ACS Catalysis
Page 10 of 12
3.
Woodward, A.; Mesrobian, R. B., Low Temperature
23.
Fillippenko, V. University of Ottawa, MSc Thesis:
1
2
3
4
5
6
7
8
Autoxidation of Hydrocarbons. The Kinetics of Tetralin
Oxidation. J. Am. Chem. Soc. 1953, 75, 6189-6195.
4.
Oxidation of Cumene (Isopropyl Benzene) in Liquid Phase. J.
Catal. 1973, 28, 236-244.
5.
an Efficient and Environmentally Friendly Solid Catalyst for
Solvent-Free Liquid-Phase Selective Oxidation of Ethylbenzene
to Acetophenone with 1 atm of Molecular Oxygen. J. Catal. 2006,
240, 268-274.
Oxygen Uptake Studies of Organic and Inorganics Oxidations,
2010.
24.
Peroxidation: Inhibiting Effects of Water Soluble Antioxidants
on Phospholipids of DIfferent Charge Types. Free Radic. Biol.
Med. 1994, 16, 779-788.
Varma, G. R.; Graydon, W. F., Heterogeneous Catalytic
Barclay, L. R. C.; Vinqvist, M. R., Membrane
Jana, S. K.; Wub, P.; Tatsumi, T., NiAl Hydrotalcite as
25.
Kharasch, M. S.; Fono, A.; Nudernberg, W., The
Chemistry of Hydroperoxide III. The Free-Radical Decomposiotn
of Hydroperoxides. J. Org. Chem. 1949, 763-774.
26.
9
Barrett, K. E.; Thomas, H. R., Kinetics of Dispersion
6.
Casemier, J. H. R.; Nieuwenhuys, B. E.; Sachlter, W. M.
Polymerization of Soluble Monomers. I. Methyl Methacrylate. J.
Polym. Sci. Pol. Chem. 1969, 7, 2621-2650.
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
H., The Oxidation of Cumene and the Decomposition of
Cumene Hydroperoxide on Silver, Copper and Platinium. J.
Catal. 1973, 29, 367-373.
27.
chemistry
Kharasch, M. S.; Fono, A.; Nuderberg, W., The
of Hydroperoxides I. The acid-catalysed
7.
Richardson, W. H., Metal Ion Decomposition of
Decomposition of alpha,alpha-Dimethylbenzyl (alpha-Cumyl)
Hydroperoxide. J. Org. Chem. 1949, 748-752.
Hydroperoxides. II. Kinetics and Mechanism of Cobalt Salt
Catalyzed Decomposition of t-Butyl Hydroperoxide. J. Am.
Chem. Soc. 1965, 87, 1096-1102.
28.
Solomon, D. H.; Murray, H. M., Acid-Base Interactions
and the Properties of Kaolinite in Non-Aqueous Media. Clays
and Clays Miner. 1972, 20, 135-141.
8.
Hereijgers, B. P. C.; Weckhuysen, P. M., Aerobic
Oxidation of Cyclohexane by Gold-Based Catalysts: New
Mechanistic Insight by Thorough Product Analysis. J. Catal.
2010, 210, 16-25.
29.
Corma, A.; Garcia, H., Supported gold nanoparticles as
catalysts for organic reactions. Chem. Soc. Rev. 2008, 37, (9),
2096-2126.
9.
Xu, Y. J.; Landon, P.; Enache, D.; Carley, A. F.; Roberts,
30.
Naya, S.-i.; Teranishi, M.; Kimurab, K.; Tada, H., A
M. W.; Hutchings, G. J., Selective Conversion of Cyclohexane to
Cyclohexanol and Cyclohexanone using a Gold Catalyst under
Mild Conditions. Cat. Lett. 2005, 101, 175-179.
strong support-effect on the catalytic activity of gold
nanoparticles for hydrogen peroxide decomposition. Chem.
Commun. 2011, 47, 3230-3232.
10.
Liu, Y.; Tsunoyama, H.; Akita, T.; Xie, S.; Tsukuda, T.,
31.
Chauvel, A.; Lefebre, G. G., Petrochemical Processes:
Aerobic Oxidation of Cyclohexane Catalyzed by Size-Controlled
Au Clusters on Hydroxyapatite: Size Effect in the Sub-2 nm
Regime. ACS Catal. 2011, 1 2-6.
Technical and Economic Characteristic. Ophrys: Paris, 1989; Vol.
2.
32.
biological molecules. 2. Autoxidation of a model membrane.
Comparison of the autoxidation of egg lecithin
Barclay, L. R. C.; Ingold, K. U., Autoxidation of
11.
Zhoua, H. J.; Luoa, H.; Zenga, C.; Lia, D.; Liu, Y.,
Synthesis, Characterization of Ag/MCM-41 and the Catalytic
Performance for Liquid-Phase Oxidation of Cyclohexane. Cat.
Lett. 2006, 108, 49-55.
12.
Industrial Chemistry. Wiley-VCH: Weinheim, Germany, 2009.
13. Van Ham, N. H. A.; Nieuwenhuys, B. E.; Sachtler, W.
M. H., The Oxidation of Cumene on Silver and Silver-Gold
Alloys. J. Catal. 1971, 20, 408-423.
14.
the Role of Metallic Copper in the Oxidation of Cumene to
Cumene Hydroperoxide J. Catal. 1976, 41, 329-332.
15.
of Cu/MgO in Liquid Oxidation of Cumene. Korean J. Chem.
Eng. 2009, 26, 1568-1573.
16.
phosphatidylcholine in water and in chlorobenzene. J. Am.
Chem. Soc. 1981, 103, (21), 6478-6485.
Centi, G.; Perathoner, S.; Trifiro, F., Sustainable
33.
Howard, J. A.; Ingold, K. U., Absolute Rate Constants
for Hydrocarbon Oxidation. XI. The Reactions of Tertiary Peroxy
Radicals. Can. J. Chem. 1968, 46, 2555-2660.
34.
Jones, A. M.; Garg, S.; He, D.; Pham, A. N.; Waite, T.
D., Superoxide-Mediated Formation and Charging of Silver
Nanoparticles. Environ. Sci. Technol. 2011, 45, 1428-1434.
Panayotava, E. N.; Dimitrov, D. I.; Petkov, A. A., On
35.
Navalon, S.; Martin, R.; Alvaro, M.; Garcia, H., Gold on
Diamond Nanoparticles as a Highly Efficient Fenton Catalyst.
Angew. Chem. Int. Ed. 2010, 49, 8403-8407.
Zu, S.; Hang, C.; Zhang, J.; Chen, B., Catalytic Activity
36.
Salukvadze, L. V.; Norikov, Y. D.; Valendo, A. Y.;
Blyumberg, E. A., The Oxidation of Cumene in the Presence of
Heterogenous Oxide Catalysts in the Liquid Phase. Russ. Chem.
Bull. 1972, 7, 1478-1482.
Lloyd, R.; Jenkins, R. L.; Piccinini, M.; He, Q.; Kiely, C.
J.; Golunski, S. E.; Bethell, D.; Bartley, J. K.; Hutchings, G. J.,
Low-temperature aerobic oxidation of decane using an oxygen-
free radical initiator. J. Catal. 2011, 283, 161-167.
37.
oxidation using gold. Chem. Soc. Rev. 2008, 37, (9), 2077-2095.
38. Maillard, B.; Ingold, K. U.; Scaiano, J. C., Rate
Della Pina, C.; Falletta, E.; Prati, L.; Rossi, M., Selective
17.
Goszner, K.; Bischof, N., The Decomposition of
Hydrogen Peroxide on Silver-Gold Alloys. J. Catal. 1974, 32, 175-
182.
18.
Garcia, H., Enhancement of the Catalytic Activity of Supported
Gold Nanoparticles for the Fenton Reaction by Light. J. Am.
Chem. Soc. 2011, 133, 2218-2226.
19.
Production. Appl. Catal. A: General 2005, 280, 89-103.
20. Mitsudome, T.; Noujima, A.; Mizugaki, T.; Jitsukawa,
Constants for the Reactions of Free Radicals with Oxygen in
Solution. J. Am. Chem. Soc. 1983, 105, 5095-5099.
Navalon, S.; de Miguel, M.; Martin, R.; Alvaro, M.;
39.
Menchon, C.; Martin, R.; Apostolova, N.; Victor, V. M.;
Alvaro, M.; Herance, J. R.; Garcia, H., Gold Nanoparticles
Supported on Nanoparticulate Ceria as a Powerful Agent against
Intracellular Oxidative Stress. Small 2012, 8, 1895-1903.
Schmidt, R. J., Industrial Catalytic Processes - Phenol
40.
Aprile, C.; Corma, A.; Domine, M. E.; Garcia, H.;
Mitchell, C., A Cascade Aerobic Epoxidation of Alkenes over
Au/CeO2 and Ti-mesoporous Material by ‘‘In Situ” Formed
Peroxides. J. Catal. 2009, 264, 44-53.
K.; Kaneda, K., Efficient Aerobic Oxidation of Alcohols using a
Hydrotalcite-Supported Gold Nanoparticle Catalyst. Adv. Synth.
Catal. 2009, 351, 1890-1896.
41.
Bar-Ziv, R.; Zilbermann, I.; Zidki, T.; Cohen, H.;
Meyerstein, D., Reactions of Alkyl Peroxyl Radicals with Metal
Nanoparticles in Aqueous Solutions. J. Phys. Chem. C. 2009, 113,
3281-3286.
21.
Mitsudome, T.; Mikami, Y.; Funai, H.; Mizugaki, T.;
Jitsukawa, K.; Kaneda, K., Supported Silver-Nanoparticle-
Catalyzed Highly Efficient Aqueous Oxidation of Phenylsilanes
to Silanols. Angew. Chem. Int. Ed. 2008, 47, 138-141.
42.
Boronat, M.; Corma, A., Molecular approaches to
catalysis: Naked gold nanoparticles as quasi-molecular catalysts
for green processes. J. Catal. 2011, 284, (2), 138-147.
22.
Howard, J. A., Advances in Free Radical Chemistry,
Volume 4. Logos Press: London, England, 1972.
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