
B0989 Bathophenanthrolinedisulfonic Acid Disodium Salt Hydrate [for Determination of Ferrous Ion]
D1678 Dipivaloylmethane
T1359 Tetraphenylporphyrin (Chlorin free)
T0434 Trifluoroacetylacetone
T0519 Triphenylphosphine

Literature

1) I. E. Markó, P. R. Giles, M. Tsukazaki, I. Chellé-Regnaut, C. J. Urch, S. M. Brown, J. Am. Chem. Soc., 1997, 119, 12661 [DOI].
2) T. Nishimura, T. Onoue, K. Ohe, S. Uemura, Tetrahedron Lett., 1998, 39, 6011 [DOI].
3) A. Miyata, M. Murakami, R. Irie, T. Katsuki, Tetrahedron Lett., 2001, 42, 7067 [DOI]; T. Katsuki, TCIMAIL, 2004, number 124, 2.
4) S. Fukuzumi, H. Kotani, K. Ohkubo, S. Ogo, N. V. Tkachenko, H. Lemmetyinen, J. Am. Chem. Soc., 2004, 126, 1600 [DOI]; H. Kotani, K. Ohkubo, S. Fukuzumi, J. Am. Chem. Soc., 2004, 126, 15999 [DOI].
5) Y. Ishii, T. Iwahama, S. Sakaguchi, K. Nakayama, Y. Nishiyama, J. Org. Chem., 1996, 61, 4520 [DOI]; Y. Ishii, S. Sakaguchi, TCIMAIL, 2002, number 116, 2; Y. Ishii, Yuki Gousei Kagaku Kyokaishi (J. Synth. Org. Chem., Jpn.), 2001, 59, 2.


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